2003
DOI: 10.1023/b:nano.0000006070.61144.93
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Nanobionics of Pharmacologically Active Derivatives of Fullerene C60

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Cited by 41 publications
(17 citation statements)
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“…132 Amino acid-modified C60s can penetrate the lipid membrane, bind to the hydrophobic domains of proteins and alter the function of membrane-bound enzymes. 140 …”
Section: Nanoparticle-biomolecule Interactionsmentioning
confidence: 99%
“…132 Amino acid-modified C60s can penetrate the lipid membrane, bind to the hydrophobic domains of proteins and alter the function of membrane-bound enzymes. 140 …”
Section: Nanoparticle-biomolecule Interactionsmentioning
confidence: 99%
“…As a result both computational and experimental studies have identified compounds that could inhibit the assembly of the HIV capsid. Various nanomaterials that include fullerene(c-60)-based structures and inorganic nanoparticles, such as gold and silver, have been shown to have anti-HIV activity in vitro [75][76][77]. While these efforts have not yet progressed beyond in vitro studies, they illustrate the potential of therapeutic nanomaterials to inhibit HIV replication.…”
Section: Nanomaterials As Therapeutic Agentsmentioning
confidence: 99%
“…This was discussed in comparison to D-or L-isomers' abilities to penetrate the phosphatidylcholine membranes and enter the liposome's interior. 53 A complete, in vivo, biopharmaceutical study was carried out by Rajagopalan et al, who utilized intravenous administration of a bis-monosuccinimide derivative, p,p′-bis(2-aminoethyl)-diphenyl-C 60 , 28 ( Figure 6D). 6 Derivative 28 displayed a higher affinity to tissues rather than a tendency to interact with the cellular membranes or other lipid-based structures.…”
Section: Membranotropic Propertiesmentioning
confidence: 99%