Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Hitesh A. Jogia"'
Publikováno v:
Chromatographia. 85:177-191
Publikováno v:
Chromatographia. 83:1197-1220
We developed a novel, rapid, sensitive, and stability-indicating UHPLC method for quantification of Perindopril (PER), Amlodipine (AML), and their impurities in pharmaceutical formulations. The optimum chromatographic separation was achieved in gradi
Publikováno v:
Analytical Chemistry Letters. 10:477-497
A simple, rapid, mass compatible, selective, stability-indicating ultra high performance liquid chromatographic method was developed for the simultaneous estimation of Perindopril (PER), Indapamide...
Publikováno v:
Oriental Journal of Chemistry. 34:1098-1104
Autor:
Hitesh A. Jogia, Kancherla Prasad, Datla Peda Varma, Khagga Bhavyasri, Khagga Mukkanti, T.S.S. Jagan Mohan
Publikováno v:
Asian Journal of Chemistry. 29:1360-1364
Autor:
Kancherla Prasad, T.S.S. Jagan Mohan, Khagga Bhavyasri, Datla Peda Varma, Khagga Mukkanti, Hitesh A. Jogia
Publikováno v:
Asian Journal of Chemistry. 29:1113-1118
Autor:
Vobalaboina Venkateswarlu, Srinivas Arutla, Surya Prakash Sola, Annarapu Malleswara Reddy, Hitesh A. Jogia, Lovleen Kumar Garg
Publikováno v:
Dissolution Technologies. 21:45-48
Biorelevant dissolution media were designed and proposed based on physiological and physicochemical properties of the small intestine luminal contents in the fastedand fed-state conditions. Biorelevant dissolution media have proved to be an excellent
Publikováno v:
Dissolution Technologies. 16:14-19
The objective of this study was to employ a tailor-made, surface-active agent (phosphonobile acid) in the design of dissolution media that more closely reflect various luminal fluid physicochemical parameters such as buffer capacity, osmolarity, surf
Publikováno v:
Scientia Pharmaceutica
Volume 81
Issue 4
Pages 1043-1056
Volume 81
Issue 4
Pages 1043-1056
A simple, fast, and sensitive reversed-phase HPLC method with UV detection was developed for the quantitation of omeprazole and its eleven related compounds (impurities) in pharmaceutical formulation using the Thermo Accucore C–18 (50 mm x 4.6 mm,
Publikováno v:
Scientia Pharmaceutica
Volume 81
Issue 2
Pages 505-518
Volume 81
Issue 2
Pages 505-518
A stability-indicating reversed-phase high-performance liquid chromatography (RP-HPLC) method was developed for the simultaneous determination of halometasone, fusidic acid, methylparaben, and propylparaben in topical pharmaceutical formulation. The