Takahashi Shuuhei, Iizuka Hideaki, Kuwabara Ryousuke, Naito Yoko, Sakamoto Tatsuya, Miyagi Aya, Onozato Mayu, Ichiba Hideaki, Fukushima Takeshi
Department of Analytical Chemistry, Faculty of Pharmaceutical Sciences, Toho University, 2-2-1 Miyama, Funabashi-shi, Chiba, 274-8510, Japan.
Biomed Chromatogr. 2016 Sep;30(9):1481-6. doi: 10.1002/bmc.3709. Epub 2016 Mar 14.
The concentrations of l-tryptophan (Trp) and the metabolite l-kynurenine (KYN) can be used to evaluate the in-vivo activity of indoleamine 2,3-dioxygenase (IDO) and tryptophan 2,3-dioxygenase (TDO). As such, a novel method involving derivatization of l-Trp and l-KYN with (R)-4-(3-isothiocyanatopyrrolidin-1-yl)-7-(N,N-dimethylaminosulfonyl)-2,1,3-benzoxadiazole (DBD-PyNCS) and separation by high-performance liquid chromatography (HPLC) with tandem mass spectrometric (MS/MS) detection on a triazole-bonded column (Cosmosil HILIC®) was developed to determine their concentrations. The optimized mobile phase, CH3 CN/10 mm ammonium formate in H2 O (pH 5.0) (90:10, v/v) eluted isocratically, resulted in satisfactory separation and MS/MS detection of the analytes. The detection limits of l-Trp and l-KYN were approximately 50 and 4.0 pm, respectively. The column temperature affected the retention behaviour of the Trp and KYN derivatives, with increased column temperatures leading to increased capacity factors; positive enthalpy changes were revealed by van't Hoff plot analyses. Using the proposed LC-MS/MS method, l-Trp and l-KYN were successfully determined in 10 μL human serum using 1-methyl-l-Trp as an internal standard. The precision and recovery of l-Trp were in the ranges 2.85-9.29 and 95.8-113%, respectively, while those of l-KYN were 2.51-16.0 and 80.8-98.2%, respectively. The proposed LC-MS/MS method will be useful for evaluating the in vivo activity of IDO or TDO. Copyright © 2016 John Wiley & Sons, Ltd.
l-色氨酸(Trp)和代谢产物l-犬尿氨酸(KYN)的浓度可用于评估吲哚胺2,3-双加氧酶(IDO)和色氨酸2,3-双加氧酶(TDO)的体内活性。因此,开发了一种新方法,该方法涉及用(R)-4-(3-异硫氰酸根合吡咯烷-1-基)-7-(N,N-二甲基氨基磺酰基)-2,1,3-苯并恶二唑(DBD-PyNCS)对l-Trp和l-KYN进行衍生化,并在三唑键合柱(Cosmosil HILIC®)上通过高效液相色谱(HPLC)与串联质谱(MS/MS)检测进行分离,以测定它们的浓度。优化后的流动相,即CH3 CN/10 mM甲酸铵水溶液(pH 5.0)(90:10,v/v)等度洗脱,实现了对分析物的满意分离和MS/MS检测。l-Trp和l-KYN的检测限分别约为50和4.0 pm。柱温影响Trp和KYN衍生物的保留行为,柱温升高导致容量因子增加;范特霍夫图分析显示焓变为正值。使用所提出的LC-MS/MS方法,以1-甲基-l-Trp作为内标,成功测定了10 μL人血清中的l-Trp和l-KYN。l-Trp的精密度和回收率分别在2.85 - 9.29和95.8 - 113%范围内,而l-KYN的精密度和回收率分别在2.51 - 16.0和80.8 - 98.2%范围内。所提出的LC-MS/MS方法将有助于评估IDO或TDO的体内活性。版权所有© 2016约翰威立父子有限公司。