journal article·2022

Porphyrin-based supramolecular nanofibres as a dynamic and activatable photosensitiser for photodynamic therapy

Nicolás M. Casellas, Gaole Dai, Evelyn Y. Xue, M. Jesús Vicente-Arana, Dennis K. P. Ng, Tomás Torres, Miguel García-Iglesias

Biomaterials Science· Volume 10· Issue 12
Publisher page

Abstract

Photodynamic therapy (PDT) represents a promising treatment modality for a range of cancers and other non-malignant diseases due to its non-invasive nature arising from the light-dependent activation. However, PDT has not been the first-line treatment of cancer thus far as a consequence of, among others, the lack of effective transport and activation strategies, and the undesired side effect caused by skin photosensitisation induced by the "always on" photosensitisers. To overcome this "Achilles' heel", we present herein a non-covalent approach to construct a one-component dynamic supramolecular nanophotosensitising system based on a carefully designed porphyrin. The control of the photoactivities of the resulting supramolecular fibres lies in the spatiotemporal control of the monomer-polymer equilibrium. Both the thermodynamics and kinetics of this nanosystem have been carefully studied by different techniques. Moreover, in vitro and in vivo studies have also been performed, showing that these supramolecular aggregates exhibit facile cell internalisation and progressive disassembly after being endocyted by targeted cells, leading to activation of the photosensitising units and eventually cell death and tumour eradication under photoirradiation.
Source: europepmc · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Nanoplatforms for cancer theranostics · Porphyrin and Phthalocyanine Chemistry · Photodynamic Therapy Research Studies

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Organic Chemistry, Universidad Autónoma de Madrid, Institute for Advanced Research in Chemical Sciences, Calle Francisco Tomás y Valiente, 7, 28049 Madrid, ES, Spain

IMDEA Nanociencia, c/Faraday 9, Cantoblanco, 28049, ES, Spain

Department of Chemistry, The Chinese University of Hong Kong, Shatin, N.T., Hong Kong, China

Servicio Interdepartamental de Investigación, Facultad de Ciencias, UAM, Spain

QUIPRE Department, Nanomedicine-IDIVAL, Universidad de Cantabria, Avd. de Los Castros, 46, 39005 Santander, Spain

Funding

Ministerio de Economía y Competitividad · Ministerio de Ciencia e Innovación

References (46)

Show source-provided references
1. Castano · Photodiagn. Photodyn. Ther. · 2004 · 1 · 27910.1016/S1572-1000(05)00007-4 ↗
2. Castano · Photodiagn. Photodyn. Ther. · 2005 · 2 · 110.1016/S1572-1000(05)00030-X ↗
3. Brown · Lancet Oncol. · 2004 · 5 · 49710.1016/S1470-2045(04)01529-3 ↗
4. Dai · Photodiagn. Photodyn. Ther. · 2009 · 6 · 17010.1016/j.pdpdt.2009.10.008 ↗
5. Dolmans · Nat. Rev. Cancer · 2003 · 3 · 38010.1038/nrc1071 ↗
6. Juarranz · Clin. Transl. Oncol. · 2008 · 10 · 14810.1007/s12094-008-0172-2 ↗
7. B.Rodríguez-Amigo , O.Planas , R.Bresolí-Obach , J.Torra , R.Ruiz-González and S.Nonell , in Photodynamic Medicine: From Bench to Clinic , ed. H. Kostron and T. Hasan , The Royal Society of Chemistry , 2016 , pp. 23–6210.1039/9781782626824-00023 ↗
8. Bae · J. Controlled Release · 2009 · 133 · 210.1016/j.jconrel.2008.09.074 ↗
9. Hu · Prog. Mater. Sci. · 2020 · 114 · 10068510.1016/j.pmatsci.2020.100685 ↗
10. Mura · Adv. Drug Delivery Rev. · 2012 · 64 · 139410.1016/j.addr.2012.06.006 ↗
11. Krieg · Chem. – Eur. J. · 2011 · 17 · 901610.1002/chem.201100809 ↗
12. Stupp · Nano Lett. · 2010 · 10 · 478310.1021/nl103567y ↗
13. Chandler · Nat. Mater. · 2016 · 15 · 1310.1038/nmat4474 ↗
14. Li · Chem. Rev. · 2018 · 118 · 535910.1021/acs.chemrev.8b00195 ↗
15. Zhao · ACS Appl. Bio Mater. · 2020 · 3 · 8610.1021/acsabm.9b00843 ↗
16. Overchuk · ACS Nano · 2019 · 13 · 456010.1021/acsnano.9b00494 ↗
17. Zheng · Adv. Mater. · 2019 · 31 · 190158610.1002/adma.201901586 ↗
18. Wang · Org. Biomol. Chem. · 2018 · 16 · 159110.1039/C7OB03108D ↗
19. Li · Chem. Soc. Rev. · 2018 · 47 · 117410.1039/C7CS00594F ↗
20. Lovell · Nat. Mater. · 2011 · 10 · 32410.1038/nmat2986 ↗
21. Li · J. Am. Chem. Soc. · 2017 · 139 · 1088010.1021/jacs.7b05916 ↗
22. Mura · Nat. Mater. · 2013 · 12 · 99110.1038/nmat3776 ↗
23. Liu · Nanoscale · 2020 · 12 · 1111910.1039/C9NR10646D ↗
24. Almeida-Marrero · Chem. – Eur. J. · 2021 · 27 · 963410.1002/chem.202100681 ↗
25. Krieg · Chem. Rev. · 2016 · 116 · 241410.1021/acs.chemrev.5b00369 ↗
26. Tian · ACS Appl. Mater. Interfaces · 2020 · 12 · 3235210.1021/acsami.0c07333 ↗
27. Liu · Polym. Chem. · 2014 · 5 · 5310.1039/C3PY01036H ↗
28. Yu · J. Am. Chem. Soc. · 2018 · 140 · 800510.1021/jacs.8b04400 ↗
29. Petkau-Milroy · J. Am. Chem. Soc. · 2012 · 134 · 808610.1021/ja3029075 ↗
30. Lee · Nat. Nanotechnol. · 2017 · 12 · 82110.1038/nnano.2017.109 ↗
31. Casellas · Chem. Commun. · 2018 · 54 · 411210.1039/C8CC01259H ↗
32. Casellas · Chem. – Eur. J. · 2021 · 27 · 1105610.1002/chem.202101660 ↗
33. Ethirajan · Chem. Soc. Rev. · 2011 · 40 · 34010.1039/B915149B ↗
34. Almeida-Marrero · Chem. Soc. Rev. · 2018 · 47 · 736910.1039/C7CS00554G ↗
35. Yu · J. Controlled Release · 2005 · 110 · 9010.1016/j.jconrel.2005.09.050 ↗
36. Helmich · J. Am. Chem. Soc. · 2011 · 133 · 1223810.1021/ja204543f ↗
37. Weyandt · Chem. – Eur. J. · 2021 · 27 · 970010.1002/chem.202101036 ↗
38. Spano · Acc. Chem. Res. · 2010 · 43 · 42910.1021/ar900233v ↗
39. de Greef · Chem. Rev. · 2009 · 109 · 568710.1021/cr900181u ↗
40. Korevaar · J. Am. Chem. Soc. · 2012 · 134 · 1348210.1021/ja305512g ↗
41. Hu · Proc. Natl. Acad. Sci. U. S. A. · 2013 · 110 · 768410.1073/pnas.1305887110 ↗
42. Lou · Nat. Commun. · 2017 · 8 · 1542010.1038/ncomms15420 ↗
43. Lafleur · J. Am. Chem. Soc. · 2020 · 142 · 1764410.1021/jacs.0c08179 ↗
44. The Porphyrin Handbook , ed. K. M. Kadish , K. M. Smith and R. Guilard , Academic Press , San Diego , 2000
45. Lou · J. Polym. Sci. · 2021 · 59 · 115110.1002/pol.20210011 ↗
46. Nombona · J. Photochem. Photobiol., B · 2012 · 107 · 3510.1016/j.jphotobiol.2011.11.007 ↗