TY - JOUR
T1 - Interaction potential between biological sensing nanoparticles determined by combining small-angle x-ray scattering and model-potential-free liquid theory
AU - Morita, Takeshi
AU - Uehara, Nobuo
AU - Kuwahata, Kenji
AU - Imamura, Hiroshi
AU - Shimada, Takeshi
AU - Ookubo, Kouki
AU - Fujita, Maki
AU - Sumi, Tomonari
N1 - Funding Information:
We are grateful to PF at KEK for providing the opportunity to perform the SAXS experiments. This work was partially supported by JSPS Grant-in-Aid for Scientific Research (KAKENHI). T.M. thanks the AGSST fund at Chiba University for financial support.
Publisher Copyright:
© 2016 American Chemical Society.
PY - 2016/11/10
Y1 - 2016/11/10
N2 - Biological sensing technology utilizing nanoparticles extends through a diverse range of fields. The nanosensing is controlled using the assembly/disassembly of nanoparticles dominated by interaction forces between them. Although the interaction potential surface gives decisive information on the sensing mechanism, evaluating the quantitative profile has been impossible due to extremely complicated interactions of conjugated soft matter. In this study, a model-potential-free determination of the interaction potential surfaces was devised by combining small-angle scattering and liquidstate theory. The model-potential-free liquid theory was developed for colloidal nanoparticles inherently with strong van der Waals attraction forces by their nanoscopic size. The present method extracts interaction potential between nanoparticles even in systems with complicated interactions due to conjugated soft matter. By applying this determination method to a glutathione-triggered biosensing reaction, interaction potential curves between biosensing nanoparticles were realized for the first time. The analysis revealed peculiar potential surfaces of the sensing nanoparticles. The mechanism of colorimetric nanosensing function based on surface plasmon resonance is discussed from the viewpoint of the assembly/disassembly of nanoparticles in nanocomposites dominated by the interaction potential surfaces.
AB - Biological sensing technology utilizing nanoparticles extends through a diverse range of fields. The nanosensing is controlled using the assembly/disassembly of nanoparticles dominated by interaction forces between them. Although the interaction potential surface gives decisive information on the sensing mechanism, evaluating the quantitative profile has been impossible due to extremely complicated interactions of conjugated soft matter. In this study, a model-potential-free determination of the interaction potential surfaces was devised by combining small-angle scattering and liquidstate theory. The model-potential-free liquid theory was developed for colloidal nanoparticles inherently with strong van der Waals attraction forces by their nanoscopic size. The present method extracts interaction potential between nanoparticles even in systems with complicated interactions due to conjugated soft matter. By applying this determination method to a glutathione-triggered biosensing reaction, interaction potential curves between biosensing nanoparticles were realized for the first time. The analysis revealed peculiar potential surfaces of the sensing nanoparticles. The mechanism of colorimetric nanosensing function based on surface plasmon resonance is discussed from the viewpoint of the assembly/disassembly of nanoparticles in nanocomposites dominated by the interaction potential surfaces.
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U2 - 10.1021/acs.jpcc.6b06487
DO - 10.1021/acs.jpcc.6b06487
M3 - Article
AN - SCOPUS:85042596160
SN - 1932-7447
VL - 120
SP - 25564
EP - 25571
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
IS - 44
ER -