Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/86288
Title: Rupturing cancer cells by the expansion of functionalized stimuli-responsive hydrogels
Authors: Fang, Yan
Tan, Jiajun
Lim, Sierin
Soh, Siowling
Keywords: Hydrogels
Cancer Cells
Issue Date: 2018
Source: Fang, Y., Tan, J., Lim, S., & Soh, S. (2018). Rupturing cancer cells by the expansion of functionalized stimuli-responsive hydrogels. NPG Asia Materials, 10(2), e465-.
Series/Report no.: NPG Asia Materials
Abstract: Using particles with different functionalities for treating cancer has many advantages over other methods (for example, better access to remote parts of the body); however, current chemical (for example, chemotherapy) and biological (for example, immunotherapy) methods still face many challenges. Here, we describe a fundamentally different approach: using the physical force of an expanding stimuli-responsive hydrogel to rupture cancer cells attached on its surface. Specifically, we coated temperature-responsive hydrogels with a layer of cell-adherent arginine-glycine-aspartate (RGD) peptides. The approach involved first allowing cancer cells to attach onto the surface of the hydrogels, and then applying a change in temperature. As the hydrogel underwent a chemical transformation and expanded due to the stimulus, the cancer cells attached to it ruptured. The results from staining the cells with trypan blue, observing them using SEM, and analyzing them using the MTT assay showed that both breast and lung cancer cells died after the hydrogel expanded; hence, we showed that this physical force from the expanding hydrogel is strong enough to rupture the cancer cells. In addition, the force derived from the expanding hydrogel was determined separately to be larger than that needed to rupture typical cells. This physical approach is conceptually simple, technically easy to implement, and potentially generalizable for rupturing a wide range of cells.
URI: https://hdl.handle.net/10356/86288
http://hdl.handle.net/10220/45241
DOI: 10.1038/am.2017.232
Rights: © 2018 The Author(s). This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SCBE Journal Articles

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