Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Manish Majumder"'
Autor:
Premsagar K M, Bhagyalakshmi C, Piyong Sola, Akramul Ansary, Tridib Kumar Das, T. Yunus Pasha, Koushik Nandan Dutta, Ramesh B, Manish Majumder
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-15 (2024)
Abstract The current study developed a method for quantifying four drugs—Sulfamethoxazole, Trimethoprim, Isoniazid, and Pyridoxine—in rabbit plasma. The method uses gradient liquid chromatography based on analytical quality by design. To achieve
Externí odkaz:
https://doaj.org/article/82ceac2feb4546da9eaa58d2d3964307
Autor:
Manoj Kumar Deka, Akramul Ansary, Tridib Kumar Das, Amit Kumar Das, Bhargab Jyoti Sahariah, Manish Majumder
Publikováno v:
Green Analytical Chemistry, Vol 8, Iss , Pp 100088- (2024)
This study evaluates three spectrophotometric techniques for quantifying a binary combination of raloxifene and aspirin in terms of whiteness and greenness. Application of green and white analytical chemistry has gained widespread acceptance in the a
Externí odkaz:
https://doaj.org/article/03711cb773d84e7c953c43ba0b5ab469
Publikováno v:
E-Journal of Chemistry, Vol 6, Iss 2, Pp 537-540 (2009)
Two new, selective and sensitive visible spectrophotometric methods (method A and B) have been developed for the estimation of tinofovir in bulk and in pharmaceutical preparations. Tinofovir was subjected to acid hydrolysis and this acid hydrolyzed d
Externí odkaz:
https://doaj.org/article/34e95fbd854541e296295d44c019b11a
Publikováno v:
International Journal of Research in Pharmaceutical Sciences. 11:3023-3032
Quality by design guided. The assay method of Boceprevir is developed in accordance with ICH Q8(R2) guideline with due validation. .In this process, the Target analytical profile (TAP) of the drug was set and critical method parameters (CMP) were inv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0624308b272f392e53fd21d95546eba3
https://doi.org/10.26452/ijrps.v11ispl4.4599
https://doi.org/10.26452/ijrps.v11ispl4.4599
Publikováno v:
International Journal of Research in Pharmaceutical Sciences. 11:3033-3041
Response surface methodology approach has been utilized for the assay of Telaprevir in pure and formulation using ion-pair chromatography. In this, A risk assessment approach (Control-Noise-Experiment) has been used for identifying the risk factors,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20bcc8ee97ee883418dfd8ce0284aaf7
https://doi.org/10.26452/ijrps.v11ispl4.4600
https://doi.org/10.26452/ijrps.v11ispl4.4600
Publikováno v:
Journal of chromatographic science. 59(7)
A simple, precise, rapid and accurate UFLC method has been developed with due validation for the simultaneous estimation of Amlodipine besylate and Celecoxib in rat plasma. The separation has been taken place by C18 Eclipse plus column at 1ml/min flo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3a12cab488b09b2f0348188d77b45d3
https://pubmed.ncbi.nlm.nih.gov/33912904
https://pubmed.ncbi.nlm.nih.gov/33912904
Publikováno v:
E-Journal of Chemistry, Vol 6, Iss 2, Pp 537-540 (2009)
Two new, selective and sensitive visible spectrophotometric methods (method A and B) have been developed for the estimation of tinofovir in bulk and in pharmaceutical preparations. Tinofovir was subjected to acid hydrolysis and this acid hydrolyzed d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::faa50aade9dd9c5c6862e8165879f509
https://doaj.org/article/34e95fbd854541e296295d44c019b11a
https://doaj.org/article/34e95fbd854541e296295d44c019b11a