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A novel enhanced dot blot immunoassay using colorimetric biosensor for detection of Toxoplasma gondii infection.
Safarpour, Hanie; Pourhassan-Moghaddam, Mohammad; Spotin, Adel; Majdi, Hassan; Barac, Aleksandra; Yousefi, Mehdi; Ahmadpour, Ehsan.
Afiliación
  • Safarpour H; Infectious and Tropical Disease Research Center, Tabriz University of Medical Sciences, Tabriz, Iran; Student Research Committee, Department of Parasitology and Mycology, Tabriz University of Medical Sciences, Tabriz, Iran.
  • Pourhassan-Moghaddam M; ARC Research Hub for Integrated Device for End-user Analysis at Low-levels (IDEAL), Faculty of Science, University of Technology Sydney, Sydney, NSW 2007, Australia; School of Life Sciences, Faculty of Science, University of Technology Sydney, Sydney, NSW 2007, Australia.
  • Spotin A; Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
  • Majdi H; Department of Medical Nanotechnology, Faculty of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran.
  • Barac A; Clinic for Infectious and Tropical Diseases, Clinical Centre of Serbia, Belgrade, Serbia; Faculty of Medicine, University of Belgrade, Belgrade, Serbia.
  • Yousefi M; Drug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
  • Ahmadpour E; Infectious and Tropical Disease Research Center, Tabriz University of Medical Sciences, Tabriz, Iran; Department of Parasitology and Mycology, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran. Electronic address: ehsanahmadpour@gmail.com.
Comp Immunol Microbiol Infect Dis ; 79: 101708, 2021 Dec.
Article en En | MEDLINE | ID: mdl-34481108
This study reports development of a novel point of care assay, namely an enhanced immuno-dot blot assay, for discrimination of anti-Toxoplasma IgG and anti-Toxoplasma IgM antibodies. This method has been designed based on formation of a sandwich complex between a gold nanoprobe (chitosan gold nanoparticle-anti-human IgG or anti-IgM) and anti- Toxoplasma lysate antigen (TLA) which holds anti-TLA antibodies, either IgG or IgM. Briefly, anti-human IgG or anti-IgM antibody was conjugated to chitosan gold nanoparticles via glutaraldehyde chemistry. Then, lysate antigen was immobilized on the surface of nitrocellulose membrane, which followed by addition of the sera sample and gold nanoprobes. The positive signals were readily detectable via observation with naked eye. This positive color change was further intensified via gold enhancement chemistry. The intensity of biosensor signal was proportional to the concentration of active antibodies on the surface of nanoparticles, titer of T. gondii antibodies in the sera samples and concentration of Toxoplasma lysate antigen coated on the nitrocellulose membrane. A minimum concentration to use the antibodies for conjugation, to detect titer of Toxoplasma IgG and IgM antibodies, and the concentration of TLA coated in nitrocellulose membrane were 0.5 mg/mL, 2 IU/mL, 10 IU/mL, and 20 µg/mL, respectively. This enhanced immuno-dot blot assay offers a simple diagnostic technique without expensive equipment requirement for distinguishing of anti- T. gondii IgM and IgG antibodies in field conditions, pregnant women, and immunocompromised patients.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Toxoplasma / Técnicas Biosensibles / Toxoplasmosis / Nanopartículas del Metal Tipo de estudio: Diagnostic_studies Límite: Animals / Pregnancy Idioma: En Revista: Comp Immunol Microbiol Infect Dis Año: 2021 Tipo del documento: Article País de afiliación: Irán Pais de publicación: Reino Unido
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Toxoplasma / Técnicas Biosensibles / Toxoplasmosis / Nanopartículas del Metal Tipo de estudio: Diagnostic_studies Límite: Animals / Pregnancy Idioma: En Revista: Comp Immunol Microbiol Infect Dis Año: 2021 Tipo del documento: Article País de afiliación: Irán Pais de publicación: Reino Unido