Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Shakil S. Sait"'
Autor:
Jyotsna Cherukuri, B. Ramadevi, Shakil S. Sait, Ch. Venkata Ramana Reddy, Chunduru Srinivasa Rao
Publikováno v:
Asian Journal of Chemistry. 28:2579-2581
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7aa4006786abc237d1aa30f2d11279b0
https://doi.org/10.14233/ajchem.2016.19253
https://doi.org/10.14233/ajchem.2016.19253
Publikováno v:
Journal of Liquid Chromatography & Related Technologies. 38:677-686
This manuscript demonstrates a Quality by Design approach using Design of Experiments to prove the robustness of a stability indicating HPLC method. The method determines the omeprazole in the presence of eight related substances and ketoprofen with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::419695a54c75e650cbea7effa14d54fb
https://doi.org/10.1080/10826076.2014.951766
https://doi.org/10.1080/10826076.2014.951766
Autor:
Shakil S. Sait, Krishnamurthi Vyas, A. Malleswara Reddy, S. Jayapal Reddy, Palavai Sripal Reddy
Publikováno v:
Journal of Liquid Chromatography & Related Technologies. 37:2490-2505
A novel gradient reversed-phase high-performance liquid chromatographic method has been developed for quantitative determination of Ropinirole hydrochloride and its six impurities in pharmaceutical dosage forms. Chromatographic separation has been ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4120b4b8058e350e809865832062f9ab
https://doi.org/10.1080/10826076.2013.850720
https://doi.org/10.1080/10826076.2013.850720
Autor:
Lovleen Kumar Garg, A. Malleswara Reddy, T. Krishnamurthy, S. Jafer Vali, Shakil S. Sait, Vajrala S. Reddy
Publikováno v:
Chromatographia. 76:1697-1706
This paper describes a systematic design of experiments (DoE) approach by applying the principle of quality by design (QbD) to determine the design space for a stability-indicating HPLC method prior to validation. By employing DoE, a simultaneous mul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b174a4939fabad2af9730a7da0055d7c
https://doi.org/10.1007/s10337-013-2509-4
https://doi.org/10.1007/s10337-013-2509-4
Publikováno v:
Scientia Pharmaceutica
Volume 81
Issue 2
Pages 475-492
Volume 81
Issue 2
Pages 475-492
A complex, sensitive, and precise high-performance liquid chromatographic method for the profiling of impurities of esomeprazole in low-dose aspirin and esomeprazole capsules has been developed, validated, and used for the determination of impurities
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d51a5e58c2022a9d1b2ec0d36ec094a8
http://europepmc.org/articles/PMC3700076
http://europepmc.org/articles/PMC3700076
Publikováno v:
Journal of Liquid Chromatography & Related Technologies. 35:1550-1564
A new stability-indicating gradient reverse phase high-performance liquid chromatographic (RP-HPLC) method was developed for the quantitative determination of Eslicarbazepine acetate (antiepileptic drug) in bulk drugs and pharmaceutical dosage forms
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::234d1763bf37e3427b5668300ff327b8
https://doi.org/10.1080/10826076.2011.619043
https://doi.org/10.1080/10826076.2011.619043
Autor:
Y. Ramakoti Reddy, Shakil S. Sait, K. Mukkanti, Dinesh Chakole, Dantu Durga Rao, A. Malleswara Reddy
Publikováno v:
Journal of Chromatographic Science. 48:819-824
A reproducible gradient reversed-phase ultra-performance liquid chromatographic method is developed for quantitative determination of duloxetine hydrochloride in pharmaceutical dosage forms. The method is also applicable for analysis of related subst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::584c65328dcd99eccad6219c7b3ebd05
https://doi.org/10.1093/chromsci/48.10.819
https://doi.org/10.1093/chromsci/48.10.819
Publikováno v:
Chromatographia. 70:647-651
A stability-indicating UPLC method was developed for the simultaneous quantitative determination of losartan potassium, atenolol, and hydrochlorothiazide in pharmaceutical dosage forms in the presence of degradation products. The separation was achie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd78053a08f881bc25c4c29c6a517de9
https://doi.org/10.1365/s10337-009-1221-x
https://doi.org/10.1365/s10337-009-1221-x
Publikováno v:
Chromatographia. 69:1133-1136
A stability-indicating LC method was developed for the simultaneous determination of ibuprofen and diphenhydramine citrate in pharmaceutical dosage forms. The chromatographic separation was achieved on an Inertsil ODS 3V, 150 × 4.6 mm, 5 μm, column
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ecce684ef1e6fd5450c3abe692649c16
https://doi.org/10.1365/s10337-009-0977-3
https://doi.org/10.1365/s10337-009-0977-3
Publikováno v:
ChemInform. 45
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed82166d89ec019a0c39a581e015a2ef
https://doi.org/10.1002/chin.201410153
https://doi.org/10.1002/chin.201410153