2020
DOI: 10.1016/j.snb.2020.128380
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Surface plasmon resonance-based aptasensor for direct monitoring of thrombin in a minimally processed human blood

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Cited by 35 publications
(44 citation statements)
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“…[7,8] Thus, the practical application of bioactive surfaces requires antifouling layers capable of preventing protein and cell fouling from complex biological media. [9,10] Antifouling coatings can be generated by immobilizing self-assembled monolayers (SAMs) or "grafted-to" or "graftedfrom" polymer coatings on a surface. [6,[11][12][13][14] SAMs are broadly applied to introduce different functionalities to the surfaces.…”
mentioning
confidence: 99%
“…[7,8] Thus, the practical application of bioactive surfaces requires antifouling layers capable of preventing protein and cell fouling from complex biological media. [9,10] Antifouling coatings can be generated by immobilizing self-assembled monolayers (SAMs) or "grafted-to" or "graftedfrom" polymer coatings on a surface. [6,[11][12][13][14] SAMs are broadly applied to introduce different functionalities to the surfaces.…”
mentioning
confidence: 99%
“…Notably most small molecules bind aptamers only with the one-site binding configuration because there is no room for the aptamer to interact with a second molecule [60]. Therefore, many SPR aptasensors have been developed based on this direct strategy [61][62][63][64][65]. For example Wu et al and Ashley et al immobilized a biotin-modified aptamer probe on an avidin modified chip through streptavidin-biotin interaction for the detection of aflatoxin in vin egar and lysozyme in milk [66,67].…”
Section: Basic Spr Assaymentioning
confidence: 99%
“…Lately, the same antifouling polymer brush (poly [HPMA-co-CBMAA]) was synthesized on a gold surface via photoinduced single-electron transfer living radical polymerization and then functionalized by including three aptamers for specific direct detection of two particular binding sites of thrombin (exosite I and II) in minimally processed 10% blood. This brush architecture exhibited a limit of detection with HD1 aptamer equal to 0.7 nM, adequate for predicting a thrombotic event and diagnosis of thrombosis [118].…”
Section: Antifouling Strategies For Spr Biosensing In Clinical Diagno...mentioning
confidence: 99%