PHARMACOKINETIC STUDY ON SATURATED HEPATO-BILIARY TRANSPORT OF ACETYL PROCAINAMIDE ETHOBROMIDE
スポンサーリンク
概要
- 論文の詳細を見る
Pharmacokinetic analysis of plasma concentration of acetyl procainamide ethobromide (APAEB) after single injection of 1.5,8.8 and 20μmol/300 g rat of APAEB showed that its elimination from plasma followed saturation kinetics. The existence of saturable step in transport of APAEB from blood to bile was also evident from the data of the biliary excretion at three dose levels. The data of the biliary excretion were well fitted to two compartment model with two saturable processes at the hepatic uptake and the biliary excretion. The Michaelis-Menten parameters were calculated according to that model. The model was also applicable to the data of biliary excretion obtained by constant infusion of APAEB. Simulation of liver and plasma content gave a good agreement to the experimental data. All these results indicate that the pharmacokinetics of APAEB is satisfactorily represented by the proposed model.
- 公益社団法人日本薬学会の論文
著者
-
MURANISHI SHOZO
Kyoto College of Pharmacy
-
Takada Kanji
Kobe Women's College Of Pharmacy
-
Asada Shozo
Kobe Women's College Of Pharmacy
-
NAKAE HIROKO
Kyoto College of Pharmacy
関連論文
- OPTIMAL DOSAGE REGIMEN CALCULATION BASED ON THE REMAINING DRUG CONCENTRATIONS IN PLASMA
- PHARMACOKINETIC PROPERTY OF HUMAN INTERFERON AFTER ADMINISTRATION BY DIFFERENT ROUTES : PROMOTION OF INTESTINAL ABSORPTION AND SPECIFIC TRANSFER INTO LYMPHATICS
- USE OF A FLUORESCENT SULFHYDRYL REAGENT, N-[p-(2-BENZIMIDAZOLYL) PHENYL] MALEIMIDE, IN INVESTIGATING ACTIVE BILIARY EXCRETION OF ORGANIC CATIONS
- PHARMACOKINETIC STUDY ON SATURATED HEPATO-BILIARY TRANSPORT OF ACETYL PROCAINAMIDE ETHOBROMIDE
- MODEL INDEPENDENT METHOD TO DESCRIBE BLOOD DISAPPEARANCE PROFILE OF DRUGS
- EVIDENCE FOR THE PULMONARY ABSORPTION OF FLUORESCENT LABELLED MACROMOLECULAR COMPOUNDS
- DEVELOPMENT OF BIFUNCTIONAL DELIVERY SYSTEM FOR SELECTIVE TRANSFER OF DRUG INTO LYMPHATICS VIA ENTERAL ROUTE AND TRANSFER MECHANISM
- The hydrolytic rate of barbituric acid and the extrathermodynamic relationship.
- The carbon-13 NMR spectra of barbituric-acid derivatives.