2016 International Conference Laser Optics (LO) 2016
DOI: 10.1109/lo.2016.7550018
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Ru(II) complex mediated PDT for bladder cancer, Biology and dosimetry

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Cited by 2 publications
(3 citation statements)
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“…There has been ongoing interest by a number of research groups in the use of the protein transferrin (Tf) to carry metal-based drugs as cargo to Tfreceptors that tend to be overexpressed on cancer cell surfaces. [152][153][154][155][156][157][158] Ru(II) transition metal complexes, including photosensitizers, have been shown to exhibit nonselective binding to both holo-and apo-Tf. This is also the case for TLD1433 and its derivatives, where Tfbinding both enhances and red-shifts the molar extinction coefficients of some of these photosensitizers under certain conditions.…”
Section: Future Directionmentioning
confidence: 99%
See 1 more Smart Citation
“…There has been ongoing interest by a number of research groups in the use of the protein transferrin (Tf) to carry metal-based drugs as cargo to Tfreceptors that tend to be overexpressed on cancer cell surfaces. [152][153][154][155][156][157][158] Ru(II) transition metal complexes, including photosensitizers, have been shown to exhibit nonselective binding to both holo-and apo-Tf. This is also the case for TLD1433 and its derivatives, where Tfbinding both enhances and red-shifts the molar extinction coefficients of some of these photosensitizers under certain conditions.…”
Section: Future Directionmentioning
confidence: 99%
“…TLT has demonstrated that the photophysical properties of TLD1433 are improved by premixing TLD1433 and Tf, which includes reduced photobleaching, and that overall PDT efficacies are improved with a significant decrease in toxicity. 154 The TLD1433-Tf conjugate was named Rutherrin ® , with a Canadian patent pending, and is currently under clinical development for glioblastoma multiforme (GBM) and non-small cell lung cancer (NSCLC). Rutherrin ® is able to cross the blood brain barrier (BBB) when sys-temically delivered to rats, with higher uptake by GBM cells relative to normal brain tissue.…”
Section: Future Directionmentioning
confidence: 99%
“…During the active targeting of a tumor, a specific interaction of a molecule, such as a signaling peptide, oligonucleotide, oligosaccharide, protein, receptor targeting moiety or an antibody, is used to transport the therapeutic molecule. [32][33][34][35][36][37][38][39][40][41][42][43][44][45][46][47] A large variety of transition metal complexes have been successfully coupled to peptides resulting in increased receptor selectivity. [48][49][50] As examples for Ru(II) polypyridine complexes, the conjugation to the peptide hormone somatostatin showed a 100-fold increased selectivity for somatostatin receptor-expressing cells relative to the free PS.…”
Section: Introductionmentioning
confidence: 99%