CHEMOMETRIC ANALYSIS AND IT’S APPLICATION IN HERBAL DRUGS
INTRODUCTION
Chemometrics is, "the chemical discipline that uses mathematical, statistical, and logical techniques to create or select optimal measurement processes and experiments, and to offer maximum chemical information by analysing chemical data."
ORIGIN AND DEVELOPMENT OF CHEMOMETRICS
Chemometrics is the English name for the Swedish term "kemometri," which was first used in 1971 by Swedish physicist Svante Wold
The following two journals were launched in the years 1986 and 1987: "Journal of Chemometrics" and "Chemometrics and Intelligent Laboratory Systems" raised the intellectualization of equipment and provided new construction techniques for new, high-dimensional hyphenated equipment
CLASSIFICATION OF CHEMOMETRICS
Monovariate
Multivariate- Supervised, Unsupervised
CHEMOMETRIC TOOLS
PCA
A multivariate tool called PCA
It is used to identify the primary cause of variability in the data sets
It is used to determine the relationship between an object and a variable and to detect cluster formatting
The main goal of PCA is reducing the dimension of a data set and multivariate compression of data
APPLICATION OF CHEMOMETRIC IN HERBAL PLANTS
Authenticity
Efficacy
Consistency
Safety evaluation
Identification of Bioactive Compounds in the acetone extract of Daedalea eleg...AI Publications
Daedalea elegans is a Nigerian wild (non-edible) higher fungus with great potentials in the pharmaceutical, textile, cosmetics and food industry. This current study investigates the bioactive compounds that can be found in the acetone extract of D. elegans using Gas Chromatography-Mass Spectrometry (GC-MS). There were twenty-eight compounds identified to be present in the acetone extract of the fungi under study and these are Benzoic acid (0.40%), Nonanoic acid (0.14%), Oxetane, 2,2,4-trimethyl- (0.28%), n-Decanoic acid (0.09%), Phthalimide (0.44%) Dodecanoic acid (0.24%), E-2-Hexenyl benzoate (0.21%), 2,4-Difluorobenzene, 1-benzyloxy- (0.16%), Tetratetracontane (0.55%), Isopropylphosphonic acid, fluoroanhydryde (0.28%), Benzene, (1-methylundecyl)- (0.21%), Tetradecanoic acid (0.76%), Cyclohexanepropanol, .alpha.,2,2,6-tetrame (0.56%), Pentadecanoic acid (0.71%), E-2-Hexenyl benzoate (0.32%), Pentadecanoic acid (0.97%), 1-Decanol, 2-hexyl- (0.46%), 9-Tetradecenal, (Z) (1.67), n-Hexadecanoic acid (23.59%) is the second most abundant, Phthalic acid, butyl undecyl ester (1.08%), Eicosanoic acid (0.79%), 9,12-Octadecadienoic acid (Z,Z)- (44.64%) was the highest in quantity, Octadecanoic acid (6.98%), Bis(2-ethylhexyl) phthalate (2.64%), 2,2,4-Trimethyl-3-(3,8,12,16-tetramethyl-heptadeca-3,7,11,15-tetraenyl)-cyclohexanol (1.95%), 9(11)-Dehydroergosteryl benzoate (8.37%), 9(11)-Dehydroergosteroltosylate (1.28%), 4,6-Decadienal, 8-ethyl-10-[4-hydroxy-8-(2-hydroxypropyl)-3,9 (0.22%). These compounds possess activities which includes but not limited to cancer chemotherapy, antifeedant against pine weevil, antifungi agent in topical therapeutic preparation, anti-inflammatory, immunomodulatory, anti-convulsant, antioxidants, hypocholesterolemic, anti-androgenic, nematicide, analgesic, intermediate for food-grade additives, lubricants, greases, rubber, dyes and plastic, antineoplastic agent, biosynthesis of prostaglandins and cell membrane to mention a few. This study has been able to show that D. elegans is a good source of bioactive compounds with great potentials that can be harnessed in various industries.
A simple visible spectrophotometric method is proposed for the determination
of ulipristal acetate present in bulk and tablet formulation. The currently
proposed method is established based on MBTH oxidation by ferric ions to
form an active coupling species (electrophile), followed by its coupling with
the ulipristal in acidic medium to form high intensiϑied green colored chromophore
having max at 609 nm. Validated the method as per the current
guidelines of ICH. Beer’s law was obeyed in the concentration range of 6.25 –
37.50 g mL 1 with a high regression coefϑicient (r > 0.999). Reproducibility,
accuracy, and precision of the method are evident from the low values of R.S.D.
This method can be used in quality control laboratories for routine analysis of
ulipristal acetate in bulk drug and pharmaceutical dosage forms.
Supercritical fluid (CO2) chromatography for quantitative determination of se...Ratnakaram Venkata Nadh
In the present study, two cancer therapeutic drugs (docetaxel and bortezomib) were separated from their
potential impurities on a chromatographic platform by utilizing CO2 gas (supercritical state) and quantified.
The chromatographic separations were achieved on two short columns BEH-2EP (100mm 3mm, 1.7 mm)
and CHIRALPAK AD-3 (100 mm 4.6 mm, 3 mm) for docetaxel and bortezomib, respectively. The present
work describes the role of organic modifiers in the separation of polar compounds by supercritical fluid
chromatography. The two new methods were fully validated in accordance with the current ICH
(International Council for Harmonization of technical requirements for pharmaceuticals for human use)
guidelines. The stability indicating power of the methods was demonstrated from the stress studies
conducted on the injection formulations of the two compounds. The methods are precise with % RSD of
0.4, linear with the correlation coefficient of r2 $ 0.999 and accurate in the range of 50–150% of the
target assay concentration. The two methods can be equally employed for the assay determination of
docetaxel and bortezomib APIs as well.
DEVELOPMENT AND VALIDATION OF SPECTROSCOPIC AND CHROMATOGRAPHIC METHOD FOR D...Dipak Reddy
A simple, precise & accurate UV spectroscopy & HPLC method was developed & validated as per ICH guideline.
In UV spectroscopy 0.1HCL used as diluent & in HPLC Methanol :ortho phosphoric acid (40:60%v/v) used.
Thus based on validation data it is concluded that present method is economical, less time consuming, precise , accurate for estimation of Pioglitazone in bulk drug & formulations.
This method can be used to determine the purity of the drug available from various sources by detecting the related impurities.
—3-Chloro-1,2-propanediol (3-chloropropanediol) is a well-known food processing contaminant found in a wide range of foods and ingredients and there has been recent concern about the levels of carcinogenic 3-chloropropanediol (3-MCPD) in some soy sauces. This paper reports on the development of an analytical method for the fast determination of 3-MCPD at trace level in commercial soy sauce using novel liquid phase extraction (LPE)/cleanup coupled with microwave-assisted derivatization (MAD) method followed by high performance liquid chromatography-ultraviolet (HPLC-UV) detection. In this method, 3-MCPD was first isolated from soy sauce sample matrix by LPE/cleanup with Extrude NT3 column cartridges and the isolated (eluent) solution was subjected to MAD with acetophenone to form 2-methyl-2-phenyl-4-(chloromethyl)-1,3-dioxolane under microwave irradiation using a specially modified domestic microwave oven, then the derivatizeddioxolane was directly analyzed with a HPLC-UV system. The optimum conditions for MAD such as the ratio of reagents, acidic catalyst, microwave irradiation power and time, as well as the chromatographic conditions were thoroughly investigated. Experimental results indicated that maximum derivatization can be achieved in 10 min under microwave irradiation at 362 watts when compared to 18 hours by conventional refluxing reaction. The proposed method provided a simple and rapid analytical procedure for 3-MCPD analysis in soy sauce with the detection limit of 80 ng mL-1. The relative standard deviations were all below 3.0 % (n = 7). Application was illustrated by the analysis of commercial sauce sample obtained from a local traditional store in central Taiwan.
Identification of Bioactive Compounds in the acetone extract of Daedalea eleg...AI Publications
Daedalea elegans is a Nigerian wild (non-edible) higher fungus with great potentials in the pharmaceutical, textile, cosmetics and food industry. This current study investigates the bioactive compounds that can be found in the acetone extract of D. elegans using Gas Chromatography-Mass Spectrometry (GC-MS). There were twenty-eight compounds identified to be present in the acetone extract of the fungi under study and these are Benzoic acid (0.40%), Nonanoic acid (0.14%), Oxetane, 2,2,4-trimethyl- (0.28%), n-Decanoic acid (0.09%), Phthalimide (0.44%) Dodecanoic acid (0.24%), E-2-Hexenyl benzoate (0.21%), 2,4-Difluorobenzene, 1-benzyloxy- (0.16%), Tetratetracontane (0.55%), Isopropylphosphonic acid, fluoroanhydryde (0.28%), Benzene, (1-methylundecyl)- (0.21%), Tetradecanoic acid (0.76%), Cyclohexanepropanol, .alpha.,2,2,6-tetrame (0.56%), Pentadecanoic acid (0.71%), E-2-Hexenyl benzoate (0.32%), Pentadecanoic acid (0.97%), 1-Decanol, 2-hexyl- (0.46%), 9-Tetradecenal, (Z) (1.67), n-Hexadecanoic acid (23.59%) is the second most abundant, Phthalic acid, butyl undecyl ester (1.08%), Eicosanoic acid (0.79%), 9,12-Octadecadienoic acid (Z,Z)- (44.64%) was the highest in quantity, Octadecanoic acid (6.98%), Bis(2-ethylhexyl) phthalate (2.64%), 2,2,4-Trimethyl-3-(3,8,12,16-tetramethyl-heptadeca-3,7,11,15-tetraenyl)-cyclohexanol (1.95%), 9(11)-Dehydroergosteryl benzoate (8.37%), 9(11)-Dehydroergosteroltosylate (1.28%), 4,6-Decadienal, 8-ethyl-10-[4-hydroxy-8-(2-hydroxypropyl)-3,9 (0.22%). These compounds possess activities which includes but not limited to cancer chemotherapy, antifeedant against pine weevil, antifungi agent in topical therapeutic preparation, anti-inflammatory, immunomodulatory, anti-convulsant, antioxidants, hypocholesterolemic, anti-androgenic, nematicide, analgesic, intermediate for food-grade additives, lubricants, greases, rubber, dyes and plastic, antineoplastic agent, biosynthesis of prostaglandins and cell membrane to mention a few. This study has been able to show that D. elegans is a good source of bioactive compounds with great potentials that can be harnessed in various industries.
A simple visible spectrophotometric method is proposed for the determination
of ulipristal acetate present in bulk and tablet formulation. The currently
proposed method is established based on MBTH oxidation by ferric ions to
form an active coupling species (electrophile), followed by its coupling with
the ulipristal in acidic medium to form high intensiϑied green colored chromophore
having max at 609 nm. Validated the method as per the current
guidelines of ICH. Beer’s law was obeyed in the concentration range of 6.25 –
37.50 g mL 1 with a high regression coefϑicient (r > 0.999). Reproducibility,
accuracy, and precision of the method are evident from the low values of R.S.D.
This method can be used in quality control laboratories for routine analysis of
ulipristal acetate in bulk drug and pharmaceutical dosage forms.
Supercritical fluid (CO2) chromatography for quantitative determination of se...Ratnakaram Venkata Nadh
In the present study, two cancer therapeutic drugs (docetaxel and bortezomib) were separated from their
potential impurities on a chromatographic platform by utilizing CO2 gas (supercritical state) and quantified.
The chromatographic separations were achieved on two short columns BEH-2EP (100mm 3mm, 1.7 mm)
and CHIRALPAK AD-3 (100 mm 4.6 mm, 3 mm) for docetaxel and bortezomib, respectively. The present
work describes the role of organic modifiers in the separation of polar compounds by supercritical fluid
chromatography. The two new methods were fully validated in accordance with the current ICH
(International Council for Harmonization of technical requirements for pharmaceuticals for human use)
guidelines. The stability indicating power of the methods was demonstrated from the stress studies
conducted on the injection formulations of the two compounds. The methods are precise with % RSD of
0.4, linear with the correlation coefficient of r2 $ 0.999 and accurate in the range of 50–150% of the
target assay concentration. The two methods can be equally employed for the assay determination of
docetaxel and bortezomib APIs as well.
DEVELOPMENT AND VALIDATION OF SPECTROSCOPIC AND CHROMATOGRAPHIC METHOD FOR D...Dipak Reddy
A simple, precise & accurate UV spectroscopy & HPLC method was developed & validated as per ICH guideline.
In UV spectroscopy 0.1HCL used as diluent & in HPLC Methanol :ortho phosphoric acid (40:60%v/v) used.
Thus based on validation data it is concluded that present method is economical, less time consuming, precise , accurate for estimation of Pioglitazone in bulk drug & formulations.
This method can be used to determine the purity of the drug available from various sources by detecting the related impurities.
—3-Chloro-1,2-propanediol (3-chloropropanediol) is a well-known food processing contaminant found in a wide range of foods and ingredients and there has been recent concern about the levels of carcinogenic 3-chloropropanediol (3-MCPD) in some soy sauces. This paper reports on the development of an analytical method for the fast determination of 3-MCPD at trace level in commercial soy sauce using novel liquid phase extraction (LPE)/cleanup coupled with microwave-assisted derivatization (MAD) method followed by high performance liquid chromatography-ultraviolet (HPLC-UV) detection. In this method, 3-MCPD was first isolated from soy sauce sample matrix by LPE/cleanup with Extrude NT3 column cartridges and the isolated (eluent) solution was subjected to MAD with acetophenone to form 2-methyl-2-phenyl-4-(chloromethyl)-1,3-dioxolane under microwave irradiation using a specially modified domestic microwave oven, then the derivatizeddioxolane was directly analyzed with a HPLC-UV system. The optimum conditions for MAD such as the ratio of reagents, acidic catalyst, microwave irradiation power and time, as well as the chromatographic conditions were thoroughly investigated. Experimental results indicated that maximum derivatization can be achieved in 10 min under microwave irradiation at 362 watts when compared to 18 hours by conventional refluxing reaction. The proposed method provided a simple and rapid analytical procedure for 3-MCPD analysis in soy sauce with the detection limit of 80 ng mL-1. The relative standard deviations were all below 3.0 % (n = 7). Application was illustrated by the analysis of commercial sauce sample obtained from a local traditional store in central Taiwan.
Abstract:
The Chronopharmacotherapy the drug administration is synchronised with circadian rhythms Formulation development of Microspheres is more reliable formulation as compare to single type dosage formulation due to it avoids dose dumping, as per required drug release profile is achieved For microspheres many polymers are used such as albumin, gelatine, starch, Eudragit, Polyacrylamide (“PAM”) these material loading capacity is high. Micro sponges which are Spherical are called as micro-balloons. Due to its hollow structure it shows good floating properties. In these systems use of Carbon-dioxide (CO2) as gas generating system which are used for floating purpose. The objective of present investigation is to prepared and evaluate a floating pulsatile drug delivery system of Aceclofenac. The strategy adopted for microspheres containing Aceclofenac as a material were prepared by emulsion solvent diffusion technique. Drug and polymer were mixed in dichloromethane and ethanol at 1:1 ratio. The drug and polymer solution were poured in water 50% W/V polyvinyl alcohol maintained at 30-40 C and the solution was stir at 500rpm using mechanical stirrer, The microspheres obtain were washed repeatedly with water until free from poly vinyl alcohol. The developed formulations were evaluated yield of floating microspheres particle size and shape, drug entrapment efficiency in-vitro evolution of floating ability, in-vitro drug release study. On the basis of these evolution parameters it was found that optimised floating pulsatile release formulation F7 showed higher drug entrapment efficiency floating time 6.8 minutes and the drug and polymer 32 1:3 ratio the particle size was increased.
Key Words: Chronopharmacotherapy, Floating pulsatile drug delivery, Aceclofenac.
Development and validation of rphplc method for nsai ds in combined pharmaceu...IJSIT Editor
The present research work includes the development and validation of High performance liquid
chromatography method for simultaneous estimation of Etirocoxib (ETX )and Paracetamol (PCM) which are
very much of useful in multiple therapies rather than the use of single drug formulation, because of multiple
actions, fever side effect ,and quicker relief. We aimed to design a quick and simple method, suitable for the
determination of identity, strength. The UV spectroscopic method were developed on standard ETX and PCM
using methanol as standard solution and also, the standard stock solution of both ETX and PCM were diluted
with 2%hydrochloric acid to obtain concentration 2.0µg/ml and 16.6µg/ml.The spectrum was recorded in the
range of 400-200nm.The RP- HPLC method were developed on standard ETX and PCM which performed on C-
18 column using mobile phase composed by acetonitrile :water 50:50(v/v) at a flow rate of 1 ml/min, with
injection volume 20µl and Ph 6.8 can be adjusted using orthophosphoric acid.
The IOSR Journal of Pharmacy (IOSRPHR) is an open access online & offline peer reviewed international journal, which publishes innovative research papers, reviews, mini-reviews, short communications and notes dealing with Pharmaceutical Sciences( Pharmaceutical Technology, Pharmaceutics, Biopharmaceutics, Pharmacokinetics, Pharmaceutical/Medicinal Chemistry, Computational Chemistry and Molecular Drug Design, Pharmacognosy & Phytochemistry, Pharmacology, Pharmaceutical Analysis, Pharmacy Practice, Clinical and Hospital Pharmacy, Cell Biology, Genomics and Proteomics, Pharmacogenomics, Bioinformatics and Biotechnology of Pharmaceutical Interest........more details on Aim & Scope).
All manuscripts are subject to rapid peer review. Those of high quality (not previously published and not under consideration for publication in another journal) will be published without delay.
Unraveling the potential phytochemical compounds of gymnema sylvestre through...University of Pretoria
ABSTRACT
Objective: To profile the chemical composition of ethanolic extract of Gymnema sylvestre through Gas Chromatography-Mass Spectrometry technique.
Methods: The chemical compositions of the plant leaf extracts of G. sylvestre were investigated using Gas Chromatography–Mass Spectroscopy (Scion 436-GC Bruker model coupled with a Triple, quadruple mass spectrophotometer) and NIST-MS library.
Results: GC-MS analysis of leaf extracts revealed the existence of Terpenes, alcohols, fatty acids, amine and sterols. The highest % Peak area is hexadecanoic acid, α-Santoline alcohol, recorded the next highest % peak area of 9.05. Major of the compounds belongs to terpeneoid group, namely 6-Octen-1-ol, 3,7-dimethyl, Isophytol, Squalene, Nerolidol, β-Amyrin and Cedrene-V6 which constitutes 30.7% of the peak area. The presence of α-Tocopherol-β-D-mannoside and Vitamin E also identified through this study.
Conclusion: From the above finding we can interpret that the G. sylvestre contained a considerable amount of phytoconstituents especially terpenoids. In future, this study will be helpful for the quantitative analysis of phytochemicals as well as formulation studies.
UV Spectrophotometric Method Development and Validation for Quantitative Esti...Sagar Savale
Aim: UV Spectrophotometric Method Development and Validation for quantitative estimation of
Diclofenac Sodium. Objective: U.V Spectrophotometric method have been widely employed for
determination of analyte in a mixture. Our aim is to develop spectroscopic method for estimation of the
diclofenac sodium in ternary mixture by using U.V spectrophotometry. Methodology: The method was
validated as per ICH guidelines. The recovery studies confirmed the accuracy and precision of the method.
Conclusion: It was successfully applied for the analysis of the drug in bulk and could be effectively used for
the routine analysis.
A HPLC-UV METHOD FOR DETEERMINATION OF THREE PESTICIDES IN WATERijac123
HPLC method is developed and validated for determination of three pesticides (abamectin, imidacloprid,
and β-cyfluthrin) in water. These pesticides are used widely in agriculture for crops protection, and may be
leached to the groundwater. Reversed-phase method with C18 column (5 µm, 250mm × 4.6 mm inner
diameter) using a mobile phase consisting of acetonitrile/water (v:v = 4:1) at a flow rate of 1.5 mL/min and
UV detection at 220 nm was used. This method is validated according to new methods which include
accuracy, precision, linearity and range, limit of detection and limit of quantitation. The current method
exhibits good linearity over the range of 1-1000 ppb for abamectin, 0.5-1000 ppb for imidacloprid, and
0.4-1000 ppb for ß-cyfluthrin with r2
greater than 0.990. The percentage recovery of the method at three
concentration levels (5, 100, and 1000 ppb) is within 97.6 to 101.5% for the three pesticides. Relative
standard deviation of the area of six replicate injections of each pesticide at three concentration levels (5.0,
100.0, and 1000.0 ppb) was found to be less than 1% which reflect the precision of the method. Limit of
quantitation of the three pesticides using this method is low (1.0, 0.5, and 0.4 ppb) for abamectin,
imidacloprid, and β-cyfluthrin, respectively which enables the determination of these three pesticides in
water at low concentration levels
UV Spectrophotometric Method Development and Validation for Quantitative Esti...Sagar Savale
U.V Spectrophotometric method have been widely employed in determination of individual components in a mixture or fixed dose combination. Our aim is to develop spectroscopic method for estimation of the paracetamol in ternary mixture by using U.V spectrophotometry.
Determination of Etodolac in Commercial Formulations by HPLC-UV Methodijtsrd
The aim of this study was to develop and verify a simple, rapid and sensitive high performance liquid chromatography method coupled with UV detector HPLC UV method for the quantitative determination of etodolac in bulk and pharmaceutical dosage forms. Chromatographic separation was performed at ambient conditions on a reverse phase ACE C8 analytical column 250 mm x 4.6 mm ID, 5 umm using the mobile phase containing acetonitrile water 80 20, v v at a flow rate of 1.0 mL min 1. A wavelength of 272 nm was used for etodolok and paracetamol IS . A retention time of 4.21 min and 2.02 min were obtained for etodolac and IS, respectively. The method showed linearity in the range of 0.08 10 µg mL 1 for etodolac R = 0.9999 . The linear regression equations obtained by least square regression method were the ratio of peak area of etodolac and IS =1.559 concentration etodolac µg mL 0.139. The intra day and inter day RE and RSD values of the method were =10.0 and =2.65 , respectively. Limit of detection LOD and limit of quantification LOQ were found to be 0.04 and 0.06 µg mL 1 for etodolac, respectively. A new, simple and sensitive high performance liquid chromatography method was developed and validated for etodolac. The method can be applied for the quantification of etodolac without derivatization in bulk solutions and commercial formulations using the internal standard. Tugrul Cagri Akman | Yucel Kadioglu "Determination of Etodolac in Commercial Formulations by HPLC-UV Method" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-4 | Issue-1 , December 2019, URL: https://www.ijtsrd.com/papers/ijtsrd29452.pdfPaper URL: https://www.ijtsrd.com/pharmacy/analytical-chemistry/29452/determination-of-etodolac-in-commercial-formulations-by-hplc-uv-method/tugrul-cagri-akman
Spectrophotometric Estimation of Rosuvastatin Calcium in Bulk and Pharmaceuti...SriramNagarajan15
Rosuvastatin calcium of the class statins is used for primary hyperlipidemias. It is a selective and competitive inhibitor of HMG-CoA reductase. In the present work, simple, sensitive and economic spectrophotometric method has been developed for quantitative determination of Rosuvastatin calcium. In the present spectrophotometric method Rosuvastatin calcium was dissolved in double distilled water. It exhibited an absorption maximum at 241 nm and obeyed Beer’s law in the concentration range of 5-25g/ml. The results of analysis have been validated and found to be sensitive, precise and accurate for quantitative determination of Rosuvastatin calcium in bulk drug and pharmaceutical formulations.
Abstract:
The Chronopharmacotherapy the drug administration is synchronised with circadian rhythms Formulation development of Microspheres is more reliable formulation as compare to single type dosage formulation due to it avoids dose dumping, as per required drug release profile is achieved For microspheres many polymers are used such as albumin, gelatine, starch, Eudragit, Polyacrylamide (“PAM”) these material loading capacity is high. Micro sponges which are Spherical are called as micro-balloons. Due to its hollow structure it shows good floating properties. In these systems use of Carbon-dioxide (CO2) as gas generating system which are used for floating purpose. The objective of present investigation is to prepared and evaluate a floating pulsatile drug delivery system of Aceclofenac. The strategy adopted for microspheres containing Aceclofenac as a material were prepared by emulsion solvent diffusion technique. Drug and polymer were mixed in dichloromethane and ethanol at 1:1 ratio. The drug and polymer solution were poured in water 50% W/V polyvinyl alcohol maintained at 30-40 C and the solution was stir at 500rpm using mechanical stirrer, The microspheres obtain were washed repeatedly with water until free from poly vinyl alcohol. The developed formulations were evaluated yield of floating microspheres particle size and shape, drug entrapment efficiency in-vitro evolution of floating ability, in-vitro drug release study. On the basis of these evolution parameters it was found that optimised floating pulsatile release formulation F7 showed higher drug entrapment efficiency floating time 6.8 minutes and the drug and polymer 32 1:3 ratio the particle size was increased.
Key Words: Chronopharmacotherapy, Floating pulsatile drug delivery, Aceclofenac.
Development and validation of rphplc method for nsai ds in combined pharmaceu...IJSIT Editor
The present research work includes the development and validation of High performance liquid
chromatography method for simultaneous estimation of Etirocoxib (ETX )and Paracetamol (PCM) which are
very much of useful in multiple therapies rather than the use of single drug formulation, because of multiple
actions, fever side effect ,and quicker relief. We aimed to design a quick and simple method, suitable for the
determination of identity, strength. The UV spectroscopic method were developed on standard ETX and PCM
using methanol as standard solution and also, the standard stock solution of both ETX and PCM were diluted
with 2%hydrochloric acid to obtain concentration 2.0µg/ml and 16.6µg/ml.The spectrum was recorded in the
range of 400-200nm.The RP- HPLC method were developed on standard ETX and PCM which performed on C-
18 column using mobile phase composed by acetonitrile :water 50:50(v/v) at a flow rate of 1 ml/min, with
injection volume 20µl and Ph 6.8 can be adjusted using orthophosphoric acid.
The IOSR Journal of Pharmacy (IOSRPHR) is an open access online & offline peer reviewed international journal, which publishes innovative research papers, reviews, mini-reviews, short communications and notes dealing with Pharmaceutical Sciences( Pharmaceutical Technology, Pharmaceutics, Biopharmaceutics, Pharmacokinetics, Pharmaceutical/Medicinal Chemistry, Computational Chemistry and Molecular Drug Design, Pharmacognosy & Phytochemistry, Pharmacology, Pharmaceutical Analysis, Pharmacy Practice, Clinical and Hospital Pharmacy, Cell Biology, Genomics and Proteomics, Pharmacogenomics, Bioinformatics and Biotechnology of Pharmaceutical Interest........more details on Aim & Scope).
All manuscripts are subject to rapid peer review. Those of high quality (not previously published and not under consideration for publication in another journal) will be published without delay.
Unraveling the potential phytochemical compounds of gymnema sylvestre through...University of Pretoria
ABSTRACT
Objective: To profile the chemical composition of ethanolic extract of Gymnema sylvestre through Gas Chromatography-Mass Spectrometry technique.
Methods: The chemical compositions of the plant leaf extracts of G. sylvestre were investigated using Gas Chromatography–Mass Spectroscopy (Scion 436-GC Bruker model coupled with a Triple, quadruple mass spectrophotometer) and NIST-MS library.
Results: GC-MS analysis of leaf extracts revealed the existence of Terpenes, alcohols, fatty acids, amine and sterols. The highest % Peak area is hexadecanoic acid, α-Santoline alcohol, recorded the next highest % peak area of 9.05. Major of the compounds belongs to terpeneoid group, namely 6-Octen-1-ol, 3,7-dimethyl, Isophytol, Squalene, Nerolidol, β-Amyrin and Cedrene-V6 which constitutes 30.7% of the peak area. The presence of α-Tocopherol-β-D-mannoside and Vitamin E also identified through this study.
Conclusion: From the above finding we can interpret that the G. sylvestre contained a considerable amount of phytoconstituents especially terpenoids. In future, this study will be helpful for the quantitative analysis of phytochemicals as well as formulation studies.
UV Spectrophotometric Method Development and Validation for Quantitative Esti...Sagar Savale
Aim: UV Spectrophotometric Method Development and Validation for quantitative estimation of
Diclofenac Sodium. Objective: U.V Spectrophotometric method have been widely employed for
determination of analyte in a mixture. Our aim is to develop spectroscopic method for estimation of the
diclofenac sodium in ternary mixture by using U.V spectrophotometry. Methodology: The method was
validated as per ICH guidelines. The recovery studies confirmed the accuracy and precision of the method.
Conclusion: It was successfully applied for the analysis of the drug in bulk and could be effectively used for
the routine analysis.
A HPLC-UV METHOD FOR DETEERMINATION OF THREE PESTICIDES IN WATERijac123
HPLC method is developed and validated for determination of three pesticides (abamectin, imidacloprid,
and β-cyfluthrin) in water. These pesticides are used widely in agriculture for crops protection, and may be
leached to the groundwater. Reversed-phase method with C18 column (5 µm, 250mm × 4.6 mm inner
diameter) using a mobile phase consisting of acetonitrile/water (v:v = 4:1) at a flow rate of 1.5 mL/min and
UV detection at 220 nm was used. This method is validated according to new methods which include
accuracy, precision, linearity and range, limit of detection and limit of quantitation. The current method
exhibits good linearity over the range of 1-1000 ppb for abamectin, 0.5-1000 ppb for imidacloprid, and
0.4-1000 ppb for ß-cyfluthrin with r2
greater than 0.990. The percentage recovery of the method at three
concentration levels (5, 100, and 1000 ppb) is within 97.6 to 101.5% for the three pesticides. Relative
standard deviation of the area of six replicate injections of each pesticide at three concentration levels (5.0,
100.0, and 1000.0 ppb) was found to be less than 1% which reflect the precision of the method. Limit of
quantitation of the three pesticides using this method is low (1.0, 0.5, and 0.4 ppb) for abamectin,
imidacloprid, and β-cyfluthrin, respectively which enables the determination of these three pesticides in
water at low concentration levels
UV Spectrophotometric Method Development and Validation for Quantitative Esti...Sagar Savale
U.V Spectrophotometric method have been widely employed in determination of individual components in a mixture or fixed dose combination. Our aim is to develop spectroscopic method for estimation of the paracetamol in ternary mixture by using U.V spectrophotometry.
Determination of Etodolac in Commercial Formulations by HPLC-UV Methodijtsrd
The aim of this study was to develop and verify a simple, rapid and sensitive high performance liquid chromatography method coupled with UV detector HPLC UV method for the quantitative determination of etodolac in bulk and pharmaceutical dosage forms. Chromatographic separation was performed at ambient conditions on a reverse phase ACE C8 analytical column 250 mm x 4.6 mm ID, 5 umm using the mobile phase containing acetonitrile water 80 20, v v at a flow rate of 1.0 mL min 1. A wavelength of 272 nm was used for etodolok and paracetamol IS . A retention time of 4.21 min and 2.02 min were obtained for etodolac and IS, respectively. The method showed linearity in the range of 0.08 10 µg mL 1 for etodolac R = 0.9999 . The linear regression equations obtained by least square regression method were the ratio of peak area of etodolac and IS =1.559 concentration etodolac µg mL 0.139. The intra day and inter day RE and RSD values of the method were =10.0 and =2.65 , respectively. Limit of detection LOD and limit of quantification LOQ were found to be 0.04 and 0.06 µg mL 1 for etodolac, respectively. A new, simple and sensitive high performance liquid chromatography method was developed and validated for etodolac. The method can be applied for the quantification of etodolac without derivatization in bulk solutions and commercial formulations using the internal standard. Tugrul Cagri Akman | Yucel Kadioglu "Determination of Etodolac in Commercial Formulations by HPLC-UV Method" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-4 | Issue-1 , December 2019, URL: https://www.ijtsrd.com/papers/ijtsrd29452.pdfPaper URL: https://www.ijtsrd.com/pharmacy/analytical-chemistry/29452/determination-of-etodolac-in-commercial-formulations-by-hplc-uv-method/tugrul-cagri-akman
Spectrophotometric Estimation of Rosuvastatin Calcium in Bulk and Pharmaceuti...SriramNagarajan15
Rosuvastatin calcium of the class statins is used for primary hyperlipidemias. It is a selective and competitive inhibitor of HMG-CoA reductase. In the present work, simple, sensitive and economic spectrophotometric method has been developed for quantitative determination of Rosuvastatin calcium. In the present spectrophotometric method Rosuvastatin calcium was dissolved in double distilled water. It exhibited an absorption maximum at 241 nm and obeyed Beer’s law in the concentration range of 5-25g/ml. The results of analysis have been validated and found to be sensitive, precise and accurate for quantitative determination of Rosuvastatin calcium in bulk drug and pharmaceutical formulations.
Palestine last event orientationfvgnh .pptxRaedMohamed3
An EFL lesson about the current events in Palestine. It is intended to be for intermediate students who wish to increase their listening skills through a short lesson in power point.
A Strategic Approach: GenAI in EducationPeter Windle
Artificial Intelligence (AI) technologies such as Generative AI, Image Generators and Large Language Models have had a dramatic impact on teaching, learning and assessment over the past 18 months. The most immediate threat AI posed was to Academic Integrity with Higher Education Institutes (HEIs) focusing their efforts on combating the use of GenAI in assessment. Guidelines were developed for staff and students, policies put in place too. Innovative educators have forged paths in the use of Generative AI for teaching, learning and assessments leading to pockets of transformation springing up across HEIs, often with little or no top-down guidance, support or direction.
This Gasta posits a strategic approach to integrating AI into HEIs to prepare staff, students and the curriculum for an evolving world and workplace. We will highlight the advantages of working with these technologies beyond the realm of teaching, learning and assessment by considering prompt engineering skills, industry impact, curriculum changes, and the need for staff upskilling. In contrast, not engaging strategically with Generative AI poses risks, including falling behind peers, missed opportunities and failing to ensure our graduates remain employable. The rapid evolution of AI technologies necessitates a proactive and strategic approach if we are to remain relevant.
Read| The latest issue of The Challenger is here! We are thrilled to announce that our school paper has qualified for the NATIONAL SCHOOLS PRESS CONFERENCE (NSPC) 2024. Thank you for your unwavering support and trust. Dive into the stories that made us stand out!
Macroeconomics- Movie Location
This will be used as part of your Personal Professional Portfolio once graded.
Objective:
Prepare a presentation or a paper using research, basic comparative analysis, data organization and application of economic information. You will make an informed assessment of an economic climate outside of the United States to accomplish an entertainment industry objective.
The French Revolution, which began in 1789, was a period of radical social and political upheaval in France. It marked the decline of absolute monarchies, the rise of secular and democratic republics, and the eventual rise of Napoleon Bonaparte. This revolutionary period is crucial in understanding the transition from feudalism to modernity in Europe.
For more information, visit-www.vavaclasses.com
Embracing GenAI - A Strategic ImperativePeter Windle
Artificial Intelligence (AI) technologies such as Generative AI, Image Generators and Large Language Models have had a dramatic impact on teaching, learning and assessment over the past 18 months. The most immediate threat AI posed was to Academic Integrity with Higher Education Institutes (HEIs) focusing their efforts on combating the use of GenAI in assessment. Guidelines were developed for staff and students, policies put in place too. Innovative educators have forged paths in the use of Generative AI for teaching, learning and assessments leading to pockets of transformation springing up across HEIs, often with little or no top-down guidance, support or direction.
This Gasta posits a strategic approach to integrating AI into HEIs to prepare staff, students and the curriculum for an evolving world and workplace. We will highlight the advantages of working with these technologies beyond the realm of teaching, learning and assessment by considering prompt engineering skills, industry impact, curriculum changes, and the need for staff upskilling. In contrast, not engaging strategically with Generative AI poses risks, including falling behind peers, missed opportunities and failing to ensure our graduates remain employable. The rapid evolution of AI technologies necessitates a proactive and strategic approach if we are to remain relevant.
Operation “Blue Star” is the only event in the history of Independent India where the state went into war with its own people. Even after about 40 years it is not clear if it was culmination of states anger over people of the region, a political game of power or start of dictatorial chapter in the democratic setup.
The people of Punjab felt alienated from main stream due to denial of their just demands during a long democratic struggle since independence. As it happen all over the word, it led to militant struggle with great loss of lives of military, police and civilian personnel. Killing of Indira Gandhi and massacre of innocent Sikhs in Delhi and other India cities was also associated with this movement.
Digital Tools and AI for Teaching Learning and Research
Chemometrics Analysis and It's application in Herbal Drugs.pptx
1. CHEMOMETRIC ANALYSIS AND IT’S
APPLICATION IN HERBAL DRUGS
Presented by
Kamini Chaturvedi
M.S. (Pharm.) – 1st Semester
Department of Natural Products
1
3. INTRODUCTION
Chemometrics is, "the chemical discipline that uses mathematical, statistical, and logical
techniques to create or select optimal measurement processes and experiments, and to offer
maximum chemical information by analysing chemical data."
ANALYSIS
SAMPLE PREPARATION RESULT PRODUCTION AND
INTERPRETATION
CHEMOMETRICS
Biancolillo, A. et. al., Compr. Anal. Chem 2018, 80, 69-104 3
4. ORIGIN AND DEVELOPMENT OF CHEMOMETRICS
Chemometrics is the English name for the Swedish term "kemometri," which was first used in
1971 by Swedish physicist Svante Wold
The following two journals were launched in the years 1986 and 1987: "Journal of
Chemometrics" and "Chemometrics and Intelligent Laboratory Systems" raised the
intellectualization of equipment and provided new construction techniques for new, high-
dimensional hyphenated equipment
Kiralj, R. et.al., J. Chemom 2006, 20, 247-272. 4
6. CHROMATOGRAPHIC FINGERPRINT AND RELATED
CHEMOMETRIC TOOLS
RAW DATA
CHEMOMETRIC
TOOL
NOISE
+
INFORMATION
NOISE
INFORMATION
Bansal, A. et. al., J. Pharm. Anal 2014, 4, 223-233 6
8. PCA
A multivariate tool called PCA
It is used to identify the primary cause of variability in the data sets
It is used to determine the relationship between an object and a variable and to detect cluster
formatting
The main goal of PCA is reducing the dimension of a data set and multivariate compression of data
Bansal, A. et. al., J. Pharm. Anal 2014, 4, 223-233 8
10. APPLICATION OF CHEMOMETRIC IN HERBAL PLANTS
• Authenticity
• Efficacy
• Consistency
• Safety evaluation
Du, J. et. al., J. Med. Plant Res 2011, 5, 4001-4008 10
11. Classification of Andrographis paniculate extracts via solvent extraction using
HPLC fingerprint and chemometric analysis
CONT…
https://www.ekgaon.com/img/p/1/8/6/4/1864-thickbox_default.jpg
Family- Acanthaceae
Synonyms- Green chiretta, King of bitters
Pharmacological activity-
Antidiabetic
Andrographis paniculate
Antimalarial
Anti-cancer
Hepatoprotective
Rafi, M. et. al., BMC Res. Notes 2020, 13, 1-6 11
12. Material: Andrographis paniculata was collected 3 months previously from the medicinal
plant garden. HPLC grade, whatman membrane filters(0.22 μm pore size)
Chemical: Ethanol (as a solvent )
Acetonitrile and formic acid (as) a mobile phase
50 µL of 0.1 M phosphate buffer (pH 7), 25 µL of 10 mM PNG ,25 µL of α-
glucosidase (0.04 µ/mL) 100 µL of 0.2 M Na2CO3 for determination
of α-glucosidase inhibition activity.
1 mL DMSO
Rafi, M. et. al., BMC Res. Notes 2020, 13, 1-6 12
13. SAMPLE PREPARATION
Sample, first arranged then clean with water
Dried and pulverized to a powder
10 g powder +100 mL solvent soaked with continuous stirring (6 h) then
left without stirring (12 h)
Water, and solutions of 30%, 50%, 70% and pure ethanol used for extraction
Filtrate collected ,concentrated and then dried
HPLC and Determination of andrographolide
Rafi, M. et. al., BMC Res. Notes 2020, 13, 1-6 13
14. Extraction and inhibition of α-glucosidase activity
Effect of solvent concentration on α-glucosidase inhibitory activity and andrographolide yield
from A. paniculata extracts
Extraction solvent Inhibition (% ± SD)a Andrographolide content
(mg/g ± SD)b
Water 54.80±4.05 25.18±1.49
30% ethanol 58.42±2.41 50.29±1.43
50% ethanol 79.66±6.45 114.56±2.30
70% ethanol 60.02±0.32 96.48±0.89
Pure ethanol 49.58±0.97 102.08±2.73
a Average of 2 replicates b Average of 3 replicates
Rafi, M. et. al., BMC Res. Notes 2020, 13, 1-6
14
15. HPLC FINGERPRINTS
HPLC chromatograms of A. paniculata extracts using different solvents:
(a) Pure ethanol
(b) 70% ethanol
(c) 50% ethanol
(d) 30% ethanol
(e) water
Rafi, M. et. al., BMC Res. Notes 2020, 13, 1-6 15
16. a. PCA plot
b. PCA biplot
PCA PLOT OF A. PANICULATA USING DIFFERENT SOLVENT
• Pure ethanol
• 70% ethanol
• 50% ethanol
• 30% ethanol
• Water
• Variable(peak no.)
+
×
Rafi, M. et. al., BMC Res. Notes 2020, 13, 1-6 16
17. CONCLUSION
Combining the HPLC fingerprint technique with PCA enabled the A. paniculata extracts to be
classified according to their solvent extraction
The HPLC fingerprint chromatograms of the A. paniculata extracts exhibited a similar pattern
which differed only in the peak height and area of each detected peak. The 50% ethanol extract
provided a higher andrographolide content and percentage α-glucosidase inhibitory activity than
the other extracts
Chemometrics is an emerging tool for increase the yield and optimized the conditions for
extraction of herbal medicines
Rafi, M. et. al., BMC Res. Notes 2020, 13, 1-6 17
