International Journal of Trend in Scientific Research and Development: Analytical Chemistry

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Showing posts with label Analytical Chemistry. Show all posts
Showing posts with label Analytical Chemistry. Show all posts

Saturday 11 September 2021

A Comprehensive Review on Drug Delivery Approach to Central Nervous System

September 11, 2021 0
A Comprehensive Review on Drug Delivery Approach to Central Nervous System
The brain is a delicate organ, and evolution built very efficient ways to protect it. Unfortunately, the same mechanisms that protect it against intrusive chemicals can also frustrate therapeutic interventions. Many existing pharmaceuticals are rendered ineffective in the treatment of cerebral diseases due to our inability to effectively deliver and sustain them within the brain. General methods that can enhance drug delivery to the brain are, therefore, of great interest. Despite aggressive research, patients suffering from fatal and or debilitating central nervous system CNS diseases, such as brain tumors, HIV encephalopathy, epilepsy, cerebrovascular diseases and neurodegenerative disorders, far outnumber those dying of all types of systemic cancer or heart disease. The clinical failure of much potentially effective therapeutics is often not due to a lack of drug potency but rather to shortcomings in the method by which the drug is delivered. Treating CNS diseases is particularly challenging because a variety of formidable obstacles often impede drug delivery to the brain and spinal cord. By localizing drugs at their desired site of action one can reduce toxicity and increase treatment efficiency. In response to the insufficiency in conventional delivery mechanisms, aggressive research efforts have recently focused on the development of new strategies to more effectively deliver drug molecules to the CNS. This review intends to detail the recent advances in the field of brain targeting, rational drug design approach and drug delivery to CNS. To illustrate the complexity of the problems that have to be overcome for successful brain targeting, a brief intercellular characterization of the blood-brain barrier BBB is also included. 
by Parth Nikam | Rishikesh Bachhav "A Comprehensive Review on Drug Delivery Approach to Central Nervous System" 

Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-5 | Issue-6 , October 2021, 



Wednesday 8 September 2021

Method Development and Validation for Estimation of Oral Hypoglycaemic Drug Dapagliflozinina Tablet Dosage form by the Employment of Rp HPLC

September 08, 2021 0
Method Development and Validation for Estimation of Oral Hypoglycaemic Drug Dapagliflozinina Tablet Dosage form by the Employment of Rp HPLC
HPLC is a chromatographic technique employed in active compound chemistry and biochemistry to separate a mixture and substances with the goal of identifying, measuring, and purifying the different components of the mixture. Its a much better variety of column and traditional chromatography. The objective of the research work is to develop and validate a simple and accurate reverse phase chromatographic method to estimate amount of drug in dosage form. The developed method successfully can be applied to estimate the amount of Dapagliflozin in tablet dosage form. After oral administration of dapagliflozin, the maximum plasma concentration Concentration max under two hours. High performance liquid chromatographic system was alleviated according to the chromatographic settings. After attaining the steady base line, to verify the system suitability, a single 40 µg ml of standard solution proportional to 100 test concentration of dapagliflozin was injected into the HPLC system. The gradient mobile phase flow rate programming assisted in optimising the lengthy run duration and resolution of sample analysis, making the approach more cost effective and quick. Validation of the developed and optimized HPLC method was carried out according to ICH guidelines with respect to parameters such as linearity, specificity, precision and accuracy. 
by Junaid Ahmed | Himanchal Sharma | Shiva Teotia "Method Development and Validation for Estimation of Oral Hypoglycaemic Drug Dapagliflozinina Tablet Dosage form by the Employment of Rp-HPLC" 

Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-5 | Issue-6 , October 2021, 



Monday 6 September 2021

Stability Indicating HPLC Method Development A Review

September 06, 2021 0
Stability Indicating HPLC Method Development A Review
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. 
by 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, 



Sunday 5 September 2021

Stability Indicating RP HPLC Method Development and Validation of Everolimus in Bulk and Pharmaceutical Dosage Form

September 05, 2021 0
Stability Indicating RP HPLC Method Development and Validation of Everolimus in Bulk and Pharmaceutical Dosage Form
Everolimus is semisynthetic derivative of sirolimus, which is isolated from Streptomyces hygroscopicus. A novel reversed phase high performnce liquid chromatography HPLC method for determination of the everolimus in the presence of degradation product or pharmaceutical excipients. Seperation was carried out using Cosmosil C18 250mm x 4. 6ID , column having particle size 5 micron using acetonitrile and methanol mixture, and pH adjusted to 3, a flow rate of 1. 0 mL min, and ultraviolet detection at 285nm. A retention time nearly 3. 806 min was observed. The calibration curve for everolimus was linear from range of 5 25 µg mL with limit of detection and limit of quantitation of 0. 0817 and 0. 2478 µg mL, respectively. Analytical validation parameters such as selectivity, specificity, linearity, accuracy and precision were evaluated and relative standard deviation value for all the key parameters were less than 2. 0 . The stability indicating method was developed by exposing the drug to stress conditions of acid and base hydrolysis, oxidation, photodegradation, and thermal degradation the obtained degraded products were successfully seperated from the APIs. This method was validated in acceptance with ICH guidelines and results within the acceptance criteria. 
by Rushikesh Mulay | Rishikesh Bachhav "Stability Indicating RP-HPLC Method Development and Validation of Everolimus in Bulk and Pharmaceutical Dosage Form" 

Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-5 | Issue-6 , October 2021, 



Curcumin Based Nanotherapy of Cancer A Review

September 05, 2021 0
Curcumin Based Nanotherapy of Cancer A Review
Cancer is the most prevalent disease not only in the United States but worldwide. The most representative polyphenol component extracted from the rhizomes of Curcuma long a known as turmeric is curcumin. The therapeutic benefits of curcumin have been demonstrated in multiple chronic diseases inflammation, arthritis, metabolic syndrome, liver disease, obesity, neurodegenerative diseases and, above all, in several cancers. Chemotherapy is a major form of treatment modality for various human diseases and disorders in both developing and developed countries. This intervention has been associated with a number of side effects and poor compliance. Therefore, in recent years, a significant effort has been put forward for finding a better treatment modality that uses natural compounds or extracts. Among many naturally occurring polyphenol compounds, curcumin is a highly safe yellow pigment molecule, widely used as a food coloring agent, and can be used to treat various pathological conditions. 
by Rushikesh Mulay | Rishikesh Bachhav "Curcumin Based Nanotherapy of Cancer - A Review" 

Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-5 | Issue-6 , October 2021, 



Thursday 10 December 2020

Application of Hydrotrophy in HPLC Hydrotrophic Solution, A Novel Cost Effective and Eco Friendly Mobile Phase for Solubilization of Poorly Water Soluble Drugs

December 10, 2020 0
Application of Hydrotrophy in HPLC Hydrotrophic Solution, A Novel Cost Effective and Eco Friendly Mobile Phase for Solubilization of Poorly Water Soluble Drugs

Hydrotrophy is a unique molecular phenomenon that posses the ability to increase the solubility of sparingly soluble and poorly soluble drugs in water. A hydrotrophic solution can be defined as adding a solute, that is Hydrotrope, eg urea to the primary one solvent and is used as mobile phase for HPLC. High solubility, easy availability, cost effectiveness, eco friendly are the major advantages which makes the solubilization technique superior. Here we use paracatamol and diclofenac sodium as example to review and conclude this topic. The current review takes the readers throughout a brief summary and features of hydrotropic agents and their different advances towards HPLC technique. It provides an insight of the future perspectives concerned with HPLC and Hydrotropism. 

by Ahammed Unais V P | P K Sahoo "Application of Hydrotrophy in HPLC; Hydrotrophic Solution, A Novel Cost Effective and Eco-Friendly Mobile Phase for Solubilization of Poorly Water Soluble Drugs" 

Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-5 | Issue-1 , December 2020, 

URL: https://www.ijtsrd.com/papers/ijtsrd38222.pdf

Paper URL : https://www.ijtsrd.com/pharmacy/analytical-chemistry/38222/application-of-hydrotrophy-in-hplc-hydrotrophic-solution--a-novel-cost-effective-and-ecofriendly-mobile-phase-for-solubilization-of-poorly-water-soluble-drugs/ahammed-unais-v-p

callforpapereconomics, economicsjournal

Thursday 24 September 2020

Review Article on Valsartan

September 24, 2020 0
Review Article on Valsartan

A simple, sensitive, rapid and reproducible HPLC method has been developed and validated for Calibration determination of Valsartan in bulk and in pharmaceutical formulation by applying Quality intentionally. For development of HPLC method for Valsartan various trials are performed by using Design Expert software by applying 3 level factorial designs. Quantitative method development by optimization from trials intentionally Expert software. The Optimized method Desirabilityis0.998 for Mobile Phase ACN Phosphate Buffer 65 35 in3.5 pH at maximum Wavelength 274nm at column oven temperature 40°C. The flow of mobile phase was adjusted 1.0 ml min. and therefore the injection volume 10 µl. Optimised Standard curve showed a parametric statistic is 0.998. Retention time was found to be 4.6 min. the half of recovery was found to be within the bounds of the acceptance criteria with average recovery of 99.4 you take care of Valsartan. The tactic was validated as per ICH guidelines. The precision and repeatability results showed RSD but 2 . The developed method was successfully validated in consistent with ICH guidelines. Hence, these methods are often conveniently adopted for the routine analysis in internal control laboratories. 

by Mr. Sandeep Markad | Dr. Amit Kasabe | Dr. Ashok Bhosale "Review Article on Valsartan" 

Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-4 | Issue-6 , October 2020, 

URL: https://www.ijtsrd.com/papers/ijtsrd33435.pdf

Paper Url: https://www.ijtsrd.com/pharmacy/analytical-chemistry/33435/review-article-on-valsartan/mr-sandeep-markad

callforpaperlifesciences, lifesciencesjournal, researchpapers

Friday 8 May 2020

Current Status and Future Perspective of Rapid Diagnostic Kits Vaccine against COVID 19

May 08, 2020 0
Current Status and Future Perspective of Rapid Diagnostic Kits Vaccine against COVID 19
Coronavirus disease 2019 COVID 19 , which causes serious respiratory illness such as pneumonia and lung failure, was first reported in Wuhan, the capital of Hubei, China. The etiological agent of COVID 19 has been confirmed as a novel coronavirus, now known as severe acute respiratory syndrome coronavirus 2 SARS CoV 2 , which is most likely originated from zoonotic coronaviruses, like SARS CoV, which emerged in 2002. Rapid diagnostics, vaccines and therapeutics are important interventions for the management of the 2019 novel coronavirus 2019 nCoV outbreak. Currently, various diagnostic kits to test for COVID 19 are available and several repurposing therapeutics for COVID 19 have shown to be clinically effective. In addition, global institutions and companies have begun to develop vaccines for the prevention of COVID 19. Here, we review the current status of, diagnosis, and vaccine development for COVID 19. 

by M A Nandedkar | R A Shinde | S S Bansode ""Current Status and Future Perspective of Rapid Diagnostic Kits / Vaccine against COVID-19""

Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-4 | Issue-4 , June 2020,

URL: https://www.ijtsrd.com/papers/ijtsrd30977.pdf

Paper Url :https://www.ijtsrd.com/pharmacy/analytical-chemistry/30977/current-status-and-future-perspective-of-rapid-diagnostic-kits--vaccine-against-covid19/m-a-nandedkar

ugclistedjournals, indexedjournal, paperpublication

Monday 16 December 2019

RP-HPLC Method Developed for the Estimation of Etodolac and Thiocolchicoside in Bulk and Combined Dosage Forms

December 16, 2019 0
RP-HPLC Method Developed for the Estimation of Etodolac and Thiocolchicoside in Bulk and Combined Dosage Forms

A new, simple, specific, sensitive, rapid, accurate and precise RP HPLC method was developed for the estimation of Etodolac ETO and Thiocolchicoside THIO in bulk and combined pharmaceutical dosage forms. Etodolac ETO and Thiocolchicoside THIO was chromatographed on a Symmetry ODS C18 4.6mm—250mm, 5µm Column in a mobile phase consisting of Acetonitrile Methanol Acetate Buffer 25 20 55 v v . The mobile phase was pumped at a flow rate of 1.0 ml min with detection at 238 nm. The detector response was linear in the concentration of 200 600µg ml 20 60µg ml for Etodolac and Thiocolchicoside respectively. The intra and inter day variation was found to be less than 2 . The mean recovery of the drug from the solution was 99.98 . The developed method was validated for sensitivity, accuracy, precision, ruggedness and robustness. The RSD results for precision and intermediate precision found less than 2.0 . The LOD and LOQ were found to be 0.86 and 1.18 µg ml for Etodolac and 2.4 and 3.54µg ml for Thiocolchicoside respectively. The proposed method is simple, fast, accurate, precise and reproducible hence it can be applied for routine quality control analysis of Etodolac ETO and Thiocolchicoside THIO in bulk and combined pharmaceutical formulations. 


by Prapulla Putta "RP-HPLC Method Developed for the Estimation of Etodolac and Thiocolchicoside in Bulk and Combined Dosage Forms"

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/ijtsrd29703.pdf

Paper URL: https://www.ijtsrd.com/pharmacy/analytical-chemistry/29703/rp-hplc-method-developed-for-the-estimation-of-etodolac-and-thiocolchicoside-in-bulk-and-combined-dosage-forms/prapulla-putta

ugc approved journals for social science, management journal, paper publication for engineering

Development and Validation of Analytical Methods for Simultaneous Spectrophotometric Determination of Pioglitazone and Glimepiride by Derivative Method

December 16, 2019 0
Development and Validation of Analytical Methods for Simultaneous Spectrophotometric Determination of Pioglitazone and Glimepiride by Derivative Method
A simple, rapid UV Visible spectrophotometric method for the quantification of Pioglitazone hydrochloride and Glimepiride in bulk drug and tablet formulation was developed and validated. UV Visible spectrophotometric methods have been developed for the Derivative Spectrophotometric Method, of Pioglitazone and glimepiride in bulk and pharmaceutical dosage forms. the sampling wavelengths selected are 210 nm and 218 nm over the concentration ranges of 1.5 7.5 µg ml and 0.2 1.0 µg ml for pioglitazone and glimepiride respectively.

by Tejaswini Kande | Pallavi Dhekale | Supriya Khatal | Priyanka Borude "Development and Validation of Analytical Methods for Simultaneous Spectrophotometric Determination of Pioglitazone and Glimepiride by Derivative 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/ijtsrd29699.pdf

Paper URL: https://www.ijtsrd.com/pharmacy/analytical-chemistry/29699/development-and-validation-of-analytical-methods-for-simultaneous-spectrophotometric-determination-of-pioglitazone-and-glimepiride-by-derivative-method/tejaswini-kande

ugc approved journals for management, mathematics journal, multidisciplinary journal

Friday 22 November 2019

Determination of Etodolac in Commercial Formulations by HPLC-UV Method

November 22, 2019 0
Determination of Etodolac in Commercial Formulations by HPLC-UV Method
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. 

by 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.pdf

Paper URL: https://www.ijtsrd.com/pharmacy/analytical-chemistry/29452/determination-of-etodolac-in-commercial-formulations-by-hplc-uv-method/tugrul-cagri-akman

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Sunday 20 October 2019

Development and Validation of RP HPLC Method for Estimation of Vortioxetine in Bulk and Pharmaceutical Dosage Form

October 20, 2019 0
Development and Validation of RP HPLC Method for Estimation of Vortioxetine in Bulk and Pharmaceutical Dosage Form
A rapid and precise reverse phase high performance liquid chromatographic method has been developed for the validated of Vortioxetine in its pure form as well as in tablet dosage form. Chromatography was carried out on ODS C18 4.6 x 250 mm, 5µm column using Acetonitrile And Methonal 70 30 as the mobile phase at a flow rate of 1.0 mL min, the detection was carried out at 274nm. The retention time of the Vortioxetine was 2.922 ±0.02min. The method produce linear responses in the concentration range of 20 µg ml of Vortioxetine. The method precision for the determination of assay was below 2.0 RSD. The method is useful in the quality control of bulk and pharmaceutical formulations. 

by Rathod K. G | Bargaje G. S | Rathod G. R | Deshpande O. V "Development and Validation of RP-HPLC Method for Estimation of Vortioxetine in Bulk and Pharmaceutical Dosage Form"

Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-3 | Issue-6 , October 2019,

URL: https://www.ijtsrd.com/papers/ijtsrd28040.pdf

Paper URL: https://www.ijtsrd.com/pharmacy/analytical-chemistry/28040/development-and-validation-of-rp-hplc-method-for-estimation-of-vortioxetine-in-bulk-and-pharmaceutical-dosage-form/rathod-k-g

peer reviewed international journal, call for paper economics, ugc approved journals for chemistry

Wednesday 16 October 2019

Development and Validation of an RP HPLC Method for Analysis of Sitagliptin

October 16, 2019 0
Development and Validation of an RP HPLC Method for Analysis of Sitagliptin

Sitagliptin is a drug used against type 2 diabetes mellitus and it is a member of class of anti diabetic drugs known as dipeptidyl peptidase 4 inhibitors or gliptins . A simple, sensitive and accurate RP HPLC method has been developed for the determination of Sitagliptin in bulk formulation. The max of the Sitagliptin was found to be 267nm in Methanol phosphate buffer 10mM pH 4.8 60 40 v v . The method shows high sensitivity with linearity 10 to 50µg ml regression equation y = 45765x 239272 r2 = 0.9996 . The various parameters according to ICH guidelines and USP are followed for validating and testing of this method. The Detection limit and quantitation limit were found to be 0.743 µg ml-1 and 2.25µgml-1 respectively. The results demonstrated that the procedure is accurate, specific and reproducible RSD 2 , and also being simple, cheap and less time consuming and appropriate for the determination of Sitagliptin in bulk and pharmaceutical formulation. 


by Pradnya Lokhande "Development and Validation of an RP-HPLC Method for Analysis of Sitagliptin"

Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-3 | Issue-6 , October 2019,

URL: https://www.ijtsrd.com/papers/ijtsrd29214.pdf

Paper URL: https://www.ijtsrd.com/chemistry/analytical-chemistry/29214/development-and-validation-of-an-rp-hplc-method-for-analysis-of-sitagliptin/pradnya-lokhande

ugc approved journals for management, mathematics journal, multidisciplinary journal

Friday 9 August 2019

Review Conductivity of Water Purified and SWFI at Different pH and Temperatures

August 09, 2019 0
Review Conductivity of Water Purified and SWFI at Different pH and Temperatures

This paper in particular mainly concerns with the conductivity of water used in pharmaceutical preparation, i.e. purified water and SWFI sterile water for injection . This paper is focused on the variation of conductivity of the water purified and SWFI with the change in pH and temperature. 


by Faiz Hashmi ""Review: Conductivity of Water (Purified and SWFI) at Different pH and Temperatures""

Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-3 | Issue-5 , August 2019,

URL: https://www.ijtsrd.com/papers/ijtsrd27942.pdf

Paper URL: https://www.ijtsrd.com/pharmacy/analytical-chemistry/27942/review-conductivity-of-water-purified-and-swfi-at-different-ph-and-temperatures/faiz-hashmi

ugc approved journals for social science, management journal, paper publication for engineering

Anti Microbiological Assay Test or Antibiotic Assay Test of Pharmaceutical Preparation Containing Antibiotics using 'Cylinder Plate Method'

August 09, 2019 0
Anti Microbiological Assay Test or Antibiotic Assay Test of Pharmaceutical Preparation Containing Antibiotics using 'Cylinder Plate Method'

In this paper, we are going to discuss the anti microbiological assay of the antibiotics. Aim of this paper is to predict the potency of the antibiotic preparation in reference with the working standard of the antibiotic and using the mathematical model in order to obtain the potency of the preparation in regards to its claim. 


by Faiz Hashmi ""Anti-Microbiological Assay Test or Antibiotic Assay Test of Pharmaceutical Preparation Containing Antibiotics using Cylinder Plate Method'"" 

Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-3 | Issue-5 , August 2019,

URL: https://www.ijtsrd.com/papers/ijtsrd27940.pdf

Paper URL: https://www.ijtsrd.com/pharmacy/analytical-chemistry/27940/anti-microbiological-assay-test-or-antibiotic-assay-test-of-pharmaceutical-preparation-containing-antibiotics-using-%E2%80%98cylinder-plate-method%E2%80%99/faiz-hashmi

ugc approved journals for science, manuscript publication, call for paper commerce

Sunday 14 July 2019

Analytical Method Development and Validation for the Estimation of Zolmitriptan by RP HPLC Method

July 14, 2019 0
Analytical Method Development and Validation for the Estimation of Zolmitriptan by RP HPLC Method

In this work the authors have proposed a simple, specific, economic and accurate reverse phase liquid chromatographic method for the estimation of Zolmitriptan as an active pharmaceutical ingredient and in pharmaceutical formulation. The main objective of the current research paper is to To develop simple, precise and accurate RP HPLC method for Zolmitriptan also to validate the developed method as per ICH guideline Q2R1 and to explore the applicability of the method in finished product formulation for estimation of Zolmitriptan during its lifecycle. The objective was achieved by optimized condition with Phonemenex C18 column 150mm×4.6mm , 5µm. And mobile phase Phosphate buffer pH 3.5 85 Methanol 15. The separation was done with a flow rate of 0.9ml min, detection with 224nm. The retention was found to be 3.57 minute. LOD and LOQ were found to be 2.45 and 7.42 respectively. So in order to obtain the correct results various validations methods are performed to get the results. The results obtained from those validation methods are plotted in the form of the charts as well as the different curves. 


by Mr. Rahul M. Sagde | Mr. Pawan N. Karwa | Mr. Vivek M. Thorat | Sanjay S. Jadhav ""Analytical Method Development and Validation for the Estimation of Zolmitriptan by RP HPLC Method""

Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-3 | Issue-5 , August 2019,

URL: https://www.ijtsrd.com/papers/ijtsrd26474.pdf

Paper URL: https://www.ijtsrd.com/pharmacy/analytical-chemistry/26474/analytical-method-development-and-validation-for-the-estimation-of-zolmitriptan-by-rp-hplc-method/mr-rahul-m-sagde

paper publication in science, call for paper medical science, ugc approved management journal

Saturday 13 July 2019

Nutritive Evaluation, Mineral Composition and Phytochemical Analysis of Leaf Protein Concentrates of Daucus carota

July 13, 2019 0
Nutritive Evaluation, Mineral Composition and Phytochemical Analysis of Leaf Protein Concentrates of Daucus carota

Fresh green leaves of Daucus Carota was harvested and processed with a view to analyse its photochemical constituents and nutritional potentials. Proximate analysis, mineral analysis and phytochemical analysis was determining using standard analytical techniques. The nutrient composition of the leaf protein concentrate revealed Moisture content 8.69±0.03 g 100g, crude protein 18.38±0.08 g 100g, crude fibre 14.81±0.02 g 100g, crude fat 5.69±0.23 g 100g, Ash 19.69±0.02g 100g , and NFE 32.74±0.43 g 100g.The mineral analysis of the sample shows the concentrations of the elements in the following descending order of magnitude Ca P Mg Na Fe K Zn Cu Mn Se while Hg was not detected in the sample. The photochemical constituents also revealed Tanin 3.66±0.16 mg 100g, Saponin 4.34±0.06 mg 100g, Alkaloid 10.49±0.02 mg 100g, Oxalate 6.89±0.04 mg 100g, Phytate 14.62±0.05 mg 100g, Phenolics 3.75±0.82 mg 100g, Flavonoids 3.62±0.43 mg 100g. High Concentration of Calcium and Phosphorus indicates that Daucus carota leaf protein concentrates is fit for consumption by children, pregnant women and weaned infants for good teeth and bone formation. The constituents of Daucus carota leaf protein concentrates present values of significant nutritional benefits and can find application in various food additives, binders, flavonoids and vitamins. It could also be used as additives in some drugs if the active compounds present in it could be analysed to detect its suitability. 


by Sodamade, A. | Raimi, S. M. | Owonikoko, A. D. | Adebimpe, A. T. ""Nutritive Evaluation, Mineral Composition and Phytochemical Analysis of Leaf Protein Concentrates of Daucus carota""

Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-3 | Issue-5 , August 2019,

URL: https://www.ijtsrd.com/papers/ijtsrd26427.pdf

Paper URL: https://www.ijtsrd.com/chemistry/analytical-chemistry/26427/nutritive-evaluation-mineral-composition-and-phytochemical-analysis-of-leaf-protein-concentrates-of-daucus-carota/sodamade-a

call for paper international journal, call for paper mathematics

Monday 6 May 2019

Analytical Methods Development and Validation of Naproxen and Sumatriptan by RP HPLC

May 06, 2019 0
Analytical Methods Development and Validation of Naproxen and Sumatriptan by RP HPLC

Aim and objective A simple, précised, accurate method was developed for the estimation of Crizotinib by RP HPLC technique. Chromatographic conditions used are stationary phase BDS 250x4.6 mm, 5µ. Mobile phase buffer Methodology Acetonitrile in the ratio of 60 40 and flow rate was maintained at1ml min, detection wave length was 267 nm, column temperature was set to 30o C and diluents was methanol water System suitability parameters were studied by injecting the standard five times and results were well 50 50 , Results and Discussion Conditions were finalized as optimized method under acceptance criteria. Linearity study was carried out between 25 to 150 levels, r2 value was found to be as 0.999. Precision was found to be 1.26 for repeatability and 0.93 for intermediate precision. LOD and LOQ are 0.080 ug ml. By using above method assay of marketed formulation was carried out 100.24 was present. 


By Prapulla Putta "Analytical Methods Development and Validation of Naproxen and Sumatriptan by RP HPLC"

Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-3 | Issue-4 , June 2019,

URL: https://www.ijtsrd.com/papers/ijtsrd23582.pdf

Paper URL: https://www.ijtsrd.com/pharmacy/analytical-chemistry/23582/analytical-methods-development-and-validation-of-naproxen-and-sumatriptan-by-rp-hplc/prapulla-putta

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Monday 25 March 2019

Solvent Extraction and Spectrophotometric Determination of Nickel II using 2 "“ Hydroxy 1 Naphthaldehyde Thiosemicarbazone HNT as an Analytical Reagent

March 25, 2019 0
Solvent Extraction and Spectrophotometric Determination of Nickel II using 2 "“ Hydroxy 1 Naphthaldehyde Thiosemicarbazone HNT as an Analytical Reagent

2 – hydroxy 1 naphthaldehyde thiosemicarbazone HNT is synthesized in laboratory and characterized by NMR, IR and elemental analysis for its purity. This reagent forms a yellowish green coloured complex with Ni II which can be quantitatively extracted into ethyl acetate at pH 7. Complex in ethyl acetate shows an intense absorption peak 430 nm. It is observed that Beers law is obeyed in the range of 10µg to 100µg of metal solution. It gives linear and reproducible graph under appropriate conditions, the complex having a molar absorptivity of 0.275 x 10 6L mol 1 cm 1, Sandells sensitivity calculated was found to be 0.275 x 102 µg cm 2 .Nature of the extracted complex, determined by Jobs continuous variation method, Slope ratio method and Mole ratio method shows that the composition of Ni II HNT is 1 1. Interference by various ions is studied and masking agents used where required. The proposed method has been applied for the determination of Ni II in various samples. The results of the analysis are found to be comparable with those obtained by standard method. 


by Pradnya Lokhande "Solvent Extraction and Spectrophotometric Determination of Nickel (II) using 2 – Hydroxy 1- Naphthaldehyde Thiosemicarbazone (HNT) as an Analytical Reagent"

Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-3 | Issue-3 , April 2019,

URL: https://www.ijtsrd.com/papers/ijtsrd22964.pdf

Paper URL: https://www.ijtsrd.com/chemistry/analytical-chemistry/22964/solvent-extraction-and-spectrophotometric-determination-of-nickel-ii-using-2-%C3%A2%E2%82%AC%E2%80%9C-hydroxy-1--naphthaldehyde-thiosemicarbazone-hnt-as-an-analytical-reagent/pradnya-lokhande

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Tuesday 12 March 2019

Analytical Method Development and Validation of Metformin Hydrochloride by using RP HPLC with ICH Guidelines

March 12, 2019 0
Analytical Method Development and Validation of Metformin Hydrochloride by using RP HPLC with ICH Guidelines

A simple and reproducible method was developed for Metformin MET by Reverse Phase High Performance Liquid Chromatography RP HPLC . Metformin was separated on C18 column 4.6x250mm, particle size 5µm , using combination of phosphate buffer with pH of 3.0 and Methanol at the UV detection of 238nm. Isocratic elution of phosphate buffer with pH of 3.0 and Methanol was used as a mobile phase with various ratios and flow rates, eventually 30 70 v v phosphate buffer with pH of 3.0 and Methanol was being set with the flow rate of 1mL min. The statistical validation parameters such as linearity, accuracy, precision, inter day and intra day variation were checked, assay studies of Metformin were within 98 to 102 indicating that the proposed method can be adoptable for quality control analysis of Metformin. 


by Mr. Nilesh Nikam | Dr. Avish Maru | Dr. Anil Jadhav | Dr. Prashant Malpure "Analytical Method Development and Validation of Metformin Hydrochloride by using RP-HPLC with ICH Guidelines"

Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-3 | Issue-3 , April 2019,

URL: https://www.ijtsrd.com/papers/ijtsrd22812.pdf

Paper URL: https://www.ijtsrd.com/pharmacy/analytical-chemistry/22812/analytical-method-development-and-validation-of-metformin-hydrochloride-by-using-rp-hplc-with-ich-guidelines/mr-nilesh-nikam

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