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通过简单可靠的统计方法合成生物相容性和可生物降解的聚酰胺胺微凝胶

Synthesis of Biocompatible and Biodegradable Polyamidoamines Microgels via a Simple and Reliable Statistical Approach.

作者信息

Mauro Nicolò, Giammona Gaetano, Ranucci Elisabetta, Ferruti Paolo

机构信息

Laboratory of Biocompatible Polymers, Department of "Scienze e Tecnologie Biologiche, Chimiche e Farmaceutiche" (STEBICEF), University of Palermo, 90123 Palermo, Italy.

Dipartimento di Chimica, Università degli Studi di Milano, 20133 Milano, Italy.

出版信息

Materials (Basel). 2022 Oct 18;15(20):7280. doi: 10.3390/ma15207280.

Abstract

Polyamidoamines (PAAs) are biocompatible and biodegradable polymers with a huge potential as biomaterials for pharmaceutical applications. They are obtained by the step-wise aza-Michael polyaddition of bifunctional or multifunctional amines with bisacrylamides in water. To the best of our knowledge, no synthetic protocols leading to hyperbranched PAAs as well as PAA microgels have been published so far. To fill this gap, a statistical approach was established in this work to fine-tune the aza-Michael polyaddition stoichiometry when a multifunctional co-monomer (b) is added to a mixture of bifunctional monomers with complementary functions (a + b), possibly even in presence of a monofunctional co-monomer (b), for obtaining either microgels or hyperbranched polymers by a one-pot reaction. For this purpose, two new equations, obtained by reworking the classic Flory-Stockmayer equations, were successfully applied to the synthesis of different model systems, obtaining biocompatible microgels with tunable size distribution (200-500 nm) and properly designed end-chains in a simple and straightforward way. The same mathematical approach allowed us to empirically evaluate the actual number of active reactive functions of the co-monomers. A number of selected systems, being evaluated for their cytotoxicity in vitro, proved highly cytocompatible and, therefore, endowed with great potential for pharmaceutical and medical applications.

摘要

聚酰胺胺(PAAs)是具有生物相容性和可生物降解性的聚合物,作为药物应用的生物材料具有巨大潜力。它们是通过双功能或多功能胺与双丙烯酰胺在水中逐步进行氮杂迈克尔加成聚合反应得到的。据我们所知,目前尚未发表任何合成超支化PAAs以及PAA微凝胶的方法。为了填补这一空白,本工作建立了一种统计方法,用于在将多功能共聚单体(b)添加到具有互补功能的双功能单体混合物(a + b)中时,甚至可能在单功能共聚单体(b)存在的情况下,微调氮杂迈克尔加成聚合反应的化学计量比,以便通过一锅法反应获得微凝胶或超支化聚合物。为此,通过对经典的弗洛里 - 斯托克迈耶方程进行重新推导得到的两个新方程,成功应用于不同模型体系的合成,以简单直接的方式获得了具有可调尺寸分布(200 - 500 nm)且末端链设计合理的生物相容性微凝胶。同样的数学方法使我们能够凭经验评估共聚单体活性反应官能团的实际数量。一些经过体外细胞毒性评估的选定体系被证明具有高度的细胞相容性,因此在药物和医学应用方面具有巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c30d/9611214/ff5aa2bfebb7/materials-15-07280-sch001.jpg

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