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Extraction of Tropical Fruit Peels and Development of HPMC Film Containing the Extracts as an Active Antibacterial Packaging Material

机译:含有提取物作为活性抗菌包装材料提取物的热带果皮剥离及肝脏膜的开发

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摘要

In recent years, instead of the use of chemical substances, alternative substances, especially plant extracts, have been characterized for an active packaging of antibacterial elements. In this study, the peels of mangosteen (Garcinia mangostana), rambutan (Nephelium lappaceum), and mango (Mangifera indica) were extracted to obtain bioactive compound by microwave-assisted extraction (MAE) and maceration with water, ethanol 95% and water–ethanol (40:60%). All extracts contained phenolics and flavonoids. However, mangosteen peel extracted by MAE and maceration with water/ethanol (MT-MAE-W/E and MT-Ma-W/E, respectively) contained higher phenolic and flavonoid contents, and exhibited greater antibacterial activity against Staphylococcus aureus and Escherichia coli. Thus, both extracts were analyzed by liquid chromatograph-mass spectrometer (LC-MS) analysis, α-mangostin conferring antibacterial property was found in both extracts. The MT-MAE-W/E and MT-Ma-W/E films exhibited 30.22 ± 2.14 and 30.60 ± 2.83 mm of growth inhibition zones against S. aureus and 26.50 ± 1.60 and 26.93 ± 3.92 mm of growth inhibition zones against E. coli. These clear zones were wider than its crude extract approximately 3 times, possibly because the film formulation enhanced antibacterial activity with sustained release of active compound. Thus, the mangosteen extracts have potential to be used as an antibacterial compound in active packaging.
机译:近年来,代替使用化学物质,替代物质,尤其是植物提取物,已经表征了抗菌元件的主动包装。在这项研究中,提取山竹(Garcinia Mangostana),红毛丹(Nephelium Lappaceum)和芒果(Mangifera indica)的剥离,通过微波辅助萃取(MAE)和用水,乙醇95%和水盐来获得生物活性化合物。乙醇(40:60%)。所有提取物都含有酚类和黄酮类化合物。然而,由Mae和Mae和乙醇(MT-MAE-W / E和MT-MA-W / E)提取的山竹果皮含有较高的酚类和黄酮含量,并对葡萄球菌和大肠杆菌的抗菌活性表现出更大的抗菌活性。因此,通过液相色谱 - 质谱仪(LC-MS)分析分析了两种提取物,在两种提取物中发现赋予抗菌性抗菌性抗菌性。 MT-MAE-W / E和MT-MA-W / E膜的生长抑制区的30.22±2.14和30.60±2.83mm。对E的生长抑制区的26.50±1.60和26.93±3.92mm。大肠杆菌。这些透明区域比其粗提物宽约3倍,可能是因为薄膜配方增强了具有活性化合物的持续释放的抗菌活性。因此,山竹提取物具有在主体包装中用作抗菌化合物的可能性。

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