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Stability of Oxytocin Preparations in Malawi and Rwanda: Stabilizing Effect of Chlorobutanol

Oxytocin is used for the prevention and treatment of postpartum hemorrhage, the leading cause of maternal mortality in low- and middle-income countries. Because of the high instability of oxytocin, most products are labeled for storage at 2–8°C. Some other products are on the market which are labele...

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Autores principales: Hagen, Nhomsai, Bizimana, Thomas, Kayumba, Pierre Claver, Khuluza, Felix, Heide, Lutz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society of Tropical Medicine and Hygiene 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7646793/
https://www.ncbi.nlm.nih.gov/pubmed/32748770
http://dx.doi.org/10.4269/ajtmh.20-0255
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author Hagen, Nhomsai
Bizimana, Thomas
Kayumba, Pierre Claver
Khuluza, Felix
Heide, Lutz
author_facet Hagen, Nhomsai
Bizimana, Thomas
Kayumba, Pierre Claver
Khuluza, Felix
Heide, Lutz
author_sort Hagen, Nhomsai
collection PubMed
description Oxytocin is used for the prevention and treatment of postpartum hemorrhage, the leading cause of maternal mortality in low- and middle-income countries. Because of the high instability of oxytocin, most products are labeled for storage at 2–8°C. Some other products are on the market which are labeled for non-refrigerated storage, but independent evaluations of their stability hardly exist. In the present study, seven brands (nine batches) of oxytocin were purchased from wholesalers and medical stores in Malawi and Rwanda and investigated by accelerated stability testing according to the ICH/WHO guidelines. Two oxytocin brands approved by a stringent regulatory authority (SRA) or by the WHO Prequalification of Medicines program and purchased in Europe were used as comparison. All investigated brands which were either produced in countries with SRAs, or were WHO-prequalified products, were labeled for storage at 2–8°C, and all of them passed stability testing with very good results. Even exposure to 25°C or 30°C for several months hardly affected their oxytocin content. However, two other investigated brands were labeled for non-refrigerated storage, and both of them had been produced in countries without SRAs. These two preparations showed not higher but lower stability than the brands labeled for storage at 2–8°C, and, for both of them, noncompliance with pharmacopoeial specifications was found after accelerated stability testing. At 40°C, and in forced degradation studies at 80°C, chlorobutanol showed a remarkable stabilizing effect on oxytocin, which may deserve further investigation. The results of the present study support the policy “Buy Quality Oxytocin, Keep It Cool.”
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spelling pubmed-76467932020-11-17 Stability of Oxytocin Preparations in Malawi and Rwanda: Stabilizing Effect of Chlorobutanol Hagen, Nhomsai Bizimana, Thomas Kayumba, Pierre Claver Khuluza, Felix Heide, Lutz Am J Trop Med Hyg Articles Oxytocin is used for the prevention and treatment of postpartum hemorrhage, the leading cause of maternal mortality in low- and middle-income countries. Because of the high instability of oxytocin, most products are labeled for storage at 2–8°C. Some other products are on the market which are labeled for non-refrigerated storage, but independent evaluations of their stability hardly exist. In the present study, seven brands (nine batches) of oxytocin were purchased from wholesalers and medical stores in Malawi and Rwanda and investigated by accelerated stability testing according to the ICH/WHO guidelines. Two oxytocin brands approved by a stringent regulatory authority (SRA) or by the WHO Prequalification of Medicines program and purchased in Europe were used as comparison. All investigated brands which were either produced in countries with SRAs, or were WHO-prequalified products, were labeled for storage at 2–8°C, and all of them passed stability testing with very good results. Even exposure to 25°C or 30°C for several months hardly affected their oxytocin content. However, two other investigated brands were labeled for non-refrigerated storage, and both of them had been produced in countries without SRAs. These two preparations showed not higher but lower stability than the brands labeled for storage at 2–8°C, and, for both of them, noncompliance with pharmacopoeial specifications was found after accelerated stability testing. At 40°C, and in forced degradation studies at 80°C, chlorobutanol showed a remarkable stabilizing effect on oxytocin, which may deserve further investigation. The results of the present study support the policy “Buy Quality Oxytocin, Keep It Cool.” The American Society of Tropical Medicine and Hygiene 2020-11 2020-08-03 /pmc/articles/PMC7646793/ /pubmed/32748770 http://dx.doi.org/10.4269/ajtmh.20-0255 Text en © The American Society of Tropical Medicine and Hygiene This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Articles
Hagen, Nhomsai
Bizimana, Thomas
Kayumba, Pierre Claver
Khuluza, Felix
Heide, Lutz
Stability of Oxytocin Preparations in Malawi and Rwanda: Stabilizing Effect of Chlorobutanol
title Stability of Oxytocin Preparations in Malawi and Rwanda: Stabilizing Effect of Chlorobutanol
title_full Stability of Oxytocin Preparations in Malawi and Rwanda: Stabilizing Effect of Chlorobutanol
title_fullStr Stability of Oxytocin Preparations in Malawi and Rwanda: Stabilizing Effect of Chlorobutanol
title_full_unstemmed Stability of Oxytocin Preparations in Malawi and Rwanda: Stabilizing Effect of Chlorobutanol
title_short Stability of Oxytocin Preparations in Malawi and Rwanda: Stabilizing Effect of Chlorobutanol
title_sort stability of oxytocin preparations in malawi and rwanda: stabilizing effect of chlorobutanol
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7646793/
https://www.ncbi.nlm.nih.gov/pubmed/32748770
http://dx.doi.org/10.4269/ajtmh.20-0255
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