Multifunctional Hybrid Magnetic Microgel Synthesis for Immune-Based Isolation and Post-Isolation Culture of Tumor Cells
Source abstract
Abstract
Circulating tumor cells are of utmost importance among various biomarkers in liquid biopsies as a prognosis indicator of metastasis as well as in chemotherapeutic monitoring. This study introduces an efficient tool composed of soft nano/hybrid immune microgels for magnetic isolation of targeted tumor cells. The development process involves the in situ synthesis of magnetic nanoparticles within the three-dimensional matrix of thermoresponsive microgels. Surface modification and anti-EpCAM conjugation are adjusted by changing the temperature, and a conjugation efficiency of around 70% is achieved by using a protein G linker. Anti-EpCAM-conjugated nano/hybrid magnetic microgels are used to isolate EpCAM-expressing breast adenocarcinoma MCF-7 cells from culture media and whole blood with an efficiency of 75 and 70%, respectively. Furthermore, we demonstrate the ability of the hybrid microgels to isolate cancer cells with a purity of 65% and culture the cells post-isolation for further drug studies. The multifunctional hybrid microcarriers reported in this work can be potentially used for continuous monitoring of cancers and in personalized medicine.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: 3D Printing in Biomedical Research · Cancer Cells and Metastasis · Microfluidic and Bio-sensing Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Advanced Magnetic Materials Research Center, College of Engineering, University of Tehran, Tehran 14399-57131, Iran
Biomaterials and Tissue Engineering Department, Breast Cancer Research Center, Motamed Cancer Institute, ACECR, Tehran 1665659911, Iran
Funding
Canada Foundation for Innovation · University of Tehran · Natural Sciences and Engineering Research Council of Canada · RepliCel Life Sciences · National Institute for Medical Research Development
References (57)
Show source-provided references
1. 10.1016/j.drudis.2017.06.01010.1016/j.drudis.2017.06.010 ↗
2. 10.3322/caac.2126210.3322/caac.21262 ↗
3. 10.1038/nrclinonc.2017.1410.1038/nrclinonc.2017.14 ↗
4. 10.1016/j.bios.2016.12.06210.1016/j.bios.2016.12.062 ↗
5. 10.1073/pnas.101253910710.1073/pnas.1012539107 ↗
6. 10.1158/0008-5472.can-10-122910.1158/0008-5472.can-10-1229 ↗
7. 10.1039/c4lc00136b10.1039/c4lc00136b ↗
8. 10.1056/nejmoa04076610.1056/nejmoa040766 ↗
9. 10.1093/annonc/mdy17210.1093/annonc/mdy172 ↗
10. 10.1126/science.123522610.1126/science.1235226 ↗
11. 10.1038/s41698-017-0039-510.1038/s41698-017-0039-5 ↗
12. Zhang X. · Am. J. Cancer Res. · 2018 · 8 · 332
13. 10.1021/acsami.8b1143610.1021/acsami.8b11436 ↗
14. 10.1039/c6nr02299e10.1039/c6nr02299e ↗
15. 10.1002/adma.20150391810.1002/adma.201503918 ↗
16. 10.1002/adma.20160361210.1002/adma.201603612 ↗
17. 10.1016/j.gpb.2016.11.00510.1016/j.gpb.2016.11.005 ↗
18. 10.1038/nature0638510.1038/nature06385 ↗
19. 10.1002/bit.2678710.1002/bit.26787 ↗
20. 10.1097/cmr.000000000000043110.1097/cmr.0000000000000431 ↗
21. 10.1002/smll.20140312610.1002/smll.201403126 ↗
22. 10.1177/184945441878261710.1177/1849454418782617 ↗
23. 10.1038/nnano.2016.23910.1038/nnano.2016.239 ↗
24. 10.1038/nprot.2016.00310.1038/nprot.2016.003 ↗
25. 10.1021/acs.analchem.5b0202310.1021/acs.analchem.5b02023 ↗
26. 10.1016/j.snb.2017.12.00310.1016/j.snb.2017.12.003 ↗
27. 10.1016/j.bios.2015.04.08010.1016/j.bios.2015.04.080 ↗
28. 10.1021/acs.analchem.6b0057010.1021/acs.analchem.6b00570 ↗
29. 10.1039/c5lc00947b10.1039/c5lc00947b ↗
30. 10.1016/j.colsurfb.2017.10.06010.1016/j.colsurfb.2017.10.060 ↗
31. 10.1371/journal.pone.005801710.1371/journal.pone.0058017 ↗
32. 10.1016/j.biotechadv.2018.03.00710.1016/j.biotechadv.2018.03.007 ↗
33. 10.1002/cncr.2944410.1002/cncr.29444 ↗
34. 10.1002/adfm.20150417610.1002/adfm.201504176 ↗
35. 10.1088/0034-4885/78/1/01660110.1088/0034-4885/78/1/016601 ↗
36. 10.3978/j.issn.2218-6751.2013.02.0610.3978/j.issn.2218-6751.2013.02.06 ↗
37. Zamay A. S. · 2017 · 6710.1007/978-3-319-55947-6_3 ↗
38. Ju H. · 2011 · 110.1007/978-1-4419-9622-0 ↗
39. 10.1021/ac070484i10.1021/ac070484i ↗
40. 10.1021/acs.analchem.5b0270210.1021/acs.analchem.5b02702 ↗
41. 10.1002/adma.20140362610.1002/adma.201403626 ↗
42. 10.1002/adma.20080139310.1002/adma.200801393 ↗
43. 10.1016/j.biomaterials.2011.08.07610.1016/j.biomaterials.2011.08.076 ↗
44. 10.1039/c8lc00708j10.1039/c8lc00708j ↗
45. 10.1016/j.polymer.2006.05.01710.1016/j.polymer.2006.05.017 ↗
46. 10.1166/jnn.2010.259610.1166/jnn.2010.2596 ↗
47. 10.1039/c3ra43919d10.1039/c3ra43919d ↗
48. 10.1103/physrevlett.73.143210.1103/physrevlett.73.1432 ↗
49. 10.1038/srep1552010.1038/srep15520 ↗
50. 10.1007/s10856-014-5159-710.1007/s10856-014-5159-7 ↗
51. 10.1371/journal.pone.008719010.1371/journal.pone.0087190 ↗
52. 10.1186/1556-276x-9-66410.1186/1556-276x-9-664 ↗
53. 10.1039/c7tb00157f10.1039/c7tb00157f ↗
54. 10.1021/acsami.5b0679110.1021/acsami.5b06791 ↗
55. 10.2147/ijn.s3611110.2147/ijn.s36111 ↗
56. 10.1186/s11671-018-2457-x10.1186/s11671-018-2457-x ↗
57. 10.1038/srep1753310.1038/srep17533 ↗