Time-Gated Raman Spectroscopy for Quantitative Determination of Solid-State Forms of Fluorescent Pharmaceuticals

dc.contributor.authorLipiäinen T
dc.contributor.authorPessi J
dc.contributor.authorMovahedi P
dc.contributor.authorKoivistoinen J
dc.contributor.authorKurki L
dc.contributor.authorTenhunen M
dc.contributor.authorYliruusi J
dc.contributor.authorJuppo AM
dc.contributor.authorHeikkonen J
dc.contributor.authorPahikkala T
dc.contributor.authorStrachan CJ
dc.contributor.organizationfi=tietojenkäsittelytiede|en=Computer Science|
dc.contributor.organization-code1.2.246.10.2458963.20.23479734818
dc.converis.publication-id36442021
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/36442021
dc.date.accessioned2022-10-27T12:11:57Z
dc.date.available2022-10-27T12:11:57Z
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 X (2) X 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.format.pagerange4832
dc.format.pagerange4839
dc.identifier.jour-issn0003-2700
dc.identifier.olddbid173855
dc.identifier.oldhandle10024/156949
dc.identifier.urihttps://www.utupub.fi/handle/11111/33081
dc.identifier.urnURN:NBN:fi-fe2021042720058
dc.language.isoen
dc.okm.affiliatedauthorMovahedi, Parisa
dc.okm.affiliatedauthorHeikkonen, Jukka
dc.okm.affiliatedauthorPahikkala, Tapio
dc.okm.discipline113 Computer and information sciencesen_GB
dc.okm.discipline116 Chemical sciencesen_GB
dc.okm.discipline113 Tietojenkäsittely ja informaatiotieteetfi_FI
dc.okm.discipline116 Kemiafi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherAMER CHEMICAL SOC
dc.publisher.countryUnited Statesen_GB
dc.publisher.countryYhdysvallat (USA)fi_FI
dc.publisher.country-codeUS
dc.relation.doi10.1021/acs.analchem.8b00298
dc.relation.ispartofjournalAnalytical Chemistry
dc.relation.issue7
dc.relation.volume90
dc.source.identifierhttps://www.utupub.fi/handle/10024/156949
dc.titleTime-Gated Raman Spectroscopy for Quantitative Determination of Solid-State Forms of Fluorescent Pharmaceuticals
dc.year.issued2018

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