Suppr超能文献

核苷脂质的反相超高效液相色谱-二极管阵列检测/串联四级杆飞行时间质谱分析。

Chromatographic study of nucleoside-lipids by RP-UHPLC-DAD/CAD.

机构信息

ChemBioPharm, ARNA Laboratory, INSERM U1212, UMR CNRS 5320, Univ. Bordeaux, 146 rue Léo Saignat, 33076, Bordeaux, France.

出版信息

Anal Bioanal Chem. 2018 Nov;410(29):7711-7721. doi: 10.1007/s00216-018-1388-9. Epub 2018 Sep 28.

Abstract

Today, one of the most popular strategies in drug delivery is the encapsulation of therapeutic agents in supramolecular nanosystems formed from amphiphilic molecules. Synthetic nucleoside-lipids, composed of one nucleoside and lipidic chains, constitute promising new amphiphilic excipients under research in the field of pharmaceutical and biomedical applications. The aim of this work was to study the chromatographic behavior of these nucleoside-lipids in reversed-phase HPLC to establish appropriate chromatographic conditions for their analysis in drug delivery systems. The effect of the stationary phase, the organic solvent, the pH* values, and pH modifier nature of the mobile phase were studied on retention, peak shape, and detection. Good chromatographic performance was achieved on both Syncronis® C18 and Acquity® BEH C18 with mobile phases composed of MeOH/water, 95:5 (v/v) mixtures at apparent pH above 5. Dual detection by diode array detection (DAD) and charged aerosol detection (CAD) was investigated. CAD signal was found to be dependent on the type of pH modifiers added to the mobile phase. In isocratic elution, the same order of magnitude of CAD responses was obtained for the tested nucleoside-lipids. This study led to suitable chromatographic conditions for purity and stability studies of nucleoside-lipids. The purity of the synthetized molecules was established to be superior to 98%. Different stability in organic solvents was noticed depending on nucleoside-lipid structure. This first study will allow quantitative applications to establish loading ratio and encapsulation yield in future drug delivery systems composed of nucleoside-lipid-based assemblies.

摘要

如今,药物传递中最流行的策略之一是将治疗剂封装在由两亲分子形成的超分子纳米系统中。合成核苷脂质由一个核苷和脂质链组成,是药物和生物医学应用领域中研究的有前途的新型两亲赋形剂。本工作的目的是研究这些核苷脂质在反相 HPLC 中的色谱行为,以建立适合其在药物传递系统中分析的色谱条件。研究了固定相、有机溶剂、pH 值和流动相 pH 调节剂性质对保留、峰形和检测的影响。在 Syncronis® C18 和 Acquity® BEH C18 上均获得了良好的色谱性能,流动相由 MeOH/水、95:5(v/v)混合物组成,表观 pH 值高于 5。研究了二极管阵列检测(DAD)和带电气溶胶检测(CAD)的双重检测。发现 CAD 信号取决于添加到流动相中的 pH 调节剂的类型。在等度洗脱中,测试的核苷脂质获得了相同数量级的 CAD 响应。这项研究为核苷脂质的纯度和稳定性研究提供了合适的色谱条件。合成分子的纯度被确定为优于 98%。根据核苷脂质结构的不同,在有机溶剂中的稳定性也不同。这项初步研究将允许进行定量应用,以在未来由核苷脂质基组装体组成的药物传递系统中建立载药量和包封率。

相似文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验