Affinity-Enhanced CTC-Capturing Hydrogel Microparticles Fabricated by Degassed Mold Lithography

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 functiona...

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Published in:Journal of Clinical Medicine
Main Authors: Nak Jun Lee, Sejung Maeng, Hyeon Ung Kim, Yoon Ho Roh, Changhyun Hwang, Jongjin Kim, Ki-Tae Hwang, Ki Wan Bong
Format: Text
Language:English
Published: Multidisciplinary Digital Publishing Institute 2020
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Online Access:https://doi.org/10.3390/jcm9020301
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author Nak Jun Lee
Sejung Maeng
Hyeon Ung Kim
Yoon Ho Roh
Changhyun Hwang
Jongjin Kim
Ki-Tae Hwang
Ki Wan Bong
author_facet Nak Jun Lee
Sejung Maeng
Hyeon Ung Kim
Yoon Ho Roh
Changhyun Hwang
Jongjin Kim
Ki-Tae Hwang
Ki Wan Bong
author_sort Nak Jun Lee
collection MDPI Open Access Publishing
container_issue 2
container_start_page 301
container_title Journal of Clinical Medicine
container_volume 9
description 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.
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op_doi https://doi.org/10.3390/jcm9020301
op_relation Oncology
https://dx.doi.org/10.3390/jcm9020301
op_rights https://creativecommons.org/licenses/by/4.0/
op_source Journal of Clinical Medicine; Volume 9; Issue 2; Pages: 301
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spelling ftmdpi:oai:mdpi.com:/2077-0383/9/2/301/ 2025-01-16T21:38:26+00:00 Affinity-Enhanced CTC-Capturing Hydrogel Microparticles Fabricated by Degassed Mold Lithography Nak Jun Lee Sejung Maeng Hyeon Ung Kim Yoon Ho Roh Changhyun Hwang Jongjin Kim Ki-Tae Hwang Ki Wan Bong 2020-01-21 application/pdf https://doi.org/10.3390/jcm9020301 EN eng Multidisciplinary Digital Publishing Institute Oncology https://dx.doi.org/10.3390/jcm9020301 https://creativecommons.org/licenses/by/4.0/ Journal of Clinical Medicine; Volume 9; Issue 2; Pages: 301 circulating tumor cell cell capture hydrogel microparticle degassed mold lithography Text 2020 ftmdpi https://doi.org/10.3390/jcm9020301 2023-07-31T23:01:38Z 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. Text DML MDPI Open Access Publishing Journal of Clinical Medicine 9 2 301
spellingShingle circulating tumor cell
cell capture
hydrogel microparticle
degassed mold lithography
Nak Jun Lee
Sejung Maeng
Hyeon Ung Kim
Yoon Ho Roh
Changhyun Hwang
Jongjin Kim
Ki-Tae Hwang
Ki Wan Bong
Affinity-Enhanced CTC-Capturing Hydrogel Microparticles Fabricated by Degassed Mold Lithography
title Affinity-Enhanced CTC-Capturing Hydrogel Microparticles Fabricated by Degassed Mold Lithography
title_full Affinity-Enhanced CTC-Capturing Hydrogel Microparticles Fabricated by Degassed Mold Lithography
title_fullStr Affinity-Enhanced CTC-Capturing Hydrogel Microparticles Fabricated by Degassed Mold Lithography
title_full_unstemmed Affinity-Enhanced CTC-Capturing Hydrogel Microparticles Fabricated by Degassed Mold Lithography
title_short Affinity-Enhanced CTC-Capturing Hydrogel Microparticles Fabricated by Degassed Mold Lithography
title_sort affinity-enhanced ctc-capturing hydrogel microparticles fabricated by degassed mold lithography
topic circulating tumor cell
cell capture
hydrogel microparticle
degassed mold lithography
topic_facet circulating tumor cell
cell capture
hydrogel microparticle
degassed mold lithography
url https://doi.org/10.3390/jcm9020301