肽
荧光
化学
检出限
劈理(地质)
纳米颗粒
费斯特共振能量转移
材料科学
生物物理学
光子上转换
分析化学(期刊)
发光
纳米技术
色谱法
生物化学
生物
光电子学
光学
复合材料
物理
断裂(地质)
作者
Lin Liu,Xiaotong Li,Hua Zhang,Hongda Chen,Murad M. A. Abualrejal,Daqian Song,Zhenxin Wang
标识
DOI:10.1016/j.snb.2021.129554
摘要
Herein, a six-in-one peptide functionalized [email protected] nanoparticle-based ratiometric fluorescence sensing platform (termed as [email protected]@Cy3-pep) has been fabricated for monitoring the anticancer efficacy of photothermal-chemotherapy in real time through detection of caspase-3 activity. In this work, the upconversion nanoparticle (UCNP) core of [email protected] was employed as an internal reference, while the PDA shell of [email protected] was used as an acceptor of fluorescence resonance energy transfer (FRET) system, photothermal therapy (PTT) agent, loading agent of chemical drug and immobilization platform of Cy3 (donor of FRET) labeled peptide (Cy3-pep), which contains a specific caspase-3 substrate (DEVD) and active tumor-targeting motif (PSP). In the presence of caspase-3, the FRET system was broken through the enzymatic cleavage of DEVD, resulting in a recovery of Cy3 fluorescence emission. Under the optimal conditions, the ratio of recovered Cy3 fluorescence intensity with upconversion luminescent (UCL) intensity was linearly dependent on the caspase-3 concentration within the range of 0.5–50 ng mL−1 and the limit of detection (LOD) was calculated as 0.065 ng mL−1. Using mouse-bearing MG-63 tumor as a model system, the capability of as-proposed [email protected]@Cy3-pep has been successfully demonstrated through a real-time noninvasive evaluation of tumor response to PTT and chemotherapy of staurosporine (STS).
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