This document provides details of projects being conducted by students of the B. Pharm VIII semester at Kamla Nehru College of Pharmacy in Nagpur, India during the summer of 2020. It lists 66 student projects, each with the student name, project title, and name of the supervising faculty member. The projects cover various areas of pharmacy including pharmaceutics, pharmacognosy, pharmacology, and pharmaceutical chemistry. They involve activities such as synthesis of drug derivatives, herbal drug formulation and evaluation, and determination of bioactivities.
ALZET osmotic pumps are implantable devices that continuously deliver solutions over a set duration at a constant rate. They offer a simple alternative to repetitive injections by providing around-the-clock exposure to test agents without needing frequent animal handling. ALZET pumps work through osmosis, using no batteries or electronics. They have various sizes to deliver agents from 1 day to 6 weeks at controlled rates. Common applications include delivering drugs, hormones, and other compounds in animal research.
It is unique in bringing together the regulatory authorities and
pharmaceutical industry to discuss scientific and technical aspects of pharmaceuticals and develop ICH guidelines.
Pilot Plant:-
“Defined as a part of pharmaceutical industry where a lab scale formula is transformed into viable product by the development of liable practical procedure for manufacture”.
Scale-up:-
“The art of designing of prototype using the data obtained from the pilot plant model”
WHO GUIDELINES FOR TECH.TRANSFER SIDHANTA SAHU.GvDurgamani
This document provides information about technology transfer in the pharmaceutical industry. It defines technology transfer as the logical procedure that controls the transfer of any process along with documentation and expertise between development and manufacturing sites. The WHO guidelines for technology transfer provide a flexible framework to guide the transfer process with a focus on quality. The scope of the WHO guidelines includes guidance for transferring manufacturing processes of APIs, packaging, and all dosage forms. Reasons for technology transfer include a lack of manufacturing capacity, resources, or marketing capabilities.
Approaches for the design of transdermal drug deliverykvineetha8
The document provides an introduction to transdermal drug delivery systems (TDDS). It discusses advantages like controlled delivery and avoidance of first-pass metabolism. Components are described, including rate-controlling polymers, drugs, permeation enhancers, adhesives and backing layers. Approaches to development include polymer membrane systems, polymer matrix systems, and adhesive or microreservoir systems. Recent approaches discussed are iontophoresis and electroporation, which use electric current to enhance skin permeation.
Bio pharmaceutical classification System [BCS]Sagar Savale
The Biopharmaceutical Classification System was first developed by in 1995, by Amidon et al & his colleagues.
Definition:
“The Biopharmaceutical Classification System is a scientific framework for classifying a drug substance based on its aqueous solubility & intestinal permeability & dissolution rate”.
To saved time fast screening is required so drug substances are classified on basis of solubility and permeability. This classification is called Biopharmaceutical Classification System
Novel drug delivery system based herbal formulationsNitin Patel
This document discusses novel drug delivery systems for herbal medicines. It begins by introducing how novel delivery can help herbal drugs be delivered at specific rates and sites of action, improving bioavailability. It then discusses various novel delivery approaches for herbal drugs like nanoparticles, liposomes, phytosomes, and nanoemulsions that can enhance solubility, bioavailability, stability and targeting of herbal medicines. Several studies examining specific herbal extract formulations employing these approaches are also summarized. The document concludes by discussing some commercialized herbal extract formulations utilizing novel delivery approaches.
ALZET osmotic pumps are implantable devices that continuously deliver solutions over a set duration at a constant rate. They offer a simple alternative to repetitive injections by providing around-the-clock exposure to test agents without needing frequent animal handling. ALZET pumps work through osmosis, using no batteries or electronics. They have various sizes to deliver agents from 1 day to 6 weeks at controlled rates. Common applications include delivering drugs, hormones, and other compounds in animal research.
It is unique in bringing together the regulatory authorities and
pharmaceutical industry to discuss scientific and technical aspects of pharmaceuticals and develop ICH guidelines.
Pilot Plant:-
“Defined as a part of pharmaceutical industry where a lab scale formula is transformed into viable product by the development of liable practical procedure for manufacture”.
Scale-up:-
“The art of designing of prototype using the data obtained from the pilot plant model”
WHO GUIDELINES FOR TECH.TRANSFER SIDHANTA SAHU.GvDurgamani
This document provides information about technology transfer in the pharmaceutical industry. It defines technology transfer as the logical procedure that controls the transfer of any process along with documentation and expertise between development and manufacturing sites. The WHO guidelines for technology transfer provide a flexible framework to guide the transfer process with a focus on quality. The scope of the WHO guidelines includes guidance for transferring manufacturing processes of APIs, packaging, and all dosage forms. Reasons for technology transfer include a lack of manufacturing capacity, resources, or marketing capabilities.
Approaches for the design of transdermal drug deliverykvineetha8
The document provides an introduction to transdermal drug delivery systems (TDDS). It discusses advantages like controlled delivery and avoidance of first-pass metabolism. Components are described, including rate-controlling polymers, drugs, permeation enhancers, adhesives and backing layers. Approaches to development include polymer membrane systems, polymer matrix systems, and adhesive or microreservoir systems. Recent approaches discussed are iontophoresis and electroporation, which use electric current to enhance skin permeation.
Bio pharmaceutical classification System [BCS]Sagar Savale
The Biopharmaceutical Classification System was first developed by in 1995, by Amidon et al & his colleagues.
Definition:
“The Biopharmaceutical Classification System is a scientific framework for classifying a drug substance based on its aqueous solubility & intestinal permeability & dissolution rate”.
To saved time fast screening is required so drug substances are classified on basis of solubility and permeability. This classification is called Biopharmaceutical Classification System
Novel drug delivery system based herbal formulationsNitin Patel
This document discusses novel drug delivery systems for herbal medicines. It begins by introducing how novel delivery can help herbal drugs be delivered at specific rates and sites of action, improving bioavailability. It then discusses various novel delivery approaches for herbal drugs like nanoparticles, liposomes, phytosomes, and nanoemulsions that can enhance solubility, bioavailability, stability and targeting of herbal medicines. Several studies examining specific herbal extract formulations employing these approaches are also summarized. The document concludes by discussing some commercialized herbal extract formulations utilizing novel delivery approaches.
Function of community pharmacy, Organization and structure of retail and wholesale drug store, Legal requirement for establishment, Maintenance of records
regulatory requirements for drug approval ( IP-2 / UNIT -3 )JAYACHANDRA AKUTHOTA
The document discusses regulatory requirements for drug approval. It covers the drug development process including non-clinical and clinical development teams. The non-clinical team conducts pre-clinical studies in animals to evaluate efficacy, safety, and viability of manufacturing. Clinical trials have multiple phases to test drugs on humans. A New Drug Application is submitted to regulatory authorities for marketing approval and includes preclinical and clinical data. The drug development process takes 10-12 years and involves interactions between scientific disciplines.
The document discusses the importance of medication history interviews. A medication history interview involves collecting detailed information from a patient about all prescribed and non-prescribed medications they have taken. This information includes allergies, adherence to treatments, and use of alternative medicines. Collecting a thorough medication history helps prevent prescription errors, detect potential drug-related issues, and allows healthcare providers to develop better treatment plans by understanding a patient's complete medication use and history. The interview collects demographic data, medical information, and details on both current and past prescription and non-prescription medication use.
COPP/CPP it certification of pharmaceutical product for reviewing QSE i.e. Quality, Sefty,Efficacy of product. it important certification for exporting it may required by importing country.
Polymers are large molecules composed of repeating structural units and can be either natural or synthetic, biodegradable or non-biodegradable. They are widely used in controlled release drug delivery systems due to their ability to control drug release rates and provide advantages like improved patient compliance. Common polymers used include natural ones like collagen and alginate as well as synthetic biodegradable polymers like PLGA. Applications include ocular inserts and transdermal patches that use polymers to regulate drug diffusion out of a matrix over time.
Application Of Polymer In Controlled Release FormulationAnindya Jana
Polymers are becoming increasingly important in the field of drug delivery. The pharmaceutical applications of polymers range from their use as binders in tablets to viscosity and flow controlling agents in liquids, suspensions and emulsions. Polymers can be used as film coatings to disguise the unpleasant taste of a drug, to enhance drug stability and to modify drug release characteristics.
As a consequence, increasing attention has been focused on methods of giving drugs continually for a prolonged time periods and in a controlled fashion.
This technology now spans many fields and includes pharmaceutical, food and agricultural applications, pesticides, cosmetics, and household products.
Copp - CERTIFICATE OF PHARMACEUTICAL PRODUCTSuraj Pamadi
The document discusses the Certificate of Pharmaceutical Product (CoPP), which is issued by regulatory authorities to help importing countries assess the quality of pharmaceutical products. It outlines the importance of the CoPP for product registration in other countries. The summary also describes the application process for obtaining a CoPP in India, including requirements for documentation, inspections, and the format of the certificate.
The document discusses quality management systems in the pharmaceutical industry. It states that quality management systems (QMS) rely on regulations and guidelines to ensure effective quality control in pharmaceutical companies. The International Council for Harmonization (ICH) guideline provides a model for an effective QMS and is intended to assist manufacturers in maintaining quality and safety of their products and services. QMS is an important aspect of the pharmaceutical industry for regulating quality and safety.
The document provides an overview of regulatory affairs (RA) in the pharmaceutical industry. It discusses that RA ensures pharmaceutical products comply with regulatory standards by acting as the link between companies and regulatory authorities. RA is responsible for guiding drug development and submissions for market approval. The document outlines the historical development of regulations from 1900 to present day. It also reviews the roles and responsibilities of RA professionals which include maintaining knowledge of regulations, preparing submissions, and ensuring compliance. Finally, it lists some major regulatory authorities around the world and their roles in overseeing drug development and approval processes.
This document discusses phytosomes, which are herbal extracts bound to phospholipids. Phytosomes have several advantages over traditional herbal extracts, including enhanced absorption and bioavailability. The document outlines the structure and properties of phytosomes, comparing them to liposomes. It also describes the preparation process, evaluation methods, and applications of various phytosome formulations. Common phytosomes include silymarin (milk thistle) for liver health, grape seed for antioxidants, green tea for antioxidants and chronic diseases, and curcumin for anti-inflammatory effects. Phytosomes allow herbal constituents to be absorbed more effectively and produce better results than conventional herbal extracts.
Pharmaceutical Licecnsing authorites of indiaAtul Bhombe
Central Drug Standard Control Organisation (CDSCO) is India's national regulatory body for pharmaceuticals and medical devices. It regulates the import of drugs, approves new drugs and clinical trials. CDSCO works with six zonal offices, seven sub-zonal offices, and thirteen port/airport offices. The Drug Controller General of India, who is responsible for new drug, medical device, and clinical trial approvals, advises CDSCO. At the state level, State Licensing Authorities regulate and control the licensing of drug manufacturing, distribution, and sale within the state.
polymer in pharmacy and application of polymersRoshan Bodhe
This document discusses the use of polymers in pharmaceutical applications. It begins with an introduction that defines polymers as large molecules formed by linking repeating structural units through covalent bonds. The document then covers the classification, properties, characteristics, advantages, and applications of polymers. Some key points include that polymers can be classified based on their source, polymerization method, degradability, nature, and properties. They have advantages like localized and sustained drug delivery to improve patient compliance. Applications mentioned are in modified drug release systems, biomedical uses like tissue engineering, and industrial/agricultural packaging.
Stability testing of herbal products involves subjecting samples to various conditions like heat, light, and humidity to determine shelf life and ensure quality over time. Key aspects of stability testing include establishing acceptance criteria and storage conditions, conducting both accelerated and long-term real-time tests, and developing a protocol that specifies test attributes, analytical methods, sampling plans, and evaluation procedures. Challenges with testing herbal products relate to their complex compositions, but can be addressed through marker analyses and fingerprinting techniques. Proper stability testing is important for determining appropriate packaging, storage, and expiry dates.
This document discusses gastroretentive drug delivery systems (GRDDS), which are oral dosage forms designed to remain in the stomach for an extended period of time to prolong drug release. It covers the rationale for using GRDDS, factors controlling gastric residence time, and various approaches for prolonging gastric retention including floating systems, high-density systems, and bioadhesive or magnetic systems. Floating systems include non-effervescent and effervescent types that float due to low density or gas generation. High-density systems do not float but remain in the stomach through bioadhesion, magnetic forces, swelling to a large size, or raft formation on gastric fluids.
The device which is used in the intrauterine drug delivery system is known as an Intrauterine device (IUD) (2). IUDs or intrauterine devices are small artificial objects or devices inserted into the uterus to prevent the occurrence of pregnancy by disrupting the fertilization process as a result of sexual intercourse. They have gained popularity in recent times and are one of the most effective methods of birth control in terms of long-term contraception. It can be easily installed and is flexible. These devices are usually small in size and inserted through the cervix. IUDs reduce the need for abortion with unwanted pregnancies by preventing the effective movement of eggs and sperm. However, it cannot confirm the spread of STIs or STDs such as HIV, gonorrhoea, etc
Topics covered
Introduction
Advantages
Disadvantages
Development of intra uterine devices (IUDs)
Applications
References
Ocuserts are solid or semisolid ocular inserts designed for ophthalmic drug delivery. They deliver drugs at a constant rate via diffusion and increase corneal contact time to prolong drug effects. This improves bioavailability and reduces dosing frequency. Ocuserts consist of a central drug reservoir, rate-controlling membrane, and outer ring. They are classified as insoluble, soluble, or bioerodible inserts depending on their composition. Insoluble inserts include diffusional and osmotic inserts that control drug release via membranes. Soluble inserts are natural or synthetic polymers that diffuse drug. Bioerodible inserts modulate drug release during erosion.
The document discusses criteria for drugs to be suitable for incorporation into controlled release formulations. It states that the drug should have a half-life between 3-4 hours, not have a short half-life under 2 hours or a long half-life over 8 hours. The drug also should not have a low therapeutic index, a high conventional dose, poor water solubility, an absorption window in the GI tract, or undergo extensive hepatic first-pass metabolism. Meeting these criteria helps ensure controlled delivery is possible without the dosage form being too large or absorption efficiency being reduced.
This document provides information on transdermal drug delivery systems (TDDS). It discusses the key components of TDDS formulations including the polymer matrix, drug, permeation enhancers, pressure sensitive adhesive, backing laminate and release liner. The document also describes the preparation methods for different types of TDDS and the evaluation methods used to test the physicochemical properties, in vitro drug release, and stability of TDDS. The evaluations help ensure the TDDS will safely and effectively deliver the drug through the skin as intended.
This document discusses the key aspects of technology transfer between a sending unit and receiving unit. It outlines the types of documentation, analytical methods, equipment, and facilities information that should be provided to properly transfer a manufacturing process. This includes details on APIs, excipients, finished products, packaging, cleaning procedures, and quality control testing. The roles and responsibilities of both units are defined to ensure a successful technology transfer.
This document summarizes the development and evaluation of taste masked tablets of drotoverine using solid dispersion technique. Drotoverine has an unpleasant bitter taste and poor aqueous solubility, resulting in incomplete absorption. Solid dispersion with carriers like urea and mannitol was used to mask the bitter taste and improve dissolution. Tablets were prepared by direct compression and evaluated for properties like hardness, friability and disintegration time. Fourier transform infrared spectroscopy and scanning electron microscopy showed no interaction between drug and carriers. Tablets using solid dispersion exhibited faster disintegration and complete taste masking. Dissolution studies also showed improved dissolution profile. Human volunteers rated the taste as tasteless. The formulated tablets thus demonstrated successful masking of bitter taste and improved
Pharmacognosy iii syllabus f inal yr b pharm-cbcs 2020-21Dr. Harshal Pawar
This document outlines the course objectives, outcomes, topics, and reading materials for the Pharmacognosy III course offered at the University of Mumbai for the Bachelor of Pharmacy program. The course covers various phytoconstituents including steroidal, triterpenoidal, anthraquinone, flavonoid glycosides and alkaloids. It aims to introduce students to the chemistry, sources, and uses of crude drugs containing these constituents. Major topics include steroidal and triterpenoidal glycosides, alkaloids, glycoproteins, glycosides, flavonoids, coumarins, herb-drug interactions, spectroscopy techniques for characterization, standardization of herbal drugs, regulatory issues, and herbal formulations.
Function of community pharmacy, Organization and structure of retail and wholesale drug store, Legal requirement for establishment, Maintenance of records
regulatory requirements for drug approval ( IP-2 / UNIT -3 )JAYACHANDRA AKUTHOTA
The document discusses regulatory requirements for drug approval. It covers the drug development process including non-clinical and clinical development teams. The non-clinical team conducts pre-clinical studies in animals to evaluate efficacy, safety, and viability of manufacturing. Clinical trials have multiple phases to test drugs on humans. A New Drug Application is submitted to regulatory authorities for marketing approval and includes preclinical and clinical data. The drug development process takes 10-12 years and involves interactions between scientific disciplines.
The document discusses the importance of medication history interviews. A medication history interview involves collecting detailed information from a patient about all prescribed and non-prescribed medications they have taken. This information includes allergies, adherence to treatments, and use of alternative medicines. Collecting a thorough medication history helps prevent prescription errors, detect potential drug-related issues, and allows healthcare providers to develop better treatment plans by understanding a patient's complete medication use and history. The interview collects demographic data, medical information, and details on both current and past prescription and non-prescription medication use.
COPP/CPP it certification of pharmaceutical product for reviewing QSE i.e. Quality, Sefty,Efficacy of product. it important certification for exporting it may required by importing country.
Polymers are large molecules composed of repeating structural units and can be either natural or synthetic, biodegradable or non-biodegradable. They are widely used in controlled release drug delivery systems due to their ability to control drug release rates and provide advantages like improved patient compliance. Common polymers used include natural ones like collagen and alginate as well as synthetic biodegradable polymers like PLGA. Applications include ocular inserts and transdermal patches that use polymers to regulate drug diffusion out of a matrix over time.
Application Of Polymer In Controlled Release FormulationAnindya Jana
Polymers are becoming increasingly important in the field of drug delivery. The pharmaceutical applications of polymers range from their use as binders in tablets to viscosity and flow controlling agents in liquids, suspensions and emulsions. Polymers can be used as film coatings to disguise the unpleasant taste of a drug, to enhance drug stability and to modify drug release characteristics.
As a consequence, increasing attention has been focused on methods of giving drugs continually for a prolonged time periods and in a controlled fashion.
This technology now spans many fields and includes pharmaceutical, food and agricultural applications, pesticides, cosmetics, and household products.
Copp - CERTIFICATE OF PHARMACEUTICAL PRODUCTSuraj Pamadi
The document discusses the Certificate of Pharmaceutical Product (CoPP), which is issued by regulatory authorities to help importing countries assess the quality of pharmaceutical products. It outlines the importance of the CoPP for product registration in other countries. The summary also describes the application process for obtaining a CoPP in India, including requirements for documentation, inspections, and the format of the certificate.
The document discusses quality management systems in the pharmaceutical industry. It states that quality management systems (QMS) rely on regulations and guidelines to ensure effective quality control in pharmaceutical companies. The International Council for Harmonization (ICH) guideline provides a model for an effective QMS and is intended to assist manufacturers in maintaining quality and safety of their products and services. QMS is an important aspect of the pharmaceutical industry for regulating quality and safety.
The document provides an overview of regulatory affairs (RA) in the pharmaceutical industry. It discusses that RA ensures pharmaceutical products comply with regulatory standards by acting as the link between companies and regulatory authorities. RA is responsible for guiding drug development and submissions for market approval. The document outlines the historical development of regulations from 1900 to present day. It also reviews the roles and responsibilities of RA professionals which include maintaining knowledge of regulations, preparing submissions, and ensuring compliance. Finally, it lists some major regulatory authorities around the world and their roles in overseeing drug development and approval processes.
This document discusses phytosomes, which are herbal extracts bound to phospholipids. Phytosomes have several advantages over traditional herbal extracts, including enhanced absorption and bioavailability. The document outlines the structure and properties of phytosomes, comparing them to liposomes. It also describes the preparation process, evaluation methods, and applications of various phytosome formulations. Common phytosomes include silymarin (milk thistle) for liver health, grape seed for antioxidants, green tea for antioxidants and chronic diseases, and curcumin for anti-inflammatory effects. Phytosomes allow herbal constituents to be absorbed more effectively and produce better results than conventional herbal extracts.
Pharmaceutical Licecnsing authorites of indiaAtul Bhombe
Central Drug Standard Control Organisation (CDSCO) is India's national regulatory body for pharmaceuticals and medical devices. It regulates the import of drugs, approves new drugs and clinical trials. CDSCO works with six zonal offices, seven sub-zonal offices, and thirteen port/airport offices. The Drug Controller General of India, who is responsible for new drug, medical device, and clinical trial approvals, advises CDSCO. At the state level, State Licensing Authorities regulate and control the licensing of drug manufacturing, distribution, and sale within the state.
polymer in pharmacy and application of polymersRoshan Bodhe
This document discusses the use of polymers in pharmaceutical applications. It begins with an introduction that defines polymers as large molecules formed by linking repeating structural units through covalent bonds. The document then covers the classification, properties, characteristics, advantages, and applications of polymers. Some key points include that polymers can be classified based on their source, polymerization method, degradability, nature, and properties. They have advantages like localized and sustained drug delivery to improve patient compliance. Applications mentioned are in modified drug release systems, biomedical uses like tissue engineering, and industrial/agricultural packaging.
Stability testing of herbal products involves subjecting samples to various conditions like heat, light, and humidity to determine shelf life and ensure quality over time. Key aspects of stability testing include establishing acceptance criteria and storage conditions, conducting both accelerated and long-term real-time tests, and developing a protocol that specifies test attributes, analytical methods, sampling plans, and evaluation procedures. Challenges with testing herbal products relate to their complex compositions, but can be addressed through marker analyses and fingerprinting techniques. Proper stability testing is important for determining appropriate packaging, storage, and expiry dates.
This document discusses gastroretentive drug delivery systems (GRDDS), which are oral dosage forms designed to remain in the stomach for an extended period of time to prolong drug release. It covers the rationale for using GRDDS, factors controlling gastric residence time, and various approaches for prolonging gastric retention including floating systems, high-density systems, and bioadhesive or magnetic systems. Floating systems include non-effervescent and effervescent types that float due to low density or gas generation. High-density systems do not float but remain in the stomach through bioadhesion, magnetic forces, swelling to a large size, or raft formation on gastric fluids.
The device which is used in the intrauterine drug delivery system is known as an Intrauterine device (IUD) (2). IUDs or intrauterine devices are small artificial objects or devices inserted into the uterus to prevent the occurrence of pregnancy by disrupting the fertilization process as a result of sexual intercourse. They have gained popularity in recent times and are one of the most effective methods of birth control in terms of long-term contraception. It can be easily installed and is flexible. These devices are usually small in size and inserted through the cervix. IUDs reduce the need for abortion with unwanted pregnancies by preventing the effective movement of eggs and sperm. However, it cannot confirm the spread of STIs or STDs such as HIV, gonorrhoea, etc
Topics covered
Introduction
Advantages
Disadvantages
Development of intra uterine devices (IUDs)
Applications
References
Ocuserts are solid or semisolid ocular inserts designed for ophthalmic drug delivery. They deliver drugs at a constant rate via diffusion and increase corneal contact time to prolong drug effects. This improves bioavailability and reduces dosing frequency. Ocuserts consist of a central drug reservoir, rate-controlling membrane, and outer ring. They are classified as insoluble, soluble, or bioerodible inserts depending on their composition. Insoluble inserts include diffusional and osmotic inserts that control drug release via membranes. Soluble inserts are natural or synthetic polymers that diffuse drug. Bioerodible inserts modulate drug release during erosion.
The document discusses criteria for drugs to be suitable for incorporation into controlled release formulations. It states that the drug should have a half-life between 3-4 hours, not have a short half-life under 2 hours or a long half-life over 8 hours. The drug also should not have a low therapeutic index, a high conventional dose, poor water solubility, an absorption window in the GI tract, or undergo extensive hepatic first-pass metabolism. Meeting these criteria helps ensure controlled delivery is possible without the dosage form being too large or absorption efficiency being reduced.
This document provides information on transdermal drug delivery systems (TDDS). It discusses the key components of TDDS formulations including the polymer matrix, drug, permeation enhancers, pressure sensitive adhesive, backing laminate and release liner. The document also describes the preparation methods for different types of TDDS and the evaluation methods used to test the physicochemical properties, in vitro drug release, and stability of TDDS. The evaluations help ensure the TDDS will safely and effectively deliver the drug through the skin as intended.
This document discusses the key aspects of technology transfer between a sending unit and receiving unit. It outlines the types of documentation, analytical methods, equipment, and facilities information that should be provided to properly transfer a manufacturing process. This includes details on APIs, excipients, finished products, packaging, cleaning procedures, and quality control testing. The roles and responsibilities of both units are defined to ensure a successful technology transfer.
This document summarizes the development and evaluation of taste masked tablets of drotoverine using solid dispersion technique. Drotoverine has an unpleasant bitter taste and poor aqueous solubility, resulting in incomplete absorption. Solid dispersion with carriers like urea and mannitol was used to mask the bitter taste and improve dissolution. Tablets were prepared by direct compression and evaluated for properties like hardness, friability and disintegration time. Fourier transform infrared spectroscopy and scanning electron microscopy showed no interaction between drug and carriers. Tablets using solid dispersion exhibited faster disintegration and complete taste masking. Dissolution studies also showed improved dissolution profile. Human volunteers rated the taste as tasteless. The formulated tablets thus demonstrated successful masking of bitter taste and improved
Pharmacognosy iii syllabus f inal yr b pharm-cbcs 2020-21Dr. Harshal Pawar
This document outlines the course objectives, outcomes, topics, and reading materials for the Pharmacognosy III course offered at the University of Mumbai for the Bachelor of Pharmacy program. The course covers various phytoconstituents including steroidal, triterpenoidal, anthraquinone, flavonoid glycosides and alkaloids. It aims to introduce students to the chemistry, sources, and uses of crude drugs containing these constituents. Major topics include steroidal and triterpenoidal glycosides, alkaloids, glycoproteins, glycosides, flavonoids, coumarins, herb-drug interactions, spectroscopy techniques for characterization, standardization of herbal drugs, regulatory issues, and herbal formulations.
Indian journal of research in pharmacy and biotechnology issue 5debjit bhowmik
This study evaluated the association between the rs8052394 polymorphism of the metalothionein-1A gene and type 2 diabetes mellitus in the Nepalese population. The rs8052394 polymorphism results in a lysine to arginine substitution at position 51 of the metalothionein-1A protein. Polymerase chain reaction-restriction fragment length polymorphism analysis was used to identify the rs8052394 polymorphism in DNA samples from 62 Nepalese patients with type 2 diabetes mellitus. The study aimed to determine if the rs8052394 polymorphism is responsible for an increased risk of developing type 2 diabetes mellitus or its complications in the Nepalese population.
Now a days everybody wants evidence or proof for any purpose.so govt.of india introduces AYUSH research portal for the devalopment and taking awareness regarding ayurveda where it consists of clinical trial and pre-clinical trial data.
This review summarizes the antimicrobial potential of the polyherbal Ayurvedic formulation Vidangadi churna. Vidangadi churna contains five ingredients - Embelia ribes, rock salt, alkali of yava, Mallotus philippinensis hairs, and Terminalia chebula fruit pulp. Each ingredient is described in detail including its Rasadi properties, pharmacological activities, and therapeutic uses as described in Ayurvedic texts. Research studies indicate the individual ingredients and the formulation as a whole have antimicrobial, antibacterial, antifungal, anthelmintic, antifilarial, and other therapeutic properties. The review concludes Vidangadi churna has significant antimicrobial potential and
This document provides a bio-data or resume for Dr. Kundan Prasad. It includes personal details like name, date of birth, addresses, qualifications including degrees earned from various universities, work experience in research projects, training programs attended, publications including research papers and abstracts, and areas of expertise in analytical techniques. The bio-data demonstrates Dr. Prasad's educational qualifications and experience in research related to phytochemical analysis of medicinal plants from the Kumaon Himalayas using techniques like HPLC, GCMS, and FTIR. He has over 25 research publications and has worked on several projects related to pesticide residue analysis and post-harvest losses of vegetables.
Indian journal of research in pharmacy and biotechnology vol 1-issue-6-nove-...Debjit Bhowmik
This document describes the development of a LAMP marker for the authentication of the traditional medicinal plant Kalongi (Nigella sativa L.). RAPD analysis was performed on different accessions of Kalongi, identifying a monomorphic fragment present in all accessions. This fragment was cloned and sequenced, and specific LAMP primers were designed. The LAMP assay specifically amplified genomic DNA of authenticated Kalongi samples, but not a negative control species. The developed LAMP marker can provide guidance for authentication of plant materials traded as Kalongi and help address issues of adulteration.
This document provides a personal profile and curriculum vitae for Dr. U. Srinivasa. It summarizes his educational qualifications including a B.Pharm, M.Pharm, and Ph.D. It details his areas of specialization, teaching experience of over 23 years, research interests, publications, seminars and workshops attended, grants and honors received, and professional affiliations.
This document is a curriculum vitae for Dr. Rajesh Yadav that provides details about his educational qualifications and professional experience. It summarizes that he has a Ph.D. in Pharmaceutical Sciences, has over 13 years of teaching experience as a lecturer and professor, and 5.5 years of research experience. He has published over 25 research papers and presented in several national and international conferences.
This document provides a curriculum vitae for Dr. Ch. Mohan that outlines his educational qualifications and experiences. He holds a Ph.D. in Botany from Osmania University, Hyderabad, as well as other degrees. His research experience includes working on a DST-PURSE project involving the micropropagation and molecular characterization of two medicinal plants. He has published over 20 papers and has teaching experience at the university level. The CV details his laboratory skills, research focus, and qualifications for plant tissue culture, phytochemical analysis, and molecular biology techniques.
Dr. Chiluveru Mohan has extensive education and experience in botany and plant biology. He holds a PhD in Botany from Osmania University and has worked as a senior research fellow at ICAR-CRIDA studying the effects of climate change on agriculture. He has over 15 years of experience in teaching, research, and publishing on topics related to plant physiology, biochemistry, molecular biology, and micropropagation of medicinal plants. He has published numerous books, book chapters, and journal articles and has experience operating various instruments and software relevant to plant research.
This document summarizes a student project on the phytochemical and antimicrobial activity of Acalypha fruticosa. The student investigated the plant's traditional use as medicine, extracted compounds from its leaves, conducted phytochemical analysis to identify alkaloids and other compounds, and tested the extract against several bacteria and a fungus using the disc diffusion method. The extract showed antimicrobial activity. The student concluded the plant may be a potential source of antimicrobial drugs and its extracts could be used to destroy pathogenic organisms and treat diseases.
Indian journal of research in pharmacy and biotechnology 4debjit bhowmik
This document discusses the controversial role of antipsychotics in the treatment of Alzheimer's disease. While atypical antipsychotics can effectively treat psychotic symptoms and behavioral issues in the short term, several placebo-controlled studies have found they nearly double the risk of death over 2-3 years due to adverse events like infections. The FDA issued a black box warning about this increased mortality risk. Currently, the only FDA-approved medications target cognitive symptoms, but they also have significant side effects. More research is needed to develop safer alternatives for managing behavioral and psychological symptoms in Alzheimer's patients. Non-pharmacological interventions should be the primary treatment approach.
Dr. Rakesh Barik.Profile.pptx profile showing details.Rakesh Barik
Dr. Rakesh Barik is an Assistant Professor at the School of Pharmacy at GITAM (Deemed to be University) in Hyderabad, India with 18 years of experience in academics and research. His areas of expertise include pharmacological evaluation of herbal and synthetic drugs, standardization of herbal drugs, phytochemical studies, and herbal drug formulations. He has published 30 papers, presented at 21 conferences, authored 10 book chapters, and given 8 invited lectures.
Evaluation of in vitro antibacterial activity of Caralluma lasiantha for scie...Ratnakaram Venkata Nadh
Caralluma lasiantha is used as a traditional medicine in India to heal body
heat and inflammations. In order to find out a scientific validation for the Indian
traditional knowledge, antibacterial activity of C. lasiantha extracts was studied
against inflammation causing bacteria (viz., Staphylococcus aureus, Escherichia coli,
Streptococcus Sp., Bacillus subtilis, Enterobacter aerogenes, Klebsiella pneumoniae)
along with other Gram-positive and Gram-negative bacteria. Solvents with different
polarity were used for extraction from dry roots and stems. Minimum inhibitory
concentrations (MIC) were also studied. Differential antibacterial activity was
exhibited by extracts and higher inhibition potential against Gram-positive bacteria
was explained. The observed antibacterial activities were correlated with the chemical
structures of phytochemicals present in C. lasiantha. Anti-inflammation activities
are related to C. lasiantha extracts through their antibacterial activities.
prathmesh shinde formulation, evaluation of herbal soapdhanashrisjadhav26
(1) The document describes the formulation and evaluation of a herbal soap using Musa spp. (banana) leaves through cold saponification method.
(2) Preliminary phytochemical tests of the Musa spp. leaves extract showed the presence of alkaloids, flavonoids, glycosides, and tannins.
(3) The herbal soap was formulated using coconut oil, sodium hydroxide, ethanol, Musa spp. leaves extract, and other ingredients. Evaluation tests found the soap to have good physical appearance, pH of 6.6, foaming ability, and significant antibacterial activity against Staphylococcus aureus.
Effect Of Many Body Interactions On Indices Of Refraction Of Alkali HalidesDr.imran aziz
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Effect Of Many Body Interactions On Indices Of Refraction Of Alkali HalidesDr.imran aziz
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1. Details of Project Report B. Pharm VIII Sem Summer 2020 Examination
Name of Institute: Kamla Nehru College of Pharmacy, Butibori, Nagpur
Sr.
No.
Name of the Student Title of Project Name of Supervisor Broad Area
1. Aarti Shankar Uprikar Evaluation of antianxiety activity of Bauhinia variegata in
mice.
Ms. Seema B. Wakodkar Pharmacology
2. Aakash Shivraya Yadpalle To formulate and evaluate Atenolol multiparticulate drug
delivery system.
Mr. Mangesh D. Godbole Pharmaceutics
3. Abhijit Madhao Padole Preparation and evaluation of zinc oxide nanoparticles of
Saraca asoca leave extract.
Mr. Lokesh T. Thote Pharmaceutics
4. Aditya Vijay Shuddhalwar A review on herbal potential for treatment of peptic ulcer. Ms. Seema B. Wakodkar Pharmacology
5. Ankit Prakash Mazumdar Synthesis and characterization of a novel Schiff’s Base
derivative of diphenylcarbazide: potential future
antimicrobial candidate.
Mrs. Kavita R. Pandey Pharmaceutical
Chemistry
6. Anwar Fateema Arif Khan Preparation and evaluation of microemulsion using model
drug.
Dr. Sunil Gupta Pharmaceutics
7. Ashwini Ramchandraji
Raghorte
Formulation and evaluation of dispersible tablet of taste
mask Mebeverine.
Dr. Parimal P. Katolkar Pharmaceutics
8. Avantika Nimbalkar To formulate and evaluate Diltiazem floating tablets. Mr. Mangesh D. Godbole Pharmaceutics
9. Bhagyashree W. Mudewar Pharmacognostic evaluation of Acacia auriculoformis
(Benth)
Mr. Manish A. Kamble Pharmacognosy
10. Bharati Ramesh Gondane Synthesis and Characterization of some Schiff’s base
containing substituted phenylhydrazine compound:
screening of antimicrobial potential.
Mrs. Ruchi S. Shivahare Pharmaceutical
chemistry
11. Chetna M. Waghale Synthesis and evaluation of thaizolidinones for analgesic
activity.
Dr. Deweshri R. Kerzare Pharmaceutical
chemistry
12. Devyani Mangesh Yenurkar Studies on Rubia cordifolia with reference to
phytopharmacology and formulation.
Dr. Jagdish R. Baheti Pharmacognosy
13. Gorakhnath Shamrao Kurude Herbal drugs in Parkinson’s disease. Dr. Mahendra C. Gunde Pharmacognosy
2. 14. Hrushikesh Ganesh Labede Synthesis of zinc oxide nanoparticles of leaf extract of
Acacia auriculiformis.
Ms. Disha M. Dhabarde Pharmaceutical
Chemistry
15. Ishank Dharmendra Kale Preparation and evaluation of microspheres using a model
drug.
Dr. Sunil Gupta Pharmaceutics
16. Kalyani Krishna Vairagade Investigation of different Bougainvillea varieties as acid
base indicators.
Mrs. Kavita R. Pandey Pharmaceutical
Chemistry
17. Kapil Rajesh Bahalani Herbal drugs in Alzeimer’s disease. Dr. Mahendra C. Gunde Pharmacognosy
18. Ketki Ashokrao Nichat To formulate and evaluate Atenolol controlled release
multiparticulate drug delivery system.
Mr. Mangesh D. Godbole Pharmaceutics
19. Khushbu Subhash Kolte Formulation and evaluation of herbal lip balm from lentil
and Tagets patula.
Mrs. Kavita R. Pandey Pharmaceutics
20. Laxman Gajanan Galat Evaluation of Anthemintic Potential of Acacia
auriculiformis Pods (Fruits) extract
Mr. Manish A. Kamble Pharmacognosy
21. Mallika Mahajan Preparation and evaluation of OTFs using a model drug. Dr. Sunil Gupta Pharmaceutics
22. Mayuresh Hirulkar Phytochemical screening and blood glucose level lowering
effect of Hydroalcoholic extract of Didymocarus
pedicellata.
Mr. Satish S. Meshram Pharmacognosy
23. Minal Maroti Katkar To formulate and evaluate Atenolol controlled release
multiparticulate drug delivery system.
Mr. Mangesh D. Godbole Pharmaceutics
24. Nandini Chandandas Gupta Synthesis of novel chalcone derivatives from 5-nitro
salicylaldehyde.
Ms. Disha M. Dhabarde Pharmaceutical
Chemistry
25. Naushin Nabi Maladhari Synthesis of benzylidene acetophenone derivatives. Ms. Disha M. Dhabarde Pharmaceutical
Chemistry
26. Niranjan Dhondiba
Bachewad
Evaluation of wound healing activity of herbal formulation
in comparison with marketed sample.
Ms. Ashwini R. Ingole Pharmaceutics
27. Nisha Chandramani
Meshram
Anxiolytic potential of acetone extract of Rubia cardifolia
Linn. on wistar albino rat.
Mr. Satish S. Meshram Pharmacognosy
28. Onkar Ramu Markunde Bateriological evaluation of drinking water samples from
different sources.
Dr. Parimal P. Katolkar Pharmaceutics
29. Payal Bharat Borkute Pharmacological development of thiazolidinones as
analgesics.
Dr. Deweshri R. Kerzare Pharmaceutical
chemistry
3. 30. Pooja Prakash Rathod Study of WHO and AYUSH Guidelines for safety
monitoring of natural medicine.
Dr. Pravinkumar B. Suruse Pharmacognosy
31. Prachi Pramod Pahade Synthesis of metal complex of 2-chloromethyl
benzimidazole derivative.
Dr. Parimal P. Katolkar Pharmaceutical
chemistry
32. Pragati Ganesh Ashtankar Formulation and evaluation of herbal cream. Ms. Ashwini R. Ingole Pharmaceutics
33. Prajakta Chandreshekhar
Dukare
Investigation of antibacterial potentials of natural product
extract in rat model.
Ms. Shilpa S. Borkar Pharmacology
34. Pranay Gunvanta Gautre A comparative evaluation of Marketed preparation of
Ashwagandha and Bramhi for anxiolytic activity.
Ms. Seema B. Wakodkar Pharmacology
35. Pranay Prem Adkine Exploring thiazolidinone derivatives for analgesic activity. Dr. Deweshri R. Kerzare Pharmaceutical
chemistry
36. Pratik Narendrarao Jadhao A review on Arka Kalpana. Mr. Lokesh T. Thote Pharmaceutical
chemistry
37. Pratiksha Bhikachande
Mundada
Formulate and evaluate topical gel of methanolic extract of
Cyperus rotundus for arthritis.
Mr. Satish S. Meshram Pharmaceutics
38. Pratiksha Suresh Makode Formulation and evaluation of herbal tablet for
hypertension.
Dr. Mahendra C. Gunde Pharmaceutics
39. Priyanka Dorwe Evaluation of in-vitro anti-inflammatory potential of
Acacia auriculiformis bark extract.
Mr. Manish A. Kamble Pharmacognosy
40. Rahul Yadaorao Kapse Synthesis of novel chalcone from 4-amino acetophenone. Ms. Disha M. Dhabarde Pharmaceutical
Chemistry
41. Rahuri Nanaji Deshbhratar Formulation of polyherbal antidiabetic suspension. Mr. Pradeep S. Raghatate Pharmaceutics
42. Ravikant Dilip Sakore Synthesis of zinc oxide nanoparticles from fruit extract of
Acacia auriculiformis.
Ms. Disha M. Dhabarde Pharmaceutical
Chemistry
43. Reena Gangadhar Bansod Formulation and evaluation of carrot beet root beverages as
probiotics.
Dr. Deweshri R. Kerzare Pharmaceutics
44. Rohan Dnyaneshwar Rathod Corona: Current status. Ms. Seema B. Wakodkar Pharmacology
45. Rushabh Prabhakar
Vairagade
Synthesis of some acetophenone and benzaldehyde
derivatives.
Dr. Parimal P. Katolkar Pharmaceutical
chemistry
46. Saloni Abhay Sakharwade Preparation and evaluation of ethosomes of some oils. Mr. Lokesh T. Thote Pharmaceutical
chemistry
4. 47. Sarang Anil Waghe Investigation of in vivo anti-infective potentials of some
common aqueous extracts.
Ms. Shilpa S. Borkar Pharmacology
48. Sarvesh Baban Fuke Design, synthesis and characterization of some Schiff’s
base containing phenylhydrazine compounds: screening of
antimicrobial potential.
Mrs. Ruchi S. Shivahare Pharmaceutical
chemistry
49. Sayali Ravindra Kotpalliwar Formulation and evaluation of polyherbal hair oil. Mrs. Ruchi S. Shivahare Pharmaceutics
50. Sejal Dilip Gadpalliwar Formulation and evaluation of polyherbal shampoo. Mrs. Ruchi S. Shivahare Pharmaceutics
51. Shailesh Sharwanji Rewatkar Evaluation and Comparison of antidandruff shampoos. Ms. Ashwini R. Ingole Pharmaceutics
52. Shejal Subhash Nikam Process automization in pharmaceutical industry with
specific reference to manufacturing of tablets.
Dr. Pravinkumar B. Suruse Pharmaceutics
53. Shubham Pankaj Singh Derivatization of natural products: A review. Mr. Pradeep S. Raghtate Pharmaceutical
chemistry
54. Shweta Bandu Kothe Review on Ranitidine, a cancer-causing agent. Mr. Lokesh T. Thote Pharmaceutical
chemistry
55. Shweta Rajesh Jaiswal Synthesis of metal complex of 2-chloromethyl
benzimidazole derivative.
Dr. Parimal P. Katolkar Pharmaceutical
chemistry
56. Simran Noordin Panjwani Scientific studies on Ficus religiosa. Dr. Jagdish R. Baheti Pharmacognosy
57. Sonali Prabhakar Derkar Formulation and evaluation of herbal gel. Ms. Ashwini R. Ingole Pharmaceutics
58. Supriya Sukhlalji Barewar Evaluation of analgesic activity of clove oil. Ms. Seema B. Wakodkar Pharmacology
59. Suraj Moundekar Use of computers in Pharmaceutical formulation
development.
Dr. Pravinkumar B. Suruse Pharmaceutics
60. Swati Devendra Shivankar Phytochemical screening and wound healing activity of
hydroalcoholic extract of Bergenia ligulata.
Mr. Satish S. Meshram Pharmacognosy
61. Sandhya Ram Exploring the antimicrobial traditional knowledge for
antiinfective activity in animal model.
Ms. Shilpa S. Borkar Pharmacology
62. Tejashree Waman Idhole 3D printing in Pharmaceutics: A novel tool for designing
customized drug activity system.
Dr. Pravinkumar B. Suruse Pharmaceutics
63. Tushar Sadanand Giri Investigating the gram positive and gram-negative
bactericidal effects of few common plant extract in rats.
Ms. Shilpa S. Borkar Pharmacology
64. Ujwala Vasanta Derkar Evaluation of analgesic potential of Acacia auriculifurmis. Mr. Pradeep S. Raghatate Pharmacognosy
5. 65. Vaishanavi Umakant
Nimbalkar
In vitro anti-inflammatory evaluation of Acacia
auriculiformis.
Mr. Manish A. Kamble Pharmacognosy
66. Vaishnavi Giridhar Vaidya Design, synthesis and characterization of 2-[(E)-4-[(Z)-
phenylmethylidene]aminophenyl)diazinyl]naphathalen-1-ol
Mrs. Kavita R. Pandey Pharmaceutical
Chemistry
67. Vikas Madhavrao Rathod Formulation and evaluation of herbal tablet for cancer. Dr. Mahendra C. Gunde Pharmaceutics
68. Vishvajit Rajeshwar Shelke Evaluation of polyherbal antidiabetic suspension. Mr. Pradeep S. Raghatate Pharmaceutics
69. Vrushali Subhash Pachpor Artificial intelligence robotics and computational fluid
dynamics.
Dr. Pravinkumar B. Suruse Pharmaceutics
Date: 09-03-20 Name & Signature of Principal with Seal
6. pctaik orProi..t Ren.rt B. Plra.m VIII Sem Surnnrer 20l9 Exarn
N!me orlrstitute: KaDla Nelnu Coll.g. ofPl!armacy, Butibori, Nagptrr.
Mi.roballons a d.usdelivc.yy*em
l svnrhesir :nd eviltr:ii.n.r 2-.hl.r.
methyl b€nzinidazole derivativ€ or
Synthesis and biological evaluation or2
.hlnr. methvlhenihid,T.!p
Formulate herbal paste and evaluare
antimicrob jal a.tivity.ontaining
3 D printing in phamraceuticak A new
standardrzalion olsome ma.keted
f.rnu!:tion Trlhla.burn:
lr Fev'ew on an!.an.er herbrl druss
Synthesis and antimi.r.bial adivity ol 2'
.hloro methvl benrimrd.zole
Development olanalytjcal method for
qualily by desisn in pharmaceuticals
t2 Cold nanoparticles lor tarseted delivery
ofdruss to lumo6: a review
Conparanve evaluatron of CNS $ihulant
HrrbstLt,uB for n! nc fluc.: rcv rw
r5 Extnction and phltocbemical
investigation of steD bark of bauhinia
Synlhesrs and evaluatron ollndole based
new s.2f lold for :ntimi.rohi:l :.tivitu
To sy.rhesize 1-(2-hyd.oxy-1,2-diphenyl
ethyldene) 3 phenyl throurea &evaluate
for 3ntimi.robi:l 3divitv.
Bonbax .eiba LDit pulp as nedi.i.al
7. canem lantana pla.t e!t.act of hediated
synthesis of silver nanopa.ti.les ahd i6
22 22 Solubrlrry enhan.emenrorN'redLII'ne
Development of wound healin3.ream
f..'nulari.n arom vrri.ns herh:l arrr:.i
2.1 F.rnrulanon of herhal.hurn:
Formulation and €valuadon of hsrbal
Formulation and evaluation of
multipu.pose hprbal cream
Synthesis ol 3-(((4-[1.3-d joxoisoindolin.
2 yll phenyl) hydroxyl) methylenel
amino).4'methyl benzoic acrd and its
lmpact olNeut.a.euti.ak on hcalth.are
Dvaluahon of herbal anhbacterial gel
Ircvjew oh ehereen(y rreatnrent
EvaluatioD of antianxiety a.iivity ol
A re iew on wound healnB herbs
Fo.mulation and evaluatioh oI fuhgal gel
lt l1
Synthesis ol4 benzamide-N' (2.4.
dinilIophe.yll benzohydrazoni. a.id and
ca.ry out its anrimicrobial activitv
Synthesis of antibacteial a.tiviry of 2.
chloro melhyl benzimidazole derivatives.
Synthes6 and annnicrobial aclivity of
Sch,ff base containinp Dhenvlthiourea.
Nano.apsules: a .ovel druE delivery
Ealuatio. of analgesic a.tiviry or
coriander fruit ext.act in rats
Rolc of novel polyner in drug delivery
Indole*cafiold Ior diverse
pharma.olosical import nce
Evaluarjon.lpdt.nhahng effe.r of herhal
druAs io the rre3tnent olanxrety.
Eval0aLion of l'.rbal anrlbrLteoal ge
Formulation and evaluatio. of
anlimicrobial gel cream with hntana
8. r5 S!andardizanon ofsome Iood stufito
,14 Fornulation and evaluanon of an!i
infl ammatory cran using psidium guava
To synthesize and evaluate lhe
a.timicrobial activiry of Z N-Benzoyl 4'
(2 (2.4 dinit.o phenyl)hyd.azinyl
henT:midi. :.id deriverivPr
Crnsens: An rnmunonodulalor in
Formulalion and evaluation of
Dolvherbal tablet use Ior multiDurDose
Slandardizatioh of soho marketed
To formulate a.d eval!ate polyhe.bal
5l A review on Licuid biopsy in can.er
Evaluation of antini.rob'31 potennal of
Lantana camera seed DulD extract
compa.ative a$esshent otaninrcrobral
effi.a.v ordif ferenr hand s3nihzerr
l0 '1
& siAn,ture of Princip.l with se.l
9. Details of Project Report B.Pharm VIII Sem
Name of Institute: Kamla Nehru College of Pharmacy, Butibori, Nagpur
Sr.
No.
Name of the student Title of Project Name of
Supervisor
Broad Area
1. Mr. Abhijit Narendra Daf To study the phytochemical
screening of guava seed extract.
Mr. L. T. Thote Pharmaceutical
Chemistry
2. Ku. Abhilasha Premlal
Ikhar
Enhancement of solubility and solid
dispersion technique
Mr. A. Y. Kanugo Pharmaceutics
3. Mr. Akshay Vijayrao
Malve
Development of nutritive biscuits
with herbal extract
Mr. M. C. Gunde Pharmacognosy
4. Ku. Ankita Subhash Pote Transdermal patches: A review Ms. A. R. Ingole Pharmaceutics
5. Mr. Anshu Thansing
Bisen
Development of natural herbal
insect repellent formulation.
Mrs. R.S. Shivhare Pharmacognosy
6. Mr. Ashish Sahadeo
Nemade
Effect of micronutrient application
through seed treatment
Dr. P. P. Katolkar Pharmacognosy
7. Mr. Ayush
Gautamprashad Sharma
Evaluation of adipic acid containing
pH-independent release matrix
tablet.
Ms. N. A. Arsod Pharmaceutics
8. Mr. Balkrushna Mohanrao
Daf
Comparative phytochemical studies
of different colour flowers of
Nerium oleander
Mr. M. C. Gunde Pharmacognosy
9. Mr. Chetan Diliprao Chute Formulation and evaluation of
antibacterial polyherbal dentifrices
Mr. S. S. Meshram Pharmacognosy
10. Mr. Dinesh Bhaskar
Kamdi
Drug solubility, Importance and
Enhancement techniques
Dr. P. B. Suruse Pharmaceutics
11. Ku. Dipti Ruprao Gurmule Enhancement of bioavailability of
Nebivolol HCl by liquisolid compoq
method
Mr. A. Y. Kanugo Pharmaceutics
12. Mr. Ganesh Balkrushnaji
Thombare
Formulation and evaluation of
polyherbal toothpaste
Mr. S. S. Meshram Pharmacognosy
13. Mr. Gaurav Sanjayrao
Mude
Evaluation of antianxiety and
antidepressant effect of herbal drug
extract
Ms. S. B.
Wakodkar
Pharmacology
14. Ku. Harpreet Kaur
Kripalsing Rajput
Synthesis of 4-(4-substituted
phenyl)-N- (4 substituted
benzylidene oxazole 2-amine
Ms. D. M.
Dhabarde
Pharmaceutical
Chemistry
15. Ku. Madhuri Sarangdhar
Chopde
Standardization of some marketed
herbal products used in arthritis
Mr. M. A. Kamble Pharmacognosy
16. Ku. Mayuri Radheshyam
Mane
Standardization of some marketed
herbal products used in diabetes
Mr. M. A. Kamble Pharmacognosy
17. Mr. Narendra Netram
Rahangdale
In vitro anti-inflammatory activity
of guava seed extract
Mr. L. T. Thote Pharmaceutical
Chemistry
18. Ms. Nayan Ashok Mule Painless insulin drug delivery
system: A review
Ms. S. B.
Wakodkar
Pharmaceutics
19. Ku. Nidhita Sharad
Kamble
Synthesis of 4-(4-substituted
phenyl) oxazole 2-amine
Ms. D. M.
Dhabarde
Pharmaceutical
Chemistry
20. Mr. Pawan Bramhadeo Design and evaluation of polyherbal Mrs. R. S. Shivhare Pharmacognosy
10. Tripathi cream for wound healing potential
21. Ku. Poonam Janardan
Karadbhajane
Metallopharmaceutical : A novel
approach for treatment of disease
Ms. D. M.
Dhabarde
Pharmaceutical
Chemistry
22. Ku. Pooja Sureshrao
Kothekar
Evaluation of Lagestromia speciosa
root extract gel
Ms. S. S. Borkar Pharmaceutics
23. Ms. Prachi Nagorao
Bhoge
Evaluation of anthelmentic potential
of fresh fruit flesh of Terminalia
catappa
Mr. M. A. Kamble Pharmacognosy
24. Ku. Purva Sanjay Bankar Screening of antianxiety activity of
Lagestromia speciosa leaves extract
Ms. S. S. Borkar Pharmacology
25. Mr. Rahul Ramdas Barai Studies of physiochemical
parameters of dripping water from
air conditioning units and its
bacteriological aspects
Mr. M. A. Kamble Pharmacognosy
26. Mr. Ratikesh A.
Wawarkar
Formulation and evaluation of
ayurvedic tablet
Mr. M. C. Gunde Pharmacognosy
27. Ku. Rohini Manohar
Chafle
Modified release oral dosage form :
A review
Mr. M. D. Godbole Pharmaceutics
28. Mr. Rohitkumar
Rameshrao Kale
Design and evaluation of pH
independent controlled release tablet
Mr. N. A. Arsod Pharmaceutics
29. Ku. Ruchita Gulab Lanje Formulation and evaluation of
herbal dye from leaves of Barelia
prionitis, Beta vulgaris leaves ,
hibiscus and amla leaves.
Mrs. K. R. Pandey Pharmaceutical
Chemistry
30. Mr. Sagar Chintaman
Kamble
A review on recent approaches in
taste masking technologies and their
regulatory considerations
Dr. P.B.Suruse Pharmaceutics
31. Ms. Sanket Ashokrao
Manekar
Formulation of gel from
Lagestromia speciosa root extract
Ms. S. S. Borkar Pharmaceutics
32. Ku. Shailaja Arvind
Latkar
Pharmacological properties of
Tabernaemontana divaricata: A
review.
Ms. S. B.
Wakodkar
Pharmacology
33. Mr. Shubham Sunilji
Balpande
Formulation and evaluation of fast
dissolving tablet
Mr. A. Y. Kanugo Pharmaceutics
34. Ku. Sonali Suresh Bobde Floating tablet: An approach of
gastroretentive drug delivery system
Mr. M. D. Godbole Pharmaceutics
35. Ku. Sonia Latif Gill Osmotically controlled drug
delivery system: A review
Ms. A. R. Ingole Pharmaceutics
36. Ku. Suchita Sanjayrao
Kale
In-situ gel: A Novel approach for
drug delivery: A review
Mr. M. D. Godbole Pharmaceutics
37. Ku. Surbhi Rajendra
Warokar
Formulation and in-vitro evaluation
of fluconazole gel containing
groundnut oil
Mr. S. S. Meshram Pharmacognosy
38. Mr. Suvek Anilrao
Sontakke
Formulation and evaluation of
herbal moisturizer
Mr. M. C. Gunde Pharmacognosy
39. Ms. Sweeti Surybhan
Kamde
Effect of micronutrient on seed
treatment on seedling growth
Mr. M. D. Godbole Pharmacognosy
40. Ku. Tanvi Mahendra
Anandpara
Screening of anti-nociceptive
activity of Lagestromia speciosa
leaves extract
Ms. S. S. Borkar Pharmacology
11. 41. Ku. Vaishanavi Suresh
Barapatre
Formulation and evaluation of
polyherbal hair dye from amla beet
root, butea monosperma flowers,
curry leaves.
Ms. K. R. Pandey Pharmacognosy
42. Ku. Vidya Shrikrushna
Kukde
Standardization and phytochemical
screening of Ficus religiosa
Dr. J. R. Baheti Pharmacognosy
43. Ku. Vijaya Jagannath
Gaidhane
Microsponge – novel drug delivery
system: A review.
Ms. A. R. Ingole Pharmaceutics
44. Mr. Vrushabh Giridhar
Sontakke
Physiochemical and phytochemical
investigation of methanolic and
hydro alcoholic extract of Bauhnia
purpuria stem bark
Mr. S. S. Meshram Pharmacognosy
45. Mr. Yogesh Maroti
Rewatkar
Formulation and evaluation of
herbal chocolate
Mr. M. C. Gunde Pharmacognosy
12. RASHTRASANT TUKADOJI MAHARAJ NAGPUR UNIVERSITY, NAGPUR
STATEMENT OF THE CANDIDATE WHO HAVE SUBMITTED THEIR DISSERTATION REPORT FOR FOLLOWING EXAMIN
SUMMER, 2019
College Name: Kamla Nehru College ofPharmacy, Butibori, Nagpur-441108
Specialization: Pharmaceutics
Faculty: Science & Technology
Sr.No Enrollment No. Name of student PG Teacher Letter Name of topic Name of guide
Details
C.S./2125
Dt:-01/07/2013
2012016600798277 | Ms. Pooja M. meshramn Formulation evaluation and validation of herbal| Mr. MangeshD.
anti arthritic transdermal patch
Formulation evaluation and validation of Mr. MangeshD. (
analgesic herbal emulgel, ointment and oil
Formulation evaluation and validation of herbal Mr.Mangesh D.
antacid suspension
2 Provisional Mr. Rupesh M. Borlawar C.S./2125
Dt:-01/07/2013
2011016600401172 Ms. YogitaM.Rahangdale C.S./2125
Dt:-01/07/2013
4 2015016601156115 Mr. Akshay R. Ladke C.S./2125 Formulation and evaluation of fast dissolving
buccal film of Sumatriptan succinet
Mr. Mangesh D.
Dt:-01/07/2013
Date:
Borthed
S e t e
PRI
Place: KAMLA NEHAU CO
BUTIBORI,1
13. RASHTRASANT TUKADOJI MAHARAJ NAGPUR UNIVERSITY, NAGPUR
STATEMENT OF THE CANDMATE WO HAVE SUBMITTED THEIR DISSERTATION REPORT FOR FOLLOWING EXAMD
SUMMER, 2019
College Name: Kamla Nehru College of Pharmacy, Butibori, Nagpur-441108
Specialization: Pharmaceutics
Faculty: Science & Technology
Sr.No Enrollment No. Name of student PG Teacher Letter Name of topic
Name of guide
Details
C.S./2125
Provisional
Ms. Vanashri S. Turke
Formulation and evaluation of controlled release Mr. Mangesh D
Dt:-01/07/2013 matrix tablets of Tramadol HCI
Formulation and evaluation of Metformin mouth Mr. Mangesh D
dissolving tablets
Formulation evaluation and optimization of Mr. MangeshD
extended release tablets of Lornoxicam
2012016601016117 Ms. PritiD.Gharde C.S./2125
Dt:-01/07/2013
2
C. 2125
3 2012016601135603 Mr. Kunal D. Bisen
Dt:-01/07/2013
Ph
Date:
colege
Place
KAMLA NEHRU CC
BUTIBOR,
14. RASHTRASANT TUKADOJI MAHARAJ NAGPUR UNIVERSITY, NAGPUR
STATEMENT OF THE CANDIDATE WHO HAVE SUBMITTED THEIR DISSERTATION REPORT FOR FOLLWING EXAMN
SUMMER, 2019
College Name: Kamla Nehru College of Pharmacy, Butibori, Nagpur-441108
Specialization: Pharmaceutical Chemistry
Faculty: Science & Technolo;
Sr.No EnrollmentNo. Name of student PG Teacher Name of topic Name of
Letter Details
C.S./1839
Dt:-30/05/2013
1 201501660171 1963 Mr. Amol A. Koche. Development of Analytical Method for Simultaneous Ms. D. M
Estimation of Pregabalin and Nortriptyline in bulk and
marketed formulations
2015016601711955 Mr.SwapnilM.Kamble C.S./1839 Synthesis and Characterisation of Metal Complexes of | Ms. D. M
Schiff Bases containing 2,4,- Disubstituted Oxazole Ring
as Potential Anti- inflammatoryagents
Dt:-30/05/2013
Date:
Colege
6
Place:
KAMLA NEHAU
b u t i n i
Nagaun
BUTIBO
15. RASHTRASANT TUKADOJI MAHARAJ NAGPUR UNIVERSITY, NAGPUR
STATEMENT OF THE CANDIDATE WHO HAVE SUBMITTED THEIR DISSERTATION REPORT FOR FOLLWING EXAMI
SUMMER, 2019
College Name: Kamla Nehru College of Pharmacy, Butibori, Nagpur-441108
Specialization: Pharmaceutical Chemistry Faculty: Science & Technole
Sr.No Enrollment No. Name of student PG Teacher Name of topic Name of
LetterDetails
12015016602186412 Ku. Kajol S. Hinganikar C.S./1839 Design, Synthesis and Biological Evaluation of Some Ms.D.M
Dt:-30/05/2013 Novel 2-Amino-benzimidazole Derivative for
Antimicrobial Activityy
Design, Synthesis and Evaluation of Some Novel Histone
Deacetylase Inhibitor as an Antimicrobial Agents
2015016602186482 Ku. MonikaP. Maske
2 C.S./1839 Ms. D. M
Dt:-30/05/2013
3 2012016600904687 Ku. Vaishanvi S. Khante C.S./1839 Stability Indicating Analytical Method Development and Ms.D.M
Dt:-30/05/2013 Validation for Estimation of Topical Corticosteroid in
Ointment Formulation by RP-HPLC
C.S/18399
Dt:-30/05/2013 bis-Phthalimides
4 Provisional Mr. Vinayak M. Shejol Synthesis and Antimicrobial Screening of Some Novel | Ms. D. M
I l e g e
P
Date:
Place: KAiLA NEHRU CO
BUTIBORI,
eu
16. RASHTRASANT TUKADOJI MAHARAJ NAGPUR UNIVERSITY, NaGPUR
STATEMENT OF THE CANDIDATE WHO HAVE SUBMITTED THEIR DISSERTATION REPORT FOR FOLLWING
EXAMINATION OF SUMMER, 2018
College Name: Kamla Nehru College of Pharmacy, Butibori, Nagpur-441108
Specialization: Pharunaceutical Chemistry Faculty: Medicine
Sr.No Earollment No Name of student Name of topic Name of guide
201501660171195 Mr. Swapnil M. Kamble Synthesis and Characterisation ofMetal Complexes of Ms. D. M. Dhabarde
Schiff Bases containing 2,4,- Disubstituted Oxazole
Ring as Potential Anti- inflammatory agents.
2015016601711963 Mr. Amol A. Koche. Development of AnalyticalMethodfor Simultaneous Ms. D.M. Dhabarde
Estimation ofPregabalin and Nortriptyline in bulk and
marketed formulations.
PRINCIPAL
KAMLA NEARU COLLEGE OF PARACY
&TBORI, NAGFUR4A1
Date:
R r t t
(Sate
Place:
20218
Ash/kakde d
17. RASHTRASANT TUKADOJI MAHARAJ NAGPUR UNIVERSITY, NAGPUR
STATEMENT OF THE CANDDATE WHO HAVE SUBMITTED THEIR DISSERTATION REPORT FOR FOLLWING
EXAMINATION OF SUMMER, 2018
College Name: Kanila Nehru College of Pharmacy, Butibori, Nagpur-441108
Specializatiou: Pharmaceutics Faculty: Medicine
Name ofstudent Name of topie Name ofguide
Sr.No nroliment No.
2012016600924846 Bvaluation ofeffectsof simultaneous consumption of Mr. M.D. Godbole
beverages on the release profile of antihypertensive
Gancsh T. jumle
Atd
drug
PAINCIPAL
KAMLA NEMRU COLLEGE OF PHARMACY.
BUTIBORI,NAGPUR-441108 2 0 2 - 1 8
18. RASHTRASANT TUKADOJI MAHARAJ NAGPUR UNIVERSITY, NAGPUR
STATEMENT OF THE CANDIDATE WHO HAVE SUBMITTED THEIR DISSERTATION REPORT FOR FOLLWING
EXAMINATION OF SUMMER, 2017
College Name: Kamla Nehru College ofPharmacy,Butibori, Nagpur-441108
Specialization: Pharmaceutical Chemistry
Faculty: M
Sr.No EnrollmentNo._
| 1.
Name of student
Mr. Prasad P. Kathade
Name oftopic
Synthesis of NewThiazole Derivatives and Evaluation
of their Antimicrobial Potential.
Name ofguide
Ms. D. M. Dhaba
2014016601151287
2015016601711955
Ms. D. M. Dhaba
Synthesis and Characterisation of Metal Complexes of
Schiff Bases containing 2,4,- Disubstituted Oxazole
Ring as Potential Anti- inflammatory agents.
2.
Mr. Swapnil M. Kamble
Development of Analytical Method for Simultaneous
Estimation of Pregabalin and Nortriptyline in bulk and
marketed formulations.
Ms. D. M. Dhaba
. 2015016601711963 Mr. Amol A. Koche.
O orFICIATINGPRiNP
Date: 30||201
Place: Buiboi, Naqpm
KAMLA NSHRU
COLLEGE
CE
BUT!8C,
har
19. RASHTRASANT TUKADOJI MAHARAJ NAGPUR UNIVERSITY, NAGPUR
STATEMENT OF THE CANDIDATE WHO HAVE SUBMITTED THEIR DISSERTATION REPORT FOR FOLLWING
EXAMINATION OF SUMMER, 2015
College Name: Kamla Nehru College ofPharmacy, Butibori, Nagpur-441108
Specialization: Pharmaceutics
Faculty: Medicine
Sr.No Enrollment No. Name of student Name of topic
Name of guide
2013016600446041
Mr. Mangesh Godbole
Formulation evaluation and optimization of tablets
containing poorly water soluble drug by moisture activated
drygranulation method.
Design and evaluation of selfemulsifying drug deivery
system ofanti-hypertensive drug
Solubility enhancement of poorly water soluble drug b
solid dispersion method.
Design optimization and evaluation ot tloating microspheres Mr. Mangesh Godbole
ofantiulcer drug
Design and evaluation of topical gel containing plant
enzymefor woundhealingactivity.
Formulation and evaluation ofantipsoriatictopical gel.
Ameya Manohar Lanjewar
2. 2013016600446087 Aslam Shakeel Riyaz
Mr. Mangesh Godbole
3. 2013016600446072 Priyanka Vijay Ingle
M: Mangesh Godbole
4.
2013016600446033 Devender Sharma
Mr. Mangesh Godbole
2012016600924815
Dipmala R Choudhari
Mr. Mangesh Godbole
6.
2012016600924831
Arvind Bhagwan Fulzele
Date: 31/07/2014
Place: Butibori
PRINCIPAL
lege
of Kamia Nahru College of PharmaCy
Borkned (Gte) Butibori Nagour