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1.成都中医药大学 药学院,西南特色中药资源国家重点实验室,成都 611137
2.河南中医药大学 第一附属医院,郑州 450000
3.四川护理职业学院,成都 610100
4.成都市三勒浆药业集团,成都 610000
5.四川省中医药科学院 国家中医药管理局 中药质量生物评价重点研究室,成都 610041
6.成都中医药大学 附属医院,成都 610072
黄浩洲,博士,从事中药药剂学研究,E-mail:1539889839@qq.com
林俊芝,硕士,助理研究员,从事中药药剂学研究,E-mail:582097013@qq.com
张定堃,博士,副教授,从事中药药剂学研究,E-mail:465790643@qq.com
纸质出版日期:2020-07-20,
网络出版日期:2019-12-31,
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黄浩洲,仇敏,唐进法等.基于UPLC-Q-TOF-MSE技术的三勒浆口服液上清液及沉淀部分化学成分分析[J].中国实验方剂学杂志,2020,26(14):143-151.
HUANG Hao-zhou,QIU Min,TANG Jin-fa,et al.Analysis of Chemical Components in Supernatant and Precipitate of Sanajon Oral Liquid Based on UPLC-Q-TOF-MSE Technology[J].Chinese Journal of Experimental Traditional Medical Formulae,2020,26(14):143-151.
黄浩洲,仇敏,唐进法等.基于UPLC-Q-TOF-MSE技术的三勒浆口服液上清液及沉淀部分化学成分分析[J].中国实验方剂学杂志,2020,26(14):143-151. DOI: 10.13422/j.cnki.syfjx.20200848.
HUANG Hao-zhou,QIU Min,TANG Jin-fa,et al.Analysis of Chemical Components in Supernatant and Precipitate of Sanajon Oral Liquid Based on UPLC-Q-TOF-MSE Technology[J].Chinese Journal of Experimental Traditional Medical Formulae,2020,26(14):143-151. DOI: 10.13422/j.cnki.syfjx.20200848.
目的
2
分析三勒浆口服液上清液和沉淀部分的主要化学成分,为建立其质量标准与沉淀控制技术提供依据。
方法
2
使用UPLC-Q-TOF-MS
E
技术分别对分离后的上清液及沉淀部分化学成分进行定性分析,采用Waters ACQUITY UPLC BEH C
18
色谱柱(2.1 mm×100 mm,1.7 μm),流动相选择0.1%甲酸水溶液(A)-乙腈(B)梯度洗脱(0~1 min,2%B;1~2 min,2%~5%B;2~4 min,5%~7%B;4~6 min,7%~24%B;6~10 min,24%~42%B;10~12 min,42%~54%B;12~15 min,54%~76%B;15~18 min,76%~100%B),流速0.3 mL·min
-1
,柱温30 ℃,进样量2 μL。质谱分析采用电喷雾离子源(ESI),负离子模式下使用时间依赖型MS
E
方式采集样品质谱数据,采集范围
m
/
z
50~1 200(上清液)和
m
/
z
50~3 000(沉淀),通过对采集数据的保留时间、精确相对分子质量和二级质谱裂解碎片进行比对后鉴定化学成分。
结果
2
在三勒浆口服液上清液中共鉴定了61个化合物,包括鞣质类、酚酸类、黄酮类、氨基酸类、有机酸类、脂肪酸类等;沉淀中共鉴定了15个化合物,包括鞣质类、酚酸类、黄酮类、脂肪酸类等。
结论
2
三勒浆口服液的水解鞣质可能是该制剂潜在的沉淀物质基础,其沉淀物很可能是以鞣花酸和鞣红为主构成的复杂沉淀。建立的UPLC-Q-TOF-MS
E
可快速、全面地分析三勒浆口服液的化学成分,可为其物质基础、沉淀机制及质量控制等研究提供科学依据。
Objective
2
To analyze the main chemical components in the supernatant and precipitate of Sanajon oral liquid
so as to provide basis for establishing its quality standard and precipitation control technology.
Method
2
UPLC-Q-TOF-MS
E
was used to analyze the chemical components in the supernatant and precipitate of this oral liquid. The analysis was performed on Waters ACQUITY UPLC BEH C
18
column (2.1 mm×100 mm
1.7 μm) with the mobile phase of 0.1% formic acid solution (A) and acetonitrile (B) for gradient elution (0-1 min
2%B; 1-2 min
2%-5%B; 2-4 min
5%-7%B; 4-6 min
7%-24%B; 6-10 min
24%-42%B; 10-12 min
42%-54%B; 12-15 min
54%-76%B; 15-18 min
76%-100%B)
the flow rate was set to 0.3 mL·min
-1
the column temperature was 30 ℃
the injection volume was 2 µL. The mass spectrographic analysis was used with electrospray ionization (ESI)
sample MS data was acquired by time-dependent MS
E
in negative ion mode
the collection range was
m
/
z
50-1 200 (supernatant) and
m
/
z
50-3 000 (precipitate). Then the chemical constituents were identified by the information of retention time
accurate relative molecular mass and secondary mass spectrum fragment.
Result
2
Totally 61 compounds were identified in the supernatant
including tannins
phenolic acids
flavonoids
amino acids
organic acids
fatty acids
etc. Totally 15 compounds were identified in the precipitate
including tannins
phenolic acids
flavonoids
fatty acids
etc.
Conclusion
2
The hydrolyzed tannin of Sanajon oral liquid may be the potential material basis of its precipitate
and its precipitate is likely to be a complex precipitate mainly composed of ellagic acid and tanned red. The established UPLC-Q-TOF-MS
E
can quickly and comprehensively analyze the chemical composition of Sanajon oral liquid
which can provide a scientific basis for the researches of its material basis
precipitation mechanism and quality control.
三勒浆口服液沉淀多酚鞣质鞣花酸鞣红
Sanajonoral liquidprecipitationpolyphenolstanninsellagic acidphlobaphene
陈明.“法出波斯”:“三勒浆”源流考[J].历史研究,2012(1):4-23,190.
杨继家,张艺,冀静,等.藏医药与印度传统医药对三果汤传统应用及现代研究概述[J].世界科学技术—中医药现代化,2012,14(1):1311-1316.
亓旗,崔雅萍,梁文仪,等.藏药余甘子与诃子化学和药理作用比较[J].世界科学技术—中医药现代化,2016,18(7):1171-1176.
TARASIUK A,MOSIŃSKA P,FICHNA J.Triphala:current applications and new perspectives onthe treatment of functional gastrointestinal disorders[J].Chin Med,2018,13:39.
SINGHAL P,NESARI T,GUPTA G S.Efficacy of herbomineral compounds and pathya (Ayurvedic dietary regime and physical exercise) in the management of Yakrt Roga (Non-alcoholic fatty liver disease)[J].Anc Sci Life,2015,34(4):216-222.
CHANDRAN U,MEHENDALE N,TILLU G,et al.Network pharmacology of Ayurvedaformulation Triphala with special reference to anti-cancer property[J].Comb Chem High T Scr,2015,18(9):846-854.
PRADEEP A R,SUKE D K,MARTANDE S S,et al.Triphala,a new herbal mouthwash for the treatment of gingivitis:a randomized controlled clinical trial[J].J Periodontol,2016,87(11):1352-1359.
黄浩洲,林俊芝,魏夕川,等.中药口服液中鞣花酸分子稳定储存的制剂学机制与调控策略[J].药学学报,2019,54(4):737-745.
陈平,左晓霜,华杰,等.不同pH条件下测定藏药三果汤中没食子酸、单宁酸、β-PGG含量变化及分析[J].中国民族医药杂志,2015,21(11):30-32.
HUANG H Z,FENG B,LIN J Z,et al.Exploration on the approaches of diverse sedimentations in polyphenol solutions:an integrated chain of evidence based on the physical phase,chemical profile,and sediment elements[J]Front Pharmacol,2019,doi:10.3389/fphar.2019.01060http://dx.doi.org/10.3389/fphar.2019.01060.
AVULA B,WANG Y H,WANG M,et al.Simultaneous determination and characterization of tannins and triterpene saponins from the fruits of various species of Terminalia and Phyllantus emblica using a UHPLC-UV-MS method:application to triphala[J].Planta Med,2013,29(2):181-188.
黄浩洲,魏夕川,林俊芝,等.余甘子回流过程中鞣质转化及药典含量测定方法合理性探讨[J].中国药学杂志,2019,54(7):581-587.
TILLER P R,YU S,CASTRO-PEREZ J,et al.High-throughput,accurate mass liquid chromatography/tandem mass spectrometry on a quadrupole time-of-flight system as a 'first-line' approach for metabolite identification studies[J].Rapid Commu Mass Sp,2010,22(7):1053-1061.
李金花,曾锐,瞿燕,等.UPLC-Q-TOF-MSE技术结合UNIFI数据库快速定性分析黄牡丹化学成分[J].中草药,2017,48(8):1529-1536.
王坤凤,袁永兵,吴玲芳,等.缩合鞣质的研究进展[J].中草药,2013,44(12):1687-1699.
冯敬文.小儿清热利肺口服液工艺优化及质量提高研究[D].广州:广东药学院,2011.
SANG S,YANG I,BUCKLEY B,et al.Autoxidat ive quinone formation in vitroand metabolite formation in vivo from tea polyphenol (-)-epigallocatechin-3-gallate:studied byreal-time mass spectrometry combined with tandem mass ion mapping[J].Free Radical Bio Med,2007,43(3):362-371.
石碧,狄莹.植物多酚[M].北京:科学出版社,2000:63,138,139-141.
程金生,黄靖瑜,万维宏,等.金樱子种核微观结构鉴别及活性成分分析[J].安徽农业科学,2018,46(24):149-151.
EL-SHITANY N A,EL-BASTAWISSY E A,EL-DESOKY K.Ellagic acid protects against carrageenan-induced acute inflammation through inhibition of nuclear factor kappa B,inducible cyclooxygenase and proinflammatory cytokines and enhancement of interleukin-10 via an antioxidant mechanism[J].Int Immunopharmacol,2014,19(2):290-299.
KESHTZAR E,KHODAYAR M J,JAVADIPOUR M,et al.Ellagic acid protects against arsenic toxicity in isolated rat mitochondria possibly through the maintaining of complex Ⅱ[J].Hum Exp Toxicol,2016,35(10):1060-1072.
HSEU Y C,CHOU C W,KUMAR K J S,et al.Ellagic acid protects human keratinocyte (HaCaT) cells against UVA-induced oxidative stress and apoptosis through the upregulation of the HO-1 and Nrf-2 antioxidant genes[J].Food Chem Toxicol,2012,50(5):1245-1255.
PFUNDSTEIN B,EL-DESOUKY S K,Hull W E,et al.Polyphenolic compounds in the fruits of Egyptian medicinal plants (Terminalia bellerica,Terminalia chebula,and Terminalia horrida):characterization,quantitation and determination of antioxidant capacities[J].Phytochemistry,2010,71(10):1132-1148.
YANG B,KORTESNIEMI M,LIU P,et al.Analysis of hydrolyzable tannins and other phenolic compounds in emblic leafflower (Phyllanthus emblica L.) fruits by high performance liquid chromatography-electrospray ionization mass spectrometry[J].J Agric Food Chem,2012,60(35):8672-8683.
BALA I,BHARDWAJ V,HARIHARAN S,et al.Analytical methods for assay ofellagic acid and its solubility studies[J].J Pharm Biomed Anal,2006,40(1):206-210.
李碧云,龚琼,张雄飞,等.中药口服液澄明度问题分析[J].中成药,2014,36(11):2384-2387.
杨笑笑,邢晓平,纪白慧,等.水解法制备石榴皮鞣花酸工艺研究[J].食品工业科技,2013,34(12):284-288.
姜红,赵生玉,黄浩洲,等.三勒浆口服液HPLC指纹图谱的建立及多成分定量测定[J].中草药,2017,48(18):3741-3747.
吴玲芳.藏药余甘子鞣质部位体内成分分析[D].北京:北京中医药大学,2014.
丁阳平,陆昌琪,候宏晓,等.儿茶素氧化产物及形成机制研究[J].中国中药杂志,2017,42(2):239-253.
李维熙,王葳,王文静.茶多酚的氧化聚合机制研究进展[J].暨南大学学报:自然科学与医学版,2016,37(3):193-200.
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