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利用杂合光介导/荧光光谱法探测,对经封装的油橄榄废渣提取物进行高羟基自由基清除性能的管理。

Managing Encapsulated Oil Extract of Date Seed Waste for High Hydroxyl Radical Scavenging Assayed via Hybrid Photo-Mediated/Spectrofluorimetric Probing.

机构信息

Chemistry Department, College of Science, Jouf University, Sakaka 72388, Saudi Arabia.

Chemistry Department, Faculty of Science, Fayoum University, Fayoum 63514, Egypt.

出版信息

Molecules. 2023 Jul 1;28(13):5160. doi: 10.3390/molecules28135160.

DOI:10.3390/molecules28135160
PMID:37446822
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10343647/
Abstract

This work addresses two research topics: the first concerns the specific/sensitive trapping of hydroxyl radicals (OH), and the second concerns the efficacy of encapsulating natural antioxidants, potentially lengthening their preservation activity. For context, nano-titania was solar-irradiated to produce OH, which was spectrofluorimetrically assessed, based on the selective aromatic hydroxylation of the non-fluorescent sodium terephthalate to 2-hydroxyterephthalate fluorophore. Fluorescence intensity is proportional to generated OH. Thus, a simple/rapid indirect method was utilized to assess OH precisely. Accordingly, novel photoluminescent system is outlined in order to assess the scavenging potentiality of OH in date seed oil (DSO) in both its pure and encapsulated formulations (ECP-DSO), i.e., when fresh and 5 months after extraction and encapsulation, respectively. With the addition of 80 μg/mL DSO or ECP-DSO, the efficacy of OH scavenging amounted to 25.12 and 63.39%, which increased to 68.65 and 92.72% when 200 μg/mL DSO or ECP-DSO, respectively, was added. Moreover, the IC50 of DSO and ECP-DSO is 136.6 and 62.1 µg/mL, respectively. Furthermore, DSO and ECP-DSO decreased the kinetics for producing OH by ≈20 and 40%, respectively, relative to OH generated in the absence of antioxidant. This demonstrates the benefits of encapsulation on the preservation activity of natural antioxidants, even after five months after extraction, in terms of its interesting activity when compared to synthetic antioxidants. The developed fluorimetric OH probing upgrades antioxidant medicines, thus paving the way for theoretical/practical insights on mechanistic hydroxyl radical-damaging biology.

摘要

这项工作涉及两个研究课题

第一个课题涉及羟基自由基(OH)的特异性/敏感性捕获,第二个课题涉及封装天然抗氧化剂的功效,可能延长其保存活性。在这个背景下,纳米二氧化钛被太阳照射产生 OH,然后通过对非荧光的对苯二甲酸钠选择性芳香族羟化生成 2-羟基对苯二甲酸荧光团来进行分光荧光评估。荧光强度与生成的 OH 成正比。因此,利用一种简单/快速的间接方法来精确评估 OH。据此,提出了一种新的光致发光体系,以评估在新鲜状态和提取及封装 5 个月后分别处于纯态和封装态的枣籽油(DSO)中 OH 的清除潜力。当添加 80μg/mL 的 DSO 或 ECP-DSO 时,OH 的清除效率分别达到 25.12%和 63.39%,当添加 200μg/mL 的 DSO 或 ECP-DSO 时,清除效率分别增加到 68.65%和 92.72%。此外,DSO 和 ECP-DSO 的 IC50 分别为 136.6 和 62.1µg/mL。此外,DSO 和 ECP-DSO 使产生 OH 的动力学分别降低了约 20%和 40%,与没有抗氧化剂时产生的 OH 相比。这表明即使在提取五个月后,封装仍能提高天然抗氧化剂的保存活性,其活性与合成抗氧化剂相比更有趣。开发的荧光 OH 探测法提升了抗氧化药物,从而为关于机械性羟自由基损伤生物学的理论/实践见解铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aed9/10343647/7c6736ebcbbb/molecules-28-05160-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aed9/10343647/0804714930ed/molecules-28-05160-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aed9/10343647/d2c1870fa9eb/molecules-28-05160-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aed9/10343647/3fc7bc2cb195/molecules-28-05160-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aed9/10343647/060b5e813a58/molecules-28-05160-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aed9/10343647/f53a6e0f0a65/molecules-28-05160-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aed9/10343647/caec44615fbb/molecules-28-05160-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aed9/10343647/cbe90b0293a1/molecules-28-05160-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aed9/10343647/7c6736ebcbbb/molecules-28-05160-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aed9/10343647/0804714930ed/molecules-28-05160-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aed9/10343647/d2c1870fa9eb/molecules-28-05160-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aed9/10343647/3fc7bc2cb195/molecules-28-05160-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aed9/10343647/060b5e813a58/molecules-28-05160-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aed9/10343647/f53a6e0f0a65/molecules-28-05160-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aed9/10343647/caec44615fbb/molecules-28-05160-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aed9/10343647/cbe90b0293a1/molecules-28-05160-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aed9/10343647/7c6736ebcbbb/molecules-28-05160-g008.jpg

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