Self-nanoemulsifying drug delivery system (SNEDDS) for oral delivery of protein drugs. III. In vivo oral absorption study

International Journal of Pharmaceutics

Volumn 362, Issue 1-2, 2008, Pages 16-19

  Rao, Sripriya Venkata Ramana ^a   Yajurvedi, Kavya ^a   Shao, Jun ^a  

^a Department of Pharmacy and Administrative Sciences   (United States)

Author keywords

Lactamase; Bioavailability; Pharmacokinetics; Protein oral administration; SNEDDS

Indexed keywords

BETA LACTAMASE; CREMOPHOR; LAUROGLYCOL FCC; NANOPARTICLE; PROTEIN; TRANSCUTOL HP; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ARTICLE; DISPERSION; DRUG ABSORPTION; DRUG BIOAVAILABILITY; DRUG BLOOD LEVEL; DRUG DELIVERY SYSTEM; IN VIVO STUDY; MAXIMUM PLASMA CONCENTRATION; MEAN RESIDENCE TIME; MICROEMULSION; NONHUMAN; PRIORITY JOURNAL; RAT; TECHNIQUE; TIME TO MAXIMUM PLASMA CONCENTRATION;

ABSORPTION; ADMINISTRATION, ORAL; ANIMALS; BETA-LACTAMASES; CHEMISTRY, PHARMACEUTICAL; DRUG CARRIERS; DRUG DELIVERY SYSTEMS; DRUG DESIGN; DRUG STABILITY; EMULSIONS; MOUTH MUCOSA; NANOPARTICLES; OILS; PARTICLE SIZE; PROTEIN STABILITY; RATS; RATS, SPRAGUE-DAWLEY; SURFACE-ACTIVE AGENTS;

EID: 50249175117     PISSN: 03785173     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ijpharm.2008.05.015     Document Type: Article

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