journal article·2019-10-22

Peptide-Based Assemblies on Electrospun Polyamide-6/Chitosan Nanofibers for Detecting Visceral Leishmaniasis Antibodies

Michelle S. Liberato, Rodrigo S. N. Mancini, Irina M. Factori, Fabio F. Ferreira, Vivian L. de Oliveira, Juliana B. T. Carnielli, Suchismita Guha, Luis A. Peroni, Marcone A. L. Oliveira, Wendel A. Alves

ACS Applied Electronic Materials· Volume 1· Issue 10
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Abstract

An alternative label-free electrochemical immunosensor for the rapid detection of Leishmania braziliensis was developed by immobilizing a peptide-based probe of the promastigote surface antigen (PSA-38S) onto electrospun polyamide-6 (PA6)/chitosan nanofibers. An increase in chitosan content in the spinning solution leads to a decrease in the diameter of the formed fibers, whereas the differential scanning calorimetry (DSC) and X-ray diffraction (XRD) data showed a decrease in crystallinity upon increasing the chitosan content in the formulation. In addition, the incorporation of chitosan into the PA6 nanofibers tends to decrease the resistance to the charge-transfer process at the electrode surface. A 40 wt % chitosan content was used for immobilization of the peptide antigen, which was characterized by scanning electron microscopy (SEM) and electrochemical impedance spectroscopy (EIS). The detection was performed by measuring the relative change in impedance before and after the anti-Leishmania braziliensis reaction by EIS. Under the optimized conditions, the relative change in impedance was proportional to the logarithmic value of PSA concentrations in the range of 2.5 to 10 pg·mL–1(r2 = 0.9946) with a detection limit of 0.2 pg·mL–1, which was slightly lower than that of the enzyme-linked immunosorbent assay. Additionally, the sensor was tested against two nonspecific antibodies (T. cruzi and β-actin), whereas multivariate analysis using unsupervised pattern recognition through principal component analysis was successfully applied to identification of the pattern relative to each antibody. Finally, the optimized electrochemical immunoassay can be a favorable approach for Leishmania detection tests, as it is able to differentiate negative and positive visceral leishmaniasis human serum samples.
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Research context

OpenAlex topics: Research on Leishmaniasis Studies · Trypanosoma species research and implications · Synthesis and Biological Evaluation

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Centro de Ciências Naturais e Humanas, Universidade Federal do ABC, Santo André, São Paulo 09210-580, Brazil

Núcleo de Doenças Infecciosas, Universidade Federal do Espírito Santo, Vitória, Espírito Santo 29047-100, Brazil

Department of Physics and Astronomy, University of Missouri, Columbia, Missouri 65211, United States

Rheabiotech Company, Campinas, São Paulo 13084-791, Brazil

Departamento de Química, Universidade Federal de Juiz de Fora, Juiz de Fora, Minas Gerais 36036-330, Brazil

Funding

Conselho Nacional de Desenvolvimento Cient?fico e Tecnol?gico · Funda??o de Amparo ? Pesquisa do Estado de S?o Paulo · Division of Electrical, Communications and Cyber Systems · Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior

References (43)

Show source-provided references
1. 10.1590/S0036-4665200900050000310.1590/S0036-46652009000500003 ↗
2. 10.1016/j.cimid.2004.03.00410.1016/j.cimid.2004.03.004 ↗
3. 10.1128/CDLI.9.5.951-958.200210.1128/CDLI.9.5.951-958.2002 ↗
4. 10.1016/j.trstmh.2010.09.00610.1016/j.trstmh.2010.09.006 ↗
5. 10.1073/pnas.90.2.77510.1073/pnas.90.2.775 ↗
6. 10.1016/j.micpath.2017.06.02010.1016/j.micpath.2017.06.020 ↗
7. 10.1186/1471-2148-8-29210.1186/1471-2148-8-292 ↗
8. 10.4049/jimmunol.172.8.490210.4049/jimmunol.172.8.4902 ↗
9. Murray P. J. · J. Immunol. · 1989 · 143 · 422110.4049/jimmunol.143.12.4221 ↗
10. 10.1073/pnas.87.21.839310.1073/pnas.87.21.8393 ↗
11. 10.1074/jbc.272.28.1736010.1074/jbc.272.28.17360 ↗
12. 10.1046/j.1432-1327.1998.2510389.x10.1046/j.1432-1327.1998.2510389.x ↗
13. McMahon-Pratt D. · Infect. Immun. · 1993 · 61 · 335110.1128/iai.61.8.3351-3359.1993 ↗
14. Handman E. · Infect. Immun. · 1995 · 63 · 426110.1128/iai.63.11.4261-4267.1995 ↗
15. 10.1016/S0928-8244(98)00015-710.1016/S0928-8244(98)00015-7 ↗
16. 10.1046/j.1365-3024.2000.00269.x10.1046/j.1365-3024.2000.00269.x ↗
17. 10.1039/C5TB02240A10.1039/C5TB02240A ↗
18. 10.4269/ajtmh.2003.68.32110.4269/ajtmh.2003.68.321 ↗
19. 10.1016/j.progpolymsci.2009.04.00110.1016/j.progpolymsci.2009.04.001 ↗
20. 10.3390/ijms1902040710.3390/ijms19020407 ↗
21. 10.1021/bm060804s10.1021/bm060804s ↗
22. 10.1002/polb.1001510.1002/polb.10015 ↗
23. 10.5772/5709910.5772/57099 ↗
24. Aharoni S. M. · 1997
25. 10.1021/ma070039p10.1021/ma070039p ↗
26. Najafi M. · 2017
27. 10.1002/pol.1955.12017840110.1002/pol.1955.120178401 ↗
28. 10.1002/pol.1965.10003013210.1002/pol.1965.100030132 ↗
29. 10.1016/j.electacta.2009.05.02110.1016/j.electacta.2009.05.021 ↗
30. 10.1016/j.polymer.2011.07.03810.1016/j.polymer.2011.07.038 ↗
31. 10.1155/2014/27841810.1155/2014/278418 ↗
32. 10.1002/elan.20050337110.1002/elan.200503371 ↗
33. 10.1016/0925-4005(94)01543-Q10.1016/0925-4005(94)01543-Q ↗
34. 10.1007/s12221-018-8062-x10.1007/s12221-018-8062-x ↗
35. 10.1039/C8CP05391J10.1039/C8CP05391J ↗
36. 10.1021/bp049735o10.1021/bp049735o ↗
37. 10.1039/b506571b10.1039/b506571b ↗
38. 10.1038/ng205310.1038/ng2053 ↗
39. 10.1021/ac101920t10.1021/ac101920t ↗
40. 10.1016/j.snb.2016.05.02310.1016/j.snb.2016.05.023 ↗
41. 10.1016/j.talanta.2016.08.03010.1016/j.talanta.2016.08.030 ↗
42. 10.1016/j.snb.2017.09.20210.1016/j.snb.2017.09.202 ↗
43. 10.1016/j.bios.2015.03.03410.1016/j.bios.2015.03.034 ↗