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. 2021 Nov 21;22(22):12549. doi: 10.3390/ijms222212549

Table 4.

Metastatic melanoma active targeting delivery systems.

PS Active PS Delivery System Cell Line Tumor Model Outcomes Ref.
Zinc phthalocyanine tetra-sulphonic acid (ZnPcS4) Anti-Melanoma Inhibitory Activity (Anti-MIA) combined with AuNPs A375 Monolayers The bioconjugate concentrated the PS within the cytoplasm and nuclei, triggering a 65% apoptotic cell population [91]
Ferrous chlorophyllin (Fe-CHL) PLGA NPs loaded with cRGDyk peptide B16-F10 Monolayers The combination therapy showed enhanced accumulation of the PS and singlet oxygen generation in B16-F10 cells [92]
Zinc ethynylphenyl porphyrin (Zn-EpPor) Cowpea mosaic virus (CPMV) bioconjugated to dendron hybrids B16-F10 Monolayers 2 PS-CPMV achieved a 2-fold increase in efficacy when compared to free PS. [93]
Methylene blue (MB) Naproxen amides (NAPs) B16-F10 Monolayers MB-NAP induced high levels of toxicity on MC-1 receptor-expressing B16-F10 cells, leaving only 4% of cells viable. [94]
BODIPY (BDP) Phenylthiourea (PTU) B16-F10 Monolayers BDP-PTU showed an enhanced cellular uptake, resulting in 20% cell viability. [95]
Rose Bengal (RB) Amphipathic peptide (AMP) C(KLAKLAK)2 B16-F10-Luc2 Monolayers, in vivo
C57 mice
The target specificity and PDT effects of RB significantly reduced the viability of B16-F10-Luc2 cells to 6%. [7]
Pyropheophorbide Perfluorocarbons (PFCs) anchored onto hyaluronic acid (HA) OM431 Monolayers, in vivo
4-week-old BALB/c male mice
The nanocomposite increased singlet oxygen production, which reduced cell viability to 30% in vitro and tumor weight to 0.05 g in vivo. [56]
Indocyanine Green (ICG)
With temozolomide (TMZ)
Hyaluronic acid (HA)-modified with Poly(amino-amine) (PAMAM) A375 Monolayers, in vivo
6–8-week-old nude BALB/c female mice
ICG active nanophotosensitizer showed the strongest tumor cell-killing effect and revealed a cell viability of 17.1%. [96]
IR820 Catalase (CAT) encapsulated in (PLGA) NPs MV3 monolayers, in vivo
6–8-week-old BALB/c nude female mice
Displayed increased cellular uptake with 10% cell viability in vitro and a significant tumor regression in vivo. [97]
Chlorin e6 (Ce6) Anti-CD25 B16-F10 In vivo, C57BL/6-Tg (Foxp3-GFP) 90Pkraj/J mice Ce6-CD25-targeted PDT induced apoptosis in 60–70% of melanoma tumors and caused tumor regression. [98]