Affinity-Enhanced CTC-Capturing Hydrogel Microparticles Fabricated by Degassed Mold Lithography.
cell capture
circulating tumor cell
degassed mold lithography
hydrogel microparticle
Journal
Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588
Informations de publication
Date de publication:
21 Jan 2020
21 Jan 2020
Historique:
received:
11
12
2019
revised:
16
01
2020
accepted:
18
01
2020
entrez:
25
1
2020
pubmed:
25
1
2020
medline:
25
1
2020
Statut:
epublish
Résumé
Technologies for the detection and isolation of circulating tumor cells (CTCs) are essential in liquid biopsy, a minimally invasive technique for early diagnosis and medical intervention in cancer patients. A promising method for CTC capture, using an affinity-based approach, is the use of functionalized hydrogel microparticles (MP), which have the advantages of water-like reactivity, biologically compatible materials, and synergy with various analysis platforms. In this paper, we demonstrate the feasibility of CTC capture by hydrogel particles synthesized using a novel method called degassed mold lithography (DML). This technique increases the porosity and functionality of the MPs for effective conjugation with antibodies. Qualitative fluorescence analysis demonstrates that DML produces superior uniformity, integrity, and functionality of the MPs, as compared to conventional stop flow lithography (SFL). Analysis of the fluorescence intensity from porosity-controlled MPs by each reaction step of antibody conjugation elucidates that more antibodies are loaded when the particles are more porous. The feasibility of selective cell capture is demonstrated using breast cancer cell lines. In conclusion, using DML for the synthesis of porous MPs offers a powerful method for improving the cell affinity of the antibody-conjugated MPs.
Identifiants
pubmed: 31973077
pii: jcm9020301
doi: 10.3390/jcm9020301
pmc: PMC7073783
pii:
doi:
Types de publication
Journal Article
Langues
eng
Subventions
Organisme : National Research Foundation of Korea
ID : NRF-2016R1A5A1010148
Organisme : Next-Generation Biogreen 21 Program
ID : PJ013158
Organisme : National Research Foundation of Korea
ID : NRF-2018R1D1A1B07046577
Organisme : Seoul National University College of Medicine
ID : 800-20160257
Organisme : Seoul National University Hospital
ID : 03-2016-0400
Organisme : National Research Foundation of Korea
ID : NRF-2017R1D1A1B03029392
Déclaration de conflit d'intérêts
The authors declare no conflict of interest.
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