Gelatin hollow type rectal suppository; Indomethacin; Rats; SES (Tween 85: ethyl oleate, 3:7)
Indexed keywords
EMULSIFYING AGENT;
INDOMETACIN;
ANIMAL EXPERIMENT;
AREA UNDER THE CURVE;
ARTICLE;
DRUG ABSORPTION;
DRUG BIOAVAILABILITY;
DRUG FORMULATION;
DRUG SOLUBILITY;
MALE;
NONHUMAN;
PARTICLE SIZE;
PRIORITY JOURNAL;
RAT;
Self-emulsifying drug delivery system: Formulation and biopharmaceutic evaluation of an investigational lipophilic compound
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Critical evaluation of potential error in pharmacokinetic studies using the linear trapezoidal rule method for the calculation of the area under the plasma level-time curve
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Pharmacokinetics of DA-125, a new anthracycline, after intravenous administration to uranyl nitrate-induced acute renal failure rats or protein-calorie malnutrition rats
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Pharmacokinetics of a new carbapenem, DA-1131, after intravenous administration to rats with uranyl nitrate-induced acute renal failure
Kim S.H., Shim H.J., Kim W.B., Lee M.G. Pharmacokinetics of a new carbapenem, DA-1131, after intravenous administration to rats with uranyl nitrate-induced acute renal failure. Antimicrob. Agents Chemother. 42:1998;1217-1221.
Preparation of sustained-release suppositories of indomethacin using a solid-dispersion system and evaluation of bioavailability in rabbits
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Particle design of tolbutamide by the spherical crystallization technique. III. Micromeritic properties and dissolution rate of tolbutamide spherical agglomerates prepared by the quasi-emulsion solvent diffusion method and the solvent change method
Sano A., Kuriki T., Kawashima Y. et al. Particle design of tolbutamide by the spherical crystallization technique. III. Micromeritic properties and dissolution rate of tolbutamide spherical agglomerates prepared by the quasi-emulsion solvent diffusion method and the solvent change method. Chem. Pharm. Bull. 38:1990;733-739.
Dissolution behavior and gastrointestinal absorption of dicoumarol from solid dispersion systems of dicoumarol-polyvinyl pyrrolidone and dicoumarol-β-cyclodextrin
Sekikawa H., Fukuda N., Takada M. et al. Dissolution behavior and gastrointestinal absorption of dicoumarol from solid dispersion systems of dicoumarol-polyvinyl pyrrolidone and dicoumarol-β-cyclodextrin. Chem. Pharm. Bull. 31:1983;1350-1356.
Self-emulsifying drug delivery systems (SEDDS) with polyglycolysed glycerides for improving in vitro dissolution and oral absorption of lipophilic drugs
Shah N.H., Carvajal M.T., Patel C.I., Infeld M.H., Malik A.W. Self-emulsifying drug delivery systems (SEDDS) with polyglycolysed glycerides for improving in vitro dissolution and oral absorption of lipophilic drugs. Int. J. Pharm. 106:1994;15-23.