Inclusion of celecoxib into fibrous ordered mesoporous carbon for enhanced oral bioavailability and reduced gastric irritancy

European Journal of Pharmaceutical Sciences

Volumn 45, Issue 5, 2012, Pages 639-647

  Zhao, Peng ^a   Jiang, Haitao ^a   Jiang, Tongying ^a   Zhi, Zhuangzhi ^a   Wu, Chao ^a   Sun, Changshan ^a   Zhang, Jinghai ^a   Wang, Siling ^a  

^a SHENYANG PHARMACEUTICAL UNIVERSITY   (China)

Author keywords

Celecoxib; Drug delivery; Fibrous ordered mesoporous carbon; Gastric damage; Improved dissolution; Oral bioavailability

Indexed keywords

BUFFER; CARBON; CELECOXIB; FIBROUS ORDERED MESOPOROUS CARBON; NANOMATERIAL; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; CRYSTALLIZATION; DRUG BIOAVAILABILITY; DRUG CAPSULE; DRUG DELIVERY SYSTEM; DRUG EFFECT; DRUG RELEASE; DRUG SOLUBILITY; MALE; NONHUMAN; PARTICLE SIZE; PH; POROSITY; PRIORITY JOURNAL; RAT; STOMACH IRRITATION; STOMACH PROTECTION; WEIGHT;

ADMINISTRATION, ORAL; ANIMALS; BIOLOGICAL AVAILABILITY; CAPSULES; CARBON; DRUG CARRIERS; DRUG COMPOUNDING; DRUG DELIVERY SYSTEMS; GASTRIC MUCOSA; MALE; NANOPARTICLES; NANOSTRUCTURES; PARTICLE SIZE; POROSITY; PYRAZOLES; RATS; RATS, SPRAGUE-DAWLEY; SOLUBILITY; SULFONAMIDES;

EID: 84862783847     PISSN: 09280987     EISSN: 18790720     Source Type: Journal    
DOI: 10.1016/j.ejps.2012.01.003     Document Type: Article

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