Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2080569 | Drug Discovery Today | 2012 | 7 Pages |
Abstract
The early promise of boron neutron capture therapy as a method for the treatment of cancer has been inhibited by the inherent toxicity associated with therapeutically useful doses of 10B-containing pharmacophores, the need for target-tissue specificity and the challenges imposed by biological barriers. Although developments in the synthetic chemistry of polyhedral boranes have addressed issues of toxicity to a considerable extent, the optimisation of the transport and the delivery of boronated agents to the site of action – the subject of this review – is a challenge that is addressed by the development of innovative formulation strategies.
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Authors
Gianpiero Calabrese, John J. Nesnas, Eugen Barbu, Dimitris Fatouros, John Tsibouklis,