Action of Carriers on Carbamazepine Dissolution
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Summary
An improved in vitro dissolution of the drug was obtained in all the binary systems that increased as the polymer content increased, and the in vitro drug availability of the systems was evaluated.
- Type
- article
- Published
- 2002-01-01
- Cited by
- 31
- References
- 17
- OpenAlex
- https://openalex.org/W2122656098
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:33808230
Keywords
Dissolution, Differential scanning calorimetry, Polyvinylpyrrolidone, Chemistry, Solubility
References
- A swellable polymer as carbamazepine dissolution rate enhancer.
- The current status of solid dispersions.
- Pharmacokinetics of carbamazepine in normal man
- Dissolution Phenomena of Organic Medicinals involving Simultaneous Phase Changes
- Physicochemical properties and X-ray structural studies of the trigonal polymorph of carbamazepine.
- The combined use of DSC and TGA for the thermal analysis of atenolol tablets.
- Carbamazepine and Polyethylene Glycol Solid Dispersions: Preparation, in Vitro Dissolution, and Characterization
- Pharmaceutical applications of solid dispersion systems.
- Solid-state study of polymorphic drugs: carbamazepine.
- Thermal behavior and dissolution properties of naproxen from binary and ternary solid dispersions.
- Formulation and Evaluation of Vinylpyrrolidone/Vinylacetate Copolymer Microspheres with Carbamazepine
- CLINICAL PHARMACOKINETICS OF CARBAMAZEPINE
- Solid dispersions of carbamazepine with Gelucire 44/14 and 50/13
- Release of carbamazepine from solid dispersions with polyvinylpyrrolidone/vinylacetate copolymer (PVP/VA)
Cited by
- Thermodynamic equilibrium solubility measurements in simulated fluids by 96-well plate method in early drug discovery.
- Influence of hydrophilic polymers on the complexation of carbamazepine with hydroxypropyl-β-cyclodextrin.
- Evaluation of Influence of Various Polymers on Dissolution and Phase Behavior of Carbamazepine-Succinic Acid Cocrystal in Matrix Tablets
- DEVELOPMENT OF HYDROPHILIC MATRIX TABLET OF CARBAMAZEPINE USING 33 FULL FACTORIAL EXPERIMENTAL DESIGNS
- Increased dissolution rates of carbamazepine – gluconolactone binary blends processed by hot melt extrusion
- Improvement of dissolution rate of aceclofenac by solid dispersion technique
- Formulation design of carbamazepine fast-release tablets prepared by melt granulation technique.
- Effect of hydrophilic swellable polymers on dissolution enhancement of carbamazepine solid dispersions studied using response surface methodology
- Physicochemical and mechanical properties of carbamazepine cocrystals with saccharin
- Nasal administration of carbamazepine using chitosan microspheres: in vitro/in vivo studies.
- Study of the solid state of carbamazepine after processing with gas anti-solvent technique.
- Investigation of in vitro release kinetics of carbamazepine from Eudragit® RS PO and RL PO matrix tablets.
- Fast disintegrating crystalline solid dispersions of simvastatin for incorporation into orodispersible tablets
- Pharmaceutical characterisation and evaluation of cocrystals: Importance of in vitro dissolution conditions and type of coformer.
- Dissolution rate enhancement and physicochemical characterization of carbamazepine-poloxamer solid dispersions
- Influence of polymorphic form, morphology, and excipient interactions on the dissolution of carbamazepine compacts.
- Impairment of the in vitro release of carbamazepine from tablets.
- The development and assessment of a generic carbamazepine sustained release dosage form
- Factors Affecting the Formulation of Carbamazepine Extended Release Tablet
- Electrosprayed Nanosystems of Carbamazepine – PVP K30 for Enhancing Its Pharmacologic Effects
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