• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

通过美拉德反应制备的用于缓解结肠炎症的巨噬细胞和线粒体双靶向虾青素纳米粒

Macrophage and mitochondrion dual-targeting astaxanthin nanoparticles prepared by Maillard reaction for colonic inflammation alleviation.

作者信息

Liu Kangjing, Tian Xueying, Fei Siyuan, Song Yukun, Abd El-Aty A M, Tan Mingqian

机构信息

State Key Laboratory of Marine Food Processing and Safety Control, Dalian Polytechnic University, Dalian, 116034 China.

School of Food Science and Technology, Academy of Food Interdisciplinary Science, Dalian Polytechnic University, Dalian, 116034 China.

出版信息

Mar Life Sci Technol. 2025 Feb 17;7(2):352-365. doi: 10.1007/s42995-024-00255-9. eCollection 2025 May.

DOI:10.1007/s42995-024-00255-9
PMID:40417255
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12102426/
Abstract

UNLABELLED

This study demonstrated the design of whey protein isolate (WPI)-mannose (Man) conjugates with triphenylphosphonium bromide (TPP) through self-assembly to prepare macrophage and mitochondrion dual-targeting astaxanthin (AXT) nanoparticles (AXT@TPP-WPI-Man). The nanoparticles displayed spherical structures with a well-dispersed size of approximately 206.1 ± 39.2 nm, with good biocompatibility, stability, and targeting capabilities. In vitro experiments demonstrated the specific accumulation of AXT@TPP-WPI-Man in mitochondria and exhibited good targeting ability toward macrophages. The AXT@TPP-WPI-Man effectively reduced reactive oxygen species and preserved the normal mitochondrial membrane potential. The AXT@TPP-WPI-Man treated ulcerative colitis mice exhibited a 52.32% increase in colon length with significant improvement in weight loss, disease activity index scores, and reduced release of inflammatory cytokines. Immunofluorescence staining indicated AXT@TPP-WPI-Man alleviated ulcerative colitis by reducing M1 polarization in colonic macrophages while promoting M2 polarization. The dual-targeting AXT@TPP-WPI-Man has the potential to improve astaxanthin bioavailability, presenting a promising delivery method for the treatment of ulcerative colitis.

SUPPLEMENTARY INFORMATION

The online version contains supplementary material available at 10.1007/s42995-024-00255-9.

摘要

未标注

本研究展示了通过自组装设计乳清分离蛋白(WPI)-甘露糖(Man)与溴化三苯基鏻(TPP)的缀合物,以制备巨噬细胞和线粒体双靶向虾青素(AXT)纳米颗粒(AXT@TPP-WPI-Man)。这些纳米颗粒呈现球形结构,尺寸约为206.1±39.2纳米,分散良好,具有良好的生物相容性、稳定性和靶向能力。体外实验表明AXT@TPP-WPI-Man在线粒体中特异性积累,并对巨噬细胞表现出良好的靶向能力。AXT@TPP-WPI-Man有效减少活性氧并维持正常的线粒体膜电位。经AXT@TPP-WPI-Man处理的溃疡性结肠炎小鼠结肠长度增加了52.32%,体重减轻、疾病活动指数评分显著改善,炎症细胞因子释放减少。免疫荧光染色表明AXT@TPP-WPI-Man通过减少结肠巨噬细胞中的M1极化同时促进M2极化来减轻溃疡性结肠炎。双靶向的AXT@TPP-WPI-Man有潜力提高虾青素的生物利用度,为溃疡性结肠炎的治疗提供了一种有前景的递送方法。

补充信息

在线版本包含可在10.1007/s42995-024-00255-9获取的补充材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85b0/12102426/b5f993eb1554/42995_2024_255_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85b0/12102426/e2cd4bb2d2cc/42995_2024_255_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85b0/12102426/88fdd5932579/42995_2024_255_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85b0/12102426/5b55aa2bd6b8/42995_2024_255_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85b0/12102426/fd62417b3480/42995_2024_255_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85b0/12102426/1665222268e4/42995_2024_255_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85b0/12102426/667b35e2ff6d/42995_2024_255_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85b0/12102426/b5f993eb1554/42995_2024_255_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85b0/12102426/e2cd4bb2d2cc/42995_2024_255_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85b0/12102426/88fdd5932579/42995_2024_255_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85b0/12102426/5b55aa2bd6b8/42995_2024_255_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85b0/12102426/fd62417b3480/42995_2024_255_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85b0/12102426/1665222268e4/42995_2024_255_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85b0/12102426/667b35e2ff6d/42995_2024_255_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85b0/12102426/b5f993eb1554/42995_2024_255_Fig7_HTML.jpg

相似文献

1
Macrophage and mitochondrion dual-targeting astaxanthin nanoparticles prepared by Maillard reaction for colonic inflammation alleviation.通过美拉德反应制备的用于缓解结肠炎症的巨噬细胞和线粒体双靶向虾青素纳米粒
Mar Life Sci Technol. 2025 Feb 17;7(2):352-365. doi: 10.1007/s42995-024-00255-9. eCollection 2025 May.
2
Orally administered dual-targeted astaxanthin nanoparticles as novel dietary supplements for alleviating hepatocyte oxidative stress.口服双靶向虾青素纳米粒作为新型膳食补充剂缓解肝细胞氧化应激
Food Funct. 2024 Feb 19;15(4):2131-2143. doi: 10.1039/d3fo05319a.
3
Hepatocytes and mitochondria dual-targeted astaxanthin WPI-SCP nanoparticles for the alleviation of alcoholic liver injury.用于减轻酒精性肝损伤的肝细胞和线粒体双靶向虾青素-乳清蛋白分离物-大豆浓缩蛋白纳米粒
Int J Biol Macromol. 2025 Jan;285:137992. doi: 10.1016/j.ijbiomac.2024.137992. Epub 2024 Nov 22.
4
Preparation and characterization of glycosylated protein nanoparticles for astaxanthin mitochondria targeting delivery.用于虾青素靶向递送至线粒体的糖基化蛋白纳米粒的制备及表征。
Food Funct. 2021 Sep 7;12(17):7718-7727. doi: 10.1039/d1fo01751a. Epub 2021 Jul 21.
5
Preparation, characterization, and stability of pectin-whey protein isolate-based nanoparticles with mitochondrial targeting ability.具有线粒体靶向能力的基于果胶-乳清分离蛋白的纳米颗粒的制备、表征及稳定性
Int J Biol Macromol. 2025 Apr;301:140383. doi: 10.1016/j.ijbiomac.2025.140383. Epub 2025 Jan 27.
6
Orally deliverable sequence-targeted astaxanthin nanoparticles for colitis alleviation.口服递呈的靶向序列虾青素纳米粒缓解结肠炎。
Biomaterials. 2023 Feb;293:121976. doi: 10.1016/j.biomaterials.2022.121976. Epub 2022 Dec 22.
7
Oral Delivery of Astaxanthin via Carboxymethyl Chitosan-Modified Nanoparticles for Ulcerative Colitis Treatment.通过羧甲基壳聚糖修饰的纳米颗粒经口递送虾青素治疗溃疡性结肠炎。
Molecules. 2024 Mar 14;29(6):1291. doi: 10.3390/molecules29061291.
8
Hepatic parenchymal cell and mitochondrial-targeted astaxanthin nanocarriers for relief of high fat diet-induced nonalcoholic fatty liver disease.用于缓解高脂饮食诱导的非酒精性脂肪性肝病的肝实质细胞和线粒体靶向虾青素纳米载体
Food Funct. 2023 Mar 20;14(6):2908-2920. doi: 10.1039/d2fo04036k.
9
Dual-Targeted Nanoparticles Hitchhiking on Bacterial Ghosts to Alleviate Nonalcoholic Steatohepatitis.搭载于细菌幽灵上的双靶点纳米颗粒用于缓解非酒精性脂肪性肝炎
ACS Nano. 2025 Apr 15;19(14):14010-14027. doi: 10.1021/acsnano.4c18280. Epub 2025 Apr 3.
10
Synthesis and application of astaxanthin-loaded procyanidins/sea cucumber peptide nanoparticles with good antioxidant and pH-responsive capacities.具有良好抗氧化和pH响应能力的虾青素负载原花青素/海参肽纳米粒的合成与应用
Food Res Int. 2025 Feb;203:115821. doi: 10.1016/j.foodres.2025.115821. Epub 2025 Jan 22.

本文引用的文献

1
A smart cauliflower-like carrier for astaxanthin delivery to relieve colon inflammation.一种智能花椰菜状载体,用于递送虾青素以缓解结肠炎症。
J Control Release. 2022 Feb;342:372-387. doi: 10.1016/j.jconrel.2022.01.014. Epub 2022 Jan 14.
2
Dioscin ameliorates murine ulcerative colitis by regulating macrophage polarization.薯蓣皂苷通过调节巨噬细胞极化改善溃疡性结肠炎。
Pharmacol Res. 2021 Oct;172:105796. doi: 10.1016/j.phrs.2021.105796. Epub 2021 Jul 31.
3
Preparation and characterization of glycosylated protein nanoparticles for astaxanthin mitochondria targeting delivery.
用于虾青素靶向递送至线粒体的糖基化蛋白纳米粒的制备及表征。
Food Funct. 2021 Sep 7;12(17):7718-7727. doi: 10.1039/d1fo01751a. Epub 2021 Jul 21.
4
Construction and evaluation of an iron delivery system by ultra-small nanoparticles from roast sturgeon (Acipenser schrenckiid).超小纳米粒从烤鲟鱼(施氏鲟)构建和评价一个铁传递系统。
Food Funct. 2021 Feb 15;12(3):1147-1155. doi: 10.1039/d0fo02746d.
5
Construction of an environmentally friendly octenylsuccinic anhydride modified pH-sensitive chitosan nanoparticle drug delivery system to alleviate inflammation and oxidative stress.构建一种环保的辛烯基琥珀酸酐修饰的 pH 敏感壳聚糖纳米粒药物传递系统,以缓解炎症和氧化应激。
Carbohydr Polym. 2020 May 15;236:115972. doi: 10.1016/j.carbpol.2020.115972. Epub 2020 Feb 12.
6
Triphenylphosphonium-modified mitochondria-targeted paclitaxel nanocrystals for overcoming multidrug resistance.用于克服多药耐药性的三苯基鏻修饰的线粒体靶向紫杉醇纳米晶体
Asian J Pharm Sci. 2019 Sep;14(5):569-580. doi: 10.1016/j.ajps.2018.06.006. Epub 2018 Sep 18.
7
Chitosan-caseinate-dextran ternary complex nanoparticles for potential oral delivery of astaxanthin with significantly improved bioactivity.壳聚糖-酪蛋白酸钠-葡聚糖三元复合纳米粒用于提高虾青素口服生物活性的潜在递送系统。
Int J Biol Macromol. 2020 May 15;151:747-756. doi: 10.1016/j.ijbiomac.2020.02.170. Epub 2020 Feb 19.
8
Macrophage-based nanotherapeutic strategies in ulcerative colitis.基于巨噬细胞的溃疡性结肠炎纳米治疗策略。
J Control Release. 2020 Apr 10;320:363-380. doi: 10.1016/j.jconrel.2020.01.047. Epub 2020 Jan 27.
9
FSGHF3 and peptides, prepared from fish skin gelatin, exert a protective effect on DSS-induced colitis via the Nrf2 pathway.鱼皮明胶制备的 FSGHF3 和肽通过 Nrf2 通路对 DSS 诱导的结肠炎发挥保护作用。
Food Funct. 2020 Jan 29;11(1):414-423. doi: 10.1039/c9fo02165e.
10
Macrophages in intestinal inflammation and resolution: a potential therapeutic target in IBD.肠道炎症和消退中的巨噬细胞:IBD 的潜在治疗靶点。
Nat Rev Gastroenterol Hepatol. 2019 Sep;16(9):531-543. doi: 10.1038/s41575-019-0172-4. Epub 2019 Jul 16.