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胆固醇调节脂质体膜的流动性和对亲水分子的通透性。

Cholesterol modulates the liposome membrane fluidity and permeability for a hydrophilic molecule.

机构信息

Bioactive Molecules Research Laboratory, Faculty of Sciences, Lebanese University, Lebanon; Laboratoire D'Automatique et de Génie des Procédés (LAGEP), Université Claude Bernard, Lyon 1, France.

Bioactive Molecules Research Laboratory, Faculty of Sciences, Lebanese University, Lebanon.

出版信息

Food Chem Toxicol. 2018 Mar;113:40-48. doi: 10.1016/j.fct.2018.01.017. Epub 2018 Jan 12.

Abstract

The effect of cholesterol (CHOL) content on the permeability and fluidity of dipalmitoylphosphatidylcholine (DPPC) liposome membrane was investigated. Liposomes encapsulating sulforhodamine B (SRB), a fluorescent dye, were prepared by reverse phase evaporation technique (REV) at various DPPC:CHOL molar ratios (from 100:0 to 100:100). The release kinetics of SRB was studied during 48 h in buffer (pH 7.4) containing NaCl at 37 °C. The DPPC:CHOL formulations were also characterized for their size, polydispersity index and morphology. Increasing CHOL concentration induced an increase in the mean liposomes size accompanying with a shape transition from irregular to nanosized, regular and spherical vesicles. The release kinetics of SRB showed a biphasic pattern; the release data was then analyzed using different mathematical models. On the overall, the SRB release was governed by a non-Fickian diffusion during the first period (0-10 h) while it followed a Fickian diffusion between 10 and 48 h. Changes in DPPC liposome membrane fluidity of various batches (CHOL% 0, 10, 20, 30 and 100) were monitored by using 5- and 16 doxyl stearic acids (DSA) as spin labels. CHOL induced a decrease in the bilayer fluidity. Concisely, CHOL represents a critical component in modulating the release of hydrophilic molecules from lipid vesicles.

摘要

研究了胆固醇(CHOL)含量对二棕榈酰磷脂酰胆碱(DPPC)脂质体膜通透性和流动性的影响。通过反相蒸发技术(REV)在不同 DPPC:CHOL 摩尔比(从 100:0 到 100:100)下制备包封了磺基罗丹明 B(SRB)的荧光染料脂质体。在 37°C 下,在含有 NaCl 的缓冲液(pH 7.4)中研究了 48 小时内 SRB 的释放动力学。还对 DPPC:CHOL 制剂的大小、多分散指数和形态进行了表征。随着 CHOL 浓度的增加,平均脂质体大小增加,并伴随着从不规则到纳米尺寸、规则和球形囊泡的形状转变。SRB 的释放动力学呈现出双相模式;然后使用不同的数学模型对释放数据进行分析。总的来说,在第一个阶段(0-10 小时),SRB 的释放由非菲克扩散控制,而在 10 到 48 小时之间,它遵循菲克扩散。使用 5-和 16 二氧芑硬脂酸(DSA)作为旋转标记监测了不同批次(CHOL%0、10、20、30 和 100)的 DPPC 脂质体膜流动性的变化。CHOL 降低了双层的流动性。简而言之,CHOL 是调节亲水分子从脂质体释放的关键成分。

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