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首页> 外文期刊>International Journal of Pharmaceutics >Cholesteryl hemisuccinate as a membrane stabilizer in dipalmitoylphosphatidylcholine liposomes containing saikosaponin-d.
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Cholesteryl hemisuccinate as a membrane stabilizer in dipalmitoylphosphatidylcholine liposomes containing saikosaponin-d.

机译:胆固醇半琥珀酸酯作为含有皂苷皂苷-d的二棕榈酰磷脂酰胆碱脂质体中的膜稳定剂。

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摘要

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.
机译:在本研究中,评估了半琥珀酸胆固醇酯(CHEMS)用作二棕榈酰磷脂酰胆碱(DPPC)脂质体中的膜稳定剂。差示扫描量热法(DSC)和钙黄绿素释放研究表明,CHEMS在提高DPPC膜稳定性方面比胆固醇(CHOL)更有效。傅立叶变换红外光谱(FT-IR)的发现还表明,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不与柴胡中的三萜皂苷saikosaponin-d(SSD)相互作用。含DPPC,CHEMS和DSPE-PEG的含SSD脂质体可大大降低SSD的溶血活性。这项研究表明,CHEMS比CHOL具有更高的稳定能力,因为CHEMS可能同时显示氢键相互作用和与DPPC膜的静电相互作用,而CHOL仅具有氢键相互作用,从而产生稳定且低溶血的SSD脂质体。

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