• 文献标题:   Milk-derived multi-fluorescent graphene quantum dot-based cancer theranostic system
  • 文献类型:   Article
  • 作  者:   THAKUR M, MEWADA A, PANDEY S, BHORI M, SINGH K, SHARON M, SHARON M
  • 作者关键词:   graphene quantum dot, cancer, drug delivery, theranostic, cell cycle, apoptosi
  • 出版物名称:   MATERIALS SCIENCE ENGINEERING CMATERIALS FOR BIOLOGICAL APPLICATIONS
  • ISSN:   0928-4931 EI 1873-0191
  • 通讯作者地址:   Walchand Coll Arts Sci
  • 被引频次:   47
  • DOI:   10.1016/j.msec.2016.05.007
  • 出版年:   2016

▎ 摘  要

An economical green-chemistry approach was used for the synthesis of aqueous soluble graphene quantum dots (GQDs) from cow milk for simultaneous imaging and drug delivery in cancer. The GQDs synthesized using one pot microwave-assisted heating were multi-fluorescent, spherical in shape having a lateral size of ca. 5 nm, The role of processing parameters such as heating time and ionic strength showed a profound effect on photoluminescence properties of GQDs. The GQDs were N-doped and oxygen-rich as confirmed by X-ray photoelectron spectroscopy (XPS) analysis. Cysteamine hydrochloride (Cys) was used to attach an anti-cancer drug berberine hydrochloride (BHC) on GQDs forming"GQDs@Cys-BHC complex with ca. 88% drug loading efficiency. In vitro drug release was studied at the acidic-basic environment and drug kinetics was studied using pharmacokinetic statistical models. The GQDs were biocompatible on L929 cells whereas theranostic GQDs@Cys-BHC complex showed a potent cytotoxic effect on different cancerous cell line models: cervical cancer cell lines such as HeLa cells and breast cancer cells such as MDA-MB-231 confirmed by Trypan blue and MTT-based cytotoxic assays. Furthermore, multi-excitation based cellular bioimaging was demonstrated using confocal laser scanning microscopy (CLSM) and fluorescence microscopy using GQDs as well as GQDs@Cys-BHC complex. Thus, drug delivery (therapeutic) and bioimaging (diagnostic),properties of GQDs@Cys-BHC complex are thought to have a potential in vitro theranostic application in cancer therapy. (C) 2016 Elsevier B.V. All rights reserved.