Centre of Biological Engineering, University of Minho, Braga, Portugal.
Centre of Biological Engineering, University of Minho, Braga, Portugal.
Colloids Surf B Biointerfaces. 2019 Jul 1;179:414-420. doi: 10.1016/j.colsurfb.2019.03.039. Epub 2019 Mar 31.
Liposomes are one of the most important and extensively studied drug delivery system due to their ability to encapsulate different kinds of drugs. Exploiting the advantages of H Nuclear Magnetic Resonance (NMR) spectrometry, we established a rapid and easy method for quantification of drugs encapsulated in liposomes. An internal standard, pyridine, was used for quantitative determination of drug concentration. Two different drugs were involved in this work, one hydrophilic, methotrexate disodium salt, and another hydrophobic, tamoxifen. The specificity and selectivity of the suggested method were evaluated by the absence of overlapping of at least one signal of each drug with pyridine in the NMR spectrum. The accuracy and precision of the method were assessed by adding a known amount of each drug to unloaded liposomes. Results obtained by quantitative NMR (qNMR) were validated and confirmed by comparing with two other traditional techniques, Ultraviolet-Visible (UV-vis) spectrophotometry and High-Performance Liquid Chromatography (HPLC). It was found that the results were consistent with the ones obtained from our proposed qNMR method. Considering all the experiments conducted in this study, we deliberate that qNMR can be a suitable tool for the determination of drugs encapsulated in liposomes.
脂质体是最重要和研究最广泛的药物传递系统之一,因为它们能够包裹不同种类的药物。利用 H 核磁共振(NMR)光谱的优势,我们建立了一种快速简便的方法来定量测定脂质体中包裹的药物。内标吡啶用于定量测定药物浓度。本工作涉及两种不同的药物,一种是亲水性的甲氨蝶呤二钠盐,另一种是疏水性的他莫昔芬。通过 NMR 光谱中每种药物与吡啶之间至少一个信号没有重叠,评估了所建议方法的特异性和选择性。通过向未载药的脂质体中加入已知量的每种药物来评估方法的准确性和精密度。通过与两种传统技术,紫外-可见(UV-vis)分光光度法和高效液相色谱法(HPLC)进行比较,验证和确认定量 NMR(qNMR)的结果。结果表明,与我们提出的 qNMR 方法获得的结果一致。考虑到本研究中进行的所有实验,我们认为 qNMR 可以作为测定脂质体中包裹的药物的合适工具。