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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2018
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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. |
format | Online Article Text |
id | pubmed-6150637 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
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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