Emulsification Using Highly Hydrophilic Surfactants Improves the Absorption of Orally Administered Coenzyme Q10
スポンサーリンク
概要
- 論文の詳細を見る
Coenzyme Q10 (CoQ10) is an essential component in the electron-transport systems of mitochondria and bacteria and is often used as a supplementary treatment for some diseases. We previously reported that the bioavailability of CoQ10 powder was less than 10%. In this study, we investigated various preparations to improve the intestinal absorption of CoQ10 with focus on the effect of emulsification. We prepared a suspension and some emulsions with four types of surfactants and investigated the plasma concentration profile after oral administration to rats. The absorption of CoQ10 was improved by an emulsion formulation although there was little absorption of CoQ10 when a suspension was administered. However, little CoQ10 was absorbed in the bile duct-ligated group even when the emulsion formulation was administered (about 50% of the control group). Bile and emulsion formulation are essential for absorption of CoQ10. When the preparations containing Tween20 (polysorbate (20) sorbitan monolaurate) and Tween80 (polyoxyethylene (20) sorbitan monooleate) were administered, plasma concentrations of CoQ10 were higher than those obtained with preparations containing Tween65 (polyoxyethylene (20) sorbitan tristearate) and Span20 (sorbitan monolaurate). Tween20 and Tween80 have higher hydrophile–lipophile balance (HLB) values than those Tween65 and Span20. Our study suggests that highly lipophilic compounds like CoQ10 would diffuse the unstirred water layer and would easily access the intestinal apical membrane by an emulsion containing a surfactant with a high HLB value. Attention must be given to CoQ10 supplementation for patients whose bile is not excreted to the intestine such as patients with cholestasis.
- 公益社団法人 日本薬学会の論文
著者
-
Sato Yuki
Faculty Of Agriculture Niigata University
-
Suzuki Mika
Faculty of Pharmaceutical Sciences, Hokkaido University
-
Iseki Ken
Faculty of Pharmaceutical Sciences, Hokkaido University
-
Mutoh Hanami
Faculty of Pharmaceutical Sciences, Hokkaido University
-
Takekuma Yoh
Faculty of Pharmaceutical Sciences, Hokkaido University
-
Sugawara Mitsuru
Faculty of Pharmaceutical Sciences, Hokkaido University
関連論文
- Two-component high-affinity nitrate transport system in barley : Membrane localization, protein expression in roots and a direct protein-protein interaction
- Development of Des-Fatty Acyl-Polymyxin B Decapeptide Analogs with Pseudomonas aeruginosa-Specific Antimicrobial Activity
- Contribution of Each Amino Acid Residue in Polymyxin B_3 to Antimicrobial and Lipopolysaccharide Binding Activity
- Des-Fatty Acyl-Polymyxin B Decapeptide Analogs with Antimicrobial Activity Specifically against Pseudomonas aeruginosa
- Semi-synthesis of Polymyxin B (2-10) and Colistin (2-10) Analogs Employing the Trichloroethoxycarbonyl (Troc) Group for Side Chain Protection of α, γ-Diaminobutyric Acid Residues
- Chemical Conversion of Natural Polymyxin B and Colistin to Their N-Terminal Derivatives
- Semi-Synthesis of Polymyxin B-(2-10) Analogs Employing the Trichloroethoxycarbonyl (Troc) Group for Side Chain Protection of 2,4-Diaminobutyric Acid Residues
- Structure-Activity Relationships of Neuromedin U. V. Study on the Stability of Porcine Neuromedin U-8 at the C-Terminal Asparagine Amide under Mild Alkaline and Acidic Conditions
- Antimicrobial Activity of Des-Fatty Acyl-Polymyxin B Decapeptide N-Terminal Analogs
- The Contribution of the N-Terminal Structure of Polymyxin B Peptides to Antimicrobial and Lipopolysaccharide Binding Activity
- Antimicrobial Activity of Polymyxin B_3 Analogs modified at the Hydrophobic Amino Acids
- Novel Des-Fatty Acyl-Polymyxin B Derivatives with Pseudomonas aeruginosa-Specific Antimicrobial Activity
- Antimicrobial Activity of Various Aminocyclohexylcarbonyl-polymyxin B (2-10) Derivatives
- Heterogeneous expression and emulsifying activity of class I hydrophobin from Pholiota nameko
- Emulsification Using Highly Hydrophilic Surfactants Improves the Absorption of Orally Administered Coenzyme Q10