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作 者:李楷 唐冰洁 柴新龙 平洋[1,2] 王丽红 苏瑾[1,2] Kai Li;Bingjie Tang;Xinlong Chai;Yang Ping;Lihong Wang;Jin Su(College of Pharmacy,Jiamusi University,Jiamusi 154007,Heilongjiang,China;Heilongjiang Provincial Key Laboratory of New Drug Development and Pharmacotoxicological Evaluation,Jiamusi 154007,Heilongjiang,China)
机构地区:[1]佳木斯大学药学院,黑龙江佳木斯154007 [2]黑龙江省新药创制与药效毒理评价重点实验室,黑龙江佳木斯154007
出 处:《Journal of Chinese Pharmaceutical Sciences》2023年第10期773-795,共23页中国药学(英文版)
基 金:“Northern Medicine and functional food”,Heilongjiang “Double first-class” specialty construction project(Grant No. 2018-TSXK-02);The project for scientific research of colleges and universities of The Department of Education of Heilongjiang Province(2020-KYYWF-0248);the Jiamusi University Science and Technology Innovation Team University-level Innovation Team(Grant No. cxtd202103)。
摘 要:靶向给药系统由于能够在特定部位实现药物的靶向释放而受到研究人员的广泛青睐,其中主动靶向给药系统被认为是最有前途的靶向给药系统。然而,用于构建多功能药物载体靶向部分的常用纳米材料存在许多缺点,如生物相容性低、易被单核吞噬细胞系统消除、不易修饰等,限制了其应用。唾液酸是一种天然配体,通常作为糖蛋白或糖脂上聚糖的末端糖存在于细胞表面。作为一种内源性物质,它具有生物安全性高、分子结构均匀清晰、易于化学修饰等特点。唾液酸功能化的纳米颗粒可携带靶向特异性表达其受体(唾液酸结合免疫球蛋白样凝集素或选择素受体)细胞的药物用以治疗疾病。在这篇综述中,我们介绍了目前发表的关于以唾液酸修饰的纳米粒子为基础并结合“唾液酸结合免疫球蛋白样凝集素或选择素受体”的靶向给药系统在肿瘤或炎症中治疗作用的文献,并讨论了天然唾液酸配体的化学修饰方法,用以提高对受体的结合亲和力和选择性。Targeted drug delivery systems are highly desirable for their ability to release drugs specifically at targeted sites.Among these systems,active targeting is considered the most promising.However,the nanomaterials commonly used for constructing the targeting moiety of multifunctional drug delivery vehicles have several disadvantages that limit their applications,such as low biocompatibility,susceptibility to elimination by the mononuclear phagocyte system,and difficulty in modification.Sialic acid,a natural ligand,is often present as the terminal sugar of glycans on glycoproteins or glycolipids on the cell surface.As an endogenous substance,it is highly biocompatible,has a clear molecular structure,and is easy to chemically modify.Sialic acid-functionalized nanoparticles can carry drugs that target cells expressing receptors(sialic acid-binding immunoglobulin-like lectin or selectin receptors)for the treatment of diseases.In the present review,we presented current literature on sialic acid-decorated nanoparticle-based targeted drug delivery systems that bind to“sialic acid-binding immunoglobulin-like lectin or selectin receptors"for therapeutic effects in tumors or inflammation.We also discussed chemical modification strategies for natural sialic acid ligands to improve binding affinity and selectivity to receptors.
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