Department of Chemistry and Department of Physiology and Functional Genomics, Shands Cancer Center and Center for Research at the Interface of Bio/Nano, UF Genetics Institute and McKnight Brain Institute, University of Florida, Gainesville, Florida 32611-7200, USA.
ACS Nano. 2012 Jun 26;6(6):5070-7. doi: 10.1021/nn300694v. Epub 2012 Jun 4.
An aptamer switch probe (ASP) linking chlorin e6 (Ce6), a photosensitizer molecule, to the surface of gold nanorods (AuNRs) was used to target cancer cells for photodynamic therapy (PDT) and photothermal therapy (PTT). In the presence of target cancer cells, the ASP changes conformation to drive Ce6 away from the gold surface, thereby producing singlet oxygen for PDT upon light irradiation. Since each AuNR is modified with many ASP-Ce6 molecules, the AuNR-ASP-Ce6 conjugate yields enhanced binding and therapeutic effect by the added ability to carry many photosensitizers. In addition, absorption of radiation by the gold nanorods enables further cell destruction by the photothermal effect. Consequently, this multimodal AuNR-ASP-Ce6 conjugate offers a remarkably improved and synergistic therapeutic effect compared to PTT or PDT alone, providing high specificity and therapeutic efficiency, which can be generalized to other types of cancer therapies.
一种适体开关探针 (ASP) 将光敏剂分子氯乙啶 (Ce6) 连接到金纳米棒 (AuNRs) 的表面,用于针对癌细胞进行光动力疗法 (PDT) 和光热疗法 (PTT)。在存在靶癌细胞的情况下,ASP 改变构象以将 Ce6 从金表面驱离,从而在光照下产生用于 PDT 的单线态氧。由于每个 AuNR 都用许多 ASP-Ce6 分子修饰,因此 AuNR-ASP-Ce6 缀合物通过增加携带许多光敏剂的能力而产生增强的结合和治疗效果。此外,金纳米棒吸收辐射可通过光热效应进一步破坏细胞。因此,与单独的 PTT 或 PDT 相比,这种多模式的 AuNR-ASP-Ce6 缀合物提供了显著改善和协同的治疗效果,具有高特异性和治疗效率,可推广应用于其他类型的癌症治疗。