American Journal of Analytical Chemistry

American Journal of Analytical Chemistry

ISSN Print: 2156-8251
ISSN Online: 2156-8278
www.scirp.org/journal/ajac
E-mail: ajac@scirp.org
"A Validated Stability Indicating RP-UPLC Method for Atrovastain Calcium"
written by Kakumani Kishore Kumar, Chimalakonda Kameswara Rao, Maddala Vijaya Lakshmi, Khagga Mukkanti,
published by American Journal of Analytical Chemistry, Vol.3 No.5, 2012
has been cited by the following article(s):
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[1]  Study of the dissolution kinetics of drugs in solid dosage form with lisinopril and atorvastatin and intestinal permeability to assess their equivalence in vitro
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[2] Review on forced degradation study of statins
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[3] Development of a Novel, Fast, Simple HPLC Method for Determination of Atorvastatin and its Impurities in Tablets
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[4] Chaotropic salts impact in HPLC approaches for simultaneous analysis of hydrophilic and lipophilic drugs
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[5] Specific Stability Indicating RP-HPLC Photodiode Array Based Method for Estimation of Novel combination Atorvastatin Calcium and Vitamin D3 for the treatment of …
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[6] ANALYTICAL METHODS FOR THE QUANTITATION OF AMLODIPINE BESYLATE AND ATORVASTATIN CALCIUM IN PHARMACEUTICAL DOSAGE FORM …
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[7] Analytical methods for the quantitation of amlodipine besylate and atorvastatin calcium in pharmaceutical dosage form and biological fluids
International Journal of Applied …, 2019
[8] Bioanalytical Method Development and Validation of Atorvastatin in Human Plasma by Using UV-Visibile Spectrophotometry
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[9] Isolation, Identification and Characterization of Degradation Impurity of Atorvastatin in Fixed Dose Combination of Atorvastatin and Ezetimibe
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[10] Forced degradation study of statins: A review
2018
[11] Optimization of a forced degradation study of atorvastatin employing an experimental design approach
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[12] Concepts in development of fast, simple, stability indicating HPLC method for analysis of atorvastatin related compounds in tablets
2018
[13] A NOVEL STABILITY-INDICATING RP-UPLC METHOD FOR THE QUANTIFICATION OF IMPURITIES AND A NEW QDa MASS DETECTOR COUPLED WITH LC-PDA FOR IDENTIFICATION OF MASS OF DEGRADATION PRODUCTS IN A FIXED DOSE COMBINATION OF EMPAGLIFLOZIN AND LANIGLIPTIN TABLETS USED AS SECOND-LINE THERAPY FOR TYPE-2 DIABETES
INTERNATIONAL RESEARCH JOURNAL OF PHARMACY, 2018
[14] METHOD DEVELOPMENT AND VALIDATION OF RP-UPLC METHOD FORTHE DETERMINATION OF SEMAGLUTIDE IN BULK ANDPHARMACEUTICAL DOSAGE FORM
International Journal of Research and Analytical Reviews, 2018
[15] Understanding unconventional routes to impurities from drugs in hydrolytic conditions
2016
[16] Comparative in vitro and in vivo Bioequivalence Analysis of some Brands of film coated Atorvastatin (a BCS Class II Compound) tablets marketed in Nigeria
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[17] Comparative in vitro and in vivo Bioequivalence Analysis of some Brands of film coated Atorvastatin (a BCS Class II Compound) tablets marketed in …
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[18] Design and study of reverse phase ultra high performance liquid chromatographic method for simultaneous estimation of two antidiabetic drugs with an …
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[19] A Compendium of Techniques for the Analysis of Pharmaceutical Impurities
Current Pharmaceutical Analysis, 2014
[20] DESIGN AND STUDY OF REVERSE PHASE ULTRA HIGH PERFORMANCE LIQUID CHROMATOGRAPHIC METHOD FOR SIMULTANEOUS ESTIMATION OF TWO ANTIDIABETIC DRUGS WITH AN ANTIHYPERLIPEMIC DRUG USING STATISTICAL APPROACH.
International Journal of Pharmacy & Pharmaceutical Sciences?, 2014
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