Issue 14, 2021, Issue in Progress

A high-performance microfluidic detection platform to conduct a novel multiple-biomarker panel for ovarian cancer screening

Abstract

Ovarian cancer is an important leading cause of cancer-related deaths among females, and a single biomarker does not have the sensitivity and specificity required for an effective ovarian cancer screening. Herein, we investigate a high-performance microfluidic detection platform to conduct a novel panel of multiple biomarkers for the early detection of ovarian carcinoma, which include CA125, HE4, OPN, MSLN, Hsp70, CA153, AFP, IL-6, and IL-8 using a microfluidic chip. High-throughput microfluidic chips and graphene oxide-assembled substrate are used to microprint repeatable capture antibody arrays and conduct multiple biomarkers in microscale volume samples. The proposed microfluidic platform achieves an ultralow detection limit of ∼1 pg mL−1 and 0.01 U mL−1 with excellent detection selectivity and a short detection time of 30 min. The analysis of serum biomarkers in 18 ovarian cancer patients and 4 healthy persons indicates a clear subgroup sorting between the high-grade serous ovarian carcinoma, borderline, and benign tumor patients, and healthy persons. The proposed detection platform and the biomarker panel are promising to conduct an early detection of ovarian cancer.

Graphical abstract: A high-performance microfluidic detection platform to conduct a novel multiple-biomarker panel for ovarian cancer screening

Article information

Article type
Paper
Submitted
03 Dec 2020
Accepted
30 Jan 2021
First published
19 Feb 2021
This article is Open Access
Creative Commons BY license

RSC Adv., 2021,11, 8124-8133

A high-performance microfluidic detection platform to conduct a novel multiple-biomarker panel for ovarian cancer screening

Y. Wu, C. Wang, P. Wang, C. Wang, Y. Zhang and L. Han, RSC Adv., 2021, 11, 8124 DOI: 10.1039/D0RA10200H

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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