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Pressurized liquid extraction of bioactive compounds from blackberry (Rubus fruticosus L.) residues: a comparison with conventional methods

机译:黑莓(Rubus fruticosus L.)残留物中加压提取生物活性化合物的方法:与常规方法的比较

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摘要

Extracts with antioxidant compounds were obtained from residues of blackberries (Rubus fruticosus L.) through pressurized liquid extraction (PLE). The influence of solvent type (water, acidified water pH = 2.5, ethanol and ethanol + water 50% v:v) and temperature (60, 80 and 100 degrees C) on global yield (X-0), total phenolics (TP), monomeric anthocyanins (MA) and antioxidant activity (AA) (by DPPH and ABTS) of the extracts was evaluated. Moreover, anthocyanins were identified and quantified by UHPLC-QToF-MS e UHPLC-UV-Vis, respectively. The best PLE condition was compared to conventional extractions (Soxhlet and maceration). Results showed positive influence of temperature on global yield, TP and AA. Ethanol + water as solvent at 100 degrees C was chosen as the best PLE condition, providing TP = 7.36 mgGAE/g fresh residue, MA = 1.02 mg C3GE/g fresh residue, AA = 76.03 mu mol TE/g fresh residue and X-0 = 633%. Excepting MA, all other results were over those of conventional extractions. Four anthocyanins were identified by UHPLC in the extracts, and their higher yields were achieved with acidified water as solvent at 60 and 80 degrees C. PLE has proved to be a promising alternative to recover bioactive compounds from blackberry residues, as well as other food by-products. (C) 2014 Elsevier Ltd. All rights reserved.
机译:通过加压液体萃取(PLE)从黑莓(Rubus fruticosus L.)残留物中获得抗氧化剂化合物的萃取物。溶剂类型(水,酸化水pH = 2.5,乙醇和乙醇+ 50%v:v的水)和温度(60、80和100摄氏度)对总产量(X-0)和总酚(TP)的影响评估了提取物的单体花色苷(MA)和抗氧化剂活性(AA)(通过DPPH和ABTS)。此外,分别通过UHPLC-QToF-MS和UHPLC-UV-Vis鉴定并定量了花色苷。将最佳PLE条件与常规提取(索氏提取法和浸渍法)进行了比较。结果表明温度对全球产量,总磷和氨基酸有积极影响。选择100°C的乙醇+水作为溶剂的最佳PLE条件,条件是TP = 7.36 mgGAE / g新鲜残余物,MA = 1.02 mg C3GE / g新鲜残余物,AA = 76.03μmolTE / g新鲜残余物和X- 0 = 633%。除MA以外,所有其他结果均超过常规提取。通过UHPLC在提取物中鉴定出四种花色苷,并用酸化水作为溶剂在60和80摄氏度下获得了更高的收率。事实证明,PLE是从黑莓残留物中回收生物活性化合物以及其他食品的有前途的替代方法。产品。 (C)2014 Elsevier Ltd.保留所有权利。

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