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...

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Published in:International Journal of Pharmaceutics
Main Authors: Jansook, Phatsawee, Prajapati, Manisha, Pruksakorn, Patamaporn, Loftsson, Thorsteinn
Other Authors: Lyfjafræðideild (HÍ), Faculty of Pharmaceutical Sciences (UI), School of Health Sciences (UI), Heilbrigðisvísindasvið (HÍ), Háskóli Íslands, University of Iceland
Format: Article in Journal/Newspaper
Language:English
Published: Elsevier 2019
Subjects:
Online Access:https://hdl.handle.net/20.500.11815/2469
https://doi.org/10.1016/j.ijpharm.2019.118896
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spelling 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
institution Open Polar
collection Opin vísindi (Iceland)
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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
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