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INVESTIGATION OF SOLUBILITY ENHANCEMENT OF PRASUGREL HYDROCHLORIDE: NANOSUSPENSIONS AND CYCLODEXTRIN INCLUSION COMPLEXES

INDIAN DRUGS, 2014
The objective of this study was to investigate nanosuspensions, hydroxypropyl-β-cyclodextrin (HPβCD) complexes and SLS powders for enhancing the solubility and dissolution rate of Prasugrel HCl (PHCl) so as to reduce the fluctuations in its oral bioavailability. PHCl nanosuspensions were prepared using evaporative precipitation method.
R. K Devara   +5 more
openaire   +1 more source

Determination of Prasugrel Hydrochloride in Bulk and Pharmaceutical Formulation Using New Ion Selective Electrodes

Research Journal of Pharmacy and Technology, 2018
The construction and performance characteristics of Prasugrel hydrochloride (PRS) selective electrodes were developed. Electrodes were based on the incorporation of PRS with pairing agents, Ammonium Molybdate (MOL) and Nessler reagent (NES). The electrodes displayed a Nernstian response with a mean calibration graphs slopes of 59.21, 27.57 mv.decade-1 ...
Amir Alhaj Sakur   +3 more
openaire   +1 more source

Solution-Mediated Polymorphic Transformation of Prasugrel Hydrochloride from Form II to Form I

Industrial & Engineering Chemistry Research, 2014
In situ Raman spectroscopy was applied for the analysis of the solution-mediated polymorphic transformation of prasugrel hydrochloride from the metastable form II to the stable form I. The solution concentration during the transition process was monitored by a gravimetric method.
Wei Du   +8 more
openaire   +1 more source

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

Pharmaceutics 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
openaire   +1 more source

Prasugrel (CS-747, LY640315) Hydrochloride, a Novel Thienopyridine Prodrug, Shows Potent Antiplatelet and Antithrombotic Effects with Rapid Onset of Action in Rats.

Blood, 2005
Abstract The thienopyridine antiplatelet prodrug clopidogrel bisulfate (C) is widely used for atherothrombotic diseases. However, several reports have described a limitation of C, namely, poor platelet inhibition in many patients following oral dosing.
Yoichi Niitsu   +7 more
openaire   +1 more source

Extractive Spectrophotometric Methods for determination of Prasugrel Hydrochloride in Pharmaceutical Formulations using some Acidic Triphenylmethane Dyes

Asian Journal of Research in Chemistry, 2016
Three simple and sensitive extractive spectrophotometric methods have been described for the assay of ondansetron hydrochloride either in pure form or in pharmaceutical formulations. The developed methods involve formation of coloured chloroform extractable ion-pair complexes of the drug with bromothymol blue (BTB), bromophenol blue (BPB) and ...
openaire   +1 more source

Analytical method development and validation of prasugrel hydrochloride in bulk and its pharmaceutical formulation using the GC-MS, HPLC method

Asian Journal of Research in Chemistry
The present work reports rapid, sensitive and specific methods for determination of Prasugrel and its impurities by gas chromatography with mass spectrometry and high-performance liquid chromatography. The proposed method presented excellent intraday precision (% RSD < 1), and accuracy 99.23 to 100.40% and 99.48 to 100.81% for Prasugrel and 2-bromo ...
Manohar Reddy Epuru   +3 more
openaire   +1 more source

Formulation and Characterization of Β-Cyclodextrin and Ethyl CelluloseBased Nanosponges for Enhanced Solubility and Sustained Delivery of Prasugrel Hydrochloride

International Journal of Drug Delivery Technology
Prasugrel hydrochloride (Prasugrel HCl), a potent thienopyridine-class antiplatelet agent, is classified as a Biopharmaceutics Classification System (BCS) Class II drug, characterized by low aqueous solubility and high permeability, which limits its oral bioavailability.
Suryawanshi A.N., Ratnaparkhi M.P.
openaire   +1 more source

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