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通过层层技术合成温敏性接枝纤维素磺酸钠的 PNIPAM 用于生物活性多层膜。

Synthesis of Thermoresponsive PNIPAM-Grafted Cellulose Sulfates for Bioactive Multilayers via Layer-by-Layer Technique.

机构信息

Sustainable Materials and Chemistry, Department of Wood Technology and Wood-based Composites, University of Göttingen, Büsgenweg 4, Göttingen D-37077, Germany.

Department Biomedical Materials, Institute of Pharmacy, Martin Luther University Halle-Wittenberg, Heinrich-Damerow-Strasse 4, Halle (Saale) 06120, Germany.

出版信息

ACS Appl Mater Interfaces. 2022 Nov 2;14(43):48384-48396. doi: 10.1021/acsami.2c12803. Epub 2022 Oct 20.

DOI:10.1021/acsami.2c12803
PMID:36264178
Abstract

The robust thermoresponsive and bioactive surfaces for tissue engineering by combining poly--isopropylacrylamide (PNIPAM) and cellulose sulfate (CS) remain highly in demand but not yet realized. Herein, PNIPAM-grafted cellulose sulfates (PCSs) with diverse degrees of substitution ascribed to sulfate groups (DS) are synthesized for the first time. Higher sulfated PCS2 generally forms larger aggregates than lower sulfated PCS1 at their cloud point temperatures (TCP) of around 33 °C, whereas PCS1 leads to larger aggregates at body temperature (37 °C). Via the layer-by-layer (LbL) technique, biocompatible polyelectrolyte multilayers (PEMs) composed of PCSs as polyanions in combination with poly-l-lysine (PLL) or quaternized chitosan (QCHI) as polycations were fabricated. The resulting surfaces contained a more intermingled structure of polyanions with both polycations, while higher sulfated cellulose derivatives (CS2 and PCS2) displayed greater stability. Studies on toxicity and biocompatibility of PEM using 3T3 mouse fibroblasts showed a lower cytotoxicity of PEM with PCS2 and CS2 than PCS1 and CS1. Furthermore, the PEM using PCS2 particularly in combination with QCHI demonstrated excellent biocompatibility that is promising for new bioactive, thermoresponsive coatings on biomaterials and substrata for culturing adhesion-dependent cells.

摘要

通过将聚 N-异丙基丙烯酰胺 (PNIPAM) 和纤维素硫酸酯 (CS) 结合在一起,用于组织工程的强热响应和生物活性表面仍然高度需求,但尚未实现。本文首次合成了具有不同硫酸根基团取代度 (DS) 的接枝纤维素硫酸盐 (PCSs)。在其浊点温度 (TCP) 约为 33°C 时,高磺化的 PCS2 通常比低磺化的 PCS1 形成更大的聚集体,而 PCS1 在体温 (37°C) 下导致更大的聚集体。通过层层 (LbL) 技术,制备了由 PCS 作为聚阴离子与聚-l-赖氨酸 (PLL) 或季铵化壳聚糖 (QCHI) 作为聚阳离子组成的生物相容性聚电解质多层 (PEM)。所得表面包含聚阴离子与两种聚阳离子的更混合结构,而更高磺化的纤维素衍生物 (CS2 和 PCS2) 表现出更大的稳定性。使用 3T3 小鼠成纤维细胞对 PEM 的毒性和生物相容性进行研究表明,与 PCS1 和 CS1 相比,具有 PCS2 和 CS2 的 PEM 的细胞毒性更低。此外,使用 PCS2 的 PEM 特别是与 QCHI 结合使用时,表现出优异的生物相容性,有望成为用于培养粘附依赖性细胞的生物活性、热响应生物材料和基底的新型涂层。

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