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基于D-Lin-MC3-DMA的LNP中蛋白质冠形成机制研究
发布时间:2025-07-16     作者:kx   分享到:
文献资料:血清热去火大肠杆菌培养大大减少 ApoE 介导的 D-Lin-MC3-DMA 脂质納米粉末的摄取量的链接://www.beilstein-journals.org/bjnano/articles/16/57诗人:德米安·范斯特拉滕, 卢克·范德·谢波普, 罗文·弗朗特, 彼得·维德和 雷蒙德·M·希弗勒斯节选:几何形的微米离子在用量递送学习中推动着至关重点的施用。微米离子给药后在其表皮型成的蛋清质冠而致对其特点方面的显著性引响而颇受关注公众号。脂质微米离子 (LNP) 依赖感蛋清质冠的型成来实现目标其靶点性。某些蛋清质-微米离子彼此之间施用基本*初施用身胃中部模板做好学习,契机*终认知 LNP 在胃中的生物学分布图和载药递送速率。在身胃中部训练中,基本会在训练基中使用胎牛血清 (FCS) 以供应膳食纤维并促进会内部潜能和出现。基本对 FCS 做好热消灭以以避免止补网络体系统提高。所以,该历程对蛋清质冠型成和因此对 LNP 模块表的引响尚不非常清楚。本诗,让.我学习了血清肺热消灭对含带 D-lin-MC3-DMA (MC3) 或 C12-200 (C12) 可电离脂质的 LNP 中蛋清质冠型成的引响。在含带未进行处理或热消灭血清的训练基中,检验了LNP的内部摄食和siRNA递送速率。从原则上讲,让.我发觉载脂蛋清E(另外一种对MC3 LNP趋近性至关重点的蛋清冠部分)在FCS热消灭后平衡性和模块表性削减,故而对MC3 LNP的摄食和运输递送生成消极引响,但对C12 LNP则无引响。让.我的学习最后透露了身体实验操作中被强化的关键因素分析的重点性,哪些关键因素分析或许会故意中引响LNP的特点方面。哪些发觉有益于整改身体学习蛋清冠型成的方法,并以避免LNP激发中的问题。

D-Lin-MC3-DMA

AbstractNanoparticles play a crucial role in drug delivery research. The protein corona that develops on the surface of nanoparticles after administration has garnered substantial attention due to the significant effects it has on their performance. Lipid nanoparticles (LNPs) depend on protein corona formation to mediate their targeting. Such protein–nanoparticle interactions are often initially studied using in vitro cellular models aiming to eventually understand biodistribution and cargo delivery efficiency of the LNPs in vivo. For in vitro cell culture, fetal calf serum (FCS) is supplemented to culture media to provide nutrients and promote cell viability and growth. Heat inactivation of FCS is often performed to prevent complement system activation. However, the effect of this process on protein corona formation and, in turn, LNP functionality is unclear. Here, we investigated the effects of serum heat inactivation on protein corona formation on LNPs containing D-lin-MC3-DMA (MC3) or C12-200 (C12) ionizable lipids. Cellular uptake and siRNA delivery efficiency of the LNPs were determined in media containing untreated or heat-inactivated serum. Mechanistically, we found that apolipoprotein E, a protein corona component that is crucial for MC3 LNP tropism, displayed reduced stability and functionality upon heat inactivation of FCS, thereby negatively influencing uptake and cargo delivery of MC3 LNPs, but not C12 LNPs. Our results underline the importance of overlooked factors in in vitro experiments that can inadvertently affect LNP performance. These findings can help to improve protocols to study protein corona formation in vitro and prevent bias in LNP development.昆明pg电子娱乐游戏app 生物制品具备各种相关车辆:DPPE-PEG-COOHDSPE-PEG-Glutamic acidmPEG-DEPEICG-PEG-DLPEDSPE-MAL,DSPE-MaleimideDSPE-PEG-RVG29  二硬脂酰基磷脂酰酒精胺-聚乙二醇-狂犬病病毒有哪些肽DSPE-PEG2K-RVG29以内小文章信息来历当下期刊杂志或论文,假如有侵权行为请联系起来自己删去!