Formation of Antihyperlipidemic Nano-Ezetimibe from Volatile Microemulsion Template for Enhanced Dissolution Profile

Nanostructures play an important role in targeting sparingly water-soluble drugs to specific sites. Because of the structural flexibility and stability, the use of template microemulsions (μEs) can produce functional nanopharmaceuticals of different sizes, shapes, and chemical properties. In this ar...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1999. - 36(2020), 27 vom: 14. Juli, Seite 7908-7915
1. Verfasser: Saleem, Muhammad Atif (VerfasserIn)
Weitere Verfasser: Yasir Siddique, Muhammad, Nazar, Muhammad Faizan, Khan, Salah Ud-Din, Ahmad, Ashfaq, Khan, Rawaiz, Hussain, Syed Zajif, Mat Lazim, Azwan, Azfaralariff, Ahmad, Mohamed, Mazlan
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2020
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Emulsions Hypolipidemic Agents Water 059QF0KO0R Ezetimibe EOR26LQQ24
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100 1 |a Saleem, Muhammad Atif  |e verfasserin  |4 aut 
245 1 0 |a Formation of Antihyperlipidemic Nano-Ezetimibe from Volatile Microemulsion Template for Enhanced Dissolution Profile 
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520 |a Nanostructures play an important role in targeting sparingly water-soluble drugs to specific sites. Because of the structural flexibility and stability, the use of template microemulsions (μEs) can produce functional nanopharmaceuticals of different sizes, shapes, and chemical properties. In this article, we report a new volatile oil-in-water (o/w) μE formulation comprising ethyl acetate/ethanol/brij-35/water to obtain the highly water-dispersible nanoparticles of an antihyperlipidemic agent, ezetimibe (EZM-NPs), to enhance its dissolution profile. A pseudoternary phase diagram was delineated in a specified brij-35/ethanol ratio (1:1) to describe the transparent, optically isotropic domain of the as-formulated μE. The water-dilutable μE formulation, comprising an optimum composition of ethyl acetate (18.0%), ethanol (25.0%), brij-35 (25.0%), and water (32.0%), showed a good dissolvability of EZM around 4.8 wt % at pH 5.2. Electron micrographs showed a fine monomodal collection of EZM-loaded μE droplets (∼45 nm) that did not coalesce even after lyophilization, forming small spherical EZM-NPs (∼60 nm). However, the maturity of nanodrug droplets observed through dynamic light scattering suggests the affinity of EZM to the nonpolar microenvironment, which was further supported through peak-to-peak correlation of infrared analysis and fluorescence measurements. Moreover, the release profile of the as-obtained EZM-nanopowder increased significantly >98% in 30 min, which indicates that a reduced drug concentration will be needed for capsules or tablets in the future and can be simply incorporated into the multidosage formulation of EZM 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
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650 7 |a Hypolipidemic Agents  |2 NLM 
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650 7 |a Ezetimibe  |2 NLM 
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700 1 |a Yasir Siddique, Muhammad  |e verfasserin  |4 aut 
700 1 |a Nazar, Muhammad Faizan  |e verfasserin  |4 aut 
700 1 |a Khan, Salah Ud-Din  |e verfasserin  |4 aut 
700 1 |a Ahmad, Ashfaq  |e verfasserin  |4 aut 
700 1 |a Khan, Rawaiz  |e verfasserin  |4 aut 
700 1 |a Hussain, Syed Zajif  |e verfasserin  |4 aut 
700 1 |a Mat Lazim, Azwan  |e verfasserin  |4 aut 
700 1 |a Azfaralariff, Ahmad  |e verfasserin  |4 aut 
700 1 |a Mohamed, Mazlan  |e verfasserin  |4 aut 
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773 1 8 |g volume:36  |g year:2020  |g number:27  |g day:14  |g month:07  |g pages:7908-7915 
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