Loading hydrophilic drug in solid lipid media as nanoparticles: Statistical modeling of entrapment efficiency and particle size

International Journal of Pharmaceutics

Volumn 424, Issue 1-2, 2012, Pages 128-137

  Ghadiri, Maryam ^a   Fatemi, Shohreh ^a   Vatanara, Alireza ^b   Doroud, Delaram ^b   Najafabadi, Abdolhossein Rouholamini ^b   Darabi, Majid ^b   Rahimi, Amir Abbas ^c  

^a UNIVERSITY OF TEHRAN   (Iran)

^b TEHRAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^c PASTEUR INSTITUTE OF IRAN   (Iran)

Author keywords

Entrapment efficiency; Paromomycin; Solid lipid nanoparticles; Statistical modeling

Indexed keywords

PALMITIC ACID CETYL ESTER; PALMITIC ACID DERIVATIVE; PAROMOMYCIN; SOLID LIPID NANOPARTICLE; SOLVENT; STEARIC ACID; SURFACTANT; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL PARAMETERS; CONTROLLED DRUG RELEASE; DIFFUSION; DRUG FORMULATION; ENTRAPMENT EFFICIENCY; HYDROPHILICITY; MICROEMULSION; PARTICLE SIZE; PRIORITY JOURNAL; PROCESS OPTIMIZATION; QUANTITATIVE ANALYSIS; RESPONSE SURFACE METHOD; SOLVENT DIFFUSION; STATISTICAL MODEL;

CHEMISTRY, PHARMACEUTICAL; DRUG CARRIERS; HEXOSES; HYDROPHOBIC AND HYDROPHILIC INTERACTIONS; MODELS, STATISTICAL; NANOPARTICLES; PALMITATES; PAROMOMYCIN; PARTICLE SIZE; POLYSORBATES; STEARIC ACIDS; SURFACE-ACTIVE AGENTS;

EID: 84856968332     PISSN: 03785173     EISSN: 18733476     Source Type: Journal    
DOI: 10.1016/j.ijpharm.2011.12.037     Document Type: Article

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