Results 1 to 10 of about 149,648 (111)

Stability-Indicating LC Method for the Determination of Prasugrel Hydrochloride in Pharmaceutical Dosage Form. [PDF]

open access: yesSci Pharm, 2012
A simple, rapid and precise method was developed for the quantitative estimation of prasugrel hydrochloride in pharmaceutical dosage form. A chromatographic separation of prasugrel and its degradants was achieved with Zorbax XDB C(8), 150 × 4.6 mm, 3.5μm analytical column using aqueous solution of 0.05 M ammonium acetate pH 4.5 with acetic acid ...
Ahirrao VK   +7 more
europepmc   +5 more sources

Process validation of prasugrel hydrochloride tablet USP

open access: yesInternational Journal of Pharmaceutical Chemistry and Analysis, 2020
Process validation is an essential part for the safety and quality of the drug products. Validation act as guidance that is intended to assist manufacturers in understanding quality management system requirements concerning process validation. It is a fundamental component for assuring the quality system used by pharmaceutical industries.
Yamuna Choudhary, Anju Goyal, Anju Goyal
openaire   +3 more sources

Preparation, Characterization and Evaluation of Prasugrel Hydrochloride Nanosuspensions: Its enhancement of dissolution rate and oral bioavailability

open access: yesPharmaceutics and Pharmacology Research, 2022
The objective of this study was to investigate nanosuspensions for enhancing the solubility and dissolution rate of Prasugrel HCl (PHCl) so as to reduce the fluctuations in its oral bioavailability. Prasugrel Hydrochloride nanosuspensions were prepared using evaporative precipitation method. After preparation, various nanosuspensions were characterized
R. Devara
openaire   +2 more sources

Preparation and Evaluation of Multi-Particulate System (Pellets) of Prasugrel Hydrochloride [PDF]

open access: yesOpen Pharmaceutical Sciences Journal, 2015
Multiparticulate systems (pellets) of prasugrel hydrochloride were prepared by extrusion spheronization method using MCC (micro crystalline cellulose). Optimum spheronization time and method of drying were selected as the process parameters for the preparation of final batches.
Navjot Kanwar, Rakesh Kumar, V.R. Sinha
openaire   +2 more sources

Identification and Synthesis of Impurities Formed During Prasugrel Hydrochloride Preparation

open access: yesAsian Journal of Chemistry, 2013
Prasugrel hydrochloride is designated chemically as 5[1(RS)-2-cyclopropyl-1-(2-fluorophenyl)-2-oxyethyl]-4,5,6,7tetrahydrothieno[3,2-c]pyridine-2-yl acetate hydrochloride (1).
T. Umasankara Sastry   +3 more
openaire   +2 more sources

An Improvement to the Preparation of Prasugrel Hydrochloride

open access: yesJournal of Chemical Research, 2013
An efficient synthesis of prasugrel, a thienopyridine ADP-receptor antagonists, is described. A thienopyridine inter-mediate was prepared by N-protection, boric acid substitution and N-substitution. After acid hydrolysis of the methyl ether and subsequent acetylation, prasugrel was obtained with a total yield of 50% after seven linear steps from 4,5,6,
Wenhua Ou   +4 more
openaire   +2 more sources

Identification and characterization of the degradation products of prasugrel hydrochloride tablets using LC-MS technique

open access: yesJournal of Liquid Chromatography & Related Technologies, 2018
New high-performance liquid chromatography method was developed for the determination of prasugrel HCl-related substances. Impurity profile of prasugrel HCl was established by studying the degradation profile of it as an active pharmaceutical ingredient, for the first time, in the tablet form.
Arar, Sharif   +2 more
openaire   +2 more sources

Estimation Of Prasugrel Hydrochloride In Bulk Dosage Form

open access: yesJournal of Medical Pharmaceutical And Allied Sciences, 2020
J. Tejaswi
openaire   +2 more sources

Dissolution Rate Improvement of Prasugrel Hydrochloride by Solid Dispersion Method Using HPMC-AS as a Polymer

open access: yesInternational Journal of Scientific Research and Reviews, 2019
Warkad S. S   +4 more
semanticscholar   +3 more sources

Home - About - Disclaimer - Privacy