Supercritical Fluid Chromatography (SFC) is a highly adaptable and potent technology for the analysis of complicated mixtures, and it stands as the epitome of separation science.
Pharmagupshup supercritical fluid chrometography and flash chromatography p...Hitesh Katariya
The document discusses supercritical fluid chromatography (SFC), including its principles and applications. SFC uses supercritical fluids like carbon dioxide as the mobile phase. It provides advantages over gas chromatography and liquid chromatography like being faster, more cost effective, and allowing better separation of some compounds. The document explains the instrumentation, process, and properties of supercritical fluids. It also gives examples of SFC applications in analyzing natural products, drugs, pesticides, lipids, and other compounds.
HPLC and its relation with mass spectroscopy IronMerc1
This document describes a PowerPoint presentation on HPLC and its relationship to mass spectrometry. The presentation was created by a group of students for their 4th semester course. It introduces HPLC and how it separates mixtures based on interactions with stationary and mobile phases. It then explains how HPLC can be combined with mass spectrometry (LC-MS) to further analyze separated compounds. The presentation covers operating principles, applications in fields like forensics and pharmaceuticals, examples of research using the techniques, and concludes that LC-MS is widely used for qualitative and quantitative analysis in various industries and research.
Difference between HPLC and HPTLC and Applications.Chothish Jayaram
HPLC and HPTLC are two types of automated chromatographic techniques used to separate components of a mixture. The main difference is that HPLC uses a column filled with a solid stationary phase, while HPTLC uses a solid stationary phase fixed to a plate. HPLC produces results with high efficiency and resolution, while HPTLC produces moderately resolved but high-efficiency results. Both techniques have applications in fields like pharmaceutical analysis, herbal drug identification, and forensic analysis.
This document presents information on preformulation studies, which involve characterizing the physicochemical properties of new drug molecules. The objectives are to generate stability and bioavailability data for formulation development. Key studies discussed include analyzing bulk properties, solubility, partitioning, hygroscopicity, ionization, dissolution, stability, and compatibility. Analytical techniques like spectroscopy, microscopy, thermal analysis, and chromatography are used to investigate properties and purity. Thorough preformulation provides critical information for designing dosage forms that are stable, safe, and effective.
A brief review on development and validation of hplc method.adhirajain
the slides in the ppt gives a brief review on product development and its validation in HPLC method. Contents are with advantages, disadvantages, application , classification and methods for development.
HPLC is a type of liquid chromatography that is used to separate, identify, and quantify components in a mixture. It works by forcing a pressurized liquid mobile phase through a column packed with solid particles or porous material. Samples are injected into the column and the different components interact differently with the stationary phase, causing them to elute from the column at different rates and allowing separation. HPLC provides efficient, high resolution separations and is commonly used in fields like pharmaceutical analysis and quality control due to its ability to analyze complex mixtures.
This document provides information about High Performance Liquid Chromatography (HPLC) and Gas Chromatography. It discusses the basic principles, instrumentation, and applications of HPLC, including the types of columns, mobile phases, pumps, injectors, detectors, and data acquisition systems used. It also summarizes the basic principles of Gas Chromatography, where a gas mobile phase is used to separate components of a vaporized sample based on interactions with a stationary phase. Key applications of HPLC mentioned include pharmaceutical analysis, environmental monitoring, clinical analysis, and food and flavor analysis.
Pharmagupshup supercritical fluid chrometography and flash chromatography p...Hitesh Katariya
The document discusses supercritical fluid chromatography (SFC), including its principles and applications. SFC uses supercritical fluids like carbon dioxide as the mobile phase. It provides advantages over gas chromatography and liquid chromatography like being faster, more cost effective, and allowing better separation of some compounds. The document explains the instrumentation, process, and properties of supercritical fluids. It also gives examples of SFC applications in analyzing natural products, drugs, pesticides, lipids, and other compounds.
HPLC and its relation with mass spectroscopy IronMerc1
This document describes a PowerPoint presentation on HPLC and its relationship to mass spectrometry. The presentation was created by a group of students for their 4th semester course. It introduces HPLC and how it separates mixtures based on interactions with stationary and mobile phases. It then explains how HPLC can be combined with mass spectrometry (LC-MS) to further analyze separated compounds. The presentation covers operating principles, applications in fields like forensics and pharmaceuticals, examples of research using the techniques, and concludes that LC-MS is widely used for qualitative and quantitative analysis in various industries and research.
Difference between HPLC and HPTLC and Applications.Chothish Jayaram
HPLC and HPTLC are two types of automated chromatographic techniques used to separate components of a mixture. The main difference is that HPLC uses a column filled with a solid stationary phase, while HPTLC uses a solid stationary phase fixed to a plate. HPLC produces results with high efficiency and resolution, while HPTLC produces moderately resolved but high-efficiency results. Both techniques have applications in fields like pharmaceutical analysis, herbal drug identification, and forensic analysis.
This document presents information on preformulation studies, which involve characterizing the physicochemical properties of new drug molecules. The objectives are to generate stability and bioavailability data for formulation development. Key studies discussed include analyzing bulk properties, solubility, partitioning, hygroscopicity, ionization, dissolution, stability, and compatibility. Analytical techniques like spectroscopy, microscopy, thermal analysis, and chromatography are used to investigate properties and purity. Thorough preformulation provides critical information for designing dosage forms that are stable, safe, and effective.
A brief review on development and validation of hplc method.adhirajain
the slides in the ppt gives a brief review on product development and its validation in HPLC method. Contents are with advantages, disadvantages, application , classification and methods for development.
HPLC is a type of liquid chromatography that is used to separate, identify, and quantify components in a mixture. It works by forcing a pressurized liquid mobile phase through a column packed with solid particles or porous material. Samples are injected into the column and the different components interact differently with the stationary phase, causing them to elute from the column at different rates and allowing separation. HPLC provides efficient, high resolution separations and is commonly used in fields like pharmaceutical analysis and quality control due to its ability to analyze complex mixtures.
This document provides information about High Performance Liquid Chromatography (HPLC) and Gas Chromatography. It discusses the basic principles, instrumentation, and applications of HPLC, including the types of columns, mobile phases, pumps, injectors, detectors, and data acquisition systems used. It also summarizes the basic principles of Gas Chromatography, where a gas mobile phase is used to separate components of a vaporized sample based on interactions with a stationary phase. Key applications of HPLC mentioned include pharmaceutical analysis, environmental monitoring, clinical analysis, and food and flavor analysis.
HPLC BMLT/ DMLT High Performance Liquid ChromatographyMdShamsTabrez4
Chromatography is a separation technique used to separate and analyze the components of a mixture. It involves the distribution of the components between two phases: a mobile phase and a stationary phase. The different affinities of the components for these phases lead to their separation based on their physical or chemical properties.
This document discusses several chromatography techniques used in forensic science analysis, including high performance liquid chromatography (HPLC), gas chromatography (GC), and inductively coupled plasma mass spectrometry (ICP-MS). It describes the basic principles, instrumentation components, and applications of each technique. HPLC uses high pressure to separate mixtures based on interactions with a stationary and mobile liquid phase. GC separates volatile compounds using an inert gas mobile phase and liquid stationary phase. ICP-MS uses plasma to ionize elements and masses to identify unknown samples at very low concentrations.
Chiral analysis and separation refers to the analysis and separation of chiral molecules that are mixed together using analytical techniques like chromatography and spectrometry. It is important because single enantiomers of chiral drug molecules and agricultural chemicals often have different effects on the human body and environment. Advanced equipment and technologies like high performance liquid chromatography (HPLC), gas chromatography (GC), supercritical fluid chromatography (SFC), and capillary electrophoresis (CE) are commonly used for chiral separations and analysis. BOC Sciences provides chiral analysis and separation services using state-of-the-art equipment and a dedicated team of experts.
1. Supercritical fluid chromatography is a form of normal phase chromatography that uses supercritical fluids like carbon dioxide as the mobile phase.
2. It has properties between liquid and gas with low viscosity and high diffusivity, allowing for more rapid separations compared to HPLC.
3. Applications include separation of chiral molecules, purification in pharmaceutical industry, and identification of pesticides and other compounds.
ntroduction to Chromatography
Chromatography is a powerful analytical technique used to separate, identify, and quantify the components of a complex mixture. This versatile method is widely used across numerous scientific fields, including chemistry, biology, environmental science, and forensics. At its core, chromatography relies on the differential distribution of analytes between a stationary phase and a mobile phase, allowing for the efficient separation and precise analysis of even the most intricate samples.
The underlying principle of chromatography is the difference in the affinity of various compounds for the stationary and mobile phases. As the sample is introduced into the system, the individual components are carried by the mobile phase and interact with the stationary phase, resulting in their differential migration and separation. This process enables scientists to not only identify the presence of specific compounds but also measure their relative concentrations with remarkable accuracy.
History and Development of Chromatography
The origins of chromatography can be traced back to the early 20th century, when the Russian botanist Mikhail Tsvet first introduced the concept in 1903. Tsvet used a glass column packed with calcium carbonate to separate plant pigments, such as chlorophyll and carotenoids, by their differential adsorption onto the stationary phase. This pioneering work laid the foundation for the development of various chromatographic techniques that would revolutionize the field of analytical chemistry.
In the following decades, chromatography continued to evolve, with scientists exploring different stationary phases, mobile phases, and separation mechanisms. The introduction of paper chromatography by Archer John Porter Martin and Richard Laurence Millington Synge in the 1940s, and the subsequent development of thin-layer chromatography (TLC) and gas chromatography (GC) in the 1950s, further expanded the capabilities of chromatographic analysis. These techniques allowed for the separation and identification of an increasingly diverse range of compounds, from small organic molecules to complex biomolecules.
The 1960s and 1970s witnessed a significant breakthrough with the introduction of high-performance liquid chromatography (HPLC), which provided higher resolution, sensitivity, and speed compared to earlier chromatographic methods. The continuous advancements in column technology, detection syst
Bioanalysis using HPLC is crucial in the pharmaceutical industry to measure drug and metabolite levels. HPLC is a powerful and versatile liquid chromatography technique that forces samples through columns at high pressures for faster, more efficient separation of components. Key components of an HPLC system include columns, pumps, detectors, and data collection systems. HPLC follows the same principles as chromatography but provides higher speed and sensitivity through the use of high pressure. It has many applications including qualitative and quantitative analysis of chemicals, drugs, and biological compounds.
This document discusses various chromatography techniques including high-performance liquid chromatography (HPLC), fast protein liquid chromatography (FPLC), ultra-performance liquid chromatography (UPLC), and rapid resolution liquid chromatography (RRLC). HPLC uses pumps to pass a pressurized liquid through a column to separate sample components. FPLC is a modified HPLC used for protein separations using aqueous buffers and resins. UPLC uses smaller particle columns (<2μm) than HPLC to improve resolution, speed, and sensitivity. RRLC also uses sub-2μm particles and high flow rates to achieve faster analysis times than HPLC while maintaining resolution.
This presentation was presented when I was MVSc 1st year student, hence this ppt will provide a piece of basic information about the use of Chromatography.in toxicology. Principle of its work and related terminology are explained in this ppt.
Method Validation Is Used To Analyze The Specific And...Laura Benitez
Here is a draft lab report for the paper chromatography experiment:
Abstract
Paper chromatography and spectrophotometry were used to separate and identify amino acids in a protein hydrolysate. Chromatography paper was used as the stationary phase with a solvent system of n-butanol, acetic acid, and water to separate the amino acids. The Rf values were calculated and used to identify the amino acids present by comparing to known standards. Spectrophotometry was then used to determine the concentration of protein in the original solution by measuring absorbance at 280 nm and applying the Beer-Lambert Law.
Introduction
Paper chromatography is a common technique used to separate and identify amino acids. The technique takes advantage of differences in how
Supercritical fluid chromatography uses a supercritical fluid such as carbon dioxide as the mobile phase to separate analytes in a column. As the density of the supercritical fluid increases with pressure, the solvating power increases, allowing for elution of components from the column similar to temperature programming in gas chromatography or solvent gradients in HPLC. Common instrumentation includes pumps to control pressure of the mobile phase, injection systems, columns, and detectors compatible with both liquid and gas chromatography such as optical or mass spectrometry detectors. Applications of supercritical fluid chromatography include separation of chiral molecules and purification in the pharmaceutical industry.
Stability Indicating HPLC Method Development A Reviewijtsrd
High performance liquid chromatography is most powerful tools in analytical chemistry which assessing drug product stability. It is most accurate method for determining the qualitative and quantitative analysis of drug product. Forced degradation plays an important role in development of stability indicating analytical methodology. Stability indicating HPLC methods are used to separate various drug related impurities that are formed during the synthesis or manufacture of drug product. This article discusses the strategies and issues regarding the development of stability indicating HPLC system for drug substance. Forced degradation studies establish degradation pathways of drug substances and drug products. Forced degradation elucidate the possible degradation pathway of the drug substance or the active pharmaceutical ingredient in the drug product. At every stage of drug development practical recommendations are provided which will help to avoid failure. Rushikesh S Mulay | Rishikesh S Bachhav "Stability Indicating HPLC Method Development - A Review" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-5 | Issue-6 , October 2021, URL: https://www.ijtsrd.com/papers/ijtsrd46342.pdf Paper URL : https://www.ijtsrd.com/pharmacy/analytical-chemistry/46342/stability-indicating-hplc-method-development--a-review/rushikesh-s-mulay
This document provides an overview of high performance liquid chromatography (HPLC). It discusses the principle, history, types, instrumentation, procedure, advantages, disadvantages and applications of HPLC. Key points include that HPLC uses high pressure to separate compounds faster and more efficiently than other chromatography techniques. Silica is commonly used as the stationary phase because it can withstand pressures over 300-400 atmospheres. The major components of HPLC instrumentation are the solvent reservoir, pump, injector, column, detector and data collector. HPLC has various applications in fields like analytical chemistry, pharmaceuticals, forensics and environmental analysis.
High Performance Liquid Chromatography HPLC is a process of separating components in a liquid mixture. A liquid sample is injected into a stream of solvent mobile phase flowing through a column packed with a separation medium stationary phase . Sample components separate from one another by a process of differential migration as they flow through the column.As bands emerge from the column, flow carries them to one or more detectors which deliver a voltage response as a function of time. This is called a chromatogram. For each peak, the time at which it emerges identifies the sample constituent with respect to a standard. The peak’s area represents the quantity .HPLC provides a highly specific, reasonably precise, and fairly rapid analytical method for a plethora of complicated samples.This is difficult in detecting compounds. Low sensitivity of some compounds towards the stationary phase in the columns is difficult. Mohd Ali | Panjak Chasta | Dr. Kausal Kishore Chandrul "High Performance Liquid Chromatography (HPLC)" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-5 | Issue-5 , August 2021, URL: https://www.ijtsrd.com/papers/ijtsrd45146.pdf Paper URL: https://www.ijtsrd.com/pharmacy/other/45146/high-performance-liquid-chromatography-hplc/mohd-ali
Supercritical fluid technology offers opportunities for pharmaceutical manufacturing but faces challenges for widespread adoption. It can be used for particle size reduction, drug delivery system design, and extraction. However, challenges include developing feasible scale-up designs, accurately modeling solute behavior, high capital costs of equipment, and difficulties producing products consistently at an industrial scale. Overcoming these challenges through continued research, development, and validation of continuous production processes could realize the full potential of this technology.
Purification method development for chiral separation in supercritical
fluid chromatography with the solubilities in supercritical fluid
chromatographic mobile phases
The document discusses High Performance Liquid Chromatography (HPLC), including its principles, types of separations, instrumentation, applications in fields like food and pharmaceuticals, and advantages like speed and accuracy over traditional chromatography techniques. HPLC uses high pressure to pass samples in liquid mobile phases through stationary phases in columns to separate mixtures based on properties like polarity, size, or ionic charge.
Development and estimation of carvedilol in oral dosage form using HPLC methodBRNSSPublicationHubI
This document describes the development and validation of a method for estimating carvedilol, a beta-blocker drug, using reverse phase high-performance liquid chromatography (RP-HPLC). The researchers developed a new RP-HPLC method because existing literature did not report a method for analyzing carvedilol this way. They determined the optimal chromatographic conditions including selecting a C18 column, mobile phase of pH 3.4 phosphate and methanol mixture, flow rate of 1.0 mL/min, and detection wavelength of 284 nm. This new method was validated for the analysis of carvedilol in pharmaceutical dosage forms.
This document discusses liquid chromatography-mass spectrometry (LC-MS). It begins with an introduction to LC-MS, explaining that it combines liquid chromatography separation with mass spectrometry detection. It then covers the history, principles, instrumentation, advantages, and applications of LC and MS. Key applications discussed include pharmacokinetics, proteomics, metabolomics, and drug development.
Basic skills training guide hplc method development and validation- an over...bmarkandeya
This document provides an overview of HPLC method development and validation. It focuses on optimizing HPLC conditions and discusses various critical steps in analytical method development and validation. These include developing a stability-indicating HPLC method to analyze degradation products during stability studies and validating the method to demonstrate its suitability for intended use. Key aspects of method development and validation covered are sample preparation, HPLC analysis, standardization, and quantitative measures of column efficiency.
The document provides an overview of high performance liquid chromatography (HPLC). It begins with defining HPLC and explaining the basic principles of chromatography. It then describes the different types of HPLC based on the mode and principle of separation. The document also discusses HPLC instrumentation, including the solvent reservoir, pump, injector, column, and various detectors. It concludes by outlining some common applications of HPLC and discussing quantitative and qualitative analysis.
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Applications of Digital Biology: 1. Genomics and Personalized Medicine 2. Drug Discovery and Development 3. Biotechnology and Agriculture 4. Environmental Monitoring
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HPLC BMLT/ DMLT High Performance Liquid ChromatographyMdShamsTabrez4
Chromatography is a separation technique used to separate and analyze the components of a mixture. It involves the distribution of the components between two phases: a mobile phase and a stationary phase. The different affinities of the components for these phases lead to their separation based on their physical or chemical properties.
This document discusses several chromatography techniques used in forensic science analysis, including high performance liquid chromatography (HPLC), gas chromatography (GC), and inductively coupled plasma mass spectrometry (ICP-MS). It describes the basic principles, instrumentation components, and applications of each technique. HPLC uses high pressure to separate mixtures based on interactions with a stationary and mobile liquid phase. GC separates volatile compounds using an inert gas mobile phase and liquid stationary phase. ICP-MS uses plasma to ionize elements and masses to identify unknown samples at very low concentrations.
Chiral analysis and separation refers to the analysis and separation of chiral molecules that are mixed together using analytical techniques like chromatography and spectrometry. It is important because single enantiomers of chiral drug molecules and agricultural chemicals often have different effects on the human body and environment. Advanced equipment and technologies like high performance liquid chromatography (HPLC), gas chromatography (GC), supercritical fluid chromatography (SFC), and capillary electrophoresis (CE) are commonly used for chiral separations and analysis. BOC Sciences provides chiral analysis and separation services using state-of-the-art equipment and a dedicated team of experts.
1. Supercritical fluid chromatography is a form of normal phase chromatography that uses supercritical fluids like carbon dioxide as the mobile phase.
2. It has properties between liquid and gas with low viscosity and high diffusivity, allowing for more rapid separations compared to HPLC.
3. Applications include separation of chiral molecules, purification in pharmaceutical industry, and identification of pesticides and other compounds.
ntroduction to Chromatography
Chromatography is a powerful analytical technique used to separate, identify, and quantify the components of a complex mixture. This versatile method is widely used across numerous scientific fields, including chemistry, biology, environmental science, and forensics. At its core, chromatography relies on the differential distribution of analytes between a stationary phase and a mobile phase, allowing for the efficient separation and precise analysis of even the most intricate samples.
The underlying principle of chromatography is the difference in the affinity of various compounds for the stationary and mobile phases. As the sample is introduced into the system, the individual components are carried by the mobile phase and interact with the stationary phase, resulting in their differential migration and separation. This process enables scientists to not only identify the presence of specific compounds but also measure their relative concentrations with remarkable accuracy.
History and Development of Chromatography
The origins of chromatography can be traced back to the early 20th century, when the Russian botanist Mikhail Tsvet first introduced the concept in 1903. Tsvet used a glass column packed with calcium carbonate to separate plant pigments, such as chlorophyll and carotenoids, by their differential adsorption onto the stationary phase. This pioneering work laid the foundation for the development of various chromatographic techniques that would revolutionize the field of analytical chemistry.
In the following decades, chromatography continued to evolve, with scientists exploring different stationary phases, mobile phases, and separation mechanisms. The introduction of paper chromatography by Archer John Porter Martin and Richard Laurence Millington Synge in the 1940s, and the subsequent development of thin-layer chromatography (TLC) and gas chromatography (GC) in the 1950s, further expanded the capabilities of chromatographic analysis. These techniques allowed for the separation and identification of an increasingly diverse range of compounds, from small organic molecules to complex biomolecules.
The 1960s and 1970s witnessed a significant breakthrough with the introduction of high-performance liquid chromatography (HPLC), which provided higher resolution, sensitivity, and speed compared to earlier chromatographic methods. The continuous advancements in column technology, detection syst
Bioanalysis using HPLC is crucial in the pharmaceutical industry to measure drug and metabolite levels. HPLC is a powerful and versatile liquid chromatography technique that forces samples through columns at high pressures for faster, more efficient separation of components. Key components of an HPLC system include columns, pumps, detectors, and data collection systems. HPLC follows the same principles as chromatography but provides higher speed and sensitivity through the use of high pressure. It has many applications including qualitative and quantitative analysis of chemicals, drugs, and biological compounds.
This document discusses various chromatography techniques including high-performance liquid chromatography (HPLC), fast protein liquid chromatography (FPLC), ultra-performance liquid chromatography (UPLC), and rapid resolution liquid chromatography (RRLC). HPLC uses pumps to pass a pressurized liquid through a column to separate sample components. FPLC is a modified HPLC used for protein separations using aqueous buffers and resins. UPLC uses smaller particle columns (<2μm) than HPLC to improve resolution, speed, and sensitivity. RRLC also uses sub-2μm particles and high flow rates to achieve faster analysis times than HPLC while maintaining resolution.
This presentation was presented when I was MVSc 1st year student, hence this ppt will provide a piece of basic information about the use of Chromatography.in toxicology. Principle of its work and related terminology are explained in this ppt.
Method Validation Is Used To Analyze The Specific And...Laura Benitez
Here is a draft lab report for the paper chromatography experiment:
Abstract
Paper chromatography and spectrophotometry were used to separate and identify amino acids in a protein hydrolysate. Chromatography paper was used as the stationary phase with a solvent system of n-butanol, acetic acid, and water to separate the amino acids. The Rf values were calculated and used to identify the amino acids present by comparing to known standards. Spectrophotometry was then used to determine the concentration of protein in the original solution by measuring absorbance at 280 nm and applying the Beer-Lambert Law.
Introduction
Paper chromatography is a common technique used to separate and identify amino acids. The technique takes advantage of differences in how
Supercritical fluid chromatography uses a supercritical fluid such as carbon dioxide as the mobile phase to separate analytes in a column. As the density of the supercritical fluid increases with pressure, the solvating power increases, allowing for elution of components from the column similar to temperature programming in gas chromatography or solvent gradients in HPLC. Common instrumentation includes pumps to control pressure of the mobile phase, injection systems, columns, and detectors compatible with both liquid and gas chromatography such as optical or mass spectrometry detectors. Applications of supercritical fluid chromatography include separation of chiral molecules and purification in the pharmaceutical industry.
Stability Indicating HPLC Method Development A Reviewijtsrd
High performance liquid chromatography is most powerful tools in analytical chemistry which assessing drug product stability. It is most accurate method for determining the qualitative and quantitative analysis of drug product. Forced degradation plays an important role in development of stability indicating analytical methodology. Stability indicating HPLC methods are used to separate various drug related impurities that are formed during the synthesis or manufacture of drug product. This article discusses the strategies and issues regarding the development of stability indicating HPLC system for drug substance. Forced degradation studies establish degradation pathways of drug substances and drug products. Forced degradation elucidate the possible degradation pathway of the drug substance or the active pharmaceutical ingredient in the drug product. At every stage of drug development practical recommendations are provided which will help to avoid failure. Rushikesh S Mulay | Rishikesh S Bachhav "Stability Indicating HPLC Method Development - A Review" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-5 | Issue-6 , October 2021, URL: https://www.ijtsrd.com/papers/ijtsrd46342.pdf Paper URL : https://www.ijtsrd.com/pharmacy/analytical-chemistry/46342/stability-indicating-hplc-method-development--a-review/rushikesh-s-mulay
This document provides an overview of high performance liquid chromatography (HPLC). It discusses the principle, history, types, instrumentation, procedure, advantages, disadvantages and applications of HPLC. Key points include that HPLC uses high pressure to separate compounds faster and more efficiently than other chromatography techniques. Silica is commonly used as the stationary phase because it can withstand pressures over 300-400 atmospheres. The major components of HPLC instrumentation are the solvent reservoir, pump, injector, column, detector and data collector. HPLC has various applications in fields like analytical chemistry, pharmaceuticals, forensics and environmental analysis.
High Performance Liquid Chromatography HPLC is a process of separating components in a liquid mixture. A liquid sample is injected into a stream of solvent mobile phase flowing through a column packed with a separation medium stationary phase . Sample components separate from one another by a process of differential migration as they flow through the column.As bands emerge from the column, flow carries them to one or more detectors which deliver a voltage response as a function of time. This is called a chromatogram. For each peak, the time at which it emerges identifies the sample constituent with respect to a standard. The peak’s area represents the quantity .HPLC provides a highly specific, reasonably precise, and fairly rapid analytical method for a plethora of complicated samples.This is difficult in detecting compounds. Low sensitivity of some compounds towards the stationary phase in the columns is difficult. Mohd Ali | Panjak Chasta | Dr. Kausal Kishore Chandrul "High Performance Liquid Chromatography (HPLC)" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-5 | Issue-5 , August 2021, URL: https://www.ijtsrd.com/papers/ijtsrd45146.pdf Paper URL: https://www.ijtsrd.com/pharmacy/other/45146/high-performance-liquid-chromatography-hplc/mohd-ali
Supercritical fluid technology offers opportunities for pharmaceutical manufacturing but faces challenges for widespread adoption. It can be used for particle size reduction, drug delivery system design, and extraction. However, challenges include developing feasible scale-up designs, accurately modeling solute behavior, high capital costs of equipment, and difficulties producing products consistently at an industrial scale. Overcoming these challenges through continued research, development, and validation of continuous production processes could realize the full potential of this technology.
Purification method development for chiral separation in supercritical
fluid chromatography with the solubilities in supercritical fluid
chromatographic mobile phases
The document discusses High Performance Liquid Chromatography (HPLC), including its principles, types of separations, instrumentation, applications in fields like food and pharmaceuticals, and advantages like speed and accuracy over traditional chromatography techniques. HPLC uses high pressure to pass samples in liquid mobile phases through stationary phases in columns to separate mixtures based on properties like polarity, size, or ionic charge.
Development and estimation of carvedilol in oral dosage form using HPLC methodBRNSSPublicationHubI
This document describes the development and validation of a method for estimating carvedilol, a beta-blocker drug, using reverse phase high-performance liquid chromatography (RP-HPLC). The researchers developed a new RP-HPLC method because existing literature did not report a method for analyzing carvedilol this way. They determined the optimal chromatographic conditions including selecting a C18 column, mobile phase of pH 3.4 phosphate and methanol mixture, flow rate of 1.0 mL/min, and detection wavelength of 284 nm. This new method was validated for the analysis of carvedilol in pharmaceutical dosage forms.
This document discusses liquid chromatography-mass spectrometry (LC-MS). It begins with an introduction to LC-MS, explaining that it combines liquid chromatography separation with mass spectrometry detection. It then covers the history, principles, instrumentation, advantages, and applications of LC and MS. Key applications discussed include pharmacokinetics, proteomics, metabolomics, and drug development.
Basic skills training guide hplc method development and validation- an over...bmarkandeya
This document provides an overview of HPLC method development and validation. It focuses on optimizing HPLC conditions and discusses various critical steps in analytical method development and validation. These include developing a stability-indicating HPLC method to analyze degradation products during stability studies and validating the method to demonstrate its suitability for intended use. Key aspects of method development and validation covered are sample preparation, HPLC analysis, standardization, and quantitative measures of column efficiency.
The document provides an overview of high performance liquid chromatography (HPLC). It begins with defining HPLC and explaining the basic principles of chromatography. It then describes the different types of HPLC based on the mode and principle of separation. The document also discusses HPLC instrumentation, including the solvent reservoir, pump, injector, column, and various detectors. It concludes by outlining some common applications of HPLC and discussing quantitative and qualitative analysis.
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Creutzfeldt-Jakob Disease (CJD) is caused by the abnormal folding of prion proteins in the brain, leading to the formation of insoluble aggregates that damage nerve cells.
Histololgy of Female Reproductive System.pptxAyeshaZaid1
Dive into an in-depth exploration of the histological structure of female reproductive system with this comprehensive lecture. Presented by Dr. Ayesha Irfan, Assistant Professor of Anatomy, this presentation covers the Gross anatomy and functional histology of the female reproductive organs. Ideal for students, educators, and anyone interested in medical science, this lecture provides clear explanations, detailed diagrams, and valuable insights into female reproductive system. Enhance your knowledge and understanding of this essential aspect of human biology.
- Video recording of this lecture in English language: https://youtu.be/kqbnxVAZs-0
- Video recording of this lecture in Arabic language: https://youtu.be/SINlygW1Mpc
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
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Abdominal trauma in pediatrics refers to injuries or damage to the abdominal organs in children. It can occur due to various causes such as falls, motor vehicle accidents, sports-related injuries, and physical abuse. Children are more vulnerable to abdominal trauma due to their unique anatomical and physiological characteristics. Signs and symptoms include abdominal pain, tenderness, distension, vomiting, and signs of shock. Diagnosis involves physical examination, imaging studies, and laboratory tests. Management depends on the severity and may involve conservative treatment or surgical intervention. Prevention is crucial in reducing the incidence of abdominal trauma in children.
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Here is the updated list of Top Best Ayurvedic medicine for Gas and Indigestion and those are Gas-O-Go Syp for Dyspepsia | Lavizyme Syrup for Acidity | Yumzyme Hepatoprotective Capsules etc
These lecture slides, by Dr Sidra Arshad, offer a quick overview of the physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar lead (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
6. Describe the flow of current around the heart during the cardiac cycle
7. Discuss the placement and polarity of the leads of electrocardiograph
8. Describe the normal electrocardiograms recorded from the limb leads and explain the physiological basis of the different records that are obtained
9. Define mean electrical vector (axis) of the heart and give the normal range
10. Define the mean QRS vector
11. Describe the axes of leads (hexagonal reference system)
12. Comprehend the vectorial analysis of the normal ECG
13. Determine the mean electrical axis of the ventricular QRS and appreciate the mean axis deviation
14. Explain the concepts of current of injury, J point, and their significance
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. Chapter 3, Cardiology Explained, https://www.ncbi.nlm.nih.gov/books/NBK2214/
7. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
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Supercritical Fluid Chromatography (SFC): Explores the Fundamentals, Uses, and Benefits | The Lifesciences Magazine
1. Supercritical Fluid Chromatography:
Unveiling the Pinnacle of Separation
Science
Source-Chromatography Online
Supercritical Fluid Chromatography (SFC) is a highly adaptable and potent technology for the
analysis of complicated mixtures, and it stands as the epitome of separation science. SFC is at the
forefront of analytical chemistry improvements as it marries conventional chromatography with
the special qualities of supercritical fluids. This paper explores the fundamentals, uses, and
benefits of SFC, revealing the secrets of its effectiveness in a range of analytical contexts.
What is the Principle of Supercritical Chromatography?
1. Chromatographic Foundations
Supercritical Fluid Chromatography operates on the fundamental principles of chromatography,
where the separation of components in a mixture is achieved based on their differential
interactions with a mobile phase and a stationary phase. However, what distinguishes SFC is the
use of supercritical fluids as the mobile phase.
2. Supercritical Fluid State
Supercritical fluids exist in a state that transcends both liquid and gas phases. By manipulating
temperature and pressure conditions, a substance can be brought into this supercritical state,
2. where it exhibits unique properties such as high diffusivity and low viscosity, crucial for efficient
chromatographic separations.
Use of Supercritical Fluid Chromatography (SFC):
The adoption of Supercritical Fluid Chromatography (SFC) heralds a transformative era in
analytical chemistry, offering a dynamic and efficient solution for the separation and analysis of
complex mixtures. As we delve into the applications of SFC, it becomes evident that this
chromatographic technique transcends conventional boundaries, providing scientists with a
versatile tool capable of addressing diverse analytical challenges.
1. SFC in Pharmaceutical Advancements
In the pharmaceutical realm, where precision and efficiency are paramount, SFC emerges as a
game-changer. Its application spans drug development and quality control, significantly
expediting the analysis of intricate pharmaceutical compounds. The unique ability of SFC to
handle chiral compounds with exceptional resolution holds immense value, ensuring the
production of pharmaceuticals with enhanced efficacy and reduced development timelines.
2. SFC’s Role in Food and Beverage Analysis
The complexities of food and beverage matrices demand an analytical approach that can navigate
through diverse compounds with accuracy. Supercritical Fluid Chromatography, with its
adaptability to various solvents and unparalleled sensitivity, becomes an indispensable asset in
assessing food additives, identifying contaminants, and maintaining stringent quality control
standards.
3. Environmental Monitoring Elevated by SFC
3. As environmental concerns intensify, the need for advanced analytical techniques becomes
paramount. SFC’s capability to analyze polar and nonpolar compounds positions it as a key
player in environmental monitoring. Whether scrutinizing water quality, investigating soil
samples, or assessing air pollutants, SFC provides a comprehensive solution for discerning the
intricate composition of environmental samples.
4. Championing Chiral Separations
A standout feature of Supercritical Fluid Chromatography lies in its proficiency in chiral
separations. In industries where enantiomeric purity is critical, such as pharmaceuticals and
agrochemicals, SFC’s prowess in efficiently separating chiral compounds elevates it to the status
of a preferred and indispensable analytical tool.
5. SFC-MS Coupling Expanding Analytical Horizons
The fusion of SFC with Mass Spectrometry (MS) creates a synergistic analytical platform that
goes beyond traditional boundaries. This coupling enhances the capabilities of both techniques,
opening new frontiers in metabolomics, proteomics, and the exploration of natural products. SFC-
MS represents a harmonious convergence of superior separation power and advanced compound
identification, propelling analytical capabilities to unprecedented heights.
In essence, the use of SFC chromatography encapsulates a transformative analytical paradigm. As
we navigate through its applications, the versatility, efficiency, and precision of SFC unfold,
showcasing its instrumental role in shaping advancements across pharmaceuticals, food analysis,
environmental monitoring, and beyond. Supercritical Fluid Chromatography stands not merely as
a technique but as a catalyst for innovation, empowering researchers and analysts with the means
to explore the complexities of diverse sample matrices with unprecedented clarity and depth.
6. Versatility in Applications
SFC finds applications across a spectrum of industries, from pharmaceuticals and food analysis to
environmental monitoring. Its ability to handle a wide range of analytes, including polar and
nonpolar compounds, makes it a go-to technique for scientists seeking reliable and efficient
separation solutions.
7. Pharmaceutical Industry
In drug development, SFC plays a pivotal role in analyzing complex mixtures, ensuring the purity
and quality of pharmaceutical compounds. Its compatibility with a diverse range of solvents and
its ability to separate chiral compounds make it indispensable in pharmaceutical research and
quality control.
8. Food and Environmental Analysis
SFC’s versatility extends to food and environmental analysis, where complex matrices demand
high-resolution separations. Its ability to operate with reduced environmental impact, compared
to traditional techniques, aligns with the growing emphasis on green analytical methods.
Why Supercritical Fluid Chromatography is Better than HPLC?
4. 1. Efficiency and Speed
SFC offers several advantages over High-Performance Liquid Chromatography (HPLC). One key
distinction lies in the efficiency and speed of separations. The lower viscosity of supercritical
fluids facilitates faster mass transfer, reducing analysis times and enhancing throughput.
2. Compatibility with Nonpolar Compounds
HPLC often struggles with the separation of nonpolar compounds due to the limitations of
aqueous mobile phases. SFC, utilizing supercritical CO2 as a mobile phase, excels in separating
both polar and nonpolar compounds with enhanced resolution.
3. Reduced Environmental Impact
SFC’s utilization of supercritical CO2 as a primary solvent aligns with the principles of green
chemistry. CO2 is non-toxic, non-flammable, and easily recyclable, contributing to reduced
environmental impact compared to the organic solvents often used in HPLC.
Difference Between SFC and GC:
1. Mobile Phase Distinctions
While both SFC and Gas Chromatography (GC) employ gases as mobile phases, the critical
difference lies in the nature of these gases. SFC uses supercritical fluids, often CO2, while GC
uses inert gases like helium or nitrogen.
2. Applicability to Analyte Types
5. GC is highly effective for volatile and thermally stable compounds, making it suitable for
applications such as environmental analysis. On the other hand, Supercritical Fluid
Chromatography’s versatility allows the analysis of a broader range of compounds, including
those that may not be suitable for GC.
3. Temperature and Pressure Conditions
GC typically requires higher temperatures, limiting its applicability to thermally stable
compounds. SFC, operating at lower temperatures, offers advantages in the analysis of thermally
labile substances.
Principle of Supercritical Fluid:
Source-Phasex Corporation
1. Understanding the Supercritical State
A substance reaches the supercritical state when subjected to specific temperature and pressure
conditions beyond its critical point. At this point, it exhibits properties of both a gas and a liquid,
possessing the density of a liquid and the diffusivity of a gas.
2. Unique Properties
Supercritical fluids, like supercritical CO2 commonly used in Supercritical Fluid
Chromatography, offer unique properties, such as high diffusivity, low viscosity, and tunable
density. These characteristics contribute to their effectiveness in chromatographic separations.
Theory of Supercritical Fluid:
6. 1. Theoretical Foundations
The theory of supercritical fluid behavior in chromatography is rooted in the principles of mass
transfer, thermodynamics, and fluid dynamics. Understanding how supercritical fluids interact
with analytes and the stationary phase is crucial for optimizing separations and achieving desired
analytical outcomes.
2. Mass Transfer Dynamics
The efficiency of SFC relies on the rapid mass transfer of analytes between the mobile phase
(supercritical fluid) and the stationary phase. The unique properties of supercritical fluids
facilitate enhanced mass transfer, contributing to the speed and efficiency of chromatographic
separations.
Conclusion:
Finally, Supercritical Fluid Chromatography provides a strong instrument with a wide range of
uses and unmatched benefits, serving as a monument to the development of separation research.
The trip through SFC reveals the revolutionary influence it has had on analytical chemistry, from
its fundamental ideas to practical applications, giving chemists an advanced way to decipher the
intricacies of various sample matrices.
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