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首页> 外文期刊>Journal of Applied Phycology >Comparison of different extraction techniques for obtaining extracts from brown seaweeds and their potential effects as angiotensin I-converting enzyme (ACE) inhibitors
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Comparison of different extraction techniques for obtaining extracts from brown seaweeds and their potential effects as angiotensin I-converting enzyme (ACE) inhibitors

机译:从褐藻中提取提取物的不同提取技术的比较及其作为血管紧张素I转化酶(ACE)抑制剂的潜在作用

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摘要

An extraction protocol was developed to maximize the amount of extracts obtained from three brown seaweeds, Lessonia nigrescens (in two stages of development), Macrocystis pyrifera, and Durvillaea antarctica, and to evaluate them as natural inhibitors of the angiotensin I-converting enzyme (ACE). Two extraction methods were used, an enzymatic method (cellulase and alpha-amylase) and a conventional method (maceration). The extracts were analyzed to determine the extraction yield (%), the total phenolic and carbohydrate concentrations, and the ACE inhibition. Juvenile L. nigrescens extracts obtained by alpha-amylase exhibited the highest extraction yield (37.72 +/- 4.13 %), the highest ACE inhibition (95.61 +/- 0.33 %), and the lowest IC50 (10.10 +/- 1.55 mu g PGE mg(-1) seaweed) among the studied extracts. Extraction by maceration produced extracts with chemical characteristics that were less favorable for inhibiting ACE than the enzymatic extraction. The presence of phlorotannins and carbohydrates in these brown seaweeds after enzymatic extraction could be responsible for the superior ACE inhibitory activity of the extracts. Thus, these molecules could be considered as potential phytopharmaceuticals for the development of new ACE inhibitors.
机译:制定了提取协议,以最大程度地从三种褐藻,雀Lesson(在两个发育阶段),大果囊藻和南极草中提取提取物,并将其评估为血管紧张素I转化酶(ACE)的天然抑制剂)。使用了两种提取方法,一种酶法(纤维素酶和α-淀粉酶)和一种常规方法(浸渍)。分析提取物以确定提取率(%),总酚和碳水化合物浓度以及ACE抑制作用。通过α-淀粉酶获得的黑曲霉幼虫提取物表现出最高的提取率(37.72 +/- 4.13%),最高的ACE抑制率(95.61 +/- 0.33%)和最低的IC50(10.10 +/- 1.55μg PGE) mg(-1)海藻)在研究的提取物中。通过浸软提取产生的提取物具有的化学特征比酶促提取更不利于抑制ACE。酶促提取后这些褐藻中的邻苯二酚单宁和碳水化合物的存在可能是提取物具有较强的ACE抑制活性的原因。因此,这些分子可以被认为是开发新的ACE抑制剂的潜在植物药。

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