2021
DOI: 10.1016/j.bioactmat.2020.10.008
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Thermo-responsive imprinted hydrogel with switchable sialic acid recognition for selective cancer cell isolation from blood

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Cited by 46 publications
(25 citation statements)
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“…The thermo-responsive hydrogel (NIPAAm) allowed to tune the capture and release of cells; at 37 °C, the binding sites are all exposed and cancer cells can bind to them, while at temperatures lower than 25 °C the sites change in shape and functionality, so that the cells may be quickly released. Results showed the selective capture of cancer cells (HepG-2) and release by changing the temperature [83]. The SA epitope is imprinted over the surface of the PNIPAAm hydrogel; at 37 °C, the epitope is exposed on the surface, so that cancer cells can bind to it.…”
Section: Epitope Imprintingmentioning
confidence: 99%
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“…The thermo-responsive hydrogel (NIPAAm) allowed to tune the capture and release of cells; at 37 °C, the binding sites are all exposed and cancer cells can bind to them, while at temperatures lower than 25 °C the sites change in shape and functionality, so that the cells may be quickly released. Results showed the selective capture of cancer cells (HepG-2) and release by changing the temperature [83]. The SA epitope is imprinted over the surface of the PNIPAAm hydrogel; at 37 °C, the epitope is exposed on the surface, so that cancer cells can bind to it.…”
Section: Epitope Imprintingmentioning
confidence: 99%
“…Finally, in ( d ) the staining of the cell on the hydrogel surface at 37 °C (captured cells) and 25 °C (released cells). Figure modified with permission from [ 83 ].…”
Section: Figurementioning
confidence: 99%
“…F I G U R E 3 Schematic illustration for the synthesis of molecularly imprinted polymer nanoparticles that specifically target a cell membrane protein [44] F I G U R E 4 (A) Schematic illustration for the imaging of sialic acid (SA) terminated glycan motifs using MIPs. (B) The surface grafting of an SA-imprinted shell on silica core particles mediated by reversible addition fragmentation chain transfer polymerization using a mixed covalent and noncovalent approach based on reversible amine catalyzed boronate esterification (1,3), hydrogen bond stabilization through a guest-responsive fluorescent reporter group (2), and electrostatic stabilization (3) [56] F I G U R E 5 Schematic illustration of targeting and imaging of cancer cells using monosaccharide-imprinted nanoparticles [62] Later, Pan and co-workers constructed an SA-imprinted thermo-responsive hydrogel layer to attain the selective capture and release of cancer cells triggered by changing temperature [57]. The generated SA-imprinted hydrogel was able to effectively capture cancer cells from the red blood samples.…”
Section: Polysaccharidementioning
confidence: 99%
“…Due to the tight correlation between human health and environmental pollution that results in various diseases, environmental monitoring of pollutants and biomedical diagnosis of biomarkers are global concerns [ 1 , 2 ]. Hence, there is an increasing demand for developing sensors for the selective detection of various targets, such as abused pesticides and overproduced mycotoxins in food samples [ 3 , 4 , 5 , 6 ], as well as biomarkers and tumor cells that represent related diseases [ 7 , 8 , 9 , 10 ]. Moreover, the obtained sensors should be fabricated cost-effectively and capable of rapid, sensitive, portable applications.…”
Section: Introductionmentioning
confidence: 99%