Degradation kinetics of artesunate for the development of an ex-tempore intravenous injection

Abstract Background Artesunate is recommended by the World Health Organization (WHO) for parenteral treatment of severe Plasmodium falciparum malaria. However, artesunate is inherently unstable in an aqueous solution and hydrolyses rapidly after its preparation for injection. Therefore, the aim of t...

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Published in:Malaria Journal
Main Authors: Fanta Gashe, Evelien Wynendaele, Bart De Spiegeleer, Sultan Suleman
Format: Article in Journal/Newspaper
Language:English
Published: BMC 2022
Subjects:
Online Access:https://doi.org/10.1186/s12936-022-04278-4
https://doaj.org/article/d7ce4dff9a214d80a92ddbc0ebe209f8
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spelling ftdoajarticles:oai:doaj.org/article:d7ce4dff9a214d80a92ddbc0ebe209f8 2023-05-15T15:17:07+02:00 Degradation kinetics of artesunate for the development of an ex-tempore intravenous injection Fanta Gashe Evelien Wynendaele Bart De Spiegeleer Sultan Suleman 2022-09-01T00:00:00Z https://doi.org/10.1186/s12936-022-04278-4 https://doaj.org/article/d7ce4dff9a214d80a92ddbc0ebe209f8 EN eng BMC https://doi.org/10.1186/s12936-022-04278-4 https://doaj.org/toc/1475-2875 doi:10.1186/s12936-022-04278-4 1475-2875 https://doaj.org/article/d7ce4dff9a214d80a92ddbc0ebe209f8 Malaria Journal, Vol 21, Iss 1, Pp 1-11 (2022) Intravenous formulations Ex-tempore Artesunate Stability Kinetics Optimization Arctic medicine. Tropical medicine RC955-962 Infectious and parasitic diseases RC109-216 article 2022 ftdoajarticles https://doi.org/10.1186/s12936-022-04278-4 2022-12-30T21:08:28Z Abstract Background Artesunate is recommended by the World Health Organization (WHO) for parenteral treatment of severe Plasmodium falciparum malaria. However, artesunate is inherently unstable in an aqueous solution and hydrolyses rapidly after its preparation for injection. Therefore, the aim of the study was to evaluate the stabilizing effects of phosphate buffer and mannitol against short-term (ex-tempore) artesunate hydrolysis. Methods A HPLC–UV isocratic method was developed using a reversed-phase fused core column (HALO RP-C18) and a mobile phase consisting of a mixture of 45% ammonium formate 10 mM in water (pH 4.5) and 55% methanol. Artesunate was formulated as aqueous solutions using a design of experiment (DOE) to investigate the artesunate stabilizing effects of pH (8–10), phosphate buffer strength (0.3–0.5 M), and mannitol (0–0.22 mmol/mL). The solutions were incubated at predefined temperatures (5, 25, and 40 °C) with subsequent analysis. Arrhenius equation was applied to model and evaluate the stability results. Results The developed HPLC-based method using fused-core stationary phase allowed to selectively quantify artesunate in the presence of its main hydrolysis degradants; namely β-dihydroartemisinin (β-DHA) and α-dihydroartemisinin (α-DHA) within 10 min. By applying the Arrhenius equation, the rate of hydrolysis of the drug increased approximately by 3.4 as the temperature raised by 10 °C. Buffer strength was found to be the main factor affecting the hydrolysis rate constants at 5 and 25 °C (p < 0.05), the activation energy (p = 0.009), and the frequency factor (p = 0.045). However, the effect of the buffer was predominant on the activation energy and hydrolysis rate constants, revealing its stabilizing effect on the drug at lower buffer strength (0.3 M). Within the investigated range (pH = 8–10), pH was found to influence the activation energy, with a positive stabilizing effect in the pH range of 8–9. The addition of mannitol as stabilizing agent into artesunate aqueous formulation did ... Article in Journal/Newspaper Arctic Directory of Open Access Journals: DOAJ Articles Arctic Malaria Journal 21 1
institution Open Polar
collection Directory of Open Access Journals: DOAJ Articles
op_collection_id ftdoajarticles
language English
topic Intravenous formulations
Ex-tempore
Artesunate
Stability
Kinetics
Optimization
Arctic medicine. Tropical medicine
RC955-962
Infectious and parasitic diseases
RC109-216
spellingShingle Intravenous formulations
Ex-tempore
Artesunate
Stability
Kinetics
Optimization
Arctic medicine. Tropical medicine
RC955-962
Infectious and parasitic diseases
RC109-216
Fanta Gashe
Evelien Wynendaele
Bart De Spiegeleer
Sultan Suleman
Degradation kinetics of artesunate for the development of an ex-tempore intravenous injection
topic_facet Intravenous formulations
Ex-tempore
Artesunate
Stability
Kinetics
Optimization
Arctic medicine. Tropical medicine
RC955-962
Infectious and parasitic diseases
RC109-216
description Abstract Background Artesunate is recommended by the World Health Organization (WHO) for parenteral treatment of severe Plasmodium falciparum malaria. However, artesunate is inherently unstable in an aqueous solution and hydrolyses rapidly after its preparation for injection. Therefore, the aim of the study was to evaluate the stabilizing effects of phosphate buffer and mannitol against short-term (ex-tempore) artesunate hydrolysis. Methods A HPLC–UV isocratic method was developed using a reversed-phase fused core column (HALO RP-C18) and a mobile phase consisting of a mixture of 45% ammonium formate 10 mM in water (pH 4.5) and 55% methanol. Artesunate was formulated as aqueous solutions using a design of experiment (DOE) to investigate the artesunate stabilizing effects of pH (8–10), phosphate buffer strength (0.3–0.5 M), and mannitol (0–0.22 mmol/mL). The solutions were incubated at predefined temperatures (5, 25, and 40 °C) with subsequent analysis. Arrhenius equation was applied to model and evaluate the stability results. Results The developed HPLC-based method using fused-core stationary phase allowed to selectively quantify artesunate in the presence of its main hydrolysis degradants; namely β-dihydroartemisinin (β-DHA) and α-dihydroartemisinin (α-DHA) within 10 min. By applying the Arrhenius equation, the rate of hydrolysis of the drug increased approximately by 3.4 as the temperature raised by 10 °C. Buffer strength was found to be the main factor affecting the hydrolysis rate constants at 5 and 25 °C (p < 0.05), the activation energy (p = 0.009), and the frequency factor (p = 0.045). However, the effect of the buffer was predominant on the activation energy and hydrolysis rate constants, revealing its stabilizing effect on the drug at lower buffer strength (0.3 M). Within the investigated range (pH = 8–10), pH was found to influence the activation energy, with a positive stabilizing effect in the pH range of 8–9. The addition of mannitol as stabilizing agent into artesunate aqueous formulation did ...
format Article in Journal/Newspaper
author Fanta Gashe
Evelien Wynendaele
Bart De Spiegeleer
Sultan Suleman
author_facet Fanta Gashe
Evelien Wynendaele
Bart De Spiegeleer
Sultan Suleman
author_sort Fanta Gashe
title Degradation kinetics of artesunate for the development of an ex-tempore intravenous injection
title_short Degradation kinetics of artesunate for the development of an ex-tempore intravenous injection
title_full Degradation kinetics of artesunate for the development of an ex-tempore intravenous injection
title_fullStr Degradation kinetics of artesunate for the development of an ex-tempore intravenous injection
title_full_unstemmed Degradation kinetics of artesunate for the development of an ex-tempore intravenous injection
title_sort degradation kinetics of artesunate for the development of an ex-tempore intravenous injection
publisher BMC
publishDate 2022
url https://doi.org/10.1186/s12936-022-04278-4
https://doaj.org/article/d7ce4dff9a214d80a92ddbc0ebe209f8
geographic Arctic
geographic_facet Arctic
genre Arctic
genre_facet Arctic
op_source Malaria Journal, Vol 21, Iss 1, Pp 1-11 (2022)
op_relation https://doi.org/10.1186/s12936-022-04278-4
https://doaj.org/toc/1475-2875
doi:10.1186/s12936-022-04278-4
1475-2875
https://doaj.org/article/d7ce4dff9a214d80a92ddbc0ebe209f8
op_doi https://doi.org/10.1186/s12936-022-04278-4
container_title Malaria Journal
container_volume 21
container_issue 1
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