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通过微流控辅助自组装控制聚合物囊泡的大小:为生物应用提供“即用型”制剂。

Controlling polymersome size through microfluidic-assisted self-assembly: Enabling 'ready to use' formulations for biological applications.

机构信息

Université de Bordeaux, CNRS, Bordeaux INP, LCPO, UMR 5629, 33600 Pessac, France.

Université de Bordeaux, CNRS, Bordeaux INP, LCPO, UMR 5629, 33600 Pessac, France.

出版信息

Int J Pharm. 2023 Jul 25;642:123157. doi: 10.1016/j.ijpharm.2023.123157. Epub 2023 Jun 20.

Abstract

The self-assembly of poly(ethylene glycol)-block-poly(trimethylene carbonate) PEG-b-PTMC copolymers into vesicles, also referred as polymersomes, was evaluated by solvent displacement using microfluidic systems. Two microfluidic chips with different flow regimes (micromixer and Herringbone) were used and the impact of process conditions on vesicle formation was evaluated. As polymersomes are sensitive to osmotic variations, their preparation under conditions allowing their direct use in biological medium is of major importance. We therefore developed a solvent exchange approach from DMSO (Dimethylsulfoxide) to aqueous media with an osmolarity of 300 mOsm L, allowing their direct use for biological evaluation. We evidenced that the organic/aqueous solvent ratio does not impact vesicle size, but the total flow rate and copolymer concentration have been observed to influence the size of polymersomes. Finally, nanoparticles with diameters ranging from 76 nm to 224 nm were confirmed to be vesicles through the use of multi-angle light scattering in combination with cryo-TEM (Cryo-Transmission Electron Microscopy) characterization.

摘要

聚乙二醇-嵌段-聚三亚甲基碳酸酯 PEG-b-PTMC 共聚物通过溶剂置换在微流控系统中自组装成囊泡,也称为聚合物囊泡。使用两种具有不同流型(微混合器和人字形)的微流控芯片评估了囊泡形成的过程条件的影响。由于聚合物囊泡对渗透压变化敏感,因此在允许其直接用于生物介质的条件下制备它们非常重要。因此,我们开发了一种从 DMSO(二甲基亚砜)到渗透压为 300 mOsm L 的水介质的溶剂交换方法,允许其直接用于生物学评估。我们证明了有机/水溶剂比对囊泡大小没有影响,但总流速和共聚物浓度已被观察到影响聚合物囊泡的大小。最后,通过使用多角度光散射结合 cryo-TEM(Cryo-Transmission Electron Microscopy)表征,证实了直径为 76nm 至 224nm 的纳米颗粒是囊泡。

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