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Developing single-entity theranostic: drug-based fluorescent nanoclusters with augmented cytotoxicity

机译:开发单一实体治疗:药物基荧光纳米能器,具有增强细胞毒性

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Aim: To develop methotrexate (MTX) templated luminescent gold nanoclusters (NCs) as a single unit nanotheranostic for cancer therapy and to assess its potential as an alternative to the parent drug, for drug delivery vehicles (DDVs). Methods: Theranostics were synthesized and extensively characterized. The stability of the theranostic and its bioimaging aptitude were evaluated. The antiproliferative propensity of the theranostic was gauged with cell viability assays and was supplemented with cytometry-based assays. Feasibility of delivering the MTX NCs instead of parent drug on a DDV was also checked. Results: MTX NCs displayed remarkable physical characteristics and augmented cytotoxicity with a robust stability in phosphate-buffered saline and serum. MTX NCs also demonstrated their amenability to being loaded on a DDV (chitosan folic acid nanoparticles) while retaining their physical and cytotoxic profile. Conclusion: Generation of next level drug-based theranostics with the potential of replacing the free drug in drug delivery platforms.
机译:目的:将甲氨蝶呤(MTX)模板化发光金纳米纳米纳米能器(NCS)作为癌症治疗的单一单位纳米移植,并评估其作为母体药物的替代品,用于药物递送载体(DDV)。方法:合成耐药性和广泛的表征。评估治疗的稳定性及其生物分析能力。通过细胞活力测定测量治疗的抗增殖倾向,并补充基于细胞术的测定。还检查了在DDV上提供MTX NCS而不是父药的可行性。结果:MTX NCS显示出显着的物理特性和增强细胞毒性,具有良好的磷酸盐缓冲盐水和血清的稳定稳定性。 MTX NCS还证明了它们在达到DDV(壳聚糖叶酸纳米粒子)上的扫抚性,同时保留其物理和细胞毒性谱。结论:在药物递送平台中替代自由药物的潜力,产生下一级药物治疗的疗效。

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