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Polymeric prodrug for bio-controllable gene and drug co-delivery 被引量:1

Polymeric prodrug for bio-controllable gene and drug co-delivery
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摘要 A polymeric polyethylenimine(PEI)-based prodrug of anticancer doxorubicin(DOX)(PEI-hyd-DOX) was designed by attaching DOX to PEI via an acid-labile hydrazone bond, for the achievement of biocontrollable gene and drug co-delivery in response to the intracellular acid microenvironments in the late endosome/lysosome compartments. The cytotoxicity of PEI-hyd-DOX was evaluated by the MTT assay and the cellular uptake was monitored using confocal laser scanning microscopy. The polymeric prodrug can respond with a high sensitivity to the specific acid condition inside cells, thus permitting the precise biocontrol over intracellular drug liberation with high drug efficacy. The chemical attachment of drug molecules also led to the relatively reduced toxicity and the enhanced transfection efficiency compared with parent PEI. The resulting data adumbrated the potential of PEI-hyd-DOX to co-deliver DOX and therapeutic gene for the combination of chemotherapy and gene therapy. A polymeric polyethylenimine(PEI)-based prodrug of anticancer doxorubicin(DOX)(PEI-hyd-DOX) was designed by attaching DOX to PEI via an acid-labile hydrazone bond, for the achievement of biocontrollable gene and drug co-delivery in response to the intracellular acid microenvironments in the late endosome/lysosome compartments. The cytotoxicity of PEI-hyd-DOX was evaluated by the MTT assay and the cellular uptake was monitored using confocal laser scanning microscopy. The polymeric prodrug can respond with a high sensitivity to the specific acid condition inside cells, thus permitting the precise biocontrol over intracellular drug liberation with high drug efficacy. The chemical attachment of drug molecules also led to the relatively reduced toxicity and the enhanced transfection efficiency compared with parent PEI. The resulting data adumbrated the potential of PEI-hyd-DOX to co-deliver DOX and therapeutic gene for the combination of chemotherapy and gene therapy.
出处 《Science China Chemistry》 SCIE EI CAS CSCD 2016年第11期1397-1404,共8页 中国科学(化学英文版)
基金 supported by the National Natural Science Foundation of China (21374085, 21174110, 51233003) the Natural Science Foundation of Hubei Province of China (2014CFB697) the Fundamental Research Funds for the Central Universities (2042014kf0193)
关键词 gene/drug co-delivery hydrazone bond p H-sensitivity polymeric prodrug transfection efficiency 基因 / 药合作交货;hydrazone 债券;pH 敏感;聚合 prodrug;transfection 效率;
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  • 1Naldini L. Nature, 2015, 526:351-360.
  • 2Wu MY, Meng QS, Chen Y, Du YY, Zhang LX, Li YP, Zhang, LL. Shi JL. Adv Mater, 2015, 27:215-222.
  • 3Yan H, Oornmen OP, Yu D, Hilborn J, Qian H, Varghese OP. Adv Funct Mater, 2015, 25:3907-3915.
  • 4Wu ZY, Zhan SY, Fan W, Ding XY, Wu X, Zhang W, Fu YH, Huang YY, Huang X, Chert RB, Li MJ, Xu NY, Zheng YX, Ding BY Nanoscale Res Lett, 2016, 11:1-13.
  • 5Klauber TCB, Sndergaard RV, Sawant RR, Torchilin VP, Andresen TL. Acta Biomaterialia, 2016, 35:248-259.
  • 6Wang RR, Hu H, Cai Q, Zhao NN, Zhu Y, Xu FJ. Sci China Chem, 2015, 58:1461-1470.
  • 7Liu C, Liu F, Feng L, Li M, Zhang J, Zhang N. Biomaterials, 2013, 34:2547-2564.
  • 8Jia HZ, Luo XH, Cheng H, Yang J, Li C, Liu CW, Feng J, Zhang XZ, Zhuo RX. JMater Chem, 2012, 22:24092-24101.
  • 9Li J, Wang Y, Zhu Y, Oupick D. J Control Release, 2013, 172: 589-600.
  • 10Lei C, Cui Y, Zheng L, Kah-Hoe Chow P, Wang CH. Biomaterials, 2013, 34:7483-7494.

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