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Automated System for Kinetic Analysis of Particle Size Distributions for Pharmaceutically Relevant Systems
Detailing the kinetics of particle formation for pharmaceutically relevant solutions is challenging, especially when considering the combination of formulations, containers, and timescales of clinical importance. This paper describes a method for using commercial software Automate with a stream-sele...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4124733/ https://www.ncbi.nlm.nih.gov/pubmed/25140276 http://dx.doi.org/10.1155/2014/810589 |
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author | Green, John-Bruce D. Carter, Phillip W. Zhang, Yingqing Patel, Dipa Kotha, Priyanka Gonyon, Thomas |
author_facet | Green, John-Bruce D. Carter, Phillip W. Zhang, Yingqing Patel, Dipa Kotha, Priyanka Gonyon, Thomas |
author_sort | Green, John-Bruce D. |
collection | PubMed |
description | Detailing the kinetics of particle formation for pharmaceutically relevant solutions is challenging, especially when considering the combination of formulations, containers, and timescales of clinical importance. This paper describes a method for using commercial software Automate with a stream-selector valve capable of sampling container solutions from within an environmental chamber. The tool was built to monitor changes in particle size distributions via instrumental particle counters but can be adapted to other solution-based sensors. The tool and methodology were demonstrated to be highly effective for measuring dynamic changes in emulsion globule distributions as a function of storage and mixing conditions important for parenteral nutrition. Higher levels of agitation induced the fastest growth of large globules (≥5 μm) while the gentler conditions actually showed a decrease in the number of these large globules. The same methodology recorded calcium phosphate precipitation kinetics as a function of [Ca(2+)] and pH. This automated system is readily adaptable to a wide range of pharmaceutically relevant systems where the particle size is expected to vary with time. This instrumentation can dramatically reduce the time and resources needed to probe complex formulation issues while providing new insights for monitoring the kinetics as a function of key variables. |
format | Online Article Text |
id | pubmed-4124733 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-41247332014-08-19 Automated System for Kinetic Analysis of Particle Size Distributions for Pharmaceutically Relevant Systems Green, John-Bruce D. Carter, Phillip W. Zhang, Yingqing Patel, Dipa Kotha, Priyanka Gonyon, Thomas J Anal Methods Chem Research Article Detailing the kinetics of particle formation for pharmaceutically relevant solutions is challenging, especially when considering the combination of formulations, containers, and timescales of clinical importance. This paper describes a method for using commercial software Automate with a stream-selector valve capable of sampling container solutions from within an environmental chamber. The tool was built to monitor changes in particle size distributions via instrumental particle counters but can be adapted to other solution-based sensors. The tool and methodology were demonstrated to be highly effective for measuring dynamic changes in emulsion globule distributions as a function of storage and mixing conditions important for parenteral nutrition. Higher levels of agitation induced the fastest growth of large globules (≥5 μm) while the gentler conditions actually showed a decrease in the number of these large globules. The same methodology recorded calcium phosphate precipitation kinetics as a function of [Ca(2+)] and pH. This automated system is readily adaptable to a wide range of pharmaceutically relevant systems where the particle size is expected to vary with time. This instrumentation can dramatically reduce the time and resources needed to probe complex formulation issues while providing new insights for monitoring the kinetics as a function of key variables. Hindawi Publishing Corporation 2014 2014-07-16 /pmc/articles/PMC4124733/ /pubmed/25140276 http://dx.doi.org/10.1155/2014/810589 Text en Copyright © 2014 John-Bruce D. Green et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Green, John-Bruce D. Carter, Phillip W. Zhang, Yingqing Patel, Dipa Kotha, Priyanka Gonyon, Thomas Automated System for Kinetic Analysis of Particle Size Distributions for Pharmaceutically Relevant Systems |
title | Automated System for Kinetic Analysis of Particle Size Distributions for Pharmaceutically Relevant Systems |
title_full | Automated System for Kinetic Analysis of Particle Size Distributions for Pharmaceutically Relevant Systems |
title_fullStr | Automated System for Kinetic Analysis of Particle Size Distributions for Pharmaceutically Relevant Systems |
title_full_unstemmed | Automated System for Kinetic Analysis of Particle Size Distributions for Pharmaceutically Relevant Systems |
title_short | Automated System for Kinetic Analysis of Particle Size Distributions for Pharmaceutically Relevant Systems |
title_sort | automated system for kinetic analysis of particle size distributions for pharmaceutically relevant systems |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4124733/ https://www.ncbi.nlm.nih.gov/pubmed/25140276 http://dx.doi.org/10.1155/2014/810589 |
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