Proniosomal gel for transdermal delivery of lornoxicam: Optimization using factorial design and in vivo evaluation in rats
Objective Clinical utility of lornoxicam in oral therapy is primarily restricted by the low
solubility and gastric adverse effects. This study evaluated the prospective of optimized …
solubility and gastric adverse effects. This study evaluated the prospective of optimized …
Formulation by design-based proniosome for accentuated transdermal delivery of risperidone: in vitro characterization and in vivo pharmacokinetic study
Aim: The aim of this work was to investigate the effects of formulation variables on the
development of risperidone proniosomal formulations as potential transdermal delivery …
development of risperidone proniosomal formulations as potential transdermal delivery …
Formulation and optimization of nanostructured lipid carriers to enhance oral bioavailability of telmisartan using Box–Behnken design
The aim of the present study was to formulate and optimize nanostructured lipid carriers
(NLC) to enhance oral bioavailability of telmisartan.“Box-Behnken design (3-factor, 3-level)” …
(NLC) to enhance oral bioavailability of telmisartan.“Box-Behnken design (3-factor, 3-level)” …
Enhancement of ocular anti-glaucomic activity of agomelatine through fabrication of hyaluronic acid modified-elastosomes: formulation, statistical optimisation, in vitro …
AA Nemr, GM El-Mahrouk, HA Badie - Journal of …, 2023 - Taylor & Francis
Aim The aim of this manuscript was to fabricate agomelatine (AGM) loaded elastosomes to
improve its corneal permeation and ocular bioavailability. AGM is a biopharmaceutical …
improve its corneal permeation and ocular bioavailability. AGM is a biopharmaceutical …
Design and evaluation of proniosomes as a carrier for ocular delivery of lomefloxacin HCl
RM Khalil, GA Abdelbary, M Basha… - Journal of liposome …, 2017 - Taylor & Francis
The current investigation aims to develop and evaluate novel ocular proniosomal gels of
lomefloxacin HCl (LXN); in order to improve its ocular bioavailability for the management of …
lomefloxacin HCl (LXN); in order to improve its ocular bioavailability for the management of …
Development of novel transdermal self-adhesive films for tenoxicam, an anti-inflammatory drug
DI Nesseem, SF Eid, SS El-Houseny - Life sciences, 2011 - Elsevier
AIM: The purpose of this study was to develop transdermal films (TFs) with the addition of
different polymer ratios that incorporated 0.5% tenoxicam in order to ensure maximum …
different polymer ratios that incorporated 0.5% tenoxicam in order to ensure maximum …
Enhanced transdermal delivery of luteolin via non-ionic surfactant-based vesicle: quality evaluation and anti-arthritic assessment
Luteolin (LUT) is a promising molecule with potential anti-arthritic activity. This investigation
presents formulation and evaluation of niosomal transgel for enhanced transdermal delivery …
presents formulation and evaluation of niosomal transgel for enhanced transdermal delivery …
Tenoxicam loaded hyalcubosomes for osteoarthritis
YE Elakkad, MK Younis, RM Allam, AF Mohsen… - International journal of …, 2021 - Elsevier
The main aim is to develop transcutaneous tenoxicam (TNX) loaded vesicles to control
osteoarthritis (OA) without common side effects. Different vesicles were prepared by the …
osteoarthritis (OA) without common side effects. Different vesicles were prepared by the …
Development and optimization of boswellic acid-loaded proniosomal gel
Abstract Context: Boswellic acids (BAs) are isolated from oleo gum of Boswellia serrata and
are mainly used as potential anti-inflammatory, hypolipidemic, immunomodulatory, and …
are mainly used as potential anti-inflammatory, hypolipidemic, immunomodulatory, and …
Nonionic surfactant-based vesicular system for transdermal drug delivery
S Ghanbarzadeh, A Khorrami, S Arami - Drug delivery, 2015 - Taylor & Francis
Objective: The objective of this study was to formulate and evaluate the Ibuprofen niosomal
formulation as a transdermal drug delivery system. Materials and methods: Niosomes were …
formulation as a transdermal drug delivery system. Materials and methods: Niosomes were …