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Sealing Effects on the Storage Stability of the Cyanide Antidotal Candidate, Dimethyl Trisulfide
BACKGROUND: Dimethyl trisulfide (DMTS) is a highly lipid-soluble cyanide (CN) antidote candidate molecule. In prior studies with various US FDA-approved co-solvents, surfactants, and their combinations, aqueous solutions containing 15% polysorbate 80 (Poly80) were found to effectively solubilize DMT...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833904/ https://www.ncbi.nlm.nih.gov/pubmed/29214385 http://dx.doi.org/10.1007/s40268-017-0220-x |
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author | Kiss, Lóránd Duke, Anna Kovacs, Kristof Barcza, Tibor Kiss, Márton Petrikovics, Ilona Thompson, David E. |
author_facet | Kiss, Lóránd Duke, Anna Kovacs, Kristof Barcza, Tibor Kiss, Márton Petrikovics, Ilona Thompson, David E. |
author_sort | Kiss, Lóránd |
collection | PubMed |
description | BACKGROUND: Dimethyl trisulfide (DMTS) is a highly lipid-soluble cyanide (CN) antidote candidate molecule. In prior studies with various US FDA-approved co-solvents, surfactants, and their combinations, aqueous solutions containing 15% polysorbate 80 (Poly80) were found to effectively solubilize DMTS in formulations for intramuscular administration. However, DMTS formulated in 15% aqueous Poly80 solutions showed gradual losses over time when stored in vials with septum-based seals. OBJECTIVE: The present study tested whether storing DMTS formulations in hermetically sealed glass ampules could mitigate storage losses. METHODS: Samples consisted of 1-mL aliquots of a 50 mg/ml stock solution of DMTS in 15% aqueous Poly80. The control samples were stored using a vial-within-a-vial system—the inner and outer vials were sealed respectively, with a snap cap, and with a crimped septum. The hermetically sealed test samples were stored in fire-sealed glass ampules. The DMTS content was measured by HPLC–UV analysis at specific time points over a 100-day period. RESULTS: While the control samples exhibited systematic DMTS losses, no DMTS losses were observed from the test samples stored in hermetically sealed glass ampules over the 100-day testing period. CONCLUSION: DMTS formulated in 15% aqueous Poly80 solution has excellent stability when stored in fire-sealed glass ampules and thus has the potential to be effectively stored as an intramuscular CN countermeasure for mass casualty scenarios. |
format | Online Article Text |
id | pubmed-5833904 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-58339042018-03-07 Sealing Effects on the Storage Stability of the Cyanide Antidotal Candidate, Dimethyl Trisulfide Kiss, Lóránd Duke, Anna Kovacs, Kristof Barcza, Tibor Kiss, Márton Petrikovics, Ilona Thompson, David E. Drugs R D Short Communication BACKGROUND: Dimethyl trisulfide (DMTS) is a highly lipid-soluble cyanide (CN) antidote candidate molecule. In prior studies with various US FDA-approved co-solvents, surfactants, and their combinations, aqueous solutions containing 15% polysorbate 80 (Poly80) were found to effectively solubilize DMTS in formulations for intramuscular administration. However, DMTS formulated in 15% aqueous Poly80 solutions showed gradual losses over time when stored in vials with septum-based seals. OBJECTIVE: The present study tested whether storing DMTS formulations in hermetically sealed glass ampules could mitigate storage losses. METHODS: Samples consisted of 1-mL aliquots of a 50 mg/ml stock solution of DMTS in 15% aqueous Poly80. The control samples were stored using a vial-within-a-vial system—the inner and outer vials were sealed respectively, with a snap cap, and with a crimped septum. The hermetically sealed test samples were stored in fire-sealed glass ampules. The DMTS content was measured by HPLC–UV analysis at specific time points over a 100-day period. RESULTS: While the control samples exhibited systematic DMTS losses, no DMTS losses were observed from the test samples stored in hermetically sealed glass ampules over the 100-day testing period. CONCLUSION: DMTS formulated in 15% aqueous Poly80 solution has excellent stability when stored in fire-sealed glass ampules and thus has the potential to be effectively stored as an intramuscular CN countermeasure for mass casualty scenarios. Springer International Publishing 2017-12-06 2018-03 /pmc/articles/PMC5833904/ /pubmed/29214385 http://dx.doi.org/10.1007/s40268-017-0220-x Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Short Communication Kiss, Lóránd Duke, Anna Kovacs, Kristof Barcza, Tibor Kiss, Márton Petrikovics, Ilona Thompson, David E. Sealing Effects on the Storage Stability of the Cyanide Antidotal Candidate, Dimethyl Trisulfide |
title | Sealing Effects on the Storage Stability of the Cyanide Antidotal Candidate, Dimethyl Trisulfide |
title_full | Sealing Effects on the Storage Stability of the Cyanide Antidotal Candidate, Dimethyl Trisulfide |
title_fullStr | Sealing Effects on the Storage Stability of the Cyanide Antidotal Candidate, Dimethyl Trisulfide |
title_full_unstemmed | Sealing Effects on the Storage Stability of the Cyanide Antidotal Candidate, Dimethyl Trisulfide |
title_short | Sealing Effects on the Storage Stability of the Cyanide Antidotal Candidate, Dimethyl Trisulfide |
title_sort | sealing effects on the storage stability of the cyanide antidotal candidate, dimethyl trisulfide |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833904/ https://www.ncbi.nlm.nih.gov/pubmed/29214385 http://dx.doi.org/10.1007/s40268-017-0220-x |
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