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超高效液相色谱-串联质谱法测定总黄酮提取物在年轻和老年大鼠中的组织分布

Tissue Distribution of Total Flavonoids Extracts of in Young and Old Rats by UPLC-MS/MS Determination.

作者信息

Zhang Yue, Lei Xia, Xu Hongdan, Liu Guoliang, Wang Yeqiu, Sun Huifeng, Geng Fang, Zhang Ning

机构信息

College of Pharmacy, Heilongjiang University of Chinese Medicine, Harbin, Heilongjiang 150040, China.

College of Jiamusi, Heilongjiang University of Chinese Medicine, Jiamusi, Heilongjiang 154007, China.

出版信息

J Anal Methods Chem. 2022 Feb 4;2022:2447945. doi: 10.1155/2022/2447945. eCollection 2022.

Abstract

(Kunze ex Mett.) J. Sm. has been extensively used in China, Japan, and Korea to treat osteoporosis and tonify kidneys. A rapid and validated UPLC-MS/MS method for simultaneous determination of the seven analytes including neoeriocitrin, luteolin-7--D-glucoside, astragalin, naringin, eriodictyol, naringenin, and kaempferol in rats' various tissues (heart, liver, spleen, lung, kidney, stomach, brain, uterus, ovary, and small intestine) using quercetin as the internal standard (IS) was developed after oral administration of TFDR to rats. Tissues samples were retreated by protein precipitation with methanol. The chromatographic separation was performed using an ACQUITY UPLC™ BEH C column (2.1 × 50 mm; 1.7 m) at 35°C. The mobile phase consisted of 1% acetic acid in water as the aqueous phase (A) and 100% acetonitrile as the organic phase (B). All analytes and IS were quantified through electrospray ionization in positive ion multiple reaction monitoring (MRM) mode. MS transitions were m/z 597.5 ⟶ 289.2 for neoeriocitrin, m/z 449.1 ⟶ 287.1 for luteolin-7--D-glucoside, m/z 449.1 ⟶ 287.1 for astragalin, m/z 581.5 ⟶ 273.2 for naringin, m/z 289.2 ⟶ 153.1 for eriodictyol, m/z 273.2 ⟶ 153.1 for naringenin, m/z 287.1 ⟶ 153.1 for kaempferol, and m/z 303.2 ⟶ 153.1 for quercetin (IS). The mean extraction recovery of the seven analytes and IS in tissue samples at three levels of quality control (QC) samples ranged from 82.72% to 118.57%, and the RSD was ≤14.98%. The intraday and interday precision (RSD) were all less than 14.98%, and the accuracy (RE) ranged from -13.96% to 14.96%, which indicated that the present method was not an issue. Tissues distribution showed neoeriocitrin, luteolin-7--D-glucoside, astragalin, naringin, and naringenin could transfer across the blood-brain barrier, which may form the basis of TFDR entering the brain to play an anti-AD role. Compared with the 8-month-old rats, a higher concentration of naringin was found in the ovaries of the 18-month-old rats; this result indicated that it may regulate the autonomic nervous dysfunction of the cerebrospinal system through the hypothalamus-pituitary-ovary axis, thus playing an anti-AD role, but further research is needed. Naringenin, eriodictyol, and kaempferol have a higher concentration in the liver and kidney; this phenomenon may be related to the traditional Chinese medicine theory that there is a definite relationship between the liver and kidney meridian. These results provide reliable data support for further study of the pharmacological mechanism of TFDR, formulation of drug delivery schemes, and development of new Chinese medicines in the treatment of AD.

摘要

(Kunze ex Mett.)J. Sm. 在中国、日本和韩国已被广泛用于治疗骨质疏松症和补肾。在给大鼠口服TFDR后,建立了一种快速且经过验证的超高效液相色谱-串联质谱法,以槲皮素为内标(IS),同时测定大鼠各种组织(心脏、肝脏、脾脏、肺脏、肾脏、胃、大脑、子宫、卵巢和小肠)中的七种分析物,包括新橙皮苷、木犀草素-7-O-D-葡萄糖苷、紫云英苷、柚皮苷、圣草酚、柚皮素和山奈酚。组织样品用甲醇进行蛋白沉淀处理。色谱分离在35°C下使用ACQUITY UPLC™ BEH C18柱(2.1×50 mm;1.7μm)进行。流动相由含1%乙酸的水作为水相(A)和100%乙腈作为有机相(B)组成。所有分析物和内标通过电喷雾电离在正离子多反应监测(MRM)模式下进行定量。新橙皮苷的质谱转换为m/z 597.5→289.2,木犀草素-7-O-D-葡萄糖苷为m/z 449.1→287.1,紫云英苷为m/z 449.1→287.1,柚皮苷为m/z 581.5→273.2,圣草酚为m/z 289.2→153.1,柚皮素为m/z 273.2→153.1,山奈酚为m/z 287.1→153.1,槲皮素(内标)为m/z 303.2→153.1。七个分析物和内标在三个质量控制(QC)样品水平的组织样品中的平均提取回收率在82.72%至118.57%之间,相对标准偏差(RSD)≤14.98%。日内和日间精密度(RSD)均小于14.98%,准确度(RE)在-13.96%至14.96%之间,这表明本方法没有问题。组织分布表明新橙皮苷、木犀草素-7-O-D-葡萄糖苷、紫云英苷、柚皮苷和柚皮素可以穿过血脑屏障,这可能是TFDR进入大脑发挥抗AD作用的基础。与8月龄大鼠相比,18月龄大鼠卵巢中柚皮苷浓度更高;该结果表明它可能通过下丘脑-垂体-卵巢轴调节脑脊液系统的自主神经功能障碍,从而发挥抗AD作用,但需要进一步研究。柚皮素、圣草酚和山奈酚在肝脏和肾脏中浓度较高;这种现象可能与中医理论中肝肾经络之间存在明确关系有关。这些结果为进一步研究TFDR的药理机制、制定给药方案以及开发治疗AD的新型中药提供了可靠的数据支持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f68f/8837432/9134892ad6ba/JAMC2022-2447945.001.jpg

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