Table 1.
Photosensitizer (s) | PS Class | Cancer Type (s) | Application | PS-PDT Effective Concentrations | Ref. |
---|---|---|---|---|---|
Upconversion nanoconstruct—targeted with folate-modified amphiphilic chitosan loaded with zinc(II) phthalocyanine (FASOC-UCNP-ZnPc) | Phthalocyanines Derivatives | Hepatocellular carcinoma and sarcoma | In vivo | <150 mg.kg−1 triggered by 660 and 980 nm light (0.2 W.cm−2, 30 min) | [51] |
Dimeric anthraquinone (–)-7,7′-biphyscion | Anthraquinones Derivatives | lung cancer, cervical cancer, stomach cancer and urinary bladder carcinoma | In vitro | 0.064 µmol.L−1 combined with 9.3 J.cm−2 light dose (λexc = 468 nm) | [52] |
6-Nitro-Quinazolin-4(3H)-one | Quinazoline Derivatives | glioblastoma and melanoma | In vitro | 50 μmol.L−1 and then irradiated at 365 nm using a UVA lamp for 1 and 2 h. | [53] |
2-(3,5-dimethyl-1Hpyrazol-1-yl)-1-arylethanones | Pyrazole Derivatives | colon cancer, prostate cancer, ovarian cancer, and lung cancer. | In vitro | Not reported. | [54] |
Hf–porphyrin nanoscale metal–organic framework, (DBP–UiO) | Porphyrin derivative | head and neck cancer | In vitro/in vivo | 5–100 μmol.L−1 and 3.5 mg.kg−1(in vivo) combined with 90–180 J.cm−2 light dose (100 mW.cm−2, 15 and 30 min). | [55] |
Cationic porphyrin-cisplatin conjugate (Pt-1)- polymeric nanoparticles (NP@Pt-1) | Porphyrin derivative | colon carcinoma | In vitro/ in vivo |
0.025–20 μmol.L−1 and 3.5 mg.kg−1(in vivo) combined with 6.95 J.cm−2 light dose (100 mW.cm−2, 15 and 30 min). | [56] |
Selenium-rubyrin (NMe2Se4N2)-loaded nanoparticles functionalized with folate (FA) | Transition metal complex | cervical carcinoma | In vitro/ in vivo |
35 μg.mL−1 and 0.5 mg.kg−1(in vivo) combined with 30 J.cm−2 light dose (635 nm and 808 nm laser, 100 mW.cm−2, 30 min). |
[57] |
Constructed homologous targeting-based nanoplatform (MH-PLGA-IR780 NPs) | NIR-absorbing PSs | osteosarcoma | In vitro/in vivo | 5 μg.mL−1, 808 nm laser, 1 and 1.5 W.cm−2. | [58] |
MnO2-capped silk fibroin (SF) nanoparticles with chlorin e6 (Ce6) encapsulated | Chlorin | breast cancer | In vitro/ in vivo |
40 μg.mL−1 and 1 mg.kg−1 (in vivo), 808/660 nm laser, 1.5/1.0 W.cm−2. | [59] |
Aluminum-phthalocyanine chloride associated with poly(methyl vinyl ether-co-maleic anhydride) nanoparticles | Phthalocyanines Derivatives | breast cancer | In vitro | 0.25 μmol.L−1 combined with 3.82 J.cm−2 light dose | [60] |
Silicon (IV) phthalocyanine (SiPC) | Phthalocyanines Derivatives | hepatocarcinoma and gastric cancer | In vitro | 9 nmol.L−1 to 33 nM combined with 27 J.cm−2 light dose (λ > 610 nm, 15 mW.cm-2, 30 min). |
[61] |
Hypocrellin A (HA) | Natural hypocrellins | lung adenocarcinoma | In vitro | 0.08 μmol.L−1, 470 nm LED light irradiation. | [62] |
Sinoporphyrin Sodium | Photofrin | eleven human cancer cell line | In vitro/ in vivo |
0.1–0.8 μg.mL−1, 630 nm laser at fluence rate of 30 mW.cm−2 total illumination power 5.4 J.well−1. 0.5–2 mg.kg−1, fluence rate of 127.7 mW.cm−2 total illumination power 60 J/animal. | [63] |
Sinoporphyrin Sodium | Photofrin | breast cancer | In vitro | 2–4 μ.mol.L− at fluence rate of 23.85 mW.cm−2 combined with 5.72 J.cm−2 light dose. | [64] |
Palmatine hydrochloride (PaH) | Quinolone-based alkaloids | breast cancer | In vitro | 0.087 μ.mol.L−1, 470 nm LED light irradiation, combined with 10.8 J.cm−2 light dose. | [65] |
Palmatine hydrochloride (PaH) | Quinolone-based alkaloids | colon adenocarcinoma | In vitro | 5 μ.mol.L−1, 470 nm LED light irradiation, combined with 10.8 J.cm−2 light dose. | [66] |
Hypericin | Perylenequinone/Natural PS | larynx carcinoma | In vitro | 11 and 25 nmol.L−1, combined with 6 and 12 J.cm−2 light dose. | [67] |
Redaporfin-P123 micelles | bacteriochlorin derivative |
melanoma | In vitro/ in vivo |
5 μ.mol.L−1, 735 nm LED light irradiation, combined with 0.97 J.cm−2 light dose. 1.5 mg.Kg−1, 750 nm LED light irradiation, combined with 74 J.cm−2. |
[68] |