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基于超临界流体乳液和羧酸甜菜碱功能化壳聚糖涂层制备的磁化聚乳酸/聚乳酸微球的新型超顺磁微器件,可实现治疗药物的可调释放。

Novel Superparamagnetic Microdevices Based on Magnetized PLGA/PLA Microparticles Obtained by Supercritical Fluid Emulsion and Coating by Carboxybetaine-Functionalized Chitosan Allowing the Tuneable Release of Therapeutics.

机构信息

Supercritical Fluids Lab., Department of Industrial Engineering, University of Salerno, Via Giovanni Paolo II, 84084 Fisciano, SA, Italy.

Brighton Studies in Tissue-mimicry and Aided Regeneration (BrightSTAR), Brighton Centre for Regenerative Medicine (BCRM), University of Brighton, Huxley Building Lewes Road, Brighton, UK.

出版信息

J Pharm Sci. 2017 Aug;106(8):2097-2105. doi: 10.1016/j.xphs.2017.05.005. Epub 2017 May 10.

DOI:10.1016/j.xphs.2017.05.005
PMID:28499877
Abstract

When superparamagnetic nanoparticles (MAG) are loaded within microcarriers of thermosensitive and injectable biopolymers, "smart" microdevices are obtained: they respond to an external magnetic field through the release of any co-encapsulated molecules with a remote on-off control. Creating reliable and effective fabrication technologies for the production of these smart nano/microdevices remains a challenge. In this work, supercritical emulsion extraction technology is proposed for the fabrication of microcapsules with a core of poly-lactic-co-glycolic acid (PLGA) or polylactic acid (PLA) covered by carboxybetaine-functionalized chitosan (f-chi) and loaded with MAG (mean size of 6.5 ± 3.0 nm) and water-soluble fluorescein (Fluo). Fluo is co-encapsulated as a fluorescent marker for the release study. Microcarriers showed a mean size of 800 ± 60 nm with an encapsulation efficiency of up to 90%. The inversion of surface charge, after the f-chi coating, suggested the presence of a uniform functionalized surface available for further chemical linkage. The external chitosan layer had a thickness of 200 ± 50 nm. An excellent MAG dispersion was confirmed within the biopolymer matrix that was shown to be responsive to external magnetic field; indeed, Fluo was released over 3 or 5 days from PLGA or f-chi-PLGA microdevices into phosphate-buffered saline medium at 37°C, whereas remote on-off controlled release was achieved when an alternating magnetic field was applied.

摘要

当超顺磁纳米粒子(MAG)被负载在热敏感和可注射生物聚合物的微载体中时,就得到了“智能”微器件:它们通过释放任何共包封的分子来对外磁场做出响应,实现远程开/关控制。创建用于生产这些智能纳米/微器件的可靠且有效的制造技术仍然是一个挑战。在这项工作中,提出了超临界乳液萃取技术来制造具有聚乳酸-共-羟基乙酸(PLGA)或聚乳酸(PLA)核的微胶囊,该核由羧基甜菜碱功能化壳聚糖(f-chi)覆盖,并负载 MAG(平均粒径为 6.5±3.0nm)和水溶性荧光素(Fluo)。Fluo 被共包封作为释放研究的荧光标记物。微载体的平均粒径为 800±60nm,包封效率高达 90%。f-chi 涂层后表面电荷的反转表明存在均匀的功能化表面,可用于进一步的化学连接。外部壳聚糖层的厚度为 200±50nm。在生物聚合物基质中证实了 MAG 的良好分散性,并且它对外部磁场有响应;事实上,在 37°C 的磷酸盐缓冲盐溶液介质中,Fluo 从 PLGA 或 f-chi-PLGA 微器件中释放超过 3 或 5 天,而当施加交变磁场时,实现了远程开/关控制释放。

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