Ding Wu-Xiao, Qi Xian-Rong, Li Ping, Maitani Yoshie, Nagai Tsuneji
Department of Pharmaceutics, School of Pharmaceutical Sciences, Peking University, Beijing 100083, China.
Int J Pharm. 2005 Aug 26;300(1-2):38-47. doi: 10.1016/j.ijpharm.2005.05.005.
In the present study, cholesteryl hemisuccinate (CHEMS) was evaluated for use as a membrane stabilizer in dipalmitoylphosphatidylcholine (DPPC) liposomes. Differential scanning calorimetry (DSC) and a calcein release study showed that CHEMS was more effective than cholesterol (CHOL) in increasing DPPC membrane stability. The findings of Fourier transform infrared spectroscopy (FT-IR) also suggested that CHEMS interacts with DPPC via both hydrogen bonding and electrostatic interaction. More importantly, CHEMS did not interact with saikosaponin-d (SSD), a triterpene saponin from Bupleurum species, unlike CHOL. SSD-containing liposomes with DPPC, CHEMS and DSPE-PEG could greatly decrease the hemolytic activity of SSD. This study demonstrated that CHEMS has more stabilization ability than CHOL since CHEMS may exhibit both hydrogen bond interaction and electrostatic interaction with DPPC membrane while CHOL only has hydrogen bond interaction, resulting in stable and low-hemolytic SSD-liposomes.
在本研究中,对胆固醇半琥珀酸酯(CHEMS)作为二棕榈酰磷脂酰胆碱(DPPC)脂质体中的膜稳定剂的用途进行了评估。差示扫描量热法(DSC)和钙黄绿素释放研究表明,在提高DPPC膜稳定性方面,CHEMS比胆固醇(CHOL)更有效。傅里叶变换红外光谱(FT-IR)的研究结果还表明,CHEMS通过氢键和静电相互作用与DPPC相互作用。更重要的是,与CHOL不同,CHEMS不与柴胡属植物中的三萜皂苷柴胡皂苷d(SSD)相互作用。含有DPPC、CHEMS和DSPE-PEG的SSD脂质体可大大降低SSD的溶血活性。本研究表明,CHEMS比CHOL具有更强的稳定能力,因为CHEMS可能与DPPC膜同时表现出氢键相互作用和静电相互作用,而CHOL仅具有氢键相互作用,从而形成稳定且低溶血的SSD脂质体。