Hunter screening design to understand the product variability of solid dispersion formulation of a peptide antibiotic

International Journal of Pharmaceutics

Volumn 456, Issue 2, 2013, Pages 572-582

  Rahman, Ziyaur ^a   Khan, Mansoor A ^a  

^a CENTER FOR DRUG EVALUATION AND RESEARCH   (United States)

Author keywords

Design of experiment; Dissolution; Polyethylene glycol; Potency; Vancomycin

Indexed keywords

GELATIN; MACROGOL; PULLULAN; SURFACTANT; VANCOMYCIN;

ARTICLE; DIFFERENTIAL SCANNING CALORIMETRY; DISPERSION; DISSOLUTION; DRUG CAPSULE; DRUG FORMULATION; DRUG POTENCY; INDEPENDENT VARIABLE; INFRARED SPECTROSCOPY; MELTING POINT; MOLECULAR WEIGHT; PHYSICAL CHEMISTRY; PRIORITY JOURNAL; SCANNING ELECTRON MICROSCOPE; SCANNING ELECTRON MICROSCOPY; SCREENING; X RAY DIFFRACTION;

DESIGN OF EXPERIMENT; DISSOLUTION; POLYETHYLENE GLYCOL; POTENCY; VANCOMYCIN;

ANTI-BACTERIAL AGENTS; CHEMISTRY, PHARMACEUTICAL; DRUG EVALUATION, PRECLINICAL; PEPTIDE FRAGMENTS; VANCOMYCIN; X-RAY DIFFRACTION;

EID: 84886723948     PISSN: 03785173     EISSN: 18733476     Source Type: Journal    
DOI: 10.1016/j.ijpharm.2013.07.062     Document Type: Article

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