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1.徐州医科大学药学院/江苏省新药研究与临床药学重点实验室,江苏 徐州 210004
2.南京医科大学第一附属医院临床药理研究室,南京 210029
3.江苏省妇幼保健院儿科,南京 210036
Received:24 April 2023,
Revised:2023-07-24,
Accepted:10 August 2023,
Published:30 September 2023
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陈相龙,赵杨,黄琼叶,等.咖啡因及代谢产物的尿药浓度测定方法建立及临床应用[J].中国药房,2023,34(18):2233-2237.
CHEN Xianglong,ZHAO Yang,HUANG Qiongye,et al.Method establishment and clinical practice for concentration determination of caffeine and its metabolites in urine[J].ZHONGGUO YAOFANG,2023,34(18):2233-2237.
陈相龙,赵杨,黄琼叶,等.咖啡因及代谢产物的尿药浓度测定方法建立及临床应用[J].中国药房,2023,34(18):2233-2237. DOI: 10.6039/j.issn.1001-0408.2023.18.11.
CHEN Xianglong,ZHAO Yang,HUANG Qiongye,et al.Method establishment and clinical practice for concentration determination of caffeine and its metabolites in urine[J].ZHONGGUO YAOFANG,2023,34(18):2233-2237. DOI: 10.6039/j.issn.1001-0408.2023.18.11.
目的
2
建立同时测定尿液中咖啡因及3种代谢产物茶碱、副黄嘌呤和可可碱浓度的方法并应用于临床。
方法
2
以咖啡因-
13
C
3
-d3为内标,尿液样本经乙腈沉淀蛋白后,采用高效液相色谱-串联质谱(HPLC-MS/MS)技术测定咖啡因及3种代谢产物的浓度。以Waters ACQUITY UPLC
®
BEH HILIC为色谱柱,60 mmol/L乙酸铵溶液(A)-乙腈(B)为流动相进行梯度洗脱,流速为0.5 mL/min,柱温为38 ℃,进样量为2 μL。采用电喷雾离子源,以多反应监测模式进行正离子扫描,用于定量分析的离子对分别为
m/z
195.1→110.0(咖啡因)、
m/z
181.1→124.0(茶碱)、
m/z
181.1→124.0(副黄嘌呤)、
m/z
181.1→138.0(可可碱)、
m/z
198.1→140.1(内标)。采用上述方法测定19例早产儿呼吸暂停(AOP)患儿尿液中咖啡因及3种代谢产物的浓度。
结果
2
咖啡因、茶碱、副黄嘌呤、可可碱检测质量浓度的线性范围分别为0.200~200、0.050~50.0、0.050~50.0、0.100~100 μg/mL(
r
均大于0.990),定量下限分别为0.200、0.050、0.050、0.100 μg/mL;日内、日间精密度的RSD均不高于10.37%,基质因子为85.68%~109.90%,提取回收率为93.53%~109.40%(RSD均小于15%),稳定性试验的RSD均小于15%。19例AOP患儿尿液中咖啡因及3种代谢产物的质量浓度分别为(27.346±7.951)、(0.351±0.223)、(0.428±0.395)、(0.472±0.374)μg/mL。
结论
2
所建HPLC-MS/MS法操作简单、灵敏度高,可用于AOP患儿尿液中咖啡因及3种代谢产物浓度的测定。
OBJECTIVE
2
To establish a method for concentration determination of caffeine and its three metabolites, theophylline, paraxanthine and theobromine in urine, and apply it in clinical practice.
METHODS
2
Using caffeine-
13
C
3
-d3 as internal standard (IS), and the urine samples were protein precipitated with acetonitrile; HPLC-MS/MS method was adopted to determine the concentrations of caffeine and its three metabolites. The determination was performed on Waters ACQUITY UPLC
®
BEH HILIC column with mobile phase consisting of 60 mmol/L ammonium acetate (A)-acetonitrile (B) (gradient elution) at the flow rate of 0.5 mL/min. The column temperature was set at 38 ℃, and the sample size was 2 μL. The electrospray ionization detection was operated in a positive mode by multiple reaction monitoring. The detection ions for quantitative analysis were
m
/
z
195.1→110.0 for caffeine,
m
/
z
181.1→124.0 for theophylline,
m
/
z
181.1→124.0 for paraxanthine,
m
/
z
181.1→138.0 for theobromine, and
m
/
z
198.1→140.1 for IS. The above method was used to determine the concentrations of caffeine and its three metabolites in the urine of 19 infants with apnea of prematurity (AOP).
RESULTS
2
The linear ranges of mass concentration of caffeine, theophylline, paraxanthin and theobromine were 0.200-200, 0.050-50.0, 0.050 0-50.0, and 0.100-100 μg/mL, respectively. The lower limits of quantification were 0.200, 0.050, 0.050 and 0.100 μg/mL (
r
>0.990), respectively. RSDs of intra-day and intra-day precision were not above 10.37%, and matrix factors were 85.68%-109.90%; extraction recoveries were 93.53%-109.40% (RSD≤15%), and RSDs of stability tests were all lower than 15%. The concentration
s of caffeine and its three metabolites in the urine of 19 cases were (27.346±7.951), (0.351±0.223), (0.428±0.395) and (0.472±0.374) μg/mL, respectively.
CONCLUSIONS
2
The established HPLC-MS/MS method is simple, sensitive and can be used for the determination of caffeine and its three metabolites in urine samples of AOP.
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