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	       <dc:title>Localized surface plasmon resonance: Nanostructures, bioassays and biosensing-A review</dc:title>
	       <dc:creator>Petryayeva, Eleonora [Chemical Sensors Group, Department of Chemical and Physical Sciences, University of Toronto Mississauga, Mississauga, Ontario, L5L 1C6 (Canada)]; Krull, Ulrich J., E-mail: urlich.krull@utoronto.ca [Chemical Sensors Group, Department of Chemical and Physical Sciences, University of Toronto Mississauga, Mississauga, Ontario, L5L 1C6 (Canada)]</dc:creator>
	       <dc:subject>77 NANOSCIENCE AND NANOTECHNOLOGY; BIOASSAY; FLUORESCENCE; NANOSTRUCTURES; RAMAN SPECTROSCOPY; RESONANCE; SENSITIVITY; EMISSION; LASER SPECTROSCOPY; LUMINESCENCE; PHOTON EMISSION; SPECTROSCOPY</dc:subject>
	       <dc:subjectRelated>EMISSION; LASER SPECTROSCOPY; LUMINESCENCE; PHOTON EMISSION; SPECTROSCOPY</dc:subjectRelated>
	       <dc:description>Highlights: {yields} An overview of fundamental physical theory is provided to explain LSPR. {yields} A survey is provided of structures that can support LSPR. {yields} Examples of applications of LSPR have emphasis on determination of biochemical and biological targets. - Abstract: Localized surface plasmon resonance (LSPR) is an optical phenomena generated by light when it interacts with conductive nanoparticles (NPs) that are smaller than the incident wavelength. As in surface plasmon resonance, the electric field of incident light can be deposited to collectively excite electrons of a conduction band, with the result being coherent localized plasmon oscillations with a resonant frequency that strongly depends on the composition, size, geometry, dielectric environment and separation distance of NPs. This review serves to describe the physical theory of LSPR formation at the surface of nanostructures, and the potential for this optical technology to serve as a basis for the development bioassays and biosensing of high sensitivity. The benefits and challenges associated with various experimental designs of nanoparticles and detection systems, as well as creative approaches that have been developed to improve sensitivity and limits of detection are highlighted using examples from the literature.</dc:description>
	       <dcq:publisher></dcq:publisher>
	       <dcq:publisherResearch></dcq:publisherResearch>
	       <dcq:publisherAvailability>Available from http://dx.doi.org/10.1016/j.aca.2011.08.020</dcq:publisherAvailability>
	       <dcq:publisherSponsor></dcq:publisherSponsor>
	       <dcq:publisherCountry>Netherlands</dcq:publisherCountry>
		   <dc:contributingOrganizations></dc:contributingOrganizations>
	       <dc:date>2011-11-07</dc:date>
	       <dc:language>English</dc:language>
	       <dc:type>Journal Article</dc:type>
	       <dcq:typeQualifier></dcq:typeQualifier>
	       <dc:relation>Journal Name: Analytica Chimica Acta; Journal Volume: 706; Journal Issue: 1; Other Information: DOI: 10.1016/j.aca.2011.08.020; PII: S0003-2670(11)01119-6; Copyright (c) 2011 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; Country of input: International Atomic Energy Agency (IAEA)</dc:relation>
	       <dc:coverage></dc:coverage>
	       <dc:format>Medium: X; Size: page(s) 8-24</dc:format>
	       <dc:doi>https://doi.org/10.1016/j.aca.2011.08.020</dc:doi>
	       <dc:identifier></dc:identifier>
		   <dc:journalName>[]</dc:journalName>
		   <dc:journalIssue>1</dc:journalIssue>
		   <dc:journalVolume>706</dc:journalVolume>
	       <dc:identifierReport></dc:identifierReport>
	       <dcq:identifierDOEcontract></dcq:identifierDOEcontract>
	       <dc:identifierOther>Journal ID: ISSN 0003-2670; ACACAM; TRN: NL12R0089069773</dc:identifierOther>
	       <dc:source>NLN</dc:source>
	       <dc:rights></dc:rights>
	       <dc:dateEntry>2012-12-11</dc:dateEntry>
	       <dc:dateAdded></dc:dateAdded>
	       <dc:ostiId>21591782</dc:ostiId>
	       <dcq:identifier-purl></dcq:identifier-purl>
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