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基于聚乙烯醇物理水凝胶的生物可吸收表面附着酶微反应器。

Bioresorbable surface-adhered enzymatic microreactors based on physical hydrogels of poly(vinyl alcohol).

机构信息

Department of Chemistry, Aarhus University, Denmark.

出版信息

Langmuir. 2013 Jan 8;29(1):344-54. doi: 10.1021/la3040903. Epub 2012 Dec 13.

Abstract

Hydrogel biomaterials based on poly(vinyl alcohol), PVA, have an extensive history of biomedical applications, yet in their current form suffer from significant shortcomings, such as a lack of mechanism of biodegradation and poor opportunities in controlled drug release. We investigate physical hydrogels of PVA as surface-adhered materials and present biodegradable matrices equipped with innovative tools in substrate-mediated drug release. Toward the final goal, PVA chains with narrow polydispersities (1.1-1.2) and molecular weights of 5, 10, and 28 kDa are synthesized via controlled radical polymerization (RAFT). These molecular weights are shown to be suitably high to afford robust hydrogel matrices and at the same time suitably low to allow gradual erosion of the hydrogels with kinetics of degradation controlled via polymer macromolecular characteristics. For opportunities in controlled drug release, hydrogels are equipped with enzymatic cargo to achieve an in situ conversion of externally added prodrug into a final product, thus giving rise to surface-adhered enzymatic microreactors. Hydrogel-mediated enzymatic activity was investigated as a function of polymer molecular weight and concentration of solution taken for assembly of hydrogels. Taken together, we present, to the best of our knowledge, the first example of bioresorbable physical hydrogel based on PVA with engineered opportunities in substrate-mediated enzymatic activity and envisioned utility in surface-mediated drug delivery and tissue engineering.

摘要

基于聚乙烯醇(PVA)的水凝胶生物材料在生物医学应用方面有着悠久的历史,但目前它们存在着明显的缺点,例如缺乏生物降解机制和在控制药物释放方面的机会有限。我们研究了 PVA 的物理水凝胶作为表面附着材料,并提出了具有创新工具的可生物降解基质,用于基质介导的药物释放。为了实现最终目标,通过可控自由基聚合(RAFT)合成了具有较窄多分散性(1.1-1.2)和分子量为 5、10 和 28 kDa 的 PVA 链。这些分子量被证明足够高,可以提供坚固的水凝胶基质,同时又足够低,可以通过聚合物大分子特性控制降解动力学,逐渐侵蚀水凝胶。为了实现控制药物释放的机会,水凝胶配备了酶载体制备原位将外加的前药转化为最终产物,从而产生表面附着的酶微反应器。研究了水凝胶介导的酶活性作为聚合物分子量和用于组装水凝胶的溶液浓度的函数。综上所述,据我们所知,这是第一个基于 PVA 的可生物吸收物理水凝胶的例子,它具有工程化的基质介导酶活性机会,并有望在表面介导的药物输送和组织工程中得到应用。

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