Drug-polymer solubility and miscibility: Stability consideration and practical challenges in amorphous solid dispersion development.
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Controlled release systems containing solid dispersions: strategies and mechanismsFundamental aspects of solid dispersion technology for poorly soluble drugsMechanistic insights into acyclovir-polyethylene glycol 20000 binary dispersions.Lipid-polymer composite microspheres for colon-specific drug delivery prepared using an ultrasonic spray freeze-drying technique.Enhancing the bioavailability of magnolol in rabbits using melting solid dispersion with polyvinylpyrrolidone.Towards improved solubility of poorly water-soluble drugs: cryogenic co-grinding of piroxicam with carrier polymers.Influence of Molecular Weight of Carriers and Processing Parameters on the Extrudability, Drug Release, and Stability of Fenofibrate Formulations Processed by Hot-Melt ExtrusionAmorphous solid dispersions of sulfonamide/Soluplus® and sulfonamide/PVP prepared by ball milling.Solid-state characterization of Felodipine-Soluplus amorphous solid dispersions.Evaluation of Three Amorphous Drug Delivery Technologies to Improve the Oral Absorption of Flubendazole.Electrosprayed core-shell solid dispersions of acyclovir fabricated using an epoxy-coated concentric spray head.Interactions between drugs and polymers influencing hot melt extrusion.Hot-melt extrusion--basic principles and pharmaceutical applications.Physical stabilization of low-molecular-weight amorphous drugs in the solid state: a material science approach.Challenges and Strategies in Thermal Processing of Amorphous Solid Dispersions: A ReviewUse of Polyvinyl Alcohol as a Solubility Enhancing Polymer for Poorly Water-Soluble Drug Delivery (Part 2)Use of Polyvinyl Alcohol as a Solubility-Enhancing Polymer for Poorly Water Soluble Drug Delivery (Part 1).In pursuit of functional electrospun materials for clinical applications in humans.Rational excipient selection for co-amorphous formulations.Use of the Flory-Huggins theory to predict the solubility of nifedipine and sulfamethoxazole in the triblock, graft copolymer Soluplus.Mucoadhesive plasticized system of branched poly(lactic-co-glycolic acid) with aciclovir.Investigation of the combined effect of MgO and PEG on the release profile of mefenamic acid prepared via hot-melt extrusion techniques.Initial Drug Dissolution from Amorphous Solid Dispersions Controlled by Polymer Dissolution and Drug-Polymer Interaction.Construction and Validation of Binary Phase Diagram for Amorphous Solid Dispersion Using Flory-Huggins TheoryKlucel™ EF and ELF polymers for immediate-release oral dosage forms prepared by melt extrusion technology.Evaluation of Influence of Various Polymers on Dissolution and Phase Behavior of Carbamazepine-Succinic Acid Cocrystal in Matrix Tablets.Atomic force microscopy-based screening of drug-excipient miscibility and stability of solid dispersions.The influence of drug physical state on the dissolution enhancement of solid dispersions prepared via hot-melt extrusion: a case study using olanzapine.Solubility advantage from amorphous etoricoxib solid dispersions.Theoretical prediction of a phase diagram for solid dispersions.Hydrogen Bonding: Between Strengthening the Crystal Packing and Improving Solubility of Three Haloperidol Derivatives.Influence of Low-Molecular-Weight Excipients on the Phase Behavior of PVPVA64 Amorphous Solid Dispersions.Impact of Drug-Polymer Miscibility on Enthalpy Relaxation of Irbesartan Amorphous Solid Dispersions.DNP-enhanced solid-state NMR spectroscopy of active pharmaceutical ingredients.Evaluation of the Crystallization Tendency of Commercially Available Amorphous Tacrolimus Formulations Exposed to Different Stress Conditions.Investigation of phase diagrams and physical stability of drug-polymer solid dispersions.Melt extrusion with poorly soluble drugs - An integrated review.Hot melt extrusion versus spray drying: hot melt extrusion degrades albendazole.Electrolyte-stimulated biphasic dissolution profile and stability enhancement for tablets containing drug-polyelectrolyte complexes.Prediction of Phase Behavior of Spray-Dried Amorphous Solid Dispersions: Assessment of Thermodynamic Models, Standard Screening Methods and a Novel Atomization Screening Device with Regard to Prediction Accuracy.
P2860
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P2860
Drug-polymer solubility and miscibility: Stability consideration and practical challenges in amorphous solid dispersion development.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on July 2010
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Drug-polymer solubility and mi ...... solid dispersion development.
@en
Drug-polymer solubility and mi ...... solid dispersion development.
@nl
type
label
Drug-polymer solubility and mi ...... solid dispersion development.
@en
Drug-polymer solubility and mi ...... solid dispersion development.
@nl
prefLabel
Drug-polymer solubility and mi ...... solid dispersion development.
@en
Drug-polymer solubility and mi ...... solid dispersion development.
@nl
P2093
P356
P1476
Drug-polymer solubility and mi ...... solid dispersion development.
@en
P2093
Munir A Hussain
P304
P356
10.1002/JPS.22074
P407
P577
2010-07-01T00:00:00Z