Enhancement of the Hypnotic Potency of Barbiturates by Inclusion Complexation with β-Cyclodextrin
スポンサーリンク
概要
- 論文の詳細を見る
The 50% effective doses of five barbiturate-β-cyclodextrin complexes on oral administration to mice were compared with those of the corresponding barbiturates. In all cases tested, the complex gave a smaller ED_<50> than the intact drug. ED_<50> of phenobarbital, which forms the most stable complex and consequently shows the greatest enhancement in solubility, was reduced most markedly by complexation. With the exception of barbital, sleeping lag (the time from oral administration to loss of righting reflex) on administration of the complex to mice was shorter than that on giving an equimolar amount of the intact drug (p<0.001), and sleeping time (the time from loss to recovery of righting reflex) was significantly increased by inclusion complexation with β-cyclodextrin.
- 社団法人日本薬学会の論文
- 1980-01-25
著者
-
窪田 洋子
Faculty Of Pharmaceutical Sciences Mukogawa Women's University
-
三木 弘子
Faculty of Pharmaceutical Sciences, Osaka University
-
小泉 京子
Faculty of Pharmaceutical Sciences, Mukogawa Women's University
-
小泉 京子
Faculty Of Pharmaceutical Sciences Mukogawa Women's University
-
三木 弘子
Faculty Of Pharmaceutical Sciences Osaka University
関連論文
- Studies on Nucleosides and Nucleotides. LXXXVIII. : Purine Cyclonucleosides. XLIII. : ^C NMR Spectra of 2'-Substituted 2'-Deoxyadenosines. Substituent Effects on the Chemical Shifts in the Furanose Ring System
- Studies on Nucleosides and Nucleotides. LXXXVIII. : Purine Cyclonucleosides. XLIII. : ^C NMR Spectra of 2'-Substituted 2'-Deoxyadenosines. Substituent Effects on the Chemical Shifts in the Furanose Ring System
- Isolation and Characterization of Hexakis(2,6-di-O-methyl)cyclomaltohexaose and Octakis(2,6-di-O-methyl)cyclomalto-octaose : and Their Over-methylated Homologues
- Some Properties and the Inclusion Behavior of Branched Cyclodextrins
- Enhancement of the Hypnotic Potency of Barbiturates by Inclusion Complexation with β-Cyclodextrin
- Preparation of 6^1,6^n-Di-O-(tert-butyldimethylsilyl)-cyclomalto-octaoses
- Preparation of Di-O-triphenylmethyl-(trityl-)cyclomalto-octaoses, and Isolation and Characterization by "Hex-5-enose Degradation" of Four Positional Isomers
- Preparation of Three Positional Isomers of Diglucosyl-cyclomaltohexaose
- Separation and Characterization of Three Positional Isomers of Dimaltosyl-cyclomaltoheptaose(Dimaltosyl-β-cyclodextrin)
- Solubilization of Lipid-Soluble Vitamins by Complexation with Glucosyl-β-cyclodextrin
- Inclusion Complexes of Lipids with Branched Cyclodextrins
- Studies of Nucleosides and Nucleotides. LXXXIV. Purine Cyclonucleosides. XL. Cyclonucleosides derived from 5´-Deoxyadenosine
- Syntheses and ^1H- and ^C-Nuclear Magnetic Resonance Spectra of All Positional Isomers of Tetra-O-acetyl-D-glucopyranoses, and Their Monobenzyl and Monotrityl Derivatives
- A Reinvestigation of the Tritylation of Maltose
- Trityl Derivatives of Cellobiose. VII. Unusual Di-O-trityl Derivatives of Cellobiose
- Trityl Derivatives of Cellobiose. VI. Unambiguous Assignments of Acetoxyl Group Resonances in the ^1H-NMR Spectra of 6,6'-Di-O-trityl-, 6-O-Trityl-, and 6'-O-Tritylcellobiose Peracetates
- Trityl Derivatives of Cellobiose. V. Selective Acetylation of 6- and 6'-Mono-O-tritylcellobiose and Their Methyl β-Glycosides
- Trityl Derivatives of Cellobiose. IV. Studies on the Relative Reactivities of the Secondary Hydroxyl Groups in 6,6'-Di-O-tritylcellobiose and Methyl 6,6'-Di-O-trityl-β-cellobioside by Selective Acetylation
- Studies of Nucleosides and Nucleotides. LXXXII. Cyclonucleosides. (39). Synthesis and Properties of 2'-Halogeno-2'-deoxyadenosines
- Studies of Nucleosides and Nucleotides. LXXXV. Purine Cyclonucleosides. (35). Synthesis of Purine Nucleosides having 2'-Azido and 2'-Amino Functions by Cleavage of Purine Cyclonucleosides
- Untersuchung der Oligosaccharide. II. Beziehung zwischen Polymerisationsgrad und Perjodatreaktionsgeschwindigkeit der Oligosaccharide der Amylosereihe.
- Untersuchung der Oligosaccharide. I. Beziehung zwischen Struktur und Perjodatverbrauch von Disacchariden.
- Uber die Bestandteile der chinesischen Droge Tanshin. IV. Zur Kenntnis der Konstitution des Tanshinons II-A.