• 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

脂质纳米粒和脂质体参考物质的研制(二):细胞毒性特征。

Development of lipid nanoparticles and liposomes reference materials (II): cytotoxic profiles.

机构信息

Metrology Research Centre, National Research Council Canada, 100 Sussex Drive, Ottawa, ON, K1A 0R6, Canada.

Integrated Nanotherapeutics, Burnaby, BC, V5G 4X4, Canada.

出版信息

Sci Rep. 2022 Oct 27;12(1):18071. doi: 10.1038/s41598-022-23013-2.

DOI:10.1038/s41598-022-23013-2
PMID:36302886
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9610362/
Abstract

Lipid based nanocarriers are one of the most effective drug delivery systems that is evident from the recent COVID-19 mRNA vaccines. The main objective of this study was to evaluate toxicity of six lipid based formulations with three surface charges-anionic, neutral or cationic, to establish certified reference materials (CRMs) for liposomes and siRNA loaded lipid nanoparticles (LNP-siRNA). Cytotoxicity was assessed by a proliferation assay in adherent and non-adherent cell lines. High concentration of three LNP-siRNAs did not affect viability of suspension cells and LNP-siRNAs were non-toxic to adherent cells at conventionally used concentration. Systematic evaluation using multiple vials and repeated test runs of three liposomes and three LNP-siRNA formulations showed no toxicity in HL60 and A549 cells up to 128 and 16 µg/mL, respectively. Extended treatment and low concentration of LNPs did not affect the viability of suspension cells and adherent cells at 96 h. Interestingly, 80% of A549 and HL60 cells in 3D conditions were viable when treated with cationic LNP-siRNA for 48 h. Taken together, anionic, cationic and neutral lipid formulations were non-toxic to cells and may be explored further in order to develop them as drug carriers.

摘要

基于脂质的纳米载体是最有效的药物递送系统之一,这一点从最近的 COVID-19 mRNA 疫苗中可见一斑。本研究的主要目的是评估六种带三种表面电荷(阴离子、中性或阳离子)的基于脂质的制剂的毒性,为脂质体和负载 siRNA 的脂质纳米颗粒 (LNP-siRNA) 建立认证参考材料 (CRM)。通过贴壁和非贴壁细胞系的增殖测定评估细胞毒性。高浓度的三种 LNP-siRNA 不会影响悬浮细胞的活力,并且在常规使用浓度下,LNP-siRNA 对贴壁细胞无毒。使用多个小瓶和三种脂质体和三种 LNP-siRNA 制剂的重复测试运行进行系统评估表明,HL60 和 A549 细胞中三种脂质体的浓度高达 128 和 16μg/mL 时无毒。延长处理时间和低浓度的 LNPs 在 96 小时内不会影响悬浮细胞和贴壁细胞的活力。有趣的是,当用阳离子 LNP-siRNA 处理 48 小时时,80%的 A549 和 HL60 细胞在 3D 条件下仍然存活。总之,阴离子、阳离子和中性脂质制剂对细胞无毒,可进一步探索用于开发它们作为药物载体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f588/9613665/82836e85a156/41598_2022_23013_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f588/9613665/886fc979d139/41598_2022_23013_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f588/9613665/9a38cb0ff8d7/41598_2022_23013_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f588/9613665/a7e8d7a756d0/41598_2022_23013_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f588/9613665/82836e85a156/41598_2022_23013_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f588/9613665/886fc979d139/41598_2022_23013_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f588/9613665/9a38cb0ff8d7/41598_2022_23013_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f588/9613665/a7e8d7a756d0/41598_2022_23013_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f588/9613665/82836e85a156/41598_2022_23013_Fig4_HTML.jpg

相似文献

1
Development of lipid nanoparticles and liposomes reference materials (II): cytotoxic profiles.脂质纳米粒和脂质体参考物质的研制(二):细胞毒性特征。
Sci Rep. 2022 Oct 27;12(1):18071. doi: 10.1038/s41598-022-23013-2.
2
Production of siRNA-Loaded Lipid Nanoparticles using a Microfluidic Device.使用微流控装置生产载 siRNA 的脂质纳米粒。
J Vis Exp. 2022 Mar 22(181). doi: 10.3791/62999.
3
Lipid nanoparticle formulations for optimal RNA-based topical delivery to murine airways.用于优化基于 RNA 的经皮递送至小鼠气道的脂质纳米颗粒制剂。
Eur J Pharm Sci. 2022 Sep 1;176:106234. doi: 10.1016/j.ejps.2022.106234. Epub 2022 Jun 8.
4
Lipid Nanoparticle and Liposome Reference Materials: Assessment of Size Homogeneity and Long-Term -70 °C and 4 °C Storage Stability.脂质纳米粒子和脂质体参考材料:大小均一性评估和长期 -70°C 和 4°C 储存稳定性。
Langmuir. 2023 Feb 21;39(7):2509-2519. doi: 10.1021/acs.langmuir.2c02657. Epub 2023 Feb 7.
5
Chemistry of Lipid Nanoparticles for RNA Delivery.脂质纳米颗粒的 RNA 递送化学。
Acc Chem Res. 2022 Jan 4;55(1):2-12. doi: 10.1021/acs.accounts.1c00544. Epub 2021 Dec 1.
6
A lipid nanoparticle platform for mRNA delivery through repurposing of cationic amphiphilic drugs.脂质纳米颗粒平台通过重新利用阳离子两亲药物实现 mRNA 递送。
J Control Release. 2022 Oct;350:256-270. doi: 10.1016/j.jconrel.2022.08.009. Epub 2022 Aug 24.
7
Influence of cationic lipid composition on gene silencing properties of lipid nanoparticle formulations of siRNA in antigen-presenting cells.阳离子脂质组成对抗原呈递细胞中 siRNA 的脂质纳米粒制剂基因沉默特性的影响。
Mol Ther. 2011 Dec;19(12):2186-200. doi: 10.1038/mt.2011.190. Epub 2011 Oct 4.
8
Microfluidic technologies and devices for lipid nanoparticle-based RNA delivery.基于脂质纳米颗粒的 RNA 递释的微流控技术和装置。
J Control Release. 2022 Apr;344:80-96. doi: 10.1016/j.jconrel.2022.02.017. Epub 2022 Feb 17.
9
Efficient Delivery of Globotriaosylceramide Synthase siRNA using Polyhistidine-Incorporated Lipid Nanoparticles.使用含多组氨酸的脂质纳米颗粒高效递送葡萄糖神经酰胺合酶小干扰RNA
Macromol Biosci. 2023 Apr;23(4):e2200423. doi: 10.1002/mabi.202200423. Epub 2023 Feb 10.
10
Lipid Nanoparticles─From Liposomes to mRNA Vaccine Delivery, a Landscape of Research Diversity and Advancement.脂质纳米颗粒——从脂质体到 mRNA 疫苗传递,研究多样性和进展的全景。
ACS Nano. 2021 Nov 23;15(11):16982-17015. doi: 10.1021/acsnano.1c04996. Epub 2021 Jun 28.

引用本文的文献

1
Long Non-coding RNA Based Therapy for Cardiovascular Disease.基于长链非编码RNA的心血管疾病治疗方法
J Cardiovasc Transl Res. 2025 Sep 3. doi: 10.1007/s12265-025-10686-z.
2
Advanced drug delivery systems for oral squamous cell carcinoma: a comprehensive review of nanotechnology-based and other innovative approaches.口腔鳞状细胞癌的先进药物递送系统:基于纳米技术及其他创新方法的综合综述
Front Drug Deliv. 2025 Jun 27;5:1596964. doi: 10.3389/fddev.2025.1596964. eCollection 2025.
3
Therapeutic and diagnostic implications of exosomes as natural nanoparticles: a new paradigm in brain cancer disease management.

本文引用的文献

1
Toxicity of transition metal nanoparticles: A review of different experimental models in the gastrointestinal tract.过渡金属纳米粒子的毒性:胃肠道不同实验模型的综述。
J Appl Toxicol. 2023 Jan;43(1):32-46. doi: 10.1002/jat.4320. Epub 2022 Apr 6.
2
Three-dimensional models: a novel approach for lymphoma research.三维模型:淋巴瘤研究的新方法。
J Cancer Res Clin Oncol. 2022 Apr;148(4):753-765. doi: 10.1007/s00432-021-03897-9. Epub 2022 Jan 29.
3
Endosomal escape of delivered mRNA from endosomal recycling tubules visualized at the nanoscale.
外泌体作为天然纳米颗粒的治疗和诊断意义:脑癌疾病管理的新范式
Front Med (Lausanne). 2025 Jul 21;12:1599392. doi: 10.3389/fmed.2025.1599392. eCollection 2025.
4
Dual-modified Liposomes Encapsulating Nucleic Acids (pApoE2 or pGFP) for Transport Studies Across a Hydrocortisone-enhanced In Vitro Blood-brain Barrier Model for CNS Therapeutic Screening.用于跨氢化可的松增强的体外血脑屏障模型进行中枢神经系统治疗筛选转运研究的双修饰脂质体(包裹核酸(pApoE2或pGFP))
Pharm Res. 2025 Aug;42(8):1331-1345. doi: 10.1007/s11095-025-03900-9. Epub 2025 Jul 28.
5
Transdermal delivery of CRISPR/Cas9-mediated melanoma gene therapy via polyamines-modified thermosensitive hydrogels.通过多胺修饰的热敏水凝胶进行CRISPR/Cas9介导的黑色素瘤基因治疗的经皮递送
J Nanobiotechnology. 2025 Jun 13;23(1):441. doi: 10.1186/s12951-025-03523-7.
6
Enhancing Intracellular Uptake of Ivermectin through Liposomal Encapsulation.通过脂质体包封增强伊维菌素的细胞内摄取
AAPS PharmSciTech. 2025 May 2;26(5):123. doi: 10.1208/s12249-025-03113-8.
7
Mechanistic Insights into Sphingomyelin Nanoemulsions as Drug Delivery Systems for Non-Small Cell Lung Cancer Therapy.对鞘磷脂纳米乳剂作为非小细胞肺癌治疗药物递送系统的机制洞察。
Pharmaceutics. 2025 Apr 2;17(4):461. doi: 10.3390/pharmaceutics17040461.
8
Nanoscale reference and test materials for the validation of characterization methods for engineered nanomaterials - current state, limitations, and needs.用于工程纳米材料表征方法验证的纳米级参考材料和测试材料——现状、局限性及需求。
Anal Bioanal Chem. 2025 May;417(12):2405-2425. doi: 10.1007/s00216-024-05719-6. Epub 2025 Jan 4.
9
Endosomal escape mechanisms of extracellular vesicle-based drug carriers: lessons for lipid nanoparticle design.基于细胞外囊泡的药物载体的内体逃逸机制:脂质纳米颗粒设计的经验教训。
Extracell Vesicles Circ Nucl Acids. 2024 Jul 5;5(3):344-357. doi: 10.20517/evcna.2024.19. eCollection 2024.
10
Tetrahydropyrimidine Ionizable Lipids for Efficient mRNA Delivery.可离子化的四氢嘧啶脂质用于高效 mRNA 递送。
ACS Nano. 2024 Oct 22;18(42):29045-29058. doi: 10.1021/acsnano.4c10154. Epub 2024 Oct 11.
纳米尺度可视化观察到从内体再循环小管中递送的 mRNA 的内体逃逸。
J Cell Biol. 2022 Feb 7;221(2). doi: 10.1083/jcb.202110137. Epub 2021 Dec 9.
4
Lipid Nanoparticle-mRNA Formulations for Therapeutic Applications.脂质纳米颗粒-mRNA 制剂在治疗中的应用。
Acc Chem Res. 2021 Dec 7;54(23):4283-4293. doi: 10.1021/acs.accounts.1c00550. Epub 2021 Nov 18.
5
Lipid nanoparticles for mRNA delivery.用于mRNA递送的脂质纳米颗粒。
Nat Rev Mater. 2021;6(12):1078-1094. doi: 10.1038/s41578-021-00358-0. Epub 2021 Aug 10.
6
Advances in culture methods for acute myeloid leukemia research.急性髓系白血病研究培养方法的进展
Oncoscience. 2021 Aug 4;8:82-90. doi: 10.18632/oncoscience.540. eCollection 2021.
7
Modular Lipid Nanoparticle Platform Technology for siRNA and Lipophilic Prodrug Delivery.用于 siRNA 和疏水性前药递送的模块化脂质纳米颗粒平台技术。
Small. 2021 Sep;17(37):e2103025. doi: 10.1002/smll.202103025. Epub 2021 Aug 1.
8
The current landscape of nucleic acid therapeutics.核酸疗法的现状。
Nat Nanotechnol. 2021 Jun;16(6):630-643. doi: 10.1038/s41565-021-00898-0. Epub 2021 May 31.
9
The Importance of Apparent pKa in the Development of Nanoparticles Encapsulating siRNA and mRNA.纳米颗粒包封 siRNA 和 mRNA 中表观 pKa 的重要性。
Trends Pharmacol Sci. 2021 Jun;42(6):448-460. doi: 10.1016/j.tips.2021.03.002. Epub 2021 Apr 16.
10
Efficacy and Safety of the mRNA-1273 SARS-CoV-2 Vaccine.mRNA-1273 新型冠状病毒疫苗的有效性和安全性。
N Engl J Med. 2021 Feb 4;384(5):403-416. doi: 10.1056/NEJMoa2035389. Epub 2020 Dec 30.