Dissolution and solid-state characterization of poorly water-soluble drugs in the presence of a hydrophilic carrier

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Dissolution and solid-state characterization of poorly water-soluble drugs in the presence of a hydrophilic carrier is …
instance of (P31):
scholarly articleQ13442814

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P6179Dimensions Publication ID1023435395
P356DOI10.1208/S12249-011-9697-8
P932PMC publication ID3225548
P698PubMed publication ID21932161
P5875ResearchGate publication ID51656176

P2093author name stringMuhammad Hussain
Chase Reed
Rahmat Talukder
Thomas Dürig
P2860cites workImproving the dissolution rate of poorly water soluble drug by solid dispersion and solid solution: pros and consQ94503211
A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailabilityQ28293773
Modern bioavailability, bioequivalence and biopharmaceutics classification system. New scientific approaches to international regulatory standardsQ33935245
Improving drug solubility for oral delivery using solid dispersionsQ33935264
Solid dispersion as an approach for bioavailability enhancement of poorly water-soluble drug ritonavir.Q33986048
Influence of physicochemical properties on dissolution of drugs in the gastrointestinal tractQ34190317
Physics of amorphous solidsQ35597371
Effect of hydrophilic swellable polymers on dissolution enhancement of carbamazepine solid dispersions studied using response surface methodologyQ37360630
In vivo evaluation of modified gum karaya as a carrier for improving the oral bioavailability of a poorly water-soluble drug, nimodipineQ41897614
Evaluation of griseofulvin binary and ternary solid dispersions with HPMCAS.Q41989095
Preparation and characterization of co-grinded mixtures of aceclofenac and neusilin US2 for dissolution enhancement of aceclofenacQ41989240
Effects of grinding with microcrystalline cellulose and cyclodextrins on the ketoprofen physicochemical propertiesQ43552164
Characterization of physicochemical properties of naproxen systems with amorphous beta-cyclodextrin-epichlorohydrin polymersQ44058043
Microcrystals for dissolution rate enhancement of poorly water-soluble drugsQ44353177
Solid dispersion of prednisolone: solid state characterization and improvement of dissolution profileQ51661394
Analytical approach for the Lucas-Washburn equation.Q51959909
Dissolution behavior and bioavailability of phenytoin from a ground mixture with microcrystalline celluloseQ67836613
Increasing dissolution rates and gastrointestinal absorption of drugs via solid solutions and eutectic mixtures. IV. Chloramphenicol--urea systemQ72813156
Physicochemical characterization and dissolution study of solid dispersions of Lovastatin with polyethylene glycol 4000 and polyvinylpyrrolidone K30Q80276454
Preparation of a solid dispersion of felodipine using a solvent wetting methodQ83915185
Changed crystallinity of mebendazole solid dispersion: improved anthelmintic activityQ85175187
P433issue4
P407language of work or nameEnglishQ1860
P304page(s)1227-1233
P577publication date2011-09-20
P1433published inAAPS PharmSciTechQ15750612
P1476titleDissolution and solid-state characterization of poorly water-soluble drugs in the presence of a hydrophilic carrier
P478volume12

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cites work (P2860)
Q64984261Bioavailability Enhancement of Poorly Water-Soluble Drugs via Nanocomposites: Formulation⁻Processing Aspects and Challenges.
Q57371724Deposition of Ibuprofen Crystals on Hydroxypropyl Cellulose/Polyacrylamide Gel: Experimental and Mathematic Modeling Releasing
Q42059847Improvement of Physico-mechanical Properties of Partially Amorphous Acetaminophen Developed from Hydroalcoholic Solution Using Spray Drying Technique
Q53295583Increased dissolution rates of carbamazepine--gluconolactone binary blends processed by hot melt extrusion.
Q28538718Topical cream-based dosage forms of the macrocyclic drug delivery vehicle cucurbit[6]uril

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