Results 11 to 20 of about 56,903 (208)

Preparation And Characterization Of Nimesulide Nanoparticles For Dissolution Improvement

open access: yesAl-Mustansiriyah Journal of Pharmaceutical Sciences, 2018
Nimesulide is one of the types of non-steroidal anti-inflammatory drugs, widely used as analgesic and antipyretic. It is classified as class II drugs according to BCS guidance because of low solubility in water that leads to decrease in dissolution rate.
Inas F. Abd-AlRazaq   +2 more
doaj   +3 more sources

Role of Solvents in Improvement of Dissolution Rate of Drugs: Crystal Habit and Crystal Agglomeration [PDF]

open access: yesAdvanced Pharmaceutical Bulletin, 2015
Crystallization is often used for manufacturing drug substances. Advances of crystallization have achieved control over drug identity and purity, but control over the physical form remains poor.
Maryam Maghsoodi
doaj   +2 more sources

Improvement of Solubility and Dissolution of Niclosamide using Metal Organic Framework 5 (MOF-5)

open access: yesIraqi Journal of Pharmaceutical Sciences
Metal-organic frameworks-5 (MOF-5) were explored for enhancement of the solubility and dissolution of the drug niclosamide (NIC). MOF-5 was synthesized by solvothermal method and NIC was loaded into it (NIC@MOF-5).
Hayder Yahya Mansoor Al-Jarsha   +1 more
doaj   +3 more sources

Influence of the Efavirenz Micronization on Tableting and Dissolution

open access: yesPharmaceutics, 2012
The purpose of this study was to propose an analytical procedure that provides the effects of particle size and surface area on dissolution of efavirenz.
Lucio Mendes Cabral   +9 more
doaj   +2 more sources

Liquisolid Systems to Improve the Dissolution of Furosemide [PDF]

open access: yesScientia Pharmaceutica, 2010
A liquisolid system has the ability to improve the dissolution properties of poorly water soluble drugs. Liquisolid compacts are flowing and compactable powdered forms of liquid medications. The aim of this study was to enhance the in vitro dissolution properties of the practically water insoluble loop diuretic furosemide, by utilising liquisolid ...
Akinlade, Babatunde   +3 more
openaire   +3 more sources

Improving Dissolution and Cytotoxicity by Forming Multidrug Crystals [PDF]

open access: yesMolecules, 2020
Both rosiglitazone and metformin have effects on blood glucose regulation and the proliferation of liver cancer cells. Combination therapy with these two drugs is common and effective for the treatment of diabetes in the clinic, however, the application of these two drugs is influenced by the poor dissolution of rosiglitazone and the gastrointestinal ...
Xufei Bian   +7 more
openaire   +3 more sources

Isostructural cocrystals of metaxalone with improved dissolution characteristics

open access: yesRSC Advances, 2021
Metaxalone forms isostructural cocrystals with nicotinamide and salicylamide that offer a solubility advantage compared to the native drug. A drug–drug homosynthon is retained in all the cocrystal structures.
Sunil Kumar Gohel   +5 more
openaire   +3 more sources

Liquisolid technique for dissolution rate enhancement of a high dose water-insoluble drug (carbamazepine) [PDF]

open access: yes, 2007
Different liquisolid formulations of carbamazepine were accomplished by dissolving the drug in the non-toxic hydrophilic liquids, and adsorbing the solution onto the surface of silica.
Yousef Javadzadeh   +8 more
core   +1 more source

SOLUBILITY AND DISSOLUTION ENHANCEMENT OF KETOTIFEN BY SOLID DISPERSION TECHNIQUE [PDF]

open access: yesBulletin of Pharmaceutical Sciences. Assiut University, 2015
Ketotifen (KT) solid dispersions and physical mixtures were prepared with the objective of solubility and dissolution improvement using Hydroxypropyl-Beta-Cyclodextrin (HP-β-CD), Pluronic 127 (PF-127), Pluronic 68 (PF-68), Polyethylene glycol 6000 (PEG ...
Omnia Mahmoud   +2 more
doaj   +1 more source

Dissolution Enhancement of Meloxicam Tablets from the Synergistic Effect of Hydrotropic and Sublimating Agent

open access: yesPolytechnic Journal, 2021
Drugs which fall into Class II of Biopharmaceutical Classification System suffer from poor aqueous solubility that limits the dissolution and oral bioavailability.
Hemn L. Qader   +2 more
doaj   +1 more source

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