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Carbon nanotubes as multifunctional biological transporters and near-infrared agents for selective cancer cell destruction

机译:碳纳米管作为多功能生物转运蛋白和近红外试剂可选择性破坏癌细胞

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摘要

Biological systems are known to be highly transparent to 700- to 1,100-nm near-infrared (NIR) light. It is shown here that the strong optical absorbance of single-walled carbon nanotubes (SWNTs) in this special spectral window, an intrinsic property of SWNTs, can be used for optical stimulation of nanotubes inside living cells to afford multifunctional nanotube biological transporters. For oligonucleotides transported inside living cells by nanotubes, the oligos can translocate into cell nucleus upon endosomal rupture triggered by NIR laser pulses. Continuous NIR radiation can cause cell death because of excessive local heating of SWNT in vitro. Selective cancer cell destruction can be achieved by functionalization of SWNT with a folate moiety, selective internalization of SWNTs inside cells labeled with folate receptor tumor markers, and NIR-triggered cell death, without harming receptor-free normal cells. Thus, the transporting capabilities of carbon nanotubes combined with suitable functionalization chemistry and their intrinsic optical properties can lead to new classes of novel nanomaterials for drug delivery and cancer therapy.
机译:众所周知,生物系统对700至1100 nm的近红外(NIR)光具有很高的透明度。在此显示,在此特殊的光谱窗口中,单壁碳纳米管(SWNT)的强光吸收是SWNT的固有特性,可用于光刺激活细胞内的纳米管,从而提供多功能纳米管生物转运蛋白。对于通过纳米管在活细胞内部转运的寡核苷酸,寡核苷酸可以在NIR激光脉冲触发的内体破裂后转移到细胞核中。连续的NIR辐射可能会由于体外SWNT局部过热而导致细胞死亡。选择性癌细胞破坏可以通过用叶酸部分将SWNT功能化,用叶酸受体肿瘤标记物标记的细胞内部SWNT的选择性内在化以及NIR触发的细胞死亡来实现,而不会损害无受体的正常细胞。因此,碳纳米管的运输能力与合适的功能化化学及其固有的光学性质相结合,可以导致新型的新型纳米材料用于药物输送和癌症治疗。

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