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dc.contributor.authorLipiäinen, Tiina
dc.contributor.authorPessi, Jenni
dc.contributor.authorMovahedi, Parisa
dc.contributor.authorKoivistoinen, Juha
dc.contributor.authorKurki, Lauri
dc.contributor.authorTenhunen, Mari
dc.contributor.authorYliruusi, Jouko
dc.contributor.authorJuppo, Anne M.
dc.contributor.authorHeikkonen, Jukka
dc.contributor.authorPahikkala, Tapio
dc.contributor.authorStrachan, Clare J.
dc.date.accessioned2018-04-16T07:39:52Z
dc.date.available2019-03-07T22:35:26Z
dc.date.issued2018
dc.identifier.citationLipiäinen, T., Pessi, J., Movahedi, P., Koivistoinen, J., Kurki, L., Tenhunen, M., Yliruusi, J., Juppo, A. M., Heikkonen, J., Pahikkala, T., & Strachan, C. J. (2018). Time-Gated Raman Spectroscopy for Quantitative Determination of Solid-State Forms of Fluorescent Pharmaceuticals. <i>Analytical Chemistry</i>, <i>90</i>(7), 4832-4839. <a href="https://doi.org/10.1021/acs.analchem.8b00298" target="_blank">https://doi.org/10.1021/acs.analchem.8b00298</a>
dc.identifier.otherCONVID_27942545
dc.identifier.otherTUTKAID_77028
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/57599
dc.description.abstractRaman spectroscopy is widely used for quantitative pharmaceutical analysis, but a common obstacle to its use is sample fluorescence masking the Raman signal. Time-gating provides an instrument-based method for rejecting fluorescence through temporal resolution of the spectral signal and allows Raman spectra of fluorescent materials to be obtained. An additional practical advantage is that analysis is possible in ambient lighting. This study assesses the efficacy of time-gated Raman spectroscopy for the quantitative measurement of fluorescent pharmaceuticals. Time-gated Raman spectroscopy with a 128 × (2) × 4 CMOS SPAD detector was applied for quantitative analysis of ternary mixtures of solid-state forms of the model drug, piroxicam (PRX). Partial least-squares (PLS) regression allowed quantification, with Raman-active time domain selection (based on visual inspection) improving performance. Model performance was further improved by using kernel-based regularized least-squares (RLS) regression with greedy feature selection in which the data use in both the Raman shift and time dimensions was statistically optimized. Overall, time-gated Raman spectroscopy, especially with optimized data analysis in both the spectral and time dimensions, shows potential for sensitive and relatively routine quantitative analysis of photoluminescent pharmaceuticals during drug development and manufacturing.
dc.language.isoeng
dc.publisherAmerican Chemical Society
dc.relation.ispartofseriesAnalytical Chemistry
dc.subject.otherRaman spectroscopy
dc.titleTime-Gated Raman Spectroscopy for Quantitative Determination of Solid-State Forms of Fluorescent Pharmaceuticals
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-201804031901
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineFysikaalinen kemiafi
dc.contributor.oppiaineNanoscience Centerfi
dc.contributor.oppiainePhysical Chemistryen
dc.contributor.oppiaineNanoscience Centeren
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.date.updated2018-04-03T12:15:23Z
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.format.pagerange4832-4839
dc.relation.issn0003-2700
dc.relation.numberinseries7
dc.relation.volume90
dc.type.versionacceptedVersion
dc.rights.copyright© 2018 American Chemical Society. This is a final draft version of an article whose final and definitive form has been published by American Chemical Society. Published in this repository with the kind permission of the publisher.
dc.rights.accesslevelopenAccessfi
dc.subject.ysospektroskopia
jyx.subject.urihttp://www.yso.fi/onto/yso/p10176
dc.relation.doi10.1021/acs.analchem.8b00298
dc.type.okmA1


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