Journal
COLLOID AND POLYMER SCIENCE
Volume 298, Issue 3, Pages 263-271Publisher
SPRINGER
DOI: 10.1007/s00396-020-04603-w
Keywords
Microemulsion; Encapsulation; Bicontinuous; Interfacial; Storage stability
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Funding
- Higher Education Commission of Pakistan [20-4557/NRPU/RD/HEC/14/481]
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Microemulsions (mu Es)-based drug delivery is known to be superior as well as effective due to customizable and easy management, efficiency and capability, and quick drug absorption over a wide range of targets. Herein, two mu E formulations were established comprising of clove oil (as oil phase), water (as aqueous phase), Tween-80 (as surfactant), isopropanol, and methanol (as cosurfactant) for formulation A (mu E-A) and formulation B (mu E-B), respectively, and further used for the encapsulation of an antimuscarinic drug, mirabegron (MBG). Multiple complementary measurements, namely, electrical conductivity (sigma), viscosity (eta), and optical microscopy, show the existence of phase transition from W/O to O/W mu E via intermediate bicontinuous channels. MBG showed long storage stability as well as good solubility i.e. 3.0 and 2.5 wt% at pH 6.4 in optimum mu E-A and mu E-B, respectively. Furthermore, no apparent aggregation of MBG was observed, as revealed by scanning transmission electron microscopy and peak correlations of IR analysis, suggesting the stability of MBG inside the formulations. Likewise, fluorescence detection senses the interfacial environment of MBG molecules in the examined formulations that could be vital for understanding the mechanism of controlled drug release.
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