This document provides a catalogue of products and services from Nanovex Biotechnologies, an innovative nanobiotechnology company. The catalogue includes various types of nanoparticles such as pronanosomes, synthetic exosomes, metallic nanoparticles including gold, silver and alloy nanoparticles, carbon dots, SPIONS, and quantum dots. It also lists services for nanoencapsulation, bioconjugation, and nanomaterial characterization. The document provides details on the different product lines including compositions, sizes, properties and applications.
This document discusses metallic nanoparticles and their applications in biomedical sciences and engineering. Metallic nanoparticles such as iron oxide nanoparticles, gold nanoparticles, and silver nanoparticles have unique properties like high surface-to-volume ratio that make them useful for applications in imaging, drug delivery, and therapy. Various methods for synthesizing these nanoparticles like chemical coprecipitation and conjugating them with ligands allow them to be used as contrast agents for MRI, CT, and other imaging modalities. Targeted delivery of nanoparticles can help image and treat diseases like cancer in a non-invasive manner.
This document summarizes the fabrication and characterization of nanowire devices. It discusses the early history of nanotechnology and how the field has progressed. Various methods for synthesizing semiconductor nanowires are described, including vapor-liquid-solid growth and electrodeposition. The document shows images of nanowires made from materials like copper, cadmium sulfide, and zinc oxide. It also discusses the unique electrical and optical properties of nanowires and their potential applications in areas such as electronics, optoelectronics, and sensing. In conclusion, the author remarks that nanowires may serve as important building blocks for next-generation electronic and optoelectronic systems by enabling new device concepts.
The document discusses developing a carbon nanotube-based drug delivery system for the anticancer drug doxorubicin. It aims to allow for controlled and targeted drug delivery while reducing side effects by loading doxorubicin onto functionalized single-walled carbon nanotubes coated with chitosan and folate ligands. The formulation would be characterized and its drug loading efficiency, release properties, and ability to target cancer cells would be evaluated.
Presentation from Andreas Hermann, Oeko-Institut, about specific project activity on the risk management measures for nanomaterials, on the "Strategic workshop on nanotechnology" in Brussels,
10th February 2015.
Nanotechnology & nanobiotechnology by kk sahuKAUSHAL SAHU
Introduction &definition
a) Nanotechnology
b) Nanobiotechnology
History
Terms related to Nanotechnology
Nanoscale technology
Some Nanoscale related terms
What are Nanosensors
How nanosensors work
DNA Nanotechnology
How Nanotechnology works in different fields
Advantages & application of Nanotechnology
Disadvantages
Conclusion
References
biomedical applications of nanofibres.pptxSudiptoBehera1
This document discusses biomedical applications of nanofiber composites. It begins by defining nanotechnology as understanding and controlling matter between 1 to 100 nanometers. Nanofibers are synthesized using various methods like electrospinning and have a wide range of biomedical applications. Specifically, nanofiber composites show promise for drug delivery, tissue engineering, cancer therapy, and wound healing. For example, drug-loaded nanofiber composites can provide sustained drug release for cancer treatment. While nanofibers demonstrate many advantages, challenges remain in large-scale production and further clinical applications.
This document discusses inorganic and organic synthesis of nanocomposites through self-assembly. It begins by defining nanocomposites and describing different types including ceramic-matrix, polymer-matrix, polymer-silicate, elastomeric, and bionanocomposites. It then discusses synthesis methods using various biomolecules as templates, such as proteins, peptides, polysaccharides, and nucleic acids. Specific examples include protein-mediated hydroxyapatite and magnetic materials formation. Peptides and polysaccharides like chitosan are also described as mediating bioinspired synthesis. Nanocomposites find applications in areas like batteries, lightweight materials, and artificial joints.
This document discusses metallic nanoparticles and their applications in biomedical sciences and engineering. Metallic nanoparticles such as iron oxide nanoparticles, gold nanoparticles, and silver nanoparticles have unique properties like high surface-to-volume ratio that make them useful for applications in imaging, drug delivery, and therapy. Various methods for synthesizing these nanoparticles like chemical coprecipitation and conjugating them with ligands allow them to be used as contrast agents for MRI, CT, and other imaging modalities. Targeted delivery of nanoparticles can help image and treat diseases like cancer in a non-invasive manner.
This document summarizes the fabrication and characterization of nanowire devices. It discusses the early history of nanotechnology and how the field has progressed. Various methods for synthesizing semiconductor nanowires are described, including vapor-liquid-solid growth and electrodeposition. The document shows images of nanowires made from materials like copper, cadmium sulfide, and zinc oxide. It also discusses the unique electrical and optical properties of nanowires and their potential applications in areas such as electronics, optoelectronics, and sensing. In conclusion, the author remarks that nanowires may serve as important building blocks for next-generation electronic and optoelectronic systems by enabling new device concepts.
The document discusses developing a carbon nanotube-based drug delivery system for the anticancer drug doxorubicin. It aims to allow for controlled and targeted drug delivery while reducing side effects by loading doxorubicin onto functionalized single-walled carbon nanotubes coated with chitosan and folate ligands. The formulation would be characterized and its drug loading efficiency, release properties, and ability to target cancer cells would be evaluated.
Presentation from Andreas Hermann, Oeko-Institut, about specific project activity on the risk management measures for nanomaterials, on the "Strategic workshop on nanotechnology" in Brussels,
10th February 2015.
Nanotechnology & nanobiotechnology by kk sahuKAUSHAL SAHU
Introduction &definition
a) Nanotechnology
b) Nanobiotechnology
History
Terms related to Nanotechnology
Nanoscale technology
Some Nanoscale related terms
What are Nanosensors
How nanosensors work
DNA Nanotechnology
How Nanotechnology works in different fields
Advantages & application of Nanotechnology
Disadvantages
Conclusion
References
biomedical applications of nanofibres.pptxSudiptoBehera1
This document discusses biomedical applications of nanofiber composites. It begins by defining nanotechnology as understanding and controlling matter between 1 to 100 nanometers. Nanofibers are synthesized using various methods like electrospinning and have a wide range of biomedical applications. Specifically, nanofiber composites show promise for drug delivery, tissue engineering, cancer therapy, and wound healing. For example, drug-loaded nanofiber composites can provide sustained drug release for cancer treatment. While nanofibers demonstrate many advantages, challenges remain in large-scale production and further clinical applications.
This document discusses inorganic and organic synthesis of nanocomposites through self-assembly. It begins by defining nanocomposites and describing different types including ceramic-matrix, polymer-matrix, polymer-silicate, elastomeric, and bionanocomposites. It then discusses synthesis methods using various biomolecules as templates, such as proteins, peptides, polysaccharides, and nucleic acids. Specific examples include protein-mediated hydroxyapatite and magnetic materials formation. Peptides and polysaccharides like chitosan are also described as mediating bioinspired synthesis. Nanocomposites find applications in areas like batteries, lightweight materials, and artificial joints.
The document discusses the use of gold nanoparticles for cancer detection and treatment. It describes how gold nanoparticles can be functionalized with antibodies to detect specific cancer types by binding to protein markers on cancer cells. Laser-activated gold nanoparticles may also be used to destroy cancer cells through localized heating. The document also mentions potential applications for targeted drug delivery and angiogenesis inhibition. Overall, the document outlines how the optical and structural properties of gold nanoparticles can be exploited for cancer diagnosis and therapy.
This document provides an overview of nanotechnology. It begins with definitions of nanotechnology as the study and manipulation of matter at the atomic scale, with a nanometer being one billionth of a meter. The document then discusses the history of nanotechnology from Richard Feynman's 1959 talk introducing the concept to modern developments like the scanning tunneling microscope. Tools and techniques used in nanotechnology like lithography and microscopes are described. Specific nanomaterials like carbon nanotubes, nanorods, and nanobots are explained. The wide applications of nanotechnology in areas like electronics, medicine, fabrics and more are outlined. The future potential of nanotechnology is also mentioned.
Bionanotechnology is an area that applies nanotechnology to biology and medicine. It uses biological materials to create nanoscale devices less than 100 nanometers in size to better understand life processes. Some examples include using nanoparticles like liposomes, dendrimers, carbon nanotubes, quantum dots and gold nanoparticles for applications in drug delivery, imaging, biosensing and gene therapy by taking advantage of their small sizes and unique properties. Bionanotechnology is a rapidly developing field that offers opportunities for new medical technologies at the nanoscale level.
This document discusses various aspects of nano drug delivery. It describes how nanoscale materials can improve drug bioavailability and minimize side effects by transporting drug molecules to targeted locations. It also discusses how nanotools have been used for medical diagnostics. Different routes of drug administration are outlined including oral, nasal, ophthalmic, parenteral, and others. Targeted drug delivery seeks to optimize a drug's effects by localizing it to the site of action. Nanoparticles can help achieve targeted delivery and enhance transdermal drug applications.
Nanotechnology has applications across many areas of national defense, including armor, sensors, weapons, vehicles, aircraft, and satellites. It can enable lightweight, strong materials for body armor and helmets. Sensors built from nanomaterials can detect chemical and biological agents. Nanotechnology may also lead to adaptive camouflage, stealth capabilities, and self-healing structures for vehicles and aircraft. While improving military capabilities, nanotechnology enables new threats like easier production of nuclear weapons and hard-to-monitor weapons. Overall the document discusses both beneficial and concerning applications of nanotechnology in national defense.
NANOPARTICLES IN CANCER DIAGNOSIS AND TREATMENTKeshav Das Sahu
This document discusses the use of nanoparticles in cancer diagnosis and treatment. It introduces several types of nanoparticles that can be used, including nanoshells, dendrimers, quantum dots, superparamagnetic nanoparticles, nanowires, nanodiamonds, and nanosponges. Nanoshells and dendrimers are highlighted as promising for targeted drug delivery. The document also discusses magnetic resonance imaging contrast agents, including both paramagnetic gadolinium agents and superparamagnetic iron oxide nanoparticles, which can enhance MRI images and improve cancer diagnosis.
Nanotechnology has potential applications for cancer detection and treatment. It involves engineering systems at the molecular scale, smaller than 100 nanometers. This small size allows nanodevices to enter cells and detect diseases. Researchers are developing nanoparticles linked to antibodies that can seek out and destroy cancer cells through heat ablation. Nanotechnology may improve cancer treatment by targeting cancer cells directly without harming healthy cells. While it offers advantages like increased detection and more effective therapies, challenges remain around toxicity, targeting specificity, and moving applications from research to human trials. Overall, nanotechnology shows promise for transforming cancer treatment if these challenges can be addressed.
This document discusses carbon nanotubes. It begins by defining carbon nanotubes as seamless cylindrical hollow fibers made of pure graphite, with diameters between 0.7-50nm. It then discusses the discovery of carbon nanotubes in the 1950s and their various types including single-walled, multi-walled, and other related structures. The document outlines the unique properties of carbon nanotubes and their applications in areas like construction materials and electronics. It concludes by listing references for further reading.
Quantum dots and application in medical sciencekeyhan *
applications of quantum dots in medicine
Pharmacy and pharmacology
Bioimaiging (in vitro labelling , in vivo imaging)
Tumor & cancer target
Pathogen and toxin detection
Photothermal therapy (PTT)
photodynamic therapy (PDT)
Targeted surgery
Immunoassay
DNA analysis
biological monitoring
drug discovery
Process design.cancer treatment using nanoparticles. pptHoang Tien
Nanoparticles show promise for improving cancer detection and treatment. They are small enough to enter cells and interact with DNA and proteins. Quantum dots and nanoshells can be used to detect cancer signatures. Nanoshells coated with cancer-targeting molecules can selectively heat and destroy cancer cells when exposed to near-infrared light, protecting healthy cells. While challenges remain around toxicity and delivery, nanoparticles may enable cheaper, less toxic cancer therapies compared to chemotherapy and improve outcomes.
Carbon nanotubes are allotropes of carbon that can be constructed as cylindrical tubes with nanometer scale diameters and millimeter lengths. They consist of graphite-like rolled graphene sheets and belong to the fullerene family of carbon structures. Carbon nanotubes exist in single-walled and multi-walled varieties and have a variety of applications due to their unique electronic, thermal, and structural properties. They show potential for use in drug delivery due to their small size and ability to penetrate cell membranes while carrying drugs. However, further research is needed to fully understand their environmental and health impacts.
This document discusses the potential applications of nanotechnology in cancer diagnosis and treatment. It begins with an overview of nanotechnology and nanomedicine. It then discusses how cancer forms and the various factors that can cause cancer like chemicals, radiation, viruses and lifestyle. The document outlines how nanotechnology can be used to more effectively deliver drugs, detect cancer at an early stage, and treat cancer through approaches like photothermal ablation using gold nanoparticles. It acknowledges challenges like ensuring nanoparticles are biocompatible and non-toxic, but envisions that human clinical trials within the next few years could demonstrate how nanotechnology allows for safer and more targeted cancer treatment.
Three key points are summarized:
1. Three-dimensional cell cultures provide a more natural environment for cells compared to traditional 2D cultures, allowing cells to behave more like they do in vivo.
2. 3D cell culture technology is used for applications like tissue engineering, drug discovery, and analysis of cell biology. It involves engineering scaffolds and growth factors to direct cell differentiation.
3. Mathematical modeling is important for understanding the complex biological and physical factors influencing 3D cell cultures, but optimization of cultures remains an ongoing area of research due to the large number of tunable parameters.
This document discusses the properties and medical applications of nanoparticles. It begins by defining nanoparticles and nanotechnology. It then discusses various methods for synthesizing nanoparticles and their unique properties at the nanoscale. The document outlines several medical applications of nanoparticles, including drug delivery, cancer treatment, surgery, and antibiotic resistance. It provides examples of how nanoparticles can be used for targeted drug delivery, photodynamic therapy, MRI contrast agents, and more. The conclusion reiterates that nanoparticles have increased surface area and novel properties that can benefit medical applications.
Biomedical Application of Magnetic NanomaterialsMahmudun Nabi
This document discusses a project to characterize magnetic nanoparticles for use in biomedical applications. The objectives are to:
1. Characterize the magnetic nanoparticles and study their AC susceptibility, size distribution, magnetic properties, and relaxation to determine parameters like magnetic moment and blocking temperature.
2. Develop a system to detect biological targets using magnetic nanoparticles and improve the system's sensitivity.
3. Validate the magnetic immunoassay technique by comparing results to conventional methods and analyzing outcomes for biological targets.
The properties of nanomaterials depend on their small size, with dimensions typically between 1 to 100 nanometers. As size decreases, the surface area to volume ratio increases, altering physical properties like melting point. Nanomaterials also exhibit unique electrical properties due to quantum confinement effects, where energy levels become discrete. Their optical, magnetic, chemical and mechanical properties also change at the nanoscale, making nanomaterials useful in applications like hydrogen storage, catalysis, and superplastic materials.
The document discusses various characterization techniques used to analyze nanomaterials. It begins by providing historical context on the origins of nanotechnology and then describes several microscopy and spectroscopy methods. Scanning electron microscopy, transmission electron microscopy, X-ray diffraction, small angle X-ray scattering, and scanning probe microscopy are some of the key techniques explained in the document.
Surface-Functionalized Nanoparticles for Controlled Drug Delivery: The effectiveness of the surface-functionalized nanoparticles, which consist of copolymers with functional molecules
Nanotechnology in diagnosis of diseases (diabetes and coronary heart diseases)TamannaAntil1
Nanotechnology shows promise for improving diabetes and heart disease diagnosis and monitoring. For diabetes, injectable nanosensors could continuously monitor glucose levels without fingerpricks. Researchers are developing nanoparticles to monitor insulin production in real-time. Implantable glucose sensors use fluorescent nanoparticles responsive to glucose binding. For heart disease, nanoparticles can serve as contrast agents to detect inflammation and unstable plaque via MRI or CT. Superparamagnetic iron oxide nanoparticles are taken up by macrophages to identify inflammation. Novel nanoparticles can specifically target calcium in plaque to identify rupture-prone blockages.
Nanosensors are tiny sensors measuring just 10-100 nanometers that can detect the presence of nanomaterials or molecules. They have a wide range of applications including in food to detect pathogens, toxins, and monitor quality. Some examples mentioned are nanosensors to detect E. coli or Salmonella in food, and smart labels using nanosensors to provide information to consumers. Nanosensors embedded in food packaging can also monitor food quality throughout the supply chain. Overall, nanosensors show promise for enhancing food safety, quality control and providing consumers important information.
Nano silver technology involves creating silver particles that are approximately 25nm in size. These silver nanoparticles have powerful antibacterial properties and can be used in a variety of applications like water treatment, healthcare products, fabrics, and more. The technology allows for more effective and widespread use of silver's antimicrobial effects compared to bulk silver due to the nanoparticles' large surface area. Some benefits of nano silver include its ability to kill bacteria, fungi, viruses, and odors. It is being researched for uses like treating contaminated food and water and developing antimicrobial fabrics and coatings.
The document discusses the use of gold nanoparticles for cancer detection and treatment. It describes how gold nanoparticles can be functionalized with antibodies to detect specific cancer types by binding to protein markers on cancer cells. Laser-activated gold nanoparticles may also be used to destroy cancer cells through localized heating. The document also mentions potential applications for targeted drug delivery and angiogenesis inhibition. Overall, the document outlines how the optical and structural properties of gold nanoparticles can be exploited for cancer diagnosis and therapy.
This document provides an overview of nanotechnology. It begins with definitions of nanotechnology as the study and manipulation of matter at the atomic scale, with a nanometer being one billionth of a meter. The document then discusses the history of nanotechnology from Richard Feynman's 1959 talk introducing the concept to modern developments like the scanning tunneling microscope. Tools and techniques used in nanotechnology like lithography and microscopes are described. Specific nanomaterials like carbon nanotubes, nanorods, and nanobots are explained. The wide applications of nanotechnology in areas like electronics, medicine, fabrics and more are outlined. The future potential of nanotechnology is also mentioned.
Bionanotechnology is an area that applies nanotechnology to biology and medicine. It uses biological materials to create nanoscale devices less than 100 nanometers in size to better understand life processes. Some examples include using nanoparticles like liposomes, dendrimers, carbon nanotubes, quantum dots and gold nanoparticles for applications in drug delivery, imaging, biosensing and gene therapy by taking advantage of their small sizes and unique properties. Bionanotechnology is a rapidly developing field that offers opportunities for new medical technologies at the nanoscale level.
This document discusses various aspects of nano drug delivery. It describes how nanoscale materials can improve drug bioavailability and minimize side effects by transporting drug molecules to targeted locations. It also discusses how nanotools have been used for medical diagnostics. Different routes of drug administration are outlined including oral, nasal, ophthalmic, parenteral, and others. Targeted drug delivery seeks to optimize a drug's effects by localizing it to the site of action. Nanoparticles can help achieve targeted delivery and enhance transdermal drug applications.
Nanotechnology has applications across many areas of national defense, including armor, sensors, weapons, vehicles, aircraft, and satellites. It can enable lightweight, strong materials for body armor and helmets. Sensors built from nanomaterials can detect chemical and biological agents. Nanotechnology may also lead to adaptive camouflage, stealth capabilities, and self-healing structures for vehicles and aircraft. While improving military capabilities, nanotechnology enables new threats like easier production of nuclear weapons and hard-to-monitor weapons. Overall the document discusses both beneficial and concerning applications of nanotechnology in national defense.
NANOPARTICLES IN CANCER DIAGNOSIS AND TREATMENTKeshav Das Sahu
This document discusses the use of nanoparticles in cancer diagnosis and treatment. It introduces several types of nanoparticles that can be used, including nanoshells, dendrimers, quantum dots, superparamagnetic nanoparticles, nanowires, nanodiamonds, and nanosponges. Nanoshells and dendrimers are highlighted as promising for targeted drug delivery. The document also discusses magnetic resonance imaging contrast agents, including both paramagnetic gadolinium agents and superparamagnetic iron oxide nanoparticles, which can enhance MRI images and improve cancer diagnosis.
Nanotechnology has potential applications for cancer detection and treatment. It involves engineering systems at the molecular scale, smaller than 100 nanometers. This small size allows nanodevices to enter cells and detect diseases. Researchers are developing nanoparticles linked to antibodies that can seek out and destroy cancer cells through heat ablation. Nanotechnology may improve cancer treatment by targeting cancer cells directly without harming healthy cells. While it offers advantages like increased detection and more effective therapies, challenges remain around toxicity, targeting specificity, and moving applications from research to human trials. Overall, nanotechnology shows promise for transforming cancer treatment if these challenges can be addressed.
This document discusses carbon nanotubes. It begins by defining carbon nanotubes as seamless cylindrical hollow fibers made of pure graphite, with diameters between 0.7-50nm. It then discusses the discovery of carbon nanotubes in the 1950s and their various types including single-walled, multi-walled, and other related structures. The document outlines the unique properties of carbon nanotubes and their applications in areas like construction materials and electronics. It concludes by listing references for further reading.
Quantum dots and application in medical sciencekeyhan *
applications of quantum dots in medicine
Pharmacy and pharmacology
Bioimaiging (in vitro labelling , in vivo imaging)
Tumor & cancer target
Pathogen and toxin detection
Photothermal therapy (PTT)
photodynamic therapy (PDT)
Targeted surgery
Immunoassay
DNA analysis
biological monitoring
drug discovery
Process design.cancer treatment using nanoparticles. pptHoang Tien
Nanoparticles show promise for improving cancer detection and treatment. They are small enough to enter cells and interact with DNA and proteins. Quantum dots and nanoshells can be used to detect cancer signatures. Nanoshells coated with cancer-targeting molecules can selectively heat and destroy cancer cells when exposed to near-infrared light, protecting healthy cells. While challenges remain around toxicity and delivery, nanoparticles may enable cheaper, less toxic cancer therapies compared to chemotherapy and improve outcomes.
Carbon nanotubes are allotropes of carbon that can be constructed as cylindrical tubes with nanometer scale diameters and millimeter lengths. They consist of graphite-like rolled graphene sheets and belong to the fullerene family of carbon structures. Carbon nanotubes exist in single-walled and multi-walled varieties and have a variety of applications due to their unique electronic, thermal, and structural properties. They show potential for use in drug delivery due to their small size and ability to penetrate cell membranes while carrying drugs. However, further research is needed to fully understand their environmental and health impacts.
This document discusses the potential applications of nanotechnology in cancer diagnosis and treatment. It begins with an overview of nanotechnology and nanomedicine. It then discusses how cancer forms and the various factors that can cause cancer like chemicals, radiation, viruses and lifestyle. The document outlines how nanotechnology can be used to more effectively deliver drugs, detect cancer at an early stage, and treat cancer through approaches like photothermal ablation using gold nanoparticles. It acknowledges challenges like ensuring nanoparticles are biocompatible and non-toxic, but envisions that human clinical trials within the next few years could demonstrate how nanotechnology allows for safer and more targeted cancer treatment.
Three key points are summarized:
1. Three-dimensional cell cultures provide a more natural environment for cells compared to traditional 2D cultures, allowing cells to behave more like they do in vivo.
2. 3D cell culture technology is used for applications like tissue engineering, drug discovery, and analysis of cell biology. It involves engineering scaffolds and growth factors to direct cell differentiation.
3. Mathematical modeling is important for understanding the complex biological and physical factors influencing 3D cell cultures, but optimization of cultures remains an ongoing area of research due to the large number of tunable parameters.
This document discusses the properties and medical applications of nanoparticles. It begins by defining nanoparticles and nanotechnology. It then discusses various methods for synthesizing nanoparticles and their unique properties at the nanoscale. The document outlines several medical applications of nanoparticles, including drug delivery, cancer treatment, surgery, and antibiotic resistance. It provides examples of how nanoparticles can be used for targeted drug delivery, photodynamic therapy, MRI contrast agents, and more. The conclusion reiterates that nanoparticles have increased surface area and novel properties that can benefit medical applications.
Biomedical Application of Magnetic NanomaterialsMahmudun Nabi
This document discusses a project to characterize magnetic nanoparticles for use in biomedical applications. The objectives are to:
1. Characterize the magnetic nanoparticles and study their AC susceptibility, size distribution, magnetic properties, and relaxation to determine parameters like magnetic moment and blocking temperature.
2. Develop a system to detect biological targets using magnetic nanoparticles and improve the system's sensitivity.
3. Validate the magnetic immunoassay technique by comparing results to conventional methods and analyzing outcomes for biological targets.
The properties of nanomaterials depend on their small size, with dimensions typically between 1 to 100 nanometers. As size decreases, the surface area to volume ratio increases, altering physical properties like melting point. Nanomaterials also exhibit unique electrical properties due to quantum confinement effects, where energy levels become discrete. Their optical, magnetic, chemical and mechanical properties also change at the nanoscale, making nanomaterials useful in applications like hydrogen storage, catalysis, and superplastic materials.
The document discusses various characterization techniques used to analyze nanomaterials. It begins by providing historical context on the origins of nanotechnology and then describes several microscopy and spectroscopy methods. Scanning electron microscopy, transmission electron microscopy, X-ray diffraction, small angle X-ray scattering, and scanning probe microscopy are some of the key techniques explained in the document.
Surface-Functionalized Nanoparticles for Controlled Drug Delivery: The effectiveness of the surface-functionalized nanoparticles, which consist of copolymers with functional molecules
Nanotechnology in diagnosis of diseases (diabetes and coronary heart diseases)TamannaAntil1
Nanotechnology shows promise for improving diabetes and heart disease diagnosis and monitoring. For diabetes, injectable nanosensors could continuously monitor glucose levels without fingerpricks. Researchers are developing nanoparticles to monitor insulin production in real-time. Implantable glucose sensors use fluorescent nanoparticles responsive to glucose binding. For heart disease, nanoparticles can serve as contrast agents to detect inflammation and unstable plaque via MRI or CT. Superparamagnetic iron oxide nanoparticles are taken up by macrophages to identify inflammation. Novel nanoparticles can specifically target calcium in plaque to identify rupture-prone blockages.
Nanosensors are tiny sensors measuring just 10-100 nanometers that can detect the presence of nanomaterials or molecules. They have a wide range of applications including in food to detect pathogens, toxins, and monitor quality. Some examples mentioned are nanosensors to detect E. coli or Salmonella in food, and smart labels using nanosensors to provide information to consumers. Nanosensors embedded in food packaging can also monitor food quality throughout the supply chain. Overall, nanosensors show promise for enhancing food safety, quality control and providing consumers important information.
Nano silver technology involves creating silver particles that are approximately 25nm in size. These silver nanoparticles have powerful antibacterial properties and can be used in a variety of applications like water treatment, healthcare products, fabrics, and more. The technology allows for more effective and widespread use of silver's antimicrobial effects compared to bulk silver due to the nanoparticles' large surface area. Some benefits of nano silver include its ability to kill bacteria, fungi, viruses, and odors. It is being researched for uses like treating contaminated food and water and developing antimicrobial fabrics and coatings.
A protocol was selected and optimized using design of experiments to produce gold nanostar particles that meet all essential parameters. Six batches of nanostar particles were then manufactured at various scales from 500ml to 5l, and all batches were characterized. Analysis found that gold nanostars can be manufactured at different volumes and have potential applications as plasmonic sensors, theranostics, and providing a blue test line in lateral flow immunoassays. Nanostars were shown to have stronger Raman scattering than nanospheres using surface enhanced Raman spectroscopy.
This document is a product catalogue from Nanoshel LLC, a nanotechnology company, that summarizes their various nanomaterials and applications. It introduces nanoscience and how materials behave differently at the nanoscale, providing opportunities in many industries including medicine, consumer goods, energy, environment, and more. The catalogue then provides details on their nanomaterials and products for applications such as diagnostics, drug delivery, tissue engineering, water treatment, energy storage, and others. It emphasizes how nanotechnology can provide benefits such as faster medical diagnostics, targeted drug delivery, and tissue regeneration.
We are an ISO 9001:2008 Certified Company established in 2009 manufactures high quality plastic labware with excellent service levels through proper accreditation and certification. We make superior quality laboratory plasticwares of International standard using virgin production material under stringent quality control conditions. Our product range has been segregated in seven different sub-categories that include Centrifuge Ware, Liquid Handling Consumables, Cryo Ware, Multipuprpose Racks & Boxes, General Laboratory Products, Microscopy Family and Organizers. New products across all sub categories that include Microscopy products, Racked & Refill Pipette tips, unique range of rotator and multi-combination racks together with high quality Cryogenic Vials.
Our product range find place in all kind of laboratories located worldwide. They are further extensively used in below categories:
Universities
Research Institutes
Environmental testing labs (sampling)
Clinical Research Labs
Clinical Diagnostic Labs
Forensic Science Labs
Public Health Labs
Bio repositories (Especially Specimen containers)
Micro Biology Labs
Biotechnology Labs
Life Science Labs
Stem Cell Research
Hospital & Diagnostic centres
Industrial Labs
A. Pharmaceuticals
B. Food Beverage (Quality, R&D, Manufacturing process labs)
C. Chemical Petroleum processEnvironment and Process Control IndustriesSchool & College Labs.
To know more visit our website www.abdoslabware.com
This document summarizes the services offered by nanoimmunotech, a European nanobiotechnology company. It offers exclusive characterization services for nanomaterials to optimize their performance for biotechnological applications. It has qualified staff, state-of-the-art labs, and standardized testing protocols. Nanoimmunotech also provides consultancy and validation for nanosystem design and production as well as biosensor design using its proprietary technologies.
Nanosensors are tiny sensors measuring at the nanoscale level between 10-100 nanometers. They can detect the presence of nanomaterials or molecules of similar size or smaller. Some examples of nanosensors discussed include biological nanosensors that can detect pathogens, chemicals, or physical properties like pressure or force at the nanoscale. Potential applications mentioned include using nanosensors to detect chemicals in pollution monitoring, for medical diagnostics, in smart food packaging to monitor food quality, and to better understand plant and brain functions. Future nanosensors may be able to more precisely identify cells in the body or macroscopic changes to communicate with other nanodevices.
This document discusses nanomedicine and its potential applications for diagnosis and treatment of diseases like Alzheimer's disease. It begins by explaining how nanotechnology allows analysis and repair of the body at the molecular level similarly to how machines are repaired today. It then discusses various nanoscale structures and materials that can be used for nanomedicine, such as liposomes, dendrimers, mesoporous silica, quantum dots, carbon nanotubes, and polymers. Examples are given of current nanomedicine products and applications being researched include drug delivery, imaging, and regenerative medicine. However, challenges are also noted around manufacturing nanoparticles for medical use, assessing their toxicity, ensuring targeted delivery, and removing nanoparticles from the body
The document discusses the synthesis of nanoparticles using microorganisms such as bacteria and fungi. It describes intracellular and extracellular synthesis methods. Intracellular synthesis involves accumulation of nanoparticles inside the cell, while extracellular synthesis uses cell secretions outside the cell. Specific examples provided include gold and silver nanoparticles synthesized using bacteria and fungi through reduction of metal ions. The nanoparticles have a variety of shapes and sizes in the 1-100 nm range and potential applications.
Revolution of Nanotechnology:
Theory and Application
2016
Dr. nat.Sci. Ahmed Abdel-Megeed
Ph.D Germany, Hamburg University
Associate Professor, Plant Protection Dept.
Faculty of ِِِAgriculture- Alexandria University
Alexandria, Egypt
P.O. BOX 21531
Homepage: http://faculty.ksu.edu.sa/75164/default.aspx
Application of nanotechnology in reference to pest managementJyoti Prakash Sahoo
Biotechnology is the application of technological innovation as it pertains to biological and life sciences.
Nanotechnology is the art and science of manipulating matter at nanoscale.
The design, characterization, production and application of structure, device and system by controlling shape and size at nanoscale. (British standard institution, 2005)
Nanotechnology uses structures sized between 1 to 100 nanometers in at least one dimension to deliver drugs. Common nanocarriers discussed include liposomes, solid lipid nanoparticles, nanostructured lipid carriers, quantum dots, nanoshells, fullerenes, carbon nanotubes, dendrimers, and potential future nanorobots. Nanocarriers can provide targeted drug delivery to specific sites, control drug release over time, and reduce side effects by limiting drug exposure to healthy tissues. Several nanomedicines are currently approved or in clinical trials using these carriers to treat cancer and other diseases.
NANOTECHNOLOGY comprises technological developments on the nanometer scale, usually 0.1 to 100 nm. Nanotechnology, the science of the small. Nano is Greek for dwarf, and nanoscience deals with the study of molecular and atomic particles.
This document discusses nanoparticulate drug delivery systems. It begins by defining nanotechnology and describing some applications in pharmaceuticals including nanoparticles, nanosuspensions, nanospheres, nanocapsules, and nanoemulsions. It then provides a brief history of using nanoparticles for drug delivery and defines different types of nanoparticles. The rest of the document discusses various types of nanoparticles in more detail, methods for their preparation, advantages of nanosizing drugs, and some limitations.
Synthesis of Silver Nano Particles from Marine Bacteria Pseudomonas aerogenosaKamalpreet Sarna
This document summarizes a study that isolated a marine bacterial strain called Pseudomonas aeruginosa and used it to synthesize silver nanoparticles. The silver nanoparticles were characterized using UV-Vis spectroscopy, SEM, FTIR, and XRD. UV-Vis analysis showed a peak at 420nm indicating the presence of silver nanoparticles. SEM images showed the nanoparticles were spherical in shape with sizes ranging from 50-80nm. FTIR and XRD further confirmed the presence of silver. The silver nanoparticles showed potent antibacterial activity against both gram-positive and gram-negative bacteria as well as antifungal activity. This study demonstrates the potential of using marine bacteria as a green synthesis method for producing silver nanoparticles with biological applications.
This document discusses several instruments and techniques used in microbiology laboratories, including:
1. The Polystainer 5300, an automated system that can stain up to 20 slides in 5-10 minutes to aid rapid diagnosis.
2. The BACTEC 9240, an automated blood culture system that can detect bacteria in blood samples within days using sensors to detect changes in oxygen and carbon dioxide levels in culture vials.
3. The Vitek 2, an automated system that uses test cards containing 64 wells with metabolic substrates to identify microbes based on their reactions over 24-48 hours.
Rosh Electroptics Ltd. is an Israeli company established in 1983 that distributes and markets electro-optics products from various global manufacturers. It carries a wide range of optical components, lasers, fibers, and precision equipment and provides custom optics. The document lists many electro-optics products and manufacturers that Rosh Electroptics represents and distributes in Israel.
Lateral flow assays using polymer microspheres have become a useful diagnostic tool for point-of-care testing due to their simplicity, low cost, and not requiring specialized equipment or training. Most lateral flow assays rely on nitrocellulose membranes and use gold particles or dyed polystyrene microspheres to capture analytes. Sensitivity can be improved by using larger or more intensely dyed microspheres. New types of fluorescent and superparamagnetic microspheres have potential to develop more sensitive lateral flow assays and quantitative readings.
This document summarizes a study that evaluated the toxicity of three engineered nanomaterials (ENMs) - silicon (Si) nanoparticles, and carbon-coated silicon carbide (SiΩC99) nanoparticles of 40nm and 75nm size - using a high throughput screening approach on marine mussel (Mytilus edulis) hemocytes. The study found that the 75nm SiΩC99 nanoparticles were generally more toxic than the 40nm SiΩC99 or 40nm Si nanoparticles, as evidenced by their effects on various biomarkers like oxidative stress, DNA damage, membrane transport, immune response and detoxification. The results indicate that both size and carbon coating influence the toxicity profile of the ENMs, with
Similar to Catalogue nanovex biotechnologies 2019 (20)
TOPIC OF DISCUSSION: CENTRIFUGATION SLIDESHARE.pptxshubhijain836
Centrifugation is a powerful technique used in laboratories to separate components of a heterogeneous mixture based on their density. This process utilizes centrifugal force to rapidly spin samples, causing denser particles to migrate outward more quickly than lighter ones. As a result, distinct layers form within the sample tube, allowing for easy isolation and purification of target substances.
Presentation of our paper, "Towards Quantitative Evaluation of Explainable AI Methods for Deepfake Detection", by K. Tsigos, E. Apostolidis, S. Baxevanakis, S. Papadopoulos, V. Mezaris. Presented at the ACM Int. Workshop on Multimedia AI against Disinformation (MAD’24) of the ACM Int. Conf. on Multimedia Retrieval (ICMR’24), Thailand, June 2024. https://doi.org/10.1145/3643491.3660292 https://arxiv.org/abs/2404.18649
Software available at https://github.com/IDT-ITI/XAI-Deepfakes
Candidate young stellar objects in the S-cluster: Kinematic analysis of a sub...Sérgio Sacani
Context. The observation of several L-band emission sources in the S cluster has led to a rich discussion of their nature. However, a definitive answer to the classification of the dusty objects requires an explanation for the detection of compact Doppler-shifted Brγ emission. The ionized hydrogen in combination with the observation of mid-infrared L-band continuum emission suggests that most of these sources are embedded in a dusty envelope. These embedded sources are part of the S-cluster, and their relationship to the S-stars is still under debate. To date, the question of the origin of these two populations has been vague, although all explanations favor migration processes for the individual cluster members. Aims. This work revisits the S-cluster and its dusty members orbiting the supermassive black hole SgrA* on bound Keplerian orbits from a kinematic perspective. The aim is to explore the Keplerian parameters for patterns that might imply a nonrandom distribution of the sample. Additionally, various analytical aspects are considered to address the nature of the dusty sources. Methods. Based on the photometric analysis, we estimated the individual H−K and K−L colors for the source sample and compared the results to known cluster members. The classification revealed a noticeable contrast between the S-stars and the dusty sources. To fit the flux-density distribution, we utilized the radiative transfer code HYPERION and implemented a young stellar object Class I model. We obtained the position angle from the Keplerian fit results; additionally, we analyzed the distribution of the inclinations and the longitudes of the ascending node. Results. The colors of the dusty sources suggest a stellar nature consistent with the spectral energy distribution in the near and midinfrared domains. Furthermore, the evaporation timescales of dusty and gaseous clumps in the vicinity of SgrA* are much shorter ( 2yr) than the epochs covered by the observations (≈15yr). In addition to the strong evidence for the stellar classification of the D-sources, we also find a clear disk-like pattern following the arrangements of S-stars proposed in the literature. Furthermore, we find a global intrinsic inclination for all dusty sources of 60 ± 20◦, implying a common formation process. Conclusions. The pattern of the dusty sources manifested in the distribution of the position angles, inclinations, and longitudes of the ascending node strongly suggests two different scenarios: the main-sequence stars and the dusty stellar S-cluster sources share a common formation history or migrated with a similar formation channel in the vicinity of SgrA*. Alternatively, the gravitational influence of SgrA* in combination with a massive perturber, such as a putative intermediate mass black hole in the IRS 13 cluster, forces the dusty objects and S-stars to follow a particular orbital arrangement. Key words. stars: black holes– stars: formation– Galaxy: center– galaxies: star formation
This presentation offers a general idea of the structure of seed, seed production, management of seeds and its allied technologies. It also offers the concept of gene erosion and the practices used to control it. Nursery and gardening have been widely explored along with their importance in the related domain.
JAMES WEBB STUDY THE MASSIVE BLACK HOLE SEEDSSérgio Sacani
The pathway(s) to seeding the massive black holes (MBHs) that exist at the heart of galaxies in the present and distant Universe remains an unsolved problem. Here we categorise, describe and quantitatively discuss the formation pathways of both light and heavy seeds. We emphasise that the most recent computational models suggest that rather than a bimodal-like mass spectrum between light and heavy seeds with light at one end and heavy at the other that instead a continuum exists. Light seeds being more ubiquitous and the heavier seeds becoming less and less abundant due the rarer environmental conditions required for their formation. We therefore examine the different mechanisms that give rise to different seed mass spectrums. We show how and why the mechanisms that produce the heaviest seeds are also among the rarest events in the Universe and are hence extremely unlikely to be the seeds for the vast majority of the MBH population. We quantify, within the limits of the current large uncertainties in the seeding processes, the expected number densities of the seed mass spectrum. We argue that light seeds must be at least 103 to 105 times more numerous than heavy seeds to explain the MBH population as a whole. Based on our current understanding of the seed population this makes heavy seeds (Mseed > 103 M⊙) a significantly more likely pathway given that heavy seeds have an abundance pattern than is close to and likely in excess of 10−4 compared to light seeds. Finally, we examine the current state-of-the-art in numerical calculations and recent observations and plot a path forward for near-future advances in both domains.
3. Nanovex Biotechnologies is an innovative technology
based spin-off founded in 2014 that provides a wide
range of products and services in the nanobiotechnology
field.
Our specialized team has great experience in the design,
development, modification, functionalization and
characterization of nanovesicles and metallic
nanoparticles for multiple applications.
6. PRONANOSOME SERIES
Nanovesicles are closed bilayer structures able to entrap a wide range of
compounds providing several advantages such as: encapsulated compound
protection, increased bioavailability, controlled delivery, target delivery, great
stability and masking undesired tastes, among others.
Pronanosomes are ready-to-use formulations to obtain nanovesicles which are able
to encapsulate different compounds (Hydrophilic and lipophilic molecules, peptides,
proteins,...) in a fast and simple way:
Size and distribution can be reduced by using vortex or homogenizer. Small Unilamellar
Vesicles (SUV) with smaller sizes and narrower distributions are obtained after sonication of
the product.
Applications
Medicine
•Infectious diseases
•Cancer therapy
•Gene therapy
•Vaccination
•Parasitic diseases
•Macrophage activation
•Others
Food
•Functional foods
•Superfoods
•Dairy products
•Others
•Biotechnology
•Diagnostics
•Cosmetics
•Bioengineering
•New pharma
products
•Transfection
Others
1-LOAD 2-SHAKE READY
1. Load
2. Shake
3. Nanovesicles are ready to use
PRONANOSOME SERIES
7. Easy and fastSize controlTargeted
delivery
ADVANTAGES
Great
stability
November
Masking
undesired tastes
PRONANOSOME SERIESPRONANOSOME SERIES
8. PRONANOSOME LIPO-CAT
Cationic liposomes
- Positive Z-potential
- Intracellular release
PRONANOSOME pH
Sensitive to pH
- Controlled release with
pH
PRONANOSOME NIO-N
Niosomes
- Stability
- Versatile
PRONANOSOME LIPO-N
Liposomes
- Natural products
PRONANOSOME NIO-CAT
Cationic niosomes
- Positive Z-potential
- Intracellular release
PRONANOSOME-DERMAL
Dermal delivery
- Improve (trans)dermal
delivery
PRONANOSOME-BBB
Blood Brain Barrier
transcytosis
- Improve brain delivery
PRONANOSOME
THERMO
Thermosensitive
- Controlled released
with T
INTRACELLULAR DELIVERY PRONANOSOMES
CONTROLLED DELIVERY PRONANOSOMES
SPECIFIC APPLICATIONS PRONANOSOMES
Our standard Pronanosomes are formulated to obtain niosomes or liposomes able to
encapsulate different compounds and to be used in multiple applications
Our intracellular delivery Pronanosomes are formulated to obtain niosomes or liposomes
able to deliver the encapsulated drug intracellularly
Our controlled delivery Pronanosomes are formulated to obtain nanovesicles able to
control the delivery of the encapsulated drug with the temperature or pH.
Our Pronanosomes BBB and dermal are formulated to obtain nanovesicles able to
vehiculate compounds through the BBB or through the skin, respectively.
STANDARD PRONANOSOMES
PRONANOSOME SERIES
9. PRONANOSOME SERIES
BIOCONJUGABLE
All nanovesicles
Readyto be
bioconjugated
FLUORESCENT
All nanovesicles
Fluorescent labeled
nanovesicles
PEGYLATED
All nanovesicles
PEGylated
nanovesicles
FOLIC ACID
All nanovesicles
Ready to be
PEGylated
All our Pronanosomes can be
ordered with other extra
characteristics shown above
(From 1 to 4 simultaneously) to
suit the needs of our customers
10. PRONANOSOME – HOW TO USE?
THE COMPOUND TO
ENCAPSULATEIS…
WATERINSOLUBLE
COMPOUND
WATERSOLUBLE
COMPOUND
THERMOSENSITIVE
COMPOUND?
Add to Pronanosome the
compound solved in
buffer/water
TYPE OF
NANOVESICLE
Shake vigorously
for 2 minutes at
60º C
Shake vigorously
for 2 minutes and
sonicate (both
processes at 60ª C
TYPE OF
NANOVESICLE
MLV SUV
Hydrate Pronanosome
product at 60ºC for 20
min using the aqueous
solution containing the
compound
Hydrate Pronanosome
product at 4ºC overnight
usingthe aqueous
solution containing the
compound
Add to Pronanosome
the compound directly
and then add
water/buffer
Add to Pronanosome
the compound solved
in ethanol and then
add water/buffer. Max.
ethanol conc. 20% (v/v)
Add to Pronanosome
the compound solved
in an organic solvent.
Remove solvent and
then add water/buffer.
YESNO
Shake vigorously
for 2 minutes at
the highest
possible
temperature
Shake vigorously
for 2 minutes and
sonicate at the
highest possible
temperature
MLV SUV
Small Unilamellar Vesicles (SUV)MultiLamellar Vesicles (MLV)
Lipid bilayer
Aqueous compartment
Lipid bilayer
Aqueous compartment
• High encapsulation efficiency
• Heterogeneous size
• Easy to obtain
• Cleared rapidly by the reticulo-
endothelial system (RES)
• High Lipid/Water ratio
• Relatively easy access to the cells of
tissue
• Homogeneous size
• Low encapsulation efficiency in
aqueous phase
Characteristics Characteristics
PRONANOSOME SERIES
12. SYNTHETIC EXOSOMES
Synthetic exosomes are a very interesting
tool to use as a standard in different
applications such as the validation of
exosome isolation tools or detection
systems, among others.
SINEX-CD9
CD9 Synthetic exosomes based on liposomes with
a composition similar to that of natural exosomes.
Fully characterized. Available with green or red
fluorescence.
CD9
CD63
SINEX-CD63
CD63 Synthetic exosomes based on liposomes
with a composition similar to that of natural
exosomes. Fully characterized. Available with
green or red fluorescence.
CD81
SINEX-CD81
CD81 Synthetic exosomes based on liposomes
with a composition similar to that of natural
exosomes. Fully characterized. Available with
green or red fluorescence.
15. As gold nanoparticles properties are
size and shape dependant, Nanovex
Biotechnologies guarantee the quality
of the supplied nanoparticles
providing its customers detailed
information of each batch.
Nanovex Gold nanoparticles have an excellent QUALITY:
•Narrow size distribution (typical CV values ≤ 15%).
•Batch-to-batch consistency (typical CV values ≤ 10%).
•Full characterization data with all products.
•Product Quality Guarantee.
•Support and service from our nanomaterials experts.
VERSATILITY: Gold nanoparticles can be used in a wide range of applications
Application Size (nm) Surface Functionalization
Protein conjugation 15-100 Citrate, streptavidine, COOH
Modification with thiolated ligands 15-100 Citrate
Western blot/ dot blot 15 Streptavidine
Inmunohistochemistry 15-40 Streptavidine
Flow cytometry 50-100 Citrate
Celular uptake 30-60 Citrate
Lateral flow immunoassays 30-80 Citrate, streptavidine, COOH
ELISA 15-30 Streptavidine
Microscopy 50-100 Streptavidine
GOLD NANOPARTICLES
16. 20 nm 30 nm 50 nm
Nanovex Biotechnologies offers SPHERICAL silver nanoparticles which are tannic acid
capped.
Our silver nanoparticles are available in different sizes: 20, 30 and 50 nm.
UV-Vis spectra showing optical properties of silver nanoparticles of different sizes.
DLS spectra showing different sizes of silver nanoparticles.
SILVER NANOPARTICLES
17. Nanovex Silver nanoparticles have an excellent QUALITY:
•Narrow size distribution .
•Batch-to-batch consistency.
•Full characterization data with all products.
•Product Quality Guarantee.
•Support and service from our nanomaterials experts.
As silver nanoparticles properties are
size and shape dependant, Nanovex
Biotechnologies guarantee the quality
of the supplied nanoparticles
providing its customers detailed
information of each batch.
VERSATILITY: Silver nanoparticles can be used in a wide range of applications
Applications
Protein conjugation
Modification with thiolated ligands
Western blot/ dot blot
Molecular Imaging
Nanotoxicology
Antibacterial
Lateral flow immunoassays
ELISA
SERS
SILVER NANOPARTICLES
18. 100 % Ag 100 % Au
Nanovex Biotechnologies gold/silver alloy nanoparticles are synthesized through citrate
reduction method in absence of additional stabilizing agents.
Au0:Ag100 Au20:Ag80
Transmission electron microscopyimages of Nanovex gold/silver alloy
nanoparticles of distinct composition.
Au50:Ag50 Au100:Ag00
Au0:Ag100 Au20:Ag80
Transmission electron microscopyimages of Nanovex gold/silver alloy
nanoparticles of distinct composition.
Au50:Ag50 Au100:Ag00
The optoelectronic properties of these alloyed nanoparticles are tunable varying the
nanoparticle composition in stead of varying nanoparticle size.
The optoelectronic properties of these alloyed nanoparticles differ from pure gold or silver
nanoparticles of the same size.
0,0
0,1
0,2
0,3
0,4
0,5
0,6
0,7
0,8
0,9
1,0
350 400 450 500 550 600 650 700
Abs
Wavelength (nm)
Au0:Ag100
Au20:Ag80
Au50:Ag50
Au80:Ag20
Au100:Ag0
40 nm
GOLD/SILVER ALLOY
NANOPARTICLES
19. Our gold/silver nanoparticle are also a alternative in the development of nanomaterial
bioconjugates, electrocatalityc applications or biosensing with multiplexed detection.
0.0E+00
2.0E+07
4.0E+07
6.0E+07
8.0E+07
1.0E+08
1.2E+08
1.4E+08
1.6E+08
0 200 400 600 800 1000
Concentration(particles/mL)
Size (nm)
Alloyed nanoparticles analyzed by Nanoparticle Tracking Analysis.
Nanovex Biotechnologies gold/silver
nanoparticles are monodispersed
nanoparticles with silver like optical
properties.
These nanoparticles maintain their optical
properties in the 400-500 nm range while
avoiding the use of silver nanoparticles of
low (< 20 nm) or high size (60-100 nm) to
have similar properties.
COMPOSITION SIZE PEAK (nm)
Au0:Ag100 40 nm 411
Au20:Ag80 40 nm 431
Au50:Ag50 40 nm 456
Au80:Ag20 40 nm 498
Au100:Ag0 40 nm 526
Application Surface Functionalization
Protein conjugation Citrate, streptavidine, COOH
Modification with thiolated ligands Citrate
Western blot/ dot blot Streptavidine
Inmunohistochemistry Streptavidine
Flow cytometry Citrate
Celular uptake Citrate
Lateral flow immunoassays Citrate, streptavidine, COOH
ELISA Streptavidine
Microscopy Streptavidine
GOLD/SILVER ALLOY
NANOPARTICLES
20. Nanovex Biotechnologies offers lipoic acid functionalized SPHERICAL gold, silver and
gold-silver alloy nanoparticles.
FUNCTIONALIZED
METALLIC NANOPARTICLES
Nanovex lipoic acid functionalized nanoparticles are ideal for conjugation of proteins
and other primary amines using EDC/NHS coupling chemistry.
•Available in different sizes and materials.
•Narrow size distribution and batch-to-batch consistency.
•Carboxyl group high density.
•Full characterization data with all products.
•Product Quality Guarantee.
•Support and service from our nanomaterials experts.
Lipoic acid nanoparticles can be used in many
applications such as protein conjugation, western
blot/dot blot, microscopy applications, lateral flow
assays, ELISA or dark field microscopy.
21. CARBON DOTS
Carbon dots is a new class of fluorescent carbon
nanomaterials.
Carbon dots possess the attractive properties of
high stability, good conductivity, low toxicity,
environmental friendliness as well as
comparable optical properties to quantum dots
Applications
•Bioimaging
•Sensing
•Drug delivery
•Catalysis
•Optoelectronics
0
100
200
300
400
500
600
700
800
300 350 400 450 500 550 600
Intensity(a.u.)
Wavelength(nm)
λ 460 nmλ 340 nm
22. Superparamagnetic iron oxide
nanoparticles (SPIONS)
Nanovex Biotechnologies offers 20 nm
superparamagnetic iron oxide
nanoparticles (SPIONS) which are oleic
acid capped and dispersed in toluene.
0
10
20
30
40
50
60
70
0 10 20 30 40 50
Particle Diamenter (nm)
Magnéticas NP M2
Application
Magnetic storage
Drug delivery
Biosensing
Magnetic separation
Contrast reagent for
imaging
Lateral flow magneto-
immunoassays
Magnetization > 20 emu/g
23. do el medio de dispersión es THF
macenamiento entre 4 y 6 ºC puede alargar hasta 12 meses e
40
PVP
Agua, alcoholes, THF
a
, DMF
Au
40
NA
NA
800
0,037
12
20 -25
a
25
200
dio de partícula (nm)
m)
ento (nm)
o de absorbancia (nm)
ad (meses)
iento (ºC)
)
(mg/mes)
s THF
ºC puede alargar hasta 12 meses el periodo mínimo de estabilidad
10 - 30
815
0.067
12
20 - 25
15
60
NA
800
0,037
12
20 -25
a
25
200
Gold nanostars
TECHNICAL SPECIFICATIONS
Technical name AuNStars@PVP
Size (nm) 40
Stabilizer PVP
Dispersion medium Water, alcohols, THF, DMF
Nucleus material Au
Nucleus size (nm) 40
Coating material -
Coating thickness (nm) -
Absorbance maximun wavelength (nm) 800
Equivalence 1OD (mg/ml) 0,037
Minimun Stability period (months) 12
Storage temperature ( °C) 20 – 25 (4 – 6 for THF)
Gold nanostars are novel star-shaped gold
nanoparticles with interesting properties for different
applications such as plasmonics, spectroscopy,
biomedicine , biosensor, medical diagnostics,
cancer therapies and energy conversion.
24. Silica coated Gold
nanostars
TECHNICAL SPECIFICATIONS
Technical name AuNStars@SiO2
Size (nm) 50
Stabilizer -
Dispersion medium Alcohols
Nucleus material Au
Nucleus size (nm) 40
Coating material SiO2
Coating thickness (nm) 10 - 30
Absorbance maximun wavelength (nm) 815
Equivalence 1OD (mg/ml) 0,067
Minimun Stability period (months) 12
Storage temperature ( °C) 20 – 25
Silica coated Gold nanostars apart from the
advantages of Gold nanostars, the silica coating
provides another versatile conjugation surface
Alcoholes
Au
40
SiO2
10 - 30
815
0.067
12
20 - 25
15
60
alcoholes, THF , DMF
Au
40
NA
NA
800
0,037
12
20 -25
a
25
200
0,11, 0,31, 0,67, 2,50
12
20 - 25
50
100
el periodo mínimo de estabilidad.
0.067
12
20 - 25
15
60
25. TECHNICAL SPECIFICATIONS
Technical name AuNRs@CTAB
Size (nm) 84x24
Stabilizer CTAB
Dispersion medium water
Nucleus material 84x24
Nucleus size (nm) 14
Coating material -
Coating thickness (nm) -
Absorbance maximun wavelength (nm) 770
Equivalence 1OD (mg/ml) 0,016
Minimun Stability period (months) 3
Storage temperature ( °C) 25 - 27
Gold nanorods, apart from the advantages of
Gold nanoparticles, the silica coating provides
another versatile conjugation surface
Gold nanorods
26. Quantum Dots (QDs) are nanoparticles (3-4 nm) of
semiconducting materials. Their luminescence
properties makes them an attractive alternative to
conventional luminophores, and for other numerous
applications.
Quantum Dots
• QDs/CdSe: Quantum Dots (QDs) with a CdSe core. Max
abs: 560 ± 5 nm, 575 ± 5 nm or 590 ± 5 nm. Dispersed in
chloroform.
• QDs/CdSe/ZnS: Quantum Dots (QDs) with a CdSe core
and a ZnS shell. Max abs: 580 ± 5 nm, 590 ± 5nm or 615 ± 5
nm. Dispersed in chloroform or water.
28. Nanovex Biotechnologies offers streptavidin conjugated SPHERICAL gold, silver and gold-
silver alloy nanoparticles.
CONJUGATED
METALLIC NANOPARTICLES
Nanovex streptavidin conjugated nanoparticles has an excellent QUALITY:
•Narrow size distribution
•Batch-to-batch consistency
•Full characterization data with all products.
•Product Quality Guarantee.
•Support and service from our nanomaterials experts.
Nanovex Biotechnologies streptavidin nanoparticles
can be employed for binding to several biotinylated
ligand, like as antibodies, peptides or other
biomolecules.
Streptavidin nanoparticles can be used in many
applications such as protein conjugation, western
blot/dot blot, immunohistochemistry, lateral flow assays,
ELISA or dark field microscopy.
29. Nanovex Biotechnologies offers streptavidin conjugated nanovesicles.
Available on all nanovesicles of our catalogue
CONJUGATED
NANOVESICLES
Nanovex streptavidin conjugated nanovesicles has an excellent QUALITY:
•Narrow size distribution
•Batch-to-batch consistency
•Full characterization data with all products.
•Product Quality Guarantee.
•Support and service from our nanomaterials experts.
Nanovex Biotechnologies streptavidin nanovesicles can
be employed for binding to several biotinylated ligand,
like as antibodies, peptides or other biomolecules.
Streptavidin nanovesicles can be used in many
applications such as protein conjugation, western
blot/dot blot, immunohistochemistry, lateral flow assays,
ELISA or dark field microscopy.
Nio-N Nio-Cat Lipo-N Lipo-cat
Thermo Pegylated Fluorescent pH
30.
31. PLGA nanoparticles
Poly(lactic-co-glycolic acid) (PLGA) is one of the most successfully developed
biodegradable polymers. PLGA is a biocompatible, biodegradable and safely
administrable polymer approved by the US FDA (Food and Drug Administration) and
EMA (European Medicines Agency).
Nanovex Biotechnologies provides plain polymeric biodegradable nanoparticles
(Nps) based on poly(lactide-co-glycolide) (PLGA) acid terminated with a
lactide/glycolide ratio of 50/50 and a molecular weight of 32000 Da. There are
different types of PLGA nanoparticles so that our clients can select the
nanoparticle that best suits their needsnanoparticles. In addition, these
nanoparticles can be externally functionalized with different compounds (NH2
+, PEI,
proteins,…)
PLGA nanoparticles are available in various sizes of 50, 100 and 200nm
32. PLGA nanoparticles
PLGA Standard nanoparticles can
encapsulate both hydrophilic and
lipophilic compounds. These
nanoparticles are negative
charged and they are available in
different sizes (50, 100 or 200 nm)
PLGA-FLUO nanoparticles can
encapsulate both hydrophilic and
lipophilic compounds. These
nanoparticles chan show different
types of fluorescence (green, red
or pH sensitive fluorescence)
and they are available in different
sizes (50, 100 or 200 nm)
PLGA-PEI nanoparticles can
encapsulate both hydrophilic and
lipophilic compounds. These
nanoparticles are positive charged
due to the surface modification
with PEI.PLGA-PEI nanoparticles are
recommended for gene or drug
delivery (intracellular delivery) and
they are available in different sizes
(100 or 200 nm)
PLGA-PEG nanoparticles can
encapsulate both hydrophilic and
lipophilic compounds. These
nanoparticles are surfacely
modified with PEG and they are
recommended for “in vivo”
assays. PLGA-PEG nanoparticles
are available in different sizes (100
or 200 nm)
PLGA-PEI-FLUO nanoparticles can
encapsulate both hydrophilic and
lipophilic compounds. These
nanoparticles are positive charged
due to the surface modification
with PEI and they can show
different types of fluorescence
(green, red or pH sensitive
fluorescence), they are
recommended for gene or drug
delivery (intracellular delivery) with
fluorescence detection. PLGA-PEI-
FLUO nanoparticles are available in
different sizes (100 or 200 nm)
PLGA-PEG-FLUO nanoparticles can
encapsulate both hydrophilic and
lipophilic compounds. These
nanoparticles are surfacely
modified with PEG and they can
show different types of
fluorescence (green, red or pH
sensitive fluorescence), they are
recommended for “in vivo”
assays with fluorescence detection.
PLGA-PEG-FLUO nanoparticles are
available in different sizes (100 or
200 nm)
Nanovex offers a customized service to design,
develop and produce specific PLGA
nanoparticles suitable for drug delivery, targeted
drug delivery, gene delivery, theranostics,
modeled to the specific needs of the customers.
34. PRACTICE KITS
Practice Nanoencapsulation kit to nanoencapsulate fluorecein into nanovesicles
and to determine entrapment efficiency.
The kit is composed by:
A. Size Exclusion Chromatography (SEC) Column
B. Pronanosome (Product to form nanovesicles)
C. Fluorescein solution (100 μM)
Elution profile obtained from a 200 μl sample of nanovesicles containing fluorescein
and unencapsulated fluorescein (1 ml fractions)
The practice nanoencapsulation
kit offers a clear and pedagogic
method for learning about
nanoencapsulation and purification
techniques.
39. NANOENCAPSULATION
NANOENCAPSULATION OF COMPOUNDS
Nanoencapsulation of compounds
/biomolecules (molecules, peptides, proteins
and DNA, among others) in nanovesicles or
PLGA nanoparticles for different applications.
CUSTOM NANOSYSTEMS
Nanovex develops custom nanovesicles
or nanoparticles in order to meet your
requirements:
• Formulation
• Size and distribution
• Z-Potential
• Surface modification
SURFACE MODIFICATION
Surface modification of nanovesicles
and nanoparticles allows to achieve
different delivery strategies such as:
• Long-circulating liposomes
• Intracellular delivery
• Targeted delivery
How do we work?
1. Select the right system
2. Send the compound to
encapsulate
3. After 2-4 weeks, Nanovex
will provide your system
with a full characterization
DELIVERY STUDIES
Delivery studies of the final
encapsulated compound, peptide or
protein, can be performed by
Nanovex, for instance, simulating
different conditions :
• Gastric conditions
• Intestinal conditions
• Dermal/Transdermal assays
Nanoencapsulation
40. BIOCONJUGATION
SURFACE MODIFICATION / BIOCONJUGATION
Nanovex has a wide experience in the field of surface modification of both
nanoparticles and nanovesicles with different biomolecules, apart from the
bioconjugation of proteins and DNA with different labels. After the surface
modification or bioconjugation process, the product is purified and fully
characterized in order to get a high quality and purified surface modified final
product.
SURFACE MODIFICATION – OPTION 1
SURFACE MODIFICATION – OPTION 2
BIOCONJUGATION
Nanomaterials to modify: Nanoparticles and
nanovesicles
Technique: Passive adsorption / Covalent
conjugation
Characterization: UV-VIS
Nanomaterials to modify: Nanoparticles and
nanovesicles
Technique: Passive adsorption / Covalent
conjugation
Characterization: ICP-MS
Biomolecules to modify: Antibodies, enzymes,
proteins, and DNA.
Technique: Covalent conjugation
Characterization: UV-VIS / ICP
Bioconjugation
41. EXOSOME CHARACTERIZATION
Exosomes are one the most interesting
biological microvesicles due to the
potential source of information contained
inside these particles.
Our facilities have the highest technology
such as the Nanoparticle Track
Analysis (NTA) Technology, based on the
analysis of Brownian motion, which is able
to determine the size, size distribution and
the exosome concentration in the sample.
SPECIFIC EXOSOME CHARACTERIZATION
Apart from the analysis of exosome size and
concentration, NTA analysis also enabled an
evaluation of a subpopulation of exosomes
which possess a specific biomarkers over their
surface. This goal can be achieved by using
an appropiate fluorescent antibody or
molecule to label the exosome of interest.
Exosome
characterization
42. NANOMATERIAL CHARACTERIZATION
NANOMATERIAL CHARACTERIZATION
The service is focused on the characterization of nanomaterials (metallic
nanoparticles, polymeric nanoparticles and nanovesicles, among others) as well
as other similar systems ranged from 0.3 nm to 100 μm. In addition to nanomaterial
characterization, Nanovex offers personalized advice and technical assistance.
The following parameters can be determined: Size, size distribution,
Nanoparticle/Nanovesicle Concentration, Z-Potential, Morphology, Entrapment
Efficiency, Structural Analysis, Fluorescence and Stability.
Nanomaterial
characterization