Article(id=1240688790629577508, tenantId=1146029695717560320, journalId=1205117023404326918, issueId=1240688783964819588, articleNumber=null, orderNo=null, doi=10.16155/j.0254-1793.2023-0775, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1701705600000, receivedDateStr=2023-12-05, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1773732858569, onlineDateStr=2026-03-17, pubDate=1727625600000, pubDateStr=2024-09-30, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1773732858569, onlineIssueDateStr=2026-03-17, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1773732858569, creator=13701087609, updateTime=1773732858569, updator=13701087609, issue=Issue{id=1240688783964819588, tenantId=1146029695717560320, journalId=1205117023404326918, year='2024', volume='44', issue='9', pageStart='1463', pageEnd='1645', issueExtLink='null', onlineDate='null', pubDate='null', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1773732856979, creator=13701087609, updateTime=1773733032821, updator=13701087609, preIssue=null, nextIssue=null, ext={EN=IssueExt(id=1240689521587712627, tenantId=1146029695717560320, journalId=1205117023404326918, issueId=1240688783964819588, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1240689521587712628, tenantId=1146029695717560320, journalId=1205117023404326918, issueId=1240688783964819588, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null}, startPage=1513, endPage=1523, ext={EN=ArticleExt(id=1240688790960927530, articleId=1240688790629577508, tenantId=1146029695717560320, journalId=1205117023404326918, language=EN, title=Study on steroids detection based on dual derivatization couple with tandem mass spectrometry, columnId=1240688785420243088, journalTitle=Chinese Journal of Pharmaceutical Analysis, columnName=Metabolism Analysis·ActivityAnalysi, runingTitle=null, highlight=null, articleAbstract=
Objective: To establish a dual derivatization method combined with tandem mass spectrometry for the simultaneous determination of 18 different steroid hormones in human serum. Methods: Serum samples were treated with hydroxylamine and 1, 2-dimethylimidazole-5-sulfonyl chloride for derivatization, and the resulting compounds were analyzed by liquid chromatography-tandem mass spectrometry in positive ion selected reaction monitoring (SRM) mode. The Kinetex®C8 column (100 mm×2.1 mm, 2.6 μm) was used for the separation. Mobile phase A (0.1% acetic acid in water) and mobile phase B (0.1% acetic acid in methanol) with gradient elution(0-0.5 min, 35% B; 0.5-5 min, 35% B→100% B; 5.0-5.1 min, 100% B→35% B; 5.1-7 min, 35% B)at the flow rate of 0.4 mL·min-1 were applied. Column temperature was set at 40 ℃. Injection volume was 20 μL and collection time was 6 min. Results: The linearity correlation coefficients for all 18 steroid hormones were greater than 0.99, the recovery rates ranged from 85% to 115%, and the precision RSD was less than 15%. This method was successfully applied to the analysis of serum samples from 156 healthy subjects (75 males and 61 females), and reference intervals were established. Conclusion: This method can be used to simultaneously determine 18 types of steroid hormones, such as pregnenolone, 17-hydroxypregnenolone, progesterone, 17-hydroxyprogesterone, corticosterone, cortisol, 11-deoxycorticosterone, 21-deoxycorticosterone, aldosterone, testosterone, androstanedione, dehydroepiandrosterone, sulfated dehydroepiandrosterone, adrenocorticotropin, 18-hydroxicorticotropin, estrone, estradiol, and estriol using non-solid-phase extraction.
, correspAuthors=Tian-fu ZENG, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, authorCompany=null, fund=null, authors=null, authorsList=Qiao-li WU, Xiao-yi TONG, Qiang HUA, Qiao-lin JIANG, Yuan SHEN, Shu-xia ZHAO, Wei LI, Tian-fu ZENG), CN=ArticleExt(id=1240688793003553613, articleId=1240688790629577508, tenantId=1146029695717560320, journalId=1205117023404326918, language=CN, title=基于双衍生-串联质谱技术检测类固醇激素研究, columnId=1240688785558655126, journalTitle=药物分析杂志, columnName=代谢分析·活性分析, runingTitle=null, highlight=null, articleAbstract=
目的:建立一种双衍生法-结合串联质谱技术同时检测人血清中18种类固醇激素的方法。方法:血清样本采用羟胺和1,2-二甲基咪唑-5-磺酰氯对进行衍生处理,采用液相色谱-串联质谱法正离子选择离子监测模式(SRM)下检测,色谱柱为Kinetex®C8(100 mm×2.1 mm,2.6 μm),以0.1%甲酸水溶液为流动相A,0.1%甲酸甲醇溶液为流动相B,梯度洗脱(0~0.5 min,35% B;0.5~5 min,35% B→100% B;5.0~5.1 min,100% B→35% B;5.1~7 min,35% B),柱温40 ℃,流速0.4 mL·min-1,进样量20 μL,采集时间为6 min。结果:18种类固醇激素的线性相关系数均>0.99,回收率均在85%~115%,精密度RSD均<15%。用该方法成功地检测了156份健康人群受试者血清样本(男性75例,女性61例)并制定了参考区间。结论:该方法可用非固相萃取法同时检测孕烯醇酮、17-羟孕烯醇酮、孕酮、17-羟孕酮、皮质酮、皮质醇、11-脱氧皮质醇、21-脱氧皮质醇、醛固酮、睾酮、雄烯二酮、脱氢表雄酮、硫酸脱氢表雄酮、皮质素、18-羟皮质酮、雌酮、雌二醇、雌三醇等18种类固醇激素。
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173(2):D1, articleTitle=Mass spectrometry and immunoassay:how to measure steroid hormones today and tomorrow, refAbstract=null), Reference(id=1240704455281267210, tenantId=1146029695717560320, journalId=1205117023404326918, articleId=1240688790629577508, doi=null, pmid=null, pmcid=null, year=2012, volume=84, issue=23, pageStart=null, pageEnd=null, url=null, language=null, rfNumber=[26], rfOrder=26, authorNames=DAI W, HUANG Q, YIN P, journalName=Anal Chem, refType=null, unstructuredReference=
DAI W,
HUANG Q,
YIN P,et al. Comprehensive and highly sensitive urinary steroid hormone profiling method based on stable isotope-labeling liquid chromatography mass spectrometry[J].
Anal Chem,
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84(23):10245, articleTitle=Comprehensive and highly sensitive urinary steroid hormone profiling method based on stable isotope-labeling liquid chromatography mass spectrometry, refAbstract=null)], funds=null, companyList=[AuthorCompany(id=1240704445416263789, tenantId=1146029695717560320, journalId=1205117023404326918, articleId=1240688790629577508, xref=1., ext=[AuthorCompanyExt(id=1240704445424652398, tenantId=1146029695717560320, journalId=1205117023404326918, articleId=1240688790629577508, companyId=1240704445416263789, language=EN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=
1.Zhejiang University of Traditional Chinese Medicine, Hangzhou 310053, China), AuthorCompanyExt(id=1240704445433041007, tenantId=1146029695717560320, journalId=1205117023404326918, articleId=1240688790629577508, companyId=1240704445416263789, language=CN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=
1.浙江中医药大学,杭州 310053)]), AuthorCompany(id=1240704445529510003, tenantId=1146029695717560320, journalId=1205117023404326918, articleId=1240688790629577508, xref=2., ext=[AuthorCompanyExt(id=1240704445537898612, tenantId=1146029695717560320, journalId=1205117023404326918, articleId=1240688790629577508, companyId=1240704445529510003, language=EN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=
2.Lanxi Hospital, Jinhua 321102, China), AuthorCompanyExt(id=1240704445546287221, tenantId=1146029695717560320, journalId=1205117023404326918, articleId=1240688790629577508, companyId=1240704445529510003, language=CN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=
2.兰溪市人民医院,金华 321102)]), AuthorCompany(id=1240704445609201783, tenantId=1146029695717560320, journalId=1205117023404326918, articleId=1240688790629577508, xref=3., ext=[AuthorCompanyExt(id=1240704445617590392, tenantId=1146029695717560320, journalId=1205117023404326918, articleId=1240688790629577508, companyId=1240704445609201783, language=EN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=
3.Shanghai Wanzi Health Medical Laboratory Co., Ltd., Shanghai 200000, China), AuthorCompanyExt(id=1240704445630173305, tenantId=1146029695717560320, journalId=1205117023404326918, articleId=1240688790629577508, companyId=1240704445609201783, language=CN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=
3.上海万子健医学检验实验室有限公司,上海 200000)])], figs=[ArticleFig(id=1240704449245663512, tenantId=1146029695717560320, journalId=1205117023404326918, articleId=1240688790629577508, language=EN, label=Fig.1, caption=
Derivative reactions of steroid hormones, figureFileSmall=69H9JtUDvof1NwdFnBEILg==, figureFileBig=vknbR128zslB3lzo/3rT5g==, tableContent=null), ArticleFig(id=1240704449455378716, tenantId=1146029695717560320, journalId=1205117023404326918, articleId=1240688790629577508, language=CN, label=图1, caption=
类固醇激素的衍生反应A.含羰基类固醇化合物的肟化反应(oximation reaction of carbonyl-containing steroid compounds) B.含酚羟基类固醇化合物的酯化反应(esterification reaction of phenolic hydroxyl-containing steroid compounds)
, figureFileSmall=69H9JtUDvof1NwdFnBEILg==, figureFileBig=vknbR128zslB3lzo/3rT5g==, tableContent=null), ArticleFig(id=1240704449597985057, tenantId=1146029695717560320, journalId=1205117023404326918, articleId=1240688790629577508, language=EN, label=Fig.2, caption=
Extracted ion chromatograms of 18 types of steroid hormones at LOQ, figureFileSmall=Jgi9XBwigUZR/KLRDVT14g==, figureFileBig=KAJNDSutxkNXiFnHr+zl2w==, tableContent=null), ArticleFig(id=1240704449677676835, tenantId=1146029695717560320, journalId=1205117023404326918, articleId=1240688790629577508, language=CN, label=图2, caption=
定量限浓度处18种类固醇激素的提取离子色谱图, figureFileSmall=Jgi9XBwigUZR/KLRDVT14g==, figureFileBig=KAJNDSutxkNXiFnHr+zl2w==, tableContent=null), ArticleFig(id=1240704449761562921, tenantId=1146029695717560320, journalId=1205117023404326918, articleId=1240688790629577508, language=EN, label=Tab.1, caption=
Optimized mass spectrometry conditions of 18 types of steroid hormones
, figureFileSmall=null, figureFileBig=null, tableContent=
化合物 (compound) | 保留时间 (retention time)/min | 母离子 (precursor) m/z | 子离子 (product ion) m/z | 驻留时间 (dwell time)/ms | 传输电压 (RF)/V | 碰撞能 (CE)/eV |
|---|
| T | 5.55 | 304.31 | 112.2 | 10 | 80 | 38 |
| T-d3 | 5.55 | 307.1 | 124.2 | 10 | 80 | 40 |
| A4 | 5.45 | 317.2 | 112.2 | 10 | 80 | 38 |
| A4-d7 | 5.43 | 324.1 | 115.2 | 10 | 80 | 40 |
| DHEA | 5.41 | 304.31 | 213.3 | 10 | 80 | 30 |
| DHEA-d6 | 5.40 | 310.2 | 259.2 | 10 | 80 | 28 |
| DHEAS | 4.66 | 384.1 | 213.2 | 10 | 80 | 36 |
| DHEAS-d6 | 4.64 | 390.2 | 292.3 | 10 | 60 | 30 |
| 17OHP4 | 5.45 | 361.1 | 112.2 | 10 | 60 | 42 |
| 17OHP4-d8 | 5.43 | 369.2 | 115.1 | 10 | 60 | 42 |
| P4 | 5.99 | 345.1 | 112.1 | 10 | 60 | 42 |
| P4-d9 | 5.98 | 354.2 | 128.1 | 10 | 60 | 45 |
| S | 5.10 | 377.31 | 112.1 | 10 | 60 | 45 |
| S-d5 | 5.09 | 382.3 | 115.2 | 10 | 60 | 48 |
| B | 4.76 | 377.3 | 91.2 | 10 | 60 | 80 |
| B-d8 | 4.76 | 385.3 | 143.3 | 10 | 60 | 48 |
| 17OHP5 | 5.26 | 330.2 | 105.2 | 10 | 60 | 42 |
| 17OHP5-d3 | 5.25 | 333.2 | 315.2 | 10 | 60 | 25 |
| E | 4.57 | 376.1 | 178.1 | 10 | 60 | 35 |
| E-d8 | 4.56 | 399.1 | 324.1 | 10 | 60 | 42 |
| F | 4.29 | 393.1 | 112.2 | 10 | 80 | 42 |
| F-d4 | 4.28 | 397.1 | 136.2 | 10 | 80 | 42 |
| P5 | 2.14 | 332 | 86 | 10 | 80 | 26 |
| P5-d4 | 2.13 | 336 | 90 | 10 | 80 | 40 |
| 21DOC | 3.27 | 377 | 105 | 10 | 80 | 30 |
| 21DOC-d8 | 3.26 | 385 | 115 | 10 | 80 | 30 |
| ALD | 1.48 | 376 | 112 | 10 | 80 | 30 |
| ALD-d7 | 1.46 | 383 | 115 | 10 | 80 | 30 |
| 18OHB | 1.74 | 378 | 138 | 10 | 80 | 26 |
| 18OHB-d4 | 1.73 | 382 | 151 | 10 | 80 | 26 |
| E1 | 4.95 | 429 | 365 | 10 | 75 | 25 |
| E1-d4 | 4.94 | 433 | 96 | 10 | 75 | 40 |
| E2 | 1.73 | 431 | 367 | 10 | 75 | 25 |
| E2-d5 | 1.71 | 436 | 96 | 10 | 75 | 40 |
| E3 | 1.19 | 447 | 383 | 10 | 100 | 25 |
| E3-d3 | 1.18 | 450 | 96 | 10 | 100 | 40 |
), ArticleFig(id=1240704449866420523, tenantId=1146029695717560320, journalId=1205117023404326918, articleId=1240688790629577508, language=CN, label=表1, caption=
18种类固醇激素质谱条件优化结果
, figureFileSmall=null, figureFileBig=null, tableContent=
化合物 (compound) | 保留时间 (retention time)/min | 母离子 (precursor) m/z | 子离子 (product ion) m/z | 驻留时间 (dwell time)/ms | 传输电压 (RF)/V | 碰撞能 (CE)/eV |
|---|
| T | 5.55 | 304.31 | 112.2 | 10 | 80 | 38 |
| T-d3 | 5.55 | 307.1 | 124.2 | 10 | 80 | 40 |
| A4 | 5.45 | 317.2 | 112.2 | 10 | 80 | 38 |
| A4-d7 | 5.43 | 324.1 | 115.2 | 10 | 80 | 40 |
| DHEA | 5.41 | 304.31 | 213.3 | 10 | 80 | 30 |
| DHEA-d6 | 5.40 | 310.2 | 259.2 | 10 | 80 | 28 |
| DHEAS | 4.66 | 384.1 | 213.2 | 10 | 80 | 36 |
| DHEAS-d6 | 4.64 | 390.2 | 292.3 | 10 | 60 | 30 |
| 17OHP4 | 5.45 | 361.1 | 112.2 | 10 | 60 | 42 |
| 17OHP4-d8 | 5.43 | 369.2 | 115.1 | 10 | 60 | 42 |
| P4 | 5.99 | 345.1 | 112.1 | 10 | 60 | 42 |
| P4-d9 | 5.98 | 354.2 | 128.1 | 10 | 60 | 45 |
| S | 5.10 | 377.31 | 112.1 | 10 | 60 | 45 |
| S-d5 | 5.09 | 382.3 | 115.2 | 10 | 60 | 48 |
| B | 4.76 | 377.3 | 91.2 | 10 | 60 | 80 |
| B-d8 | 4.76 | 385.3 | 143.3 | 10 | 60 | 48 |
| 17OHP5 | 5.26 | 330.2 | 105.2 | 10 | 60 | 42 |
| 17OHP5-d3 | 5.25 | 333.2 | 315.2 | 10 | 60 | 25 |
| E | 4.57 | 376.1 | 178.1 | 10 | 60 | 35 |
| E-d8 | 4.56 | 399.1 | 324.1 | 10 | 60 | 42 |
| F | 4.29 | 393.1 | 112.2 | 10 | 80 | 42 |
| F-d4 | 4.28 | 397.1 | 136.2 | 10 | 80 | 42 |
| P5 | 2.14 | 332 | 86 | 10 | 80 | 26 |
| P5-d4 | 2.13 | 336 | 90 | 10 | 80 | 40 |
| 21DOC | 3.27 | 377 | 105 | 10 | 80 | 30 |
| 21DOC-d8 | 3.26 | 385 | 115 | 10 | 80 | 30 |
| ALD | 1.48 | 376 | 112 | 10 | 80 | 30 |
| ALD-d7 | 1.46 | 383 | 115 | 10 | 80 | 30 |
| 18OHB | 1.74 | 378 | 138 | 10 | 80 | 26 |
| 18OHB-d4 | 1.73 | 382 | 151 | 10 | 80 | 26 |
| E1 | 4.95 | 429 | 365 | 10 | 75 | 25 |
| E1-d4 | 4.94 | 433 | 96 | 10 | 75 | 40 |
| E2 | 1.73 | 431 | 367 | 10 | 75 | 25 |
| E2-d5 | 1.71 | 436 | 96 | 10 | 75 | 40 |
| E3 | 1.19 | 447 | 383 | 10 | 100 | 25 |
| E3-d3 | 1.18 | 450 | 96 | 10 | 100 | 40 |
), ArticleFig(id=1240704449958695215, tenantId=1146029695717560320, journalId=1205117023404326918, articleId=1240688790629577508, language=EN, label=Tab.2, caption=
Linearities and quantitation limits of 18 types of steroid hormones
, figureFileSmall=null, figureFileBig=null, tableContent=
化合物 (compound) | 线性范围 (linear range)/(ng·mL-1) | r | 定量限(LOQ) |
|---|
| 均值(mean)/(ng·mL-1) | 信噪比(S/N) | RSD/% | 准确度(bias)/% |
|---|
| T | 0.05~10 | 0.998 1 | 0.044 | 99 | 6.7 | -11.6 |
| A4 | 0.1~20 | 0.998 0 | 0.092 | 126 | 7.9 | -8.0 |
| DHEA | 0.1~20 | 0.998 9 | 0.097 | 971 | 9.9 | -2.8 |
| DHEAS | 50~10 000 | 0.999 4 | 48.621 | 524 | 2.9 | -2.8 |
| 17OHP4 | 0.1~20 | 0.997 5 | 0.106 | 30 | 7.4 | 6.4 |
| P4 | 0.05~10 | 0.997 3 | 0.060 | 1 107 | 11.3 | 19.6 |
| S | 0.1~20 | 0.998 2 | 0.094 | 63 | 8.7 | -5.6 |
| B | 0.1~20 | 0.993 9 | 0.098 | 36 | 10.7 | -1.8 |
| 17OHP5 | 0.1~20 | 0.998 9 | 0.093 | 52 | 8.9 | -7.0 |
| E | 0.1~20 | 0.997 6 | 0.095 | 1 110 | 13.6 | -5.0 |
| F | 1~200 | 0.999 0 | 1.103 | 3 110 | 4.9 | 10.3 |
| P5 | 0.05~10 | 0.996 5 | 0.043 | 276 | 11.7 | -14.0 |
| 21DOC | 0.05~10 | 0.999 3 | 0.053 | 108 | 15.3 | 5.2 |
| ALD | 0.05~10 | 0.996 4 | 0.043 | 14 | 12.5 | -13.6 |
| 18OHB | 0.02~4 | 0.993 7 | 0.021 | 1 783 | 12.4 | 4.0 |
| E1 | 0.02~4 | 0.997 8 | 0.019 | 24 | 18.9 | -3.0 |
| E2 | 0.05~10 | 0.998 6 | 0.048 | 1 080 | 13.0 | -4.0 |
| E3 | 0.05~10 | 0.993 3 | 0.044 | 5 754 | 10.8 | -11.2 |
), ArticleFig(id=1240704450055164210, tenantId=1146029695717560320, journalId=1205117023404326918, articleId=1240688790629577508, language=CN, label=表2, caption=
18种类固醇激素的线性定量限
, figureFileSmall=null, figureFileBig=null, tableContent=
化合物 (compound) | 线性范围 (linear range)/(ng·mL-1) | r | 定量限(LOQ) |
|---|
| 均值(mean)/(ng·mL-1) | 信噪比(S/N) | RSD/% | 准确度(bias)/% |
|---|
| T | 0.05~10 | 0.998 1 | 0.044 | 99 | 6.7 | -11.6 |
| A4 | 0.1~20 | 0.998 0 | 0.092 | 126 | 7.9 | -8.0 |
| DHEA | 0.1~20 | 0.998 9 | 0.097 | 971 | 9.9 | -2.8 |
| DHEAS | 50~10 000 | 0.999 4 | 48.621 | 524 | 2.9 | -2.8 |
| 17OHP4 | 0.1~20 | 0.997 5 | 0.106 | 30 | 7.4 | 6.4 |
| P4 | 0.05~10 | 0.997 3 | 0.060 | 1 107 | 11.3 | 19.6 |
| S | 0.1~20 | 0.998 2 | 0.094 | 63 | 8.7 | -5.6 |
| B | 0.1~20 | 0.993 9 | 0.098 | 36 | 10.7 | -1.8 |
| 17OHP5 | 0.1~20 | 0.998 9 | 0.093 | 52 | 8.9 | -7.0 |
| E | 0.1~20 | 0.997 6 | 0.095 | 1 110 | 13.6 | -5.0 |
| F | 1~200 | 0.999 0 | 1.103 | 3 110 | 4.9 | 10.3 |
| P5 | 0.05~10 | 0.996 5 | 0.043 | 276 | 11.7 | -14.0 |
| 21DOC | 0.05~10 | 0.999 3 | 0.053 | 108 | 15.3 | 5.2 |
| ALD | 0.05~10 | 0.996 4 | 0.043 | 14 | 12.5 | -13.6 |
| 18OHB | 0.02~4 | 0.993 7 | 0.021 | 1 783 | 12.4 | 4.0 |
| E1 | 0.02~4 | 0.997 8 | 0.019 | 24 | 18.9 | -3.0 |
| E2 | 0.05~10 | 0.998 6 | 0.048 | 1 080 | 13.0 | -4.0 |
| E3 | 0.05~10 | 0.993 3 | 0.044 | 5 754 | 10.8 | -11.2 |
), ArticleFig(id=1240704450168410423, tenantId=1146029695717560320, journalId=1205117023404326918, articleId=1240688790629577508, language=EN, label=Tab.3, caption=
Intra-batch and inter-batch precision of 18 types of steroid hormones
, figureFileSmall=null, figureFileBig=null, tableContent=
化合物 (compound) | 批内(intra-batch) | 批间(inter-batch) |
|---|
| 均值(mean)/(ng·mL-1) | SD | RSD/% | 均值(mean)/(ng·mL-1) | SD | RSD/% |
|---|
| T | 0.21 | 0.025 | 12.1 | 0.23 | 0.03 | 12.2 |
| 6.01 | 0.542 | 9.0 | 5.94 | 0.20 | 3.4 |
| A4 | 0.56 | 0.066 | 11.8 | 0.59 | 0.05 | 7.7 |
| 11.70 | 0.765 | 6.5 | 11.43 | 0.37 | 3.3 |
| DHEA | 0.59 | 0.078 | 13.2 | 0.62 | 0.03 | 5.1 |
| 10.82 | 1.080 | 10.0 | 10.91 | 0.30 | 2.7 |
| DHEAS | 396.31 | 16.777 | 4.2 | 411.89 | 20.74 | 5.0 |
| 978.84 | 57.869 | 5.9 | 950.32 | 34.90 | 3.7 |
| 17OHP4 | 0.74 | 0.070 | 9.4 | 0.80 | 0.06 | 7.6 |
| 8.00 | 0.374 | 4.7 | 8.34 | 0.35 | 4.2 |
| P4 | 1.57 | 0.120 | 7.6 | 1.56 | 0.08 | 5.0 |
| 16.08 | 1.006 | 6.3 | 16.67 | 0.76 | 4.6 |
| S | 1.22 | 0.086 | 7.0 | 1.30 | 0.12 | 9.3 |
| 16.84 | 0.696 | 4.1 | 17.06 | 0.36 | 2.1 |
| B | 0.71 | 0.035 | 4.9 | 0.71 | 0.01 | 2.0 |
| 14.38 | 0.608 | 4.2 | 14.72 | 0.99 | 6.7 |
| 17OHP5 | 0.80 | 0.086 | 10.8 | 0.77 | 0.09 | 11.4 |
| 12.69 | 0.936 | 7.4 | 13.38 | 1.04 | 7.8 |
| E | 0.55 | 0.048 | 8.7 | 0.59 | 0.03 | 5.9 |
| 18.89 | 0.989 | 5.2 | 19.36 | 0.46 | 2.4 |
| F | 4.47 | 0.426 | 9.5 | 4.92 | 0.42 | 8.5 |
| 45.67 | 2.332 | 5.1 | 47.00 | 1.38 | 2.9 |
| P5 | 0.62 | 0.063 | 10.2 | 0.65 | 0.05 | 7.8 |
| 15.65 | 1.058 | 6.8 | 16.42 | 0.66 | 4.0 |
| 21DOC | 0.82 | 0.090 | 11.0 | 0.82 | 0.03 | 3.9 |
| 15.92 | 1.048 | 6.6 | 16.53 | 0.73 | 4.4 |
| ALD | 0.09 | 0.011 | 12.1 | 0.10 | 0.00 | 4.6 |
| 2.69 | 0.307 | 11.4 | 2.88 | 0.21 | 7.1 |
| 18OHB | 0.17 | 0.018 | 10.4 | 0.18 | 0.01 | 8.1 |
| 2.33 | 0.211 | 9.1 | 2.33 | 0.01 | 0.2 |
| E1 | 0.27 | 0.035 | 12.8 | 0.28 | 0.00 | 1.7 |
| 2.75 | 0.127 | 4.6 | 2.73 | 0.04 | 1.6 |
| E2 | 0.12 | 0.013 | 11.0 | 0.13 | 0.01 | 10.7 |
| 1.26 | 0.123 | 9.8 | 1.26 | 0.02 | 1.3 |
| E3 | 0.36 | 0.043 | 12.2 | 0.37 | 0.02 | 4.8 |
| 1.46 | 0.066 | 4.5 | 1.48 | 0.02 | 1.0 |
), ArticleFig(id=1240704450298433855, tenantId=1146029695717560320, journalId=1205117023404326918, articleId=1240688790629577508, language=CN, label=表3, caption=
18种类固醇激素的批内和批间精密度
, figureFileSmall=null, figureFileBig=null, tableContent=
化合物 (compound) | 批内(intra-batch) | 批间(inter-batch) |
|---|
| 均值(mean)/(ng·mL-1) | SD | RSD/% | 均值(mean)/(ng·mL-1) | SD | RSD/% |
|---|
| T | 0.21 | 0.025 | 12.1 | 0.23 | 0.03 | 12.2 |
| 6.01 | 0.542 | 9.0 | 5.94 | 0.20 | 3.4 |
| A4 | 0.56 | 0.066 | 11.8 | 0.59 | 0.05 | 7.7 |
| 11.70 | 0.765 | 6.5 | 11.43 | 0.37 | 3.3 |
| DHEA | 0.59 | 0.078 | 13.2 | 0.62 | 0.03 | 5.1 |
| 10.82 | 1.080 | 10.0 | 10.91 | 0.30 | 2.7 |
| DHEAS | 396.31 | 16.777 | 4.2 | 411.89 | 20.74 | 5.0 |
| 978.84 | 57.869 | 5.9 | 950.32 | 34.90 | 3.7 |
| 17OHP4 | 0.74 | 0.070 | 9.4 | 0.80 | 0.06 | 7.6 |
| 8.00 | 0.374 | 4.7 | 8.34 | 0.35 | 4.2 |
| P4 | 1.57 | 0.120 | 7.6 | 1.56 | 0.08 | 5.0 |
| 16.08 | 1.006 | 6.3 | 16.67 | 0.76 | 4.6 |
| S | 1.22 | 0.086 | 7.0 | 1.30 | 0.12 | 9.3 |
| 16.84 | 0.696 | 4.1 | 17.06 | 0.36 | 2.1 |
| B | 0.71 | 0.035 | 4.9 | 0.71 | 0.01 | 2.0 |
| 14.38 | 0.608 | 4.2 | 14.72 | 0.99 | 6.7 |
| 17OHP5 | 0.80 | 0.086 | 10.8 | 0.77 | 0.09 | 11.4 |
| 12.69 | 0.936 | 7.4 | 13.38 | 1.04 | 7.8 |
| E | 0.55 | 0.048 | 8.7 | 0.59 | 0.03 | 5.9 |
| 18.89 | 0.989 | 5.2 | 19.36 | 0.46 | 2.4 |
| F | 4.47 | 0.426 | 9.5 | 4.92 | 0.42 | 8.5 |
| 45.67 | 2.332 | 5.1 | 47.00 | 1.38 | 2.9 |
| P5 | 0.62 | 0.063 | 10.2 | 0.65 | 0.05 | 7.8 |
| 15.65 | 1.058 | 6.8 | 16.42 | 0.66 | 4.0 |
| 21DOC | 0.82 | 0.090 | 11.0 | 0.82 | 0.03 | 3.9 |
| 15.92 | 1.048 | 6.6 | 16.53 | 0.73 | 4.4 |
| ALD | 0.09 | 0.011 | 12.1 | 0.10 | 0.00 | 4.6 |
| 2.69 | 0.307 | 11.4 | 2.88 | 0.21 | 7.1 |
| 18OHB | 0.17 | 0.018 | 10.4 | 0.18 | 0.01 | 8.1 |
| 2.33 | 0.211 | 9.1 | 2.33 | 0.01 | 0.2 |
| E1 | 0.27 | 0.035 | 12.8 | 0.28 | 0.00 | 1.7 |
| 2.75 | 0.127 | 4.6 | 2.73 | 0.04 | 1.6 |
| E2 | 0.12 | 0.013 | 11.0 | 0.13 | 0.01 | 10.7 |
| 1.26 | 0.123 | 9.8 | 1.26 | 0.02 | 1.3 |
| E3 | 0.36 | 0.043 | 12.2 | 0.37 | 0.02 | 4.8 |
| 1.46 | 0.066 | 4.5 | 1.48 | 0.02 | 1.0 |
), ArticleFig(id=1240704450399097156, tenantId=1146029695717560320, journalId=1205117023404326918, articleId=1240688790629577508, language=EN, label=Tab.4, caption=
Recovery rates of 18 types of steroid hormones
, figureFileSmall=null, figureFileBig=null, tableContent=
化合物 (compound) | 加标量 (added)/(ng·mL-1) | 测定值 (measured)/(ng·mL-1) | 理论值 (theoretical)/(ng·mL-1) | 加标 回收率 (recovery)/% | RSD/% |
|---|
| T | 0 | 4.32 | 4.32 | / | 9.8 |
| 0.4 | 3.79 | 4.72 | 80.3 | 8.6 |
| 2 | 5.67 | 6.32 | 89.7 | 4.1 |
| 10 | 12.91 | 14.32 | 90.2 | 7.8 |
| A4 | 0 | 0.56 | 0.56 | / | 12.9 |
| 0.2 | 0.81 | 0.76 | 106.6 | 11.6 |
| 1 | 1.45 | 1.56 | 92.9 | 10.0 |
| 5 | 5.45 | 5.56 | 98.0 | 8.5 |
| DHEA | 0 | 3.46 | 3.46 | / | 7.7 |
| 0.2 | 2.99 | 3.66 | 81.7 | 5.4 |
| 1 | 4.63 | 4.46 | 103.8 | 4.9 |
| 5 | 8.12 | 8.46 | 96.0 | 3.2 |
| DHEAS | 0 | 745.31 | 745.31 | / | 5.5 |
| 50 | 889.23 | 795.31 | 111.8 | 4.2 |
| 250 | 1121.09 | 995.31 | 112.6 | 4.9 |
| 750 | 1573.24 | 1 495.31 | 105.2 | 6.9 |
| 17OHP4 | 0 | 1.23 | 1.23 | / | 7.4 |
| 0.2 | 1.63 | 1.43 | 114.0 | 10.6 |
| 1 | 1.98 | 2.23 | 88.8 | 7.9 |
| 5 | 5.56 | 6.23 | 89.2 | 7.8 |
| P4 | 0 | 0.36 | 0.36 | / | 11.3 |
| 0.2 | 0.49 | 0.56 | 87.5 | 12.5 |
| 1 | 1.34 | 1.36 | 98.5 | 5.1 |
| 5 | 4.39 | 5.36 | 81.9 | 9.5 |
| S | 0 | 0.56 | 0.56 | / | 12.4 |
| 0.2 | 0.65 | 0.76 | 85.5 | 13.5 |
| 1 | 1.39 | 1.56 | 89.1 | 9.5 |
| 5 | 5.57 | 5.56 | 100.2 | 4.9 |
| B | 0 | 7.34 | 7.34 | / | 11.6 |
| 0.2 | 6.49 | 7.54 | 86.1 | 8.1 |
| 1 | 8.02 | 8.34 | 96.2 | 3.4 |
| 5 | 11.8 | 12.34 | 95.6 | 4.6 |
| 17OHP5 | 0 | 2.25 | 2.25 | / | 6.2 |
| 0.2 | 2.9 | 2.45 | 118.4 | 3.5 |
| 1 | 2.63 | 3.25 | 80.9 | 11.7 |
| 5 | 7.99 | 7.25 | 110.2 | 7.8 |
| E | 0 | 0.54 | 0.54 | / | 8.7 |
| 0.2 | 0.9 | 0.74 | 121.6 | 10.4 |
| 1 | 1.24 | 1.54 | 80.5 | 8.5 |
| 5 | 5.34 | 5.54 | 96.4 | 4.5 |
| F | 0 | 0.93 | 0.93 | / | 9.1 |
| 0.2 | 1.02 | 1.13 | 90.3 | 8.7 |
| 1 | 2.12 | 1.93 | 109.8 | 8.3 |
| 5 | 5.31 | 5.93 | 89.5 | 3.0 |
| P5 | 0 | 0 | 0 | / | / |
| 0.2 | 0.15 | 0.2 | 75.0 | 6.7 |
| 1 | 1.12 | 1 | 112.0 | 8.8 |
| 5 | 4.07 | 5 | 81.4 | 2.6 |
| 21DOC | 0 | 0.05 | 0.05 | / | 14.1 |
| 0.2 | 0.17 | 0.25 | 68.0 | 12.5 |
| 1 | 1.13 | 1.05 | 107.6 | 10.0 |
| 5 | 4.57 | 5.05 | 90.5 | 5.2 |
| ALD | 0 | 0.47 | 0.47 | / | 14.0 |
| 0.2 | 0.48 | 0.67 | 71.6 | 10.8 |
| 1 | 1.54 | 1.47 | 104.8 | 6.7 |
| 5 | 5.93 | 5.47 | 108.4 | 9.1 |
| 18OHB | 0 | 0.82 | 0.82 | / | 12.1 |
| 0.1 | 1.08 | 0.92 | 117.4 | 12.3 |
| 0.5 | 1.29 | 1.32 | 97.7 | 6.9 |
| 2.5 | 2.97 | 3.32 | 89.5 | 6.3 |
| E1 | 0 | 0.36 | 0.36 | / | 8.1 |
| 0.1 | 0.52 | 0.46 | 113.0 | 11.3 |
| 0.5 | 0.91 | 0.86 | 105.8 | 10.1 |
| 2.5 | 3.13 | 2.86 | 109.4 | 4.7 |
| E2 | 0 | 0.61 | 0.61 | / | 13.0 |
| 0.1 | 0.84 | 0.71 | 118.3 | 10.6 |
| 0.5 | 1.24 | 1.21 | 102.5 | 4.5 |
| 2.5 | 3.5 | 3.71 | 94.3 | 8.8 |
| E3 | 0 | 0.72 | 0.72 | / | 14.3 |
| 0.1 | 0.72 | 0.82 | 87.8 | 10.4 |
| 0.5 | 1.38 | 1.22 | 113.1 | 9.4 |
| 2.5 | 3.42 | 3.22 | 106.2 | 6.9 |
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18种类固醇激素的回收率
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化合物 (compound) | 加标量 (added)/(ng·mL-1) | 测定值 (measured)/(ng·mL-1) | 理论值 (theoretical)/(ng·mL-1) | 加标 回收率 (recovery)/% | RSD/% |
|---|
| T | 0 | 4.32 | 4.32 | / | 9.8 |
| 0.4 | 3.79 | 4.72 | 80.3 | 8.6 |
| 2 | 5.67 | 6.32 | 89.7 | 4.1 |
| 10 | 12.91 | 14.32 | 90.2 | 7.8 |
| A4 | 0 | 0.56 | 0.56 | / | 12.9 |
| 0.2 | 0.81 | 0.76 | 106.6 | 11.6 |
| 1 | 1.45 | 1.56 | 92.9 | 10.0 |
| 5 | 5.45 | 5.56 | 98.0 | 8.5 |
| DHEA | 0 | 3.46 | 3.46 | / | 7.7 |
| 0.2 | 2.99 | 3.66 | 81.7 | 5.4 |
| 1 | 4.63 | 4.46 | 103.8 | 4.9 |
| 5 | 8.12 | 8.46 | 96.0 | 3.2 |
| DHEAS | 0 | 745.31 | 745.31 | / | 5.5 |
| 50 | 889.23 | 795.31 | 111.8 | 4.2 |
| 250 | 1121.09 | 995.31 | 112.6 | 4.9 |
| 750 | 1573.24 | 1 495.31 | 105.2 | 6.9 |
| 17OHP4 | 0 | 1.23 | 1.23 | / | 7.4 |
| 0.2 | 1.63 | 1.43 | 114.0 | 10.6 |
| 1 | 1.98 | 2.23 | 88.8 | 7.9 |
| 5 | 5.56 | 6.23 | 89.2 | 7.8 |
| P4 | 0 | 0.36 | 0.36 | / | 11.3 |
| 0.2 | 0.49 | 0.56 | 87.5 | 12.5 |
| 1 | 1.34 | 1.36 | 98.5 | 5.1 |
| 5 | 4.39 | 5.36 | 81.9 | 9.5 |
| S | 0 | 0.56 | 0.56 | / | 12.4 |
| 0.2 | 0.65 | 0.76 | 85.5 | 13.5 |
| 1 | 1.39 | 1.56 | 89.1 | 9.5 |
| 5 | 5.57 | 5.56 | 100.2 | 4.9 |
| B | 0 | 7.34 | 7.34 | / | 11.6 |
| 0.2 | 6.49 | 7.54 | 86.1 | 8.1 |
| 1 | 8.02 | 8.34 | 96.2 | 3.4 |
| 5 | 11.8 | 12.34 | 95.6 | 4.6 |
| 17OHP5 | 0 | 2.25 | 2.25 | / | 6.2 |
| 0.2 | 2.9 | 2.45 | 118.4 | 3.5 |
| 1 | 2.63 | 3.25 | 80.9 | 11.7 |
| 5 | 7.99 | 7.25 | 110.2 | 7.8 |
| E | 0 | 0.54 | 0.54 | / | 8.7 |
| 0.2 | 0.9 | 0.74 | 121.6 | 10.4 |
| 1 | 1.24 | 1.54 | 80.5 | 8.5 |
| 5 | 5.34 | 5.54 | 96.4 | 4.5 |
| F | 0 | 0.93 | 0.93 | / | 9.1 |
| 0.2 | 1.02 | 1.13 | 90.3 | 8.7 |
| 1 | 2.12 | 1.93 | 109.8 | 8.3 |
| 5 | 5.31 | 5.93 | 89.5 | 3.0 |
| P5 | 0 | 0 | 0 | / | / |
| 0.2 | 0.15 | 0.2 | 75.0 | 6.7 |
| 1 | 1.12 | 1 | 112.0 | 8.8 |
| 5 | 4.07 | 5 | 81.4 | 2.6 |
| 21DOC | 0 | 0.05 | 0.05 | / | 14.1 |
| 0.2 | 0.17 | 0.25 | 68.0 | 12.5 |
| 1 | 1.13 | 1.05 | 107.6 | 10.0 |
| 5 | 4.57 | 5.05 | 90.5 | 5.2 |
| ALD | 0 | 0.47 | 0.47 | / | 14.0 |
| 0.2 | 0.48 | 0.67 | 71.6 | 10.8 |
| 1 | 1.54 | 1.47 | 104.8 | 6.7 |
| 5 | 5.93 | 5.47 | 108.4 | 9.1 |
| 18OHB | 0 | 0.82 | 0.82 | / | 12.1 |
| 0.1 | 1.08 | 0.92 | 117.4 | 12.3 |
| 0.5 | 1.29 | 1.32 | 97.7 | 6.9 |
| 2.5 | 2.97 | 3.32 | 89.5 | 6.3 |
| E1 | 0 | 0.36 | 0.36 | / | 8.1 |
| 0.1 | 0.52 | 0.46 | 113.0 | 11.3 |
| 0.5 | 0.91 | 0.86 | 105.8 | 10.1 |
| 2.5 | 3.13 | 2.86 | 109.4 | 4.7 |
| E2 | 0 | 0.61 | 0.61 | / | 13.0 |
| 0.1 | 0.84 | 0.71 | 118.3 | 10.6 |
| 0.5 | 1.24 | 1.21 | 102.5 | 4.5 |
| 2.5 | 3.5 | 3.71 | 94.3 | 8.8 |
| E3 | 0 | 0.72 | 0.72 | / | 14.3 |
| 0.1 | 0.72 | 0.82 | 87.8 | 10.4 |
| 0.5 | 1.38 | 1.22 | 113.1 | 9.4 |
| 2.5 | 3.42 | 3.22 | 106.2 | 6.9 |
), ArticleFig(id=1240704450654949716, tenantId=1146029695717560320, journalId=1205117023404326918, articleId=1240688790629577508, language=EN, label=Tab.5, caption=
Concentration ranges of 18 types of steroid hormones in male and female populations
, figureFileSmall=null, figureFileBig=null, tableContent=
化合物 (compound) | P5~P95/(ng·mL-1) |
|---|
| 男性(male) | 女性(female) |
|---|
| T | 2.17~9.32 | 0.18~1.40 |
| A4 | 0.30~3.64 | 0.2~3.47 |
| DHEA | 0.42~6.15 | 0.43~6.08 |
| DHEAS | 461.9~3 680.7 | 347.1~3 660.2 |
| 17-OHP4 | 0.30~3.06 | 0.30~3.12 |
| P4) | 0.06~0.62 | 0.05~0.61 |
| S | 0.69~1.02 | 0.70~1.01 |
| B | 0.74~20.93 | 0.24~20.2 |
| 17-OHP5 | 3.47~60.68 | 1.85~63.14 |
| E | 0.10~0.93 | 0.13~0.88 |
| F | 11.15~196.42 | 11.29~195.20 |
| P5 | 0.23~2.59 | 0.29~2.66 |
| 21DOC | <0.069 | <0.069 |
| ALD | <0.137 | <0.136 |
| 18OHB | 0.03~0.35 | 0.04~0.36 |
| E1 | <0.052 | 0.024~0.311 |
| E2 | <0.051 | <0.128 |
| E3 | <0.088 | <9.34 |
), ArticleFig(id=1240704450768195932, tenantId=1146029695717560320, journalId=1205117023404326918, articleId=1240688790629577508, language=CN, label=表5, caption=
18种类固醇激素在男性和女性人群中的浓度区间
, figureFileSmall=null, figureFileBig=null, tableContent=
化合物 (compound) | P5~P95/(ng·mL-1) |
|---|
| 男性(male) | 女性(female) |
|---|
| T | 2.17~9.32 | 0.18~1.40 |
| A4 | 0.30~3.64 | 0.2~3.47 |
| DHEA | 0.42~6.15 | 0.43~6.08 |
| DHEAS | 461.9~3 680.7 | 347.1~3 660.2 |
| 17-OHP4 | 0.30~3.06 | 0.30~3.12 |
| P4) | 0.06~0.62 | 0.05~0.61 |
| S | 0.69~1.02 | 0.70~1.01 |
| B | 0.74~20.93 | 0.24~20.2 |
| 17-OHP5 | 3.47~60.68 | 1.85~63.14 |
| E | 0.10~0.93 | 0.13~0.88 |
| F | 11.15~196.42 | 11.29~195.20 |
| P5 | 0.23~2.59 | 0.29~2.66 |
| 21DOC | <0.069 | <0.069 |
| ALD | <0.137 | <0.136 |
| 18OHB | 0.03~0.35 | 0.04~0.36 |
| E1 | <0.052 | 0.024~0.311 |
| E2 | <0.051 | <0.128 |
| E3 | <0.088 | <9.34 |
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