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From Mini to Micro Scale—Feasibility of Raman Spectroscopy as a Process Analytical Tool (PAT)

BACKGROUND: Active coating is an important unit operation in the pharmaceutical industry. The quality, stability, safety and performance of the final product largely depend on the amount and uniformity of coating applied. Active coating is challenging regarding the total amount of coating and its un...

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Autores principales: Wirges, Markus, Müller, Joshua, Kása, Péter, Regdon, Géza, Pintye-Hódi, Klára, Knop, Klaus, Kleinebudde, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3857055/
https://www.ncbi.nlm.nih.gov/pubmed/24309305
http://dx.doi.org/10.3390/pharmaceutics3040723
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author Wirges, Markus
Müller, Joshua
Kása, Péter
Regdon, Géza
Pintye-Hódi, Klára
Knop, Klaus
Kleinebudde, Peter
author_facet Wirges, Markus
Müller, Joshua
Kása, Péter
Regdon, Géza
Pintye-Hódi, Klára
Knop, Klaus
Kleinebudde, Peter
author_sort Wirges, Markus
collection PubMed
description BACKGROUND: Active coating is an important unit operation in the pharmaceutical industry. The quality, stability, safety and performance of the final product largely depend on the amount and uniformity of coating applied. Active coating is challenging regarding the total amount of coating and its uniformity. Consequently, there is a strong demand for tools, which are able to monitor and determine the endpoint of a coating operation. In previous work, it was shown that Raman spectroscopy is an appropriate process analytical tool (PAT) to monitor an active spray coating process in a pan coater [1]. Using a multivariate model (Partial Least Squares—PLS) the Raman spectral data could be correlated with the coated amount of the API diprophylline. While the multivariate model was shown to be valid for the process in a mini scale pan coater (batch size: 3.5 kg cores), the aim of the present work was to prove the robustness of the model by transferring the results to tablets coated in a micro scale pan coater (0.5 kg). METHOD: Coating experiments were performed in both, a mini scale and a micro scale pan coater. The model drug diprophylline was coated on placebo tablets. The multivariate model, established for the process in the mini scale pan coater, was applied to the Raman measurements of tablets coated in the micro scale coater for six different coating levels. Then, the amount of coating, which was predicted by the model, was compared with reference measurements using UV spectroscopy. RESULTS: For all six coating levels the predicted coating amount was equal to the amounts obtained by UV spectroscopy within the statistical error. Thus, it was possible to predict the total coating amount with an error smaller than 3.6%. The root mean squares of errors for calibration and prediction (root mean square of errors for calibration and prediction—RMSEC and RMSEP) were 0.335 mg and 0.392 mg, respectively, which means that the predictive power of the model is not dependent on the scale or the equipment. CONCLUSION: The scale-down experiment showed that it was possible to transfer the PLS model developed on a mini scale coater to a micro scale coater.
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spelling pubmed-38570552013-12-16 From Mini to Micro Scale—Feasibility of Raman Spectroscopy as a Process Analytical Tool (PAT) Wirges, Markus Müller, Joshua Kása, Péter Regdon, Géza Pintye-Hódi, Klára Knop, Klaus Kleinebudde, Peter Pharmaceutics Article BACKGROUND: Active coating is an important unit operation in the pharmaceutical industry. The quality, stability, safety and performance of the final product largely depend on the amount and uniformity of coating applied. Active coating is challenging regarding the total amount of coating and its uniformity. Consequently, there is a strong demand for tools, which are able to monitor and determine the endpoint of a coating operation. In previous work, it was shown that Raman spectroscopy is an appropriate process analytical tool (PAT) to monitor an active spray coating process in a pan coater [1]. Using a multivariate model (Partial Least Squares—PLS) the Raman spectral data could be correlated with the coated amount of the API diprophylline. While the multivariate model was shown to be valid for the process in a mini scale pan coater (batch size: 3.5 kg cores), the aim of the present work was to prove the robustness of the model by transferring the results to tablets coated in a micro scale pan coater (0.5 kg). METHOD: Coating experiments were performed in both, a mini scale and a micro scale pan coater. The model drug diprophylline was coated on placebo tablets. The multivariate model, established for the process in the mini scale pan coater, was applied to the Raman measurements of tablets coated in the micro scale coater for six different coating levels. Then, the amount of coating, which was predicted by the model, was compared with reference measurements using UV spectroscopy. RESULTS: For all six coating levels the predicted coating amount was equal to the amounts obtained by UV spectroscopy within the statistical error. Thus, it was possible to predict the total coating amount with an error smaller than 3.6%. The root mean squares of errors for calibration and prediction (root mean square of errors for calibration and prediction—RMSEC and RMSEP) were 0.335 mg and 0.392 mg, respectively, which means that the predictive power of the model is not dependent on the scale or the equipment. CONCLUSION: The scale-down experiment showed that it was possible to transfer the PLS model developed on a mini scale coater to a micro scale coater. MDPI 2011-10-14 /pmc/articles/PMC3857055/ /pubmed/24309305 http://dx.doi.org/10.3390/pharmaceutics3040723 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Wirges, Markus
Müller, Joshua
Kása, Péter
Regdon, Géza
Pintye-Hódi, Klára
Knop, Klaus
Kleinebudde, Peter
From Mini to Micro Scale—Feasibility of Raman Spectroscopy as a Process Analytical Tool (PAT)
title From Mini to Micro Scale—Feasibility of Raman Spectroscopy as a Process Analytical Tool (PAT)
title_full From Mini to Micro Scale—Feasibility of Raman Spectroscopy as a Process Analytical Tool (PAT)
title_fullStr From Mini to Micro Scale—Feasibility of Raman Spectroscopy as a Process Analytical Tool (PAT)
title_full_unstemmed From Mini to Micro Scale—Feasibility of Raman Spectroscopy as a Process Analytical Tool (PAT)
title_short From Mini to Micro Scale—Feasibility of Raman Spectroscopy as a Process Analytical Tool (PAT)
title_sort from mini to micro scale—feasibility of raman spectroscopy as a process analytical tool (pat)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3857055/
https://www.ncbi.nlm.nih.gov/pubmed/24309305
http://dx.doi.org/10.3390/pharmaceutics3040723
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