2018
DOI: 10.1016/j.msec.2018.03.017
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Amphiphilic prodrug-decorated graphene oxide as a multi-functional drug delivery system for efficient cancer therapy

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Cited by 40 publications
(24 citation statements)
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“…The natural structure of GO destroys covalent bonds. Conversely, non-covalent methods disrupt the internal structure of GO and are therefore more versatile and sensible than covalent methods [142]. Drug release systems can be modulated by stimulus-responsive systems, i.e., specific signals (pH, redox potential, temperature, and light).…”
Section: Drug Delivery Systemsmentioning
confidence: 99%
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“…The natural structure of GO destroys covalent bonds. Conversely, non-covalent methods disrupt the internal structure of GO and are therefore more versatile and sensible than covalent methods [142]. Drug release systems can be modulated by stimulus-responsive systems, i.e., specific signals (pH, redox potential, temperature, and light).…”
Section: Drug Delivery Systemsmentioning
confidence: 99%
“…Furthermore, PP was conjugated with DOX through disulfide bonding (SS) and mPEG with folic acid (FA). The resulting complex GO/PP-SS-DOX/PEG-FA showed that it has sufficient dispersibility and that it can serve as a stabilizing agent of GO and an active carrier for a target drug delivery [142].…”
Section: Drug Delivery Systemsmentioning
confidence: 99%
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“…However, a multiple drug loaded and bioresorbable patch that possesses on-demand antibiosis and anti-inflammatory abilities still has not been achieved, which would have great potential in skin regeneration applications.Herein, to address this issue, we report on an effective and industrially scalable approach to obtain a composite highly biodegradable patch with near infrared (NIR)-triggered antimicrobial and anti-inflammatory properties and cell proliferation ability, so as to promote wound healing through graphene oxide (GO) covalently deposited onto a PCL scaffold. Indeed, GO exhibits multifunctional properties that are useful in drug delivery applications, including enhancement of drug loading owing to the huge surface area and on-demand electrical/near infrared (NIR)-triggered drug release in the site of action [13][14][15][16][17][18]. In addition, GO coating has been proposed as a cell adhesion and proliferation promoter though nonspecific interaction with living cells [19,20].…”
mentioning
confidence: 99%