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利用超声辅助提取从枣核中制备纳米颗粒并提高其酚类含量和抗氧化性能的新策略:基于多元的优化研究。

A novel strategy for producing nano-particles from date seeds and enhancing their phenolic content and antioxidant properties using ultrasound-assisted extraction: A multivariate based optimization study.

机构信息

Department of Food Science, College of Agriculture and Veterinary Medicine, United Arab Emirates University, Al-Ain 15551, United Arab Emirates.

Department of Food Science, College of Agriculture and Veterinary Medicine, United Arab Emirates University, Al-Ain 15551, United Arab Emirates.

出版信息

Ultrason Sonochem. 2022 Jun;87:106017. doi: 10.1016/j.ultsonch.2022.106017. Epub 2022 Apr 28.

DOI:10.1016/j.ultsonch.2022.106017
PMID:35636154
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9157257/
Abstract

Date seeds from the date palm fruit are considered as a waste and they are known to contain several bioactive compounds. Producing nanoparticles from the date seeds can enhances their effectiveness and their utilization as novel functional food ingredients. In this study, date seed nanoparticles (DSNPs) synthesized using acid (HCl) hydrolysis method (HCl concentration of 38% and hydrolysis time of 4 days) was found to have particle size between 50 and 150 nm. The obtained DSNPs were characterized by measuring particle size and particle charge (Zetasizer), morphology using scanning electron microscope (SEM), and determination of the functional groups using fourier-transform infrared spectroscopy (FTIR). DSNPs were further treated with green extraction technology [ultrasound-assisted extraction (UAE)] using water-based and methanol-based solvent for optimizing the extraction of the bioactive compounds by implementing response surface methodology (RSM). The UAE of DSNPs were analysed for set of responses including total phenolic content (TPC), total flavonoid content (TFC), 1,1-diphenyl-2-picrlthydrazyl (DPPH) radical scavenging activity, ferric ion reducing antioxidant power (FRAP), and 2,2'-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) radical scavenging activity. Three-factor and four-factor Box-Behnken design (BBD) of three models (Synthesis of DSNPs, UAE with water, and UAE with methanol) was performed. The results showed that in UAE of DSNPs using water-based solvent, the key independent factors effecting the TPC and TFC and antioxidant activities were S:L ratio (40:1 mg/ml) and treatment time (9 min). Whereas the methanol-based UAE of DSNPs was mostly affected by US amplitude/power (90%) and methanol concentration (80%). All models were further optimized using response optimizer in Minitab and the generated predicted values were very comparable to the actual obtained results which confirm the significance and validity of all RSM models used. The phenolic compounds identified from DSNPs consisted mainly of 3,4-Dihydroxy benzoic acid, ferulic acid, and p-coumaric acid. The present study demonstrated a successful method for synthesising DSNPs as well as documented the optimum UAE conditions to maximize the extraction of polyphenolic compounds from DSNPs and enhancing their antioxidant activities to be used in food application.

摘要

从枣椰果实中提取的枣仁被认为是一种废物,但已知其中含有几种生物活性化合物。从枣仁中制备纳米颗粒可以提高其功效,并将其用作新型功能性食品成分。在这项研究中,使用酸(HCl)水解法(HCl 浓度为 38%,水解时间为 4 天)合成的枣仁纳米颗粒(DSNPs)的粒径在 50 至 150nm 之间。通过测量粒径和颗粒电荷(Zetasizer)、使用扫描电子显微镜(SEM)观察形态以及使用傅里叶变换红外光谱(FTIR)测定官能团来表征所得的 DSNPs。进一步用绿色提取技术[超声辅助提取(UAE)]处理 DSNPs,使用水基和甲醇基溶剂,通过实施响应面法(RSM)来优化生物活性化合物的提取。对 UAE 下的 DSNPs 进行了一组响应分析,包括总酚含量(TPC)、总黄酮含量(TFC)、1,1-二苯基-2-苦基肼(DPPH)自由基清除活性、铁离子还原抗氧化能力(FRAP)和 2,2'-联氮-双(3-乙基苯并噻唑啉-6-磺酸)(ABTS)自由基清除活性。对三个模型(DSNPs 的合成、水基 UAE 和甲醇基 UAE)进行了三因素和四因素 Box-Behnken 设计(BBD)。结果表明,在水基溶剂的 UAE 中,影响 TPC、TFC 和抗氧化活性的关键独立因素是 S:L 比(40:1mg/ml)和处理时间(9min)。而甲醇基 UAE 主要受 US 幅度/功率(90%)和甲醇浓度(80%)影响。所有模型均使用 Minitab 中的响应优化器进一步优化,生成的预测值与实际获得的结果非常接近,这证实了所用所有 RSM 模型的重要性和有效性。从 DSNPs 中鉴定出的酚类化合物主要由 3,4-二羟基苯甲酸、阿魏酸和对香豆酸组成。本研究成功地开发了一种合成 DSNPs 的方法,并记录了从 DSNPs 中最大限度提取多酚化合物并提高其抗氧化活性以用于食品应用的最佳 UAE 条件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1622/9157257/2a8bd3ed1877/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1622/9157257/7e856fc1d2f9/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1622/9157257/66491ccd9f29/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1622/9157257/dd2ec60b3bad/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1622/9157257/2a8bd3ed1877/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1622/9157257/7e856fc1d2f9/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1622/9157257/66491ccd9f29/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1622/9157257/dd2ec60b3bad/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1622/9157257/2a8bd3ed1877/gr4.jpg

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