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

[Image: see text] Raman 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 signa...

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Autores principales: Lipiäinen, Tiina, Pessi, Jenni, Movahedi, Parisa, Koivistoinen, Juha, Kurki, Lauri, Tenhunen, Mari, Yliruusi, Jouko, Juppo, Anne M., Heikkonen, Jukka, Pahikkala, Tapio, Strachan, Clare J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6150637/
https://www.ncbi.nlm.nih.gov/pubmed/29513001
http://dx.doi.org/10.1021/acs.analchem.8b00298
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author Lipiäinen, Tiina
Pessi, Jenni
Movahedi, Parisa
Koivistoinen, Juha
Kurki, Lauri
Tenhunen, Mari
Yliruusi, Jouko
Juppo, Anne M.
Heikkonen, Jukka
Pahikkala, Tapio
Strachan, Clare J.
author_facet Lipiäinen, Tiina
Pessi, Jenni
Movahedi, Parisa
Koivistoinen, Juha
Kurki, Lauri
Tenhunen, Mari
Yliruusi, Jouko
Juppo, Anne M.
Heikkonen, Jukka
Pahikkala, Tapio
Strachan, Clare J.
author_sort Lipiäinen, Tiina
collection PubMed
description [Image: see text] Raman 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.
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spelling pubmed-61506372018-09-24 Time-Gated Raman Spectroscopy for Quantitative Determination of Solid-State Forms of Fluorescent Pharmaceuticals Lipiäinen, Tiina Pessi, Jenni Movahedi, Parisa Koivistoinen, Juha Kurki, Lauri Tenhunen, Mari Yliruusi, Jouko Juppo, Anne M. Heikkonen, Jukka Pahikkala, Tapio Strachan, Clare J. Anal Chem [Image: see text] Raman 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. American Chemical Society 2018-03-07 2018-04-03 /pmc/articles/PMC6150637/ /pubmed/29513001 http://dx.doi.org/10.1021/acs.analchem.8b00298 Text en Copyright © 2018 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Lipiäinen, Tiina
Pessi, Jenni
Movahedi, Parisa
Koivistoinen, Juha
Kurki, Lauri
Tenhunen, Mari
Yliruusi, Jouko
Juppo, Anne M.
Heikkonen, Jukka
Pahikkala, Tapio
Strachan, Clare J.
Time-Gated Raman Spectroscopy for Quantitative Determination of Solid-State Forms of Fluorescent Pharmaceuticals
title Time-Gated Raman Spectroscopy for Quantitative Determination of Solid-State Forms of Fluorescent Pharmaceuticals
title_full Time-Gated Raman Spectroscopy for Quantitative Determination of Solid-State Forms of Fluorescent Pharmaceuticals
title_fullStr Time-Gated Raman Spectroscopy for Quantitative Determination of Solid-State Forms of Fluorescent Pharmaceuticals
title_full_unstemmed Time-Gated Raman Spectroscopy for Quantitative Determination of Solid-State Forms of Fluorescent Pharmaceuticals
title_short Time-Gated Raman Spectroscopy for Quantitative Determination of Solid-State Forms of Fluorescent Pharmaceuticals
title_sort time-gated raman spectroscopy for quantitative determination of solid-state forms of fluorescent pharmaceuticals
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6150637/
https://www.ncbi.nlm.nih.gov/pubmed/29513001
http://dx.doi.org/10.1021/acs.analchem.8b00298
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