Amphiphilic Cationic Phthalocyanines for Photodynamic Therapy of Cancer

. 2022 Jul 26 ; 87 (9) : e202200133. [epub] 20220726

Status PubMed-not-MEDLINE Jazyk angličtina Země Německo Médium print-electronic

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid35880676

Grantová podpora
SVV 260 547 Charles University
PRIMUS/20/SCI/013 Charles University
GAUK 1620219 Charles University
19-14758Y Czech Science Foundation
21-14919J Czech Science Foundation

Effective interaction with biomembranes is essential for activity of photosensitizers; however, majority of them are highly charged symmetrical species. Amphiphilic cationic phthalocyanines differing in bulkiness of substitution on lipophilic part (-H, -SMe, -StBu) were therefore prepared. Compounds had high singlet oxygen production (ΦΔ =0.38-0.46, DMSO), good fluorescence emission (ΦF =0.21-0.26, DMSO), and log P values ranging -0.07-1.1 (1-octanol/PBS). Study of interaction with liposomes revealed that also bulky -StBu derivatives are able to enter biomembranes. Detail in vitro studies (toxicity, subcellular localization, type of cell death, and morphology) were performed. Compounds were characterized by excellent EC50 values in range of dozens of nM (HeLa, EA.hy926, MCF-7, HCT116), which were dependent on drug-light interval and reached plateau after 4 h on HeLa cells. Well-balanced lipophilicity with ability to interact with biomembranes rank these derivatives among perspective photosensitizers, even for vascular-targeted PDT (VTP) since they kill EA.hy926 without any preincubation time.

Zobrazit více v PubMed

C. G. Claessens, U. Hahn, T. Torres, Chem. Rec. 2008, 8, 75–97;

R. C. H. Wong, P. C. Lo, D. K. P. Ng, Coord. Chem. Rev. 2019, 379, 30–46;

M. Urbani, M. E. Ragoussi, M. K. Nazeeruddin, T. Torres, Coord. Chem. Rev. 2019, 381, 1–64;

G. Simonneaux, P. Tagliatesta, J. Porphyrins Phthalocyanines 2004, 8, 1166–1171;

C. M. Allen, W. M. Sharman, J. E. Van Lier, J. Porphyrins Phthalocyanines 2001, 5, 161–169;

L. Lochman, M. Machacek, M. Miletin, S. Uhlirova, K. Lang, K. Kirakci, P. Zimcik, V. Novakova, ACS Sens. 2019, 4, 1552–1559;

G. de la Torre, P. Vaquez, F. Agullo-Lopez, T. Torres, Chem. Rev. 2004, 104, 3723–3750.

M. R. Hamblin, Photochem. Photobiol. 2020, 96, 506–516.

V. Novakova, M. P. Donzello, C. Ercolani, P. Zimcik, P. A. Stuzhin, Coord. Chem. Rev. 2018, 361, 1–73.

J. F. Lovell, T. W. B. Liu, J. Chen, G. Zheng, Chem. Rev. 2010, 110, 2839–2857;

N. Mehraban, H. S. Freeman, Materials 2015, 8, 4421–4456;

T. Hoshi, N. Kobayashi, Coord. Chem. Rev. 2017, 345, 31–41;

M. B. Spesia, E. N. Durantini, Chem. Rec. 2022, 22.

M. Machacek, J. Demuth, P. Cermak, M. Vavreckova, L. Hruba, A. Jedlickova, P. Kubat, T. Simunek, V. Novakova, P. Zimcik, J. Med. Chem. 2016, 59, 9443–9456.

B. Ghazal, M. Machacek, M. A. Shalaby, V. Novakova, P. Zimcik, S. Makhseed, J. Med. Chem. 2017, 60, 6060–6076.

J. D. Huang, S. Q. Wang, P. C. Lo, W. P. Fong, W. H. Ko, D. K. P. Ng, New J. Chem. 2004, 28, 348–354;

J. T. F. Lau, P.-C. Lo, W.-P. Fong, D. K. P. Ng, Chem. Eur. J. 2011, 17, 7569–7577;

M. Göksel, M. Durmuş, Z. Biyiklioglu, Dalton Trans. 2021, 50, 2570–2584;

K. Mitra, M. C. T. Hartman, Org. Biomol. Chem. 2021, 19, 1168–1190;

S. Y. Al-Raqa, K. Khezami, E. N. Kaya, M. Durmus, Polyhedron 2021, 194.

J. Kollar, M. Machacek, M. Halaskova, J. Lenco, R. Kucera, J. Demuth, M. Rohlickova, K. Hasonova, M. Miletin, V. Novakova, P. Zimcik, J. Med. Chem. 2020, 63, 7616–7632.

K. A. D. F. Castro, J. A. Prandini, J. C. Biazzotto, J. P. C. Tomé, R. S. da Silva, L. M. O. Lourenço, Front. Chem. 2022, 10, article 825716;

H. Li, T. J. Jensen, F. R. Fronczek, M. G. Vicente, J. Med. Chem. 2008, 51, 502–511.

V. Novakova, P. Zimcik, M. Miletin, K. Kopecky, J. Ivincová, Tetrahedron Lett. 2010, 51, 1016–1018.

S. Makhseed, M. Machacek, W. Alfadly, A. Tuhl, M. Vinodh, T. Simunek, V. Novakova, P. Kubat, E. Rudolf, P. Zimcik, Chem. Commun. 2013, 49, 11149–11151.

M. Macháček, K. A. Carter, F. Kostelanský, D. Miranda, A. Seffouh, J. Ortega, T. Šimůnek, P. Zimčík, J. F. Lovell, J. Mater. Chem. B 2018, 6, 7298–7305.

G. De La Torre, C. G. Claessens, T. Torres, Eur. J. Org. Chem. 2000, 2821–2830.

D. Nawrot, M. Kolenič, J. Kuneš, F. Kostelansky, M. Miletin, V. Novakova, P. Zimcik, Tetrahedron 2018, 74, 594–599.

Y. Arslanoglu, A. M. Sevim, E. Hamuryudan, A. Gul, Dyes Pigm. 2006, 68, 129–132;

T. Nyokong, in: Functional Phthalocyanine Molecular Materials, Vol. 135 (Ed.: J. Jiang), 2010, pp. 45–87.

S. Tuncel, F. Dumoulin, J. Gailer, M. Sooriyaarachchi, D. Atilla, M. Durmus, D. Bouchu, H. Savoie, R. W. Boyle, V. Ahsen, Dalton Trans. 2011, 40, 4067–4079;

T. Nyokong, H. Isago, J. Porphyrins Phthalocyanines 2004, 8, 1083–1090;

A. Ogunsipe, T. Nyokong, J. Mol. Struct. 2004, 689, 89–97.

M. Durmus, T. Nyokong, Polyhedron 2007, 26, 2767–2776.

R. W. Redmond, J. N. Gamlin, Photochem. Photobiol. 1999, 70, 391–475.

P. C. Lo, B. Z. Zhao, W. B. Duan, W. P. Fong, W. H. Ko, D. K. P. Ng, Bioorg. Med. Chem. Lett. 2007, 17, 1073–1077.

B. Chen, B. W. Pogue, P. J. Hoopes, T. Hasan, Crit. Rev. Eukaryotic Gene Expression 2006, 16, 279–305;

G. R. Reddy, M. S. Bhojani, P. McConville, J. Moody, B. A. Moffat, D. E. Hall, G. Kim, Y. E. L. Koo, M. J. Woolliscroft, J. V. Sugai, T. D. Johnson, M. A. Philbert, R. Kopelman, A. Rehemtulla, B. D. Ross, Clin. Cancer Res. 2006, 12, 6677–6686.

V. Novakova, M. Miletin, T. Filandrová, J. Lenčo, A. Růžička, P. Zimcik, J. Org. Chem. 2014, 79, 2082–2093.

Nejnovějších 20 citací...

Zobrazit více v
Medvik | PubMed

Elucidating the Supramolecular Interaction of Positively Supercharged Fluorescent Protein with Anionic Phthalocyanines

. 2025 May ; 9 (5) : e2400308. [epub] 20241016

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...