Detection of bleomycin and its hydrolase by the cationic surfactant-doped liquid crystal-based sensing platform.

5CB Bleomycin Bleomycin hydrolase Interface Liquid crystal Sensing

Journal

Analytica chimica acta
ISSN: 1873-4324
Titre abrégé: Anal Chim Acta
Pays: Netherlands
ID NLM: 0370534

Informations de publication

Date de publication:
15 Mar 2021
Historique:
received: 08 12 2020
revised: 18 01 2021
accepted: 19 01 2021
entrez: 15 2 2021
pubmed: 16 2 2021
medline: 15 5 2021
Statut: ppublish

Résumé

Bleomycin (BLM) is a broadly used antibiotic to treat different types of cancer. It can be hydrolyzed by bleomycin hydrolase (BLMH), which eventually influences the anti-tumor efficacy of BLM. Therefore, it is particularly important to detect BLM and BLMH. Herein, we demonstrated highly sensitive detection of BLM and BLMH by a simple and convenient liquid crystal (LC)-based sensing platform for the first time. 5CB (a nematic LC) doped with the cationic surfactant OTAB was working as the sensing platform. When the OTAB-laden 5CB interface was in contact with an aqueous solution of ssDNA, LCs displayed a bright image due to disruption of the arrangement of OTAB monolayers by ssDNA, indicating the planar orientation of LCs at the aqueous/LC interface. When BLM·Fe(II) and ssDNA were both present in the aqueous solution, ssDNA underwent irreversible cleavage, which prevented disruption of the arrangement of OTAB monolayers. Accordingly, LCs showed a dark image, suggesting the homeotropic orientation of LCs at the aqueous/LC interface. However, when BLM·Fe(II) was enzymatically hydrolyzed by BLMH, LCs remained the bright image. This approach showed high sensitivity for the detection of BLM and BLMH with the limits of detection of 0.2 nM and 0.3 ng/mL, respectively. Besides, the detection of BLM and BLMH was successfully achieved in human serum. This method has the advantages of high sensitivity, robust stability, simple operation, low cost, and easy detection through naked eyes, which makes it a potential candidate for applications in clinical analysis.

Identifiants

pubmed: 33583545
pii: S0003-2670(21)00073-8
doi: 10.1016/j.aca.2021.338247
pii:
doi:

Substances chimiques

DNA, Single-Stranded 0
Surface-Active Agents 0
Bleomycin 11056-06-7
Hydrolases EC 3.-

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

338247

Informations de copyright

Copyright © 2021 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Supan Cheng (S)

School of Pharmaceutical Sciences, Qilu University of Technology (Shandong Academy of Sciences), Jinan, 250014, China.

Mashooq Khan (M)

School of Pharmaceutical Sciences, Qilu University of Technology (Shandong Academy of Sciences), Jinan, 250014, China; Department of Chemistry, Tsinghua University, Ministry of Education, Beijing, 100084, China.

Limei Luo (L)

Maternal and Child Health Development Research Center, Shandong Provincial Maternal and Child Health Care Hospital, Jinan, 250014, China.

Li Wang (L)

School of Mechanical & Automotive Engineering, Qilu University of Technology (Shandong Academy of Sciences), Jinan, Shandong, 250353, China.

Shuhua Liu (S)

School of Pharmaceutical Sciences, Qilu University of Technology (Shandong Academy of Sciences), Jinan, 250014, China.

Jiantao Ping (J)

School of Pharmaceutical Sciences, Qilu University of Technology (Shandong Academy of Sciences), Jinan, 250014, China.

Jin-Ming Lin (JM)

Department of Chemistry, Tsinghua University, Ministry of Education, Beijing, 100084, China.

Qiongzheng Hu (Q)

School of Pharmaceutical Sciences, Qilu University of Technology (Shandong Academy of Sciences), Jinan, 250014, China. Electronic address: huqz@qlu.edu.cn.

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Classifications MeSH