Siddiqui Nasir A, Mothana Ramzi A, Al-Rehaily Adnan J, Alam Perwez, Yousaf Muhammad, Ahmed Sarfaraz, Alatar Abdulrahman
Department of Pharmacognosy, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.
Department of Botany and Microbiology, College of Science, King Saud University, Riyadh, Saudi Arabia.
Saudi Pharm J. 2017 Jul;25(5):696-702. doi: 10.1016/j.jsps.2016.09.006. Epub 2016 Sep 30.
The biomarkers are needed to be defined for standardization purposes so that safe and effective herbal formulations can be catered to the society. There is an urgent need for statistical support of herbal drugs because most of the herbal products are still used in the non-standardized form. This study is based on the development of a simple and sensitive RP-HPTLC method for concurrent estimation of two biomarkers -phyllanthidine and rutin in the methanol extract of aerial parts of . The developed method was found to be simple, economic and sensitive. Separation and quantification were performed with acetonitrile: water (4:6 /) used as the mobile phase on glass-backed RP-HPTLC plate. Detection of absorption maxima and quantification was done at 310 nm of UV region. The developed chromatographic system was found to give a sharp band for -phyllanthidine and rutin at 0.73 ± 0.01 and 0.68 ± 0.01, respectively. The linearity ranges for -phyllanthidine, and rutin were found to be 200-1600 ngband and 100-1400 ngband, respectively, with correlation coefficients ( values) of 0.998 and 0.997, respectively. The percentage of -phyllanthidine and rutin was found to be 9.121 ± 0.02% and 1.018 ± 0.04% (w/w), respectively. The resolution of bands and separation of constituents in FVME exhibited the perfect optimization of the developed method. The validation statistics supports the proposed method for standardizing crude drugs as well as formulations of a natural product containing -phyllanthidine and rutin.
为了实现标准化,需要定义生物标志物,以便能够为社会提供安全有效的草药配方。对草药药物的统计支持迫在眉睫,因为大多数草药产品仍以非标准化形式使用。本研究基于开发一种简单灵敏的反相高效薄层色谱法,用于同时测定地上部分甲醇提取物中的两种生物标志物——叶下珠碱和芦丁。结果发现所开发的方法简单、经济且灵敏。使用乙腈∶水(4∶6)作为流动相,在玻璃背反相高效薄层色谱板上进行分离和定量。在紫外区域310nm处进行最大吸收检测和定量。所开发的色谱系统在0.73±0.01和0.68±0.01处分别为叶下珠碱和芦丁给出了尖锐的色带。叶下珠碱和芦丁的线性范围分别为200 - 1600ng/斑和100 - 1400ng/斑,相关系数(r值)分别为0.998和0.997。叶下珠碱和芦丁的含量分别为9.121±0.02%和1.018±0.04%(w/w)。FVME中的色带分辨率和成分分离显示了所开发方法的完美优化。验证统计数据支持所提出的用于标准化含有叶下珠碱和芦丁的天然产物的粗药以及制剂的方法。