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Analysis of the Physical Characteristics of an Anhydrous Vehicle for Compounded Pediatric Oral Liquids
The paucity of suitable drug formulations for pediatric patients generates a need for customized, compounded medications. This research study was set out to comprehensively analyze the physical properties of the new, proprietary anhydrous oral vehicle SuspendIt(®) Anhydrous, which was designed for c...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10674891/ https://www.ncbi.nlm.nih.gov/pubmed/38004620 http://dx.doi.org/10.3390/pharmaceutics15112642 |
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author | Banov, Daniel Liu, Yi Ip, Kendice Shan, Ashley Vu, Christine Zdoryk, Oleksandr Bassani, August S. Carvalho, Maria |
author_facet | Banov, Daniel Liu, Yi Ip, Kendice Shan, Ashley Vu, Christine Zdoryk, Oleksandr Bassani, August S. Carvalho, Maria |
author_sort | Banov, Daniel |
collection | PubMed |
description | The paucity of suitable drug formulations for pediatric patients generates a need for customized, compounded medications. This research study was set out to comprehensively analyze the physical properties of the new, proprietary anhydrous oral vehicle SuspendIt(®) Anhydrous, which was designed for compounding pediatric oral liquids. A wide range of tests was used, including sedimentation volume, viscosity, droplet size after dispersion in simulated gastric fluid, microscopic examination and content uniformity measurements to evaluate the properties of the anhydrous vehicle. The results showed that the vehicle exhibited consistent physical properties under varying conditions and maintained stability over time. This can be attributed to the unique blend of excipients in its formulation, which not only maintain its viscosity but also confer thixotropic behavior. The unique combination of viscous, thixotropic and self-emulsifying properties allows for rapid redispersibility, sedimentation stability, accurate dosing, potential drug solubility, dispersion and promotion of enhanced gastrointestinal distribution and absorption. Furthermore, the vehicle demonstrated long-term sedimentation stability and content uniformity for a list of 13 anhydrous suspensions. These results suggest that the anhydrous oral vehicle could serve as a versatile base for pediatric formulation, potentially filling an important gap in pediatric drug delivery. Future studies can further investigate its compatibility, stability and performance with other drugs and in different clinical scenarios. |
format | Online Article Text |
id | pubmed-10674891 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-106748912023-11-20 Analysis of the Physical Characteristics of an Anhydrous Vehicle for Compounded Pediatric Oral Liquids Banov, Daniel Liu, Yi Ip, Kendice Shan, Ashley Vu, Christine Zdoryk, Oleksandr Bassani, August S. Carvalho, Maria Pharmaceutics Article The paucity of suitable drug formulations for pediatric patients generates a need for customized, compounded medications. This research study was set out to comprehensively analyze the physical properties of the new, proprietary anhydrous oral vehicle SuspendIt(®) Anhydrous, which was designed for compounding pediatric oral liquids. A wide range of tests was used, including sedimentation volume, viscosity, droplet size after dispersion in simulated gastric fluid, microscopic examination and content uniformity measurements to evaluate the properties of the anhydrous vehicle. The results showed that the vehicle exhibited consistent physical properties under varying conditions and maintained stability over time. This can be attributed to the unique blend of excipients in its formulation, which not only maintain its viscosity but also confer thixotropic behavior. The unique combination of viscous, thixotropic and self-emulsifying properties allows for rapid redispersibility, sedimentation stability, accurate dosing, potential drug solubility, dispersion and promotion of enhanced gastrointestinal distribution and absorption. Furthermore, the vehicle demonstrated long-term sedimentation stability and content uniformity for a list of 13 anhydrous suspensions. These results suggest that the anhydrous oral vehicle could serve as a versatile base for pediatric formulation, potentially filling an important gap in pediatric drug delivery. Future studies can further investigate its compatibility, stability and performance with other drugs and in different clinical scenarios. MDPI 2023-11-20 /pmc/articles/PMC10674891/ /pubmed/38004620 http://dx.doi.org/10.3390/pharmaceutics15112642 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Banov, Daniel Liu, Yi Ip, Kendice Shan, Ashley Vu, Christine Zdoryk, Oleksandr Bassani, August S. Carvalho, Maria Analysis of the Physical Characteristics of an Anhydrous Vehicle for Compounded Pediatric Oral Liquids |
title | Analysis of the Physical Characteristics of an Anhydrous Vehicle for Compounded Pediatric Oral Liquids |
title_full | Analysis of the Physical Characteristics of an Anhydrous Vehicle for Compounded Pediatric Oral Liquids |
title_fullStr | Analysis of the Physical Characteristics of an Anhydrous Vehicle for Compounded Pediatric Oral Liquids |
title_full_unstemmed | Analysis of the Physical Characteristics of an Anhydrous Vehicle for Compounded Pediatric Oral Liquids |
title_short | Analysis of the Physical Characteristics of an Anhydrous Vehicle for Compounded Pediatric Oral Liquids |
title_sort | analysis of the physical characteristics of an anhydrous vehicle for compounded pediatric oral liquids |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10674891/ https://www.ncbi.nlm.nih.gov/pubmed/38004620 http://dx.doi.org/10.3390/pharmaceutics15112642 |
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