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首页> 外文期刊>Journal of AOAC International >Single-laboratory validated method for determination of nordihydroguaiaretic acid in chaparral-containing dietary supplements
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Single-laboratory validated method for determination of nordihydroguaiaretic acid in chaparral-containing dietary supplements

机译:经单实验室验证的含有山核桃的膳食补充剂中去甲二氢愈创木酸的测定方法

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摘要

Nordihydroguaiaretic acid (NDGA) occurs naturally in chaparral (Larrea tridentate Coville), a plant which commonly grows in the Southwest United States and has been used for medicinal purposes by Native Americans indigenous to that region. In addition to its traditional use as a tea, manufacturers of dietary supplements have marketed chaparral-containing products in a variety of formulations. Because of the hepatotoxicity of NDGA, and its occurrence in regulated products, we have developed a method for the determination of NDGA in dietary supplements and have tested this method in several dietary supplement formulations. Products were extracted with 80% methanol, filtered, and analyzed by high-performance liquid chromatography. NDGA was detected and determined with both a diode array detector and negative-ion electrospray. Fragmentation in the triple-quadru pole mass spectrometer was obtained by collisional activation of the [M-H](-) ion. Collisional activation produced sufficient fragmentation to provide unambiguous identification. Lack of a stable isotope labeled internal standard has led us to compare quantitations based on UV detection with quantitations based on tandem mass spectrometry (MS/MS). Presence of NDGA was confirmed in several dietary supplement products. Quantitative results from the 2 detection methods were comparable for most products. The limit of quantitation using MS/MS was lower and fewer interferences were observed, although UV detection provided better linearity.
机译:去甲去氢愈创木酸(NDGA)自然存在于丛林中(拉雷亚三齿科维尔(Larrea tridentate Coville)),该植物通常在美国西南部生长,并已被该地区的原住民用于药用。除了作为茶的传统用途外,膳食补充剂制造商还以各种配方销售了含有丛林动物的产品。由于NDGA的肝毒性及其在限定产品中的存在,我们开发了一种测定膳食补充剂中NDGA的方法,并已在几种膳食补充剂配方中对该方法进行了测试。用80%甲醇萃取产物,过滤,并通过高效液相色谱法分析。使用二极管阵列检测器和负离子电喷雾检测并确定了NDGA。通过[M-H](-)离子的碰撞活化获得三重四极杆质谱仪中的碎片。碰撞激活产生足够的碎片以提供明确的鉴定。缺乏稳定的同位素标记的内标物,导致我们将基于UV检测的定量与基于串联质谱(MS / MS)的定量进行了比较。几种膳食补充剂产品中均证实了NDGA的存在。两种检测方法的定量结果对于大多数产品而言都是可比的。尽管使用UV检测可以提供更好的线性,但使用MS / MS的定量限较低,并且观察到的干扰较少。

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