Color-encoded multicompartmental hydrogel microspheres for multiplexed bioassays

IF 5.6 1区 化学 Q1 CHEMISTRY, ANALYTICAL
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Abstract

We develop color-encoded multicompartmental hydrogel (MH) microspheres tailored for multiplexed bioassays using a drop-based microfluidic approach. Our method involves the creation of triple emulsion drops that feature thin sacrificial oil layers separating two prepolymer phases. This configuration leads to the formation of poly(ethylene glycol) (PEG) multi-compartmental core-shell microspheres through photopolymerization, followed by the removal of the thin oil layers. The core compartments stably incorporate pigments, ensuring their retention within the hydrogel network without leakage, which facilitates reliable color encoding across varying spatial positions. Additionally, we introduce small molecule fluorescent labeling into the chemically functionalized shell compartments, achieving consistent distribution of functional components without the core's contamination. Importantly, our integrated one-pot conjugation of these color-encoded microspheres with affinity peptides enables the highly sensitive and selective detection of influenza virus antigens using a fluorescence bioassay, resulting in an especially low detection limit of 0.18 nM and 0.66 nM for influenza virus H1N1 and H5N1 antigens, respectively. This approach not only highlights the potential of our microspheres in clinical diagnostics but also paves the way for their application in a wide range of multiplexed assays.

Abstract Image

用于多重生物测定的彩色编码多室水凝胶微球
我们采用一种基于液滴的微流体方法,开发出专为多重生物测定定制的彩色编码多室水凝胶(MH)微球。我们的方法包括创建三重乳液液滴,其特点是以薄薄的牺牲油层分隔两个预聚物相。这种配置通过光聚合作用形成聚乙二醇(PEG)多室核壳微球,然后去除薄油层。核壳稳定地结合了颜料,确保它们保留在水凝胶网络中而不会泄漏,这有助于在不同的空间位置进行可靠的颜色编码。此外,我们还将小分子荧光标记引入化学功能化的外壳区块,实现了功能成分的一致分布,而不会污染核心。重要的是,我们将这些颜色编码微球与亲和肽进行了一体化的一次共轭,利用荧光生物测定法实现了对流感病毒抗原的高灵敏度和高选择性检测,使流感病毒 H1N1 和 H5N1 抗原的检测限特别低,分别为 0.18 nM 和 0.66 nM。这种方法不仅凸显了我们的微球在临床诊断中的潜力,还为其在各种多重检测中的应用铺平了道路。
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来源期刊
Talanta
Talanta 化学-分析化学
CiteScore
12.30
自引率
4.90%
发文量
861
审稿时长
29 days
期刊介绍: Talanta provides a forum for the publication of original research papers, short communications, and critical reviews in all branches of pure and applied analytical chemistry. Papers are evaluated based on established guidelines, including the fundamental nature of the study, scientific novelty, substantial improvement or advantage over existing technology or methods, and demonstrated analytical applicability. Original research papers on fundamental studies, and on novel sensor and instrumentation developments, are encouraged. Novel or improved applications in areas such as clinical and biological chemistry, environmental analysis, geochemistry, materials science and engineering, and analytical platforms for omics development are welcome. Analytical performance of methods should be determined, including interference and matrix effects, and methods should be validated by comparison with a standard method, or analysis of a certified reference material. Simple spiking recoveries may not be sufficient. The developed method should especially comprise information on selectivity, sensitivity, detection limits, accuracy, and reliability. However, applying official validation or robustness studies to a routine method or technique does not necessarily constitute novelty. Proper statistical treatment of the data should be provided. Relevant literature should be cited, including related publications by the authors, and authors should discuss how their proposed methodology compares with previously reported methods.
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