scispace - formally typeset
P

Praveen Kumar Gaur

Researcher at Jodhpur National University

Publications -  44
Citations -  705

Praveen Kumar Gaur is an academic researcher from Jodhpur National University. The author has contributed to research in topics: Transdermal & Solid lipid nanoparticle. The author has an hindex of 13, co-authored 38 publications receiving 539 citations. Previous affiliations of Praveen Kumar Gaur include Uttar Pradesh Technical University & ULTra.

Papers
More filters
Journal ArticleDOI

Phytochemical, therapeutic, and ethnopharmacological overview for a traditionally important herb: Boerhavia diffusa Linn.

TL;DR: A detailed account of chemical constituents and pharmacological activities of Boerhavia diffusa has been presented in this article to highlight its chemical and therapeutic potential along with its ethnopharmacological considerations.
Journal ArticleDOI

Enhanced Oral Bioavailability of Efavirenz by Solid Lipid Nanoparticles: In Vitro Drug Release and Pharmacokinetics Studies

TL;DR: This work illustrates development of an SLN formulation for Efavirenz with increased bioavailability and shows good stability at 40°C ± 2°C and 75 ± 5% relative humidity for 180 days.
Journal ArticleDOI

Formulation and evaluation of controlled-release of telmisartan microspheres: In vitro/in vivo study.

TL;DR: The controlled release of drug from TMRS-3 also provides for higher plasma drug content and improved bioavailability, and can be explained using the Higuchi model.

Transdermal drug delivery system: a review

TL;DR: In this article, a review deals with a brief insight on physiological properties of the skin, several techniques for drug permeation enhancement and regulatory issues over transdermal drug delivery, and several approaches in form of carriers/vehicles are also developed for efficient delivery of drugs.
Journal ArticleDOI

Solid lipid nanoparticles for nose to brain delivery of donepezil: formulation, optimization by Box–Behnken design, in vitro and in vivo evaluation

TL;DR: Optimal formulation was evaluated for particle size, zeta potential, entrapment efficiency, drug loading, morphological analysis, crystallinity, in vitro drug release, in vivo (biodistribution, pharmacokinetic and Gama scintigraphy) studies and result revealed the localization of drug in brain.