STUDY OF THE REUSABILITY AND STABILITY OF NYLON NANOFIBRES AS AN ANTIBODY IMMOBILISATION SURFACE

Submitting author affiliation:
INTA, Madrid, Spain

Beilstein Arch. 2023, 202342. https://doi.org/10.3762/bxiv.2023.42.v1

Published 09 Oct 2023

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Abstract

In the case of a biological threat, early, rapid and specific detection is critical. In addition, ease of handling, use in the field and low-cost production are important considerations. Immunological devices are able to respond to these needs. In the design of these immunological devices, surface antibody immobilisation is crucial. Nylon nanofibres have been described as a very good option because they allow an increase in the surface-to-volume ratio, leading to an increase in immunocapture efficiency. In this paper, we want to deepen the study of other key points, such as the reuse and stability of these nanofibres, in order to assess their profitability. On the one hand, the re-use of nanofibres has been studied using different stripping treatments based on different pH on the nylon nanofibres with well-oriented antibodies anchored by protein A/G. Our study shows that stripping with glycine buffer, pH 2.5, allows nanofibres to be reused as long as protein A/G is previously anchored, leaving both nanofibre and protein A/G unchanged. On the other hand, we investigated the stability of nylon nanofibres. To achieve this, we analysed any loss of immunocapture ability of well-oriented antibodies anchored both to the nylon nanofibres and to a specialised surface with high protein binding capacity. This immunocapture system maintained its immunocapture ability unchanged for a longer time than a planar specialised surface. In conclusion, nylon nanofibres seem to be a very good choice as an antibody immobilisation surface, offering not only higher immunocapture efficiency, but also more cost efficiency as they are reusable and stable.

Keywords: biothreat; biosensor, nanofibre, nylon, immunodetection.

How to Cite

When a peer-reviewed version of this preprint is available, this information will be updated in the information box above. If no peer-reviewed version is available, please cite this preprint using the following information:

Peraile, I.; Gil-García, M.; González-López, L.; Dabbagh-Escalante, N. A.; Cabria-Ramos, J. C.; Lorenzo-Lozano, P. Beilstein Arch. 2023, 202342. doi:10.3762/bxiv.2023.42.v1

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