Effect of Phosphatidylserine Content on the Partition Coefficients of Diazepam and Flurazepam between Phosphatidylcholine-Phosphatidylserine Bilayer of Small Unilamellar Vesicles and Water Studied by Second Derivative Spectrophotometry
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概要
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The affinity of the psychotropic benzodiazepine drugs diazepam (DZ) and flurazepam (FZ) to phosphatidylserine (PS) was examined since PS is abundantly contained in brain membranes. The effect of PS content on the partition coefficients (K_ps) of these drugs between phosphatidylcholine (PC)-PS bilayer membranes of small unilamellar vesicles (SUV) and water was measured using second derivative spectrophotometry. The second derivative spectra of DZ and FZ measured in the solutions containing various amounts of PC-PS SUV clearly showed derivative isosbestic points and a distinct derivative intensity change depending on the amount of the SUV added. The derivative intensity differences (ΔD) of the drugs before and after addition of the SUV suspension were measured at a specific wavelength. Using the ΔD values, the K_p values were calculated and obtained with relative standard deviation of below 10%. The K_p values of both drugs increased according to the PS content in the PS-PC bilayer membranes of the SUV proving that both have higher affinity to the PC-PS bilayer membranes than to PC membranes. The effect was much larger for FZ, i.e., the K_p value of FZ at 30 mol% PS content increased to about five times the value for the PC SUV. This can be explained by the fact that at the experimental pH of 7.4,80% of FZ molecules are in a cationic form (pK_a=8.1), so that these molecules are highly accessible to the negatively charged PS molecules. The results support the rapid and high distribution of DZ and FZ in the central nervous system after their administration.
- 公益社団法人日本薬学会の論文
- 2002-03-01
著者
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Mohamed Mahmoud
Department of Pharmacognosy, Faculty of Pharmacy, Al-Azhar University, Assiut Branch
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北村 和則
富山化学工業株式会社綜合研究所
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Mohamed Mahmoud
Department Of Chemistry Faculty Of Education Assuit University
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Mohamed Mahmoud
Department Of Pharmacognosy Faculty Of Pharmacy Al-azhar University
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Kitamura Keisuke
Kyoto Pharmaceutical University
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KITADE Tatsuya
Kyoto Pharmaceutical University
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TAKEGAMI Shigehiko
Kyoto Pharmaceutical University
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Kitamura K
Kyoto Pharmaceutical University
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OMRAN Ahmed
Kyoto Pharmaceutical University
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EL-SAYED Abdel-Aziz
Department of Chemistry, Faculty of Science, Al-Azhar University
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ABDEL-MOTTALEB Mohamed
Department of Chemistry, Faculty of Science, Al-Azhar University
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北村 和則
Kyoto Pharmaceutical University
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Abdel-mottaleb Mohamed
Department Of Chemistry Faculty Of Science Al-azhar University
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El-sayed Abdel-aziz
Department Of Chemistry Faculty Of Science Al-azhar University
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Kitamura Keisuke
Kyoto College of Pharmacy
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