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富勒醇在肿瘤学研究二十年之后的潜在医学用途。

Potential Medical Use of Fullerenols After Two Decades of Oncology Research.

机构信息

Faculty of Pharmacy, Pharmaceutical Biology, University of Ljubljana, Ljubljana, Slovenia.

出版信息

Technol Cancer Res Treat. 2023 Jan-Dec;22:15330338231201515. doi: 10.1177/15330338231201515.

DOI:10.1177/15330338231201515
PMID:37724005
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10510368/
Abstract

Fullerenes are carbon molecules that are found in nature in various forms. They are composed of hexagonal and pentagonal rings that create closed structures. Almost 4 decades ago, fullerenes were identified in the form of C and C, and following the award of the Nobel Prize in Chemistry for this discovery in 1996, many laboratories started working on their water-soluble derivatives that could be used in different industries, including pharmaceutical industries. One of the first fullerene forms that was the focus of different research groups was fullerenol, C(OH) (  =  2-44). Both in-vitro and in-vivo studies have shown that polyhydroxylate fullerene derivatives can potentially be used as either antioxidative agents or cytostatics (depending on their co-administration, forms, and concentration/dose) in biological systems. The current review aimed to present a critical view of the potential applications and limitations of fullerenols in oncology, as understood from the past 2 decades of research.

摘要

富勒烯是自然界中以各种形式存在的碳分子。它们由六边形和五边形环组成,形成封闭结构。大约 40 年前,以 C 和 C 的形式发现了富勒烯,1996 年因这一发现获得诺贝尔化学奖后,许多实验室开始研究其水溶性衍生物,这些衍生物可用于不同行业,包括制药行业。首批成为不同研究小组关注焦点的富勒烯形式之一是富勒醇,C(OH)(  =  2-44)。体外和体内研究均表明,多羟化富勒烯衍生物在生物系统中可能作为抗氧化剂或细胞抑制剂(取决于它们的联合给药、形式和浓度/剂量)使用。本综述旨在从过去 20 年的研究中,对富勒醇在肿瘤学中的潜在应用和局限性提出批判性看法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51d5/10510368/b6c91911ae6d/10.1177_15330338231201515-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51d5/10510368/b6c91911ae6d/10.1177_15330338231201515-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51d5/10510368/b6c91911ae6d/10.1177_15330338231201515-fig1.jpg

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