In Vivo Bioorthogonal Chemistry Enables Local Hydrogel and Systemic Pro-Drug To Treat Soft Tissue Sarcoma
Author(s) -
José M. Mejía Oneto,
Irfan Khan,
Leah M. Seebald,
Maksim Royzen
Publication year - 2016
Publication title -
acs central science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.893
H-Index - 76
eISSN - 2374-7951
pISSN - 2374-7943
DOI - 10.1021/acscentsci.6b00150
Subject(s) - bioorthogonal chemistry , doxorubicin , soft tissue sarcoma , in vivo , limiting , drug , chemistry , cancer research , sarcoma , endogeny , fibrosarcoma , biomaterial , systemic administration , immunosuppression , pharmacology , medicine , chemotherapy , biochemistry , pathology , biology , immunology , combinatorial chemistry , click chemistry , microbiology and biotechnology , mechanical engineering , organic chemistry , engineering
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 pro-drug against xenograft tumors of a type of soft tissue sarcoma (HT1080).
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