Minz Sunita, Kaurav Monika, Sahu Kantrol Kumar, Mandal Vivekananda, Pandey Ravi Shankar
SLT Institute of Pharmaceutical sciences, Guru Ghasidas Vishwavidyalaya, Bilaspur, C.G., 495009, India.
Biomed Chromatogr. 2015 Oct;29(10):1473-9. doi: 10.1002/bmc.3444. Epub 2015 Feb 24.
A simple, sensitive, selective and precise high-performance thin-layer chromatographic method was developed for determination of lipid A (MPLA) adjuvant as a bulk and in solid fat nanoemulsions. Chromatographic separations were performed on thin-layer chromatography aluminum plates precoated with silica gel 60 F-254 as stationary phase and chloroform-methanol-ethyl acetate solution (10:2:4, v/v/v) as mobile phase. With this solvent system, compact spots for MPLA at Rf value 0.80 ± 0.02 were obtained. Densitometric analysis of MPLA was carried out in absorbance mode at 357 nm. Linear regression analysis for the calibration plots showed good linear relationship with r = 0.9996 in the concentration range of 20-100 ng/spot. The mean values (±SD) of slope and intercept were found to be 7.355 ± 0.006 and 109.52 ± 0.170, respectively. Limits of detection (LOD) and quantitation (LOQ) were observed at 3.096 and 9.382 ng/spot, respectively.The method was validated for precision, accuracy, robustness and recovery as per the International Conference on Harmonization guidelines. Statistical analysis proved that the developed method for quantification of MPLA as a bulk and in solid fat nanoemulsions is reproducible, selective and economical. This method could be applied for quantitative assay of MPLA in lipid-based vaccine formulations.
开发了一种简单、灵敏、选择性好且精确的高效薄层色谱法,用于测定作为原料药的脂多糖A(MPLA)佐剂以及固体脂肪纳米乳剂中的MPLA。色谱分离在预涂硅胶60 F - 254的薄层色谱铝板上进行,以其作为固定相,氯仿 - 甲醇 - 乙酸乙酯溶液(10:2:4,v/v/v)作为流动相。使用该溶剂系统,获得了Rf值为0.80±0.02的MPLA致密斑点。在357 nm处采用吸光度模式对MPLA进行光密度分析。校准曲线的线性回归分析表明,在20 - 100 ng/斑点的浓度范围内具有良好的线性关系,r = 0.9996。斜率和截距的平均值(±SD)分别为7.355±0.006和109.52±0.170。检测限(LOD)和定量限(LOQ)分别为3.096和9.382 ng/斑点。按照国际协调会议指南对该方法的精密度、准确度、稳健性和回收率进行了验证。统计分析证明,所开发的用于定量测定原料药形式以及固体脂肪纳米乳剂中MPLA的方法具有可重复性、选择性且经济。该方法可用于脂质基疫苗制剂中MPLA的定量测定。