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二棕榈酰磷脂酰胆碱(DPPC)与具有全氟烷基末端基团的半遥爪聚(甘油甲基丙烯酸酯)的相互作用。

Interactions of DPPC with semitelechelic poly(glycerol methacrylate)s with perfluoroalkyl end groups.

机构信息

Institute of Chemistry, Martin-Luther University Halle-Wittenberg, Saale, Germany.

出版信息

Langmuir. 2012 Nov 6;28(44):15651-62. doi: 10.1021/la3028226. Epub 2012 Oct 18.

DOI:10.1021/la3028226
PMID:23046205
Abstract

Semitelechelic poly(glycerol methacrylate)s having a perfluoroalkyl end group (PGMA(n)-F(9)) were synthesized by ATRP. The interactions of these polymers with different degrees of polymerization with chiral or racemic dipalmitoylphosphatidylcholine (l-DPPC, d-DPPC, or rac-DPPC) monolayers at the air/water interface were studied. Langmuir trough measurements coupled with epifluorescence microscopy allowed for the observation of domain formation within the coexistence region of liquid-expanded (LE) and liquid-condensed (LC) states of DPPC in mixed DPPC-polymer films prepared by spreading a solution of both compounds in the same organic solvent (cospread films). Because of the incorporation of PGMA(n)-F(9) polymers into the LE phase and their line-active behavior, a formation of novel types of domains could be observed. During compression, a thinning out of the tips of two- to six-lobed flowerlike domain structures and consecutive spiral formation appeared for l- and d-DPPC within the two-phase coexistence region (LE/LC) of the monolayer. When rac-DPPC was used, symmetrical stripe formation was induced at the vertices of the domains and fingerprint-like structures were created by convection-inducing movements of the domains at the air/water interface. Additional investigations of the interaction of PGMA(n)-F(9) with DPPC vesicles using differential scanning calorimetry (DSC) supported the finding on the monolayer system that the incorporation of the polymers into the lipid monolayers is not solely driven by the perfluoroalkyl chain but significantly by the hydrophilic polymer part. Apparently, interactions of the PGMA chain with the lipid headgroups are important as the interactions increase with the elongation of the polymer chain, indicating that the polymer also has hydrophobic character.

摘要

具有全氟烷基端基的半端基聚(甘油甲基丙烯酸酯)(PGMA(n)-F(9))通过 ATRP 合成。研究了这些聚合物与不同聚合度的手性或外消旋二棕榈酰磷脂酰胆碱(l-DPPC、d-DPPC 或 rac-DPPC)单层在空气/水界面的相互作用。Langmuir 槽测量结合荧光显微镜允许在 DPPC 的液态扩展(LE)和液态凝聚(LC)状态共存区域内观察到畴形成,这些 DPPC 是通过在相同有机溶剂中展开两种化合物的溶液来制备的 DPPC-聚合物混合薄膜(共铺展薄膜)。由于 PGMA(n)-F(9)聚合物掺入 LE 相及其线活性行为,可以观察到新型畴的形成。在压缩过程中,对于 l-和 d-DPPC,在单层的两相共存区域(LE/LC)内,两到六叶花状畴结构的尖端变薄,并出现连续的螺旋形成。当使用 rac-DPPC 时,在畴的顶点诱导形成对称条纹,并通过畴在空气/水界面上的对流诱导运动产生指纹状结构。使用差示扫描量热法(DSC)对 PGMA(n)-F(9)与 DPPC 囊泡相互作用的进一步研究支持了在单层系统中的发现,即聚合物掺入脂质单层不仅仅是由全氟烷基链驱动,而是显著地由亲水聚合物部分驱动。显然,PGMA 链与脂质头部基团的相互作用很重要,因为相互作用随着聚合物链的延长而增加,这表明聚合物也具有疏水性。

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