Results 11 to 20 of about 50,651 (209)

Application of flash nanoprecipitation to fabricate poorly water-soluble drug nanoparticles [PDF]

open access: yesActa Pharmaceutica Sinica B, 2019
Nanoparticles are considered to be a powerful approach for the delivery of poorly water-soluble drugs. One of the main challenges is developing an appropriate method for preparation of drug nanoparticles. As a simple, rapid and scalable method, the flash
Jinsong Tao, Shing Fung Chow, Ying Zheng
doaj   +2 more sources

Orodispersible Polymer Films with the Poorly Water-Soluble Drug, Olanzapine: Hot-Melt Pneumatic Extrusion for Single-Process 3D Printing [PDF]

open access: yesPharmaceutics, 2020
Amorphous solid dispersions (ASDs) improve the oral delivery of poorly water-soluble drugs. ASDs of olanzapine (OLZ), which have a high melting point and low solubility, are performed using a complicated process.
Hui-Won Cho   +3 more
doaj   +2 more sources

Preclinical Bioavailability Assessment of a Poorly Water-Soluble Drug, HGR4113, Using a Stable Isotope Tracer [PDF]

open access: yesPharmaceutics, 2023
Drug solubility limits intravenous dosing for poorly water-soluble medicines, which misrepresents their bioavailability estimation. The current study explored a method using a stable isotope tracer to assess the bioavailability of drugs that are poorly ...
Eun Ji Ha   +5 more
doaj   +2 more sources

Surfactant Mediated Accelerated and Discriminatory In Vitro Drug Release Method for PLGA Nanoparticles of Poorly Water-Soluble Drug [PDF]

open access: yesPharmaceuticals, 2022
In vitro drug release testing is an important quality control tool for formulation development. However, the literature has evidence that poly-lactide-co-glycolide (PLGA)-based formulations show a slower in vitro drug release than a real in vivo drug ...
Ritu Gupta   +3 more
doaj   +2 more sources

Influence of Solid Drug Delivery System Formulation on Poorly Water-Soluble Drug Dissolution and Permeability [PDF]

open access: yesMolecules, 2015
The majority of drugs have a low dissolution rate, which is a limiting step for their absorption. In this manuscript, solid dispersions (SD), solid self-microemulsifying drug delivery systems (S-SMEDDS) and solid self-nanoemulsifying drug delivery ...
Marko Krstić   +3 more
doaj   +2 more sources

Effect of Cyclodextrin Types and Co-Solvent on Solubility of a Poorly Water Soluble Drug [PDF]

open access: yesScientia Pharmaceutica, 2016
The aim of the study was to investigate the solubility of piroxicam (Prx) depending on the inclusion complexation with various cyclodextrins (CDs) and on ethanol as a co-solvent.
Suporn Charumanee   +4 more
doaj   +2 more sources

Multicomponent cyclodextrin system for improvement of solubility and dissolution rate of poorly water soluble drug [PDF]

open access: yesAsian Journal of Pharmaceutical Sciences, 2019
The purpose of the present study was to investigate the interaction of Cinnarizine (CIN) with Hydroxypropyl-β-Cyclodextrin (HPβCD) in the presence of Hydroxy Acids (HA).
Mayank Patel, Rajashree Hirlekar
doaj   +2 more sources

Nanoconjugation and Encapsulation Strategies for Improving Drug Delivery and Therapeutic Efficacy of Poorly Water-Soluble Drugs

open access: yesPharmaceutics, 2019
Nanoconjugations have been demonstrated to be a dominant strategy for drug delivery and biomedical applications. In this review, we intend to describe several strategies for drug formulation, especially to improve the bioavailability of poorly water ...
Thao T. D. Tran, Phuong H. L. Tran
doaj   +3 more sources

FLOATING IN-SITU RAFT FORMING LIQUID GASTRORETENTIVE DRUG DELIVERY SYSTEM CONTAINING POORLY WATER-SOLUBLE DRUG [PDF]

open access: yesBulletin of Pharmaceutical Sciences. Assiut University, 2021
Present work was aimed to develop a liquid in-situ raft forming floating gastroretentive system of repaglinide using gellan gum, pectin, and sodium alginate.
Rajendra Awasthi
doaj   +1 more source

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