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Photophysicochemical Light Antiproliferative vs cancer

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Photophysicochemical Light Antiproliferative vs cancer ( photophysicochemical-light-antiproliferative-vs-cancer )

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Materials 2020, 13, 2646 23 of 24 55. Da ̨browski, J.M.; Pucelik, B.; Regiel-Futyra, A.; Brindell, M.; Mazuryk, O.; Kyzioł, A.; Stochel, G.; Macyk, W.; Arnaut, L.G. Engineering of relevant photodynamic processes through structural modifications of metallotetrapyrrolic photosensitizers. Coord. Chem. Rev. 2016, 325, 67–101. [CrossRef] 56. Dempsey, J.; Zhang, Q.-W.; Oliver, A.G.; Smith, B.D. New tetralactam hosts for squaraine dyes. Org. Biomol. Chem. 2018, 16, 8976–8983. [CrossRef] [PubMed] 57. Paternò, G.M.; Barbero, N.; Galliano, S.; Barolo, C.; Lanzani, G.; Scotognella, F.; Borrelli, R. Excited state photophysics of squaraine dyes for photovoltaic applications: An alternative deactivation scenario. J. Mater. Chem. C 2018, 6, 2778–2785. [CrossRef] 58. Pascal, S.; Haefele, A.; Monnereau, C.; Charaf-Eddin, A.; Jacquemin, D.; Le Guennic, B.; Andraud, C.; Maury, O. Expanding the Polymethine Paradigm: Evidence for the Contribution of a Bis-Dipolar Electronic Structure. J. Phys. Chem. A 2014, 118, 4038–4047. [CrossRef] [PubMed] 59. Hassan, G.F.; Saad, N.E.H.; Hmadeh, M.; Karam, P. Enhancing porphyrin photostability when locked in metal—Organic frameworks. Dalton Trans. 2018, 47, 15765–15771. [CrossRef] [PubMed] 60. Merchan, M.; Ouk, T.-S.; Kubát, P.; Lang, K.; Coelho, C.; Verney, V.; Commereuc, S.; Leroux, F.; Sol, V.; Taviot-Gueho, C. Photostability and photobactericidal properties of porphyrin-layered double hydroxide-polyurethane composite films. J. Mater. Chem. B 2013, 1, 2139–2146. [CrossRef] [PubMed] 61. Da ̨browski, J.M.; Arnaut, L.G.; Pereira, M.; Monteiro, C.; Urbanska, K.; Simoes, S.; Stochel, G. New Halogenated Water-Soluble Chlorin and Bacteriochlorin as Photostable PDT Sensitizers: Synthesis, Spectroscopy, Photophysics, and in vitro Photosensitizing Efficacy. ChemMedChem 2010, 5, 1770–1780. [CrossRef] [PubMed] 62. Ferreira, J.; Menezes, P.F.C.; Sibata, C.H.; Allison, R.R.; Zucoloto, S.; E Silva, O.C.; Bagnato, V.S.; Silva, O.C.E., Jr.; Bagnato, V.S. Can efficiency of the photosensitizer be predicted by its photostability in solution? Laser Phys. 2009, 19, 1932–1938. [CrossRef] 63. Menezes, P.F.C.; Imasato, H.; Ferreira-Strixino, J.; Bagnato, V.S.; Sibata, C.H.; Perussi, J.R. Aggregation susceptibility on phototransformation of hematoporphyrin derivatives. Laser Phys. Lett. 2008, 5, 227–235. [CrossRef] 64. Ahmad, I.; Ahmed, S.; Anwar, Z.; Sheraz, M.A.; Sikorski, M. Photostability and Photostabilization of Drugs and Drug Products. Int. J. Photoenergy 2016, 2016, 8135608. [CrossRef] 65. Welankiwar, A.; Saudagar, S.; Kumar, J.; Barabde, A. Photostability Testing of Pharmaceutical Products. Int. Res. J. Pharm. 2013, 2, 11–15. [CrossRef] 66. Krasnovsky, A.J. Singlet oxygen and primary mechanisms of photodynamic therapy and photodynamic diseases. In Photodynamic Therapy at the Cellular Level; Research Signpost: Thiruvananthapuram, India, 2007; pp. 17–62. ISBN 978-81-308-0174-2. 67. DeRosa, M.; Crutchley, R.J. Photosensitized singlet oxygen and its applications. Coord. Chem. Rev. 2002, 233, 351–371. [CrossRef] 68. Wu, W.; Shao, X.; Zhao, J.; Wu, M. Controllable Photodynamic Therapy Implemented by Regulating Singlet Oxygen Efficiency. Adv. Sci. 2017, 4, 1700113. [CrossRef] [PubMed] 69. Sari, C.; Eyüpog ̆lu, F.C.; Deg ̆irmenciog ̆lu, I.; Bayrak, R. Synthesis of axially disubstituted silicon phthalocyanines and investigation of photodynamic effects on HCT-116 colorectal cancer cell line. Photodiagn. Photodyn. Ther. 2018, 23, 83–88. [CrossRef] [PubMed] 70. Serpe, L.; Ellena, S.; Barbero, N.; Foglietta, F.; Prandini, F.; Gallo, M.P.; Levi, R.; Barolo, C.; Canaparo, R.; Visentin, S. Squaraines bearing halogenated moieties as anticancer photosensitizers: Synthesis, characterization and biological evaluation. Eur. J. Med. Chem. 2016, 113, 187–197. [CrossRef] [PubMed] 71. Rusche, B. The 3Rs and animal welfare—Conflict or the way forward? Altex 2003, 20, 63–76. [PubMed] 72. Dai, X.; Cheng, H.; Bai, Z.; Li, J. Breast Cancer Cell Line Classification and Its Relevance with Breast Tumor Subtyping. J. Cancer 2017, 8, 3131–3141. [CrossRef] [PubMed] 73. Balaji, S.A.; Udupa, N.; Chamallamudi, M.R.; Gupta, V.; Rangarajan, A. Role of the Drug Transporter ABCC3 in Breast Cancer Chemoresistance. PLoS ONE 2016, 11, e0155013. [CrossRef] [PubMed] 74. International Standard (ISO). Biological Evaluation of Medical Devices. Part 5: Tests for In Vitro Cytotoxicity, 3rd ed.; ISO 10993 5; International Standard (ISO): Geneva, Switzerland, 2009. 75. Doktorovova, S.; Souto, E.B.; Silva, A.M. Nanotoxicology applied to solid lipid nanoparticles and nanostructured lipid carriers—A systematic review of in vitro data. Eur. J. Pharm. Biopharm. 2014, 87, 1–18. [CrossRef] [PubMed]

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