An oral controlled release matrix pellet formulation containing nanocrystalline ketoprofen.
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Summary
A controlled release pellet formulation using a NanoCrystal colloidal dispersion of ketoprofen using a mixture of microcrystalline wax and starch derivatives resulted in a sustained but complete release of nanocrystalline ketofen from the matrix pellet formulations.
- Type
- article
- Published
- 2001-05-21
- Cited by
- 154
- References
- 7
- OpenAlex
- https://openalex.org/W1971744532
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:21010358
Keywords
Ketoprofen, Pellet, Microcrystalline cellulose, Maltodextrin, Chemical engineering
References
- Nanosuspensions for the formulation of poorly soluble drugs: I. Preparation by a size-reduction technique
- Development of Controlled Release Formulations of Ketoprofen for Oral Use
- A simple equation for description of solute release I. Fickian and non-fickian release from non-swellable devices in the form of slabs, spheres, cylinders or discs
- Drug particle size reduction for decreasing gastric irritancy and enhancing absorption of naproxen in rats
- Matrix pellets based on the combination of waxes, starches and maltodextrins
- In vivo evaluation of rapid release and sustained release Gelucire capsule formulations
- Wettability of a hydrophobic drug by surfactant solutions
Cited by
- Desenvolvimento e caracterização de comprimidos matriciais de dupla camada contendo Paracetamol
- Conformational study of ketoprofen by combined DFT calculations and Raman spectroscopy.
- The effect of the ratio of two acrylic polymers on the in vitro release kinetics of ketoprofen from pellets prepared by extrusion and spheronisation technique.
- Pellets formulation of crystalline nanoparticles. A formulation process and characterization study.
- NANOSUSPENSION TECHNOLOGY: A INNOVATIVE SLANT FOR DRUG DELIVERY SYSTEM AND PERMEABILITY ENHANCER FOR POORLY WATER SOLUBLE DRUGS
- Nanocrystal formulation for poorly soluble drugs
- Nanosuspension technologies for delivery of poorly soluble drugs
- SELF EMULSIFYING DRUG DELIVERY SYSTEM: A CONVENTIONAL ANDALTERNATIVE APPPROACH TO IMPROVE ORAL BIOAVAILABILITY OFLIPOPHILIC DRUGS
- Self Emulsifying Drug Delivery System: A Gentle Approach for drug delivery
- Properties of spherical pellets produced by a hot-melt extrusion and spheronization process
- Preparation and in vitro/in vivo evaluation of a ketoprofen orally disintegrating/sustained release tablet
- Ketoprofen Spray-dried Microspheres Based on Eudragit® RS and RL: Study of the Manufacturing Parameters
- Colon-specific drug delivery: Influence of solution reticulation properties upon pectin beads performance.
- Development and in vitro evaluation of an enteric-coated multiparticulate drug delivery system for the administration of piroxicam to dogs.
- Improved oral bioavailability of core-shell structured beads by redispersion of the shell-forming nanoparticles: preparation, characterization and in vivo studies.
- Solubility enhancement of Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) using polypolypropylene oxide core PAMAM dendrimers.
- What are parameters affecting Leu-enkephalin loading and release from poly(isobutylcyanoacrylate) nanoparticles coated with thiolated chitosan?
- Preparation and characterization of ketoprofen-loaded solid lipid nanoparticles made from beeswax and carnauba wax.
- Factors influencing the release kinetics of drug nanocrystal-loaded pellet formulations
- Preparation of sustained release matrix pellets by melt agglomeration in the fluidized bed: influence of formulation variables and modelling of agglomerate growth.
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