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Co-delivery of siRNA and doxorubicin to cancer cells from additively manufactured implants†
Dang Q. S. Le,Cody Bünger
RSC Advances Pub Date : 11/16/2015 00:00:00 , DOI:10.1039/C5RA23748C
Abstract

Tumors in load bearing bone tissue are a major clinical problem, in part because surgical resection invokes a dilemma whether to resect aggressively, risking mechanical failure, or to resect conservatively, risking cancer recurrence due to residual malignant cells. A chemo-functionalized implant, capable of physically supporting the void while killing residual cancer cells, would be an attractive solution. Here we describe a novel additively manufactured implant that can be functionalized with chitosan/siRNA nanoparticles. These induce long term gene silencing in adjacent cancer cells without showing toxicity to normal cells. When scaffolds are functionalized with siRNA/chitosan nanoparticles and doxorubicin in combination, their effects synergized leading to cancer cell death. This technology may be used to target resistance genes by RNA interference and thereby re-sensitizing the cancer cells to co-delivered chemotherapy.

Graphical abstract: Co-delivery of siRNA and doxorubicin to cancer cells from additively manufactured implants
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