A research on aspirin sustained-release formulation

Drug Development and Industrial Pharmacy

Volumn 23, Issue 8, 1997, Pages 741-747

  Xu, G J ^a   Fang, F ^a   Zhang, R H ^b   Sunada, H ^c  

^a BEIJING INSTITUTE OF PHARMACOLOGY AND TOXICOLOGY   (China)

^b SHENYANG PHARMACEUTICAL UNIVERSITY   (China)

^c NONE

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLSALICYLIC ACID; HYDROXYPROPYLMETHYLCELLULOSE; STARCH;

ANIMAL EXPERIMENT; ARTICLE; CONTROLLED STUDY; DISSOLUTION; DOG; DRUG BIOAVAILABILITY; DRUG BLOOD LEVEL; DRUG FORMULATION; FEMALE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; MALE; METHODOLOGY; NONHUMAN; ORAL DRUG ADMINISTRATION; QUALITY CONTROL; REGRESSION ANALYSIS; STATISTICAL ANALYSIS; SUSTAINED RELEASE FORMULATION; TABLET; VISCOSITY;

EID: 0030834103     PISSN: 03639045     EISSN: None     Source Type: Journal    
DOI: 10.3109/03639049709150545     Document Type: Article

References (2)

1. U. V. Banaker, Drug and the pharmaceutical Science, Volume 49, Pharmaceutical dissolution testing, Marcel Dekker, New York, 1991, p. 322.
2. J. E. Knoben and P. O. Anderson, Handbook of Clinical Drug Data, fifth edition, Drug Intelligence, Inc., Hamilton, 1983, pp. 456-457.