近红外荧光核糖核酸酶 A 包裹的金纳米团簇:制备、表征、癌症靶向和成像。
Near-infrared fluorescent ribonuclease-A-encapsulated gold nanoclusters: preparation, characterization, cancer targeting and imaging.
机构信息
School of Chemistry and The Astbury Centre for Structural Molecular Biology, University of Leeds, Leeds LS2 9JT, UK.
出版信息
Nanoscale. 2013 Feb 7;5(3):1009-17. doi: 10.1039/c2nr32760k. Epub 2012 Dec 18.
Ultra-small gold nanoclusters (AuNCs) have unique size-dependent optical, electrical and chemical properties. They have emerged as a new nanomaterial with broad applications in optoelectronics, catalysis, biosensing, and bioimaging. Several strategies have been exploited to prepare AuNCs of different "magic number" sizes, using different templates e.g. dendrimers, polyethyleneimines, peptides, and more recently, proteins. Notwithstanding, almost all bio-template-protected AuNCs reported so far exhibit fairly low fluorescence quantum yields (QYs), typically <5%, which is especially true for AuNCs prepared using the protein templates. In this paper, we report a facile, one-pot aqueous synthesis of highly fluorescent AuNCs using bovine pancreatic ribonuclease A (RNase-A) as the bio-template. The as-prepared AuNCs not only fluoresce strongly at the near-infrared (NIR) region (λ(em) = 682 nm), but also exhibit an elevated QY of ∼12%. Additionally, the RNase-A-encapsulated AuNC (RNase-A-AuNC) displays an exceptionally large Stokes shift of ∼210 nm as well as a single dominant fluorescence lifetime of ∼1.5 μs, about three orders of magnitude longer than biological autofluorescence. Furthermore, by coupling vitamin B(12) (VB(12)) to the RNase-A-AuNC, we develop a multifunctional nanoplatform that is suitable for simultaneous targeting and imaging of cancer at the cellular level using Caco-2 cell lines as an in vitro model. Since VB(12) has effective uptake pathways in the digestive system, this nanoplatform may have potential for targeted oral drug delivery in vivo.
超小的金纳米团簇(AuNCs)具有独特的尺寸依赖性光学、电学和化学性质。它们已经成为一种具有广泛应用前景的新型纳米材料,可用于光电、催化、生物传感和生物成像等领域。已经开发了几种策略来制备不同“幻数”尺寸的 AuNCs,使用不同的模板,例如树状大分子、聚乙烯亚胺、肽,以及最近的蛋白质。尽管如此,到目前为止,几乎所有报道的生物模板保护的 AuNCs 都表现出相当低的荧光量子产率(QYs),通常<5%,对于使用蛋白质模板制备的 AuNCs 尤其如此。在本文中,我们报告了一种使用牛胰腺核糖核酸酶 A(RNase-A)作为生物模板的简便、一锅水相合成高荧光 AuNCs 的方法。所制备的 AuNCs 不仅在近红外(NIR)区域(λ(em)=682nm)强烈荧光,而且表现出约 12%的升高的 QY。此外,RNase-A 包封的 AuNC(RNase-A-AuNC)显示出异常大的斯托克斯位移(约 210nm)以及单一主导荧光寿命(约 1.5μs),比生物自体荧光长约三个数量级。此外,通过将维生素 B(12)(VB(12))偶联到 RNase-A-AuNC 上,我们开发了一种多功能纳米平台,该平台可用于通过 Caco-2 细胞系作为体外模型在细胞水平上同时进行癌症的靶向和成像。由于 VB(12)在消化系统中有有效的摄取途径,因此该纳米平台可能具有用于体内靶向口服药物递送的潜力。