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Fabrication of Poly(ethylene glycol) Capsules via Emulsion Templating Method for Targeted Drug Delivery

机译:通过乳液模板法制备靶向药物的聚乙二醇胶囊

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摘要

To reduce nonspecific interactions and circumvent biological barriers, low-fouling material of poly(ethylene glycol) (PEG) is most used for the modification of drug nanocarriers. Herein, we report the fabrication of PEG capsules via the free-radical polymerization of linear PEG or 8-arm-PEG using an emulsion templating method for targeted drug delivery. Doxorubicin (DOX) could be loaded in capsules via electrostatic interactions. The obtained capsules composed of 8-arm-PEG result in a lower cell association (2.2%) compared to those composed of linear PEG (7.3%) and, therefore, demonstrate the stealth property. The functionalization of cyclic peptides containing Arg-Gly-Asp (cRGD) on PEG capsules induce high cell targeting to U87 MG cells. A cell cytotoxicity assay demonstrates the biocompatibility of PEG capsules and high drug delivery efficacy of the targeted capsules. The reported capsules with the stealth and targeting property provide a potential platform for improved drug delivery.
机译:为了减少非特异性相互作用并规避生物学障碍,聚(乙二醇)(PEG)的低污染材料最常用于修饰药物纳米载体。在本文中,我们报道了通过使用乳液模板法靶向药物递送的线性PEG或8臂PEG的自由基聚合来制备PEG胶囊。阿霉素(DOX)可以通过静电相互作用装入胶囊。与由线性PEG组成的胶囊(7.3%)相比,由8臂PEG组成的胶囊导致较低的细胞缔合(2.2%),因此具有隐身性。在PEG胶囊上含有Arg-Gly-Asp(cRGD)的环状肽的功能化可诱导将细胞靶向U87 MG细胞。细胞毒性试验证明了PEG胶囊的生物相容性和目标胶囊的高药物传递功效。报道的具有隐形和靶向性质的胶囊提供了改善药物递送的潜在平台。

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