UV-assisted punching of microgel shapes for oral biomacromolecule delivery

IF 2.8 Q2 ENGINEERING, ELECTRICAL & ELECTRONIC
Shahana Bishnoi , Xiaoli Liu , Lasse Højlund Eklund Thamdrup , Ritika Singh Petersen , Leticia Hosta-Rigau , Stephan Sylvest Keller
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引用次数: 0

Abstract

Hydrogel based carriers have been predominantly investigated to combat the prominent challenges faced by oral biomacromolecule delivery. Several micromolding, microfluidic and photolithographic techniques have been described for the fabrication of non-spherical hydrogel based microcarriers. However, these techniques are unsuitable for loading biomacromolecules as integral part of the fabrication process due to the use of high temperatures, solvents and multiple processing steps. Here, we introduce UV-assisted punching as a novel two-step fabrication technique for the development of biocompatible microgel shapes for oral drug administration. Poly-ethylene glycol (PEG) microgel shapes with lateral dimensions of 25–100 μm and a height of 25 μm were fabricated on a flexible poly vinyl alcohol (PVA) substrate with a robust cycloolefin polymer (COP) stamp. The proposed process uses UV-initiated crosslinking of aqueous solutions at ambient temperatures, thereby providing a highly attractive method for the fabrication of biomacromolecule loaded hydrogel based carriers. For the proof-of-concept, the microgel shapes were loaded with the fluorescently labelled model biomacromolecule bovine serum albumin without any additional steps. The successful loading is demonstrated by fluorescence microscopy. In vitro studies are performed to quantify the macromolecular content and the release profile associated with the fabricated microgel shapes.

Abstract Image

用于口服生物大分子递送的微凝胶形状的紫外线辅助打孔
基于水凝胶的载体主要用于对抗口服生物大分子递送所面临的突出挑战。已经描述了几种用于制备基于非球形水凝胶的微载体的微成型、微流体和光刻技术。然而,由于使用高温、溶剂和多个处理步骤,这些技术不适合作为制造过程的组成部分装载生物大分子。在这里,我们介绍了紫外线辅助打孔作为一种新的两步制备技术,用于开发用于口服给药的生物相容性微凝胶形状。在柔性聚乙烯醇(PVA)基底上制备了横向尺寸为25–100μm、高度为25μm的聚乙二醇(PEG)微凝胶形状,并带有坚固的环烯烃聚合物(COP)印章。所提出的方法在环境温度下使用UV引发的水溶液交联,从而为制备负载生物大分子的水凝胶基载体提供了一种极具吸引力的方法。为了验证概念,在没有任何额外步骤的情况下,用荧光标记的模型生物大分子牛血清白蛋白加载微凝胶形状。荧光显微镜证明了成功的装载。进行体外研究以量化与所制造的微凝胶形状相关的大分子含量和释放曲线。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Micro and Nano Engineering
Micro and Nano Engineering Engineering-Electrical and Electronic Engineering
CiteScore
3.30
自引率
0.00%
发文量
67
审稿时长
80 days
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