装载酶的棒状微凝胶形状:向制造用于血液解毒的特定形状微反应器迈出了一步。

IF 6.1 3区 医学 Q1 MATERIALS SCIENCE, BIOMATERIALS Journal of Materials Chemistry B Pub Date : 2024-04-23 DOI:10.1039/D3TB02905K
Shahana Bishnoi, Michelle Maria Theresia Jansman, Jiantao Chen, Peter Waaben Thulstrup, Stephan Sylvest Keller and Leticia Hosta-Rigau
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引用次数: 0

摘要

快速清除有毒物质对于恢复人体正常功能和确保生存至关重要。由于酶具有高度的底物特异性和催化效率,因此是清除有毒化合物的独特候选物质。虽然酶有一些局限性,包括稳定性低和免疫原性高,但可以通过将酶包裹在各种载体中来克服这些局限性。由此产生的微型/纳米反应器能使酶免受周围环境的影响,防止酶的错误折叠或变性,从而使酶能够发挥其功能。微型/纳米反应器必须在血流中长时间循环,以确保完全清除毒剂。令人惊讶的是,虽然人们普遍认为非球形载体在血液中的停留时间比球形载体长,但迄今为止,所有报道的微型/纳米反应器都是以球形结构组装而成的。在这里,我们通过开创首个特定形状的微反应器来解决这一重要问题。我们利用紫外线辅助打孔技术制造出了尺寸为 8 μm × 1 μm × 2 μm 的棒状微凝胶,并通过对巨噬细胞和内皮细胞系进行溶血和细胞存活率检测,证明了它们的生物相容性。封装模型酶 β-内酰胺酶后,棒状微反应器将黄色硝基蝶呤底物转化为其水解产物的能力证明了这种微反应器的成功制造。
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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Enzyme-loaded rod-like microgel shapes: a step towards the creation of shape-specific microreactors for blood detoxification purposes

Rapid removal of toxic substances is crucial to restore the normal functions of our body and ensure survival. Due to their high substrate specificity and catalytic efficiency, enzymes are unique candidates to deplete toxic compounds. While enzymes display several limitations including low stability and high immunogenicity, these can be overcome by entrapping them in a diverse range of carriers. The resulting micro/nanoreactors shield the enzymes from their surroundings, preventing their misfolding or denaturation thus allowing them to conduct their function. The micro/nanoreactors must circulate in the blood stream for extended periods of time to ensure complete depletion of the toxic agents. Surprisingly, while it is widely acknowledged that non-spherical carriers exhibit longer residence time in the bloodstream than their spherical counterparts, so far, all the reported micro/nanoreactors have been assembled with a spherical architecture. Herein, we address this important issue by pioneering the first shape-specific microreactors. We use UV-assisted punching to create rod-like microgel shapes with dimensions of 8 μm × 1 μm × 2 μm and demonstrate their biocompatibility by conducting hemolysis and cell viability assays with a macrophage and an endothelial cell line. Upon encapsulation of the model enzyme β-lactamase, the successful fabrication of rod-shaped microreactors is demonstrated by their ability to convert the yellow nitrocefin substrate into its hydrolyzed product.

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来源期刊
Journal of Materials Chemistry B
Journal of Materials Chemistry B MATERIALS SCIENCE, BIOMATERIALS-
CiteScore
11.50
自引率
4.30%
发文量
866
期刊介绍: Journal of Materials Chemistry A, B & C cover high quality studies across all fields of materials chemistry. The journals focus on those theoretical or experimental studies that report new understanding, applications, properties and synthesis of materials. Journal of Materials Chemistry A, B & C are separated by the intended application of the material studied. Broadly, applications in energy and sustainability are of interest to Journal of Materials Chemistry A, applications in biology and medicine are of interest to Journal of Materials Chemistry B, and applications in optical, magnetic and electronic devices are of interest to Journal of Materials Chemistry C.Journal of Materials Chemistry B is a Transformative Journal and Plan S compliant. Example topic areas within the scope of Journal of Materials Chemistry B are listed below. This list is neither exhaustive nor exclusive: Antifouling coatings Biocompatible materials Bioelectronics Bioimaging Biomimetics Biomineralisation Bionics Biosensors Diagnostics Drug delivery Gene delivery Immunobiology Nanomedicine Regenerative medicine & Tissue engineering Scaffolds Soft robotics Stem cells Therapeutic devices
期刊最新文献
Back cover Back cover Correction: Bioreducible and acid-labile polydiethylenetriamines with sequential degradability for efficient transgelin-2 siRNA delivery Correction: Development and characterization of a novel poly(N-isopropylacrylamide)-based thermoresponsive photoink and its applications in DLP bioprinting Back cover
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