通过激光直接写入 3d 打印技术实现控释给药微载体。

Sunandita Sarker, Kimia Forghani, Ziteng Wen, Ryan N Halli, Stephen Hoag, Sharon Flank, Ryan D Sochol
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引用次数: 0

摘要

控释,尤其是长效给药系统有望改善多种疾病的治疗。此前,我们曾报道过一种增材制造或 "三维(3D)打印 "方法,用于制造由标准光刻胶组成的液芯壳帽微载体。在此,我们探索了扩展这一策略的潜力,以实现由生物可降解材料组成的微载体,作为控释给药选择的新途径。具体来说,我们研究了使用 "双光子直接激光写入(DLW)"作为三维打印微载体的方法,微载体由以下部分组成:(i) 带孔的瓶形 "外壳",(ii) 水性液体 "内核",(iii) 可生物降解的 "盖子"。瓶盖是直接用 DLW 印刷在外壳的孔口上的,其设计目的是使其在体内随着时间的推移而降解--例如,降解时间与瓶盖的厚度成正比--最终促进液体核心在所需的时间点释放出来。使用可生物降解的聚(乙二醇)二丙烯酸酯(PEGDA)光材料制作瓶盖的结果表明,包含微流体阻塞结构的外壳设计似乎能限制液相 PEGDA 以不希望的方式进入外壳(即直接在瓶盖打印之前),从而在瓶盖打印过程完成后改善液芯的保留。这些结果标志着我们迈出了重要的第一步,即评估所提出的 DLW 3D 打印策略在可能的药物输送应用中的实用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
TOWARD CONTROLLED-RELEASE DRUG DELIVERY MICROCARRIERS ENABLED BY DIRECT LASER WRITING 3D PRINTING.

Controlled-release, and especially long-acting, drug delivery systems hold promise for improving treatments for numerous medical conditions. Previously, we reported an additive manufacturing or "three-dimensional (3D) printing" approach for fabricating liquid-core-shell-cap microcarriers comprising standard photoresists. Here we explore the potential to extend this strategy to achieve microcarriers comprising biodegradable materials as a new pathway to controlled-release drug delivery options. Specifically, we investigate the use of "Two-Photon Direct Laser Writing (DLW)" as a means to 3D print microcarriers composed of: (i) a bottle-shaped "shell" with an orifice, (ii) an aqueous liquid "core", and (iii) a biodegradable "cap". The cap, which is DLW-printed directly onto the shell's orifice, is designed to degrade over time in the body-e.g., with degradation time proportional to cap thickness-to ultimately facilitate release of the liquid core at desired time points. Fabrication results based on the use of a biodegradable poly(ethylene glycol) diacrylate (PEGDA) photomaterial for the cap revealed that shell designs incorporating microfluidic obstruction structures appeared to limit undesired entry of the liquid-phase PEGDA into the shell (i.e., directly preceding cap printing), thereby resulting in improved retention of the liquid core after completion of the cap printing process. These results mark an important first step toward evaluating the utility of the presented DLW 3D printing strategy for possible drug delivery applications.

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