Drug-drug interactions for UDP-glucuronosyltransferase substrates: a pharmacokinetic explanation for typically observed low exposure (AUCi/AUC) ratios

JA Williams, R Hyland, BC Jones, DA Smith… - Drug Metabolism and …, 2004 - ASPET
Glucuronidation is a listed clearance mechanism for 1 in 10 of the top 200 prescribed drugs.
The objective of this article is to encourage those studying ligand interactions with UDP …

The characterisation of a novel, covalently modified, amphiphilic alginate derivative, which retains gelling and non-toxic properties

E Broderick, H Lyons, T Pembroke, H Byrne… - Journal of Colloid and …, 2006 - Elsevier
The characterisation of a novel amphiphilic material, Alg-C4, produced from butanol linked
by esterification to alginate is presented. The novel derivative retains the gelling and non …

[HTML][HTML] Preparation and comparative evaluation of sustained release metoclopramide hydrochloride matrix tablets

SI Abdel-Rahman, GM Mahrous, M El-Badry - Saudi Pharmaceutical …, 2009 - Elsevier
Metoclopramide hydrochloride (MCP) is commonly used for the management of
gastrointestinal disorders. Frequent administration and the undesired side effects (extra …

In Vitro Release Kinetics and Bioavailability of Gastroretentive Cinnarizine Hydrochloride Tablet

RC Nagarwal, DN Ridhurkar, JK Pandit - Aaps PharmSciTech, 2010 - Springer
An oral sustained release dosage form of cinnarizine HCl (CNZ) based on gastric floating
matrix tablets was studied. The release of CNZ from different floating matrix formulations …

A randomized, double-blind, placebo-controlled trial of metoclopramide for the treatment of Tourette's disorder

R Nicolson, B Craven-Thuss, J Smith… - Journal of the American …, 2005 - Elsevier
OBJECTIVE: The pattern of dopamine antagonism by metoclopramide suggests benefits in
the treatment of tic disorders. The purpose of this study was to examine the efficacy and …

[HTML][HTML] Formulation of metoclopramide HCl gastroretentive film and in vitro-in silico prediction using Gastroplus® PBPK software

DS Hamdi, MBM Mohamed - Saudi Pharmaceutical Journal, 2022 - Elsevier
The new trends in pharmaceutical studies focus on targeting drug delivery and computer
software that help in the body environment simulation, such as Gastroplus® software. The …

Cyclodextrin multicomponent complexation and controlled release delivery strategies to optimize the oral bioavailability of vinpocetine

LSS Ribeiro, AC Falcão, JAB Patrício… - Journal of …, 2007 - Elsevier
In the present work, to maintain a suitable blood level of vinpocetine (VP) for a long period of
time, VP‐cyclodextrin‐tartaric acid multicomponent complexes were prepared and …

[HTML][HTML] The role of nanoparticle in brain permeability: An in-vitro BBB model

N Nikandish, L Hosseinzadeh… - Iranian Journal of …, 2016 - ncbi.nlm.nih.gov
Membrane permeability and P-glycoprotein (P-gp) efflux system are regulating factors in the
drug brain penetration. Recently, some drug delivery systems have been developed to …

Application of N-hexoyl chitosan derivatives with high degree of substitution in the preparation of super-disintegrating pharmaceutical matrices

M Al-Remawi - Journal of Drug Delivery Science and Technology, 2015 - Elsevier
The present work investigated the utilization of degree of substitution in preparing N-hexoyl
chitosan matrices with superdisintegration power. Different degrees of substitution of N …

Evaluation of Prosopis africana Seed Gum as an Extended Release Polymer for Tablet Formulation

S Nadaf, P Nnamani, N Jadhav - AAPS PharmSciTech, 2015 - Springer
In the present work, an attempt has been made to screen Prosopis africana seed gum (PG),
anionic polymer for extended release tablet formulation. Different categories of drugs …