Formulation and evaluation of proniosome based drug delivery system of the antifungal drug clotrimazole
S Pankaj, T Rini, PM Dandagi - International Journal of …, 2013 - ijpsnonline.com
In the present study proniosomal gel of clotrimazole was formulated by using lecithin,
cholesterol as encapsulating agents, nonionic surfactants Span and Tween with different …
cholesterol as encapsulating agents, nonionic surfactants Span and Tween with different …
Design and dermatokinetic evaluation of Apremilast loaded nanostructured lipid carriers embedded gel for topical delivery: A potential approach for improved …
The present study aimed to develop Apremilast loaded nanostructured lipid carriers (NLCs)
for topical delivery to overcome the limitations of oral therapy and increase the efficacy …
for topical delivery to overcome the limitations of oral therapy and increase the efficacy …
Design, synthesis of novel vesicular systems using turpentine as a skin permeation enhancer
AB Oskuie, SA Nasrollahi, S Nafisi - Journal of Drug Delivery Science and …, 2018 - Elsevier
Addition of skin penetration enhancer in a formulation is the simplest and most common
technique to improve transdermal permeation. We aimed to develop novel liposome and …
technique to improve transdermal permeation. We aimed to develop novel liposome and …
Design, evaluation and in vivo pharmacokinetic study of a cationic flexible liposomes for enhanced transdermal delivery of pramipexole
Pramipexole is a widely preferred antiparkinsonian agent because of its several
advantages, one being the delayed onset of motor fluctuations and dyskinesia observed …
advantages, one being the delayed onset of motor fluctuations and dyskinesia observed …
FORMULATION, DEVELOPMENT AND EVALUATION OF NIOSOMAL DRUG DELIVERY SYSTEM FOR CLINDAMYCIN PHOSPHATE.
SD Jivrani, VK Patel - Pharma Science Monitor, 2014 - search.ebscohost.com
To formulate and evaluate Niosomal drug delivery system for Clindamycin phosphate to
increase its effectiveness by increasing penetration through skin and reducing its side …
increase its effectiveness by increasing penetration through skin and reducing its side …
Ultradeformable liposomes: a novel vesicular carrier for enhanced transdermal delivery of procyanidins: effect of surfactants on the formation, stability, and …
R Chen, R Li, Q Liu, C Bai, B Qin, Y Ma, J Han - AAPS PharmSciTech, 2017 - Springer
The aims of this work were to develop a novel vesicular carrier, procyanidins,
ultradeformable liposomes (PUDLs), to expand the applications for procyanidins, and …
ultradeformable liposomes (PUDLs), to expand the applications for procyanidins, and …
Formulation and evaluation of lisinopril dihydrate transdermal proniosomal gels
M Sabareesh, PR Khan, B Sudheer - Journal of applied …, 2011 - japsonline.com
In the present study transdermal Lisinopril proniosomal gels was formulated by using
Lecithin, Cholesterol as encapsulating agents, Surfactant, Span and permeation enhancers …
Lecithin, Cholesterol as encapsulating agents, Surfactant, Span and permeation enhancers …
Nonionic surfactant vesicles as a carrier for transdermal delivery of frusemide
A Azeem, FJ Ahmad, ZI Khan… - Journal of dispersion …, 2008 - Taylor & Francis
The aim of the present study was to formulate and evaluate the nonionic surfactant vesicles
of frusemide in order to enhance its skin permeation. The process variables which could …
of frusemide in order to enhance its skin permeation. The process variables which could …
Statistically designed nonionic surfactant vesicles for dermal delivery of itraconazole: Characterization and in vivo evaluation using a standardized Tinea pedis …
N Kumar, S Goindi - International journal of pharmaceutics, 2014 - Elsevier
The study aims to statistically develop a hydrogel of itraconazole loaded nonionic surfactant
vesicles (NSVs) for circumventing the shortcomings and adverse effects of currently used …
vesicles (NSVs) for circumventing the shortcomings and adverse effects of currently used …