Abstract
The ability to activate drugs only at desired locations avoiding systemic immunosuppression and other dose limiting toxicities is highly desirable. Here we present a new approach, named local drug activation, that uses bioorthogonal chemistry to concentrate and activate systemic small molecules at a location of choice. This method is independent of endogenous cellular or environmental markers and only depends on the presence of a preimplanted biomaterial near a desired site (e.g., tumor). We demonstrate the clear therapeutic benefit with minimal side effects of this approach in mice over systemic therapy using a doxorubicin prodrug against xenograft tumors of a type of soft tissue sarcoma (HT1080).
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CITATION STYLE
Oneto, J. M. M., Khan, I., Seebald, L., & Royzen, M. (2016). In vivo bioorthogonal chemistry enables local hydrogel and systemic pro-drug to treat soft tissue sarcoma. ACS Central Science, 2(7), 476–482. https://doi.org/10.1021/acscentsci.6b00150
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