4.7 Article

Three-dimensional porous calcium alginate fluorescence bead-based immunoassay for highly sensitive early diagnosis of breast cancer

Journal

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
Volume 414, Issue 3, Pages 1359-1373

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-021-03758-x

Keywords

Breast cancer; Multiplexed immunoassay; HER2; CA125; Calcium alginate bead; Sandwich immunoassay

Funding

  1. [ST003-2019]

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A novel method of multiplex analysis was proposed using three-dimensional porous calcium alginate beads for detecting serum-HER2 and serum-CA125 breast cancer biomarkers, with high sensitivity and improved linear dynamic range. The developed system showed good agreement with standard methods when analyzing real clinical samples, and the analysis only required approximately 30 minutes. This approach has the potential for use in multiplex assays and biosensors.
A sensitive biosensor capable of detecting trace concentrations of several cancer biomarkers in clinical samples is critical for early detection of cancer because different cancer biomarkers may be expressed at different stages of cancer. Previous multiplex studies using microarrays or color-coded beads had limited multiplex detection in a single well, and difficulty in optimizing and unifying the incubation parameters for all tests made in different wells had posed challenges to small sample size and lengthened assay time. Herein, we proposed a novel approach to achieve multiplex analysis on a single three-dimensional porous calcium alginate bead. Because of the high surface area to volume ratio of the calcium alginate immuno-bead, the sensitivity and linear dynamic range of the as-proposed multiplex analysis method are significantly improved. Based on the direct sandwich immunoassay principle, dual-capturing antibodies were encapsulated into a single 3D porous calcium alginate bead as a proof-of-concept for multiplexity detection of serum-HER2 and serum-CA125 breast cancer biomarkers. High sensitivity was attained, with LODs of 0.004 ng mL(-1) for serum HER2, and 0.005 U mL(-1) for serum CA125, both of which are below the clinical cutoff values, enabling for early breast cancer diagnosis. Stability tests revealed that the 3D immuno-beads were stable at 4 degrees C and room temperature (25 degrees C) for at least 14 days. Most importantly, the results obtained using the developed system were in good agreement with those obtained using standard methods while analyzing real clinical samples. In addition, the analysis required only approximately 30 min, which was much less time than typical ELISA techniques. When endogenous interferences were introduced, no cross-reactivity was observed. We anticipate this approach to be potentially used in the multiplex assays and biosensors.

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