Preliminary In Vitro Evaluation of Some Porphyrins Using Human Breast Tumor Cells

Author:

Boscencu Rica1ORCID,Socoteanu Radu2ORCID,Manda Gina3ORCID,Vasiliu Georgiana1,Lupuleasa Dumitru4ORCID,Burloiu Andreea Mihaela4,Neagoe Ionela Victoria3ORCID,Olariu Laura5ORCID

Affiliation:

1. Department of Inorganic Chemistry, Faculty of Pharmacy, “Carol Davila” University of Medicine and Pharmacy, Bucharest, Romania

2. “Ilie Murgulescu” Institute of Physical Chemistry, Romanian Academy, Bucharest, Romania

3. Radiobiology Laboratory,” Victor Babes” National Institute of Pathology, Bucharest, Romania

4. Department of Pharmaceutical Technology and Biopharmaceutics, Faculty of Pharmacy, “Carol Davila” University of Medicine and Pharmacy, Bucharest, Romania

5. “SC. Biotehnos SA”, Bucharest, Romania

Abstract

Background:: Tetrapyrrolic compounds, such as porphyrins and metalloporphyrins, are highly interesting for pharmaceutical chemistry designs considering their good biocompatibility and therapeutic potential. Objective:: The aim of the present work was a preliminary in vitro evaluation of some unsymmetrical porphyrins and the corresponding symmetrical structures as potential candidates for the photodynamic therapy of malignant tumors. Methods:: The biocompatibility of compounds was assessed in terms of their in vitro effect on the viability and proliferation of breast human carcinoma MCF-7 cells and human normal peripheral blood mononuclear cells. Results:: Results indicated that unsymmetrical and symmetrical porphyrins were non-toxic against tumor MCF-7 cells in the concentration range of 0.2–2μM, making them valuable candidates for further development as photosensitizers for PDT in tumors. Moreover, unsymmetrical compounds tended to restore the response of normal and tumor cells affected by the vehicle (dimethyl sulfoxide) used for the initial solubilization of porphyrins, while the symmetrical compounds were less active in this respect. Conclusion:: Unsymmetrical A3B type porphyrins prove enhanced capacity as potential theranostic agents in interaction with human carcinoma MCF-7 cells, despite reduced differences with the corresponding symmetrical form.

Publisher

Bentham Science Publishers Ltd.

Subject

Drug Discovery,Pharmaceutical Science,Molecular Medicine

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