Takegami S, Kitamura K, Kitade T, Hasegawa K, Nishihira A
Kyoto Pharmaceutical University, 5 Nakauchicho, Misasagi, Yamashina-ku, Kyoto, 607-8414, Japan
J Colloid Interface Sci. 1999 Dec 1;220(1):81-87. doi: 10.1006/jcis.1999.6505.
Phosphatidylcholine(PC)-cholesterol (0-30 mol%) unilamellar vesicles of several sizes (20-600 nm) were prepared in buffer (pH 7.4) solutions by sonication or extrusion methods. The vesicle size was measured by a dynamic light-scattering method. Absorption spectra of chlorpromazine (CPZ) and triflupromazine (TFZ) in the presence of these vesicles showed a bathochromic shift according to the increase in vesicle concentration, but the counterbalance of the baseline was incomplete due to the intensive light scattering by the vesicles; thus, no isosbestic point could be observed. In the second-derivative spectra, the residual background signal effects were eliminated and three derivative isosbestic points were clearly observed for both drugs. The derivative intensity change (DeltaD) induced by the addition of the vesicles was measured at the lambda(max) of each drug. From the relationship between the DeltaD value and the lipid concentration, the partition coefficients (K(p)) of CPZ and TFZ between these vesicles and water (buffer) were calculated. The results revealed that the vesicle size (20-600 nm) and preparation method do not affect the K(p) values, and although the incorporation of cholesterol into the PC bilayers induces a decrease of the K(p) values, the vesicle size also did not affect the K(p) values in vesicles of the same cholesterol content. Copyright 1999 Academic Press.
通过超声处理或挤压法,在缓冲液(pH 7.4)溶液中制备了几种大小(20 - 600 nm)的磷脂酰胆碱(PC)-胆固醇(0 - 30 mol%)单层囊泡。通过动态光散射法测量囊泡大小。在这些囊泡存在的情况下,氯丙嗪(CPZ)和三氟拉嗪(TFZ)的吸收光谱随囊泡浓度增加呈现红移,但由于囊泡强烈的光散射,基线的平衡不完全;因此,未观察到等吸收点。在二阶导数光谱中,消除了残留的背景信号影响,两种药物均清晰地观察到三个导数等吸收点。在每种药物的最大吸收波长(λmax)处测量加入囊泡引起的导数强度变化(ΔD)。根据ΔD值与脂质浓度的关系,计算了CPZ和TFZ在这些囊泡与水(缓冲液)之间的分配系数(Kp)。结果表明,囊泡大小(20 - 600 nm)和制备方法不影响Kp值,并且尽管将胆固醇掺入PC双层中会导致Kp值降低,但在相同胆固醇含量的囊泡中,囊泡大小也不影响Kp值。版权所有1999年学术出版社。