Patnala Srinivas, Kanfer Isadore
Department of Chemistry, Rhodes University, Grahamstown, South Africa.
J Pharm Pharm Sci. 2015;18(4):414-23. doi: 10.18433/j3330x.
Sceletium plants have been used for its medicinal properties for centuries. However, there is a wide range of Sceletium plant species in which various alkaloidal components such as ∆7mesembrenone, mesembrenol, mesembranol, mesembrenone, mesembrine hydrochloride, epimesembranol and, sceletium A4 differ between species. Hence, to ensure the quality of Sceletium products used as a medicine, it is imperative to identify the appropriate species using both botanical and chemical methods. The chemical approach to identify and characterize the phytochemical composition of a particular species facilitates the choice of species that will provide the purported therapeutic outcome. Hence, specific analytical methods to identify relevant constituents from complex matrices are necessary. Although HPLC-UV detection is commonly used to identify and estimate phytochemical content of medicinal plants, use of mass spectroscopy (MS) and tandem mass spectroscopy (MS/MS) can unequivocally confirm their presence/absence based on characteristic ions and fragmentation patterns.
The various alkaloidal components were characterized by electrospray ionization (ESI) MS and MS/MS using an ionizing medium of 0.1% ammonium hydroxide in water mixed with acetonitrile. Compounds were purified and characterized for use as reference standards to identify the relevant alkaloidal constituents of several Sceletium plant species using HPLC with on-line UV-MS detection.
ESI-MS provided the M+H ions with respective m/z values that related to the respective molecular weights 287, 289, 291, 287, 289, 324 and 291 for the above mentioned alkaloids, whereas, ESI MS/MS provided the characteristic fragment ions to confirm the structural identity of the individual alkaloids and subsequently used to confirm the presence and/or absence of specific alkaloids in various Sceletium plant samples.
Whilst HPLC-UV detection has been a widely-used conventional analytical technique for both qualitative and quantitative analyses, the results highlight the necessity of ESI-MS detection to avoid erroneous identification of phytochemical components, particularly with mesembrine-type compounds which have closely related chemical structures. This article is open to POST-PUBLICATION REVIEW. Registered readers (see "For Readers") may comment by clicking on ABSTRACT on the issue's contents page.
几个世纪以来,南非钩枝藤属植物因其药用特性而被使用。然而,南非钩枝藤属植物种类繁多,其中诸如∆7去甲美登木酮、美登木醇、去甲美登木醇、美登木酮、盐酸美登木碱、表美登木醇和南非钩枝藤A4等各种生物碱成分在不同物种之间存在差异。因此,为确保用作药物的南非钩枝藤属产品的质量,必须使用植物学和化学方法来鉴定合适的物种。通过化学方法鉴定和表征特定物种的植物化学成分,有助于选择能提供预期治疗效果的物种。因此,需要特定的分析方法从复杂基质中鉴定相关成分。虽然高效液相色谱 - 紫外检测通常用于鉴定和估计药用植物的植物化学成分,但使用质谱(MS)和串联质谱(MS/MS)可以根据特征离子和碎片模式明确确认它们的存在与否。
使用0.1%氢氧化铵在水中与乙腈混合的电离介质,通过电喷雾电离(ESI)MS和MS/MS对各种生物碱成分进行表征。化合物经过纯化和表征后用作参考标准品,通过带有在线紫外 - MS检测的高效液相色谱法鉴定几种南非钩枝藤属植物物种的相关生物碱成分。
ESI - MS为上述生物碱提供了M + H离子,其各自的m/z值与各自的分子量287、289、291、287、289、324和291相关,而ESI MS/MS提供了特征碎片离子,以确认各个生物碱的结构身份,并随后用于确认各种南非钩枝藤属植物样品中特定生物碱的存在与否。
虽然高效液相色谱 - 紫外检测一直是广泛用于定性和定量分析的传统分析技术,但结果突出了ESI - MS检测的必要性,以避免植物化学成分的错误鉴定,特别是对于具有密切相关化学结构的美登木碱型化合物。本文接受出版后审查。注册读者(见“读者须知”)可通过点击本期目录页面上的“摘要”进行评论。