The DOI matches its Crossref record; 1,197 of the 1,199 references it cites were found in a registry or an index.
Recent Strategies to Develop Innovative Photosensitizers for Enhanced Photodynamic Therapy
Abstract
This review presents a robust strategy to design photosensitizers (PSs) for various species. Photodynamic therapy (PDT) is a photochemical-based treatment approach that involves the use of light combined with a light-activated chemical, referred to as a PS. Attractively, PDT is one of the alternatives to conventional cancer treatment due to its noninvasive nature, high cure rates, and low side effects. PSs play an important factor in photoinduced reactive oxygen species (ROS) generation. Although the concept of photosensitizer-based photodynamic therapy has been widely adopted for clinical trials and bioimaging, until now, to our surprise, there has been no relevant review article on rational designs of organic PSs for PDT. Furthermore, most of published review articles in PDT focused on nanomaterials and nanotechnology based on traditional PSs. Therefore, this review aimed at reporting recent strategies to develop innovative organic photosensitizers for enhanced photodynamic therapy, with each example described in detail instead of providing only a general overview, as is typically done in previous reviews of PDT, to provide intuitive, vivid, and specific insights to the readers.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“PDT utilizing next-generation metal-based photosensitizers with extended excitation and emission spectra holds significant promise for antibacterial applications16,241.”
From Organic small-molecule NIR-II fluorophores for tumor phototheranostics (2026) · cites this paper as [16]
In the citing paper
“This is a very important detail because phototoxicity from PDT is dependent on both oxygen tension and photosensitizer concentration. 440 , 441”
From Hypoxia signaling in cancer: Implications for therapeutic interventions (2023) · cites this paper as [440]
Citations
Cites
Items 801–1,000 of 1,197
Xu, W., Zuo, J., Wang, L., Ji, L., & Chao, H. (2014) · Chemical Communications · doi:10.1039/c3cc48916g · Cited by 76
A Glutathione‐Activated Phthalocyanine‐Based Photosensitizer for Photodynamic Therapy
He, H., Lo, P., & Ng, D. K. P. (2014) · Chemistry - A European Journal · doi:10.1002/chem.201400001 · Cited by 76
Bhattacharyya, U., Kumar, B., Garai, A., Bhattacharyya, A., Kumar, A., Banerjee, S., Kondaiah, P., & Chakravarty, A. R. (2017) · Inorganic Chemistry · doi:10.1021/acs.inorgchem.7b01924 · Cited by 76
Lv, C., Liu, W., Luo, Q., Yi, H., Yu, H., Yang, Z., Zou, B., & Zhang, Y. (2020) · Chemical Science · doi:10.1039/d0sc01095b · Cited by 76
Mara, M. W., Bowman, D. N., Büyükçakır, O., Shelby, M. L., Haldrup, K., Huang, J., Harpham, M. R., Stickrath, A. B., Zhang, X., Stoddart, J. F., et al. (2015) · Journal of the American Chemical Society · doi:10.1021/jacs.5b04612 · Cited by 75
Zhao, Q. R., Li, J., Zhang, X., Li, Z., & Tang, Y. (2015) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.5b11264 · Cited by 75
Zou, Q., Zhao, H., Zhao, Y., Fang, Y., Chen, D., Ren, J., Wang, X., Wang, Y., Gu, Y., & Wu, F. (2015) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.5b00731 · Cited by 75
Qiu, K., Ouyang, M., Liu, Y., Huang, H., Liu, C., Chen, Y., Ji, L., & Chao, H. (2017) · Journal of Materials Chemistry B · doi:10.1039/c7tb00731k · Cited by 75
Zheng, Y., Lu, H., Jiang, Z., Guan, Y., Zou, J., Wang, X., Cheng, R., & Gao, H. (2017) · Journal of Materials Chemistry B · doi:10.1039/c7tb01443k · Cited by 75
Dual-Functional NIR AIEgens for High-Fidelity Imaging of Lysosomes in Cells and Photodynamic Therapy
Dai, Y., He, F., Ji, H., Zhao, X., Misal, S., & Qi, Z. (2019) · ACS Sensors · doi:10.1021/acssensors.9b02090 · Cited by 75
Rehmat, N., Toffoletti, A., Mahmood, Z., Zhang, X., Zhao, J., & Barbon, A. (2020) · Journal of Materials Chemistry C · doi:10.1039/c9tc06429j · Cited by 75
Weiss, E. A., Ahrens, M. J., Sinks, L. E., Ratner, M. A., & Wasielewski, M. R. (2004) · Journal of the American Chemical Society · doi:10.1021/ja047205i · Cited by 74
Krumova, K., Friedland, S. N., & Cosa, G. (2012) · Journal of the American Chemical Society · doi:10.1021/ja301680m · Cited by 74
Gadolinium(III) Porpholactones as Efficient and Robust Singlet Oxygen Photosensitizers
Ke, X., Ning, Y., Tang, J., Hu, J., Yin, H., Wang, G., Yang, Z., Jie, J., Liu, K., Meng, Z., et al. (2016) · Chemistry - A European Journal · doi:10.1002/chem.201601517 · Cited by 74
Glucose-Appended Platinum(II)-BODIPY Conjugates for Targeted Photodynamic Therapy in Red Light
Ramu, V., Gautam, S., Garai, A., Kondaiah, P., & Chakravarty, A. R. (2018) · Inorganic Chemistry · doi:10.1021/acs.inorgchem.7b02249 · Cited by 74
Nkepang, G. N., Bio, M., Rajaputra, P., Awuah, S. G., & You, Y. (2014) · Bioconjugate Chemistry · doi:10.1021/bc500376j · Cited by 73
Hossain, S., Nisbett, L., & Boon, E. M. (2017) · Accounts of Chemical Research · doi:10.1021/acs.accounts.7b00095 · Cited by 73
Macrophage-Instructed Intracellular Staphylococcus aureus Killing by Targeting Photodynamic Dimers
Cai, Q., Fei, Y., An, H., Zhao, X., Ma, Y., Cong, Y., Hu, L., Li, L., & Wang, H. (2018) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.7b19056 · Cited by 73
Roberts, J., Smylie, M., Walker, J. W. T., Basappa, N. S., Chu, Q. S.-C., Kolinsky, M. P., Lyddell, C., & Ye, C. (2019) · Clinical Rheumatology · doi:10.1007/s10067-019-04451-2 · Cited by 73
Silva, P. D., Saad, M. A., Thomsen, H., Bano, S., Ashraf, S., & Hasan, T. G. (2020) · Journal of Porphyrins and Phthalocyanines · doi:10.1142/s1088424620300098 · Cited by 73
Zhang, F., Huang, Q., Zheng, K., Li, J., Liu, J.-Y., & Xue, J. (2013) · Chemical Communications · doi:10.1039/c3cc45487h · Cited by 72
Synthesis and cellular studies of PEG-functionalized meso-tetraphenylporphyrins
Sibrian‐Vazquez, M., Jensen, T. J., & Vicente, M. G. H. (2006) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2006.08.004 · Cited by 72
Naasz, R., Arnold, L. A., Minnaard, A. J., & Feringa, B. L. (2001) · PubMed · doi:10.1002/1521-3773(20010302)40:5 · Cited by 72
Schmitt, J., Heitz, V., Sour, A., Bolze, F., Kessler, P., Flamigni, L., Ventura, B., Bonnet, C. S., & Tóth, É. (2016) · Chemistry - A European Journal · doi:10.1002/chem.201503433 · Cited by 72
A histochemical approach to the mechanism of action of cisplatin and its analogues.
Aggarwal, S. K. (1993) · Journal of Histochemistry & Cytochemistry · doi:10.1177/41.7.8515048 · Cited by 71
Zhao, Z., Chan, P.-S., Li, H., Wong, K., Wong, R. N., Mak, N. K., Zhang, J., Tam, H. L., Wong, W., Kwong, D. W. J., et al. (2011) · Inorganic Chemistry · doi:10.1021/ic201178e · Cited by 71
Raza, M. K., Gautam, S., Garai, A., Mitra, K., Kondaiah, P., & Chakravarty, A. R. (2017) · Inorganic Chemistry · doi:10.1021/acs.inorgchem.7b01346 · Cited by 71
Lv, Z., Zou, L., Wei, H., Liu, S., Huang, W., & Zhao, Q. (2018) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.8b05944 · Cited by 71
Yang, M., Cao, S., Sun, X., Su, H., Li, H., Liu, G., Luo, X., & Wu, F. (2019) · Bioconjugate Chemistry · doi:10.1021/acs.bioconjchem.9b00819 · Cited by 71
Vugts, D. J., Vervoort, A., van Walsum, M., Visser, G. W. M., Robillard, M. S., Versteegen, R. M., Vulders, R. C. M., Herscheid, J. D. M., & van Dongen, G. A. M. S. (2011) · Bioconjugate Chemistry · doi:10.1021/bc200298v · Cited by 70
Hammerer, F., Garcia, G., Chen, S., Poyer, F., Achelle, S., Fiorini‐Debuisschert, C., Teulade‐Fichou, M., & Maillard, P. (2014) · The Journal of Organic Chemistry · doi:10.1021/jo402658h · Cited by 70
Supramolecular Nanostructures of Structurally Defined Graphene Nanoribbons in the Aqueous Phase
Huang, Y., Dou, W., Xu, F., Ru, H., Gong, Q., Wu, D., Yan, D., Tian, H., He, X., Mai, Y., et al. (2018) · Angewandte Chemie International Edition · doi:10.1002/anie.201712637 · Cited by 70
Acid-Triggered Nanoexpansion Polymeric Micelles for Enhanced Photodynamic Therapy
Zhong, S., Chen, C., Yang, G., Zhu, Y., Cao, H., Xu, B., Luo, Y., Gao, Y., & Zhang, W. (2019) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.9b12620 · Cited by 70
Enhancing Intersystem Crossing in Phenotiazinium Dyes by Intercalation into DNA
Nogueira, J. J., Oppel, M., & González, L. (2015) · Angewandte Chemie International Edition · doi:10.1002/anie.201411456 · Cited by 69
Novel photodynamic effects of a benzophenothiazine on two different murine sarcomas.
Cincotta, L., Foley, J. W., MacEachern, T. A., Lampros, E., & Cincotta, A. H. (1994) · PubMed · Cited by 69
da Silva, A. F., Borges, A. D. S., Giaouris, E. D., Mikcha, J. M. G., & Simões, M. V. (2018) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2018.1491528 · Cited by 69
Noncovalent DNA‐Binding Metallo‐Supramolecular Cylinders Prevent DNA Transactions in vitro
Ducani, C., Łęczkowska, A., Hodges, N. J., & Hannon, M. J. (2010) · Angewandte Chemie International Edition · doi:10.1002/anie.201004471 · Cited by 68
Tian, X., Zhang, Q., Zhang, M., Uvdal, K., Wang, Q., Chen, J., Du, W., Huang, B., Wu, J., & Tian, Y. (2016) · Chemical Science · doi:10.1039/c6sc02342h · Cited by 68
Dual-Responsive Molecular Probe for Tumor Targeted Imaging and Photodynamic Therapy
Meng, X., Yang, Y., Zhou, L., Zhang, L., Lv, Y., Li, S., Wu, Y., Zheng, M., Li, W., Gao, G., et al. (2017) · Theranostics · doi:10.7150/thno.18437 · Cited by 68
Liu, B., Monro, S. M. A., Li, Z., Jabed, M. A., Ramírez, D. C., Cameron, C. G., Colón, K. L., Roque, J. A., KILINA, S. V., Tian, J., et al. (2019) · ACS Applied Bio Materials · doi:10.1021/acsabm.9b00312 · Cited by 68
Saha, S., Mallick, D., Majumdar, R., Roy, M., Dighe, R. R., Jemmis, E. D., & Chakravarty, A. R. (2011) · Inorganic Chemistry · doi:10.1021/ic1024229 · Cited by 67
Zhang, F., Song, M., Yuan, G., Ye, H.-N., Tian, Y., Huang, M., Xue, J., Zhang, Z., & Liu, J.-Y. (2017) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.7b00682 · Cited by 67
Zhang, P., Wang, Y., Qiu, K., Zhao, Z., Hu, R., He, C., Zhang, Q., & Chao, H. (2017) · Chemical Communications · doi:10.1039/c7cc07776a · Cited by 67
Kang, M., Kwok, R. T. K., Wang, J., Zhang, H., Lam, J. W. Y., Li, Y., Zhang, P., Zou, H., Gu, X., Li, F., et al. (2018) · Journal of Materials Chemistry B · doi:10.1039/c8tb00572a · Cited by 67
Tugrak, M., Gul, H. I., Sakagami, H., Gülçın, İ., & Supuran, C. T. (2018) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2018.09.013 · Cited by 67
Kim, S., Ye, S., Adamo, A., Orizondo, R. A., Jo, J., Cho, S. K., & Wagner, W. R. (2020) · Journal of Materials Chemistry B · doi:10.1039/d0tb01220c · Cited by 67
Fluorescent microplate assay for cancer cell‐associated cathepsin B
Hulkower, K. I., Butler, C., Linebaugh, B. E., Klaus, J. L., Keppler, D., Giranda, V. L., & Sloane, B. F. (2000) · European Journal of Biochemistry · doi:10.1046/j.1432-1327.2000.01458.x · Cited by 66
Lai, Y.-C., Su, S.-Y., & Chang, C. (2013) · ACS Applied Materials & Interfaces · doi:10.1021/am403593m · Cited by 66
A pH-responsive fluorescent probe and photosensitiser based on a self-quenched phthalocyanine dimer
Ke, M., Ng, D. K. P., & Lo, P. (2012) · Chemical Communications · doi:10.1039/c2cc34327d · Cited by 66
Rosen, G. M., Beselman, A., Tsai, P., Pou, S., Mailer, C., Ichikawa, K., Robinson, B. H., Nielsen, R. D., Halpern, H. J., & MacKerell, A. D. (2004) · The Journal of Organic Chemistry · doi:10.1021/jo0354894 · Cited by 66
Dual Role of Subphthalocyanine Dyes for Optical Imaging and Therapy of Cancer
van de Winckel, E., Mascaraque, M., Zamarrón, A., Juarranz, Á., Torres⊗, T., & de la Escosura, A. (2018) · Advanced Functional Materials · doi:10.1002/adfm.201705938 · Cited by 66
Li, B., Xiao, H. P., Cai, M., Li, M., Xu, X., Wang, S., Huang, S. Q., Wang, Y., Cheng, D., Pang, P., et al. (2020) · Advanced Functional Materials · doi:10.1002/adfm.201909117 · Cited by 66
Xiao, Q., Lin, H., Wu, J., Pang, X., Zhou, Q., Jiang, Y., Wang, P., Leung, A. W., Lee, H., Jiang, S., et al. (2020) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.0c00280 · Cited by 66
Li, X., Ke, M., Zhang, M., Tang, Q., Zheng, B., & Huang, J. (2015) · Chemical Communications · doi:10.1039/c4cc09934f · Cited by 65
Ke, M., Yeung, S., Fong, W., Ng, D. K. P., & Lo, P. (2012) · Chemistry - A European Journal · doi:10.1002/chem.201103516 · Cited by 65
Selenorhodamine Photosensitizers for Photodynamic Therapy of P-Glycoprotein-Expressing Cancer Cells
Hill, J. E., Linder, M. K., Davies, K. S., Sawada, G. A., Morgan, J., Ohulchanskyy, T. Y., & Detty, M. R. (2014) · Journal of Medicinal Chemistry · doi:10.1021/jm501259v · Cited by 65
Galstyan, A., Kauscher, U., Block, D., Ravoo, B. J., & Strassert, C. A. (2016) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.6b02132 · Cited by 65
Orthogonal Bodipy Trimers as Photosensitizers for Photodynamic Action
Özdemir, T., Bila, J. L., Sözmen, F., Yildirim, L. T., & Akkaya, E. U. (2016) · Organic Letters · doi:10.1021/acs.orglett.6b02418 · Cited by 65
Razi, S. S., Koo, Y. H., Kim, W., Yang, W., Wang, Z., Gobeze, H. B., D'Souza, F. W., Zhao, J., & Kim, D. (2018) · Inorganic Chemistry · doi:10.1021/acs.inorgchem.7b02989 · Cited by 65
Some activities of PorphyChem illustrated by the applications of porphyrinoids in PDT, PIT and PDI
Habermeyer, B., & Guilard, R. (2018) · Photochemical & Photobiological Sciences · doi:10.1039/c8pp00222c · Cited by 65
Lam, T., Tong, K., Yang, C., Kwong, W., Guan, X., Li, M., Lo, V. K., Chan, S. L., Phillips, D. L., Lok, C., et al. (2018) · Chemical Science · doi:10.1039/c8sc02920b · Cited by 65
He, L., Zhang, M.-F., Pan, Z., Wang, K., Zhao, Z.-J., Li, Y., & Mao, Z. (2019) · Chemical Communications · doi:10.1039/c9cc04871e · Cited by 65
Zhang, C., Guan, R., Liao, X., Ouyang, C., Rees, T. W., Liu, J., Chen, Y., Ji, L., & Chao, H. (2019) · Chemical Communications · doi:10.1039/c9cc05998a · Cited by 65
Lau, J. T. F., Lo, P., Tsang, Y., Fong, W., & Ng, D. K. P. (2011) · Chemical Communications · doi:10.1039/c1cc13783b · Cited by 64
Toward Singlet Oxygen Delivery at a Measured Rate: A Self-Reporting Photosensitizer
Erbaş-Çakmak, S., & Akkaya, E. U. (2014) · Organic Letters · doi:10.1021/ol501084n · Cited by 64
He, H., Lo, P., Yeung, S., Fong, W., & Ng, D. K. P. (2011) · Journal of Medicinal Chemistry · doi:10.1021/jm101637g · Cited by 64
Borisov, S. M., Alemayehu, A. B., & Ghosh, A. (2016) · Journal of Materials Chemistry C · doi:10.1039/c6tc01126h · Cited by 64
Intermolecular Structural Change for Thermoswitchable Polymeric Photosensitizer
Park, W., Park, S.-J., Cho, S., Shin, H., Jung, Y.-S., Lee, B., Na, K., & Kim, D. (2016) · Journal of the American Chemical Society · doi:10.1021/jacs.6b04875 · Cited by 64
Ji, S., Gao, H., Mu, W., Ni, X., Yi, X., Shen, J. Q., Liu, Q., Bao, P., & Ding, D. (2017) · Journal of Materials Chemistry B · doi:10.1039/c7tb02685d · Cited by 64
A Cross‐linked Conjugated Polymer Photosensitizer Enables Efficient Sunlight‐Induced Photooxidation
Wu, W., Xu, S., Qi, G., Zhu, H., Hu, F., Liu, Z., Zhang, D., & Liu, B. (2018) · Angewandte Chemie International Edition · doi:10.1002/anie.201811067 · Cited by 64
Zhao, N., Li, P., Zhuang, J., Liu, Y., Xiao, Y., Qin, R., & Li, N. (2019) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.9b01655 · Cited by 64
Radunz, S., Wedepohl, S., Röhr, M., Calderón, M., Tschiche, H. R., & Resch‐Genger, U. (2020) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.9b01873 · Cited by 64
Pham, T. C., Heo, S., Nghĩa, N. V., Lee, M. W., Yoon, J., & Lee, S. (2021) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.0c22174 · Cited by 64
Self-citationBasu, U., Pant, I., Hussain, A., Kondaiah, P., & Chakravarty, A. R. (2015) · Inorganic Chemistry · doi:10.1021/ic5027625 · Cited by 63
Cheng, S., Hsieh, C., Chen, N., Chu, C.-H., Huang, C., Chou, P., Tseng, F., Yang, C., Mou, C., & Lo, L. (2011) · Nano Today · doi:10.1016/j.nantod.2011.10.003 · Cited by 63
Parker, L. J., Ciccone, S., Italiano, L. C., Primavera, A., Oakley, A. J., Morton, C. J., Hancock, N. C., Bello, M. L., & Parker, M. W. (2008) · Journal of Molecular Biology · doi:10.1016/j.jmb.2008.04.066 · Cited by 63
Lau, J. T. F., Lo, P., Fong, W., & Ng, D. K. P. (2011) · Chemistry - A European Journal · doi:10.1002/chem.201100621 · Cited by 63
Zang, Q., Yu, J., Yu, W., Qian, J., Hu, R., & Tang, B. Z. (2018) · Chemical Science · doi:10.1039/c8sc00633d · Cited by 63
Zhu, J., Zou, J., Zhang, J., Sun, Y., Dong, X., & Zhang, Q. (2019) · Journal of Materials Chemistry B · doi:10.1039/c9tb00180h · Cited by 63
Self-Assembly of Porphyrin-Containing Metalla-Assemblies and Cancer Photodynamic Therapy
Jiang, X., Zhou, Z., Huang, Y., Shan, C., Yu, H., Wojtas, Ł., Zhang, M., Mao, Z., Wang, M., & Stang, P. J. (2020) · Inorganic Chemistry · doi:10.1021/acs.inorgchem.9b02775 · Cited by 63
Photophysical and Photobiological Properties of Dinuclear Iridium(III) Bis-tridentate Complexes
Liu, B., Monro, S. M. A., Lystrom, L., Cameron, C. G., Colón, K. L., Yin, H., KILINA, S. V., McFarland, S. A., & Sun, W. (2018) · Inorganic Chemistry · doi:10.1021/acs.inorgchem.8b00789 · Cited by 62
Kim, J., Park, W., Kim, D., Lee, E. S., Lee, D. H., Jeong, S. W., Park, J. M., & Na, K. (2019) · Advanced Functional Materials · doi:10.1002/adfm.201900084 · Cited by 62
Wang, J., Zhu, X., Zhang, J., Wang, H., Liu, G., Bu, Y., Yu, J., Tian, Y., & Zhou, H. (2019) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.9b15577 · Cited by 62
Nguyen, V.-N., Baek, G., Qi, S., Heo, S., Yim, Y., & Yoon, J. (2020) · Dyes and Pigments · doi:10.1016/j.dyepig.2020.108265 · Cited by 62
Self-citationRajaputra, P., Nkepang, G. N., Watley, R. L., & You, Y. (2012) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2012.11.032 · Cited by 61
pH‐ and Thiol‐Responsive BODIPY‐Based Photosensitizers for Targeted Photodynamic Therapy
Jiang, X., Lau, J. T. F., Wang, Q., Ng, D. K. P., & Lo, P. (2016) · Chemistry - A European Journal · doi:10.1002/chem.201600452 · Cited by 61
Unique Triphenylphosphonium Derivatives for Enhanced Mitochondrial Uptake and Photodynamic Therapy
Hu, Z., Sim, Y., Kon, O. L., Ng, W. H., Ribeiro, A. J. M., Ramos, M. J., Fernandes, P. A., Ganguly, R., Xing, B., Garcı́a, F., et al. (2017) · Bioconjugate Chemistry · doi:10.1021/acs.bioconjchem.6b00682 · Cited by 61
Ru(II)-Complex-Based DNA Photocleaver Having Intense Absorption in the Phototherapeutic Window
Zhang, Y., Zhou, Q., Tian, N., Li, C., & Wang, X. (2017) · Inorganic Chemistry · doi:10.1021/acs.inorgchem.6b02459 · Cited by 61
Mirror‐Image Dependence: Targeting Enantiomeric G‐Quadruplex DNA Using Triplex Metallohelices
Zhao, C., Song, H. L., Scott, P., Zhao, A., Tateishi‐Karimata, H., Sugimoto, N., Ren, J., & Qu, X. (2018) · Angewandte Chemie International Edition · doi:10.1002/anie.201809207 · Cited by 61
BODIPY-Based Fluorescent Surfactant for Cell Membrane Imaging and Photodynamic Therapy
Wang, H., Zhao, W., Liu, X., Wang, S., & Wang, Y. (2019) · ACS Applied Bio Materials · doi:10.1021/acsabm.9b00977 · Cited by 61
Karges, J., Li, J. X., Zeng, L., Chao, H., & Gasser, G. (2020) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.0c16119 · Cited by 61
Jin, C., Liu, J., Chen, Y., Guan, R., Ouyang, C., Zhu, Y., Ji, L., & Chao, H. (2016) · Scientific Reports · doi:10.1038/srep22039 · Cited by 60
A ratiometric theranostic probe for tumor targeting therapy and self-therapeutic monitoring
Li, S., Cheng, H. B., Xie, B., Qiu, W., Song, L.-L., Zhuo, R., & Zhang, X. (2016) · Biomaterials · doi:10.1016/j.biomaterials.2016.07.024 · Cited by 60
Sun, J., Qi, X., Yang, Y., Shah, H., Cao, H., Qi, Y., Gong, J. R., & Li, J. (2017) · Chemical Communications · doi:10.1039/c7cc08820e · Cited by 60
Zhao, Y., Li, X., Wang, Z., Yang, W., Chen, K., Zhao, J., & Gurzadyan, G. G. (2018) · The Journal of Physical Chemistry C · doi:10.1021/acs.jpcc.7b11872 · Cited by 60
Ferino, A., Nicoletto, G., D’Este, F., Zorzet, S., Lago, S., Richter, S. N., Tikhomirov, A. S., Shchekotikhin, A. E., & Xodo, L. E. (2020) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.9b01577 · Cited by 60
Li, G., Chen, Y., Wu, J., Ji, L., & Chao, H. (2013) · Chemical Communications · doi:10.1039/c3cc38687b · Cited by 59
Zhang, R., Feng, G., Zhang, C., Cai, X., Cheng, X., & Liu, B. (2016) · Analytical Chemistry · doi:10.1021/acs.analchem.6b00524 · Cited by 59
Sour, A., Jenni, S., Ortí-Suárez, A., Schmitt, J., Heitz, V., Bolze, F., de Sousa, P. L., Po, C., Bonnet, C. S., Pallier, A., et al. (2016) · Inorganic Chemistry · doi:10.1021/acs.inorgchem.6b00381 · Cited by 59
Meng, Z., Yu, B., Han, G., Liu, M., Shan, B., Dong, G., Miao, Z., Jia, N., Tan, Z., Li, B., et al. (2016) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.6b00352 · Cited by 59
Sudheesh, K. V., Jayaram, P. S., Samanta, A., Bejoymohandas, K. S., Jayasree, R. S., & Ajayaghosh, A. (2018) · Chemistry - A European Journal · doi:10.1002/chem.201801918 · Cited by 59
Drug Targeting Strategies for Photodynamic Therapy
Schmitt, F., & Juillerat‐Jeanneret, L. (2012) · Anti-Cancer Agents in Medicinal Chemistry · doi:10.2174/187152012800617830 · Cited by 58
Single Near‐Infrared Emissive Polymer Nanoparticles as Versatile Phototheranostics
Guo, L., Niu, G., Zheng, X., Ge, J., Liu, W., Jia, Q., Zhang, P., Zhang, H., & Wang, P. (2017) · Advanced Science · doi:10.1002/advs.201700085 · Cited by 58
Li, G., Mark, M. F., Lv, H., McCamant, D. W., & Eisenberg, R. (2018) · Journal of the American Chemical Society · doi:10.1021/jacs.7b11581 · Cited by 58
Guo, L., Zhang, X., Zhao, W., Zhao, W., Li, F., Xiao, K., Yu, Q., Liu, S., & Zhao, Q. (2020) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.0c01695 · Cited by 58
Galstyan, A., Schiller, R., & Dobrindt, U. (2017) · Angewandte Chemie · doi:10.1002/ange.201703398 · Cited by 58
Dosselli, R., Ruiz‐González, R., Moret, F., Agnolon, V., Compagnin, C., Mognato, M., Sella, V., Agut, M., Nonell, S., Gobbo, M., et al. (2014) · Journal of Medicinal Chemistry · doi:10.1021/jm401653r · Cited by 57
Hou, A., Feng, G., Zhuo, J., & Sun, G. Z. (2015) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.5b09993 · Cited by 57
Jing, C., Wang, R., Ou, H., Li, A., An, Y., Guo, S., & Shi, L. (2018) · Chemical Communications · doi:10.1039/c7cc09954a · Cited by 57
Tian, N., Sun, W., Guo, X., Lu, J., Li, C., Hou, Y., Wang, X., & Zhou, Q. (2019) · Chemical Communications · doi:10.1039/c8cc09186b · Cited by 57
Efficient light absorbers based on thiophene-fused boron dipyrromethene (BODIPY) dyes
Tanaka, K., Yamane, H., Yoshii, R., & Chujo, Y. (2013) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2013.03.050 · Cited by 56
Multilayer Microcapsules for FRET Analysis and Two‐Photon‐Activated Photodynamic Therapy
Yang, Y., Liu, H., Han, M., Sun, B., & Li, J. (2016) · Angewandte Chemie International Edition · doi:10.1002/anie.201605905 · Cited by 56
Galland, M., Bahers, T. L., Bányász, Á., Lascoux, N., Duperray, A., Grichine, A., Tripier, R., Guyot, Y., Maynadier, M., Nguyen, C., et al. (2019) · Chemistry - A European Journal · doi:10.1002/chem.201901047 · Cited by 56
A biotinylated ruthenium( ii ) photosensitizer for tumor-targeted two-photon photodynamic therapy
Li, J. X., Zeng, L., Xiong, K., Rees, T. W., Jin, C., Wu, W., Chen, Y., Ji, L., & Chao, H. (2019) · Chemical Communications · doi:10.1039/c9cc05826e · Cited by 56
Li, D., Wang, X., Yang, L., Li, S., Hu, Q., Li, X., Zheng, B., Ke, M., & Huang, J. (2019) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.9b13861 · Cited by 56
Zhao, X., Yang, Y., Yu, Y., Guo, S., Wang, W., & Zhu, S. (2019) · Chemical Communications · doi:10.1039/c9cc06157f · Cited by 56
Lin, W., Zhang, W., Liu, S., Li, Z., Hu, X., Xie, Z., Duan, C., & Han, G. (2019) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.9b16403 · Cited by 56
Rose Bengal–Amphiphilic Peptide Conjugate for Enhanced Photodynamic Therapy of Malignant Melanoma
Dhillon, S. K., Porter, S. L., Rizk, N., Sheng, Y., McKaig, T., Burnett, K., White, B. C., Nesbitt, H., Matin, R., McHale, A. P., et al. (2020) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.9b01802 · Cited by 56
Liu, Y., Xu, C., Teng, L., Liu, H., Ren, T., Xu, S., Lou, X., Guo, H., Yuan, L., & Zhang, X. (2020) · Chemical Communications · doi:10.1039/c9cc09790b · Cited by 56
Cationic Versus Anionic Phthalocyanines for Photodynamic Therapy: What a Difference the Charge Makes
Kollár, J., Macháček, M., Halašková, M., Lenčo, J., Kučera, R., Demuth, J., Rohlickova, M., Hasonova, K., Miletín, M., Novakova, V., et al. (2020) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.0c00481 · Cited by 56
Zhang, J.-X., Li, H., Chan, C., Lan, R., Chan, W., Law, G., Wong, W., & Wong, K. (2012) · Chemical Communications · doi:10.1039/c2cc34963a · Cited by 55
Xiao, T., Fan, J. K., Huang, H. L., Gu, J. F., Li, L., & Liu, X. (2009) · Cell Research · doi:10.1038/cr.2009.126 · Cited by 55
BODIPY–Au(I): A Photosensitizer for Singlet Oxygen Generation and Photodynamic Therapy
Üçüncü, M., Karakuş, E., Demirci, E. K., Sayar, M., Dartar, S., & Emrullahoğlu, M. (2017) · Organic Letters · doi:10.1021/acs.orglett.7b00791 · Cited by 55
Two-Photon Excited FRET Dyads for Lysosome-Targeted Imaging and Photodynamic Therapy
Zhu, M., Zhang, J., Zhou, Y., Xing, P., Gong, L., Su, C., Qi, D., Du, H., Bian, Y., & Jiang, J. (2018) · Inorganic Chemistry · doi:10.1021/acs.inorgchem.8b01581 · Cited by 55
Lysosome-targeted photoactivation reveals local sphingosine metabolism signatures
Feng, S., 原山, 武., Chang, D., Hannich, J. T., Winssinger, N., & Riezman, H. (2018) · Chemical Science · doi:10.1039/c8sc03614d · Cited by 55
Self-destructive PEG–BODIPY nanomaterials for photodynamic and photothermal therapy
Li, C., Lin, W., Liu, S., Zhang, W., & Xie, Z. (2019) · Journal of Materials Chemistry B · doi:10.1039/c9tb00752k · Cited by 55
Morales, E. H., Pinto, C. A., Luraschi, R., Muñoz-Villagrán, C., Cornejo, F. A., Simpkins, S. W., Nelson, J., Arenas, F., Piotrowski, J. S., Myers, C. L., et al. (2017) · Nature Communications · doi:10.1038/ncomms15320 · Cited by 54
Bis(pyrene)-Doped Cationic Dipeptide Nanoparticles for Two-Photon-Activated Photodynamic Therapy
Sun, B., Wang, L., Li, Q., He, P., Liu, H., Wang, H., Yang, Y., & Li, J. (2017) · Biomacromolecules · doi:10.1021/acs.biomac.7b00780 · Cited by 54
Ramu, V., Gautam, S., Kondaiah, P., & Chakravarty, A. R. (2019) · Inorganic Chemistry · doi:10.1021/acs.inorgchem.9b00567 · Cited by 54
Liu, Z., Xue, Y., Wu, M., Yang, G., Lan, M., & Zhang, W. (2019) · Biomacromolecules · doi:10.1021/acs.biomac.9b01368 · Cited by 54
Qin, Q., Wei, Z., Wang, Z., Huang, X., Tan, M., Zou, H., & Liang, H. (2020) · Chemical Communications · doi:10.1039/d0cc00524j · Cited by 54
Cardillo, J. A., Jorge, R., Costa, R. A., Nunes, S., Lavinsky, D., Kuppermann, B. D., Tedesco, A. C., & Farah, M. E. (2008) · British Journal of Ophthalmology · doi:10.1136/bjo.2007.129395 · Cited by 53
Zhang, C., & Zhao, J. (2016) · Journal of Materials Chemistry C · doi:10.1039/c5tc03193a · Cited by 53
Lan, M., Zhao, S., Xie, Y., Zhao, J., Guo, L., Niu, G., Li, Y., Sun, H., Zhang, H., Liu, W., et al. (2017) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.6b15537 · Cited by 53
Dai, X., Chen, X., Zhao, Y., Yu, Y., Wei, X., Zhang, X., & Li, C. (2017) · Biomacromolecules · doi:10.1021/acs.biomac.7b01316 · Cited by 53
Covalently Attached Antimicrobial Surfaces Using BODIPY: Improving Efficiency and Effectiveness
Peveler, W. J., Noimark, S., Al-Azawi, H., Hwang, G. B., Crick, C. R., Allan, E., Edel, J. B., Ivanov, A. P., MacRobert, A. J., & Parkin, I. P. (2017) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.7b13273 · Cited by 53
Feng, X., Shi, Y. P., Xie, L., Zhang, K., Wang, X., Liu, Q., & Wang, P. (2018) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.8b00547 · Cited by 53
Enhanced Energy Transfer in a Donor–Acceptor Photosensitizer Triggers Efficient Photodynamic Therapy
Zhao, Y., Zhang, Z., Lu, Z., Wang, H., & Tang, Y. (2019) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.9b12375 · Cited by 53
Wang, C., & Qian, Y. (2019) · Biomaterials Science · doi:10.1039/c9bm01709g · Cited by 53
A charge-switchable, four-armed polymeric photosensitizer for photodynamic cancer therapy
Lee, C., Park, W., Jo, Y. U., & Na, K. (2014) · Chemical Communications · doi:10.1039/c4cc00746h · Cited by 52
BODIPY-based macromolecular photosensitizer with cation-enhanced antibacterial activity
Lu, Z., Zhang, X., Zhao, Y., Xue, Y., Zhai, T., Wu, Z., & Li, C. (2014) · Polymer Chemistry · doi:10.1039/c4py00715h · Cited by 52
Translocation of Bioactive Molecules through Carbon Nanotubes Embedded in the Lipid Membrane
Sahoo, A. K., Kanchi, S., Mandal, T., Dasgupta, C., & Maiti, P. K. (2018) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.7b18498 · Cited by 52
Water-Soluble Chlorin/Arylaminoquinazoline Conjugate for Photodynamic and Targeted Therapy
Otvagin, V. F., Kuzmina, N. S., Krylova, L. V., Volovetsky, A. B., Nyuchev, A. V., Gavryushin, A. E., Meshkov, I. N., Gorbunova, Y. G., Romanenko, Y. V., Койфман, О. И., et al. (2019) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.9b01294 · Cited by 52
Xiao, F., Cao, B., Wen, L., Su, Y., Zhan, M., Lu, L., & Hu, X. (2020) · Chinese Chemical Letters · doi:10.1016/j.cclet.2020.06.038 · Cited by 52
Nghĩa, N. V., Park, S. J., Qi, S., Ha, J., Heo, S., Yim, Y., Baek, G., Lim, C. S., Lee, D. J., Kim, H. M., et al. (2020) · Chemical Communications · doi:10.1039/d0cc04644b · Cited by 52
Self-citationCancer patients opt for unapproved drug
Pearson, H. (2007) · Nature · doi:10.1038/446474a · Cited by 51
Tuncel, S., Trivella, A., Atílla, D., Bennis, K., Savoie, H., Albrieux, F., Delort, L., Billard, H., Dubois, V., Ahsen, V., et al. (2013) · Molecular Pharmaceutics · doi:10.1021/mp400207v · Cited by 51
Zhang, J. C., Mu, Y., Ma, Z., Han, K., & Han, H. (2018) · Biomaterials · doi:10.1016/j.biomaterials.2018.08.026 · Cited by 51
Tuning photochemical properties of phosphorus( v ) porphyrin photosensitizers
Meshkov, I. N., Bulach, V., Gorbunova, Y. G., Gostev, F. E., Nadtochenko, V. A., Tsivadze, A. Y., & Hosseini, M. W. (2017) · Chemical Communications · doi:10.1039/c7cc06052a · Cited by 50
Solovieva, A. O., Kirakci, K., Ivanov, A. A., Kubát, P., Pozmogova, T. N., Miroshnichenko, S. M., Воронцова, Е. В., Владимирович, Ч. А., Trifonova, K. E., Fufaeva, M. S., et al. (2017) · Inorganic Chemistry · doi:10.1021/acs.inorgchem.7b02212 · Cited by 50
Chen, H., Bi, Q., Yao, Y., & Tan, N. (2018) · Journal of Materials Chemistry B · doi:10.1039/c8tb00665b · Cited by 50
Zhou, Z., Ergene, C., Lee, J. Y., Shirley, D. J., Carone, B. R., Caputo, G. A., & Palermo, E. F. (2018) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.8b19098 · Cited by 50
Mei, E., Vinogradov, S. A., & Hochstrasser, R. M. (2003) · Journal of the American Chemical Society · doi:10.1021/ja030271k · Cited by 49
Rsk‐mediated phosphorylation and 14‐3‐3ε binding of Apaf‐1 suppresses cytochrome c‐induced apoptosis
Kim, J., Parrish, A. B., Kurokawa, M., Matsuura, K., Freel, C. D., Andersen, J. L., Johnson, C. E., & Kornbluth, S. A. (2012) · The EMBO Journal · doi:10.1038/emboj.2011.491 · Cited by 49
Hu, W., He, T., Jiang, R., Yin, J. L., Li, L., Lu, X., Zhao, H., Zhang, L., Huang, L., Sun, H., et al. (2017) · Chemical Communications · doi:10.1039/c6cc09473b · Cited by 49
Platinum(II) Ring-Fused Chlorins as Near-Infrared Emitting Oxygen Sensors and Photodynamic Agents
Pereira, N. A. M., Laranjo, M., Casalta‐Lopes, J., Serra, A. C., Piñeiro, M., Pina, J., de Melo, J. S. S., Senge, M. O., Botelho, M. F., Martelo, L., et al. (2017) · ACS Medicinal Chemistry Letters · doi:10.1021/acsmedchemlett.6b00476 · Cited by 49
Chow, M. J., Alfiean, M., Pastorin, G., Gaiddon, C., & Ang, W. H. (2017) · Chemical Science · doi:10.1039/c7sc00497d · Cited by 49
Allison, S. J., Cooke, D. J., Davidson, F. S., Elliott, P. I. P., Faulkner, R. A., Griffiths, H. B. S., Harper, O. J., Hussain, O. A., Owen‐Lynch, P. J., Phillips, R. M., et al. (2018) · Angewandte Chemie International Edition · doi:10.1002/anie.201805510 · Cited by 49
Zhang, C., Zhao, Y., Li, D., Liu, J., Han, H., He, D., Tian, X., Li, S., Wu, J., & Tian, Y. (2019) · Chemical Communications · doi:10.1039/c8cc09230c · Cited by 49
Conti, L., Bencini, A., Ferrante, C., Gellini, C., Paoli, P., Parri, M., Pietraperzia, G., Valtancoli, B., & Giorgi, C. (2019) · Chemistry - A European Journal · doi:10.1002/chem.201901570 · Cited by 49
Photocytotoxic Copper(II) Complexes with Schiff‐Base Scaffolds for Photodynamic Therapy
Lin, R., Chiu, C., Hsu, C., Lai, Y., Venkatesan, P., Huang, P., Lai, P., & Lin, C. (2017) · Chemistry - A European Journal · doi:10.1002/chem.201705640 · Cited by 48
Read, T., Smith, A., Thomas, J. M., David, M., Foote, M. C., Wagels, M., Barbour, A. P., & Smithers, B. M. (2018) · Journal of Surgical Oncology · doi:10.1002/jso.24921 · Cited by 48
Ni, J., Lee, M. M. S., Zhang, P., Chen, G., Chen, Y., Wang, D., Yu, Z., Kwok, R. T. K., Lam, J. W. Y., & Tang, B. Z. (2018) · Analytical Chemistry · doi:10.1021/acs.analchem.8b04736 · Cited by 48
Mitochondrial Alterations During Carcinogenesis
Wang, X., Peralta, S., & Moraes, C. T. (2013) · Advances in cancer research · doi:10.1016/b978-0-12-407190-2.00004-6 · Cited by 47
Mikeš, J., Kleban, J., Sačková, V., Horváth, V., Jamborová, E., Vaculová, A. H., Kozubı́k, A., Hofmanová, J., & Fedoročko, P. (2007) · Photochemical & Photobiological Sciences · doi:10.1039/b700350a · Cited by 47
Kim, J., Tung, C., & Choi, Y. (2014) · Chemical Communications · doi:10.1039/c4cc04166f · Cited by 47
Self-citationWang, P., Qin, F., Zhang, Z., & Cao, W. (2015) · Optics Express · doi:10.1364/oe.23.022991 · Cited by 47
Programming Supramolecular Biohybrids as Precision Therapeutics
Ng, D. Y. W., Wu, Y., Kuan, S. L., & Weil, T. (2014) · Accounts of Chemical Research · doi:10.1021/ar5002445 · Cited by 47
Ruan, Z., Liu, L., Jiang, W., Li, S., Wang, Y., & Yan, L. (2016) · Biomaterials Science · doi:10.1039/c6bm00787b · Cited by 47
Zhao, S., Niu, G., Wu, F., Yan, L., Zhang, H., Zhao, J., Zeng, L., & Lan, M. (2017) · Journal of Materials Chemistry B · doi:10.1039/c7tb00371d · Cited by 47
Palao, E., Llano, R. S., Tabero, A., Manzano, H., Agarrabeitia, A. R., Villanueva, Á., López‐Arbeloa, Í., Martínez‐Martínez, V., & Ortiz, M. J. (2017) · Chemistry - A European Journal · doi:10.1002/chem.201701347 · Cited by 47
Porphyrins Conjugated with Peripheral Thiolato Gold(I) Complexes for Enhanced Photodynamic Therapy
Longevial, J., Cheikh, K. E., Aggad, D., Lebrun, A., van der Lee, A., Tielens, F., Clément, S., Morère, A., Garcia, M., Gary‐Bobo, M., et al. (2017) · Chemistry - A European Journal · doi:10.1002/chem.201702975 · Cited by 47
Hu, F., Yuan, Y., Wu, W., Mao, D., & Liu, B. (2018) · Analytical Chemistry · doi:10.1021/acs.analchem.8b00547 · Cited by 47
Zhao, X., Huang, Y., Yuan, G., Zuo, K., Huang, Y., Chen, J., Li, J., & Xue, J. (2018) · Chemical Communications · doi:10.1039/c8cc09456j · Cited by 47
Zhu, J., Zou, J., Zhang, Z., Zhang, J., Sun, Y., Dong, X., & Zhang, Q. (2019) · Materials Chemistry Frontiers · doi:10.1039/c9qm00044e · Cited by 47
Polymyxin-based photosensitizer for the potent and selective killing of Gram-negative bacteria
Üçüncü, M., Mills, B., Duncan, S., Staderini, M., Dhaliwal, K., & Bradley, M. (2020) · Chemical Communications · doi:10.1039/d0cc00155d · Cited by 47
Nano theranostics platforms that utilize proteins
Lee, S., Pham, T. C., Bae, C., Choi, Y., Kim, Y. K., & Yoon, J. (2020) · Coordination Chemistry Reviews · doi:10.1016/j.ccr.2020.213258 · Cited by 47
Self-citationLiu, B., Gao, Y., Jabed, M. A., KILINA, S. V., Liu, G., & Sun, W. (2020) · ACS Applied Bio Materials · doi:10.1021/acsabm.0c00647 · Cited by 47
A Self‐Assembled Metallomacrocycle Singlet Oxygen Sensitizer for Photodynamic Therapy
Walker, M. G., Jarman, P. J., Gill, M. R., Tian, X., Ahmad, H., Reddy, P. A. N., McKenzie, L. K., Weinstein, J. A., Meijer, A. J. H. M., Battaglia, G., et al. (2016) · Chemistry - A European Journal · doi:10.1002/chem.201600852 · Cited by 46
Development of an Azoreductase-based Reporter System with Synthetic Fluorogenic Substrates
Shin, N., Hanaoka, K., Piao, W., Miyakawa, T., Fujisawa, T., Takeuchi, S., Takahashi, S., Komatsu, T., Ueno, T., Terai, T., et al. (2016) · ACS Chemical Biology · doi:10.1021/acschembio.6b00852 · Cited by 46
A water-soluble phosphorescent conjugated polymer brush for tumor-targeted photodynamic therapy
Sun, P., Wang, G., Hou, H., Yuan, P., Deng, W., Wang, C., Lü, X., Fan, Q., & Huang, W. (2017) · Polymer Chemistry · doi:10.1039/c7py01248a · Cited by 46
Chokkalingam, P., Pavithra, M. K., Vinod Kumar Reddy, L., Sen, D., Melvin Samuel, S., & Singh, N. D. P. (2018) · ACS Applied Nano Materials · doi:10.1021/acsanm.8b01495 · Cited by 46
Gao, X., Mao, D., Zuo, X., Hu, F., Cao, J., Zhang, P., Sun, J. Z., Liu, J., Liu, B., & Tang, B. Z. (2019) · Analytical Chemistry · doi:10.1021/acs.analchem.9b01053 · Cited by 46
Strong Visible‐Light‐Absorbing Cuprous Sensitizers for Dramatically Boosting Photocatalysis
Chen, K., Guo, S., Liu, H., Li, X., Zhang, Z., & Lu, T. (2020) · Angewandte Chemie International Edition · doi:10.1002/anie.202003251 · Cited by 46
Mitochondria‐Targeting Oxidovanadium(IV) Complex as a Near‐IR Light Photocytotoxic Agent
Prasad, P., Khan, I., Kondaiah, P., & Chakravarty, A. R. (2013) · Chemistry - A European Journal · doi:10.1002/chem.201303487 · Cited by 45
Zhang, Q., Lu, X., Wang, H., Tian, X., Wang, A., Zhou, H., Wu, J., & Tian, Y. (2018) · Chemical Communications · doi:10.1039/c8cc00908b · Cited by 45
Huang, Y. L., He, N., Wang, Y., Shen, D., Kang, Q., Zhao, R., & Chen, L. (2019) · Journal of Materials Chemistry B · doi:10.1039/c8tb03054e · Cited by 45
Zhao, Y., Chen, K., Yıldız, E. A., Li, S., Hou, Y., Zhang, X., Wang, Z., Zhao, J., Barbon, A., Yaglioglu, H. G., et al. (2020) · Chemistry - A European Journal · doi:10.1002/chem.201905248 · Cited by 45
Zhuang, J., Yang, H., Li, Y., Wang, B., Li, N., & Zhao, N. (2020) · Chemical Communications · doi:10.1039/d0cc00394h · Cited by 45
Tekdaş, D. A., Garifullin, R., Şentürk, B., Zorlu, Y., Gündoğdu, U., Atalar, E., Tekinay, A. B., Chernonosov, A. А., Yerli, Y., Dumoulin, F., et al. (2014) · Photochemistry and Photobiology · doi:10.1111/php.12332 · Cited by 44
Huang, L. F., Yang, W., & Zhao, J. (2014) · The Journal of Organic Chemistry · doi:10.1021/jo5019014 · Cited by 44
Yang, W., Karatay, A., Zhao, J., Song, J., Zhao, L. Z., Xing, Y., Zhang, C., He, C., Yaglioglu, H. G., Hayvalı, M., et al. (2015) · Inorganic Chemistry · doi:10.1021/acs.inorgchem.5b01107 · Cited by 44
Fan, J., Guo, S., Wang, S., Kang, Y., Yao, Q., Wang, J., Gao, X., Wang, H., Du, J., & Peng, X. (2017) · Chemical Communications · doi:10.1039/c7cc01798g · Cited by 44
Liu, X., Yang, Z., Xu, W., Chu, Y., Yang, J., Yan, Y., Hu, Y., Wang, Y., & Hua, J. (2019) · Journal of Materials Chemistry C · doi:10.1039/c9tc04427b · Cited by 44
Zhao, N., Li, Y., Yin, W., Zhuang, J., Jia, Q., Wang, Z., & Li, N. (2019) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.9b18666 · Cited by 44
Bioorthogonal Turn‐On BODIPY‐Peptide Photosensitizers for Tailored Photodynamic Therapy
Linden, G., & Vázquez, O. (2020) · Chemistry - A European Journal · doi:10.1002/chem.202001718 · Cited by 44
Shackley, D., Whitehurst, C., Moore, J., George, N. J. R., Betts, C. D., & Clarke, N. W. (2000) · British Journal of Urology · doi:10.1046/j.1464-410x.2000.00872.x · Cited by 43
Near‐IR‐Triggered, Remote‐Controlled Release of Metal Ions: A Novel Strategy for Caged Ions
Atilgan, A., Eçik, E. T., Guliyev, R., Uyar, T. B., Erbaş-Çakmak, S., & Akkaya, E. U. (2014) · Angewandte Chemie International Edition · doi:10.1002/anie.201405462 · Cited by 43
Structure and Function of the Energy‐Converting System of Mitochondria
von JAGOW, G., & Engel, W. D. (1980) · Angewandte Chemie International Edition in English · doi:10.1002/anie.198006593 · Cited by 43
Saeed, H. K., Jarman, P. J., Archer, S. A., Sreedharan, S., Saeed, I. Q., McKenzie, L. K., Weinstein, J. A., Buurma, N. J., Smythe, C., & Thomas, J. A. (2017) · Angewandte Chemie International Edition · doi:10.1002/anie.201707350 · Cited by 43
Flagged first, then by citations
2 of the 1199 references couldn’t be matched to a known paper.
Research works printed but not linked: 20
- Jodlbauer A. V. T. H., 1904, Münch. Med. Wochenschr., 52, 1139
- 10.1039/C5SC01733E · DOI
- Gerweck L. E., 1996, Cancer Res., 56, 1194
- 10.1021/jacs.6b04875 · DOI
- 10.1002/anie.201807602 · DOI
- 10.1039/C6CC09473B · DOI
- Wolpert M. K., 1973, J. Pharmacol. Exp. Ther., 185, 202
- 10.1021/jacs.7b05019 · DOI
- 10.1016/j.ccr.2017.08.003 · DOI
- 10.1002/chem.201605822 · DOI
- Jakel C. E., 2012, In Vivo, 26, 419
- 10.1039/C9TB00721K · DOI
- 10.1021/acsabm.9b00631 · DOI
- Tonissi F., 2016, Anticancer Res., 36, 2211
- Giatromanolaki A., 2001, Cancer Res., 61, 7992
- 10.1039/C6CC09473B · DOI
- Abolhoda A., 1999, Clin. Cancer Res., 5, 3352
- 10.1002/adfm.202002546 · DOI · Paper page
- Cincotta L., 1994, Cancer Res., 54, 1249
- 10.1021/acsabm.9b00977 · DOI
Cited by
Sorted by citations
Theranostic Fluorescent Probes
Sharma, A. K., Verwilst, P., Li, M., Ma, D., Singh, N., Yoo, J., Kim, Y., Yang, Y., Zhu, J., Huang, H., et al. (2024) · Chemical Reviews · doi:10.1021/acs.chemrev.3c00778 · Cited by 512
Hang, Y., Wang, A., & Wu, N. (2024) · Chemical Society Reviews · doi:10.1039/d3cs00793f · Cited by 515
Organic photosensitizers for antimicrobial phototherapy
Nghĩa, N. V., Zhao, Z., Tang, B. Z., & Yoon, J. (2022) · Chemical Society Reviews · doi:10.1039/d1cs00647a · Cited by 464
Self-citationTeng, K., Niu, L., & Yang, Q. (2023) · Journal of the American Chemical Society · doi:10.1021/jacs.2c11868 · Cited by 411
Aggregation-Induced Emission (AIE), Life and Health
Wang, H., Li, Q., Alam, P., Bai, H., Bhalla, V., Bryce, M. R., Cao, M., Chen, C., Chen, S., Chen, X., et al. (2023) · ACS Nano · doi:10.1021/acsnano.3c03925 · Cited by 404
Self-citation
Metadata
- Authors
- Pham, T. C., Nguyen, V.-N., Choi, Y., Lee, S., & Yoon, J.
- Affiliations
- Pukyong National University (KR)
- Department of Chemistry and Nanoscience, Ewha Womans University, Seoul 03760, Korea
- Ewha Womans University (KR)
- Corresponding author
- Lee, Songyi
- Yoon, Juyoung
- Venue
- Chemical Reviews
- Publisher
- American Chemical Society (ACS)
- Published
- 2021-09-28
- Volume
- 121
- Issue
- 21
- Pages
- 13454-13619
- ISSN
- 0009-2665 (ISSN-L)
- 1520-6890
- OpenAlex
- W3204360553
- Cited by
- 1,813
- References
- 1,199
- Citations by year
- 2026: 308 · 2025: 457 · 2024: 466 · 2023: 338 · 2022: 240 · 2021: 4
- FWCI
- 42.14
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- Chemical Reviews (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Research Foundation of Korea (2012R1A3A2048814, 2017R1A6A3A04004954, 2021R1A6A1A10039823)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Photodynamic Therapy Research Studies
- Physical Sciences › Engineering › Biomedical Engineering › Nanoplatforms for cancer theranostics
- Physical Sciences › Materials Science › Materials Chemistry › Porphyrin and Phthalocyanine Chemistry
- Keywords
- photosensitizers, photodynamic therapy, organic photosensitizers, reactive oxygen species, cancer therapy, rational design
- MeSH terms
- Humans, Neoplasms, Photochemotherapy, Photosensitizing Agents, Reactive Oxygen Species, Nanotechnology
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review