Potential Medical Use of Fullerenols After Two Decades of Oncology Research

被引:6
|
作者
Injac, Rade [1 ]
机构
[1] Univ Ljubljana, Pharmaceut Biol, Fac Pharm, Askerceva Cesta 7, Ljubljana 1000, Slovenia
关键词
fullerenol; toxicity; oxidative stress; organ protection; cytostatic; oncology; DOXORUBICIN-INDUCED CARDIOTOXICITY; INDUCED ACUTE HEPATOTOXICITY; RADICAL SCAVENGING ACTIVITY; POLYHYDROXYLATED C-60; MALIGNANT NEOPLASM; INTERPENETRATED POLYANILINES; C-60(OH)(24) NANOPARTICLES; ANTIOXIDATIVE ENZYMES; CONDUCTIVE BEHAVIOR; AQUEOUS-SOLUTIONS;
D O I
10.1177/15330338231201515
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 C60 and C70, 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, C60(OH)n (n = 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.
引用
收藏
页数:21
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