Win Htun-Htun, Teethaisong Yothin, Ketudat-Cairns James R, Ketudat-Cairns Mariena
School of Biotechnology, Institute of Agricultural Technology, Suranaree University of Technology, Nakhon Ratchasima, Thailand.
Department of Medical Sciences, Faculty of Allied Health Sciences, Burapha University, Chon Buri, Thailand.
J Food Sci. 2025 Jan;90(1):e17624. doi: 10.1111/1750-3841.17624. Epub 2024 Dec 28.
Black rice bran (BRB), a valuable byproduct from the rice milling process, possesses numerous pharmacological activities, including antioxidant potential, but information regarding highly efficient extraction methods is scarce. To enhance the extraction efficiency, ultrasonic-assisted extraction coupled with Box-Behnken design (BBD) was used in this study to maximize the total phenolic content (TPC), total flavonoid content (TFC), total anthocyanin content (TAC), and antioxidant capacity of BRB extract. The BBD results showed that 57% ethanol at 50°C and pH 3.1 were best for TPC (136.2 mg GAE/g dry weight), TAC (2.3 mg cyanidin-3-O-glucoside equivalents/g dry weight), and TFC (38.6 mg quercetin equivalents/g dry weight). In vitro antioxidant capacities of BRB extract determined by 2,2-azinobis (3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) and 2,2-diphenyl-1-picrylhydrazyl (DPPH) assays revealed free radical scavenging potentials with EC values of 67.62 and 1149 µg/mL, respectively. The cytotoxic effect of BRB extract on human skin HaCaT keratinocytes was determined by a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, which revealed no significant cytotoxicity and a significant increase in cell viability at a concentration of 500 µg/mL. Ultra-high performance liquid chromatography (UHPLC) analysis identified syringic acid, gallic acid, protocatechuic acid, vanillic acid, p-coumaric acid, and ferulic acid in BRB extract. This study provides the optimal conditions to extract antioxidant bioactive compounds from BRB and supports the use of BRB as a source of antioxidants. Due to BRB showing no significant cytotoxicity to human skin cells, it could potentially be further developed for topical applications.
黑米麸皮(BRB)是碾米过程中一种有价值的副产品,具有多种药理活性,包括抗氧化潜力,但关于高效提取方法的信息却很少。为了提高提取效率,本研究采用超声辅助提取结合Box-Behnken设计(BBD)来最大化黑米麸皮提取物的总酚含量(TPC)、总黄酮含量(TFC)、总花青素含量(TAC)和抗氧化能力。BBD结果表明,50℃、pH 3.1的57%乙醇对TPC(136.2毫克没食子酸当量/克干重)、TAC(2.3毫克矢车菊素-3-O-葡萄糖苷当量/克干重)和TFC(38.6毫克槲皮素当量/克干重)最为适宜。通过2,2-联氮-双-(3-乙基苯并噻唑啉-6-磺酸)(ABTS)和2,2-二苯基-1-苦基肼(DPPH)测定法测定的黑米麸皮提取物的体外抗氧化能力显示出自由基清除潜力,其EC值分别为67.62和1149微克/毫升。通过3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)测定法测定了黑米麸皮提取物对人皮肤HaCaT角质形成细胞的细胞毒性作用,结果显示在浓度为500微克/毫升时无明显细胞毒性且细胞活力显著增加。超高效液相色谱(UHPLC)分析鉴定出黑米麸皮提取物中的丁香酸、没食子酸、原儿茶酸、香草酸、对香豆酸和阿魏酸。本研究提供了从黑米麸皮中提取抗氧化生物活性化合物的最佳条件,并支持将黑米麸皮用作抗氧化剂来源。由于黑米麸皮对人皮肤细胞无明显细胞毒性,它有可能进一步开发用于局部应用。