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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Rapid and sensitive LC-MS/MS method for simultaneous quantification of capsaicin and dihydrocapsaicin in microdialysis samples following dermal application
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Rapid and sensitive LC-MS/MS method for simultaneous quantification of capsaicin and dihydrocapsaicin in microdialysis samples following dermal application

机译:快速敏感的LC-MS / MS方法,用于在皮肤应用后微透析样品中同时定量辣椒素和二氢胶囊的方法

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A bioanalytical LC-MS/MS method was developed and validated for the simultaneous quantification of capsaicin (CAPS) and dihydrocapsaicin (D-CAPS) in dermal microdialysis samples from rats. Capsaicinoids were separated by using a C18 column, with a mobile phase of water and acetonitrile, both with 0.1% of formic acid, eluted as a gradient. Compounds were detected by using an electrospray ionization source operating in the positive mode (ESI+) to monitor the m/z transitions of 306.1 > 137.0 for CAPS and 308.1 > 137.0 for D-CAPS. The method showed linearity in the concentration range of 0.5-100 ng/ml for CAPS and 0.25-100 ng/ml for D-CAPS, with coefficients of determination of >= 0.99. The inter- and intra-day precision, accuracy, and compound stability in different conditions were in accordance with the limits established by the US Food and Drug Administration guidelines. The recovery of the drugs by microdialysis were dependent on the flow rate, but independent of drug concentration. For CAPS, calibration of the in vitro microdialysis probes by dialysis and retrodialysis resulted in statistically similar drug recovery of 68.5% +/- 5.9% and 77.8% +/- 6.6%, respectively, at a flow rate of 0.5 mu l/min. For D-CAPS, the recovery by dialysis was lower than by retrodialysis, at 51.4% +/- 6.6% and 92.6% +/- 2.4%, respectively. This difference was attributed to the binding of D-CAPS to the plastic tubing, which was experimentally evaluated and mathematically modeled. In vivo recoveries were 75.7% +/- 6.3% for CAPS and 81.9% +/- 1.5% for D-CAPS at the same flow rate. The analytical method showed high specificity, accuracy, and sensitivity, and suitability for dermatopharmacokinetic studies. These results will allow the determination of the actual free concentration of these drugs in dermatopharmacokinetic experiments, as shown in a pilot experiment with a commercial cream containing capsaicinoids. (C) 2019 Elsevier B.V. All rights reserved.
机译:开发生物分析LC-MS / MS方法,并验证了从大鼠的皮肤微透析样品中同时定量辣椒素(盖子)和二氢胶囊蛋白(D-Caps)。通过使用C18柱分离胶囊纤维素,其中水和乙腈的流动相,含有0.1%的甲酸,作为梯度洗脱。通过使用在阳性模式(ESI +)中操作的电喷雾电离源来检测化合物,以监测306.1> 137.0的M / Z转变,用于D-Caps的308.1> 137.0。该方法显示出胶囊浓度范围为0.5-100ng / ml的线性,对于D-帽,0.25-100ng / ml,测定系数> = 0.99。不同条件下的日期和内部精度和复合稳定性符合美国食品和药物管理指南的限制。通过微透析的药物的回收取决于流速,但与药物浓度无关。对于盖子,透析和逆转录的体外微透析探针的校准导致统计学上类似的药物回收率为68.5%+/- 5.9%和77.8%+/- 6.6%,流速为0.5μmL/ min。对于D-Caps,透析的回收率低于逆转录,分别为51.4%+/- 6.6%和92.6%+/- 2.4%。这种差异归因于D帽对塑料管的结合,其在实验评估和数学上建模。在相同的流速下,体内复苏率为75.7%+/- 6.3%,D-Caps的81.9%+/- 1.5%。分析方法显示出高特异性,准确性和灵敏度,适合DermatopharmoconeCocetic研究。这些结果将允许测定这种药物在Dermatopharmococketic实验中的实际自由浓度,如先行试验实验所示,其中含有含胶囊胆碱的商业乳腺。 (c)2019 Elsevier B.v.保留所有权利。

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