Influence of precursor solvent properties on matrix crystallinity and drug release rates from nanoparticle aerosol lipid matrices

International Journal of Pharmaceutics

Volumn 430, Issue 1-2, 2012, Pages 228-237

  Pawar, Amol Ashok ^a   Chen, Da Ren ^b   Venkataraman, Chandra ^a  

^a INDIAN INSTITUTE OF TECHNOLOGY BOMBAY   (India)

^b WASHINGTON UNIVERSITY IN ST LOUIS   (United States)

Author keywords

Aerosol synthesis; Anticancer drug; Droplet evaporation; Lipid crystallinity

Indexed keywords

ACETIC ACID ETHYL ESTER; CHLOROFORM; DICHLOROMETHANE; GEFITINIB; NANOPARTICLE; STEARIC ACID;

AEROSOL; ARTICLE; CRYSTALLIZATION; DIFFERENTIAL SCANNING CALORIMETRY; DRUG RELEASE; DRUG SOLUBILITY; EVAPORATION; PARTICLE SIZE; PH; PRIORITY JOURNAL; SOLVENT EFFECT; TRANSMISSION ELECTRON MICROSCOPY; VAPOR PRESSURE; X RAY DIFFRACTION;

ACETATES; AEROSOLS; ANTINEOPLASTIC AGENTS; CALORIMETRY, DIFFERENTIAL SCANNING; CHEMISTRY, PHARMACEUTICAL; CHLOROFORM; CRYSTALLIZATION; CRYSTALLOGRAPHY, X-RAY; DELAYED-ACTION PREPARATIONS; DRUG CARRIERS; DRUG COMPOUNDING; HYDROGEN-ION CONCENTRATION; KINETICS; METHYLENE CHLORIDE; MICROSCOPY, ELECTRON, TRANSMISSION; NANOPARTICLES; NANOTECHNOLOGY; PARTICLE SIZE; QUINAZOLINES; SOLUBILITY; SOLVENTS; STEARIC ACIDS; TECHNOLOGY, PHARMACEUTICAL; VAPOR PRESSURE;

EID: 84860757240     PISSN: 03785173     EISSN: 18733476     Source Type: Journal    
DOI: 10.1016/j.ijpharm.2012.03.030     Document Type: Article

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