Increased dissolution rates of carbamazepine--gluconolactone binary blends processed by hot melt extrusion.

scientific article published on 11 March 2015

Increased dissolution rates of carbamazepine--gluconolactone binary blends processed by hot melt extrusion. is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.3109/10837450.2015.1022783
P698PubMed publication ID25757644
P5875ResearchGate publication ID273430689

P50authorAli NokhodchiQ38318363
P2093author name stringDennis Douroumis
Hiren G Moradiya
Michael S A Bradley
R Farnish
P2860cites workCrystalline solidsQ34233888
A kinetic study of the polymorphic transformation of nimodipine and indomethacin during high shear granulationQ35100389
Effect of hydrophilic swellable polymers on dissolution enhancement of carbamazepine solid dispersions studied using response surface methodologyQ37360630
Melt extrusion with poorly soluble drugsQ38062266
A review of pharmaceutical extrusion: critical process parameters and scaling-up.Q38301014
Dissolution and solid-state characterization of poorly water-soluble drugs in the presence of a hydrophilic carrierQ39424063
Glucosamine HCl as a new carrier for improved dissolution behaviour: effect of grindingQ42950820
Influence of crystal structure on the tableting properties of sulfamerazine polymorphsQ43665601
Influence of polyethylene glycol and povidone on the polymorphic transformation and solubility of carbamazepineQ44026141
Action of carriers on Carbamazepine dissolutionQ44135410
Comparison of the four anhydrous polymorphs of carbamazepine and the crystal structure of form I.Q44645970
Effect of glucosamine HCl on dissolution and solid state behaviours of piroxicam upon millingQ44680360
Modeling and monitoring of polymorphic transformations during the drying phase of wet granulationQ44923738
Relative bioavailability estimation of carbamazepine crystal forms using an artificial stomach-duodenum modelQ46825687
Drug-polymer intermolecular interactions in hot-melt extruded solid dispersions.Q48105089
Physicochemical properties and bioavailability of carbamazepine polymorphs and dihydrate.Q52132105
ABSTRACTS FROM THE UK-PHARMSCI CONFERENCE, 1-3 SEPTEMBER 2010Q56031000
Influence of Polymorphic Form, Morphology, and Excipient Interactions on the Dissolution of Carbamazepine CompactsQ59235055
The influence of various excipients on the conversion kinetics of carbamazepine polymorphs in aqueous suspensionQ59235102
P433issue4
P304page(s)445-452
P577publication date2015-03-11
P1433published inPharmaceutical Development and TechnologyQ7180729
P1476titleIncreased dissolution rates of carbamazepine--gluconolactone binary blends processed by hot melt extrusion.
P478volume21

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