Zobrazeno 1 - 10
of 13
pro vyhledávání: '"P. N., Sanjay Pai"'
Publikováno v:
E-Journal of Chemistry, Vol 7, Iss 4, Pp 1435-1439 (2010)
A series of quinoxaline derivatives was prepared and evaluated for antitubercular, antibacterial and antifungal activities. The title compounds were prepared by condensation of substituted aromatic aldehydes and substituted acetophenones with 2-(3-me
Externí odkaz:
https://doaj.org/article/2e195dfdd8e14c60bb0b9b091c6e3516
Challenges in Simultaneous Analysis of Hydrolytically Sensitive Ester drugs in Combined Dosage Forms
Publikováno v:
Indian Journal of Pharmaceutical Education and Research. 53:97-103
Publikováno v:
Indian Journal of Chemistry (0019-5103); 2022, Vol. 61 Issue 11, p1169-1172, 4p
Autor:
P. N. Sanjay Pai, Neelam Sawant
Publikováno v:
Indian Journal of Pharmaceutical Education and Research. 51:388-392
Autor:
P. N. Sanjay Pai, Anjaly Pillai
Publikováno v:
Oriental Journal Of Chemistry. 29:771-775
A validated simple, accurate and rapid spectrophotometric method was developed for the estimation of isosorbide mononitrate in bulk and tablet formulation. The method is based on the reduction of nitrate group of isosorbide mononitrate to nitrite ion
Publikováno v:
E-Journal of Chemistry, Vol 7, Iss 4, Pp 1435-1439 (2010)
A series of quinoxaline derivatives was prepared and evaluated for antitubercular, antibacterial and antifungal activities. The title compounds were prepared by condensation of substituted aromatic aldehydes and substituted acetophenones with 2-(3-me
Publikováno v:
Journal of Pharmacology and Toxicology. 2:248-255
Autor:
Neelam Sawant, P. N. Sanjay Pai
Publikováno v:
Journal of Pharmaceutical Research. 15:79
Purpose : A new stability-indicating RP-HPLC assay method for estimation of indomethacin and its degradation products formed under various stress conditions was developed and validated for routine analysis of indomethacin in its marketed dosage forms
Autor:
P. N. Sanjay Pai
Publikováno v:
Journal of Pharmaceutical Research. 15:26
Publikováno v:
Pakistan journal of pharmaceutical sciences. 22(4)
GMP conditions commands to control adequately the quality of APIs by checking the levels of residual solvents. Organic solvents such as acetone, ethyl acetate, isopropyl alcohol, methanol, tetrahydrofuran and toluene frequently used in pharmaceutical