Semi-solid dosage form of clonazepam for rapid oral mucosal absorption

Drug Development and Industrial Pharmacy

Volumn 37, Issue 7, 2011, Pages 809-814

  Sakata, Osamu ^a   MacHida, Yoshiharu ^a   Onishi, Hiraku ^a  

^a HOSHI UNIVERSITY   (Japan)

Author keywords

buccal administration; Clonazepam; oral mucosal absorption; physical stability; semi solid dosage form

Indexed keywords

CLONAZEPAM; MACROGOL; MACROGOL 1500; OLEIC ACID; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; AREA UNDER THE CURVE; ARTICLE; CHEMICAL COMPOSITION; CRYSTALLIZATION; DRUG ABSORPTION; DRUG BLOOD LEVEL; DRUG FORMULATION; DRUG STABILITY; DRUG SYNTHESIS; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; MALE; MAXIMUM PLASMA CONCENTRATION; MOUTH MUCOSA; NONHUMAN; RAT; ROOM TEMPERATURE; THERMOSTABILITY; TIME TO MAXIMUM PLASMA CONCENTRATION;

ABSORPTION; ADMINISTRATION, ORAL; ANIMALS; ANTICONVULSANTS; CLONAZEPAM; DOSAGE FORMS; DRUG COMPOUNDING; DRUG STABILITY; HUMANS; MALE; MOUTH MUCOSA; OLEIC ACID; POLYETHYLENE GLYCOLS; RATS; RATS, WISTAR;

EID: 79958748183     PISSN: 03639045     EISSN: 15205762     Source Type: Journal    
DOI: 10.3109/03639045.2010.545069     Document Type: Article

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