Size-exclusion chromatography for the characterization of urinary extracellular vesicles.

In recent years, extracellular vesicles (EVs) have gained attention for their potential as biomarkers for the early diagnosis and treatment of various diseases. Traditionally, EV isolation has relied exclusively on ultracentrifugation. However, alternative enrichment methods such as size-exclusion c...

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Main Authors: Park, Sanghwi, Jalaludin, Iqbal, Hwang, Hyojin, Ko, Minjeong, Adelipour, Maryam, Hwan, Myung, Cho, Namjoon, Kim, Kee K., Lubman, David M., Kim, Jeongkwon
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Published: Elsevier B.V. 2023
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Online Access:http://eprints.utm.my/106349/
http://dx.doi.org/10.1016/j.jchromb.2023.123828
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spelling my.utm.1063492024-07-09T06:11:05Z http://eprints.utm.my/106349/ Size-exclusion chromatography for the characterization of urinary extracellular vesicles. Park, Sanghwi Jalaludin, Iqbal Hwang, Hyojin Ko, Minjeong Adelipour, Maryam Hwan, Myung Cho, Namjoon Kim, Kee K. Lubman, David M. Kim, Jeongkwon QD Chemistry In recent years, extracellular vesicles (EVs) have gained attention for their potential as biomarkers for the early diagnosis and treatment of various diseases. Traditionally, EV isolation has relied exclusively on ultracentrifugation. However, alternative enrichment methods such as size-exclusion chromatography (SEC) and polyethylene glycol-based precipitation have been introduced. This study utilized SEC as a characterization tool to assess the efficiency of EV isolation. Urinary EVs isolated from human urine using centrifugation (40,000 × g) were analyzed using an SEC column with a pore size of 1000 Å, an inner diameter of 7.8 mm, and a length of 300 mm. The EVs were detected sequentially using UV (280 nm) and fluorescence (λex/em = 550 nm/565 nm); the EVs were observed at approximately 6 min, while the proteins were observed at approximately 12 min. The repeated centrifugation enrichment steps resulted in an increase in EV peaks and a decrease in protein peaks. SEC analysis of the enriched EV samples confirmed that a four-cycle repetition of centrifugation is necessary for successful EV enrichment and removal of non-EV proteins from 40 mL of human urine. Elsevier B.V. 2023-08-01 Article PeerReviewed Park, Sanghwi and Jalaludin, Iqbal and Hwang, Hyojin and Ko, Minjeong and Adelipour, Maryam and Hwan, Myung and Cho, Namjoon and Kim, Kee K. and Lubman, David M. and Kim, Jeongkwon (2023) Size-exclusion chromatography for the characterization of urinary extracellular vesicles. Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences, 1228 (123828). NA-NA. ISSN 1570-0232 http://dx.doi.org/10.1016/j.jchromb.2023.123828 DOI:10.1016/j.jchromb.2023.123828
institution Universiti Teknologi Malaysia
building UTM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Teknologi Malaysia
content_source UTM Institutional Repository
url_provider http://eprints.utm.my/
topic QD Chemistry
spellingShingle QD Chemistry
Park, Sanghwi
Jalaludin, Iqbal
Hwang, Hyojin
Ko, Minjeong
Adelipour, Maryam
Hwan, Myung
Cho, Namjoon
Kim, Kee K.
Lubman, David M.
Kim, Jeongkwon
Size-exclusion chromatography for the characterization of urinary extracellular vesicles.
description In recent years, extracellular vesicles (EVs) have gained attention for their potential as biomarkers for the early diagnosis and treatment of various diseases. Traditionally, EV isolation has relied exclusively on ultracentrifugation. However, alternative enrichment methods such as size-exclusion chromatography (SEC) and polyethylene glycol-based precipitation have been introduced. This study utilized SEC as a characterization tool to assess the efficiency of EV isolation. Urinary EVs isolated from human urine using centrifugation (40,000 × g) were analyzed using an SEC column with a pore size of 1000 Å, an inner diameter of 7.8 mm, and a length of 300 mm. The EVs were detected sequentially using UV (280 nm) and fluorescence (λex/em = 550 nm/565 nm); the EVs were observed at approximately 6 min, while the proteins were observed at approximately 12 min. The repeated centrifugation enrichment steps resulted in an increase in EV peaks and a decrease in protein peaks. SEC analysis of the enriched EV samples confirmed that a four-cycle repetition of centrifugation is necessary for successful EV enrichment and removal of non-EV proteins from 40 mL of human urine.
format Article
author Park, Sanghwi
Jalaludin, Iqbal
Hwang, Hyojin
Ko, Minjeong
Adelipour, Maryam
Hwan, Myung
Cho, Namjoon
Kim, Kee K.
Lubman, David M.
Kim, Jeongkwon
author_facet Park, Sanghwi
Jalaludin, Iqbal
Hwang, Hyojin
Ko, Minjeong
Adelipour, Maryam
Hwan, Myung
Cho, Namjoon
Kim, Kee K.
Lubman, David M.
Kim, Jeongkwon
author_sort Park, Sanghwi
title Size-exclusion chromatography for the characterization of urinary extracellular vesicles.
title_short Size-exclusion chromatography for the characterization of urinary extracellular vesicles.
title_full Size-exclusion chromatography for the characterization of urinary extracellular vesicles.
title_fullStr Size-exclusion chromatography for the characterization of urinary extracellular vesicles.
title_full_unstemmed Size-exclusion chromatography for the characterization of urinary extracellular vesicles.
title_sort size-exclusion chromatography for the characterization of urinary extracellular vesicles.
publisher Elsevier B.V.
publishDate 2023
url http://eprints.utm.my/106349/
http://dx.doi.org/10.1016/j.jchromb.2023.123828
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