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Suresh Purohit

Researcher at Institute of Medical Sciences, Banaras Hindu University

Publications -  39
Citations -  416

Suresh Purohit is an academic researcher from Institute of Medical Sciences, Banaras Hindu University. The author has contributed to research in topics: Transdermal & Drug carrier. The author has an hindex of 10, co-authored 39 publications receiving 359 citations. Previous affiliations of Suresh Purohit include Birla Institute of Technology and Science & Jodhpur National University.

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Formulation, evaluation and 3(2) full factorial design-based optimization of ondansetron hydrochloride incorporated taste masked microspheres.

TL;DR: Full factorial design and in vitro taste assessment approach, coupled together, was successfully applied to develop and optimize batches of ONS incorporated taste-masked microspheres.
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Revalidation of the neuroprotective effects of a United States patented polyherbal formulation on scopolamine induced learning and memory impairment in rats.

TL;DR: The ability of the test formulation to reverse scopolamine-induced learning and memory deficits in rats is demonstrated, which may at least partially be explained by the reversal of scopolamines-induced reductions in brain acetylcholine levels and antioxidant activities by the test formulations.
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Simultaneous Determination of Atenolol-Amlodipine and Haloperidol–Trihexyphenidyl in Combined Tablet Preparations by Derivative Spectroscopy

TL;DR: A derivative spectrophotometric procedure for simultaneous determination of atenolol-amlodipine and haloperidol-trihexyphenidyl HCl in combined tablet preparations was developed as discussed by the authors.
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Spectrophotometric determination of nateglinide in bulk and tablet dosage forms

TL;DR: In this article, two simple, reproducible and efficient UV spectrophotometric methods for the estimation of nateglinide in bulk and pharmaceutical dosage forms have been developed, which were validated using ANOVA.
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Formulation and evaluation of lipid based taste masked granules of ondansetron HCl.

TL;DR: The dissolution tests displayed the significant retardation of drug release from the granules compared to pure drug and additionally indicated the attainment of matrix system via appearance of unbroken granules during in vitro testing.