2001
DOI: 10.1002/1616-5195(20011101)1:8<329::aid-mabi329>3.0.co;2-m
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DNA-Cleavage by Fullerene-Based Synzymes

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Cited by 26 publications
(10 citation statements)
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“…This fact pointed out that CD not only furnished water solubility to the final polymer but also prevented further branching in the C 60 cage due to its bulkiness. Interestingly, this polymer has been successfully employed as a highly efficient DNA-cleaving agent under visible light conditions . The quantitative DNA-cleaving achieved suggests strong application prospects of water-soluble C 60 -polymers in photodynamic cancer therapy.…”
Section: Main-chain Polymersmentioning
confidence: 99%
“…This fact pointed out that CD not only furnished water solubility to the final polymer but also prevented further branching in the C 60 cage due to its bulkiness. Interestingly, this polymer has been successfully employed as a highly efficient DNA-cleaving agent under visible light conditions . The quantitative DNA-cleaving achieved suggests strong application prospects of water-soluble C 60 -polymers in photodynamic cancer therapy.…”
Section: Main-chain Polymersmentioning
confidence: 99%
“…In recent years, several groups have developed different synthetic strategies with the aim to obtain water‐soluble C 60 polymers able to exploit the unique features of fullerenes in a hostile environment such as the aqueous one, in which fullerenes are practically insoluble. The interest of these water soluble C 60 ‐containing polymers lies in their use as efficient DNA‐cleaving agents in the photodynamic cancer therapy (PCT),7 as mimic of the superoxide dismutase,8 as carriers for drug/gene delivery applications,9 and for biological studies in general10 just to name a few potential applications. Among the different strategies used to solubilize fullerenes in water, the covalent linkage of a polysaccharide such as pullulans11 or curdlan sulfates12 to the C 60 cage has been very successful.…”
Section: Water Soluble C60‐polymersmentioning
confidence: 99%
“…78 Similarly, polymeric fullerocyclodextrins, synthesised by reaction of diamines with [60]fullerene complexed with cyclodextrin, have efficient DNA-cleavage properties in the presence of visible light. 79 Fullerene malonates have been shown to interact with nitric oxide synthase (NOS) distorting its structure, and in doing so, provide a unique mechanism for the isoform-selective inhibition of nNOS. 80 Studies on other water soluble [60]fullerene malonates indicate that this class of molecule is capable of eliminating both superoxide anion and H 2 O 2 and are effective inhibitors of lipid peroxidation.…”
Section: Organic Chemistrymentioning
confidence: 99%