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超声辅助提取法用于利用深水粉虾(长喙拟对虾)加工废弃物:富含类胡萝卜素虾青素提取物的综合表征

Ultrasound-Assisted Extraction (UAE) for the Utilization of Deep-Water Pink Shrimp (Parapenaeus longirostris) Processing Waste: Comprehensive Characterization of Carotenoid Astaxanthin Rich Extract.

作者信息

Dikel Çiğdem, Yanar Yasemen

机构信息

Department of Biotechnology, Cukurova University, Adana, Türkiye.

Department of Seafood Processing Technology, Faculty of Fisheries, Cukurova University, Adana, Türkiye.

出版信息

Vet Med Sci. 2025 Jul;11(4):e70498. doi: 10.1002/vms3.70498.

DOI:10.1002/vms3.70498
PMID:40644491
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12249226/
Abstract

In this study, astaxanthin extract was obtained from deep-water pink shrimp (Parapenaeus longirostris) shell wastes by ultrasound-assisted extraction method using six different organic solvents, characterized and compared with commercial astaxanthin standard. Astaxanthin extractions were performed under different time conditions (2 and 4 h) using selected apolar/polar solvents (petroleum ether, hexane, isopropanol, ethanol, methanol, acetone). All extracts were quantitatively tested by high-performance liquid chromatography. The results show that solvents with higher polarity are more suitable for astaxanthin extraction, and the effect of time on extraction yield varies with the type of solvent. The highest astaxanthin concentration was obtained after 2 h of extraction using methanol (310 ±2.00 µg/g) and the lowest value after 4 h of extraction using petroleum ether (104 ± 30.00 µg/g) (p < 0.05).The UV-Vis spectra of astaxanthin extract showed maximum absorbance in the visible region in the range of 480-520 nm, which is the characteristic absorbance of astaxanthin. Fourier transform infrared spectrometry (FTIR) spectrometry was used to confirm the fingerprint region of astaxanthin extract with C = O stretching vibration, methyl group (aliphatic) (-CH), ketone group (-C = O) (6-membered ring), alkenes (C-C, C = C) and C-CH stretching bonds. In the Raman spectrum, all characteristic values reflect the molecular vibrations of the conjugated polyene chain and its bonded groups, providing a distinct spectral fingerprint for the astaxanthin extract.

摘要

在本研究中,采用超声辅助萃取法,使用六种不同的有机溶剂从深水粉虾(长喙仿对虾)的壳废料中获得虾青素提取物,对其进行表征并与市售虾青素标准品进行比较。使用选定的非极性/极性溶剂(石油醚、己烷、异丙醇、乙醇、甲醇、丙酮)在不同时间条件(2小时和4小时)下进行虾青素萃取。所有提取物均通过高效液相色谱进行定量测试。结果表明,极性较高的溶剂更适合虾青素萃取,时间对萃取产率的影响因溶剂类型而异。使用甲醇萃取2小时后获得的虾青素浓度最高(310±2.00微克/克),使用石油醚萃取4小时后获得的值最低(104±30.00微克/克)(p<0.05)。虾青素提取物的紫外可见光谱在480 - 520纳米范围内的可见光区域显示出最大吸光度,这是虾青素的特征吸光度。利用傅里叶变换红外光谱(FTIR)光谱法确认虾青素提取物的指纹区域,其具有C = O伸缩振动、甲基(脂肪族)(-CH)、酮基(-C = O)(六元环)、烯烃(C-C、C = C)和C-CH伸缩键。在拉曼光谱中,所有特征值反映了共轭多烯链及其键合基团的分子振动,为虾青素提取物提供了独特的光谱指纹。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9c0/12249226/c163299cd061/VMS3-11-e70498-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9c0/12249226/a913f15370e9/VMS3-11-e70498-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9c0/12249226/67b5360023a8/VMS3-11-e70498-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9c0/12249226/3265e811d740/VMS3-11-e70498-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9c0/12249226/e8eb3bddfebd/VMS3-11-e70498-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9c0/12249226/496ef497b590/VMS3-11-e70498-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9c0/12249226/674a16399554/VMS3-11-e70498-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9c0/12249226/c163299cd061/VMS3-11-e70498-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9c0/12249226/a913f15370e9/VMS3-11-e70498-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9c0/12249226/67b5360023a8/VMS3-11-e70498-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9c0/12249226/3265e811d740/VMS3-11-e70498-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9c0/12249226/e8eb3bddfebd/VMS3-11-e70498-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9c0/12249226/496ef497b590/VMS3-11-e70498-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9c0/12249226/674a16399554/VMS3-11-e70498-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9c0/12249226/c163299cd061/VMS3-11-e70498-g004.jpg

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Natural Astaxanthin Is a Green Antioxidant Able to Counteract Lipid Peroxidation and Ferroptotic Cell Death.
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