纳米粒子在多发性硬化症诊断和治疗中的应用:范围综述

Edson Kenzo Takei
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摘要

多发性硬化症(MS)是一种自身免疫性疾病,目前尚无根治方法。该病的诊断主要通过分析脱髓鞘病变及其在空间和时间上的分布来进行。纳米粒子(NPs)因其独特的物理和化学特性,目前正被研究用于多发性硬化症的诊断和治疗。本综述旨在研究 NPs 在中枢神经系统疾病的诊断和治疗中的应用,调查 NPs 在多发性硬化症的诊断和治疗中的适用性。在这篇范围界定综述中,分析了 24 项关于 NPs 在多发性硬化症诊断和治疗中不同应用的研究,以及关于其体内和体外安全性的研究。结果表明,关于 NPs 不同应用的大多数研究都选择了静脉注射和腹膜内给药途径,NP 尺寸从 5.6 纳米到 500 纳米不等。通过标记免疫细胞,NPs 被用于更好地增强和识别中枢神经系统(CNS)的脱髓鞘病变。在给药应用方面,NPs 可延长药物的半衰期,实现药物的可控释放。对其安全性的研究表明,虽然粒度、浓度和目标组织对 NP 的生物相容性有很大影响,但短期使用还是相对安全的。这些结果表明,应进一步研究 NPs 在脱髓鞘疾病实验模型中的成功应用,以便将来应用于多发性硬化症患者的辅助诊断和治疗。在考虑临床应用之前,还需要进一步分析长期不良反应、不同研究采用的实验模型、使用各种化合物增强 NPs 在中枢神经系统中的作用,以及研究 NPs 未来在治疗学中的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The use of nanoparticles in the diagnosis and treatment of multiple sclerosis: A scoping review
Multiple sclerosis (MS) is an autoimmune disease for which there is no existing cure. Diagnosis of the disease occurs primarily by analysis of demyelinated lesions, and their dissemination in space and time. Nanoparticles (NPs) are currently being investigated for diagnostic and therapeutic applications for MS due to their unique physical and chemical properties. This review aims to investigate the use of NPs for the diagnosis and treatment of CNS disorders, to investigate the applicability of NPs to assist in the diagnosis and treatment of MS. In this scoping review, 24 studies on different applications of NPs for diagnosis and treatment of MS as well as studies on their safety both in vivo and vitro were analyzed. The results indicate that the majority of studies on the different applications of NPs opted for intravenous and intraperitoneal administration routes with NP size varying from 5.6-500 nm. NPs were used for better enhancement and identification of demyelinating lesions in the central nervous system (CNS) by labelling immune cells. As for drug delivery applications, NPs were shown to increase cargo half-life, and enable the controllable release of drugs. Studies on their safety indicates that while particle size, concentration, and the target tissue greatly influence a NP’s biocompatibility, they are relatively safe for short-term use. These results indicate that NPs’ success in experimental models of demyelinating diseases should be further studied for its future application to assist in the diagnosis and treatment of patients with MS. Further analysis of long-term adverse effects, experimental models employed by different studies, use of various compounds to enhance NPs’ effect in the CNS, and the study of future use of NPs in theranostic applications are needed before clinical application can be considered.
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