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Hypericin cytotoxicity in tumor and non-tumor cell lines: A chemometric study.
- Source :
-
Photodiagnosis and photodynamic therapy [Photodiagnosis Photodyn Ther] 2017 Dec; Vol. 20, pp. 86-90. Date of Electronic Publication: 2017 Aug 12. - Publication Year :
- 2017
-
Abstract
- Hypericin (HY) is an excellent photoactive compound that has been investigated for the photodynamic treatment of cancer as well as for microorganism inactivation. In this study, chemometric analysis was applied for the first time on photodynamic assays to investigate the cytotoxicity of HY in tumor (HEp-2) and non-tumor (Vero and HUVEC) cell lines. The experimental planning was based on eight assays using the 2 <superscript>3</superscript> full factorial design combining three important variables for PDT: photosensitizer concentrations, incubation time of cells in HY solutions and employed light dose (λ=590±10nm). The statistical data analysis evidenced the relative significance of such variables and the correlations among them on the cell death. The chemometric results suggested that long incubation time and a low HY concentration and/or light dose allow killing selectively tumor cells. The chemometric analysis could be a new useful empiric method to a previous prediction of the IC <subscript>50</subscript> . In this study, the estimated values were in agreement with the experimental IC <subscript>50</subscript> values.<br /> (Copyright © 2017 Elsevier B.V. All rights reserved.)
- Subjects :
- Animals
Anthracenes
Apoptosis drug effects
Cell Line, Tumor
Cell Survival
Chlorocebus aethiops
Dose-Response Relationship, Drug
Haplorhini
Hep G2 Cells
Human Umbilical Vein Endothelial Cells
Humans
Perylene pharmacology
Vero Cells
Perylene analogs & derivatives
Photochemotherapy methods
Photosensitizing Agents pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1873-1597
- Volume :
- 20
- Database :
- MEDLINE
- Journal :
- Photodiagnosis and photodynamic therapy
- Publication Type :
- Academic Journal
- Accession number :
- 28811224
- Full Text :
- https://doi.org/10.1016/j.pdpdt.2017.08.005