Phase-separated cationic giant unilamellar vesicles as templates for the polymerization of tetraethyl orthosilicate (TEOS)

IF 2.8 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Biochimica et biophysica acta. Biomembranes Pub Date : 2025-02-01 DOI:10.1016/j.bbamem.2024.184403
Kohei Shiomi , Keita Hayashi , Haruyuki Ishii , Toshiyuki Kamei , Toshinori Shimanouchi , Hidemi Nakamura , Sosaku Ichikawa
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Abstract

Unlike homogeneous liposomes, phase-separated liposomes have the potential to be attractive soft materials because they exhibit different properties for each phase. In this study, phase separation was observed when liposomes were prepared using 1,2-dioleoyloxy-3-trimethylammonium propane chloride (DOTAP), 1,2-distearoyl-sn-glycero-3-phosphocholine (DSPC), and cholesterol. The pH of the DOTAP-rich phase was evaluated using a coumarin derivative, and measurements showed that DOTAP molecules accumulated hydroxyl ions (OH) in the DOTAP-rich phase. Such accumulation of OH was not observed when homogeneous DSPC liposomes were used. The difference in local concentration of OH in each phase was applied to prepare hollow silica particles with large pores. The OH promotes the polymerization of tetraethyl orthosilicate (TEOS). Therefore, TEOS polymerized preferentially in the DOTAP-rich phase, whereas a silica membrane barely formed in the DSPC-rich phase.

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相分离阳离子巨型单层囊泡作为正硅酸四乙酯(TEOS)聚合模板的研究。
与均相脂质体不同,相分离脂质体具有成为有吸引力的软材料的潜力,因为它们在每个相中表现出不同的性质。在本研究中,用1,2-二聚氧氧基-3-三甲基丙烷氯铵(DOTAP)、1,2-二硬脂酰-sn-甘油-3-磷酸胆碱(dsc)和胆固醇制备脂质体时,观察到相分离。利用香豆素衍生物对富含DOTAP相的pH值进行了评估,结果表明,DOTAP分子在富含DOTAP相中积累了羟基离子(OH-)。当使用均匀的DSPC脂质体时,没有观察到OH-的积累。利用各相局部OH-浓度的差异制备了具有大孔隙的空心二氧化硅颗粒。OH-促进正硅酸四乙酯(TEOS)的聚合。因此,TEOS在富含dotap相中优先聚合,而二氧化硅膜在富含dspc相中几乎不形成。
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来源期刊
Biochimica et biophysica acta. Biomembranes
Biochimica et biophysica acta. Biomembranes 生物-生化与分子生物学
CiteScore
8.20
自引率
5.90%
发文量
175
审稿时长
2.3 months
期刊介绍: BBA Biomembranes has its main focus on membrane structure, function and biomolecular organization, membrane proteins, receptors, channels and anchors, fluidity and composition, model membranes and liposomes, membrane surface studies and ligand interactions, transport studies, and membrane dynamics.
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