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硫酸化海藻酸盐在生物医学中的应用。

Sulfated Alginate for Biomedical Applications.

机构信息

School of Chemistry and Molecular Biosciences, The University of Queensland, Australia.

出版信息

Macromol Biosci. 2024 Nov;24(11):e2400237. doi: 10.1002/mabi.202400237. Epub 2024 Jul 30.

DOI:10.1002/mabi.202400237
PMID:39078625
Abstract

Alginate (Alg) polymers have received much attention due to the mild conditions required for gel formation and their good bio-acceptability. However, due to limited interactions with cells, many drugs, and biomolecules, chemically modified alginates are of great interest. Sulfated alginate (S-Alg) is a promising heparin-mimetic that continues to be investigated both as a drug molecule and as a component of biomaterials. Herein, the S-Alg literature of the past five years (2017-2023) is reviewed. Several methods used to synthesize S-Alg are described, with a focus on new advances in characterization and stereoselectivity. Material fabrication is another focus and spans bulk materials, particles, scaffolds, coatings, and part of multicomponent biomaterials. The new application of S-Alg as an antitumor agent is highlighted together with studies evaluating safety and biodistribution. The high binding affinity of S-Alg for various drugs and heparin-binding proteins is exploited extensively in biomaterial design to tune the encapsulation and release of these agents and this aspect is covered in detail. Recommondations include publishing key material properties to allow reproducibility, careful selection of appropriate sulfation strategies, the use of cross-linking strategies other than ionic cross-linking for material fabrication, and more detailed toxicity and biodistribution studies to inform future work.

摘要

由于凝胶形成所需的温和条件和良好的生物可接受性,藻酸盐(Alg)聚合物受到了广泛关注。然而,由于与细胞、许多药物和生物分子的相互作用有限,因此化学修饰的藻酸盐非常受关注。硫酸化藻酸盐(S-Alg)是一种有前途的肝素类似物,作为药物分子和生物材料的组成部分,它的研究仍在继续。本文综述了过去五年(2017-2023 年)S-Alg 的文献。描述了几种用于合成 S-Alg 的方法,重点介绍了在表征和立体选择性方面的新进展。材料制备是另一个重点,涵盖了块状材料、颗粒、支架、涂层和多组分生物材料的一部分。突出了 S-Alg 作为抗肿瘤剂的新应用,以及评估安全性和生物分布的研究。S-Alg 与各种药物和肝素结合蛋白的高结合亲和力在生物材料设计中得到了广泛的利用,以调节这些药物的包封和释放,这方面的内容有详细介绍。建议包括发表关键材料特性以实现可重复性、仔细选择适当的硫酸化策略、在材料制备中使用除离子交联以外的交联策略,以及进行更详细的毒性和生物分布研究,为未来的工作提供信息。

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