Development of Microemulsion Containing Alpinia galanga Oil and Its Major Compounds: Enhancement of Antimicrobial Activities

被引:13
作者
Khumpirapang, Nattakanwadee [1 ]
Klayraung, Srikanjana [2 ]
Tima, Singkome [3 ,4 ]
Okonogi, Siriporn [4 ,5 ]
机构
[1] Naresuan Univ, Fac Pharmaceut Sci, Dept Pharmaceut Chem & Pharmacognosy, Phitsanulok 65000, Thailand
[2] Maejo Univ, Fac Sci, Program Biotechnol, Chiang Mai 50290, Thailand
[3] Chiang Mai Univ, Fac Associated Med Sci, Dept Med Technol, Chiang Mai 50200, Thailand
[4] Chiang Mai Univ, Fac Pharm, Res Ctr Pharmaceut Nanotechnol, Chiang Mai 50200, Thailand
[5] Chiang Mai Univ, Fac Pharm, Dept Pharmaceut Sci, Chiang Mai 50200, Thailand
关键词
antibacterial activity; antifungal activity; killing kinetics; essential oil; 1; 8-cineole; methyl eugenol; drug delivery system; phase diagram;
D O I
10.3390/pharmaceutics13020265
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of the present study was to develop a microemulsion (ME) containing Alpinia galanga oil (AGO), 1,8-cineole (C), or methyl eugenol (M) as an active pharmaceutical ingredient (API) for enhancing their antimicrobial activities. Agar diffusion, broth microdilution, and killing kinetics were used for antimicrobial evaluations. The ME composed of 30% API, 33.4% Tween 80, 16.6% ethanol, and 20% water appeared as translucent systems with droplet size and polydispersity index of 101.1 +/- 1.3 nm and 0.3 +/- 0.1, 80.9 +/- 1.1 nm and 0.4 +/- 0.1, and 96.6 +/- 2.0 nm and 0.2 +/- 0.1 for ME-AGO, ME-C, and ME-M, respectively. These ME formulations showed minimum bacterial concentrations of 3.91-31.25 mu g/mL and 50% fungal inhibition concentrations of 1.83 +/- 0.27-0.46 +/- 0.13 mu g/mL, 2-4 times stronger, and faster kinetic killing rate than their respective API alone. Keeping the ME formulations at 4 degrees C, 25 degrees C, and 40 degrees C for 12 weeks did not affect their activities against fungi and Gram-negative bacteria, but the high temperature of 40 degrees C decreased their activities against Gram-positive bacteria. It is concluded that ME is a promising delivery system for AGO and its major compounds to enhance their water miscibility and antimicrobial activities.
引用
收藏
页码:1 / 16
页数:16
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