Enhanced bioavailability of lacidipine via microemulsion based transdermal gels: formulation optimization, ex vivo and in vivo characterization
R Gannu, CR Palem, VV Yamsani, SK Yamsani… - International journal of …, 2010 - Elsevier
The purpose of the present study was to develop and optimize the microemulsion based
transdermal therapeutic system for lacidipine (LCDP), a poorly water soluble and low …
transdermal therapeutic system for lacidipine (LCDP), a poorly water soluble and low …
Enhancement of dissolution and skin permeability of pentazocine by proniosomes and niosomal gel
A Madni, MA Rahim, MA Mahmood, A Jabar… - AAPS …, 2018 - Springer
Proniosomes (PN) are the dry water-soluble carrier systems that may enhance the oral
bioavailability, stability, and topical permeability of therapeutic agents. The low solubility and …
bioavailability, stability, and topical permeability of therapeutic agents. The low solubility and …
Proniosomal gel as a carrier for improved transdermal delivery of griseofulvin: preparation and in-vitro characterization
S Gupta, D Ahirwar, NK Sharma… - Research Journal of …, 2009 - indianjournals.com
The present investigation aimed at formulation, and performance evaluation of vesicular
drug carrier system proniosomal gel for transdermal delivery of antifungal agent …
drug carrier system proniosomal gel for transdermal delivery of antifungal agent …
Preparation of a ligustrazine ethosome patch and its evaluation in vitro and in vivo
X Liu, H Liu, J Liu, Z He, C Ding, G Huang… - International journal …, 2011 - Taylor & Francis
Background The purpose of this study was to develop a transdermal ligustrazine patch
containing a stable formulation and with good entrapment efficiency, release rate, and …
containing a stable formulation and with good entrapment efficiency, release rate, and …
[引用][C] Development and characterization of apremilast transethosomal gel for transdermal delivery
M Rahangdale, P Pandey - International Journal of Pharmaceutical Sciences and …, 2021
Development and in-vitro characterization of sorbitan monolaurate and poloxamer 184 based niosomes for oral delivery of diacerein
MI Khan, A Madni, L Peltonen - European Journal of Pharmaceutical …, 2016 - Elsevier
The aim of the study was to develop a niosomal drug delivery system for poorly soluble
drugs with sorbitan monolaurate, poloxamer 184 and their mixture (sorbitan monolaurate …
drugs with sorbitan monolaurate, poloxamer 184 and their mixture (sorbitan monolaurate …
Formulation and evaluation of fluconazole pro-niosomal gel for topical administration
G Sandeep, SR Devireddy - Journal of Applied Pharmaceutical …, 2014 - japsonline.com
The present investigation was aimed to explore the potential of proniosomal gel for the
topical delivery of fluconazole. Fluconazole-loaded proniosomes were prepared by the …
topical delivery of fluconazole. Fluconazole-loaded proniosomes were prepared by the …
Proniosome based transdermal delivery of levonorgestrel for effective contraception
B Vora, AJ Khopade, NK Jain - Journal of controlled release, 1998 - Elsevier
A proniosome based transdermal drug delivery system of levonorgestrel (LN) was
developed and extensively characterized both in vitro and in vivo. The proniosomal structure …
developed and extensively characterized both in vitro and in vivo. The proniosomal structure …