Design and testing of a new photosensitizer based on an ytterbium porphyrazine complex

• Published in: Biophysics (Oxford) 2011-12, Vol.56 (6), p.1083-1087
• Main Authors: Shirmanova, M. V., Balalaeva, I. V., Lekanova, N. Yu, Mysyagin, S. A., Brilkina, A. A., Klapshina, L. G., Zagaynova, E. V.
• Format: Article
• Language: English
• Subjects: Biological and Medical Physics; Biophysics; Cancer; Chemical compounds; Complex Systems Biophysics; Fluorescence; Photodynamic therapy; Physics; Physics and Astronomy
• ISSN: 0006-3509; 1555-6654
• DOI: 10.1134/S0006350911060182

The ytterbium tetraphenyltetracyanoporphyrazine complex (YbPz) has been studied as a potential photosensitizer for fluorescence diagnostics and photodynamic therapy of cancer. A water-miscible formulation of YbPz has been prepared using PEG 6000. The new compound shows intense absorption and fluorescence in the “optical window” of biological tissues (absorption maximum ∼590 nm, emission maximum ∼625 nm). Fluorescence enhancement (a 50-fold increase in YbPz quantum yield) is observed in blood serum. In cultured human cancer cells, YbPz quickly accumulates around the nuclei, presumably in lysosomes. The distribution and pharmacokinetics of YbPz in mice have been investigated by a novel method of in vivo transillumination fluorescence imaging. The highest level of YbPz in grafted mouse cervical carcinoma is maintained from 3 to 6 h after i.v. injection, its half-life in the tumor being ∼24 h. However, the selectivity of YbPz for the tumor vs. normal tissue is not high enough. Most of the drug is cleared from the body (mainly via liver and intestine) in two days. Conventional ex vivo methods (confocal microscopy and point spectroscopic measurements) have revealed the largest content of YbPz in the intestine, liver, tumor, and skin. In general, the optical characteristics of YbPz as well as the features of its interaction with biological objects make it a promising candidate drug for photodynamic therapy and/or fluorescence diagnostics of cancer, though searching for formulations with higher tumor selectivity remains a topical task.