An efficient direct competitive nano-ELISA for residual BSA determination in vaccines

• Published in: Analytical and bioanalytical chemistry 2017-07, Vol.409 (19), p.4607-4614
• Main Authors: Wang, Qian-Long, Li, Jie, Li, Xing-De, Tao, Wan-Jun, Ding, Li-Sheng, Luo, Pei, Qing, Lin-Sen
• Format: Article
• Language: English
• Subjects: Analytical Chemistry; Antigens; Biochemistry; Bovine serum albumin; Characterization and Evaluation of Materials; Chemistry; Chemistry and Materials Science; Coefficient of variation; Enzyme-linked immunosorbent assay; Food Science; Horseradish peroxidase; Laboratory Medicine; Methods; Monitoring/Environmental Analysis; Nanomaterials; Nanoparticles; Nanotechnology; Peroxidase; Properties; Quality control; Research Paper; Serum albumin; Silicon dioxide; Testing; Vaccines
• ISSN: 1618-2642; 1618-2650
• DOI: 10.1007/s00216-017-0403-x

A simple, fast, and highly sensitive direct competitive enzyme-linked immunosorbent assay (ELISA) based on bovine serum albumin (BSA) antigen labeled amine-terminated silicon dioxide (SiO 2 –NH–BSA) nanoparticles was developed to determine residual BSA in vaccines. As nano-ELISA using nanomaterials with a very high surface-to-volume ratio has emerged as a promising strategy, SiO 2 –NH–BSA nanoparticles were prepared in this study by the coupling of BSA to SiO 2 nanoparticles modified with amidogen, followed by the quantification of BSA via a direct competitive binding of BSA-antigen-labeled SiO 2 nanoparticles to anti-BSA antibody conjugated with horseradish peroxidase. The validation study showed that the linear range of this method was from 1 to 90 ng/mL ( r  = 0.998) and the limit of detection was 0.67 ng/mL. The intra-assay and interassay coefficients of variation were less than 10% at three concentrations (10, 40, and 70 ng/mL), and the recovery was 92.4%, indicating good specificity. As a proof of principle, this new method was applied in the analysis of residual BSA in five different vaccines. Bland–Altman plots revealed that there was no significant difference in the accuracy and precision between our new method and the most commonly used sandwich ELISA. From the results taken together, the new method developed in this study is more sensitive and facile with lower cost and thus demonstrated potential to be applied in the quality control of biological products. Graphical Abstract Illustration of the procedures of the direct competitive enzyme immunoassay