Beurer G, Galla H J
Eur Biophys J. 1987;14(7):403-8. doi: 10.1007/BF00254863.
Binding of the positively charged drug chlorpromazine to phospholipid monolayers was investigated. A preferential uptake was observed near the phase transition of the corresponding lipid. Cholesterol considerably diminishes the chlorpromazine uptake, again particularly near a lipid phase transition. The binding properties depend on the chlorpromazine concentration in the subphase. A critical concentration is 5 X 10(-5) M, where higher uptake occurs in the liquid condensed than in the liquid expanded state of the monolayer at pressures of about 10 mN/m. Dipalmitoylphosphatidylcholine monolayers spread on a subphase containing chlorpromazine are comparable to monolayers at higher temperature but in the absence of chlorpromazine. These data are in agreement with previous fluorescence and electron paramagnetic resonance experiments on lipid bilayer membranes (Luxnat and Galla 1986).
研究了带正电荷的药物氯丙嗪与磷脂单层的结合情况。在相应脂质的相变附近观察到优先摄取现象。胆固醇显著减少了氯丙嗪的摄取,同样特别在脂质相变附近。结合特性取决于氯丙嗪在亚相中浓度。临界浓度为5×10⁻⁵ M,在此浓度下,在约10 mN/m的压力下,单层处于液晶态时比处于液态扩张态时摄取量更高。铺展在含有氯丙嗪的亚相上的二棕榈酰磷脂酰胆碱单层与在较高温度但不存在氯丙嗪时的单层相当。这些数据与先前关于脂质双分子层膜的荧光和电子顺磁共振实验结果一致(Luxnat和Galla,1986年)。