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Holy basil essential oil (HBEO) can be applied as a feed additive; however, its benefits depend on the available amount in the gastrointestinal tract. In this study, the physicochemical properties, including the release properties of three different microcapsules, HBEO-loaded gelatin microcapsules (UC), UC coated with aluminum carboxymethyl cellulose (CC), and UC coated with aluminum carboxymethyl cellulose-beeswax composite (CB), were compared. The encapsulation efficiency, HBEO content, and 2,2-diphenyl-2-picrylhydrazyl radical scavenging activity for the microcapsules were 95.4 ± 0.17%, 66.7-67.7%, and 94.3-96.5%, respectively. Scanning electron microscopy and confocal laser scanning microscopy (CLSM) revealed nonuniform HBEO distributions in honeycomb-like networks in the microcapsules. An X-ray diffraction analysis determined that UC and CC microcapsules were amorphous, but CB microcapsules were semicrystalline. UV-vis spectrophotometer and CLSM analyses results determined that HBEO was released from CC and CB microcapsules in greater amounts than from UC microcapsules in simulated intestinal fluid. Therefore, the HBEO amount reaching the intestine can be controlled using the optimal encapsulation system.

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The challenge of using essential oils possessing antioxidant and antimicrobial properties in food industry is to maintain their chemical stability. This research examined the roles of emulsion coating in preventing the degradation of holy basil essential oils (HBEO) during storage. The uncoated HBEO-loaded gelatin microcapsules and those coated with 1, 2, and 3 % palmitic acid emulsified in carboxymethyl cellulose, denoted as UC, C-1P, C-2P, and C-3P, respectively, had HBEO contents of 76.35, 76.09, 68.96, and 59.39 % with the surface oils of 1.31, 0.65, 0.65, and 0.84 %, respectively. The increase in the palmitic acid concentrations caused a significant increase in the L * values (p < 0.05). After 90 days of storage at 30°C, the surface oils of UC, C-1P, C-2P, and C-3P significantly increased to 3.65, 2.43, 2.15, and 3.03 %, respectively, coincident with the decrease in the L * values. Xray diffraction studies revealed that the crystalline structures of the microcapsules were influenced by gelatin renaturation and palmitic acid polymorphism. The antioxidant activities, expressed as IC 50 , of the free and encapsulated HBEO before storage were 0.30 mg/ml. After storage, IC 50 of only C-2P remained constant, while those of the rest significantly increased (p < 0.05). The minimum inhibitory concentrations (MICs) and minimum bactericidal concentrations (MBCs) of all the samples against pathogenic bacteria did not change over storage. C-3P exhibited the strongest antimicrobial activity of MIC of 0.625 mg/ml and MBC of 1.25 mg/ml. These findings suggest that the emulsion coating enables shelf life extension of HBEO-loaded gelatin microcapsules.