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Published July 1, 2022 | Supplemental Material
Journal Article Open

Magnetic‐Powered Janus Cell Robots Loaded with Oncolytic Adenovirus for Active and Targeted Virotherapy of Bladder Cancer

Abstract

A unique robotic medical platform is designed by utilizing cell robots as the active "Trojan horse" of oncolytic adenovirus (OA), capable of tumor-selective binding and killing. The OA-loaded cell robots are fabricated by entirely modifying OA-infected 293T cells with cyclic arginine–glycine–aspartic acid tripeptide (cRGD) to specifically bind with bladder cancer cells, followed by asymmetric immobilization of Fe₃O₄ nanoparticles (NPs) on the cell surface. OA can replicate in host cells and induce cytolysis to release the virus progeny to the surrounding tumor sites for sustainable infection and oncolysis. The asymmetric coating of magnetic NPs bestows the cell robots with effective movement in various media and wireless manipulation with directional migration in a microfluidic device and bladder mold under magnetic control, further enabling steerable movement and prolonged retention of cell robots in the mouse bladder. The biorecognition of cRGD and robust, controllable propulsion of cell robots work synergistically to greatly enhance their tissue penetration and anticancer efficacy in the 3D cancer spheroid and orthotopic mouse bladder tumor model. Overall, this study integrates cell-based microrobots with virotherapy to generate an attractive robotic system with tumor specificity, expanding the operation scope of cell robots in biomedical community.

Additional Information

© 2022 Wiley-VCH. Issue Online: 01 July 2022. Version of Record online: 27 May 2022. Accepted manuscript online: 22 April 2022. Manuscript revised: 09 April 2022. Manuscript received: 31 January 2022. This work was supported by National Key Research and Development Program of China (Grant No. 2017YFA0105900), Guangdong Special Support Program of Youth Talent with Scientific and Technological Innovation, National Natural Science Foundation Fund of China (Grant Nos. 81922046, 61931024, 81802741, and 32101133), Special Funds for Strategic Emerging Industries Development in Shenzhen (Grant No. 20180309163446298), Shenzhen Science and Technology Innovation Commission (Grant No. RCJC20200714114557005), Shenzhen Science and Technology Program (Grant No. JCYJ20210324125006019), Shenzhen Key Laboratory Program (Grant No. ZDSYS20190902092857146), and China Postdoctoral Council International Postdoctoral Exchange Fellowship Program (Grant No. PC2021078). All animal experiments were strictly conducted in compliance with the guidelines of the Animal Use and Care Administrative Advisory Committee of Shenzhen Luohu Hospital Group. The authors declare no conflict of interest. Data Availability Statement. The data that support the findings of this study are available from the corresponding author upon reasonable request.

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Additional details

Created:
August 22, 2023
Modified:
October 24, 2023