2019
DOI: 10.1371/journal.pone.0218686
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Antibody conjugation to carboxyl-modified microspheres through N-hydroxysuccinimide chemistry for automated immunoassay applications: A general procedure

Abstract: Immunochemical techniques are the workhorse for sample enrichment and detection of a large variety of analytes. In contrast to classical microtiter plate-based assays, microparticles are a next generation solid support, as they promote automation of immunoassays using flow-based techniques. Antibody immobilization is a crucial step, as these reagents are expensive, and inefficient coupling can result in low sensitivities. This paper proposes a general procedure for efficient immobilization of antibodies onto T… Show more

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Cited by 11 publications
(7 citation statements)
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“…MCP-6, whose structure is shown in Figure 1a, satisfies both requirements as its DMA-based backbone maintains the antifouling properties of the progenitor polymer copoly(DMA-NAS-MAPS, while the azide functionality allows the immobilization of the biomolecules via strain-promoted azide-alkyne cycloaddition (SPAAC) reaction. The active esters used to immobilize the biomolecules via amine coupling suffer from hydrolysis in aqueous media [21]. This phenomenon leads to poor reproducibility and low immobilization yields, thus impairing the performance of downstream applications [22].…”
Section: Resultsmentioning
confidence: 99%
“…MCP-6, whose structure is shown in Figure 1a, satisfies both requirements as its DMA-based backbone maintains the antifouling properties of the progenitor polymer copoly(DMA-NAS-MAPS, while the azide functionality allows the immobilization of the biomolecules via strain-promoted azide-alkyne cycloaddition (SPAAC) reaction. The active esters used to immobilize the biomolecules via amine coupling suffer from hydrolysis in aqueous media [21]. This phenomenon leads to poor reproducibility and low immobilization yields, thus impairing the performance of downstream applications [22].…”
Section: Resultsmentioning
confidence: 99%
“…In this reaction, the antibody is modified to carboxyl‐NPs by the reaction of its amino groups with NHS. Then, carboxyl groups are activated into NHS esters using classical NHS/EDC chemistry to form stable amide bonds (Carl et al., 2019). These antibody–carboxyl‐NPs are applied to the development of LFAs.…”
Section: Competitive Immobilizationmentioning
confidence: 99%
“…Here, the reaction of carboxylates with the EDC reagent produces an unstable reactive O-acylisourea ester, while subsequent reaction with sulfo-NHS enhances the coupling efficiency by producing semi-stable amine-reactive NHS-ester prior to the formation of the stable amide crosslinks with the amine groups of the protein. [31][32][33] Meanwhile, noncovalent 5-FU loading via the electron cloud of p back-bonded carbonyl oxygen of PEGylated AuNPs allows sustained drug release to enhance chemotherapeutic effects. 34 In order to reinvigorate the chemotherapeutic effects of 5-FU, it is pivotal to timely design the right drug carrier system with improved selectivity, effectiveness and controlled release of the drug into systemic circulation.…”
Section: Introductionmentioning
confidence: 99%