• 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

在人血清中对多功能纳米药物递送系统进行原位、定量评估。

In Situ, Quantitative Assessment of Multifunctional Nanoscale Drug Delivery Systems in Human Serum.

机构信息

Laboratory of Organic and Macromolecular Chemistry (IOMC), Friedrich Schiller University Jena, Humboldtstraße 10, 07743 Jena, Germany.

Jena Center for Soft Matter (JCSM), Friedrich Schiller University Jena, Philosophenweg 7, 07743 Jena, Germany.

出版信息

Anal Chem. 2020 Jun 2;92(11):7932-7939. doi: 10.1021/acs.analchem.0c01323. Epub 2020 May 19.

DOI:10.1021/acs.analchem.0c01323
PMID:32372636
Abstract

The large volume and diversified nanomedicine market, undergoing a rapid growth, relies not only on the creation and applicative exploration of nanocarrier-based medicines showing significant potential, but in particular, demands a quantitative assessment of their physicochemical properties. In this study, we demonstrate the in situ assessment of multifunctional biodegradable nanoparticle (NP) entries as core components of nanoscale drug delivery systems (NDDSs) by making use of analytical ultracentrifugation (AUC). We determine and elucidate the following characteristics of NPs in NDDSs: NP density and size, targeting dye functionality, encapsulated and free drug, surfactant, and also NP drug release dynamics, quantitatively interconnected to NP degradation. In concept, we demonstrate this by multidetection AUC experiments at variable speed and time profiles. We could verify the quantitative and accurate nature of AUC for assessment of NDDSs, that is, also future nanomedicines. This concerns modeled and real life solution application formats such as cell culture media and human serum.

摘要

庞大且多样化的纳米医学市场正在快速增长,不仅依赖于具有显著潜力的基于纳米载体药物的创新和应用探索,还特别需要对其物理化学性质进行定量评估。在这项研究中,我们通过分析超速离心(AUC)原位评估多功能可生物降解纳米颗粒(NP)作为纳米药物递送系统(NDDS)的核心组件。我们确定并阐明了 NDDS 中 NPs 的以下特性:NP 密度和尺寸、靶向染料功能、包封和游离药物、表面活性剂,以及 NP 药物释放动力学,与 NP 降解定量相关联。从概念上讲,我们通过在不同速度和时间分布下进行多检测 AUC 实验来证明这一点。我们可以验证 AUC 用于评估 NDDS 的定量和准确性,也可以用于未来的纳米药物。这涉及到模型和实际生活中的溶液应用格式,如细胞培养基和人血清。

相似文献

1
In Situ, Quantitative Assessment of Multifunctional Nanoscale Drug Delivery Systems in Human Serum.在人血清中对多功能纳米药物递送系统进行原位、定量评估。
Anal Chem. 2020 Jun 2;92(11):7932-7939. doi: 10.1021/acs.analchem.0c01323. Epub 2020 May 19.
2
Nanoparticle-based drug delivery systems: What can they really do ?基于纳米颗粒的药物递送系统:它们究竟能做什么?
F1000Res. 2017 May 16;6:681. doi: 10.12688/f1000research.9690.1. eCollection 2017.
3
Nuclear Delivery of Nanoparticle-Based Drug Delivery Systems by Nuclear Localization Signals.基于核定位信号的纳米药物传递系统的核递送。
Cells. 2023 Jun 15;12(12):1637. doi: 10.3390/cells12121637.
4
Analytical ultracentrifugation for analysis of doxorubicin loaded liposomes.用于分析载有阿霉素脂质体的分析型超速离心法。
Int J Pharm. 2017 May 15;523(1):320-326. doi: 10.1016/j.ijpharm.2017.03.046. Epub 2017 Mar 22.
5
Statistical prediction of nanoparticle delivery: from culture media to cell.纳米颗粒递送的统计预测:从培养基到细胞
Nanotechnology. 2015 Apr 17;26(15):155101. doi: 10.1088/0957-4484/26/15/155101. Epub 2015 Mar 23.
6
Measuring agglomerate size distribution and dependence of localized surface plasmon resonance absorbance on gold nanoparticle agglomerate size using analytical ultracentrifugation.使用分析超速离心法测量团聚体的大小分布和局域表面等离子体共振吸收与金纳米粒子团聚体大小的关系。
ACS Nano. 2011 Oct 25;5(10):8070-9. doi: 10.1021/nn202645b. Epub 2011 Sep 29.
7
Toxicological assessment of nanoparticle interactions with the pulmonary system.纳米颗粒与肺部系统相互作用的毒理学评估。
Nanotoxicology. 2020 Feb;14(1):21-58. doi: 10.1080/17435390.2019.1661043. Epub 2019 Sep 10.
8
Bridging the Gap between Macroscale Drug Delivery Systems and Nanomedicines: A Nanoparticle-Assembled Thermosensitive Hydrogel for Peritumoral Chemotherapy.弥合宏观药物输送系统与纳米医学之间的差距:用于瘤周化疗的纳米颗粒组装的温敏水凝胶。
ACS Appl Mater Interfaces. 2016 Nov 2;8(43):29323-29333. doi: 10.1021/acsami.6b10416. Epub 2016 Oct 19.
9
Nanoparticles in drug delivery: mechanism of action, formulation and clinical application towards reduction in drug-associated nephrotoxicity.药物递送中的纳米颗粒:作用机制、制剂以及降低药物相关性肾毒性的临床应用。
Expert Opin Drug Deliv. 2014 Oct;11(10):1661-80. doi: 10.1517/17425247.2014.938046. Epub 2014 Jul 23.
10
Target Site Delivery and Residence of Nanomedicines: Application of Quantitative Systems Pharmacology.纳米药物的靶部位递药与驻留:定量系统药理学的应用。
Pharmacol Rev. 2019 Apr;71(2):157-169. doi: 10.1124/pr.118.016816.

引用本文的文献

1
Differences in Physico-Chemical Properties and Immunological Response in Nanosimilar Complex Drugs: The Case of Liposomal Doxorubicin.纳米类似复杂药物中物理化学性质和免疫反应的差异:以脂质体多柔比星为例。
Int J Mol Sci. 2023 Sep 2;24(17):13612. doi: 10.3390/ijms241713612.
2
PEG-Lipids: Quantitative Study of Unimers and Aggregates Thereof by the Methods of Molecular Hydrodynamics.PEG-脂质:分子流体力学方法对单体及其聚集体的定量研究。
Anal Chem. 2023 Jul 18;95(28):10795-10802. doi: 10.1021/acs.analchem.3c01999. Epub 2023 Jul 7.
3
Nanoparticle Formulation Composition Analysis by Liquid Chromatography on Reversed-Phase Monolithic Silica.
反相整体硅胶液相色谱法分析纳米粒子配方组成。
Anal Chem. 2023 Jan 17;95(2):565-569. doi: 10.1021/acs.analchem.2c04277. Epub 2022 Dec 22.
4
Ethoxy acetalated dextran-based nanocarriers accomplish efficient inhibition of leukotriene formation by a novel FLAP antagonist in human leukocytes and blood.乙氧基乙酰化葡聚糖基纳米载体通过新型 FLAP 拮抗剂在人白细胞和血液中有效抑制白三烯的形成。
Cell Mol Life Sci. 2021 Dec 31;79(1):40. doi: 10.1007/s00018-021-04039-7.
5
Targeted delivery of a phosphoinositide 3-kinase γ inhibitor to restore organ function in sepsis.靶向递送磷酸肌醇 3-激酶 γ 抑制剂以恢复脓毒症器官功能。
EMBO Mol Med. 2021 Oct 7;13(10):e14436. doi: 10.15252/emmm.202114436. Epub 2021 Sep 2.
6
Formulation of Liver-Specific PLGA-DY-635 Nanoparticles Loaded with the Protein Kinase C Inhibitor Bisindolylmaleimide I.负载蛋白激酶C抑制剂双吲哚马来酰胺I的肝脏特异性聚乳酸-羟基乙酸共聚物-DY-635纳米颗粒的制剂
Pharmaceutics. 2020 Nov 18;12(11):1110. doi: 10.3390/pharmaceutics12111110.