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Anticancer Efficacy of Photodynamic Therapy with Lung Cancer-Targeted Nanoparticles
Published on: December 1, 2016
Cationic diarylporphyrins: In vitro versatile anticancer and antibacterial photosensitizers
Enrico Caruso1, Miryam Chiara Malacarne2, Stefano Banfi2
1Department of Biotechnology and Life Sciences (DBSV), University of Insubria, Via J.H. Dunant 3, 21100 Varese, VA, Italy..
Abstract:
The visible light combined with photosensitizers (PSs) is exploited in both antitumoral and antimicrobial fields inducing a photo-oxidative stress within the target cells. Among the different PSs, porphyrins belong to the family of the most promising compounds to be used in clinical photodynamic applications. Although in the last years many porphyrins have been synthesised and tested, only a few reports concern the in vitro effects of the 5,15-diarylporphyrins. In this work, the activity of four 5,15-diarylporphyrins (compounds 7-10), bearing alkoxy-linked pyridinium appendixes, have been tested on cancer cell lines and against bacterial cultures. Among the synthetized PSs, compounds 7 and 9 are not symmetrically substituted porphyrins showing one cationic charge tethered at the end of one 4C or 8C carbon chains, respectively. On the other hand, compounds 8 and 10 are symmetrically substituted and show two chains of C4 and C8 carbons featuring a cationic charge at the end of both chains. The dicationic 8 and 10 were more hydrophilic than monocationic 7 and 9, outlining that the presence of two pyridinium salts have a higher impact on the solubility in the aqueous phase than the lipophilic effect exerted by the length of the alkyl chains. Furthermore, these four PSs showed a similar rate of photobleaching, irrespective of the length and number of chains and the number of positive charges. Among the eukaryotic cell lines, the SKOV3 cells were particularly sensitive to the photodynamic activity of all the tested diarylporphyrins, while the HCT116 cells were found more sensitive to PSs bearing C4 chain (7 and 8), regardless the number of cationic charges. The photo-induced killing effect of these porphyrins was also tested against two different bacterial cultures. As expected, the Gram positive Bacillus subtilis was more sensitive than the Gram negative Escherichia coli, and the dicationic porphyrin 8, bearing two C4 chains, was the most efficient on both microorganisms. In conclusion, the new compound 8 seems to be an optimal candidate to deepen as versatile anticancer and antibacterial photosensitizer.
Insights
This study tested novel 5,15-diarylporphyrins as photosensitizers (PSs) for cancer and bacterial infections. Compound 8, a dicationic PS, demonstrated potent anticancer and antibacterial activity, making it a promising candidate for photodynamic therapy.
Area of Science:
- Photodynamic therapy
- Medicinal chemistry
- Antimicrobial research
Background:
- Visible light combined with photosensitizers (PSs) induces photo-oxidative stress for antitumoral and antimicrobial applications.
- Porphyrins are promising PSs for clinical photodynamic applications.
- Limited research exists on the in vitro effects of 5,15-diarylporphyrins.
Purpose of the Study:
- To evaluate the anticancer and antibacterial activity of four novel 5,15-diarylporphyrins (compounds 7-10).
- To investigate the structure-activity relationship, focusing on cationic charge and alkyl chain length.
- To identify a versatile photosensitizer for photodynamic applications.
Main Methods:
- Synthesis and characterization of four 5,15-diarylporphyrins with varying pyridinium appendixes.
- In vitro testing against human cancer cell lines (SKOV3, HCT116) and bacterial cultures (Bacillus subtilis, Escherichia coli).
- Assessment of photobleaching rates and solubility in aqueous phases.
Main Results:
- Dicationic porphyrins (8, 10) showed higher hydrophilicity than monocationic ones (7, 9).
- All tested PSs exhibited similar photobleaching rates.
- SKOV3 cells were sensitive to all diarylporphyrins; HCT116 cells were more sensitive to C4-chain porphyrins (7, 8).
- Gram-positive Bacillus subtilis was more susceptible than Gram-negative Escherichia coli.
- Dicationic porphyrin 8 with two C4 chains was the most effective against both bacterial types.
Conclusions:
- The novel 5,15-diarylporphyrins show significant potential as photosensitizers.
- Compound 8, a dicationic porphyrin with two C4 chains, is a versatile candidate for anticancer and antibacterial photodynamic therapy.
- Hydrophilicity, influenced by the number of cationic charges, plays a key role in PS efficacy.
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