Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Muthadi Radhika Reddy"'
Publikováno v:
Future Journal of Pharmaceutical Sciences, Vol 8, Iss 1, Pp 1-20 (2022)
Abstract Background Pemigatinib is a small molecule tyrosine kinase inhibitor of fibroblast growth factor receptor inhibitors. The oral bioavailability of Pemigatinib is constricted due to its limited solubility at physiological pH. It is essential t
Externí odkaz:
https://doaj.org/article/094253457ce34e0b8d4e95ffc49effd7
Publikováno v:
BioNanoScience. 13:521-540
Publikováno v:
International Journal of Applied Pharmaceutics. :16-33
The most fundamental important extensive constitutive of drug molecules to be available for systemic absorption is aqueous solubility; subsequently, that is the nature of GIT fluid. When the drug molecules become solubilized, it has to reach the syst
Publikováno v:
Challenges and Advances in Pharmaceutical Research Vol. 10 ISBN: 9788195958566
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::997a14f41bdead2cf7638eb808b7adb9
https://doi.org/10.9734/bpi/capr/v10/8708f
https://doi.org/10.9734/bpi/capr/v10/8708f
Publikováno v:
Asian Journal of Pharmaceutical and Clinical Research. :40-44
Lipid-based drug delivery systems are extensively reported in the literature for enhancing drug solubility, permeability, and bioavailability. Self-nanoemulsifying drug delivery systems (SNEDDS) are a superior strategy for enhancing solubility and bi
Entrectinib is a novel potent anticancer drug with poor aqueous solubility. A supersaturable self nano emulsifying drug delivery system of entrectinib is developed using a super saturation promoter. The components of the isotropic mixture of SNEDDS w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f44d7adddb2598fe84895a4318e527ae
https://doi.org/10.21203/rs.3.rs-1955940/v1
https://doi.org/10.21203/rs.3.rs-1955940/v1
Publikováno v:
Asian Journal of Pharmaceutical and Clinical Research. :242-251
Objective: Flutrimazole is a topical antifungal agent which displays potent broad spectrum in vitro activity against dermatophytes, filamentous fungi, and yeasts. The purpose of the present study is to formulate and evaluate microspheres loaded topic
Autor:
Muthadi Radhika Reddy
Publikováno v:
World Journal of Pharmacy and Pharmaceutical Sciences. :229-260
The objective of the present work was to formulate and to characterize controlled release matrix tablets of Fexofenadine in order to improve bioavailability and to minimize the frequency of administration and increase the patient compliance. A matrix
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::301e1e4e332f8298e0e5c9041ed22d0c