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Electrodeposited Assembly of Additive-Free Silk Fibroin Coating from Pre-Assembled Nanospheres for Drug Delivery

机译:从预组装的纳米球中电沉积的无添加丝素蛋白涂层组装用于药物递送

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摘要

Electrophoretically deposited (EPD) polymer- based coatings have been extensively reported as reservoirs in medical devices for delivery of therapeutic agents, but control over drug release remains a challenge. Here, a simple but uncommon assembly strategy for EPD polymer coatings was proposed to improve drug release without introducing any additives except the EPD matrix polymer precursor. The added value of the proposed strategy was demonstrated by developing a novel EPD silk fibroin (SF) coating assembled from pre-assembled SF nanospheres for an application model, that is, preventing infections around percutaneous orthopedic implants via local delivery of antibiotics. The EPD mechanism of this nanosphere coating involved oxidation of water near the substrate to neutralize SF nanospheres, resulting in irreversible deposition. The deposition process and mass could be easily controlled using the applied EPD parameters. In comparison with the EPD SF coating assembled in a conventional way (directly obtained from SF molecule solutions), this novel coating had a similar adhesion strength but exhibited a more hydrophobic nanotopography to induce better fibroblastic response. Moreover, the use of nanospheres as building blocks enabled 1.38 and 21 times enhancement on the antibiotic release amount and time (of 95% maximum dug release), respectively, while retaining drug effectiveness and showing undetectable cytotoxicity. This unexpected release kinetics was found attributable to the electrostatic and hydrophobic interactions between the drug and nanospheres and a negligible initial dissolution effect on the nanosphere coating. These results illustrate the promising potential of the pre-assembled strategy on EPD polymer coatings for superior control over drug delivery.
机译:电泳沉积的(EPD)基于聚合物的涂料已被广泛报道作为医疗装置的储层,用于递送治疗剂,但对药物释放的控制仍然是一个挑战。这里,提出了一种简单但不常见的环氧聚合物涂料的组装策略,以改善药物释放,而不引入除了EPD基质聚合物前体之外的任何添加剂。通过开发从预组装的SF纳米球组装的新型EPD丝素蛋白(SF)涂层来证明所提出的策略的附加值,即应用模型,即通过局部递送抗生素来防止经皮整形植入物周围的感染。该纳米晶涂层的EPD机理涉及底物附近的水氧化以中和SF纳米球,导致不可逆的沉积。可以使用所应用的EPD参数容易地控制沉积过程和质量。与以常规方式组装的EPD SF涂层相比(直接从SF分子溶液中获得),这种新涂层具有类似的粘合强度,但表现出更疏水的纳米术以诱导更好的纤维细胞反应。此外,使用纳米球作为构建块,分别使抗生素释放量和时间(最大挖出释放的时间为95%的时间(95%的最大挖出释放)增强了1.38和21倍,同时保留药物效果并显示出不可检测的细胞毒性。这种意外的释放动力学被发现可归因于药物和纳米球之间的静电和疏水相互作用以及对纳米涂层的可忽略次溶出作用。这些结果说明了对EPD聚合物涂料上预装配策略的有希望的潜力,用于对药物递送的优异控制。

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