Antifungal Activity of Econazole Nitrate/Cyclodextrin Complex: Effect of pH 2 and Formation of Complex Aggregates
Econazole nitrate (ECN) is a weakly basic drug with very low aqueous solubility that hampers its permeation through biological membranes and results in low ECN bioavailability. Formation of drug/cyclodextrin (drug/CD) inclusion complexes is a formulation technology that can be applied to enhance dru...
Published in: | International Journal of Pharmaceutics |
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Online Access: | https://hdl.handle.net/20.500.11815/2469 https://doi.org/10.1016/j.ijpharm.2019.118896 |
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ftopinvisindi:oai:opinvisindi.is:20.500.11815/2469 2023-05-15T16:51:38+02:00 Antifungal Activity of Econazole Nitrate/Cyclodextrin Complex: Effect of pH 2 and Formation of Complex Aggregates Jansook, Phatsawee Prajapati, Manisha Pruksakorn, Patamaporn Loftsson, Thorsteinn Lyfjafræðideild (HÍ) Faculty of Pharmaceutical Sciences (UI) School of Health Sciences (UI) Heilbrigðisvísindasvið (HÍ) Háskóli Íslands University of Iceland 2019-11 118896 https://hdl.handle.net/20.500.11815/2469 https://doi.org/10.1016/j.ijpharm.2019.118896 en eng Elsevier info:eu-repo/grantAgreement/EC/H2020/765441 International Journal of Pharmaceutics;574 https://doi.org/10.1016/j.ijpharm.2019.118896 Jansook, P., Prajapati, M., Pruksakorn, P., & Loftsson, T. (2020). Antifungal activity of econazole nitrate/cyclodextrin complex: Effect of pH and formation of complex aggregates. International Journal of Pharmaceutics, 574, 118896. doi:https://doi.org/10.1016/j.ijpharm.2019.118896 0378-5173 https://hdl.handle.net/20.500.11815/2469 International Journal of Pharmaceutics doi:10.1016/j.ijpharm.2019.118896 info:eu-repo/semantics/embargoedAccess info:eu-repo/semantics/article 2019 ftopinvisindi https://doi.org/20.500.11815/2469 https://doi.org/10.1016/j.ijpharm.2019.118896 2022-11-18T06:52:08Z Econazole nitrate (ECN) is a weakly basic drug with very low aqueous solubility that hampers its permeation through biological membranes and results in low ECN bioavailability. Formation of drug/cyclodextrin (drug/CD) inclusion complexes is a formulation technology that can be applied to enhance drug solubility in aqueous media. The aim of this study was to determine the effect of CD complexation and pH adjustments on the ECN solubility. The ECN pHsolubility and ECN/CD phase-solubility profiles were determined. The solubility of ECN in aqueous acidic solutions containing α-cyclodextrin (αCD) was relatively high and much higher than in aqueous γ-cyclodextrin (γCD) solutions under same conditions. The complexation efficiency of the ECN/CD complex was relatively low for the unionized drug. Formation of ECN/CD inclusion complex was verified by proton nuclear magnetic resonance spectroscopy. Formation of ECN/CD complexes enhanced the drug stability during autoclaving. γCD complexes self-assembled to form nanoand microparticles whereas αCD complexes had negligible tendency to selfassemble. Formation of CD complex nano- and microparticles was investigated by dynamic light scattering and by drug permeation through semipermeable membranes of different molecular weight cut-off. The largest aggregate fraction was observed for the unionized ECN in aqueous pH 7.5 solution containing high CD concentration, that is 10% (w/v) CD. It was shown that in acidic solutions ECN/αCD can enhance the antifungal activity to filamentous fungi. This was associated with the increased ECN solubility and increase of readily available ECN molecules in aqueous αCD solutions. This work was financially supported by European Union grant No. MSCA-ITN-2017-765441 (transMed), Thailand Research Fund grant No. RSA5980050 and Faculty of Pharmaceutical Sciences, University of Iceland. Peer-reviewed (accepted version) Article in Journal/Newspaper Iceland Opin vísindi (Iceland) International Journal of Pharmaceutics 574 118896 |
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Opin vísindi (Iceland) |
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ftopinvisindi |
language |
English |
description |
Econazole nitrate (ECN) is a weakly basic drug with very low aqueous solubility that hampers its permeation through biological membranes and results in low ECN bioavailability. Formation of drug/cyclodextrin (drug/CD) inclusion complexes is a formulation technology that can be applied to enhance drug solubility in aqueous media. The aim of this study was to determine the effect of CD complexation and pH adjustments on the ECN solubility. The ECN pHsolubility and ECN/CD phase-solubility profiles were determined. The solubility of ECN in aqueous acidic solutions containing α-cyclodextrin (αCD) was relatively high and much higher than in aqueous γ-cyclodextrin (γCD) solutions under same conditions. The complexation efficiency of the ECN/CD complex was relatively low for the unionized drug. Formation of ECN/CD inclusion complex was verified by proton nuclear magnetic resonance spectroscopy. Formation of ECN/CD complexes enhanced the drug stability during autoclaving. γCD complexes self-assembled to form nanoand microparticles whereas αCD complexes had negligible tendency to selfassemble. Formation of CD complex nano- and microparticles was investigated by dynamic light scattering and by drug permeation through semipermeable membranes of different molecular weight cut-off. The largest aggregate fraction was observed for the unionized ECN in aqueous pH 7.5 solution containing high CD concentration, that is 10% (w/v) CD. It was shown that in acidic solutions ECN/αCD can enhance the antifungal activity to filamentous fungi. This was associated with the increased ECN solubility and increase of readily available ECN molecules in aqueous αCD solutions. This work was financially supported by European Union grant No. MSCA-ITN-2017-765441 (transMed), Thailand Research Fund grant No. RSA5980050 and Faculty of Pharmaceutical Sciences, University of Iceland. Peer-reviewed (accepted version) |
author2 |
Lyfjafræðideild (HÍ) Faculty of Pharmaceutical Sciences (UI) School of Health Sciences (UI) Heilbrigðisvísindasvið (HÍ) Háskóli Íslands University of Iceland |
format |
Article in Journal/Newspaper |
author |
Jansook, Phatsawee Prajapati, Manisha Pruksakorn, Patamaporn Loftsson, Thorsteinn |
spellingShingle |
Jansook, Phatsawee Prajapati, Manisha Pruksakorn, Patamaporn Loftsson, Thorsteinn Antifungal Activity of Econazole Nitrate/Cyclodextrin Complex: Effect of pH 2 and Formation of Complex Aggregates |
author_facet |
Jansook, Phatsawee Prajapati, Manisha Pruksakorn, Patamaporn Loftsson, Thorsteinn |
author_sort |
Jansook, Phatsawee |
title |
Antifungal Activity of Econazole Nitrate/Cyclodextrin Complex: Effect of pH 2 and Formation of Complex Aggregates |
title_short |
Antifungal Activity of Econazole Nitrate/Cyclodextrin Complex: Effect of pH 2 and Formation of Complex Aggregates |
title_full |
Antifungal Activity of Econazole Nitrate/Cyclodextrin Complex: Effect of pH 2 and Formation of Complex Aggregates |
title_fullStr |
Antifungal Activity of Econazole Nitrate/Cyclodextrin Complex: Effect of pH 2 and Formation of Complex Aggregates |
title_full_unstemmed |
Antifungal Activity of Econazole Nitrate/Cyclodextrin Complex: Effect of pH 2 and Formation of Complex Aggregates |
title_sort |
antifungal activity of econazole nitrate/cyclodextrin complex: effect of ph 2 and formation of complex aggregates |
publisher |
Elsevier |
publishDate |
2019 |
url |
https://hdl.handle.net/20.500.11815/2469 https://doi.org/10.1016/j.ijpharm.2019.118896 |
genre |
Iceland |
genre_facet |
Iceland |
op_relation |
info:eu-repo/grantAgreement/EC/H2020/765441 International Journal of Pharmaceutics;574 https://doi.org/10.1016/j.ijpharm.2019.118896 Jansook, P., Prajapati, M., Pruksakorn, P., & Loftsson, T. (2020). Antifungal activity of econazole nitrate/cyclodextrin complex: Effect of pH and formation of complex aggregates. International Journal of Pharmaceutics, 574, 118896. doi:https://doi.org/10.1016/j.ijpharm.2019.118896 0378-5173 https://hdl.handle.net/20.500.11815/2469 International Journal of Pharmaceutics doi:10.1016/j.ijpharm.2019.118896 |
op_rights |
info:eu-repo/semantics/embargoedAccess |
op_doi |
https://doi.org/20.500.11815/2469 https://doi.org/10.1016/j.ijpharm.2019.118896 |
container_title |
International Journal of Pharmaceutics |
container_volume |
574 |
container_start_page |
118896 |
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1766041747279839232 |