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Silver-Assembled Silica Nanoparticles in Lateral Flow Immunoassay for Visual Inspection of Prostate-Specific Antigen

Prostate-specific antigen (PSA) is the best-known biomarker for early diagnosis of prostate cancer. For prostate cancer in particular, the threshold level of PSA <4.0 ng/mL in clinical samples is an important indicator. Quick and easy visual detection of the PSA level greatly helps in early detec...

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Autores principales: Kim, Hyung-Mo, Kim, Jaehi, Bock, Sungje, An, Jaehyun, Choi, Yun-Sik, Pham, Xuan-Hung, Cha, Myeong Geun, Seong, Bomi, Kim, Wooyeon, Kim, Yoon-Hee, Song, Hobeom, Kim, Jung-Won, Park, Seung-min, Lee, Sang Hun, Rho, Won-Yeop, Lee, Sangchul, Jeong, Dae Hong, Lee, Ho-Young, Jun, Bong-Hyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8232291/
https://www.ncbi.nlm.nih.gov/pubmed/34203603
http://dx.doi.org/10.3390/s21124099
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author Kim, Hyung-Mo
Kim, Jaehi
Bock, Sungje
An, Jaehyun
Choi, Yun-Sik
Pham, Xuan-Hung
Cha, Myeong Geun
Seong, Bomi
Kim, Wooyeon
Kim, Yoon-Hee
Song, Hobeom
Kim, Jung-Won
Park, Seung-min
Lee, Sang Hun
Rho, Won-Yeop
Lee, Sangchul
Jeong, Dae Hong
Lee, Ho-Young
Jun, Bong-Hyun
author_facet Kim, Hyung-Mo
Kim, Jaehi
Bock, Sungje
An, Jaehyun
Choi, Yun-Sik
Pham, Xuan-Hung
Cha, Myeong Geun
Seong, Bomi
Kim, Wooyeon
Kim, Yoon-Hee
Song, Hobeom
Kim, Jung-Won
Park, Seung-min
Lee, Sang Hun
Rho, Won-Yeop
Lee, Sangchul
Jeong, Dae Hong
Lee, Ho-Young
Jun, Bong-Hyun
author_sort Kim, Hyung-Mo
collection PubMed
description Prostate-specific antigen (PSA) is the best-known biomarker for early diagnosis of prostate cancer. For prostate cancer in particular, the threshold level of PSA <4.0 ng/mL in clinical samples is an important indicator. Quick and easy visual detection of the PSA level greatly helps in early detection and treatment of prostate cancer and reducing mortality. In this study, we developed optimized silica-coated silver-assembled silica nanoparticles (SiO(2)@Ag@SiO(2) NPs) that were applied to a visual lateral flow immunoassay (LFIA) platform for PSA detection. During synthesis, the ratio of silica NPs to silver nitrate changed, and as the synthesized NPs exhibited distinct UV spectra and colors, most optimized SiO(2)@Ag@SiO(2) NPs showed the potential for early prostate cancer diagnosis. The PSA detection limit of our LFIA platform was 1.1 ng/mL. By applying each SiO(2)@Ag@SiO(2) NP to the visual LFIA platform, optimized SiO(2)@Ag@SiO(2) NPs were selected in the test strip, and clinical samples from prostate cancer patients were successfully detected as the boundaries of non-specific binding were clearly seen and the level of PSA was <4 ng/mL, thus providing an avenue for quick prostate cancer diagnosis and early treatment.
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spelling pubmed-82322912021-06-26 Silver-Assembled Silica Nanoparticles in Lateral Flow Immunoassay for Visual Inspection of Prostate-Specific Antigen Kim, Hyung-Mo Kim, Jaehi Bock, Sungje An, Jaehyun Choi, Yun-Sik Pham, Xuan-Hung Cha, Myeong Geun Seong, Bomi Kim, Wooyeon Kim, Yoon-Hee Song, Hobeom Kim, Jung-Won Park, Seung-min Lee, Sang Hun Rho, Won-Yeop Lee, Sangchul Jeong, Dae Hong Lee, Ho-Young Jun, Bong-Hyun Sensors (Basel) Article Prostate-specific antigen (PSA) is the best-known biomarker for early diagnosis of prostate cancer. For prostate cancer in particular, the threshold level of PSA <4.0 ng/mL in clinical samples is an important indicator. Quick and easy visual detection of the PSA level greatly helps in early detection and treatment of prostate cancer and reducing mortality. In this study, we developed optimized silica-coated silver-assembled silica nanoparticles (SiO(2)@Ag@SiO(2) NPs) that were applied to a visual lateral flow immunoassay (LFIA) platform for PSA detection. During synthesis, the ratio of silica NPs to silver nitrate changed, and as the synthesized NPs exhibited distinct UV spectra and colors, most optimized SiO(2)@Ag@SiO(2) NPs showed the potential for early prostate cancer diagnosis. The PSA detection limit of our LFIA platform was 1.1 ng/mL. By applying each SiO(2)@Ag@SiO(2) NP to the visual LFIA platform, optimized SiO(2)@Ag@SiO(2) NPs were selected in the test strip, and clinical samples from prostate cancer patients were successfully detected as the boundaries of non-specific binding were clearly seen and the level of PSA was <4 ng/mL, thus providing an avenue for quick prostate cancer diagnosis and early treatment. MDPI 2021-06-15 /pmc/articles/PMC8232291/ /pubmed/34203603 http://dx.doi.org/10.3390/s21124099 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kim, Hyung-Mo
Kim, Jaehi
Bock, Sungje
An, Jaehyun
Choi, Yun-Sik
Pham, Xuan-Hung
Cha, Myeong Geun
Seong, Bomi
Kim, Wooyeon
Kim, Yoon-Hee
Song, Hobeom
Kim, Jung-Won
Park, Seung-min
Lee, Sang Hun
Rho, Won-Yeop
Lee, Sangchul
Jeong, Dae Hong
Lee, Ho-Young
Jun, Bong-Hyun
Silver-Assembled Silica Nanoparticles in Lateral Flow Immunoassay for Visual Inspection of Prostate-Specific Antigen
title Silver-Assembled Silica Nanoparticles in Lateral Flow Immunoassay for Visual Inspection of Prostate-Specific Antigen
title_full Silver-Assembled Silica Nanoparticles in Lateral Flow Immunoassay for Visual Inspection of Prostate-Specific Antigen
title_fullStr Silver-Assembled Silica Nanoparticles in Lateral Flow Immunoassay for Visual Inspection of Prostate-Specific Antigen
title_full_unstemmed Silver-Assembled Silica Nanoparticles in Lateral Flow Immunoassay for Visual Inspection of Prostate-Specific Antigen
title_short Silver-Assembled Silica Nanoparticles in Lateral Flow Immunoassay for Visual Inspection of Prostate-Specific Antigen
title_sort silver-assembled silica nanoparticles in lateral flow immunoassay for visual inspection of prostate-specific antigen
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8232291/
https://www.ncbi.nlm.nih.gov/pubmed/34203603
http://dx.doi.org/10.3390/s21124099
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