2013
DOI: 10.1016/j.biomaterials.2013.08.058
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Cholesteryl hyaluronic acid-coated, reduced graphene oxide nanosheets for anti-cancer drug delivery

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Cited by 170 publications
(77 citation statements)
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References 33 publications
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“…Fan et al 223 developed a water-soluble novel nanocarrier of magnetic Fe(3)O(4)-graphene nanocomposites, which showed excellent dispersibility and stability in aqueous solution and also exhibited superparamagnetic properties. Miao et al 224 fabricated cholesteryl hyaluronic acid-reduced graphene oxide (CHA-rGO) nanosheets that showed increased colloidal stability, safety, and drug-loading capacity in mice. The in vivo antitumor efficacy of DOX delivered by CHA-rGO was significantly increased compared with free DOX or DOX-loaded rGO.…”
mentioning
confidence: 99%
“…Fan et al 223 developed a water-soluble novel nanocarrier of magnetic Fe(3)O(4)-graphene nanocomposites, which showed excellent dispersibility and stability in aqueous solution and also exhibited superparamagnetic properties. Miao et al 224 fabricated cholesteryl hyaluronic acid-reduced graphene oxide (CHA-rGO) nanosheets that showed increased colloidal stability, safety, and drug-loading capacity in mice. The in vivo antitumor efficacy of DOX delivered by CHA-rGO was significantly increased compared with free DOX or DOX-loaded rGO.…”
mentioning
confidence: 99%
“…HA has been previously reported to increase the tumor cell delivery of nanoparticles by interacting with CD44 receptors; when conjugated to ASOs, it enhances their cellular delivery [22]. Moreover, surface coating of graphene nanosheets with HA has been shown to enhance cellular delivery through CD44 receptors [23], and HA-coated nanocarriers have been designed for delivery of anticancer drug to tumors expressing CD44 receptors [24].…”
Section: Discussionmentioning
confidence: 98%
“…22 Cholesteryl hyaluronic acid (HA) conjugated GO loaded with doxorubicin was developed by Miao et al for targeted delivery of doxorubicin to KB epidermal carcinoma cells both in in vitro and in vivo. 23 In vitro studies showed that the targeted nanocomposite induced 40.3% increase in cell death as compared to the non-targeted one. Similarly, subcutaneous injection of the targeted nanocomposites in tumor bearing athymic mice resulted in 14.1% decrease in the tumor volume within 24 days.…”
Section: Targeted Drug Deliverymentioning
confidence: 99%