Wang Peng, Zhang Cheng, Liu Hong-Wen, Xiong Mengyi, Yin Sheng-Yan, Yang Yue, Hu Xiao-Xiao, Yin Xia, Zhang Xiao-Bing, Tan Weihong
Molecular Science and Biomedicine Laboratory , State Key Laboratory of Chemo/Biosensing and Chemometrics , College of Chemistry and Chemical Engineering , Collaborative Innovation Center for Chemistry and Molecular Medicine , Hunan University , Changsha , Hunan 410082 , China . Email:
Molecular Science and Biomedicine Laboratory , State Key Laboratory of Chemo/Biosensing and Chemometrics , College of Life Sciences , Hunan University , Changsha , Hunan 410082 , China.
Chem Sci. 2017 Dec 1;8(12):8214-8220. doi: 10.1039/c7sc03977h. Epub 2017 Oct 9.
Fluorescence quantitative analyses for vital biomolecules are in great demand in biomedical science owing to their unique detection advantages with rapid, sensitive, non-damaging and specific identification. However, available fluorescence strategies for quantitative detection are usually hard to design and achieve. Inspired by supramolecular chemistry, a two-photon-excited fluorescent supramolecular nanoplatform () was designed for quantitative analysis with three parts: host molecules (β-CD polymers), a guest fluorophore of sensing probes (Np-Ad) and a guest internal reference (NpRh-Ad). In this strategy, the possesses the merits of (i) improved water-solubility and biocompatibility; (ii) increased tissue penetration depth for bioimaging by two-photon excitation; (iii) quantitative and tunable assembly of functional guest molecules to obtain optimized detection conditions; (iv) a common approach to avoid the limitation of complicated design by adjustment of sensing probes; and (v) accurate quantitative analysis by virtue of reference molecules. As a proof-of-concept, we utilized the two-photon fluorescent probe NHS-Ad-based to realize accurate quantitative analysis of hydrogen sulfide (HS), with high sensitivity and good selectivity in live cells, deep tissues and -dissected organs, suggesting that the is an ideal quantitative indicator for clinical samples. What's more, will pave the way for designing and preparing advanced supramolecular sensors for biosensing and biomedicine.
由于其在快速、灵敏、无损和特异性识别方面的独特检测优势,对重要生物分子的荧光定量分析在生物医学科学中有着巨大需求。然而,现有的用于定量检测的荧光策略通常难以设计和实现。受超分子化学启发,设计了一种双光子激发荧光超分子纳米平台()用于定量分析,它由三部分组成:主体分子(β-环糊精聚合物)、传感探针的客体荧光团(Np-Ad)和客体内参(NpRh-Ad)。在该策略中,该纳米平台具有以下优点:(i)提高了水溶性和生物相容性;(ii)通过双光子激发增加了用于生物成像的组织穿透深度;(iii)功能客体分子的定量和可调组装以获得优化的检测条件;(iv)通过调整传感探针避免复杂设计限制的通用方法;(v)借助参考分子进行准确的定量分析。作为概念验证,我们利用基于双光子荧光探针NHS-Ad的该纳米平台实现了对硫化氢(HS)的准确定量分析,在活细胞、深部组织和离体器官中具有高灵敏度和良好的选择性,表明该纳米平台是临床样本的理想定量指标。此外,它将为设计和制备用于生物传感和生物医学的先进超分子传感器铺平道路。