Quality by design (QbD) approach to develop fast-dissolving tablets using melt-dispersion paired with surface-adsorption method: formulation and pharmacokinetics of …

SK Vemula, B Daravath, M Repka - Drug Delivery and Translational …, 2023 - Springer
Developing amorphous solid dispersions with good flow properties is always challenging for
formulation scientists to convert into tablets. Hence, the present study investigates the impact …

Melt dispersion granules: formulation and evaluation to improve oral delivery of poorly soluble drugs–a case study with valsartan

N Chella, R Tadikonda - Drug Development and Industrial …, 2015 - Taylor & Francis
Solid dispersion (SD) technique is a promising strategy to improve the solubility and
dissolution of BCS class II drugs. However, only few products are marketed till today based …

[PDF][PDF] Effect of superdisintegrants in rapidly disintegrating flurbiprofen sodium orodispersible tablets via direct compression and camphor sublimation

SL Shid, SP Hiremath, SN Borkar… - Journal of Global …, 2010 - researchgate.net
Orodispersible or Mouth dissolving tablets are those when put on tongue, disintegrates
instantaneously, releasing the drug, which dissolves or disperses in the saliva. The faster …

Controlled precipitation for enhanced dissolution rate of flurbiprofen: Development of rapidly disintegrating tablets

EA Essa, AO Elmarakby, AMA Donia… - Drug Development …, 2017 - Taylor & Francis
Objective: The aim of this work was to investigate the potential of controlled precipitation of
flurbiprofen on solid surface, in the presence or absence of hydrophilic polymers, as a tool …

[PDF][PDF] Formulation, evaluation and pharmacokinetics of flurbiprofen fast dissolving tablets

SR Mettu, PR Veerareddy - Brit J Pharm Res, 2013 - academia.edu
Aim: The intent of present study is to formulate fast dissolving tablets of flurbiprofen using
different superdisintegrants to improve the dissolution and bioavailability. Place and …

Preparation and characterization of fast dissolving flurbiprofen and esomeprazole solid dispersion using spray drying technique

R Pradhan, TH Tran, SY Kim, KB Woo, YJ Choi… - International Journal of …, 2016 - Elsevier
We aimed to develop an immediate-release flurbiprofen (FLU) and esomeprazole (ESO)
combination formulation with enhanced gastric aqueous solubility and dissolution rate …

Physicochemical characterization and in vivo evaluation of flurbiprofen-loaded solid dispersion without crystalline change

DH Oh, YJ Park, JH Kang, CS Yong, HG Choi - Drug Delivery, 2011 - Taylor & Francis
To develop a novel flurbiprofen-loaded solid dispersion without crystalline change, various
flurbiprofen-loaded solid dispersions were prepared with water, sodium carboxylmethyl …

Development and evaluation of novel solid nanodispersion system for oral delivery of poorly water-soluble drugs

P Nkansah, A Antipas, Y Lu, M Varma, C Rotter… - Journal of controlled …, 2013 - Elsevier
The aim of the present study was to develop and evaluate a novel drug solubilization
platform (so-called solid nanodispersion) prepared by a simple co-grinding and solvent-free …

[HTML][HTML] Exploitation of design-of-experiment approach for design and optimization of fast-disintegrating tablets for sublingual delivery of sildenafil citrate with …

AS AlAli, MF Aldawsari, A Alalaiwe, BK Almutairy… - Pharmaceutics, 2021 - mdpi.com
Sildenafil citrate undergoes first-pass metabolism, resulting in poor oral bioavailability at 25–
41% of the administered dose. This study aimed to design and optimize fast-disintegrating …

Solid dispersion technology as a formulation strategy for the fabrication of modified release dosage forms: A comprehensive review

K Patel, S Shah, J Patel - DARU Journal of Pharmaceutical Sciences, 2022 - Springer
Solubility limited bioavailability is one of the crucial parameters that affect the formulation
development of the new chemical entities. Thus the major constraint in the pharmaceutical …