Literature DB >> 23352802

A chitosan-modified graphene nanogel for noninvasive controlled drug release.

Chunyan Wang1, Jaya Mallela, Ujjwala Sree Garapati, Sowndharya Ravi, Vignesh Chinnasamy, Yvonne Girard, Mark Howell, Subhra Mohapatra.   

Abstract

A near infrared (NIR) triggered drug delivery platform based on the chitosan-modified chemically reduced graphene oxide (CRGO) incorporated into a thermosensitive nanogel (CGN) was developed. CGN exhibited an NIR-induced thermal effect similar to that of CRGO, reversible thermo-responsive characteristics at 37-42 °C and high doxorubicin hydrochloride (DOX) loading capacity (48 wt%). The DOX loaded CGN (DOX-CGN) released DOX faster at 42 °C than at 37 °C. The fluorescence images revealed DOX expression in the cytoplasm of cancer cells when incubated with DOX-CGN at 37 °C but in the nucleus at 42 °C. Upon irradiation with NIR light (808 nm), a rapid, repetitive DOX release from the DOX-CGN was observed. Furthermore, the cancer cells incubated with DOX-CGN and irradiated with NIR light displayed significantly greater cytotoxicity than without irradiation owing to NIR-triggered increase in temperature leading to nuclear DOX release. These results demonstrate CGN's promising application for on-demand drug release by NIR light. FROM THE CLINICAL EDITOR: These investigators report the successful development of a novel near infrared triggered drug delivery platform based on chitosan-modified chemically reduced graphene oxide (CRGO) incorporated into a thermosensitive nanogel (CGN).
Copyright © 2013 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Drug release; Graphene; NIR; Nanogel; Photothermal; Thermosensitive

Mesh:

Substances:

Year:  2013        PMID: 23352802      PMCID: PMC3783966          DOI: 10.1016/j.nano.2013.01.003

Source DB:  PubMed          Journal:  Nanomedicine        ISSN: 1549-9634            Impact factor:   5.307


  32 in total

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10.  Combined Adsorption and Covalent Linking of Paclitaxel on Functionalized Nano-Graphene Oxide for Inhibiting Cancer Cells.

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