刘珍宝 - 中南大学 - 湘雅药学院

个人简介

教育经历： 2002年9月～2006年7月，沈阳药科大学，药学专业，本科 2006年9月～2011年12月，清华大学医学部，北京协和医学院，生物医学工程专业，博士 2010年10月～2011年10月，University of California，Berkeley，联合培养博士 2013年1月～2015年1月，中南大学，药学院，药剂学系，博士后 2015年1月～2016年1月，University of Florida，化学系，生物/纳米交叉研究中心，癌症研究中心，博士后工作经历： 2012年7月～2015年9月，中南大学，药学院，药剂学系，讲师，硕士生导师 2015年9月～中南大学，药学院，药剂学系，副教授，硕士生导师

研究领域

分子药剂学，功能核酸及纳米材料在药物传递系统和分子诊断中的应用。

近期论文

查看导师新发文章（温馨提示：请注意重名现象，建议点开原文通过作者单位确认）

1. Liu Z.,Zhao H., He L., YaoY., Zhou Y., Wu J., Liu J., and Ding J., Aptamer density dependent cellularuptake of lipid capped polymer nanoparticles for polyvalent targeted deliveryof vinorelbine to cancer cells,RSC Advance.2015, 5, 16931-16939. 2.Liu Z., Chen S.,Liu B., Wu J., Zhou Y., He L., Ding J., and Liu J., Intracellular detection ofATP using an aptamer beacon covalently linked to graphene oxide resistingnonspecific probe displacement,AnalyticalChemistry. 2014, 86(24):12229-35. 3.Liu Z., Liu B.,Ding J., Liu J., Fluorescent sensors using DNA-functionalized graphene oxide,Analytical and Bioanalytical Chemistry.2014, 406(27):6885-902. 4.Liu Z., Liu Y.,Peng D., Hydroxylation of multi-walled carbon nanotubes reduces theircytotoxicity by limiting the activation of mitochondrial mediated apoptoticpathway,Journal of Materials Science,Materials in Medicine.2014. 25: 1033-1044. 5.Liu Z., Liu Y.,Peng D., Carboxylation of multi-walled carbon nanotube attenuated thecytotoxicity by limiting the oxidative stress initiated cell membrane integritydamage, cell cycle arrestment, and death receptor mediated apoptotic pathway,Journal of Biomedical Materials Research, Part A.2015. 103(8):2770-7. 6.Liu Z., Dong X.,Song L., Zhang H., Liu L., Zhu D., Song C., Leng X., Carboxylation ofmulti-walled carbon nanotube enhanced its biocompatibility with L02 cellsthrough decreased activation of mitochondrial apoptotic pathway,Journal of Biomedical Materials Research, Part A.2014, 102 (3):665-73. 7.Liu Z.,Zhou B., Wang H., LuF., Liu T., Song C., Leng X., Highly sensitive detection of human IgG using anovel bio-barcode assay combined with DNA chip technology,Journal of Nanoparticle Research. 2013,15(9):1964. 8. Cai R., Yang D., Peng S., Chen X., Huan Y., Liu Y., Hou W., Yang S.,LiuZ., Tan W., Single Nanoparticles to 3D Supercage: Framing for an ArtificialEnzyme System,J. Am. Chem. Soc., 2015,137(43):13957-13963. 9. Tang J.,Liu Z.,Zhang Y., Wang L., Li D., Ding J., and Jiang X., Fluorofenidone-loaded PLGAmicrospheres for targeted treatment of paraquat-induced acute lung injury inrats,RSC advances, 2015, 5,30153-30159. 10. Zhou W., Zhou Y., Wu J.,Liu Z.,Zhao H., Liu J., Ding J., Aptamer-nanoparticle bioconjugates enhanceintracellular delivery of vinorelbine to breast cancer cells,Journal of drug targeting, 2014,22(1):57-66. 11. Zhang H., Zhu D., Song L., Liu L., Dong X.,Liu Z., Leng X., Arginine conjugationaffects the endocytic pathways of chitosan/DNA nanoparticles,Journal of Biomedical Materials Research, Part A,2011, 98(2):296-302. 12. Liu Y., Peng D., Huang K., Liu S.,Liu Z., Preparation and thermal degradation kinetics ofterpolymer poly (e-caprolactone-co-1,2-butylene carbonate),Polymer Degradation and Stability, 2010, 95:2453-2460. 13. Liu Y., Peng D., Huang K., Liu S.,Liu Z., Preparation and properties of poly(propylenecarbonate maleate) microcapsules for controlled release ofpazufloxacinmesilate,Journal of AppliedPolymer Science, 2011, 122(5), 3248-3254.