Zobrazeno 1 - 10 of 27 pro vyhledávání: '"Saeed A Qureshi"'
2
'Quality' of pharmaceutical products for human use—underlying concepts and required practices
Autor: Saeed A. Qureshi
The term quality of pharmaceutical products is frequently used in the literature interchangeably with safety and efficacy without a clear description. The lack of clarity and relevant use of these terminologies appear not only to cause confusion, but
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d38d0c9102fbd01ceb8fa10908135109
https://doi.org/10.1016/b978-0-12-817870-6.00009-2
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5
A Simple and Economical Approach/Concept to Evaluate Quality of Pharmaceutical Products Based on an Improved Dissolution Testing Methodology
Autor: Saeed A. Qureshi
Publikováno v: The Open Drug Delivery Journal. 2:33-37
Often the quality of drug products is evaluated based on chemical tests, commonly described in different phar- macopeias such as the USP. These tests includes: assay (potency), uniformity of dosage form and dissolution test. Pres- ently, these tests
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::039751c7e6fdcd9ae07ef1a0ea961957
https://doi.org/10.2174/1874126600802010033
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6
A Critical Assessment of Current Practices of Drug Dissolution Testing – Irrelevancies, their Causes and Suggestions to Address These
Autor: Saeed A Qureshi
Publikováno v: Journal of Applied Pharmacy.
In principle, drug dissolution testing should be one of the simplest analytical techniques, however, in practice it is perhaps the most confusing, complex and frustrating techniques often lacking scientific and/or logical considerations. Perhaps the
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ef56578e44359913ccf3c044282ac47c
https://doi.org/10.4172/1920-4159.1000208
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7
Comparative Impact of Stirring and Shearing in Drug Dissolution Testing with USP Paddle and Crescent-Shaped Spindles
Autor: Saeed A. Qureshi
Publikováno v: Dissolution Technologies. 13:25-30
Introduction Drug dissolution testing is an integral part of drug product development and quality assessment. Often drug dissolution testing is a regulatory requirement to establish the quality of a drug product [1-3]. In reality,drug dissolution tes
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::44d2a0bcc6675473491fad669ae1e8d4
https://doi.org/10.14227/dt130106p25
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9
Quantification of ketoprofen enantiomers in human plasma based on solid-phase extraction and enantioselective column chromatography
Autor: Saeed A Qureshi, Iain J. McGilveray, Gilles Caillé, Julie Boisvert
Publikováno v: Journal of Chromatography B: Biomedical Sciences and Applications. 690:189-193
An HPLC method for the quantification of ketoprofen enantiomers in human plasma is described. Following extraction with a disposable C 18 solid-phase extraction column, separation of ketoprofen enantiomers and I.S. (3,4-dimethoxy benzoic acid) was ac
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dca013191db67ce2cd71366b40d4c972
https://doi.org/10.1016/s0378-4347(96)00402-1
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10
Calibration—The USP Dissolution Apparatus Suitability Test
Autor: Saeed A. Qureshi
Publikováno v: Drug Information Journal. 30:1055-1061
This report summarizes some trends observed in drug dissolution testing, based upon the United States Pharmacopeia (USP) dissolution Apparatus Suitability Test results and the preliminary data obta...
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4563ccf9ffd3826b66e286a3d52a34da
https://doi.org/10.1177/009286159603000422
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