Recent Strategies to Develop Innovative Photosensitizers for Enhanced Photodynamic Therapy

Understanding the Warburg Effect: The Metabolic Requirements of Cell Proliferation

Vander Heiden, M. G., Cantley, L. C., & Thompson, C. B. (2009) · Science · doi:10.1126/science.1160809 · Cited by 16,197

Apoptosis: A Review of Programmed Cell Death

Elmore, S. (2007) · Toxicologic Pathology · doi:10.1080/01926230701320337 · Cited by 13,853

The biofilm matrix

Flemming, H.-C., & Wingender, J. (2010) · Nature Reviews Microbiology · doi:10.1038/nrmicro2415 · Cited by 10,137

Visible Light Photoredox Catalysis with Transition Metal Complexes: Applications in Organic Synthesis

Prier, C. K., Rankic, D. A., & MacMillan, D. W. C. (2013) · Chemical Reviews · doi:10.1021/cr300503r · Cited by 9,590

Aggregation-induced emission of 1-methyl-1,2,3,4,5-pentaphenylsilole

Luo, J., Xie, Z., Lam, J. W. Y., Cheng, L., Tang, B. Z., Chen, H., Qiu, C., Kwok, H. S., Zhan, X., Liu, Y., et al. (2001) · Chemical Communications · doi:10.1039/b105159h · Cited by 8,358

Aggregation-Induced Emission: Together We Shine, United We Soar!

Mei, J., Leung, N. L. C., Kwok, R. T. K., Lam, J. W. Y., & Tang, B. Z. (2015) · Chemical Reviews · doi:10.1021/acs.chemrev.5b00263 · Cited by 8,270

Highly efficient organic light-emitting diodes from delayed fluorescence

Uoyama, H., Goushi, K., Shizu, K., Nomura, H., & Adachi, C. (2012) · Nature · doi:10.1038/nature11687 · Cited by 8,219

Fluorine in medicinal chemistry

Purser, S., Moore, P. R., Swallow, S., & Gouverneur, V. (2007) · Chemical Society Reviews · doi:10.1039/b610213c · Cited by 7,678

Photodynamic therapy for cancer

Dolmans, D. E. J. G. J., Fukumura, D., & Jain, R. K. (2003) · Nature reviews. Cancer · doi:10.1038/nrc1071 · Cited by 6,850

Aggregation-induced emission

Hong, Y., Lam, J. W. Y., & Tang, B. Z. (2011) · Chemical Society Reviews · doi:10.1039/c1cs15113d · Cited by 6,363

Multidrug resistance in cancer: role of ATP–dependent transporters

Gottesman, M. M., Fojo, T., & Bates, S. E. (2002) · Nature Reviews Cancer · doi:10.1038/nrc706 · Cited by 5,536

BODIPY Dyes and Their Derivatives: Syntheses and Spectroscopic Properties

Loudet, A., & Burgess, K. (2007) · Chemical Reviews · doi:10.1021/cr078381n · Cited by 5,238

Photodynamic therapy of cancer: An update

Agostinis, P., Berg, K., Cengel, K. A., Foster, T. H., Girotti, A. W., Gollnick, S. O., Hahn, S. M., Hamblin, M. R., Juzeniene, A., Kessel, D., et al. (2011) · CA: A Cancer Journal for Clinicians · doi:10.3322/caac.20114 · Cited by 5,145

Why Do Cancers Have High Aerobic Glycolysis?

Gatenby, R. A., & Gillies, R. J. (2004) · Nature reviews. Cancer · doi:10.1038/nrc1478 · Cited by 4,784

Antibiotic resistance of bacteria in biofilms

Stewart, P. S., & Costerton, J. W. (2001) · The Lancet · doi:10.1016/s0140-6736(01)05321-1 · Cited by 4,596

Gadolinium(III) Chelates as MRI Contrast Agents: Structure, Dynamics, and Applications

Caravan, P. D., Ellison, J. J., McMurry, T. J., & Lauffer, R. B. (1999) · Chemical Reviews · doi:10.1021/cr980440x · Cited by 4,571

Chemical Sensors Based on Amplifying Fluorescent Conjugated Polymers

Thomas, S. W., Joly, G. D., & Swager, T. M. (2007) · Chemical Reviews · doi:10.1021/cr0501339 · Cited by 4,208

Mechanisms of biofilm resistance to antimicrobial agents

Mah, T.-F. C., & O'Toole, G. A. (2001) · Trends in Microbiology · doi:10.1016/s0966-842x(00)01913-2 · Cited by 3,921

Nonlinear magic: multiphoton microscopy in the biosciences

Zipfel, W. R., Williams, R. M., & Webb, W. W. (2003) · Nature Biotechnology · doi:10.1038/nbt899 · Cited by 3,911

Glutathione Metabolism and Its Implications for Health

Wu, G., Lupton, J. R., Turner, N. D., Fang, Y.-Z., & Yang, S. (2004) · The Journal of Nutrition · doi:10.1093/jn/134.3.489 · Cited by 3,842

Atomic structure and chemistry of human serum albumin

He, X. M., & Carter, D. C. (1992) · Nature · doi:10.1038/358209a0 · Cited by 3,833

Conjugated Polymer-Based Chemical Sensors

McQuade, D. T., Pullen, A. E., & Swager, T. M. (2000) · Chemical Reviews · doi:10.1021/cr9801014 · Cited by 3,734

Handbook Of Biological Confocal Microscopy

Pawley, J. B. (2006) · Springer eBooks · doi:10.1007/978-0-387-45524-2 · Cited by 3,685

Liposome: classification, preparation, and applications

Akbarzadeh, A., Rezaei-Sadabady, R., Davaran, S., Joo, S. W., Zarghami, N., Hanifehpour, Y., Samiei, M., Kouhi, M., & Nejati‐Koshki, K. (2013) · Nanoscale Research Letters · doi:10.1186/1556-276x-8-102 · Cited by 3,648

Targeting multidrug resistance in cancer

Szakács, G., Paterson, J. K., Ludwig, J. A., Booth-Genthe, C., & Gottesman, M. M. (2006) · Nature Reviews Drug Discovery · doi:10.1038/nrd1984 · Cited by 3,609

GLUTATHIONE TRANSFERASES

Hayes, J. D., Flanagan, J. U., & Jowsey, I. R. (2004) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.45.120403.095857 · Cited by 3,565

Malignant Gliomas in Adults

Wen, P. Y., & Kesari, S. (2008) · New England Journal of Medicine · doi:10.1056/nejmra0708126 · Cited by 3,511

Effect of pegylation on pharmaceuticals

Harris, J. M., & Chess, R. B. (2003) · Nature Reviews Drug Discovery · doi:10.1038/nrd1033 · Cited by 3,431

Carbonic anhydrases: novel therapeutic applications for inhibitors and activators

Supuran, C. T. (2008) · Nature Reviews Drug Discovery · doi:10.1038/nrd2467 · Cited by 3,226

Control of apoptosis by the BCL-2 protein family: implications for physiology and therapy

Czabotar, P. E., Lessene, G., Strasser, A., & Adams, J. M. (2014) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3722 · Cited by 3,219

RGD AND OTHER RECOGNITION SEQUENCES FOR INTEGRINS

Ruoslahti, E. (1996) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.12.1.697 · Cited by 3,191

N-Heterocyclic Carbenes in Late Transition Metal Catalysis

Díez‐González, S., Marion, N., & Nolan, S. P. (2009) · Chemical Reviews · doi:10.1021/cr900074m · Cited by 3,074

Nanoparticles in Photodynamic Therapy

Lucky, S. S., Soo, K. C., & Zhang, Y. (2015) · Chemical Reviews · doi:10.1021/cr5004198 · Cited by 2,999

Second window for in vivo imaging

Smith, A. M., Mancini, M. C., & Nie, S. (2009) · Nature Nanotechnology · doi:10.1038/nnano.2009.326 · Cited by 2,848

Über Elementarakte mit zwei Quantensprüngen

Göppert-Mayer, M. (1931) · Annalen der Physik · doi:10.1002/andp.19314010303 · Cited by 2,695

Effects of particle size and surface charge on cellular uptake and biodistribution of polymeric nanoparticles

He, C., Hu, Y., Yin, L., Tang, C., & Yin, C. (2010) · Biomaterials · doi:10.1016/j.biomaterials.2010.01.065 · Cited by 2,607

J‐Aggregates: From Serendipitous Discovery to Supramolecular Engineering of Functional Dye Materials

Würthner, F., Kaiser, T. E., & Saha‐Möller, C. R. (2011) · Angewandte Chemie International Edition · doi:10.1002/anie.201002307 · Cited by 2,597

Mitochondria and cell death: outer membrane permeabilization and beyond

Tait, S. W. G., & Green, D. R. (2010) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2952 · Cited by 2,593

The Next Generation of Platinum Drugs: Targeted Pt(II) Agents, Nanoparticle Delivery, and Pt(IV) Prodrugs

Johnstone, T. C., Suntharalingam, K., & Lippard, S. J. (2016) · Chemical Reviews · doi:10.1021/acs.chemrev.5b00597 · Cited by 2,508

Reactive Oxygen Species (ROS)-Based Nanomedicine

Yang, B., Chen, Y., & Shi, J. (2019) · Chemical Reviews · doi:10.1021/acs.chemrev.8b00626 · Cited by 2,477

Functional Nanomaterials for Phototherapies of Cancer

Cheng, L., Wang, C., Feng, L., Yang, K., & Liu, Z. (2014) · Chemical Reviews · doi:10.1021/cr400532z · Cited by 2,438

Mitochondria and cancer

Wallace, D. C. (2012) · Nature Reviews Cancer · doi:10.1038/nrc3365 · Cited by 2,404

Review of iron-free Fenton-like systems for activating H2O2 in advanced oxidation processes

Bokare, A. D., & Choi, W. (2014) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2014.04.054 · Cited by 2,402

Imaging and Photodynamic Therapy: Mechanisms, Monitoring, and Optimization

Celli, J. P., Spring, B. Q., Rizvi, I., Evans, C. L., Samkoe, K. S., Verma, S., Pogue, B. W., & Hasan, T. G. (2010) · Chemical Reviews · doi:10.1021/cr900300p · Cited by 2,359

Histone deacetylase inhibitors and the promise of epigenetic (and more) treatments for cancer

Minucci, S., & Pelicci, P. G. (2006) · Nature reviews. Cancer · doi:10.1038/nrc1779 · Cited by 2,234

New Strategies for Fluorescent Probe Design in Medical Diagnostic Imaging

Kobayashi, H., Ogawa, M., Alford, R. E., Choyke, P. L., & Urano, Y. (2009) · Chemical Reviews · doi:10.1021/cr900263j · Cited by 2,205

Understanding the diversity of membrane lipid composition

原山, 武., & Riezman, H. (2018) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm.2017.138 · Cited by 2,140

Physical Mechanisms of Generation and Deactivation of Singlet Oxygen

Schweitzer, C., & Schmidt, R. (2003) · Chemical Reviews · doi:10.1021/cr010371d · Cited by 2,123

Reactive oxygen species generating systems meeting challenges of photodynamic cancer therapy

Zhou, Z., Song, J., Nie, L., & Chen, X. S. (2016) · Chemical Society Reviews · doi:10.1039/c6cs00271d · Cited by 2,121

New photosensitizers for photodynamic therapy

Abrahamse, H., & Hamblin, M. R. (2016) · Biochemical Journal · doi:10.1042/bj20150942 · Cited by 2,112

BODIPY dyes in photodynamic therapy

Kamkaew, A., Lim, S. H., Lee, H. B., Kiew, L. V., Chung, L. Y., & Burgess, K. (2013) · Chem. Soc. Rev. · doi:10.1039/c2cs35216h · Cited by 2,104

The role of porphyrin chemistry in tumor imaging and photodynamic therapy

Ethirajan, M., Chen, Y., Joshi, P., & Pandey, R. K. (2010) · Chemical Society Reviews · doi:10.1039/b915149b · Cited by 2,038

Phase III Trial of Carboplatin and Paclitaxel Compared With Cisplatin and Paclitaxel in Patients With Optimally Resected Stage III Ovarian Cancer: A Gynecologic Oncology Group Study

Ozols, R. F., Bundy, B. N., Greer, B. E., Fowler, J. M., Clarke‐Pearson, D. L., Burger, R. A., Mannel, R. S., DeGeest, K., Hartenbach, E. M., & Baergen, R. N. (2003) · Journal of Clinical Oncology · doi:10.1200/jco.2003.02.153 · Cited by 2,034

Two‐Photon Absorption and the Design of Two‐Photon Dyes

Pawlicki, M., Collins, H. A., Denning, R. G., & Anderson, H. L. (2009) · Angewandte Chemie International Edition · doi:10.1002/anie.200805257 · Cited by 2,022

Fluorescent Chemosensors Based on Spiroring-Opening of Xanthenes and Related Derivatives

Chen, X., Pradhan, T., Wang, F., Kim, J. S., & Yoon, J. (2011) · Chemical Reviews · doi:10.1021/cr200201z · Cited by 1,997

Mitochondria: More Than Just a Powerhouse

McBride, H. M., Neuspiel, M., & Wasiak, S. (2006) · Current Biology · doi:10.1016/j.cub.2006.06.054 · Cited by 1,985

The inflammasome: a caspase-1-activation platform that regulates immune responses and disease pathogenesis

Franchi, L., Eigenbrod, T., Muñoz-Planillo, R., & Nuñez, G. (2009) · Nature Immunology · doi:10.1038/ni.1703 · Cited by 1,834

Nanotechnology for Multimodal Synergistic Cancer Therapy

Fan, W., Yung, B. C., Huang, P., & Chen, X. S. (2017) · Chemical Reviews · doi:10.1021/acs.chemrev.7b00258 · Cited by 1,813

Signals from the lysosome: a control centre for cellular clearance and energy metabolism

Settembre, C., Fraldi, A., Medina, D. L., & Ballabio, A. (2013) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3565 · Cited by 1,755

Activatable Photosensitizers for Imaging and Therapy

Lovell, J. F., Liu, T. W. B., Chen, J., & Zheng, G. (2010) · Chemical Reviews · doi:10.1021/cr900236h · Cited by 1,718

Hypoxia, HIF1 and glucose metabolism in the solid tumour

Denko, N. C. (2008) · Nature Reviews Cancer · doi:10.1038/nrc2468 · Cited by 1,707

Overcoming the Achilles' heel of photodynamic therapy

Fan, W., Huang, P., & Chen, X. S. (2016) · Chemical Society Reviews · doi:10.1039/c6cs00616g · Cited by 1,693

Mitochondria-Targeted Triphenylphosphonium-Based Compounds: Syntheses, Mechanisms of Action, and Therapeutic and Diagnostic Applications

Zielonka, J., Joseph, J., Sikora, A., Hardy, M., Ouari, O., Vasquez-Vivar, J., Cheng, G., Lopez, M., & Kalyanaraman, B. (2017) · Chemical Reviews · doi:10.1021/acs.chemrev.7b00042 · Cited by 1,683

Targeting mitochondria for cancer therapy

Fulda, S., Galluzzi, L., & Kroemer, G. (2010) · Nature Reviews Drug Discovery · doi:10.1038/nrd3137 · Cited by 1,678

Activating efficient phosphorescence from purely organic materials by crystal design

Bolton, O., Lee, K., Kim, H.-J., Lin, K. Y., & Kim, J. (2011) · Nature Chemistry · doi:10.1038/nchem.984 · Cited by 1,662

A new trend in rhodamine-based chemosensors: application of spirolactam ring-opening to sensing ions

Kim, H. N., Lee, M. H., Kim, H. J., Kim, J. S., & Yoon, J. (2008) · Chemical Society Reviews · doi:10.1039/b802497a · Cited by 1,652

A brief history of the antibiotic era: lessons learned and challenges for the future

Aminov, R. I. (2010) · Frontiers in Microbiology · doi:10.3389/fmicb.2010.00134 · Cited by 1,628

Nanoshell-Enabled Photothermal Cancer Therapy: Impending Clinical Impact

Lal, S., Clare, S. E., & Halas, N. J. (2008) · Accounts of Chemical Research · doi:10.1021/ar800150g · Cited by 1,627

Organic molecule-based photothermal agents: an expanding photothermal therapy universe

Jung, H. S., Verwilst, P., Sharma, A. K., Shin, J. W., Sessler, J. L., & Kim, J. S. (2018) · Chemical Society Reviews · doi:10.1039/c7cs00522a · Cited by 1,592

Intraoperative tumor-specific fluorescence imaging in ovarian cancer by folate receptor-α targeting: first in-human results

van Dam, G. M., Themelis, G., Crane, L. M. A., Harlaar, N. J., Pleijhuis, R. G., Kelder, W., Sarantopoulos, A., de Jong, J. S., Arts, H. J. G., van der Zee, A. G. J., et al. (2011) · Nature Medicine · doi:10.1038/nm.2472 · Cited by 1,585

Triplet photosensitizers: from molecular design to applications

Zhao, J., Wu, W., Sun, J., & Guo, S. (2013) · Chemical Society Reviews · doi:10.1039/c3cs35531d · Cited by 1,579

Smart micro/nanoparticles in stimulus-responsive drug/gene delivery systems

Karimi, M., Ghasemi, A., Zangabad, P. S., Rahighi, R., Basri, S. M. M., Mirshekari, H., Amiri, M., Shafaei, Z., Aslani, A., Bozorgomid, M., et al. (2016) · Chemical Society Reviews · doi:10.1039/c5cs00798d · Cited by 1,557

Nanochemistry and Nanomedicine for Nanoparticle-based Diagnostics and Therapy

Chen, G., Roy, I., Yang, C., & Prasad, P. N. (2016) · Chemical Reviews · doi:10.1021/acs.chemrev.5b00148 · Cited by 1,528

The role of apoptosis in response to photodynamic therapy: what, where, why, and how

Oleinick, N. L., Morris, R. L., & Belitchenko, I. (2002) · Photochemical & Photobiological Sciences · doi:10.1039/b108586g · Cited by 1,502

Cholesterol and the cell membrane

Yèagle, P. L. (1985) · Biochimica et Biophysica Acta (BBA) - Reviews on Biomembranes · doi:10.1016/0304-4157(85)90011-5 · Cited by 1,492

Hollow MnO2 as a tumor-microenvironment-responsive biodegradable nano-platform for combination therapy favoring antitumor immune responses

Yang, G., Xu, L., Chao, Y., Xu, J., Sun, X., Wu, Y., Peng, R., & Liu, Z. (2017) · Nature Communications · doi:10.1038/s41467-017-01050-0 · Cited by 1,491

Transition Metal Complexes and Photodynamic Therapy from a Tumor-Centered Approach: Challenges, Opportunities, and Highlights from the Development of TLD1433

Monro, S. M. A., Colón, K. L., Yin, H., Roque, J. A., Konda, P., Gujar, S. A., Thummel, R. P., Lilge, L. D., Cameron, C. G., & McFarland, S. A. (2018) · Chemical Reviews · doi:10.1021/acs.chemrev.8b00211 · Cited by 1,479

In vivo photodynamic therapy using upconversion nanoparticles as remote-controlled nanotransducers

Idris, N. M., Gnanasammandhan, M. K., Zhang, J., Ho, P. C., Mahendran, R., & Zhang, Y. (2012) · Nature Medicine · doi:10.1038/nm.2933 · Cited by 1,467

A review of NIR dyes in cancer targeting and imaging

Luo, S., Zhang, E., Su, Y., Cheng, T., & Shi, C. (2011) · Biomaterials · doi:10.1016/j.biomaterials.2011.06.024 · Cited by 1,459

Lysosomal membrane permeabilization in cell death

Boya, P., & Kroemer, G. (2008) · Oncogene · doi:10.1038/onc.2008.310 · Cited by 1,456

Facile Catalyst Separation Without Water: Fluorous Biphase Hydroformylation of Olefins

Horváth, I. T., & Rábai, J. (1994) · Science · doi:10.1126/science.266.5182.72 · Cited by 1,430

Carbon Nanomaterials for Biological Imaging and Nanomedicinal Therapy

Hong, G., Diao, S., Antaris, A. L., & Dai, H. (2015) · Chemical Reviews · doi:10.1021/acs.chemrev.5b00008 · Cited by 1,403

BODIPY-based probes for the fluorescence imaging of biomolecules in living cells

Kowada, T., Maeda, H., & Kikuchi, K. (2015) · Chemical Society Reviews · doi:10.1039/c5cs00030k · Cited by 1,387

Glutathione-responsive nano-vehicles as a promising platform for targeted intracellular drug and gene delivery

Cheng, R., Feng, F., Meng, F., Deng, C., Feijén, J., & Zhong, Z. (2011) · Journal of Controlled Release · doi:10.1016/j.jconrel.2011.01.030 · Cited by 1,367

Structural modification strategies for the rational design of red/NIR region BODIPYs

Lü, H., Mack, J. P., Yang, Y., & Shen, Z. (2014) · Chemical Society Reviews · doi:10.1039/c4cs00030g · Cited by 1,343

Two-Photon Excitation in Ca F 2 : Eu 2 +

Kaiser, W., & Garrett, C. G. B. (1961) · Physical Review Letters · doi:10.1103/physrevlett.7.229 · Cited by 1,342

Biosensing by luminogens with aggregation-induced emission characteristics

Kwok, R. T. K., Leung, C. W. T., Lam, J. W. Y., & Tang, B. Z. (2014) · Chemical Society Reviews · doi:10.1039/c4cs00325j · Cited by 1,303

Klebsiella pneumoniae: a major worldwide source and shuttle for antibiotic resistance

Navon‐Venezia, S., Kondratyeva, K., & Carattoli, A. (2017) · FEMS Microbiology Reviews · doi:10.1093/femsre/fux013 · Cited by 1,302

Singlet oxygen: there is indeed something new under the sun

Ogilby, P. R. (2010) · Chemical Society Reviews · doi:10.1039/b926014p · Cited by 1,292

Recent progress in photosensitizers for overcoming the challenges of photodynamic therapy: from molecular design to application

Zhao, X., Liu, J., Fan, J., Chao, H., & Peng, X. (2021) · Chemical Society Reviews · doi:10.1039/d0cs00173b · Cited by 1,278

Phosphorescent heavy-metal complexes for bioimaging

Zhao, Q., Huang, C., & Li, F. (2011) · Chemical Society Reviews · doi:10.1039/c0cs00114g · Cited by 1,262

Phosphorescent chemosensors based on heavy-metal complexes

Zhao, Q., Li, F., & Huang, C. (2010) · Chemical Society Reviews · doi:10.1039/b915340c · Cited by 1,257

Cancer biomarker detection: recent achievements and challenges

Wu, L. J., & Qu, X. (2015) · Chemical Society Reviews · doi:10.1039/c4cs00370e · Cited by 1,252

Biomedical Applications of Supramolecular Systems Based on Host–Guest Interactions

Ma, X., & Zhao, Y. (2014) · Chemical Reviews · doi:10.1021/cr500392w · Cited by 1,252

Synthesis and Characterization of Phosphorescent Cyclometalated Iridium Complexes

Lamansky, S., Djurovich, P. I., Murphy, D. L., Abdel-Razzaq, F., Kwong, R. C., Tsyba, I. M., Bortz, M., Mui, B., Bau, R., & Thompson, M. E. (2001) · Inorganic Chemistry · doi:10.1021/ic0008969 · Cited by 1,240

The integrins

Takada, Y., Ye, X., & Simon, S. I. (2007) · Genome biology · doi:10.1186/gb-2007-8-5-215 · Cited by 1,204

Nanoparticles in photodynamic therapy: An emerging paradigm

Chatterjee, D. K., Fong, E. L. S., & Zhang, Y. (2008) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2008.08.003 · Cited by 1,202

Stem-cell therapy for cardiac disease

Segers, V. F. M., & Lee, R. T. (2008) · Nature · doi:10.1038/nature06800 · Cited by 1,192

Blood–brain barrier delivery

Pardridge, W. M. (2007) · Drug Discovery Today · doi:10.1016/j.drudis.2006.10.013 · Cited by 1,191

Porphyrin and Nonporphyrin Photosensitizers in Oncology: Preclinical and Clinical Advances in Photodynamic Therapy

O’Connor, A. E., Gallagher, W. M., & Byrne, A. T. (2009) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.2009.00585.x · Cited by 1,191

Molecular Design of Benzodithiophene-Based Organic Photovoltaic Materials

Yao, H., Ye, L., Zhang, H., Li, S., Zhang, S., & Hou, J. (2016) · Chemical Reviews · doi:10.1021/acs.chemrev.6b00176 · Cited by 1,188

Inverse electron demand Diels–Alder reactions in chemical biology

Oliveira, B. L., Guo, Z., & Bernardes, G. J. L. (2017) · Chemical Society Reviews · doi:10.1039/c7cs00184c · Cited by 1,186

Lipid droplets: a unified view of a dynamic organelle

Martin, S., & Parton, R. G. (2006) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1912 · Cited by 1,179

Innovative Strategies for Hypoxic‐Tumor Photodynamic Therapy

Li, X., Kwon, N., Guo, T., Liu, Z., & Yoon, J. (2018) · Angewandte Chemie International Edition · doi:10.1002/anie.201805138 · Cited by 1,178

Discovery and Development of Folic-Acid-Based Receptor Targeting for Imaging and Therapy of Cancer and Inflammatory Diseases

Low, P. S., Henne, W. A., & Doorneweerd, D. D. (2007) · Accounts of Chemical Research · doi:10.1021/ar7000815 · Cited by 1,174

Water-Soluble Conjugated Polymers for Imaging, Diagnosis, and Therapy

Zhu, C., Liu, L., Yang, Q., Lv, F., & Wang, S. (2012) · Chemical Reviews · doi:10.1021/cr200263w · Cited by 1,171

Antimicrobial strategies centered around reactive oxygen species – bactericidal antibiotics, photodynamic therapy, and beyond

Vatansever, F., Melo, W., Avci, P., Vecchio, D., Sadasivam, M., Gupta, A., Chandran, R., Karimi, M., Parizotto, N. A., Yin, R., et al. (2013) · FEMS Microbiology Reviews · doi:10.1111/1574-6976.12026 · Cited by 1,157

Peptide Receptors as Molecular Targets for Cancer Diagnosis and Therapy

Reubi, J. C. (2003) · Endocrine Reviews · doi:10.1210/er.2002-0007 · Cited by 1,144

Untitled work

(1996) · PubMed · Cited by 1,141

Apoptosis and Clearance of Apoptotic Cells

Nagata, S. (2018) · Annual Review of Immunology · doi:10.1146/annurev-immunol-042617-053010 · Cited by 1,135

Energy metabolism in tumor cells

Moreno‐Sánchez, R., Rodríguez‐Enríquez, S., Marín‐Hernández, Á., & Saavedra, E. (2007) · FEBS Journal · doi:10.1111/j.1742-4658.2007.05686.x · Cited by 1,121

Recent Development of Chemosensors Based on Cyanine Platforms

Sun, W. C., Guo, S., Hu, C., Fan, J., & Peng, X. (2016) · Chemical Reviews · doi:10.1021/acs.chemrev.6b00001 · Cited by 1,121

Supramolecular photosensitizers rejuvenate photodynamic therapy

Li, X., Lee, S., & Yoon, J. (2018) · Chemical Society Reviews · doi:10.1039/c7cs00594f · Cited by 1,117

The unique role of nanoparticles in nanomedicine: imaging, drug delivery and therapy

Doane, T. L., & Burda, C. (2012) · Chemical Society Reviews · doi:10.1039/c2cs15260f · Cited by 1,113

From Mechanism to Mouse: A Tale of Two Bioorthogonal Reactions

Sletten, E. M., & Bertozzi, C. R. (2011) · Accounts of Chemical Research · doi:10.1021/ar200148z · Cited by 1,095

Photothermally Enhanced Photodynamic Therapy Delivered by Nano-Graphene Oxide

Tian, B., Wang, C., Zhang, S., Feng, L., & Liu, Z. (2011) · ACS Nano · doi:10.1021/nn201560b · Cited by 1,082

Engineered T cells: the promise and challenges of cancer immunotherapy

Fesnak, A. D., June, C. H., & Levine, B. L. (2016) · Nature Reviews Cancer · doi:10.1038/nrc.2016.97 · Cited by 1,074

Cancer cell–selective in vivo near infrared photoimmunotherapy targeting specific membrane molecules

Mitsunaga, M., Ogawa, M., Kosaka, N., Rosenblum, L. T., Choyke, P. L., & Kobayashi, H. (2011) · Nature Medicine · doi:10.1038/nm.2554 · Cited by 1,064

Cellular Incorporation of Unnatural Amino Acids and Bioorthogonal Labeling of Proteins

Lang, K., & Chin, J. W. (2014) · Chemical Reviews · doi:10.1021/cr400355w · Cited by 1,051

Integrins in angiogenesis and lymphangiogenesis

Avraamides, C. J., Garmy-Susini, B., & Varner, J. A. (2008) · Nature Reviews Cancer · doi:10.1038/nrc2353 · Cited by 1,050

The Bacterial Glycocalyx in Nature and Disease

Costerton, J. W., Irvin, R. T., & Cheng, K.-J. (1981) · Annual Review of Microbiology · doi:10.1146/annurev.mi.35.100181.001503 · Cited by 1,040

Zwitterionic hydrogels implanted in mice resist the foreign-body reaction

Zhang, L., Cao, Z., Bai, T., Carr, L., Ella-Menye, J.-R., Irvin, C., Ratner, B. D., & Jiang, S. (2013) · Nature Biotechnology · doi:10.1038/nbt.2580 · Cited by 1,035

The development of anticancer ruthenium( ii ) complexes: from single molecule compounds to nanomaterials

Zeng, L., Gupta, P., Chen, Y., Wang, E., Ji, L., Chao, H., & Chen, Z. (2017) · Chemical Society Reviews · doi:10.1039/c7cs00195a · Cited by 1,027

Functionalized Nano-MoS2 with Peroxidase Catalytic and Near-Infrared Photothermal Activities for Safe and Synergetic Wound Antibacterial Applications

Yin, W., Yu, J., Lv, F., Yan, L., Zheng, L., Gu, Z., & Zhao, Y. (2016) · ACS Nano · doi:10.1021/acsnano.6b05810 · Cited by 1,005

The impact of the unfolded protein response on human disease

Wang, S., & Kaufman, R. J. (2012) · The Journal of Cell Biology · doi:10.1083/jcb.201110131 · Cited by 992

The biophysics and cell biology of lipid droplets

Thiam, A. R., Farese Jr, R. V., & Walther, T. C. (2013) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3699 · Cited by 986

The In Vitro Migration Capacity of Human Bone Marrow Mesenchymal Stem Cells: Comparison of Chemokine and Growth Factor Chemotactic Activities

Ponte, A. L., Marais, E., Gallay, N., Langonné, A., Delorme, B., Hérault, O., Charbord, P., & Domenech, J. (2007) · Stem Cells · doi:10.1634/stemcells.2007-0054 · Cited by 943

Perfluorocarbon nanoparticles enhance reactive oxygen levels and tumour growth inhibition in photodynamic therapy

Cheng, Y., Cheng, H., Jiang, C., Qiu, X., Wang, K., Huan, W., Yuan, A., Wu, J., & Hu, Y. (2015) · Nature Communications · doi:10.1038/ncomms9785 · Cited by 941

In Vitro Demonstration of the Heavy-Atom Effect for Photodynamic Therapy

Gorman, A., KILLORAN, J. J., O'Shea, C., Kenna, T., Gallagher, W. M., & O’Shea, D. F. (2004) · Journal of the American Chemical Society · doi:10.1021/ja047649e · Cited by 920

Functionalized cucurbiturils and their applications

Kim, K., Selvapalam, N., Ko, Y. H., Park, K. M., Kim, D., & Kim, J. (2006) · Chemical Society Reviews · doi:10.1039/b603088m · Cited by 919

Monitoring of relative mitochondrial membrane potential in living cells by fluorescence microscopy.

Johnson, L. V., Walsh, M. L., Bockus, B. J., & Chen, L. B. (1981) · The Journal of Cell Biology · doi:10.1083/jcb.88.3.526 · Cited by 914

Antimicrobial photodynamic therapy – what we know and what we don’t

Cieplik, F., Deng, D., Crielaard, W., Buchalla, W., Hellwig, E., Al-Ahmad, A., & Maisch, T. (2018) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2018.1467876 · Cited by 902

Proteomic applications for the early detection of cancer

Wulfkuhle, J. D., Liotta, L. A., & Petricoin, E. F. (2003) · Nature reviews. Cancer · doi:10.1038/nrc1043 · Cited by 902

Lanthanide-doped upconversion nano-bioprobes: electronic structures, optical properties, and biodetection

Zheng, W., Huang, P., Tu, D., Ma, E., Zhu, H., & Chen, X. (2014) · Chemical Society Reviews · doi:10.1039/c4cs00178h · Cited by 894

The triplet excited state of Bodipy: formation, modulation and application

Zhao, J., Xu, K., Yang, W., Wang, Z., & Zhong, F. (2015) · Chemical Society Reviews · doi:10.1039/c5cs00364d · Cited by 875

Photosensitizers with Aggregation‐Induced Emission: Materials and Biomedical Applications

Hu, F., Xu, S., & Liu, B. (2018) · Advanced Materials · doi:10.1002/adma.201801350 · Cited by 859

Highly Efficient and Photostable Photosensitizer Based on BODIPY Chromophore

Yogo, T., Urano, Y., Ishitsuka, Y., Maniwa, F., & Nagano, T. (2005) · Journal of the American Chemical Society · doi:10.1021/ja0528533 · Cited by 854

Oncologic photodynamic therapy photosensitizers: A clinical review

Allison, R. R., & Sibata, C. H. (2010) · Photodiagnosis and Photodynamic Therapy · doi:10.1016/j.pdpdt.2010.02.001 · Cited by 840

Inhibition of Glycolysis in Cancer Cells: A Novel Strategy to Overcome Drug Resistance Associated with Mitochondrial Respiratory Defect and Hypoxia

Xu, R., Pelicano, H., Zhou, Y. N., Carew, J. S., Feng, L., Bhalla, K. N., Keating, M. J., & Huang, P. (2005) · Cancer Research · doi:10.1158/0008-5472.613.65.2 · Cited by 835

Deep blue phosphorescent organic light-emitting diodes with very high brightness and efficiency

Lee, J., Chen, H., Batagoda, T., Coburn, C., Djurovich, P. I., Thompson, M. E., & Forrest, S. R. (2015) · Nature Materials · doi:10.1038/nmat4446 · Cited by 834

Disulfide-Cleavage-Triggered Chemosensors and Their Biological Applications

Lee, M. H., Yang, Z., Lim, C. W., Lee, Y. H., Dongbang, S., Kang, C., & Kim, J. S. (2013) · Chemical Reviews · doi:10.1021/cr300358b · Cited by 829

Fluorescent chemical probes for accurate tumor diagnosis and targeting therapy

Gao, M., Yu, F., Lv, C., Choo, J., & Chen, L. (2017) · Chemical Society Reviews · doi:10.1039/c6cs00908e · Cited by 827

Mitochondria and Mitophagy

Kubli, D. A., & Gustafsson, Å. B. (2012) · Circulation Research · doi:10.1161/circresaha.112.265819 · Cited by 825

Mechanisms in photodynamic therapy: part two—cellular signaling, cell metabolism and modes of cell death

Castaño, A. P., Demidova, T. N., & Hamblin, M. R. (2005) · Photodiagnosis and Photodynamic Therapy · doi:10.1016/s1572-1000(05)00030-x · Cited by 797

Opportunities and challenges of radiotherapy for treating cancer

Schaue, D., & McBride, W. H. (2015) · Nature Reviews Clinical Oncology · doi:10.1038/nrclinonc.2015.120 · Cited by 784

EGF receptor trafficking: consequences for signaling and cancer

Tomas, A., Futter, C. E., & Eden, E. R. (2014) · Trends in Cell Biology · doi:10.1016/j.tcb.2013.11.002 · Cited by 779

The Medicinal Applications of Imidazolium Carbene−Metal Complexes

Hindi, K. M., Panzner, M. J., Tessier, C. A., Cannon, C. L., & Youngs, W. J. (2009) · Chemical Reviews · doi:10.1021/cr800500u · Cited by 776

Antimicrobial photodynamic inactivation: a bright new technique to kill resistant microbes

Hamblin, M. R. (2016) · Current Opinion in Microbiology · doi:10.1016/j.mib.2016.06.008 · Cited by 776

Intermolecular Atom Transfer Radical Addition to Olefins Mediated by Oxidative Quenching of Photoredox Catalysts

Nguyen, J. D., Tucker, J. W., Konieczynska, M. D., & Stephenson, C. R. J. (2011) · Journal of the American Chemical Society · doi:10.1021/ja108560e · Cited by 774

Photodynamic therapy of cancer. Basic principles and applications

Juarranz, Á., Jaén, P., Sanz-Rodrı́guez, F., Cuevas, J., & González, S. (2008) · Clinical & Translational Oncology · doi:10.1007/s12094-008-0172-2 · Cited by 765

Specific light-up bioprobes based on AIEgen conjugates

Liang, J., Tang, B. Z., & Liu, B. (2015) · Chemical Society Reviews · doi:10.1039/c4cs00444b · Cited by 762

The unique features and promises of phthalocyanines as advanced photosensitisers for photodynamic therapy of cancer

Lo, P., Rodríguez‐Morgade, M. S., Pandey, R. K., Ng, D. K. P., Torres⊗, T., & Dumoulin, F. (2019) · Chemical Society Reviews · doi:10.1039/c9cs00129h · Cited by 759

Weekly nab -Paclitaxel in Combination With Carboplatin Versus Solvent-Based Paclitaxel Plus Carboplatin as First-Line Therapy in Patients With Advanced Non–Small-Cell Lung Cancer: Final Results of a Phase III Trial

Socinski, M. A., Bondarenko, I., Karaseva, N. A., Makhson, A. M., Vynnychenko, I. O., Okamoto, I., Hon, J. K., Hirsh, V., Bhar, P., Zhang, H., et al. (2012) · Journal of Clinical Oncology · doi:10.1200/jco.2011.39.5848 · Cited by 758

Nanoscale Metal–Organic Framework for Highly Effective Photodynamic Therapy of Resistant Head and Neck Cancer

Lu, K., He, C., & Lin, W. (2014) · Journal of the American Chemical Society · doi:10.1021/ja508679h · Cited by 747

Ruthenium(ii) polypyridyl complexes and DNA—from structural probes to cellular imaging and therapeutics

Gill, M. R., & Thomas, J. A. (2012) · Chemical Society Reviews · doi:10.1039/c2cs15299a · Cited by 747

Emerging Strategies of Cancer Therapy Based on Ferroptosis

Shen, Z., Song, J., Yung, B. C., Zhou, Z., Wu, A., & Chen, X. S. (2018) · Advanced Materials · doi:10.1002/adma.201704007 · Cited by 744

Cell Death Pathways in Photodynamic Therapy of Cancer

Mróz, P., Yaroslavsky, A., Kharkwal, G. B., & Hamblin, M. R. (2011) · Cancers · doi:10.3390/cancers3022516 · Cited by 738

Nanoparticles of Conjugated Polymers

Pecher, J., & Mecking, S. (2010) · Chemical Reviews · doi:10.1021/cr100132y · Cited by 725

Enzyme-responsive polymeric assemblies, nanoparticles and hydrogels

Hu, J., Zhang, G., & Liu, S. (2012) · Chemical Society Reviews · doi:10.1039/c2cs35103j · Cited by 725

Smart Human Serum Albumin-Indocyanine Green Nanoparticles Generated by Programmed Assembly for Dual-Modal Imaging-Guided Cancer Synergistic Phototherapy

Sheng, Z., Hu, D., Zheng, M., Zhao, P., Liu, H., Gao, D., Gong, P., Gao, G., Zhang, P., Ma, Y., et al. (2014) · ACS Nano · doi:10.1021/nn5062386 · Cited by 724

Subcellular targeting strategies for drug design and delivery

Rajendran, L., Knölker, H., & Simons, K. (2009) · Nature Reviews Drug Discovery · doi:10.1038/nrd2897 · Cited by 714

Organically Modified Silica Nanoparticles Co-encapsulating Photosensitizing Drug and Aggregation-Enhanced Two-Photon Absorbing Fluorescent Dye Aggregates for Two-Photon Photodynamic Therapy

Kim, S., Ohulchanskyy, T. Y., Pudavar, H. E., Pandey, R. K., & Prasad, P. N. (2007) · Journal of the American Chemical Society · doi:10.1021/ja0680257 · Cited by 712

Free radicals and antioxidants – quo vadis?

Halliwell, B. (2011) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2010.12.002 · Cited by 706

Aggregation‐Induced Emission (AIE): A Historical Perspective

Würthner, F. (2020) · Angewandte Chemie International Edition · doi:10.1002/anie.202007525 · Cited by 696

Highly Conjugated, Acetylenyl Bridged Porphyrins: New Models for Light-Harvesting Antenna Systems

Lin, V. S. ‐., DiMagno, S. G., & Therien, M. J. (1994) · Science · doi:10.1126/science.8178169 · Cited by 694

Linear Side Chains in Benzo[1,2-b:4,5-b′]dithiophene–Thieno[3,4-c]pyrrole-4,6-dione Polymers Direct Self-Assembly and Solar Cell Performance

Cabanetos, C., Labban, A. E., Bartelt, J. A., Douglas, J. D., Mateker, W. R., Fréchet, J. M. J., McGehee, M. D., & Beaujuge, P. M. (2013) · Journal of the American Chemical Society · doi:10.1021/ja400365b · Cited by 691

Recent advances in the development of 1,8-naphthalimide based DNA targeting binders, anticancer and fluorescent cellular imaging agents

Banerjee, S., Veale, E. B., Phelan, C. M., Murphy, S. A., Tocci, G. M., Gillespie, L. J., Frimannsson, D. O., Kelly, J. M., & Gunnlaugsson, T. (2013) · Chemical Society Reviews · doi:10.1039/c2cs35467e · Cited by 691

Principles in the design of ligand-targeted cancer therapeutics and imaging agents

Srinivasarao, M., Galliford, C. V., & Low, P. S. (2015) · Nature Reviews Drug Discovery · doi:10.1038/nrd4519 · Cited by 687

Finding the Right (Bioorthogonal) Chemistry

Patterson, D. M., Nazarova, L. A., & Prescher, J. A. (2014) · ACS Chemical Biology · doi:10.1021/cb400828a · Cited by 679

Near-Infrared Light-Initiated Molecular Superoxide Radical Generator: Rejuvenating Photodynamic Therapy against Hypoxic Tumors

Li, M., Xia, J., Tian, R., Wang, J., Fan, J., Du, J., Long, S., Song, X., Foley, J. W., & Peng, X. (2018) · Journal of the American Chemical Society · doi:10.1021/jacs.8b08658 · Cited by 677

Photosensitizer-Loaded Gold Vesicles with Strong Plasmonic Coupling Effect for Imaging-Guided Photothermal/Photodynamic Therapy

Lin, J., Wang, S., Huang, P., Wang, Z., Chen, S., Niu, G., Li, W., He, J., Cui, D., Lu, G., et al. (2013) · ACS Nano · doi:10.1021/nn4011686 · Cited by 661

Enhanced Cisplatin Chemotherapy by Iron Oxide Nanocarrier-Mediated Generation of Highly Toxic Reactive Oxygen Species

Ma, P., Xiao, H., Chang, Y., Liu, J., Cheng, Z., Song, H., Zhang, X., Li, C., Wang, J., Gu, Z., et al. (2017) · Nano Letters · doi:10.1021/acs.nanolett.6b04269 · Cited by 654

Stimuli-Responsive Therapeutic Metallodrugs

Wang, X., Wang, X., Jin, S., Nafees, M., & Guo, Z. (2018) · Chemical Reviews · doi:10.1021/acs.chemrev.8b00209 · Cited by 654

Mitochondria in cancer cells: what is so special about them?

Gogvadze, V. G., Orrenius, S., & Zhivotovsky, B. (2008) · Trends in Cell Biology · doi:10.1016/j.tcb.2008.01.006 · Cited by 651

Heavy-Atom-Free Photosensitizers: From Molecular Design to Applications in the Photodynamic Therapy of Cancer

Nguyen, V.-N., Yan, Y., Zhao, J., & Yoon, J. (2021) · Accounts of Chemical Research · doi:10.1021/acs.accounts.0c00606 · Cited by 650

A Targetable Fluorescent Probe for Imaging Hydrogen Peroxide in the Mitochondria of Living Cells

Dickinson, B. C., & Chang, C. J. (2008) · Journal of the American Chemical Society · doi:10.1021/ja802355u · Cited by 646

Natural Products as Platforms To Overcome Antibiotic Resistance

Rossiter, S. E., Fletcher, M. H., & Wuest, W. M. (2017) · Chemical Reviews · doi:10.1021/acs.chemrev.7b00283 · Cited by 622

Molecular Interactions in Organic Nanoparticles for Phototheranostic Applications

Ng, K. K., & Zheng, G. (2015) · Chemical Reviews · doi:10.1021/acs.chemrev.5b00140 · Cited by 621

Bifunctionalized Mesoporous Silica‐Supported Gold Nanoparticles: Intrinsic Oxidase and Peroxidase Catalytic Activities for Antibacterial Applications

Tao, Y., Ju, E., Ren, J., & Qu, X. (2014) · Advanced Materials · doi:10.1002/adma.201405105 · Cited by 621

Critical Overview of the Use of Ru(II) Polypyridyl Complexes as Photosensitizers in One-Photon and Two-Photon Photodynamic Therapy

Heinemann, F., Karges, J., & Gasser, G. (2017) · Accounts of Chemical Research · doi:10.1021/acs.accounts.7b00180 · Cited by 615

Surface-Initiated Polymer Brushes in the Biomedical Field: Applications in Membrane Science, Biosensing, Cell Culture, Regenerative Medicine and Antibacterial Coatings

Krishnamoorthy, M., Hakobyan, S., Ramstedt, M., & Gautrot, J. E. (2014) · Chemical Reviews · doi:10.1021/cr500252u · Cited by 613

The molecular biology of cancer

Bertram, J. S. (2000) · Molecular Aspects of Medicine · doi:10.1016/s0098-2997(00)00007-8 · Cited by 610

Glutathione levels in human tumors

Gamcsik, M. P., Kasibhatla, M. S., Teeter, S. D., & Colvin, O. M. (2012) · Biomarkers · doi:10.3109/1354750x.2012.715672 · Cited by 608

Influence of Interchain Interactions on the Absorption and Luminescence of Conjugated Oligomers and Polymers: A Quantum-Chemical Characterization

Cornil, J., dos Santos, D. A., Xavier Crispin, A., Silbey, R., & Brédas, J. (1998) · Journal of the American Chemical Society · doi:10.1021/ja973761j · Cited by 603

DNA Cross-Linking Agents as Antitumor Drugs

Rajski, S. R., & Williams, R. M. (1998) · Chemical Reviews · doi:10.1021/cr9800199 · Cited by 596

Real-Time Monitoring of Cell Apoptosis and Drug Screening Using Fluorescent Light-Up Probe with Aggregation-Induced Emission Characteristics

Shi, H., Kwok, R. T. K., Liu, J., Xing, B., Tang, B. Z., & Liu, B. (2012) · Journal of the American Chemical Society · doi:10.1021/ja3064588 · Cited by 595

Recent developments in ruthenium anticancer drugs

Levina, A., Mitra, A., & Lay, P. A. (2009) · Metallomics · doi:10.1039/b904071d · Cited by 591

Organoiridium Complexes: Anticancer Agents and Catalysts

Liu, Z., & Sadler, P. J. (2014) · Accounts of Chemical Research · doi:10.1021/ar400266c · Cited by 580

UV-Emitting Upconversion-Based TiO 2 Photosensitizing Nanoplatform: Near-Infrared Light Mediated in Vivo Photodynamic Therapy via Mitochondria-Involved Apoptosis Pathway

Hou, Z., Zhang, Y., Deng, K., Chen, Y., Li, X., Deng, X., Cheng, Z., Lian, H., Li, C., & Lin, J. (2015) · ACS Nano · doi:10.1021/nn506107c · Cited by 578

Two-photon excitation nanoparticles for photodynamic therapy

Shen, Y., Shuhendler, A. J., Ye, D., Xu, J., & Chen, H. (2016) · Chemical Society Reviews · doi:10.1039/c6cs00442c · Cited by 577

Glycosylated Porphyrins, Phthalocyanines, and Other Porphyrinoids for Diagnostics and Therapeutics

Singh, S., Aggarwal, A., Bhupathiraju, N. V. S. D. K., Arianna, G., Tiwari, K., & Drain, C. M. (2015) · Chemical Reviews · doi:10.1021/acs.chemrev.5b00244 · Cited by 573

Luminescent Rhenium(I) and Iridium(III) Polypyridine Complexes as Biological Probes, Imaging Reagents, and Photocytotoxic Agents

Lo, K. K. (2015) · Accounts of Chemical Research · doi:10.1021/acs.accounts.5b00211 · Cited by 569

Targeted zwitterionic near-infrared fluorophores for improved optical imaging

Choi, H. S., Gibbs, S. L., Lee, J. H., Kim, S. H., Ashitate, Y., Liu, F., Hyun, H., Park, G., Xie, Y., Bae, S., et al. (2013) · Nature Biotechnology · doi:10.1038/nbt.2468 · Cited by 566

Nanomedicine and advanced technologies for burns: Preventing infection and facilitating wound healing

Jahromi, M. A. M., Zangabad, P. S., Basri, S. M. M., Zangabad, K. S., Ghamarypour, A., Aref, A. R., Karimi, M., & Hamblin, M. R. (2017) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2017.08.001 · Cited by 566

Release of High-Energy Water as an Essential Driving Force for the High-Affinity Binding of Cucurbit[n]urils

Biedermann, F., Uzunova, V. D., Scherman, O. A., Nau, W. M., & Simone, A. D. (2012) · Journal of the American Chemical Society · doi:10.1021/ja303309e · Cited by 565

Photodynamic therapy: a clinical reality in the treatment of cancer

Hopper, C. (2000) · The Lancet Oncology · doi:10.1016/s1470-2045(00)00166-2 · Cited by 563

High-efficiency electroluminescence and amplified spontaneous emission from a thermally activated delayed fluorescent near-infrared emitter

Kim, D.-H., D’Aléo, A., Chen, X., Sandanayaka, A. S. D., Yao, D., Zhao, L., Komino, T., Zaborova, E., Canard, G., Tsuchiya, Y., et al. (2018) · Nature Photonics · doi:10.1038/s41566-017-0087-y · Cited by 554

De Novo Design of Antimicrobial Polymers, Foldamers, and Small Molecules: From Discovery to Practical Applications

Tew, G. N., Scott, R. W., Klein, M. L., & DeGrado, W. F. (2009) · Accounts of Chemical Research · doi:10.1021/ar900036b · Cited by 553

Optimising the luminescence of platinum(II) complexes and their application in organic light emitting devices (OLEDs)☆

Williams, J. A. G., Develay, S., Rochester, D. L., & MURPHY, L. (2008) · Coordination Chemistry Reviews · doi:10.1016/j.ccr.2008.03.014 · Cited by 552

Activatable Photosensitizers: Agents for Selective Photodynamic Therapy

Li, X., Kolemen, S., Yoon, J., & Akkaya, E. U. (2017) · Advanced Functional Materials · doi:10.1002/adfm.201604053 · Cited by 544

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

Plasmonic silver and gold nanoparticles: shape- and structure-modulated plasmonic functionality for point-of-caring sensing, bio-imaging and medical therapy

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

Supramolecular Photosensitizer Enables Oxygen-Independent Generation of Hydroxyl Radicals for Photodynamic Therapy

Teng, 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

Recent advances in organic photosensitizers for tumor photodynamic therapy

Jin, Q., Huang, Y., Wang, W., Lan, H., Xiao, S., Zhang, W., & Geng, P. (2026) · Biofunctional Materials · doi:10.55092/bm20260006

Evolution and multifunctional engineering of photosensitizers: Advancing precision cancer therapy through photodynamic combinatorial strategies

Guo, J., Liu, J., Zhang, L., Zhu, D., Yan, T., & Zheng, Z. (2026) · Journal of Molecular Structure · doi:10.1016/j.molstruc.2026.145414 · Cited by 3

Role of Photosensitizers in Photodynamic Therapy of Cancer Treatment: A Comprehensive Review

Muruganantham, S. (2026) · German Journal of Pharmaceuticals and Biomaterials · doi:10.5530/gjpb.2025.4.11

Photosensitizers for Photodynamic Therapy

Lan, M., Zhao, S., Liu, W., Lee, C., Zhang, W., & Wang, P. (2019) · Advanced Healthcare Materials · doi:10.1002/adhm.201900132 · Cited by 1,105

Advances in photosensitizer-related design for photodynamic therapy

Zhou, Z., Zhang, L., Zhang, Z., & Liu, Z. (2021) · Asian Journal of Pharmaceutical Sciences · doi:10.1016/j.ajps.2020.12.003 · Cited by 100