Uptake of Liposomes Surface-Modified with Glycyrrhizin by Primary Cultured Rat Hepatocytes
スポンサーリンク
概要
- 論文の詳細を見る
Previously, we synthesized 30-stearyl glycyrrhizin (GLOSt) and reported that small unilamellar liposomes containing GLOSt (GLOSt-SUV) accumulated in the liver several times more than the control liposomes (control-SUV). In the present study, to determine the interaction between GLOSt-SUV and hepatocytes, in vitro uptake experiments were achieved with primary cultured rat hepatocytes. The uptake amount of GLOSt-SUV by rat hepatocytes was considerably higher compared to the control-SUV, while GLOSt-SUV showed about a 10-fold higher uptake level than the control-SUV during 2 h of incubation. It was assumed that GLOSt-SUV not only bind to the surface of the hepatocytes but are internalized and degraded in the cells, because at 37℃, GLOSt-SUV were taken up and the level of the degradable marker was lower than the inert marker, and this did not occur at 4℃. Since the uptake of GLOSt-SUV was inhibited by glycyrrhizin (GL), it was suggested that a binding-site for GL is present on the surface of hepatocytes, and GLOSt-SUV are likely to be internalized via this site by the hepatocytes. Furthermore, it was confirmed that the efficacy of GLOSt on liposomes is not affected by the fluidity of the liposomal membrane.
- 公益社団法人日本薬学会の論文
- 1994-07-15
著者
-
辻 秀樹
Faculty of Pharmaceutical Sciences, Toyama Medical and Pharmaceutical University
-
際田 弘志
Faculty Of Pharmaceutical Sciences University Of Tokushima
-
辻 秀樹
Faculty Of Pharmaceutical Sciences University Of Tokushima
-
逢坂 佐代子
Faculty of Pharmaceutical Sciences, University of Tokushima
-
際田 弘志
Faculty Of Pharmaceutical Sciences Tokushima University
-
逢坂 佐代子
Faculty Of Pharmaceutical Sciences University Of Tokushima
-
Kiwada H
Faculty Of Pharmaceutical Sciences University Of Tokushima
関連論文
- Chemical and Pharmaceutical Studies on Medicinal Plants in Paraguay. I. : Isolation and Identification of Lens Aldose Reductase Inhibitor from "Tapecue," Acanthospermum australe O.K.(Pharmacological)
- Anti-inflammatory Constituents of Topically Applied Crude Drugs. II. : Constituents and Anti-inflammatory Effect of Cryptomeria japonica D. DON
- Anti-inflammatory Constituents of Topically Applied Crude Drugs. I. : Constituents and Anti-inflammatory Effect of Eriobotrya japonica LINDL.
- Effects of Ascorbic Acid on Iproniazid-Induced Hepatitis in Phenobarbital-Treated Rats
- Studies on the Uptake Mechanism of Liposomes by Perfused Rat Liver. I. : An Investigation of Effluent Profiles with Perfusate Containing No Blood Component
- Effects of Fluidity and Vesicle Size on Antitumor Activity and Myelosuppressive Activity of Liposomes Loaded with Daunorubicin
- Application of Synthetic Alkyl Glycoside Vesicles as Drug Carriers. III. : Plasma Components Affecting Stability of the Vesicles
- Application of Synthetic Liposomes Based on Acyl Amino Acids or Acyl Peptides as Drug Carriers. I. Their Preparation and Transport of Glutathione into the Liver(Pharmaceutical)
- Studies on the Uptake Mechanism of Liposomes by Perfused Rat Liver. II. : An Indispensable Factor for Liver Uptake in Serum(Pharmaceutical)
- Feasibility of Magnetic Liposomes as a Targeting Device for Drugs
- Effects of Dose and Vesicle Size on the Pharmacokinetics of Liposomes
- Effects of Glucose and Ascorbic Acid on Absorption and First Pass Metabolism of Isoniazid in Rats
- Uptake of Liposomes Surface-Modified with Glycyrrhizin by Primary Cultured Rat Hepatocytes
- Targeting of Liposomes Surface-Modified with Glycyrrhizin to the Liver. I. Preparation and Biological Disposition
- Effect of Cetylmannoside Modification on the Alternative Complement Pathway Activation by Liposomes in Rat Serum
- Tissue Distribution and Pharmacokinetic Evaluation of the Targeting Efficiency of Synthetic Alkyl Glycoside Vesicles
- Application of Synthetic Alkyl Glycoside Vesicles as Drug Carriers. I. Preparation and Physical Properties
- Correlations between in Vivo and in Vitro Dissolution Rates of (α-Bromoisovaleryl) urea Polymorphs
- Pharmacokinetic Study on the Polymorphs of (α-Bromoisovaleryl) urea in the Rat
- The Determination of (α-Bromoisovaleryl) urea in Plasma and the Bioavailabilities of Its Polymorphic Forms in the Rat
- The Dissolution Properties and Physico-chemical Properties of Polymorphic Forms of (α-Bromoisovaleryl) urea
- The Preparation and Properties of a New Polymorphic Form of (α-Bromoisovaleryl) urea
- The Pharmacokinetic Study on the Fate of 8-Hydroxyquinoline in Rat
- A New Numerical Calculation Method for Deconvolution in Linear Compartment Analysis of Pharmacokinetics
- Effect of Vesicle Size on in Vivo Release of Daunorubicin from Hydrogenated Egg Phosphatidylcholine-Based Liposomes into Blood Circulation