REQUIMTE, Departamento de Ciências Químicas, Faculdade de Farmácia, Universidade do Porto, Portugal.
REQUIMTE, Departamento de Ciências Químicas, Faculdade de Farmácia, Universidade do Porto, Portugal.
Int J Pharm. 2014 May 15;466(1-2):190-7. doi: 10.1016/j.ijpharm.2014.03.005. Epub 2014 Mar 5.
This work aims to study the biophysical interactions of rifampicin (RIF) with three-dimensional macrophage membrane models, under environments with physiological and pathological relevance. The interaction of RIF with liposomes formed by 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) in different pH values (i.e., 5.0, 6.2 and 7.4) was investigated by several biophysical techniques. The RIF's membrane concentration was quantified by partition coefficient (Kp) using derivative spectrophotometry. To predict the drug's location across the membrane, fluorescence quenching studies were performed using liposomes labeled with two different fluorescence probes. The effect of the drug on the biophysical parameters of the membrane was carried out by dynamic light scattering (DLS), and small-angle X-ray scattering (SAXS). The overall results confirm that the interactions of RIF with membranes are pH-dependent, being much more pronounced at the acidic pH. A correlation between the effect of RIF on the biophysical properties of the membranes and the pH was found, which may be useful in the development of novel analogs with higher efficacy and fewer side effects, and also to understand the higher selectivity of RIF to the membranes of the infected cells, as well as its side effects.
这项工作旨在研究利福平(RIF)与三维巨噬细胞膜模型在生理和病理相关环境下的生物物理相互作用。通过多种生物物理技术研究了 RIF 在不同 pH 值(即 5.0、6.2 和 7.4)下与由 1,2-二棕榈酰-sn-甘油-3-磷酸胆碱(DPPC)形成的脂质体的相互作用。通过导数分光光度法用分配系数(Kp)定量测定 RIF 的膜浓度。为了预测药物在膜中的位置,使用两种不同荧光探针标记的脂质体进行荧光猝灭研究。通过动态光散射(DLS)和小角 X 射线散射(SAXS)研究药物对膜的生物物理参数的影响。总体结果证实,RIF 与膜的相互作用依赖于 pH 值,在酸性 pH 值下更为明显。发现 RIF 对膜生物物理性质的影响与 pH 值之间存在相关性,这对于开发具有更高疗效和更少副作用的新型类似物以及理解 RIF 对感染细胞的膜的更高选择性及其副作用可能有用。