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 >Simultaneous determination of metronidazole and spiramycin I in human plasma, saliva and gingival crevicular fluid by LC-MS/MS.
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Simultaneous determination of metronidazole and spiramycin I in human plasma, saliva and gingival crevicular fluid by LC-MS/MS.

机译:通过LC-MS / MS同时测定人血浆,唾液和龈沟液中的甲硝唑和螺旋霉素I。

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摘要

An analytical validation of a new liquid chromatographic-mass spectrometric (LC-MS/MS) method for simultaneous determination of metronidazole and spiramycin I concentrations in human plasma, saliva and gingival crevicular fluid (GCF) is presented. Ornidazole was used as an internal standard, and sample pre-treatment consisted of a liquid-liquid extraction. Chromatographic separation was achieved on a 5mum Kromasil C(18) column (150mmx4.6mm i.d., particle size 5mum), with a gradient using acetonitrile, water and formic acid at a flow rate of 0.9ml/min. The methods were validated in terms of intra- and inter-batch precision (<7.1% in plasma, 12% in saliva and 9.2% in GCF, respectively) and accuracy (within +/-8.7% in plasma, within +/-8.7%, except LDQ level within +/-15.4% in saliva and within +/-10.7% in GCF), linearity, specificity, recovery (extraction efficiency), matrix effect, dilution process, stability in human plasma and saliva after three freeze-thaw cycles, stability in human plasma and salivaat ambient temperature and stability of the extracts in the automatic injector of the HPLC system. The methods are applicable for accurate and simultaneous monitoring of the plasma, saliva and gingival crevicular fluid levels of metronidazole and spiramycin I from pharmacokinetic studies.
机译:介绍了一种同时测定人血浆,唾液和龈沟液(GCF)中甲硝唑和螺旋霉素I浓度的新液相色谱质谱(LC-MS / MS)方法的分析验证。奥硝唑用作内标,样品前处理由液-液萃取组成。在5毫米Kromasil C(18)色谱柱(内径150mmx4.6毫米,粒径5微米)上进行色谱分离,使用乙腈,水和甲酸以0.9毫升/分钟的流速进行梯度洗脱。批内和批间精度(分别在血浆中<7.1%,唾液中的12%和GCF中的9.2%)和准确度(血浆中的+/- 8.7%之内,+ /-8.7之内)进行了验证百分比,除了LDQ水平在唾液中+/- 15.4%内和GCF +/- 10.7%内),线性,特异性,回收率(提取效率),基质效应,稀释过程,三次冷冻后在人血浆和唾液中的稳定性解冻循环,人体血浆和唾液在室温下的稳定性以及在HPLC系统自动进样器中提取物的稳定性。该方法适用于从药代动力学研究中准确,同时监测甲硝唑和螺旋霉素I的血浆,唾液和龈沟液水平。

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