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Photodynamic anticancer activity evaluation of novel 5-aminolevulinic acid and 3-hydroxypyridinone conjugates.
- Source :
-
Bioorganic & medicinal chemistry [Bioorg Med Chem] 2024 May 01; Vol. 105, pp. 117726. Date of Electronic Publication: 2024 Apr 15. - Publication Year :
- 2024
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Abstract
- 5-Aminolevulinic acid (ALA) and its derivatives, serving as the endogenous precursor of the photosensitizer (PS) protoporphyrin IX (PpIX), successfully applied in tumor imaging and photodynamic therapy (PDT). ALA and its derivatives have been used to treat actinic keratosis (AK), basal cell carcinoma (BCC), and improve the detection of superficial bladder cancer. However, the high hydrophilicity of ALA and the conversion of PpIX to heme have limited the accumulation of PpIX, hindering the efficiency and potential application of ALA-PDT. This study aims to evaluate the PDT activity of three rationally designed series of ALA-HPO prodrugs, which were based on enhancing the lipophilicity of the prodrugs and reducing the labile iron pool (LIP) through HPO iron chelators to promote PpIX accumulation. Twenty-four ALA-HPO conjugates, incorporating amide, amino acid, and ester linkages, were synthesized. Most of the conjugates, exhibited no dark-toxicity to cells, according to bioactivity evaluation. Ester conjugates 19a-g showed promoted phototoxicity when tested on tumor cell lines, and this increased phototoxicity was strongly correlated with elevated PpIX levels. Among them, conjugate 19c emerged as the most promising (HeLa, IC <subscript>50</subscript>  = 24.25 ± 1.43 μM; MCF-7, IC <subscript>50</subscript>  = 43.30 ± 1.76 μM; A375, IC <subscript>50</subscript>  = 28.03 ± 1.00 μM), displaying superior photodynamic anticancer activity to ALA (IC <subscript>50</subscript>  > 100 μM). At a concentration of 80 μM, the fluorescence intensity of PpIX induced by compound 19c in HeLa, MCF-7, and A375 cells was 18.9, 5.3, and 2.8 times higher, respectively, than that induced by ALA. In conclusion, cellular phototoxicity showed a strong correlation with intracellular PpIX fluorescence levels, indicating the potential application of ALA-HPO conjugates in ALA-PDT.<br />Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Yuanyuan Xie reports administrative support was provided by Zhejiang University of Technology. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 Elsevier Ltd. All rights reserved.)
- Subjects :
- Humans
Structure-Activity Relationship
Molecular Structure
Pyridones pharmacology
Pyridones chemistry
Pyridones chemical synthesis
Cell Line, Tumor
Protoporphyrins chemistry
Protoporphyrins pharmacology
Cell Proliferation drug effects
Dose-Response Relationship, Drug
Cell Survival drug effects
Prodrugs pharmacology
Prodrugs chemistry
Prodrugs chemical synthesis
Aminolevulinic Acid pharmacology
Aminolevulinic Acid chemistry
Photosensitizing Agents pharmacology
Photosensitizing Agents chemistry
Photosensitizing Agents chemical synthesis
Photochemotherapy
Antineoplastic Agents pharmacology
Antineoplastic Agents chemistry
Antineoplastic Agents chemical synthesis
Drug Screening Assays, Antitumor
Subjects
Details
- Language :
- English
- ISSN :
- 1464-3391
- Volume :
- 105
- Database :
- MEDLINE
- Journal :
- Bioorganic & medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 38626642
- Full Text :
- https://doi.org/10.1016/j.bmc.2024.117726