journal article·2018-01-24

meso-Tetrahydroxyphenylchlorin-Conjugated Gold Nanoparticles as a Tool To Improve Photodynamic Therapy

Elina Haimov, Hana Weitman, Shlomi Polani, Hadas Schori, David Zitoun, Orit Shefi

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Abstract

Photodynamic therapy (PDT) is a promising therapeutic modality for cancer. However, current protocols using bare drugs suffer from several limitations that impede its beneficial clinical effects. Here, we introduce a new approach for an efficient PDT treatment. It involves conjugating a PDT agent, meso-tetrahydroxyphenylchlorin (mTHPC) photosensitizer, to gold nanoparticles (AuNPs) that serve as carriers for the drug. AuNPs have a number of characteristics that make them highly suitable to function as drug carriers: they are biocompatible, serve as biomarkers, and function as contrast agents in vitro and in vivo. We synthesized AuNPs and covalently conjugated the mTHPC drug molecules through a linker. The resultant functional complex, AuNP-mTHPC, is a stable, soluble compound. SH-SY5Y human neuroblastoma cells were incubated with the complex, showing possible administration of higher doses of drug when conjugated to the AuNPs. Then cells were irradiated with a laser beam at 650 nm to mimic the PDT procedure. Our study shows higher rates of cell death in cells incubated with the AuNP-mTHPC complex compared to the incubation with the free drug. Using the new complex may form the basis for a better PDT strategy for a wide range of cancers.
Source: openalex_inverted_index · Quality: baseline

Research context

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

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

Affiliations

Faculty of Engineering, ‡Department of Physics, §Department of Chemistry, and ∥Bar Ilan Institute of Nanotechnology and Advanced Materials, Bar Ilan University, 5290002 Ramat Gan, Israel

Funding

Israel Science Foundation

References (59)

Show source-provided references
1. 10.1111/j.1751-1097.1992.tb04222.x10.1111/j.1751-1097.1992.tb04222.x ↗
2. Peng Q. · Anticancer Res. · 2003 · 23 · 3591
3. 10.1039/b311429e10.1039/b311429e ↗
4. Pandey, R. K.; Zheng, G.Porphyrins as photosensitizers in photodynamic therapy;Kadish, K. M.; Smith, K. M.; Guilard, R., Eds.The Porphyrin Handbook;Academic Press:Boston, 2000; Vol.6, pp157–230.
5. 10.2174/09298670878487240110.2174/092986708784872401 ↗
6. 10.1021/ja070070710.1021/ja0700707 ↗
7. 10.1016/S1470-2045(04)01529-310.1016/S1470-2045(04)01529-3 ↗
8. 10.1177/15440591070860080310.1177/154405910708600803 ↗
9. 10.1016/j.jphotobiol.2010.06.00410.1016/j.jphotobiol.2010.06.004 ↗
10. 10.1093/jnci/90.12.88910.1093/jnci/90.12.889 ↗
11. 10.1111/j.1751-1097.1985.tb01554.x10.1111/j.1751-1097.1985.tb01554.x ↗
12. 10.1016/S1572-1000(05)00007-410.1016/S1572-1000(05)00007-4 ↗
13. 2005
14. Peng Q. · Cancer Res. · 1995 · 55 · 2620
15. 10.1177/15330346050040030810.1177/153303460500400308 ↗
16. 10.1111/j.1751-1097.2011.00986.x10.1111/j.1751-1097.2011.00986.x ↗
17. 10.1002/lsm.2242910.1002/lsm.22429 ↗
18. Bonnett R. · 200010.1201/9781482296952 ↗
19. 10.1002/ijc.291057061810.1002/ijc.2910570618 ↗
20. 10.1002/(SICI)1097-0215(19971009)73:2<230::AID-IJC12>3.0.CO;2-J10.1002/(SICI)1097-0215(19971009)73:2<230::AID-IJC12>3.0.CO;2-J ↗
21. 10.1111/j.1751-1097.2005.tb01453.x10.1111/j.1751-1097.2005.tb01453.x ↗
22. 10.1117/12.20344110.1117/12.203441 ↗
23. 10.1046/j.1365-2168.1997.02543.x10.1046/j.1365-2168.1997.02543.x ↗
24. 10.1042/bj261027710.1042/bj2610277 ↗
25. 10.1021/ja108846h10.1021/ja108846h ↗
26. 10.1142/S108842460300020310.1142/S1088424603000203 ↗
27. 10.1016/j.biomaterials.2009.07.04810.1016/j.biomaterials.2009.07.048 ↗
28. 10.1021/ja908117a10.1021/ja908117a ↗
29. 10.1016/j.addr.2009.11.00710.1016/j.addr.2009.11.007 ↗
30. 10.1038/srep0249910.1038/srep02499 ↗
31. 10.1039/C4RA15291C10.1039/C4RA15291C ↗
32. 10.1021/acsami.5b0431810.1021/acsami.5b04318 ↗
33. Patra C. R. · J. Biomed. Nanotechnol. · 2008 · 4 · 9910.1166/jbn.2008.016 ↗
34. 10.1021/acsnano.5b0193910.1021/acsnano.5b01939 ↗
35. 10.1002/anie.20040065110.1002/anie.200400651 ↗
36. 10.1002/adhm.20177007510.1002/adhm.201770075 ↗
37. 10.1002/cyto.a.2300510.1002/cyto.a.23005 ↗
38. 10.1259/bjr/1316988210.1259/bjr/13169882 ↗
39. 10.1016/j.jconrel.2014.03.05710.1016/j.jconrel.2014.03.057 ↗
40. 10.1259/bjr/5944883310.1259/bjr/59448833 ↗
41. 10.1016/j.ijbiomac.2013.04.01810.1016/j.ijbiomac.2013.04.018 ↗
42. 10.1021/la051371210.1021/la0513712 ↗
43. 10.1038/nbt137710.1038/nbt1377 ↗
44. Matsumura Y. · Cancer Res. · 1986 · 46 · 6387
45. 10.1038/nnano.2007.38710.1038/nnano.2007.387 ↗
46. 10.1155/2015/64671310.1155/2015/646713 ↗
47. 10.1039/df951110005510.1039/df9511100055 ↗
48. 10.1063/1.55596510.1063/1.555965 ↗
49. 10.1016/1010-6030(92)85132-E10.1016/1010-6030(92)85132-E ↗
50. 10.1021/ja01072a06210.1021/ja01072a062 ↗
51. 10.1246/cl.1973.74310.1246/cl.1973.743 ↗
52. 10.1063/1.55565510.1063/1.555655 ↗
53. Bevington, P. R.Data Reduction and Error Analysis for the Physical Sciences;McGraw-Hill:New York, 1969; Chapter 5, pp75–97.
54. 10.1016/0022-2852(61)90236-310.1016/0022-2852(61)90236-3 ↗
55. 10.1016/S1011-1344(98)00177-810.1016/S1011-1344(98)00177-8 ↗
56. 10.1088/0957-4484/21/6/06510210.1088/0957-4484/21/6/065102 ↗
57. 10.2217/nnm.11.13010.2217/nnm.11.130 ↗
58. 10.1016/j.jare.2010.02.00210.1016/j.jare.2010.02.002 ↗
59. 10.2217/17435889.1.4.47310.2217/17435889.1.4.473 ↗