Voriconazole-loaded self-nanoemulsifying drug delivery system (SNEDDS) to improve transcorneal permeability

The aim of this study was to develop self- nanoemulsifying drug delivery system (SNEDDS) to improve the transcorneal permeability of voriconazole. A 'mixture design around a reference mixture' approach was applied. This latter included four components, namely, isopropyl myristate, PEG 400,...

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Veröffentlicht in:Pharmaceutical development and technology 2020-07, Vol.25 (6), p.694-703
Hauptverfasser: Rasoanirina, Bakoliarisoa Nivomalala Voahangy, Lassoued, Mohamed Ali, Kamoun, Amel, Bahloul, Badr, Miladi, Karim, Sfar, Souad
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container_issue 6
container_start_page 694
container_title Pharmaceutical development and technology
container_volume 25
creator Rasoanirina, Bakoliarisoa Nivomalala Voahangy
Lassoued, Mohamed Ali
Kamoun, Amel
Bahloul, Badr
Miladi, Karim
Sfar, Souad
description The aim of this study was to develop self- nanoemulsifying drug delivery system (SNEDDS) to improve the transcorneal permeability of voriconazole. A 'mixture design around a reference mixture' approach was applied. This latter included four components, namely, isopropyl myristate, PEG 400, Tween ® 80 and Span ® 80 as oil, co-solvent, surfactant and co-surfactant, respectively. Droplet size was selected as response. The effect of mixture components on droplet size was analyzed by means of response trace method. Optimal formulation was subjected to stability studies and characterized for droplet size, polydispersity index (PDI), pH, osmolarity, viscosity and percentage of transmittance. Ex-vivo transcorneal permeation of the optimal and the marketed formulations was carried out on excised bovine cornea using Franz cell diffusion apparatus. Optimal voriconazole loaded-SNEDDS showed moderate emulsification efficiency and was characterized by a droplet size of 21.447 ± 0.081 nm, a PDI of 0.156 ± 0.004, a pH of 7.205 ± 0.006, an osmolarity of 310 mosmol/Kg and a viscosity of 8.818 ± 0.076 cP. Moreover, it presented an excellent stability and exhibited a significant improvement (p 
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Moreover, it presented an excellent stability and exhibited a significant improvement (p &lt; 0.05) in apparent permeability coefficient (1.982 ± 0.187 × 10 −6  cm/s) when compared to commercialized formulation (1.165 ± 0.106 × 10 −6  cm/s). 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dosage</topic><topic>Emulsions - metabolism</topic><topic>mixture design</topic><topic>Mycotic keratitis</topic><topic>Nanoparticles - administration &amp; dosage</topic><topic>Nanoparticles - metabolism</topic><topic>Organ Culture Techniques</topic><topic>Permeability - drug effects</topic><topic>response trace</topic><topic>SNEDDS</topic><topic>transcorneal permeability</topic><topic>voriconazole</topic><topic>Voriconazole - administration &amp; dosage</topic><topic>Voriconazole - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rasoanirina, Bakoliarisoa Nivomalala Voahangy</creatorcontrib><creatorcontrib>Lassoued, Mohamed Ali</creatorcontrib><creatorcontrib>Kamoun, Amel</creatorcontrib><creatorcontrib>Bahloul, Badr</creatorcontrib><creatorcontrib>Miladi, Karim</creatorcontrib><creatorcontrib>Sfar, Souad</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Pharmaceutical development and technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rasoanirina, Bakoliarisoa Nivomalala Voahangy</au><au>Lassoued, Mohamed Ali</au><au>Kamoun, Amel</au><au>Bahloul, Badr</au><au>Miladi, Karim</au><au>Sfar, Souad</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Voriconazole-loaded self-nanoemulsifying drug delivery system (SNEDDS) to improve transcorneal permeability</atitle><jtitle>Pharmaceutical development and technology</jtitle><addtitle>Pharm Dev Technol</addtitle><date>2020-07-02</date><risdate>2020</risdate><volume>25</volume><issue>6</issue><spage>694</spage><epage>703</epage><pages>694-703</pages><issn>1083-7450</issn><eissn>1097-9867</eissn><abstract>The aim of this study was to develop self- nanoemulsifying drug delivery system (SNEDDS) to improve the transcorneal permeability of voriconazole. 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Moreover, it presented an excellent stability and exhibited a significant improvement (p &lt; 0.05) in apparent permeability coefficient (1.982 ± 0.187 × 10 −6  cm/s) when compared to commercialized formulation (1.165 ± 0.106 × 10 −6  cm/s). These results suggest that SNEDDS is a promising carrier for voriconazole ocular delivery.</abstract><cop>England</cop><pub>Taylor &amp; Francis</pub><pmid>32064993</pmid><doi>10.1080/10837450.2020.1731532</doi><tpages>10</tpages></addata></record>
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subjects Animals
Antifungal Agents - administration & dosage
Antifungal Agents - metabolism
Cattle
Cornea - drug effects
Cornea - metabolism
Drug Delivery Systems - methods
Emulsions - administration & dosage
Emulsions - metabolism
mixture design
Mycotic keratitis
Nanoparticles - administration & dosage
Nanoparticles - metabolism
Organ Culture Techniques
Permeability - drug effects
response trace
SNEDDS
transcorneal permeability
voriconazole
Voriconazole - administration & dosage
Voriconazole - metabolism
title Voriconazole-loaded self-nanoemulsifying drug delivery system (SNEDDS) to improve transcorneal permeability
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