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基于完全可生物降解弹性体的口服大分子递药装置。

Fully Biodegradable Elastomer-Based Device for Oral Macromolecule Delivery.

机构信息

The Danish National Research Foundation and Villum Foundation's Center for Intelligent Drug Delivery and Sensing Using Microcontainers and Nanomechanics (IDUN), Department of Health Technology, Technical University of Denmark, 2800 Kgs Lyngby, Denmark.

出版信息

ACS Appl Bio Mater. 2024 Jun 17;7(6):3777-3785. doi: 10.1021/acsabm.4c00147. Epub 2024 May 16.

Abstract

Oral devices, such as foil-type devices, show great potential for the delivery of poorly permeable macromolecules by enabling unidirectional release of the loaded pharmaceutical composition in close proximity to the epithelium in the small intestine or colon. However, one of the primary concerns associated with the use of foil-type devices so far has been the utilization of nonbiodegradable elastomers in the fabrication of the devices. Therefore, research into biodegradable substitute materials with similar characteristics enables drug delivery in a sustainable and environmentally friendly manner. In this study, a biodegradable elastomer, polyoctanediol citrate (POC), was synthesized via a one-pot reaction, with subsequent purification and microscale pattern replication via casting. The microstructure geometry was designed to enable fabrication of foil-type devices with the selected elastomer, which has a high intrinsic surface free energy. The final elastomer was demonstrated to have an elastic modulus ranging up to 2.2 ± 0.1 MPa, with strain at failure up to 110.1 ± 1.5%. Devices were loaded with acetaminophen and enterically coated, demonstrating 100% release at 2.5 h, following dissolution for 1 h in 0.1 M hydrochloric acid and 1.5 h in pH 6.8 phosphate-buffered saline. The elastomer demonstrated promising properties based on mechanical testing, surface free energy evaluation, and degradation studies.

摘要

口腔内给药装置,如箔片型装置,通过使负载药物组合物在靠近小肠或结肠上皮的近距离单向释放,显示出对递送难渗透大分子的巨大潜力。然而,到目前为止,箔片型装置使用中一个主要关注的问题一直是装置制造中使用不可生物降解的弹性体。因此,研究具有相似特性的可生物降解替代材料可实现可持续和环保的药物输送。在这项研究中,通过一锅法反应合成了可生物降解的弹性体聚辛二醇柠檬酸酯(POC),随后通过浇铸进行纯化和微尺度图案复制。微结构几何形状的设计使能够用选定的弹性体制备箔片型装置,该弹性体具有高的固有表面自由能。最终的弹性体表现出高达 2.2±0.1 MPa 的弹性模量,失效应变为 110.1±1.5%。将对乙酰氨基酚载入装置并进行肠溶性包衣,在 0.1 M 盐酸中溶解 1 小时和在 pH 6.8 的磷酸盐缓冲盐中溶解 1.5 小时后,在 2.5 小时内实现了 100%的释放。该弹性体在机械测试、表面自由能评估和降解研究方面表现出了有前景的性能。

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