Refine your search
Collections
Co-Authors
Journals
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z All
Saravanan, V. S.
- Stability Indicating RP-HPLC Method for the Estimation of Emtricitabine and Tenofovir Disoproxil Fumerate in Tablet Dosage Form
Abstract Views :788 |
PDF Views:0
Authors
Affiliations
1 Department of Pharmaceutical Analysis, The Erode College of Pharmacy and Research, Erode- 638112, IN
1 Department of Pharmaceutical Analysis, The Erode College of Pharmacy and Research, Erode- 638112, IN
Source
Research Journal of Pharmacy and Technology, Vol 6, No 1 (2013), Pagination: 80-85Abstract
A simple, accurate and precise reverse phase high performance liquid chromatographic (RP-HPLC) method was developed for the simultaneous quantitative estimation of Emtricitabine (EMT) and Tenofovir disoproxil fumerate (TDF) in tablet dosage form. Quantitation was carried on an ACE (150 mm x 4.6mm, 5μ) column using gradient composition of 0.01 M citric acid monohydrate buffer pH 4.5 as mobile phase A and methanol as mobile phase B at a flow rate of 1.0 mL/min with detection at 260 nm. Determination of the different validation parameters such as precision, linearity, accuracy, specificity, robustness, limit of detection, limit of quantification and filter validation was done. The system suitability parameters such as retention time, theoretical plates and tailing factor were found to be 3.181min, 13438, 0.14 and 6.090min, 48847, 1.05 respectively for EMT and TDF. The detector response is linear from 16 μg/mL to 64 μg/mL for EMT and 24 μg/mL to 96 μg/mL TDF. The limit of detection and limit of quantification was 0.101, 0.189 μg/mLand 0.306, 0.575 μg/mL for EMT and TDF respectively. The percentage recovery for average of three different concentrations (50, 100 and 150%) was 101.1, 100.6, 99.8 and 99.7, 99.4, 99.6% for EMT and TDF respectively.The high percentage of recovery and low % RSD confirms the suitability of the method for the simultaneous estimation of EMT and TDF in tablet dosage form.The method could effectively separate the drugs from their degradation products, it can be regarded as stability indicating method.Keywords
RP-HPLC, Simultaneous Estimation, EMT, TDF, Forced Degradation StudiesReferences
- www.drugbank.com
- Appala NR, Rao VJ, Vanitha PK, Mukilteo K and Srinivasu K. Simultaneous estimation of tenofovir disoproxil, emtricitabine and efavirenz in tablet dosage form by RP- HPLC. Orient J Chem. 24(2); 2008: in press.
- Appala Raju N and Shabana Begum. Simultaneous RP-HPLC method for the estimation of the emtricitabine, tenofovir disoproxil fumerate and efavirenz in tablet dosage forms. Research Journal of Pharmacy and Technology. 1(4); 2008: 522-525.
- Shirkhedkar AA, Bhirud CH and Surana SJ. Application of UV spectrophotmetric methods for estimation of tenofovir disoproxil fumarate in tablets. Pak. J. Pharm. Sci. 22(1); 2009: 27-29.
- Sparidans RW, Crommentuyn KML, Schellens JHM and Beijnen JH. Liquid chromatographic assay for the antiviral nucleotide analogue tenofovir in plasma using derivatization with chloroacetaldehyde. Journal of Chromatography B. 791 (1-2); 2003: 227–233.
- Sentenac S, Fernandez C, Thuillier A, Lechat P and Aymard G. Sensitive determination of tenofovir in human plasma samples using reversed-phase liquid chromatography. Journal of ChromatographyB. 793 (2); 2003: 317–324.
- Kandagal PB, Manjunatha DH and Seetharamappa J. RP-HPLC Method for the determination of tenofovir in pharmaceutical formulations and spiked human plasma. Analytical letters. 41(4); 2008: 561-570.
- Delahunty T, Bushman L and Fletcher CV. Sensitive assay for determining plasma Tenofovir concentrations by LC/MS/MS. Journal of Chromatography B. 830; 2006: 6–12
- Masaaki T,Yuichi K, Naoya O, Atsushi H, Kazuhide B and Tsuguhiro K. Determination of plasma tenofovir concentrations using a conventional LC-MS method. Biological & Pharmaceutical Bulletin. 30; 2007:1784.
- King T, Bushman L, Kiser J, Anderson PL, Ray M, Delahunty T and Fletcher CV. Liquid chromatography tandem mass spectrometric determination of tenofovir diphosphate in human peripheral blood mononuclear cells. Journal of ChromatographyB. 843 (2); 2006: 147–156.
- Droste JAH, Aarnoutse RE and Burger DM. Determination of emtricitabine in human plasma using HPLC with fluorometric detection. Journal of Liquid Chromatography & Related Technologies. 30 (18); 2007: 2769 – 2778.
- Unnam S, Bodepudi H, Kottapalli B and Chandrasekhar. Development and validation of a stability-indicating liquid chromatographic method for determination of emtricitabine and related impurities in drug substance. Journal of Separation Science. 30; 2007:999 – 1004
- Rezk NL,Crutchley RD, Kashuba ADM. Simultaneous quantification of emtricitabine and tenofovir in human plasma using high performance liquid chromatography after solid phase extraction. Journal of Chromatography B. 822; 2005: 201.
- Gomes NA, Vaidya VV, Pudage A, Joshi SS, Parekh SA. Liquid chromatography–tandem mass spectrometry (LC–MS/MS) method for simultaneous determination of tenofovir and emtricitabine in human plasma and its application to a bioequivalence study. Journal of Pharmaceutical and Biomedical Analysis. 48; 2008: 918–926.
- Maithilee Joshi, Nikalje AP, Shahed M and Dehghan M. HPTLC method for the simultaneous estimation of emtricitabine and tenofovir in tablet dosage form. Indian Journal of Pharmaceutical Sciences. 71(1); 2009: 95–97.
- RP-HPLC Analysis for Quantitation of Candesartan Cilexetil in Solid Dosage Forms
Abstract Views :316 |
PDF Views:0
Authors
Affiliations
1 Department of Pharmaceutical Analysis, The Erode College of Pharmacy and Research, Erode, Tamil Nadu, IN
2 Department of Pharmaceutics, The Erode College of Pharmacy and Research, Erode, Tamil Nadu, IN
1 Department of Pharmaceutical Analysis, The Erode College of Pharmacy and Research, Erode, Tamil Nadu, IN
2 Department of Pharmaceutics, The Erode College of Pharmacy and Research, Erode, Tamil Nadu, IN
Source
Asian Journal of Pharmaceutical Analysis, Vol 3, No 4 (2013), Pagination: 115-118Abstract
A simple reverse phase liquid chromatographic method was developed and validated as per the ICH guidelines for the quantitative determination of candesartan cilexetil in pharmaceutical dosage forms. The mobile phase consisted of 0.02 M mono basic potassium phosphate buffer: acetonitrile: triethyl amine (40:60:0.2) and adjust pH to 6.0 with ortho phosphoric acid. The eluent was monitored at 254 nm, at a flow rate of 2 mL/min and retention time was observed at 9.153 min. The linearity was observed from 0.08071-0.24213 mg/mL with R2= 0.998. The LOD and LOQ were found to be 0.00005 mg/mL and 0.00017 mg/mL respectively. This method was also validated and can be successfully applied for routine analysis.Keywords
Candesartan Cilexetil, RP-HPLC, Validation.- Hepatoprotective Activity of Prunus persica Peaches against Paracetamol Induced Hepatotoxicity
Abstract Views :231 |
PDF Views:0
Authors
Affiliations
1 Dept. of Pharmacognosy, The Erode College of Pharmacy, Veppampalayam, Vallipurathan Palayam (PO), Erode – 638 112 Tamilnadu, IN
2 The Erode College of Pharmacy, Tamilnadu, IN
1 Dept. of Pharmacognosy, The Erode College of Pharmacy, Veppampalayam, Vallipurathan Palayam (PO), Erode – 638 112 Tamilnadu, IN
2 The Erode College of Pharmacy, Tamilnadu, IN
Source
Research Journal of Pharmacognosy and Phytochemistry, Vol 3, No 2 (2011), Pagination: 75-76Abstract
Hepato- toxicity is a common toxicity happening during the treatment of chronic disease like tuberculosis, diabetics. Prunus persica belongs to Rosaceae is a plant growing in temperate region has laxative , sedative, anticancer property and also consist of glycosides, flavonoids, anthocyanins, vitamins. It also posses hepato-protactent property. To prove the activity scientifically the ethanolic extract of Prunus persica was studied against paracetamol induced hepatotoxicity in albino rats. The extract when evaluated at dose of 100mg/ kg was found to significantly reduce the elevated levels of serum lysosomal enzyme Sgpt, Sgot, Alp and Bilirubin when compared with standard silymarin.
Keywords
Prunus persica, Paracetamol, Albino Rats, Serum Enzymes.- Haematological Activity of Cucurbita maxima Linn. Pulp in Phenylhydrazine Induced Anaemic Rats
Abstract Views :203 |
PDF Views:0
Authors
Affiliations
1 Dept. of Pharmacognosy, The Erode College of Pharmacy, Veppampalayam, Vallipurathan Palayam (PO), Erode – 638 112, Tamilnadu, IN
2 The Erode College of Pharmacy, Erode, IN
1 Dept. of Pharmacognosy, The Erode College of Pharmacy, Veppampalayam, Vallipurathan Palayam (PO), Erode – 638 112, Tamilnadu, IN
2 The Erode College of Pharmacy, Erode, IN
Source
Research Journal of Pharmacognosy and Phytochemistry, Vol 2, No 5 (2010), Pagination: 395-396Abstract
The hydro-alcoholic extract of Cucurbita maxima pulp shows the haematological activity against phenyl hydrazine induced anaemic rat. The hydro alcoholic extract of 150 mg/kg and 300 mg/kg are shown significant action against the anaemia, when compared to the 10 mg/kg of phenylhydrazine induced group after 4 weeks of treatment. The parameters determined are haemaglobulin content, RBC, WBC.Keywords
Haematinic Activity, Cucurbita maxima Pulp, Phenylhydrazine, Haematological Parameters.- Pitfalls in the Syllabus of B Sc (Honours) Microbiology Courses Proposed under Choice-Based Credit System by University Grants Commission, India
Abstract Views :340 |
PDF Views:109
Authors
Affiliations
1 Department of Microbiology, Indira Gandhi College of Arts and Science, Kathirkamam, Puducherry 605 009, IN
1 Department of Microbiology, Indira Gandhi College of Arts and Science, Kathirkamam, Puducherry 605 009, IN
Source
Current Science, Vol 112, No 07 (2017), Pagination: 1318-1319Abstract
Recently, the University Grants Commission, India has provided a structure of the model curriculum for B Sc (Honours) programme in Microbiology. It is based on the choice-based credit system pattern aiming to improve the academic standards and quality of microbiology education in the country. The structure of the programme has been divided into core courses, discipline-centric elective courses, generic electives, ability enhancement compulsory courses and skill enhancement elective courses. Most of the basic papers related to microbiology are well covered under the core courses and care has been taken to include the recently published books as references. However, certain terms that could bring confusion among the teachers and students have been included, and some topics that are important to microbiology are missing. The subject contents offered under the generic electives seem to be mere repetition of the core courses. Here, I provide a few suggestions to improve the standards of the above-mentioned programme.- UV Spectrophotometric Determination of Norethisterone in Tablets
Abstract Views :208 |
PDF Views:0
Authors
A. Rama Chandra Reddy
1,
K. Roshna
1,
P. Mohanraj
1,
T. M. Kulanthavel
1,
V. S. Saravanan
1,
V. Ganesh
1
Affiliations
1 Department of Pharmaceutical Analysis, The Erode College of Pharmacy, Veppampalayam, Erode-638112, TN, IN
1 Department of Pharmaceutical Analysis, The Erode College of Pharmacy, Veppampalayam, Erode-638112, TN, IN
Source
Asian Journal of Research in Chemistry, Vol 3, No 1 (2010), Pagination: 172-174Abstract
A new simple, sensitive, precise and economical spectrophotometric method of analysis for a bulk drug was developed and validated. The method employed methanol as solvent. The drug was then estimated at 270 nm. The linear regression analysis data for the calibration plots showed good linear relationship with r2=0.999 in the concentration range 0.5-3.0 μg/ml. The mean value of correlation coefficient, slope and intercept were 0.999, 0.0332 and 0.0002 respectively. The method was validated for precision, accuracy and recovery studies. LOD and LOQ for norethisterone was found to be 0.01987 (μg/ml) and 0.06024 (μg/ml) respectively. The method has been successfully applied in the analysis of marketed formulations.Keywords
Norethisterone, UV Spectrophotometric Analysis.- Comparative Analysis of Climbazole in Pharmaceutical Formulation
Abstract Views :215 |
PDF Views:0
Authors
Affiliations
1 Department of Analytical Chemistry, Erode College of Pharmacy, Erode-112, IN
2 Department of Pharmaceutical Bio-Technology, Nandha College of Pharmacy, Erode-52, IN
1 Department of Analytical Chemistry, Erode College of Pharmacy, Erode-112, IN
2 Department of Pharmaceutical Bio-Technology, Nandha College of Pharmacy, Erode-52, IN