Enhancing the Solubility of Isoconazole Nitrate Using Methyl-β-Cyclodextrin: Formulation and Characterization of Inclusion Complexes

Isoconazole nitrate (ISN) is a broad-spectrum antifungal agent whose therapeutic potential is limited by poor aqueous solubility and low bioavailability. This study aimed to enhance the solubility and physicochemical properties of ISN through the formation of inclusion complexes with methyl-β-cyclod...

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Main Authors: Tarek Alloush, Gülsel Yurtdaş Kırımlıoğlu
Format: Article
Language:English
Published: MDPI AG 2025-04-01
Series:Molecules
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Online Access:https://www.mdpi.com/1420-3049/30/8/1654
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author Tarek Alloush
Gülsel Yurtdaş Kırımlıoğlu
author_facet Tarek Alloush
Gülsel Yurtdaş Kırımlıoğlu
author_sort Tarek Alloush
collection DOAJ
description Isoconazole nitrate (ISN) is a broad-spectrum antifungal agent whose therapeutic potential is limited by poor aqueous solubility and low bioavailability. This study aimed to enhance the solubility and physicochemical properties of ISN through the formation of inclusion complexes with methyl-β-cyclodextrin (M-β-CD) using freeze-drying (FD) and spray-drying (SD) methods. The prepared inclusion complexes were comprehensively characterized by high-performance liquid chromatography (HPLC), phase solubility analysis, scanning electron microscopy (SEM), differential scanning calorimetry (DSC), Fourier-transform infrared spectroscopy (FT-IR), and proton nuclear magnetic resonance (<sup>1</sup>H-NMR). Phase solubility studies revealed an AL-type solubility diagram with a 1:1 molar ratio and an apparent stability constant (<i>K<sub>S</sub></i>) of 2711 M<sup>−1</sup>. Structural and thermal analyses confirmed successful inclusion complex formation and reduced crystallinity. The solubility assessment showed that ISN/M-β-CD complexes prepared by SD exhibited an approximately seven-fold higher aqueous solubility than ISN and performed better than those prepared by FD. Moreover, SD complexes demonstrated a higher drug content. These findings highlight the potential of M-β-CD-based inclusion complexation, particularly via spray-drying, as an effective strategy to enhance the solubility and bioavailability of poorly water-soluble drugs, such as ISN.
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spelling doaj-art-72f2cf13d0474d7fbb4186c4446ce9c92025-08-20T02:18:10ZengMDPI AGMolecules1420-30492025-04-01308165410.3390/molecules30081654Enhancing the Solubility of Isoconazole Nitrate Using Methyl-β-Cyclodextrin: Formulation and Characterization of Inclusion ComplexesTarek Alloush0Gülsel Yurtdaş Kırımlıoğlu1Department of Pharmaceutical Technology, Institute of Health Sciences, Istanbul University, Istanbul 34126, TürkiyeDepartment of Pharmaceutical Technology, Faculty of Pharmacy, Anadolu University, Eskişehir 26470, TürkiyeIsoconazole nitrate (ISN) is a broad-spectrum antifungal agent whose therapeutic potential is limited by poor aqueous solubility and low bioavailability. This study aimed to enhance the solubility and physicochemical properties of ISN through the formation of inclusion complexes with methyl-β-cyclodextrin (M-β-CD) using freeze-drying (FD) and spray-drying (SD) methods. The prepared inclusion complexes were comprehensively characterized by high-performance liquid chromatography (HPLC), phase solubility analysis, scanning electron microscopy (SEM), differential scanning calorimetry (DSC), Fourier-transform infrared spectroscopy (FT-IR), and proton nuclear magnetic resonance (<sup>1</sup>H-NMR). Phase solubility studies revealed an AL-type solubility diagram with a 1:1 molar ratio and an apparent stability constant (<i>K<sub>S</sub></i>) of 2711 M<sup>−1</sup>. Structural and thermal analyses confirmed successful inclusion complex formation and reduced crystallinity. The solubility assessment showed that ISN/M-β-CD complexes prepared by SD exhibited an approximately seven-fold higher aqueous solubility than ISN and performed better than those prepared by FD. Moreover, SD complexes demonstrated a higher drug content. These findings highlight the potential of M-β-CD-based inclusion complexation, particularly via spray-drying, as an effective strategy to enhance the solubility and bioavailability of poorly water-soluble drugs, such as ISN.https://www.mdpi.com/1420-3049/30/8/1654isoconazole nitratemethyl-β-cyclodextrinspray-dryingfreeze-dryinginclusion complexphase solubility
spellingShingle Tarek Alloush
Gülsel Yurtdaş Kırımlıoğlu
Enhancing the Solubility of Isoconazole Nitrate Using Methyl-β-Cyclodextrin: Formulation and Characterization of Inclusion Complexes
Molecules
isoconazole nitrate
methyl-β-cyclodextrin
spray-drying
freeze-drying
inclusion complex
phase solubility
title Enhancing the Solubility of Isoconazole Nitrate Using Methyl-β-Cyclodextrin: Formulation and Characterization of Inclusion Complexes
title_full Enhancing the Solubility of Isoconazole Nitrate Using Methyl-β-Cyclodextrin: Formulation and Characterization of Inclusion Complexes
title_fullStr Enhancing the Solubility of Isoconazole Nitrate Using Methyl-β-Cyclodextrin: Formulation and Characterization of Inclusion Complexes
title_full_unstemmed Enhancing the Solubility of Isoconazole Nitrate Using Methyl-β-Cyclodextrin: Formulation and Characterization of Inclusion Complexes
title_short Enhancing the Solubility of Isoconazole Nitrate Using Methyl-β-Cyclodextrin: Formulation and Characterization of Inclusion Complexes
title_sort enhancing the solubility of isoconazole nitrate using methyl β cyclodextrin formulation and characterization of inclusion complexes
topic isoconazole nitrate
methyl-β-cyclodextrin
spray-drying
freeze-drying
inclusion complex
phase solubility
url https://www.mdpi.com/1420-3049/30/8/1654
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