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Adenosine Triphosphate-Encapsulated Liposomes with Plasmonic Nanoparticles for Surface Enhanced Raman Scattering-Based Immunoassays

In this study, we prepared adenosine triphosphate (ATP) encapsulated liposomes, and assessed their applicability for the surface enhanced Raman scattering (SERS)-based assays with gold-silver alloy (Au@Ag)-assembled silica nanoparticles (NPs; SiO(2)@Au@Ag). The liposomes were prepared by the thin fi...

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Detalles Bibliográficos
Autores principales: Pham, Xuan-Hung, Hahm, Eunil, Kim, Tae Han, Kim, Hyung-Mo, Lee, Sang Hun, Lee, Yoon-Sik, Jeong, Dae Hong, Jun, Bong-Hyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5539552/
https://www.ncbi.nlm.nih.gov/pubmed/28644380
http://dx.doi.org/10.3390/s17071480
Descripción
Sumario:In this study, we prepared adenosine triphosphate (ATP) encapsulated liposomes, and assessed their applicability for the surface enhanced Raman scattering (SERS)-based assays with gold-silver alloy (Au@Ag)-assembled silica nanoparticles (NPs; SiO(2)@Au@Ag). The liposomes were prepared by the thin film hydration method from a mixture of l-α-phosphatidylcholine, cholesterol, and PE-PEG2000 in chloroform; evaporating the solvent, followed by hydration of the resulting thin film with ATP in phosphate-buffered saline (PBS). Upon lysis of the liposome, the SERS intensity of the SiO(2)@Au@Ag NPs increased with the logarithm of number of ATP-encapsulated liposomes after lysis in the range of 8 × 10(6) to 8 × 10(10). The detection limit of liposome was calculated to be 1.3 × 10(−17) mol. The successful application of ATP-encapsulated liposomes to SiO(2)@Au@Ag NPs based SERS analysis has opened a new avenue for Raman label chemical (RCL)-encapsulated liposome-enhanced SERS-based immunoassays.