[HTML][HTML] Lipid nanoparticles for transdermal delivery of flurbiprofen: formulation, in vitro, ex vivo and in vivo studies
…, V Ravichandiran, V Venkateswarlu, YM Rao - Lipids in health and …, 2009 - Springer
The aim of the study is to prepare aqueous dispersions of lipid nanoparticles – flurbiprofen
solid lipid nanoparticles (FLUSLN) and flurbiprofen nanostructured lipid carriers (FLUNLC) by …
solid lipid nanoparticles (FLUSLN) and flurbiprofen nanostructured lipid carriers (FLUNLC) by …
Development and evaluation of nitrendipine loaded solid lipid nanoparticles: influence of wax and glyceride lipids on plasma pharmacokinetics
…, S Ramakrishna, V Kishan, YM Rao… - International journal of …, 2007 - Elsevier
Nitrendipine is an antihypertensive drug with poor oral bioavailability ranging from 10 to 20%
due to the first pass metabolism. For improving the oral bioavailability of nitrendipine, …
due to the first pass metabolism. For improving the oral bioavailability of nitrendipine, …
Enhanced bioavailability of lacidipine via microemulsion based transdermal gels: formulation optimization, ex vivo and in vivo characterization
…, VV Yamsani, SK Yamsani, MR 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 …
Development of SLN and NLC enriched hydrogels for transdermal delivery of nitrendipine: in vitro and in vivo characteristics
…, SJ Mohan, V Venkateswarlu, YM Rao… - Drug development …, 2009 - Taylor & Francis
The purpose of this research was to investigate novel particulate carrier systems such as
solid lipid nanoparticles (SLN) and nanostructured lipid carrier (NLC) for transdermal delivery …
solid lipid nanoparticles (SLN) and nanostructured lipid carrier (NLC) for transdermal delivery …
Development and evaluation of gastroretentive norfloxacin floating tablets
Floating matrix tablets of norfloxacin were developed to prolong gastric residence time,
leading to an increase in drug bioavailability. Tablets were prepared by the wet granulation …
leading to an increase in drug bioavailability. Tablets were prepared by the wet granulation …
Transmucosal delivery of domperidone from bilayered buccal patches: In Vitro, Ex Vivo and In Vivo characterization
…, N Doodipala, VV Yamsani, MR Yamsani - Archives of pharmacal …, 2011 - Springer
Bilayered mucoadhesive buccal patches for systemic administration of domperidone (DOM),
a dopamine-receptor (D 2 ) antagonist, were developed using hydroxy propyl methyl …
a dopamine-receptor (D 2 ) antagonist, were developed using hydroxy propyl methyl …
Development, optimization and in vivo characterization of domperidone-controlled release hot-melt-extruded films for buccal delivery
Objective: The aim of the present investigation was the development and in vivo characterization
of domperidone (DOM) hot-melt extruded (HME) controlled release films by central …
of domperidone (DOM) hot-melt extruded (HME) controlled release films by central …
Oral transmucosal delivery of domperidone from immediate release films produced via hot-melt extrusion technology
…, R Gannu, MA Repka, MR Yamsani - Pharmaceutical …, 2013 - Taylor & Francis
The objective of the study was to prepare and characterize the domperidone (DOM) hot-melt
extruded (HME) buccal films by both in vitro and in vivo techniques. The HME film …
extruded (HME) buccal films by both in vitro and in vivo techniques. The HME film …
Preparation of a Matrix Type Multiple-Unit Gastro Retentive Floating Drug Delivery System for Captopril Based on Gas Formation Technique: In Vitro Evaluation
…, KM Chinnala, V Vobalaboina, MR Yamsani - Aaps Pharmscitech, 2008 - Springer
A gastro retentive floating drug delivery system with multiple-unit minitab’s based on gas
formation technique was developed in order to prolong the gastric residence time and to …
formation technique was developed in order to prolong the gastric residence time and to …
Improved bioavailability of albendazole following oral administration of nanosuspension in rats
M Pavan Kumar, Y Madhusudan Rao… - Current …, 2007 - ingentaconnect.com
Albendazole, a lipophilic anthelmintic drug, has low solubility and bioavailability. Albendazole
nanosuspensions (ABZNS) were developed using different surfactants (Polysorbate 80 & …
nanosuspensions (ABZNS) were developed using different surfactants (Polysorbate 80 & …