Photothermal Intracellular Delivery Using Gold Nanodisk Arrays AITranslate
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Local heating using pulsed-laser-induced photothermal effects on plasmonic nanostructured substrates can be used for intracellular delivery applications. However, the fabrication of plasmonic nanostructured interfaces is hampered by complex nanomanufacturing schemes. Here, we demonstrate the fabrication of large-area plasmonic gold (Au) nanodisk arrays that enable photothermal intracellular delivery of biomolecular cargo at high efficiency. The Au nanodisks (350 nm in diameter) were fabricated using chemical lift-off lithography (CLL). Nanosecond laser pulses were used to excite the plasmonic nanostructures, thereby generating transient pores at the outer membranes of targeted cells that enable the delivery of biomolecules via diffusion. Delivery efficiencies of >98% were achieved using the cell impermeable dye calcein (0.6 kDa) as a model payload, while maintaining cell viabilities at >98%. The highly efficient intracellular delivery approach demonstrated in this work will facilitate translational studies targeting molecular screening and drug testing that bridge laboratory and clinical investigations.
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DOI:https://doi.org/10.1021/acsmaterialslett.0c00428
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Local heating using pulsed-laser-induced photothermal effects on plasmonic nanostructured substrates can be used for intracellular delivery applications. However, the fabrication of plasmonic nanostructured interfaces is hampered by complex nanomanufacturing schemes. Here, we demonstrate the fabrication of large-area plasmonic gold (Au) nanodisk arrays that enable photothermal intracellular delivery of biomolecular cargo at high efficiency. The Au nanodisks (350 nm in diameter) were fabricated using chemical lift-off lithography (CLL). Nanosecond laser pulses were used to excite the plasmonic nanostructures, thereby generating transient pores at the outer membranes of targeted cells that enable the delivery of biomolecules via diffusion. Delivery efficiencies of >98% were achieved using the cell impermeable dye calcein (0.6 kDa) as a model payload, while maintaining cell viabilities at >98%. The highly efficient intracellular delivery approach demonstrated in this work will facilitate translational studies targeting molecular screening and drug testing that bridge laboratory and clinical investigations.
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| GB/T 7714-2015 | [1] Chuanzhen Zhao, Tianxing Man, Xiaobin Xu, et al. ACS Materials Letters, 2020(2). DOI:10.1021/acsmaterialslett.0c00428. |
| MLA | [1] Chuanzhen Zhao, et al., ACS Materials Letters, no. 2, 2020, https://doi.org/10.1021/acsmaterialslett.0c00428. |
| APA | [1] Chuanzhen Zhao, Tianxing Man, Xiaobin Xu, Qing Yang, Wenfei Liu, Steven J. Jonas, Michael A. Teitell, PeiYu Chiou, & Paul S. Weiss. (2020). ACS Materials Letters(2). https://doi.org/10.1021/acsmaterialslett.0c00428 |
| IEEE | [1] Chuanzhen Zhao, Tianxing Man, Xiaobin Xu, Qing Yang, Wenfei Liu, Steven J. Jonas, Michael A. Teitell, PeiYu Chiou, and Paul S. Weiss, ACS Materials Letters, no. 2, 2020, doi: 10.1021/acsmaterialslett.0c00428. |
