Biocompatible microemulsions for improved dermal delivery of sertaconazole nitrate: Phase behavior study and microstructure influence on drug biopharamaceutical properties
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2018
Authors
Pajic, Natasa BubicNikolić, Ines

Mitsou, Evgenia

Papadimitriou, Vassiliki

Xenakis, Aristotelis

Randjelović, Danijela

Dobricic, Vladimir
Smitran, Aleksandra
Cekic, Nebojsa

Calija, Bojan
Savić, Snežana D.

Article (Published version)

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The aim of this study was development of biocompatible topical microemulsions (MEs) for incorporation and improved dermal delivery of sertaconazole nitrate (SN). For this purpose, phase behavior and microstructure of pseudo-ternary glycereth-7-caprylate/caprate (Emanon EV-E, EV)/cosurfactant/Capryol (TM) 90/water systems were investigated. Furhermore, the influence of these properties on the drug skin delivery was also assessed. Expansion of ME single-phase regions with the use of short chain alcohols was a consequence of the more fluid interface when compared to other investigated systems, which was confirmed by electron paramagnetic resonance spectroscopy-EPR. The chosen bicontinuous to inverted bicontinuous formulations were assessed against the ME based on polysorbate 80 as referent sample. Despite incorporation of SN within the selected formulations induced similar alternations in electrical conductivity, viscosity and pH values, obtained EPR spectra suggested different SN localiz...ation: within the oil phase (for most of the EV based formulations), or interacting with the interface (polysorbate 80 based formulation). Due to higher in vitro drug release (12.24%-18.53%), ex vivo SN penetration into porcine ear skin (dermal retention Enhancement Ratio (ERO) ranged from 2.66 to 4.25) and pronounced antifungal activity, the chosen MEs represent promising vehicles for dermal delivery of SN in treatment of cutaneous fungal infections. The biopharmaceutical and skin performance differences obtained with different formulations were possible to be explained on the basis of their physicochemical characteristics.
Keywords:
Glycereth-7-caprylate/caprate / Sertaconazole nitrate / Microemulsion / Electron paramagnetic resonance spectroscopy / in vitro release / PenetrationSource:
Journal of Molecular Liquids, 2018, 272, 746-758Publisher:
- Elsevier
Funding / projects:
Note:
- The peer-reviewed version: https://cer.ihtm.bg.ac.rs/handle/123456789/4291
DOI: 10.1016/j.molliq.2018.10.002
ISSN: 0167-7322
WoS: 000451494700083
Scopus: 2-s2.0-85054321735
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IHTMTY - JOUR AU - Pajic, Natasa Bubic AU - Nikolić, Ines AU - Mitsou, Evgenia AU - Papadimitriou, Vassiliki AU - Xenakis, Aristotelis AU - Randjelović, Danijela AU - Dobricic, Vladimir AU - Smitran, Aleksandra AU - Cekic, Nebojsa AU - Calija, Bojan AU - Savić, Snežana D. PY - 2018 UR - https://cer.ihtm.bg.ac.rs/handle/123456789/2360 AB - The aim of this study was development of biocompatible topical microemulsions (MEs) for incorporation and improved dermal delivery of sertaconazole nitrate (SN). For this purpose, phase behavior and microstructure of pseudo-ternary glycereth-7-caprylate/caprate (Emanon EV-E, EV)/cosurfactant/Capryol (TM) 90/water systems were investigated. Furhermore, the influence of these properties on the drug skin delivery was also assessed. Expansion of ME single-phase regions with the use of short chain alcohols was a consequence of the more fluid interface when compared to other investigated systems, which was confirmed by electron paramagnetic resonance spectroscopy-EPR. The chosen bicontinuous to inverted bicontinuous formulations were assessed against the ME based on polysorbate 80 as referent sample. Despite incorporation of SN within the selected formulations induced similar alternations in electrical conductivity, viscosity and pH values, obtained EPR spectra suggested different SN localization: within the oil phase (for most of the EV based formulations), or interacting with the interface (polysorbate 80 based formulation). Due to higher in vitro drug release (12.24%-18.53%), ex vivo SN penetration into porcine ear skin (dermal retention Enhancement Ratio (ERO) ranged from 2.66 to 4.25) and pronounced antifungal activity, the chosen MEs represent promising vehicles for dermal delivery of SN in treatment of cutaneous fungal infections. The biopharmaceutical and skin performance differences obtained with different formulations were possible to be explained on the basis of their physicochemical characteristics. PB - Elsevier T2 - Journal of Molecular Liquids T1 - Biocompatible microemulsions for improved dermal delivery of sertaconazole nitrate: Phase behavior study and microstructure influence on drug biopharamaceutical properties VL - 272 SP - 746 EP - 758 DO - 10.1016/j.molliq.2018.10.002 ER -
@article{ author = "Pajic, Natasa Bubic and Nikolić, Ines and Mitsou, Evgenia and Papadimitriou, Vassiliki and Xenakis, Aristotelis and Randjelović, Danijela and Dobricic, Vladimir and Smitran, Aleksandra and Cekic, Nebojsa and Calija, Bojan and Savić, Snežana D.", year = "2018", abstract = "The aim of this study was development of biocompatible topical microemulsions (MEs) for incorporation and improved dermal delivery of sertaconazole nitrate (SN). For this purpose, phase behavior and microstructure of pseudo-ternary glycereth-7-caprylate/caprate (Emanon EV-E, EV)/cosurfactant/Capryol (TM) 90/water systems were investigated. Furhermore, the influence of these properties on the drug skin delivery was also assessed. Expansion of ME single-phase regions with the use of short chain alcohols was a consequence of the more fluid interface when compared to other investigated systems, which was confirmed by electron paramagnetic resonance spectroscopy-EPR. The chosen bicontinuous to inverted bicontinuous formulations were assessed against the ME based on polysorbate 80 as referent sample. Despite incorporation of SN within the selected formulations induced similar alternations in electrical conductivity, viscosity and pH values, obtained EPR spectra suggested different SN localization: within the oil phase (for most of the EV based formulations), or interacting with the interface (polysorbate 80 based formulation). Due to higher in vitro drug release (12.24%-18.53%), ex vivo SN penetration into porcine ear skin (dermal retention Enhancement Ratio (ERO) ranged from 2.66 to 4.25) and pronounced antifungal activity, the chosen MEs represent promising vehicles for dermal delivery of SN in treatment of cutaneous fungal infections. The biopharmaceutical and skin performance differences obtained with different formulations were possible to be explained on the basis of their physicochemical characteristics.", publisher = "Elsevier", journal = "Journal of Molecular Liquids", title = "Biocompatible microemulsions for improved dermal delivery of sertaconazole nitrate: Phase behavior study and microstructure influence on drug biopharamaceutical properties", volume = "272", pages = "746-758", doi = "10.1016/j.molliq.2018.10.002" }
Pajic, N. B., Nikolić, I., Mitsou, E., Papadimitriou, V., Xenakis, A., Randjelović, D., Dobricic, V., Smitran, A., Cekic, N., Calija, B.,& Savić, S. D.. (2018). Biocompatible microemulsions for improved dermal delivery of sertaconazole nitrate: Phase behavior study and microstructure influence on drug biopharamaceutical properties. in Journal of Molecular Liquids Elsevier., 272, 746-758. https://doi.org/10.1016/j.molliq.2018.10.002
Pajic NB, Nikolić I, Mitsou E, Papadimitriou V, Xenakis A, Randjelović D, Dobricic V, Smitran A, Cekic N, Calija B, Savić SD. Biocompatible microemulsions for improved dermal delivery of sertaconazole nitrate: Phase behavior study and microstructure influence on drug biopharamaceutical properties. in Journal of Molecular Liquids. 2018;272:746-758. doi:10.1016/j.molliq.2018.10.002 .
Pajic, Natasa Bubic, Nikolić, Ines, Mitsou, Evgenia, Papadimitriou, Vassiliki, Xenakis, Aristotelis, Randjelović, Danijela, Dobricic, Vladimir, Smitran, Aleksandra, Cekic, Nebojsa, Calija, Bojan, Savić, Snežana D., "Biocompatible microemulsions for improved dermal delivery of sertaconazole nitrate: Phase behavior study and microstructure influence on drug biopharamaceutical properties" in Journal of Molecular Liquids, 272 (2018):746-758, https://doi.org/10.1016/j.molliq.2018.10.002 . .