%0 Journal Article
%@ 19994923
%A Islam, M.R.
%A Chowdhury, M.R.
%A Wakabayashi, R.
%A Kamiya, N.
%A Moniruzzaman, M.
%A Goto, M.
%D 2020
%F scholars:13279
%I MDPI AG
%J Pharmaceutics
%K aciclovir; carboxylic acid derivative; choline derivative; ionic liquid; oil; sorbitan laurate, animal tissue; Article; cell survival; controlled study; drug delivery system; Fourier transform infrared spectroscopy; human; human tissue; hydrophilicity; in vitro study; microemulsion; nonhuman; particle size; physical phase; pig; process optimization; survival rate; thermodynamics
%N 4
%R 10.3390/pharmaceutics12040392
%T Ionic liquid-in-oil microemulsions prepared with biocompatible choline carboxylic acids for improving the transdermal delivery of a sparingly soluble drug
%U https://khub.utp.edu.my/scholars/13279/
%V 12
%X The transdermal delivery of sparingly soluble drugs is challenging due to of the need for a drug carrier. In the past few decades, ionic liquid (IL)-in-oil microemulsions (IL/O MEs) have been developed as potential carriers. By focusing on biocompatibility, we report on an IL/O ME that is designed to enhance the solubility and transdermal delivery of the sparingly soluble drug, acyclovir. The prepared MEs were composed of a hydrophilic IL (choline formate, choline lactate, or choline propionate) as the non-aqueous polar phase and a surface-active IL (choline oleate) as the surfactant in combination with sorbitan laurate in a continuous oil phase. The selected ILs were all biologically active ions. Optimized pseudo ternary phase diagrams indicated the MEs formed thermodynamically stable, spherically shaped, and nano-sized (<100 nm) droplets. An in vitro drug permeation study, using pig skin, showed the significantly enhanced permeation of acyclovir using the ME. A Fourier transform infrared spectroscopy study showed a reduction of the skin barrier function with the ME. Finally, a skin irritation study showed a high cell survival rate (>90) with the ME compared with Dulbecco�s phosphate-buffered saline, indicates the biocompatibility of the ME. Therefore, we conclude that IL/O ME may be a promising nano-carrier for the transdermal delivery of sparingly soluble drugs. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.
%Z cited By 48