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Determination of Methotrexate in pH-Sensitive Chitosan Nanoparticles by Validated RP-LC and UV Spectrophotometric Methods

机译:验证的RP-LC和紫外分光光度法测定pH敏感的壳聚糖纳米颗粒中的甲氨蝶呤

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摘要

Nanotechnology-based drug delivery systems are in constant development and, therefore, it is of great importance to have rapid, efficient and accurate analytical methodology to quantify the encapsulated drugs. Here, simple and fast methods, by reversed-phase liquid chromatography (RP-LC) and UV spectrophotometry, were developed and validated for the determination of methotrexate (MTX) in pH-sensitive chitosan nanoparticles (CS-NPs). NPs were prepared using a modified ionotropic complexation process, in which was included a surfactant derived from Nα,Nε-dioctanoyl lysine with an inorganic sodium counterion. The RP-LC method was carried out on a Waters XBridgeTM C18 column (250 mm x 4.6 mm I.D., 5μm), with mobile phase consisted of potassium phosphate buffer (0.05 M, pH 3.2): acetonitrile (86:14, v/v), and UV detection set at 303 nm. The analyses of MTX content by the UV method were also accomplished at 303 nm, using 0.1 M sodium hydroxide as diluent. The measurements were linearly correlated with concentration for both methods in the 1 - 30 μg/mL range (r > 0.9999). The specificity tests showed that there was no interference of the NP components on the quantitative analyses. Precision (repeatability and intermediate precision) was demonstrated by a relative standard deviation lower than 1.5%, whereas the accuracy was assessed by the recovery of MTX from sample matrices, given mean value of ~99%. The proposed methods were applied for the analyses of MTX in different batches of NPs, and the results showed non-significant differences (p > 0.05) between the values obtained with both methodologies. Moreover, the RP-LC method was successfully used to determine the drug entrapment efficiency, and to quantify MTX during in vitro release assays and photolytic degradation studies. In conclusion, the validated methods are suitable to assay MTX in pH-sensitive CS-NPs without any interference from the polymer or surfactant.
机译:基于纳米技术的药物输送系统正在不断发展,因此,具有快速,高效和准确的分析方法来定量所包封的药物非常重要。在这里,通过反相液相色谱(RP-LC)和紫外分光光度法,开发了简单快速的方法,并验证了其对pH敏感的壳聚糖纳米颗粒(CS-NPs)中甲氨蝶呤(MTX)的测定。使用改进的离子络合工艺制备NP,其中包括衍生自Nα,Nε-二辛酰基赖氨酸和无机钠抗衡离子的表面活性剂。 RP-LC方法在Waters XBridgeTM C18色谱柱(250 mm x 4.6 mm内径,5μm)上进行,流动相由磷酸钾缓冲液(0.05 M,pH 3.2):乙腈(86:14,v / v ),并将UV检测设置为303 nm。使用0.1 M氢氧化钠作为稀释剂,还在303 nm处通过UV方法完成了MTX含量的分析。两种方法的测量值均与浓度在1-30μg/ mL范围内线性相关(r> 0.9999)。特异性测试表明,NP成分在定量分析中没有干扰。相对标准偏差低于1.5%,证明了精密度(可重复性和中等精密度),而准确度则通过平均值为99%的样品基质中MTX的回收率进行评估。所提出的方法用于不同批次NPs中MTX的分析,结果显示两种方法获得的值之间无显着差异(p> 0.05)。此外,RP-LC方法已成功用于确定药物的包封效率,并在体外释放测定和光解降解研究过程中定量了MTX。总之,经过验证的方法适用于测定pH敏感的CS-NP中的MTX,而不会受到聚合物或表面活性剂的干扰。

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