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首页> 外文期刊>BioMed research international >Gold Nanotheranostics: Photothermal Therapy and Imaging of Mucin 7 Conjugated Antibody Nanoparticles for Urothelial Cancer
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Gold Nanotheranostics: Photothermal Therapy and Imaging of Mucin 7 Conjugated Antibody Nanoparticles for Urothelial Cancer

机译:金纳米纳米菌:粘液7缀合抗体纳米粒子的光热疗和成像进行尿路上皮癌

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Objective. To kill urothelial cancer cells while preserving healthy cells, this study used photothermal therapy (PTT). PTT techniques target urothelial cancer cells using gold nanoparticles (GNPs) and a green light laser. Materials and Methods. The GNPs were conjugated with anti-Mucin 7 antibodies, which acted as a probe for targeting tumor cells. Conjugated GNPs were exposed to a green light laser (532 nm) with sufficient thermal energy to kill the transitional cell carcinomas (TCCs). Results. According to our results, nanoparticles conjugated with Mucin 7 antibodies damaged all types of cancer cells (MBT2, T24, 9202, and 8301) at relatively low energy levels (i.e., 500 laser shots at 10 W/cm~2 in power, 1.6 Hz in frequency, and 300 ms in duration). Nonconjugated nanoparticles required 30 W/cm~2 or more to achieve the same effect. Cell damage was directly related to irradiation time and applied laser energy. Conclusions. The minimally invasive PTT procedure combined with Mucin 7 targeted GNPs is able to kill cancer cells and preserve healthy cells. The success of this treatment technique can likely be attributed to the lower amount of energy required to kill targeted cancer cells compared with that required to kill nontargeted cancer cells. Our in vitro pilot study yielded promising results; however, additional animal studies are required to confirm these findings.
机译:客观的。为了在保留健康细胞的同时杀死尿液癌细胞,本研究使用了光热疗法(PTT)。 PTT技术使用金纳米颗粒(GNP)和绿光激光靶向尿液癌细胞。材料和方法。将GNP与抗粘蛋白7抗体缀合,其作为靶向肿瘤细胞的探针。将共轭的GNP暴露于绿光激光器(532nm),具有足够的热能以杀死过渡细胞癌(TCC)。结果。根据我们的结果,与粘蛋白7抗体缀合的纳米颗粒在相对低的能量水平下损坏了所有类型的癌细胞(MBT2,T24,9202和8301)(即,500个激光射击,在功率为1.6 Hz。在频率和300 ms的持续时间内)。非共轭纳米颗粒需要30W / cm〜2以上以达到相同的效果。细胞损伤与照射时间和应用激光能量直接相关。结论。微创PTT程序与粘蛋白7靶向GNP结合能够杀死癌细胞并保持健康的细胞。与杀死非靶向癌细胞的需要相比,这种处理技术的成功可能归因于杀死靶向癌细胞所需的较低的能量。我们的体外试点研究产生了有希望的结果;但是,需要额外的动物研究来确认这些发现。

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