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Biosensors Based on Porous Cellulose Nanocrystal-Poly(vinyl Alcohol) Scaffolds

机译:基于多孔纤维素纳米晶体-聚乙烯醇支架的生物传感器

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Cellulose nanocrystals (CNCs), which offer a high aspect ratio, large specific surface area, and large number of reactive surface groups, are well suited for the facile immobilization of high density biological probes. We here report functional high surface area scaffolds based on cellulose nanocrystals (CNCs) and poly(vinyl alcohol) (PVA) and demonstrate that this platform is useful for fluorescence-based sensing schemes. Porous CNC/PVA nanocomposite films with a thickness of 25—70 nm were deposited on glass substrates by dip-coating with an aqueous mixture of the CNCs and PVA, and the porous nanostructure was fixated by heat treatment. In a subsequent step, a portion of the scaffold's hydroxyl surface groups was reacted with 2-(acryloxy)ethyl (3-isocyanato-4-methylphenyl)carbamate to permit the immobilization of thiolated fluorescein-substituted lysine, which was used as a first sensing motif, via nucleophile-based thiol—ene Michael addition. The resulting sensor films exhibit a nearly instantaneous and pronounced change of their fluorescence emission intensity in response to changes in pH. The approach was further extended to the detection of protease activity by immobilizing a Forster-type resonance energy transfer chromophore pair via a labile peptide sequence to the scaffold. This sensing scheme is based on the degradation of the protein linker in the presence of appropriate enzymes, which separate the chrdmophores and causes a turn-on of the originally quenched fluorescence. Using a standard benchtop spectrometer to monitor the increase in fluorescence intensity, trypsin was detected at a concentration of 250 μg/mL, i.e., in a concentration that is typical for abnormal proteolytic activity in wound fluids.
机译:纤维素纳米晶体(CNC)具有高的长宽比,大的比表面积和大量的反应性表面基团,非常适合于轻松固定高密度生物探针。我们在这里报告基于纤维素纳米晶体(CNCs)和聚乙烯醇(PVA)的功能性高表面积支架,并证明该平台可用于基于荧光的传感方案。通过浸涂CNC和PVA的水性混合物,在玻璃基板上沉积厚度为25-70 nm的多孔CNC / PVA纳米复合膜,并通过热处理固定多孔纳米结构。在随后的步骤中,将支架的一部分羟基表面基团与2-(丙烯酰氧基)乙基(3-异氰酸根合-4-甲基苯基)氨基甲酸酯反应,以固定化巯基化的荧光素取代的赖氨酸,将其用作第一检测方法通过基于亲核试剂的硫醇-迈克尔基加成得到的基序。所得的传感器膜响应于pH的变化而显示出其荧光发射强度的几乎瞬时且明显的变化。通过将不稳定的肽序列将Forster型共振能量转移生色团对固定在支架上,该方法进一步扩展到蛋白酶活性的检测。该检测方案基于蛋白质连接子在适当酶的存在下的降解,该酶将色团分离并导致最初淬灭的荧光开启。使用标准台式光谱仪监测荧光强度的增加,检测到的胰蛋白酶浓度为250μg/ mL,即伤口液体中异常蛋白水解活性的典型浓度。

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