Results 41 to 50 of about 147,210 (303)

Molecular Interactions in Solid Dispersions of Poorly Water-Soluble Drugs [PDF]

open access: yesPharmaceutics, 2020
Physicochemical characterization is a crucial step for the successful development of solid dispersions, including the determination of drug crystallinity and molecular interactions. Typically, the detection of molecular interactions will assist in the explanation of different drug performances (e.g., dissolution, solubility, stability) in solid ...
Thao T. D. Tran, Phuong H. L. Tran
openaire   +3 more sources

Positively Charged Nanostructured Lipid Carriers and Their Effect on the Dissolution of Poorly Soluble Drugs

open access: yesMolecules, 2016
The objective of this study is to develop suitable formulations to improve the dissolution rate of poorly water soluble drugs. We selected lipid-based formulation as a drug carrier and modified the surface using positively charged chitosan derivative ...
Kyeong-Ok Choi   +3 more
doaj   +1 more source

Albendazole Solid Dispersions: Influence of Dissolution Medium Composition on In Vitro Drug Release [PDF]

open access: yes, 2014
The rate-limiting step to drug absorption is often dissolution from the dosage form, especially for poorly soluble com-pounds. Two possibilities for improving the dissolution of these drugs are to increase the available surface area and to im-prove their
Allemandi, Daniel Alberto   +4 more
core   +1 more source

Improved oral bioavailability of poorly water-soluble vorinostat by self-microemulsifying drug delivery system

open access: yesBeni-Suef University Journal of Basic and Applied Sciences, 2022
Background Vorinostat is a histone deacetylase inhibitor suberoylanilide hydroxamic acid (SAHA) with anticancer properties. However, it is plagued by low water solubility, low permeability (BCS class IV drug), and suboptimal pharmacokinetics. The purpose
Ashok Kumar Janakiraman   +4 more
doaj   +1 more source

Formulation of thermoresponsive and buccal adhesive in situ gel for treatment of oral thrush containing poorly water soluble drug bifonazole

open access: yesJournal of Pharmacy and Bioallied Sciences, 2012
The aim of the present work is to formulate and evaluate in situ oral topical gels of poorly water soluble drug Bifonazole based on temperature induced systems for the treatment of oral candidiasis.
Dimendra Patel   +4 more
doaj   +1 more source

Enhancement of solubility of poorly water soluble anti hypertensive drug by nanosizing approach

open access: yesJournal of Pharmacy and Bioallied Sciences, 2012
The objective of this research study was to optimize formulation and process variables affecting characteristic of nanosuspension in bead milling process.
Divyesh Thakar   +2 more
doaj   +1 more source

Polysaccharide-based self-assembling nanohydrogels: An overview on 25-years research on pullulan [PDF]

open access: yes, 2015
The aim of this overview is to review the evolution of the studies carried out, during more than 25 years, on nanohydrogels obtained by self-assembling of pullulan (PUL) using several hydrophobization strategies.
ALHAIQUE, Franco   +4 more
core   +1 more source

Pharmaceutical particle technologies: An approach to improve drug solubility, dissolution and bioavailability

open access: yesAsian Journal of Pharmaceutical Sciences, 2014
Pharmaceutical particle technology is employed to improve poor aqueous solubility of drug compounds that limits in vivo bioavailability owing to their low dissolution rate in the gastrointestinal fluids following oral administration.
Prakash Khadka   +8 more
doaj   +1 more source

A novel method for quantitative determination of aceclofenac in bulk drug and tablets using sodium salicylate as a hydrotropic solubilizing agent

open access: yesJournal of Advanced Pharmaceutical Technology & Research, 2010
In titrimetric analysis costlier organic solvents are more often employed to solubilize the poorly water-soluble drugs. Volatility and pollution are drawbacks of such solvents.
R K Maheshwari, Shruti Moondra
doaj   +2 more sources

A new self-emulsifying formulation of mefenamic acid with enhanced drug dissolution

open access: yesAsian Journal of Pharmaceutical Sciences, 2015
To enhance the dissolution of poorly soluble mefenamic acid, self-emulsifying formulation (SEF), composing of oil, surfactant and co-surfactant, was formulated.
Pornsak Sriamornsak   +4 more
doaj   +1 more source

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