Progress in Organic Fluorescent Probes and Photocontrolled Releasers for Carbon Monoxide

doi:10.6023/A20080383

Acta Chimica Sinica ›› 2021, Vol. 79 ›› Issue (1): 36-44.DOI: 10.6023/A20080383 Previous Articles Next Articles

Special Issue: 分子探针、纳米生物学与生命分析化学

Original article

一氧化碳有机荧光探针和光控释放剂研究进展

李勇¹, 王栩^a^,^*(), 解希雷^a, 张建^a, 唐波^a^,^*()

a 山东师范大学化学化工与材料科学学院分子与纳米探针教育部重点实验室化学成像功能探针协同创新中心济南 250014

投稿日期:2020-08-21 发布日期:2020-10-24
通讯作者: 王栩, 唐波

作者简介:

李勇, 博士研究生. 研究方向为一氧化碳有机荧光探针和光控释放剂的设计、合成及应用.

王栩, 教授、博士生导师. 2006年于中国科学院生态环境研究中心获理学博士学位, 2006年至2008年在清华大学化学系从事博士后研究. 2008年进入山东师范大学化学化工与材料科学学院工作. 现主要从事光学功能探针设计、合成及其在成像、诊疗中的应用研究.

解希雷, 副教授、硕士生导师. 2014年7月于北京协和医学院(清华大学医学部)药物研究所获博士学位. 2014年9月进入山东师范大学化学化工与材料科学学院工作. 主要研究方向为新型荧光染料及分子诊疗试剂的设计合成与生物应用.

张建, 讲师、硕士生导师. 2015年7月于中国科学院大学获博士学位. 2015年10月到2017年11月在复旦大学从事博士后研究. 2017年12月到2018年7月在中国科学院国家纳米科学中心从事研究工作. 2018年8月进入山东师范大学化学化工与材料科学学院工作. 主要研究方向为正交化学与分子诊疗平台的构建及应用.

唐波, 教授、博士生导师. 国家杰出青年基金获得者, “万人计划”百千万人才工程领军人才, 973计划首席科学家. 1994年于南开大学化学系获理学博士, 同年进入山东师范大学化学系工作、任职教授. 现主要从事分子及纳米荧光探针的合成及其在生物成像中的应用、微流控芯片与质谱分析以及太阳能化学转化与储存等方面研究工作.

* E-mail: wangxu@sdnu.edu.cn; tangb@sdnu.edu.cn

基金资助:
国家自然科学基金(Nos. 91753111); 国家自然科学基金(21927811); 国家自然科学基金(21775093); 国家自然科学基金(21877076); 国家自然科学基金(21907060); 山东省重大科技创新工程项目(2018YFJH0502)

Progress in Organic Fluorescent Probes and Photocontrolled Releasers for Carbon Monoxide

Yong Li¹, Xu Wang^a^,^*(), Xilei Xie^a, Jian Zhang^a, Bo Tang^a^,^*()

a College of Chemistry, Chemical Engineering and Materials Science, Key Laboratory of Molecular and Nano Probes, Ministry of Education, Collaborative Innovation Center of Functionalized Probes for Chemical Imaging in Universities of Shandong, Institute of Molecular and Nano Science, Shandong Normal University, Jinan 250014, China

Received:2020-08-21 Published:2020-10-24
Contact: Xu Wang, Bo Tang
Supported by:
the National Natural Science Foundation of China(Nos. 91753111); the National Natural Science Foundation of China(21927811); the National Natural Science Foundation of China(21775093); the National Natural Science Foundation of China(21877076); the National Natural Science Foundation of China(21907060); the Key Research and Development Program of Shandong Province(2018YFJH0502)

Carbon monoxide (CO), an extremely important gasotransmitter, plays a critical role in a variety of physiological and pathological events, thus having been considered as a pharmaceutical activity compound with broad medical application. The physiological effects of CO are determined by its dose and spatial location. Therefore, the specific recognition of CO and its controllable supplying are of great significance for understanding and effectively utilizing its physiological and pathological effects. Fluorescence detection and photocontrolled releasing have been widely applied to track and carry active molecules in cells, tissues and in vivo in view of their unique spatiotemporal controllability and noninvasive capacity. Herein, the research progress of CO organic fluorescent probes and photocontrolled releasers in recent years is reviewed, focusing on their recognition mechanism, release mechanism and biological applications. Finally, the application prospects and challenges are discussed.

Key words: carbon monoxide, fluorescent probe, photocontrolled releasing

Cite this article

Yong Li, Xu Wang, Xilei Xie, Jian Zhang, Bo Tang. Progress in Organic Fluorescent Probes and Photocontrolled Releasers for Carbon Monoxide[J]. Acta Chimica Sinica, 2021, 79(1): 36-44.

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Fig. & Tab. 7

Figure 1. Schematic diagram of carbonylation or protonation hydrolysis reaction (a) and structure of CO probes 1~7 (b)

Figure 2. Pd(0)-mediated Tsuji-Trost reaction (a) and molecular structures of probes 8~24 (b)

Figure 3. Reduction mechanism of nitro with CO (a) and molecular structures of probes 25~28 (b)

Figure 4. Proposed response mechanism of probe 29

Figure 5. Molecular structures of photoCORMs 30~35

Figure 6. Molecular structures of photoCORMs 36~38

Figure 7. Molecular structures of photoCORMs 39~49

References 94

[1]	SjÖStrand, T. Nature 1949, 164, 580.
[2]	Fagone, P.; Mangano, K.; Coco, M.; Perciavalle, V.; Garotta, G.; Romao, C.C.; Nicoletti, F. Clin. Exp. Immunol. 2012, 167, 179.
[3]	Landaw, S.A.; Callahan, E.W., Jr.; Schmid, R.J. Clin. Invest. 1970, 49, 914.
[4]	Motterlini, R.; Otterbein, L.E. Nat. Rev. Drug Discov. 2010, 9, 728.
[5]	Ryter, S.W.; Alam, J.; Choi, A.M. Physiol. Rev. 2006, 86, 583.
[6]	Piantadosi, C.A. Free Radic. Biol. Med. 2008, 45, 562.
[7]	Hanafy, K.A.; Oh, J.; Otterbein, L.E. Curr. Pharm. Des. 2013, 19, 2771.
[8]	Wu, L.; Wang, R. Pharmacol. Rev. 2005, 57, 585.
[9]	Kim, H.J.; Joe, Y.; Surh, Y.J.; Chung, H.T. Cell. Mol. Immunol. 2018, 15, 1085.
[10]	Almeida, A.S.; Soares, N.L.; Sequeira, C.O.; Pereira, S.A.; Sonnewald, U.; Vieira, H.L.A. Redox Biol. 2018, 17, 338.
[11]	Ji, X.Y.; Wang, B.H. Acc. Chem. Res. 2018, 51, 1377.
[12]	Wegiel, B.; Gallo, D.; Csizmadia, E.; Harris, C.; Belcher, J.; Vercellotti, G.M.; Penacho, N.; Seth, P.; Sukhatme, V.; Ahmed, A.; Pandolfi, P.P.; Helczynski, L.; Bjartell, A.; Persson, J.L.; Otterbein, L.E. Cancer Res. 2013, 73, 7009.
[13]	Wu, L.H.; Cai, X.J.; Zhu, H.F.; Li, J.H.; Shi, D.X.; Su, D.F.; Yue, D.; Gu, Z.W. Adv. Funct. Mater. 2018, 28, 1804324.
[14]	Tsoyi, K.; Lee, T.Y.; Lee, Y.S.; Kim, H.J.; Seo, H.G.; Lee, J.H.; Chang, K.C. Mol. Pharmacol. 2009, 76, 173.
[15]	Long, R.; Salouage, I.; Berdeaux, A.; Motterlini, R.; Morin, D. Biochim. Biophys. Acta 2014, 1837, 201.
[16]	Yang, X.-X.; Ke, B.-W.; Lu, W.; Wang, B.-H. Chin. J. Nat. Med. 2020, 18, 284.
[17]	Yang, M.; Fan, J.; Du, J.; Peng, X. Chem. Sci. 2020, 11, 5127.
[18]	Jiao, X.; Li, Y.; Niu, J.; Xie, X.; Wang, X.; Tang, B. Anal. Chem. 2017, 90, 533.
[19]	Nakagawa, H. Chem. Pharm. Bull. 2016, 64, 1249.
[20]	Xie, X.; Fan, J.; Liang, M.; Li, Y.; Jiao, X.; Wang, X.; Tang, B. Chem. Commun. 2017, 53, 11941.
[21]	Yan, P.; Wang, T.; Zhang, D.; Ma, X. Chin. J. Org. Chem. 2019, 39, 916 . (in Chinese)
	闫沛沛, 王婷, 张丹, 马晓雪, 有机化学, 2019, 39, 916.
[22]	Chen, S.; Pang, C.; Chen, X.; Yan, Z.; Huang, S.; Li, X.; Zhong, Y.; Wang, Z. Chin. J. Org. Chem. 2019, 39, 1846 . (in Chinese)
	陈思鸿, 庞楚明, 陈孝云, 严智浩, 黄诗敏, 李香弟, 钟雅婷, 汪朝阳, 有机化学, 2019, 39, 1846.
[23]	Huang, C.; Chen, H.; Li, F.; An, S. Chin. J. Org. Chem. 2019, 39, 2467 . (in Chinese)
	黄池宝, 陈会, 李福琴, 安思雅, 有机化学, 2019, 39, 2467.
[24]	Wei, C.; Zhang, P.; Li, X. Chin. J. Org. Chem. 2019, 39, 3375 . (in Chinese)
	魏超, 张平竹, 李小六, 有机化学, 2019, 39, 3375.
[25]	Ohata, J.; Bruemmer, K.J.; Chang, C.J. Acc. Chem. Res. 2019, 52, 2841.
[26]	Tang, Y.; Ma, Y.; Yin, J.; Lin, W. Chem. Soc. Rev. 2019, 48, 4036.
[27]	Abeyrathna, N.; Washington, K.; Bashur, C.; Liao, Y. Org. Biomol. Chem. 2017, 15, 8692.
[28]	Lee, Y.; Kim, J. Anal. Chem. 2007, 79, 7669.
[29]	Collison, H.A.; Rodkey, F.L.; O'Neal, J.D. Clin. Chem. 1968, 14, 162.
[30]	Moragues, M.E.; Esteban, J.; Ros-Lis, J.V.; Martínez-Máñez, R.; Marcos, M.D.; Martínez, M.; Soto, J.; Sancenón, F. J. Am. Chem. Soc. 2011, 133, 15762.
[31]	Sun, L.Y.; An, Y.Y.; Ma, L.L.; Han, Y.F. Chin. J. Chem. 2019, 37, 763.
[32]	Yang, S.; Jiang, J.; Zhou, A.; Zhou, Y.; Ye, W.; Cao, D.-S.; Yang, R. Anal. Chem. 2020, 92, 7194.
[33]	Xie, X.; Liu, G.; Su, X.; Li, Y.; Liu, Y.; Jiao, X.; Wang, X.; Tang, B. Anal. Chem. 2019, 91, 6872.
[34]	Luo, X.; Chen, M.; Yang, Q. Acta Chim. Sinica 2020, 78, 373 . (in Chinese)
	罗兴蕊, 陈敏文, 杨晴来, 化学学报, 2020, 78, 373.
[35]	Yang, L.; Liu, B.; Li, N.; Tang, B. Acta Chim. Sinica 2017, 75, 1047 . (in Chinese)
	杨立敏, 刘波, 李娜, 唐波, 化学学报, 2017, 75, 1047.
[36]	Michel, B.W.; Lippert, A.R.; Chang, C.J. J. Am. Chem. Soc. 2012, 134, 15668.
[37]	Wang, K.H.; Majewska, A.; Schummers, J.; Farley, B.; Hu, C.; Sur, M.; Tonegawa, S. Cell 2006, 126, 389.
[38]	Li, Y.; Xie, X.; Yang, X.; Li, M.; Jiao, X.; Sun, Y.; Wang, X.; Tang, B. Chem. Sci. 2017, 8, 4006.
[39]	Yang, S.; Wen, X.; Yang, X.; Li, Y.; Guo, C.; Zhou, Y.; Li, H.; Yang, R. Anal. Chem. 2018, 90, 14514.
[40]	Yang, S.; Guo, C.; Li, Y.; Guo, J.; Xiao, J.; Qing, Z.; Li, J.; Yang, R. ACS Sens. 2018, 3, 2415.
[41]	Zheng, K.; Lin, W.; Tan, L.; Chen, H.; Cui, H. Chem. Sci. 2014, 5, 3439.
[42]	Li, Y.; Wang, X.; Yang, J.; Xie, X.; Li, M.; Niu, J.; Tong, L.; Tang, B. Anal. Chem. 2016, 88, 11154.
[43]	Liu, K.; Kong, X.; Ma, Y.; Lin, W. Angew. Chem., Int. Ed. 2017, 56, 13489.
[44]	Moody, B.F.; Calvert, J.W. Med. Gas Res. 2011, 1, 3.
[45]	Xu, S.; Liu, H.-W.; Yin, X.; Yuan, L.; Huan, S.-Y.; Zhang, X.-B. Chem. Sci. 2019, 10, 320.
[46]	Sun, M.; Yu, H.; Zhang, K.; Wang, S.; Hayat, T.; Alsaedi, A.; Huang, D. ACS Sens. 2018, 3, 285.
[47]	Pal, S.; Mukherjee, M.; Sen, B.; Mandal, S.K.; Lohar, S.; Chattopadhyay, P.; Dhara, K. Chem. Commun. 2015, 51, 4410.
[48]	Feng, W.; Liu, D.; Feng, S.; Feng, G. Anal. Chem. 2016, 88, 10648.
[49]	Feng, S.; Liu, D.; Feng, W.; Feng, G. Anal. Chem. 2017, 89, 3754.
[50]	Xu, Z.; Yan, J.; Li, J.; Yao, P.; Tan, J.; Zhang, L. Tetrahedron Lett. 2016, 57, 2927.
[51]	Yan, J.-W.; Zhu, J.-Y.; Tan, Q.-F.; Zhou, L.-F.; Yao, P.-F.; Lu, Y.-T.; Tan, J.-H.; Zhang, L. RSC Adv. 2016, 6, 65373.
[52]	Feng, W.; Liu, D.; Zhai, Q.; Feng, G. Sens. Actuator B-Chem. 2017, 240, 625.
[53]	Wang, X.; Sun, J.; Zhang, W.; Ma, X.; Lv, J.; Tang, B. Chem. Sci. 2013, 4, 2551.
[54]	Fan, J.; Hu, M.; Zhan, P.; Peng, X. Chem. Soc. Rev. 2013, 42, 29.
[55]	Feng, W.; Hong, J.; Feng, G. Sens. Actuator B-Chem. 2017, 251, 389.
[56]	Zhou, E.; Gong, S.; Hong, J.; Feng, G. Spectrochim. Acta A Mol. Biomol. Spectrosc. 2020, 227, 117657.
[57]	Wang, Z.; Geng, Z.; Zhao, Z.; Sheng, W.; Liu, C.; Lv, X.; He, Q.; Zhu, B. New J. Chem. 2018, 42, 14417.
[58]	Xie, X.; Yang, X.; Wu, T.; Li, Y.; Li, M.; Tan, Q.; Wang, X.; Tang, B. Anal. Chem. 2016, 88, 8019.
[59]	Feng, W.; Feng, G. Sens. Actuator B-Chem. 2018, 255, 2314.
[60]	Gong, S.; Hong, J.; Zhou, E.; Feng, G. Talanta 2019, 201, 40.
[61]	Deng, Y.; Hong, J.; Zhou, E.; Feng, G. Dyes Pigm. 2019, 170, 107634.
[62]	Hong, J.; Xia, Q.; Zhou, E.; Feng, G. Talanta 2020, 120914.
[63]	Zhou, E.; Gong, S.; Feng, G. Sens. Actuator B-Chem. 2019, 301, 127075.
[64]	Li, S.-J.; Zhou, D.-Y.; Li, Y.-F.; Yang, B.; OuYang, J.; Jie, J.; Liu, J.; Li, C.-Y. Talanta 2018, 188, 691.
[65]	Wang, Z.; Zhao, Z.; Wang, R.; Yuan, R.; Liu, C.; Duan, Q.; Zhu, W.; Li, X.; Zhu, B. Anal. Methods 2019, 11, 288.
[66]	Mei, J.; Leung, N.L.; Kwok, R.T.; Lam, J.W.; Tang, B.Z. Chem. Rev. 2015, 115, 11718.
[67]	Niu, J.; Fan, J.; Wang, X.; Xiao, Y.; Xie, X.; Jiao, X.; Sun, C.; Tang, B. Anal. Chem. 2017, 89, 7210.
[68]	Wang, J.; Li, C.; Chen, Q.; Li, H.; Zhou, L.; Jiang, X.; Shi, M.; Zhang, P.; Jiang, G.; Tang, B.Z. Anal. Chem. 2019, 91, 9388.
[69]	Das, B.; Lohar, S.; Patra, A.; Ahmmed, E.; Mandal, S.K.; Bhakta, J.N.; Dhara, K.; Chattopadhyay, P. New J. Chem. 2018, 42, 13497.
[70]	Dhara, K.; Lohar, S.; Patra, A.; Roy, P.; Saha, S.K.; Sadhukhan, G.C.; Chattopadhyay, P. Anal. Chem. 2018, 90, 2933.
[71]	Wang, Z.; Liu, C.; Wang, X.; Duan, Q.; Jia, P.; Zhu, H.; Li, Z.; Zhang, X.; Ren, X.; Zhu, B.; Sheng, W. Sens. Actuator B-Chem. 2019, 291, 329.
[72]	Feng, W.; Feng, S.; Feng, G. Anal. Chem. 2019, 91, 8602.
[73]	Yuan, Z.; Yang, X.; De La Cruz, L.K.; Wang, B. Chem. Commun. 2020, 56, 2190.
[74]	Zhang, C.; Xie, H.; Zhan, T.; Zhang, J.; Chen, B.; Qian, Z.; Zhang, G.; Zhang, W.; Zhou, J. Chem. Commun. 2019, 55, 9444.
[75]	Knauert, M.; Vangala, S.; Haslip, M.; Lee, P.J. Oxid. Med. Cell. Longev. 2013, 2013, 360815.
[76]	Hess, D.R. Respir. Care 2017, 62, 1333.
[77]	Ryter, S.W.; Choi, A.M.K. Curr. Opin. Pharmacol. 2006, 6, 257.
[78]	Mondal, R.; Okhrimenko, A.N.; Shah, B.K.; Neckers, D.C. J. Phys. Chem. B 2008, 112, 11.
[79]	Peng, P.; Wang, C.; Shi, Z.; Johns, V.K.; Ma, L.; Oyer, J.; Copik, A.; Igarashi, R.; Liao, Y. Org. Biomol. Chem. 2013, 11, 6671.
[80]	Aotake, T.; Suzuki, M.; Tahara, K.; Kuzuhara, D.; Aratani, N.; Tamai, N.; Yamada, H. Chem. Eur. J. 2015, 21, 4966.
[81]	Michael, E.; Abeyrathna, N.; Patel, A.V.; Liao, Y.; Bashur, C.A. Biomed. Mater. 2016, 11, 025009.
[82]	Antony, L.A.P.; Slanina, T.; Šebej, P.; Šolomek, T.; Klán, P. Org. Lett. 2013, 15, 4552.
[83]	Palao, E.; Slanina, T.; Muchová, L.; Šolomek, T.; Vítek, L.; Klán, P. J. Am. Chem. Soc. 2016, 138, 126.
[84]	Romano, B.; Pagano, E.; Montanaro, V.; Fortunato, A.L.; Milic, N.; Borrelli, F. Phytother. Res. 2013, 27, 1588.
[85]	Perez-Vizcaino, F.; Duarte, J. Mol. Asp. Med. 2010, 31, 478.
[86]	Fetzner, S. Appl. Environ. Microbiol. 2012, 78, 2505.
[87]	Anderson, S.N.; Richards, J.M.; Esquer, H.J.; Benninghoff, A.D.; Arif, A.M.; Berreau, L.M. ChemistryOpen 2015, 4, 590.
[88]	Soboleva, T.; Esquer, H.J.; Benninghoff, A.D.; Berreau, L.M. J. Am. Chem. Soc. 2017, 139, 9435.
[89]	Popova, M.; Soboleva, T.; Ayad, S.; Benninghoff, A.D.; Berreau, L.M. J. Am. Chem. Soc. 2018, 140, 9721.
[90]	Li, Y.; Shu, Y.; Liang, M.; Xie, X.; Jiao, X.; Wang, X.; Tang, B. Angew. Chem., Int. Ed. 2018, 57, 12415.
[91]	Li, Y.; Shu, Y.; Wang, X.; Jiao, X.; Xie, X.; Zhang, J.; Tang, B. Chem. Commun. 2019, 55, 6301.
[92]	Soboleva, T.; Esquer, H.J.; Anderson, S.N.; Berreau, L.M.; Benninghoff, A.D. ACS Chem. Biol. 2018, 13, 2220.
[93]	Feng, W.; Feng, S.; Feng, G. Chem. Commun. 2019, 55, 8987.
[94]	Cheng, J.; Zheng, B.; Cheng, S.; Zhang, G.; Hu, J. Chem. Sci. 2020, 11, 4499.

一氧化碳有机荧光探针和光控释放剂研究进展

Progress in Organic Fluorescent Probes and Photocontrolled Releasers for Carbon Monoxide

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