Quaternized Chitosan/Heparin Polyelectrolyte Multilayer Films for Protein Delivery

聚电解质 壳聚糖 生物材料 化学 单宁酸 生物物理学 表面等离子共振 化学工程 双层 肝素 聚合物 生物高聚物 高分子化学 材料科学 生物化学 纳米技术 有机化学 纳米颗粒 工程类 生物
作者
Tomasz Urbaniak,Gabriela S. García‐Briones,Alexander Zhigunov,Sviatoslav Hladysh,Edyta Adrian,Volodymyr Lobaz,Tereza Krunclová,Olga Janoušková,Ognen Pop‐Georgievski,Dana Kubies
出处
期刊:Biomacromolecules [American Chemical Society]
卷期号:23 (11): 4734-4748 被引量:12
标识
DOI:10.1021/acs.biomac.2c00926
摘要

Layer-by-layer (LbL) polyelectrolyte coatings are intensively studied as reservoirs of bioactive proteins for modulating interactions between biomaterial surfaces and cells. Mild conditions for the incorporation of growth factors into delivery systems are required to maintain protein bioactivity. Here, we present LbL films composed of water-soluble N-[(2-hydroxy-3-trimethylammonium)propyl] chitosan chloride (HTCC), heparin (Hep), and tannic acid (TA) fabricated under physiological conditions with the ability to release heparin-binding proteins. Surface plasmon resonance analysis showed that the films formed on an anchoring HTCC/TA bilayer, with TA serving as a physical crosslinker, were more stable during their assembly, leading to increased film thickness and increased protein release. X-ray reflectivity measurements confirmed intermixing of the deposited layers. Protein release also increased when the proteins were present as an integral part of the Hep layers rather than as individual protein layers. The 4-week release pattern depended on the protein type; VEGF, CXCL12, and TGF-β1 exhibited a typical high initial release, whereas FGF-2 was sustainably released over 4 weeks. Notably, the films were nontoxic, and the released proteins retained their bioactivity, as demonstrated by the intensive chemotaxis of T-lymphocytes in response to the released CXCL12. Therefore, the proposed LbL films are promising biomaterial coating candidates for stimulating cellular responses.

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