Cargando…
Predictive Model-Based Process Start-Up in Pharmaceutical Continuous Granulation and Drying
Continuous manufacturing (CM) is a promising strategy to achieve various benefits in the context of quality, flexibility, safety and cost in pharmaceutical production. One of the main technical challenges of CM is that the process needs to handle transient conditions such as the start-up phase befor...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7022419/ https://www.ncbi.nlm.nih.gov/pubmed/31952206 http://dx.doi.org/10.3390/pharmaceutics12010067 |
_version_ | 1783498011281719296 |
---|---|
author | Pauli, Victoria Kleinebudde, Peter Krumme, Markus |
author_facet | Pauli, Victoria Kleinebudde, Peter Krumme, Markus |
author_sort | Pauli, Victoria |
collection | PubMed |
description | Continuous manufacturing (CM) is a promising strategy to achieve various benefits in the context of quality, flexibility, safety and cost in pharmaceutical production. One of the main technical challenges of CM is that the process needs to handle transient conditions such as the start-up phase before state of control operation is reached, which can potentially cause out-of-specification (OOS) material. In this context, the presented paper aims to demonstrate that suitable process control strategies during start-up of a continuous granulation and drying operation can limit or even avoid OOS material production and hence can ensure that the provided benefits of CM are not compromised by poor production yields. In detail, heat-up of the drying chamber prior the start of production can lead to thermal energy being stored inside of the stainless-steel housing, acting as an energy buffer that is known to cause over-dried granules in the first few minutes of the drying process. To compensate this issue, an automatic ramping procedure of dryer rotation speed (and hence drying time) was introduced into the plant’s process control system, which counteracts the excessive drying capacity during start-up. As a result, dry granules exiting the dryer complied with the targeted intermediate critical quality attribute loss-on-drying (LOD) from the very beginning of production. |
format | Online Article Text |
id | pubmed-7022419 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70224192020-03-09 Predictive Model-Based Process Start-Up in Pharmaceutical Continuous Granulation and Drying Pauli, Victoria Kleinebudde, Peter Krumme, Markus Pharmaceutics Article Continuous manufacturing (CM) is a promising strategy to achieve various benefits in the context of quality, flexibility, safety and cost in pharmaceutical production. One of the main technical challenges of CM is that the process needs to handle transient conditions such as the start-up phase before state of control operation is reached, which can potentially cause out-of-specification (OOS) material. In this context, the presented paper aims to demonstrate that suitable process control strategies during start-up of a continuous granulation and drying operation can limit or even avoid OOS material production and hence can ensure that the provided benefits of CM are not compromised by poor production yields. In detail, heat-up of the drying chamber prior the start of production can lead to thermal energy being stored inside of the stainless-steel housing, acting as an energy buffer that is known to cause over-dried granules in the first few minutes of the drying process. To compensate this issue, an automatic ramping procedure of dryer rotation speed (and hence drying time) was introduced into the plant’s process control system, which counteracts the excessive drying capacity during start-up. As a result, dry granules exiting the dryer complied with the targeted intermediate critical quality attribute loss-on-drying (LOD) from the very beginning of production. MDPI 2020-01-15 /pmc/articles/PMC7022419/ /pubmed/31952206 http://dx.doi.org/10.3390/pharmaceutics12010067 Text en © 2020 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Pauli, Victoria Kleinebudde, Peter Krumme, Markus Predictive Model-Based Process Start-Up in Pharmaceutical Continuous Granulation and Drying |
title | Predictive Model-Based Process Start-Up in Pharmaceutical Continuous Granulation and Drying |
title_full | Predictive Model-Based Process Start-Up in Pharmaceutical Continuous Granulation and Drying |
title_fullStr | Predictive Model-Based Process Start-Up in Pharmaceutical Continuous Granulation and Drying |
title_full_unstemmed | Predictive Model-Based Process Start-Up in Pharmaceutical Continuous Granulation and Drying |
title_short | Predictive Model-Based Process Start-Up in Pharmaceutical Continuous Granulation and Drying |
title_sort | predictive model-based process start-up in pharmaceutical continuous granulation and drying |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7022419/ https://www.ncbi.nlm.nih.gov/pubmed/31952206 http://dx.doi.org/10.3390/pharmaceutics12010067 |
work_keys_str_mv | AT paulivictoria predictivemodelbasedprocessstartupinpharmaceuticalcontinuousgranulationanddrying AT kleinebuddepeter predictivemodelbasedprocessstartupinpharmaceuticalcontinuousgranulationanddrying AT krummemarkus predictivemodelbasedprocessstartupinpharmaceuticalcontinuousgranulationanddrying |