Fullerenes in vivo. Toxicity and protective effects.

IF 3.4 3区 医学 Q3 NANOSCIENCE & NANOTECHNOLOGY
Nanotoxicology Pub Date : 2025-05-01 Epub Date: 2025-02-27 DOI:10.1080/17435390.2025.2471273
Olga Bolshakova, Olga Zherebyatieva, Svetlana V Sarantseva
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引用次数: 0

Abstract

The data available in the literature on the toxicity of fullerenes are numerous but contradictory. The ambiguity of research results hinders the transition from scientific research to real-world drug development. The ability of fullerenes to accumulate in some organs and tissues is interpreted in most cases as their disadvantage, while a number of studies have shown that there is no relationship between the accumulation of fullerenes and toxic effects. Moreover, fullerenes often exert potent protective effects. The pharmacokinetics and toxicity of fullerenes depend on the route of administration and are closely related to their functionalization, since pristine fullerenes are generally harmless. These factors, as well as the risk-benefit ratio, need to be considered when developing fullerene-based drugs. In this review, open-source data on in vivo toxicity, biodistribution, metabolism, and some protective properties of both native fullerene and a number of its derivatives are collected and analyzed. The problems and prospects for using fullerenes through various methods of delivery to the body, such as through the gastrointestinal tract, intravenous administration, intraperitoneal administration, dermal application or respiratory exposure are described.

富勒烯在体内。毒性和保护作用。
文献中关于富勒烯毒性的数据虽多但相互矛盾。研究结果的模糊性阻碍了从科学研究到现实世界药物开发的过渡。富勒烯在某些器官和组织中积累的能力在大多数情况下被解释为它们的缺点,而许多研究表明,富勒烯的积累与毒性作用之间没有关系。此外,富勒烯经常发挥强大的保护作用。富勒烯的药代动力学和毒性取决于给药途径,并与其功能化密切相关,因为原始的富勒烯通常是无害的。在开发基于富勒烯的药物时,需要考虑这些因素以及风险收益比。本文收集和分析了天然富勒烯及其衍生物的体内毒性、生物分布、代谢和一些保护特性的开源数据。介绍了富勒烯通过胃肠道、静脉给药、腹腔给药、皮肤给药或呼吸暴露等多种给药方式给药的问题和前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Nanotoxicology
Nanotoxicology 医学-毒理学
CiteScore
10.10
自引率
4.00%
发文量
45
审稿时长
3.5 months
期刊介绍: Nanotoxicology invites contributions addressing research relating to the potential for human and environmental exposure, hazard and risk associated with the use and development of nano-structured materials. In this context, the term nano-structured materials has a broad definition, including ‘materials with at least one dimension in the nanometer size range’. These nanomaterials range from nanoparticles and nanomedicines, to nano-surfaces of larger materials and composite materials. The range of nanomaterials in use and under development is extremely diverse, so this journal includes a range of materials generated for purposeful delivery into the body (food, medicines, diagnostics and prosthetics), to consumer products (e.g. paints, cosmetics, electronics and clothing), and particles designed for environmental applications (e.g. remediation). It is the nano-size range if these materials which unifies them and defines the scope of Nanotoxicology . While the term ‘toxicology’ indicates risk, the journal Nanotoxicology also aims to encompass studies that enhance safety during the production, use and disposal of nanomaterials. Well-controlled studies demonstrating a lack of exposure, hazard or risk associated with nanomaterials, or studies aiming to improve biocompatibility are welcomed and encouraged, as such studies will lead to an advancement of nanotechnology. Furthermore, many nanoparticles are developed with the intention to improve human health (e.g. antimicrobial agents), and again, such articles are encouraged. In order to promote quality, Nanotoxicology will prioritise publications that have demonstrated characterisation of the nanomaterials investigated.
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