Application of factorial and response surface methodology in modern experimental design and optimization

G Hanrahan, K Lu - Critical reviews in analytical chemistry, 2006 - Taylor & Francis
This article critically examines the use of factorial and response surface methodology in
modern experimental design and optimization. A survey of important screening and …

The science of USP 1 and 2 dissolution: present challenges and future relevance

V Gray, G Kelly, M Xia, C Butler, S Thomas… - Pharmaceutical …, 2009 - Springer
Since its inception, the dissolution test has come under increasing levels of scrutiny
regarding its relevance, especially to the correlation of results to levels of drug in blood. The …

Quality by design approach for developing chitosan-Ca-alginate microspheres for colon delivery of celecoxib-hydroxypropyl-β-cyclodextrin-PVP complex

N Mennini, S Furlanetto, M Cirri, P Mura - European journal of …, 2012 - Elsevier
The aim of the present work was to develop a new multiparticulate system, designed for
colon-specific delivery of celecoxib for both systemic (in chronotherapic treatment of arthritis) …

Pharmaceutical application and development of fixed-dose combination: Dosage form review

DW Kim, KY Weon - Journal of Pharmaceutical Investigation, 2021 - Springer
Background Fixed dose combination (FDC) products are common in the treatment of various
disease such as hypertension, diabetes, HIV and HCV, Pain, Respiratory disease for …

Development and characterization of functionalized niosomes for brain targeting of dynorphin-B

M Bragagni, N Mennini, S Furlanetto, S Orlandini… - European Journal of …, 2014 - Elsevier
A niosomal formulation, functionalized with N-palmitoylglucosamine, was developed as
potential brain targeted delivery system of dynorphin-B. In fact, this endogenous …

Application of melt granulation technology using twin-screw extruder in development of high-dose modified-release tablet formulation

M Vasanthavada, Y Wang, T Haefele… - Journal of …, 2011 - Elsevier
Development of modified-release oral tablets of drug products usually requires release-
modifying polymers at the level of above 50% of the total weight. This makes the …

In Situ Forming Formulation: Development, Evaluation, and Optimization Using 33 Factorial Design

RC Nagarwal, A Srinatha, JK Pandit - Aaps Pharmscitech, 2009 - Springer
The present investigation concerns with the development and optimization of an in situ
forming formulation using 3 3 full factorial design experimentation. Metformin, an antidiabetic …

Application of pharmaceutical QbD for enhancement of the solubility and dissolution of a class II BCS drug using polymeric surfactants and crystallization inhibitors …

EB Basalious, W El-Sebaie, O El-Gazayerly - Aaps Pharmscitech, 2011 - Springer
The aim of this study was to apply quality by design (QbD) for pharmaceutical development
of felodipine solid mixture (FSM) containing hydrophilic carriers and/or polymeric …

Product and process understanding of a novel pediatric anti-HIV tenofovir niosomes with a high-pressure homogenizer

AS Zidan, Z Rahman, MA Khan - European Journal of Pharmaceutical …, 2011 - Elsevier
A variety of factors were systemically evaluated in order to establish the characteristics of the
niosomes obtained with a high-pressure homogenizer. The vesicular sizing parameters …

[HTML][HTML] Continuous melt granulation to develop high drug loaded sustained release tablet of Metformin HCl

P Vaingankar, P Amin - asian journal of pharmaceutical sciences, 2017 - Elsevier
The present work explores the application of melt granulation technology to develop a high
drug loaded sustained release matrix tablet of Metformin HCl using hydroxypropylcellulose …