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3D Superhydrophobic Electrospun Meshes as Reinforcement Materials for Sustained Local Drug Delivery Against Colorectal Cancer Cells

机译:3D超疏水电纺成型作为增强材料用于持续局部药物输送对抗结肠直肠癌细胞

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摘要

In this work we expand upon a recently reported local drug delivery device, where air is used as a degradable component of our material to control drug release (J. Am. Chem. Soc. 2012, 134, 2016-2019). We consider its potential use as a drug loaded strip to provide both mechanical stability to the anastomosis, and as a means to release drug locally over prolonged periods for prevention of locoregional recurrence in colorectal cancer. Specifically, we electrospun poly(ε-caprolactone) (PCL) with the hydrophobic polymer dopant poly(glycerol monostearate-co-ε-caprolactone) (PGC-C18) and used the resultant mesh to control the release of two anticancer drugs (CPT-11 and SN-38). The increase in mesh hydrophobicity with PGC-C18 addition slows drug release both by the traditional means of drug diffusion, as well as by increasing the stability of the entrapped air layer to delay drug release. We demonstrate that superhydrophobic meshes have mechanical properties appropriate for surgical buttressing of the anastomosis, permit non-invasive assessment of mesh location and documentation of drug release via ultrasound, and release chemotherapy over a prolonged period of time (>90 days) resulting in significant tumor cytotoxicity against a human colorectal cell line (HT-29).
机译:在这项工作中,我们在最近报告的本地药物递送装置上进行扩展,其中空气被用作我们材料的可降解组分,以控制药物释放(J.IM。Chem。Soc。2012,134,2016-2019)。我们认为其潜在用途作为药物装载的条带,以提供吻合术的机械稳定性,并且作为局部释放药物的手段,以预防结直肠癌中的招脑复发。具体地,用疏水聚合物掺杂剂聚(甘油单稳态-co-Co-Caprolacterone(PGC-C18)进行电纺运源(ε-己内酯)(PCL)并使用所得网格来控制两种抗癌药物的释放(CPT- 11和SN-38)。通过传统的药物扩散方法增加了与PGC-C18的疏水性的增加减慢药物释放,以及通过增加夹带空气层的稳定性延迟药物释放。我们证明,超疏水网格具有适合于吻合术的外科障碍的机械性能,允许通过超声波的网格地点和药物释放文献的非侵入性评估,并在长时间(> 90天)上释放化疗,导致显着的肿瘤对人结肠直肠细胞系(HT-29)的细胞毒性。

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