Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 2018 Sep;47(6):601-609.
doi: 10.1007/s00249-018-1283-5. Epub 2018 Feb 16.

Comparative study of phototoxicity of protoporphyrin IX synthetic and extracted from ssp Rattus novergicus albinus rats toward murine melanoma cells

Affiliations
Comparative Study

Comparative study of phototoxicity of protoporphyrin IX synthetic and extracted from ssp Rattus novergicus albinus rats toward murine melanoma cells

E R Reis et al. Eur Biophys J. 2018 Sep.

Abstract

Protoporphyrin IX (PpIX) is a precursor of heme synthesis and is known to be an active photosensitizer and precursor of photosensitizers applied in photodynamic therapy (PDT) and photodynamic diagnostics (PDD). On irradiation with visible light, PpIX undergoes phototransformation, producing photoproducts which may also be phototoxic and increase its efficacy. The mechanism of PpIX phototransformation depends on environmental characteristics and can be different in vitro and in vivo. In this paper, we present a comparative study of the photoactivity of synthetic PpIX and PpIX extracted from the Harderian gland of ssp Rattus novergicus albinus rats, along with their photoproducts toward murine B16F-10 melanoma cells. It was observed that when irradiated with visible light the endogenous PpIX demonstrates photocytotoxicity ten times higher than the synthetic PpIX. The photoproduct of endogenous PpIX also possesses phototoxicity, though slightly lower than that of PpIX itself. The rate of cell internalization for both endogenous PpIX and its photoproduct was eightfold greater than that obtained for the synthetic porphyrin. This difference might result from a complexation of the native PpIX with some amphiphilic compounds during its synthesis within the Harderian glands, which facilitates the cell uptake of PpIX. Fluorescence microscopy images show that both endogenous and synthetic porphyrins are localized after uptake predominantly in the mitochondrial region of cells.

Keywords: Harderian gland; Photodynamic therapy and diagnostics; Photoproduct; Phototoxicity; Synthetic and endogenous protoporphyrin IX.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Photochem Photobiol Sci. 2006 Jan;5(1):73-81 - PubMed
    1. Phys Med Biol. 2004 Nov 7;49(21):4837-60 - PubMed
    1. Photochem Photobiol. 1995 Sep;62(3):383-8 - PubMed
    1. Lasers Med Sci. 2003;18(1):56-62 - PubMed
    1. J Photochem Photobiol B. 1993 May;18(2-3):287-90 - PubMed

Publication types

MeSH terms

LinkOut - more resources