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Intrant ELISA: A Novel Approach to Fabrication of Electrospun Fiber Mat-Assisted Biosensor Platforms and Their Integration within Standard Analytical Well Plates

机译:酶联免疫吸附测定法:一种新型的电纺纤维垫辅助生物传感器平台制造方法及其在标准分析孔板上的整合

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A combination of far-field electrospinning (FFES) and free-radical polymerization has been used to fabricate coated electrospun polymer fiber mats as a new type of biosensor platform. Poly (3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) electrospun fibers were dip-coated with different compositions of poly methyl methacrylate-co-methacrylic acid (poly(MMA-co-MAA)). This synergistic approach utilizes large specific surface area of PHBV fibers and co-polymer coatings that feature an optimum concentration of surface carboxyl (–COOH) groups. The platform surface morphology, porosity and tunable hydrophobicity enhance biomolecular interactions via plurality of molecular forces. These customized fiber mats have been integrated into a newly designed 96-well plate called an “intrant enzyme-linked immunosorbent assay” or i-ELISA. I-ELISA allows colorimetric sandwich assay to be carried out without any modifications or additional steps in ELISA methodology. By introducing the fiber mats in fabrication of i-ELISA via extensions on the lid, we address some of the limitations of the previous designs while demonstrating an enhanced signal intensity up to 12 times higher than that of conventional assays. With improved sensitivity, specificity and accuracy in the detection of dengue virus, i-ELISA has proven to be a reliable platform for biomolecular recognition. The proposed fiber mat-assisted well plate in this study holds great potential as a universal approach for integration of different types of fiber mats with pre-designed specific properties in order to enhance the detection sensitivity of the assay.
机译:远场静电纺丝(FFES)和自由基聚合的结合已被用于制造涂覆的静电纺聚合物纤维垫,作为一种新型的生物传感器平台。将聚(3-羟基丁酸酯-共-3-羟基戊酸酯)(PHBV)电纺纤维浸涂有不同组成的聚甲基丙烯酸甲酯-共-甲基丙烯酸(聚(MMA-共MAA))。这种协同方法利用PHBV纤维和共聚物涂层的大比表面积,这些涂层具有最佳的表面羧基(–COOH)浓度。平台的表面形态,孔隙率和可调的疏水性通过多种分子力增强了生物分子的相互作用。这些定制的纤维垫已整合到新设计的96孔板中,称为“酶联免疫吸附测定法”或i-ELISA。 I-ELISA可以进行比色夹心测定,而无需对ELISA方法进行任何修改或其他步骤。通过在盖子上加长盖来在i-ELISA的制造过程中引入纤维垫,我们解决了先前设计的一些局限性,同时证明了增强的信号强度是传统测定方法的12倍。通过提高登革热病毒检测的灵敏度,特异性和准确性,i-ELISA已被证明是用于生物分子识别的可靠平台。在这项研究中,提出的纤维垫辅助孔板具有巨大的潜力,可以作为一种通用方法来整合具有预先设计的特定特性的不同类型的纤维垫,以提高测定的检测灵敏度。

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