Advances in constructing biocompatible nanocarriers.

IF 5.7 3区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Xuehui Duan, Xinlei Chu, Yan Du, Yixuan Tang
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引用次数: 0

Abstract

The design of effective drug nanocarriers requires the prevention of adverse biological interactions such as immune activation and cytotoxicity, making superior biocompatibility a critical determinant for clinical success. While existing reviews predominantly focus on the therapeutic applications of nanomedicines, systematic analyses of biocompatibility optimization strategies remain scarce. To address this gap, we present a review of three primary approaches for constructing biocompatible nanocarriers: (1) inert-material-based frameworks, (2) polymer surface engineering techniques, and (3) biomimetic functionalization methodologies. By evaluating the structural designs and biological mechanisms of commonly employed materials, we elucidated how these strategies leverage inherent material properties and biological interaction principles to regulate biocompatibility. Furthermore, we analyzed the advantages and limitations of each approach, offering guidance for selecting the optimal biocompatibility enhancement methods. This work not only synthesizes current advancements in biocompatible nanocarrier development but also provides actionable insights to advance nanomedicine research and clinical translation.

构建生物相容性纳米载体的研究进展。
设计有效的药物纳米载体需要防止不良的生物相互作用,如免疫激活和细胞毒性,使优越的生物相容性成为临床成功的关键决定因素。虽然现有的评论主要集中在纳米药物的治疗应用上,但对生物相容性优化策略的系统分析仍然很少。为了解决这一差距,我们回顾了构建生物相容性纳米载体的三种主要方法:(1)基于惰性材料的框架,(2)聚合物表面工程技术,(3)仿生功能化方法。通过评估常用材料的结构设计和生物学机制,我们阐明了这些策略如何利用材料固有特性和生物相互作用原理来调节生物相容性。分析了每种方法的优点和局限性,为选择最佳的生物相容性增强方法提供指导。这项工作不仅综合了当前生物相容性纳米载体的发展进展,而且为推进纳米医学研究和临床转化提供了可行的见解。
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来源期刊
Drug Delivery and Translational Research
Drug Delivery and Translational Research MEDICINE, RESEARCH & EXPERIMENTALPHARMACOL-PHARMACOLOGY & PHARMACY
CiteScore
11.70
自引率
1.90%
发文量
160
期刊介绍: The journal provides a unique forum for scientific publication of high-quality research that is exclusively focused on translational aspects of drug delivery. Rationally developed, effective delivery systems can potentially affect clinical outcome in different disease conditions. Research focused on the following areas of translational drug delivery research will be considered for publication in the journal. Designing and developing novel drug delivery systems, with a focus on their application to disease conditions; Preclinical and clinical data related to drug delivery systems; Drug distribution, pharmacokinetics, clearance, with drug delivery systems as compared to traditional dosing to demonstrate beneficial outcomes Short-term and long-term biocompatibility of drug delivery systems, host response; Biomaterials with growth factors for stem-cell differentiation in regenerative medicine and tissue engineering; Image-guided drug therapy, Nanomedicine; Devices for drug delivery and drug/device combination products. In addition to original full-length papers, communications, and reviews, the journal includes editorials, reports of future meetings, research highlights, and announcements pertaining to the activities of the Controlled Release Society.
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