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Toxicology and Pharmacokinetics of BOPP in a Canine Model

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Cancer Neutron Capture Therapy

Abstract

The development of new tumor-selective boron compounds for the treatment of glioblastoma multiforme, melanoma and other malignancies only begins with the synthesis of new compounds. Compounds that show initial promise as a result of cell culture and small animal studies face the further requirement that they exhibit acceptable levels of toxicity in larger animal models. Furthermore the pharmacokinetic behavior of such compounds as determined in small animals must be re-examined at the level of larger mammals in order to more closely approximate their expected behavior in human Phase 1 biodistribution trials.

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References

  1. J.S. Hill, S.B. Kahl, A.H. Kaye, S.S. Stylli, M.S. Koo, M.F. Gonzales, N.J. Vardaxis and C.l. Johnson, Selective tumor uptake of a boronated porphyrinin animal model of cerebral glioma, Proc. Natl. Acad. Sci. USA 89: 1785–1789 1992.

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  3. L.G. Salford, personal communication.

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© 1996 Springer Science+Business Media New York

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Kahl, S.B., Tibbitts, J., Fike, J. (1996). Toxicology and Pharmacokinetics of BOPP in a Canine Model. In: Mishima, Y. (eds) Cancer Neutron Capture Therapy. Springer, Boston, MA. https://doi.org/10.1007/978-1-4757-9567-7_86

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  • DOI: https://doi.org/10.1007/978-1-4757-9567-7_86

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4757-9569-1

  • Online ISBN: 978-1-4757-9567-7

  • eBook Packages: Springer Book Archive

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