Unsymmetrical cyanine dye via in vivo hitchhiking endogenous albumin affords high-performance NIR-II/photoacoustic imaging and photothermal therapy.
Unsymmetrical cyanine dye via in vivo hitchhiking endogenous albumin affords high-performance NIR-II/photoacoustic imaging and photothermal therapy.
复制标题
通过体内搭便车内源性白蛋白的不对称花青染料提供高性能 NIR-II/光声成像和光热治疗
DOI:
10.1186/s12951-021-01075-0
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发表时间:
2021-10-24
影响因子:
10.2
通讯作者:
Wang J
中科院分区:
文献类型:
--
作者:
Xu P;Hu L;Yu C;Yang W;Kang F;Zhang M;Jiang P;Wang J
Herein, an unprecedented synergistic strategy for the development of high-performance NIR-II fluorophore is proposed and validated. Based on an unsymmetrical cyanine dye design strategy, the NIR-II emissive dye NIC was successfully developed by replacing only one of the indoline donors of symmetrical cyanine dye ICG with a fully conjugated benz[c,d]indole donor. This minor structural change maximally maintains the high extinction coefficient advantage of cyanine dyes. NIC-ER with endogenous albumin-hitchhiking capability was constructed to further enhance its in vivo fluorescence brightness. In the presence of HSA (Human serum albumin), NIC-ER spontaneously resides in the albumin pocket, and a brilliant ~89-fold increase in fluorescence was observed. Due to its high molar absorptivity and moderate quantum yield, NIC-ER in HSA exhibits bright NIR-II emission with high photostability and significant Stokes shift (>110 nm). Moreover, NIC-ER was successfully employed for tumor-targeted NIR-II/PA imaging and efficient photothermal tumor elimination. Overall, our strategy may open up a new avenue for designing and constructing high-performance NIR-II fluorophores. The online version contains supplementary material available at 10.1186/s12951-021-01075-0.
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影响因子:
--
作者:
Liu R;Tang J;Xu Y;Zhou Y;Dai Z
通讯作者:
Dai Z
影响因子:
16.6
作者:
Antaris AL;Chen H;Diao S;Ma Z;Zhang Z;Zhu S;Wang J;Lozano AX;Fan Q;Chew L;Zhu M;Cheng K;Hong X;Dai H;Cheng Z
通讯作者:
Cheng Z
影响因子:
29.4
作者:
Li, Shengliang;Deng, Qingyuan;Lee, Chun-Sing
通讯作者:
Lee, Chun-Sing
影响因子:
16.6
作者:
Naczynski, D. J.;Tan, M. C.;Zevon, M.;Wall, B.;Kohl, J.;Kulesa, A.;Chen, S.;Roth, C. M.;Riman, R. E.;Moghe, P. V.
通讯作者:
Moghe, P. V.
影响因子:
46.2
作者:
Jung HS ;Verwilst P ;Sharma A ;Shin J ;Sessler JL ;Kim JS
通讯作者:
Kim JS