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 >Investigation of the disposition of loxapine, amoxapine and their hydroxylated metabolites in different brain regions, CSF and plasma of rat by LC-MS/MS.
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Investigation of the disposition of loxapine, amoxapine and their hydroxylated metabolites in different brain regions, CSF and plasma of rat by LC-MS/MS.

机译:LC-MS / MS法研究洛沙平,阿莫沙平及其羟基化代谢物在大鼠不同脑区,脑脊液和血浆中的分布。

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Loxapine represents an interesting example of old "new" drug and is recently drawing attention for its novel inhalation formulation for the treatment of both psychiatric and non-psychiatric disorders. It is extensively metabolized to several active metabolites with diverging pharmacological properties. To further pursue the contribution of metabolites to the overall outcome after loxapine administration, quantification of both loxapine and its active metabolites is essential. The current study developed a rapid liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for the simultaneous quantification of loxapine and its five metabolites (amoxapine, 7-hydroxy-loxapine, 8-hydroxy-loxapine, 7-hydroxy-amoxapine and 8-hydroxy-amoxapine) in rat brain tissues, plasma and cerebrospinal fluid (CSF). By evaluating the effects of perchloric acid and methanol on analyte recovery, the extraction methods were optimized and only small amounts of sample (100 μl for plasma and less than 100mg for brain tissue) were required. The lower limits of quantification (LLOQs) in brain tissue were 3 ng/g for loxapine and amoxapine and 5 ng/g for the four hydroxylated metabolites of loxapine. The LLOQs were 1 ng/ml for loxapine and amoxapine and 2 ng/ml for the four hydroxylated metabolites in plasma, and 10 ng/ml for all analytes in CSF. The developed method was applied to a pharmacokinetic study on rats treated with a low-dose loxapine by oral administration. Four hours after loxapine dosing, high levels of 7-hydroxy-loxapine were found throughout the ten brain regions examined (68-124 ng/g), while only trace amount of loxapine was measured in brain (<5 ng/g) and plasma (<3 ng/ml). The method provides a useful tool for both preclinical and clinical investigations on the dispositions of loxapine and its metabolites, which would help to elucidate their roles in neurotherapeutics.
机译:洛沙平代表了一个古老的“新”药物的有趣例子,并且最近因其新颖的吸入剂用于精神病和非精神病治疗而受到关注。它被广泛代谢为具有不同药理特性的几种活性代谢物。为了进一步追踪洛沙平给药后代谢物对总体结果的贡献,定量洛沙平及其活性代谢物至关重要。当前的研究开发了一种快速液相色谱-串联质谱(LC-MS / MS)方法,用于同时定量洛沙平及其五种代谢物(阿莫沙平,7-羟基-洛沙平,8-羟基-洛沙平,7-羟基-阿莫沙平和8-羟基-阿莫沙平)在大鼠脑组织,血浆和脑脊液(CSF)中的分布。通过评估高氯酸和甲醇对分析物回收的影响,优化了提取方法,只需要少量样品(血浆为100μl,脑组织为100mg以下)。脑组织中的定量下限(LLOQs)为洛沙平和阿莫沙平为3 ng / g,洛沙平的四种羟基化代谢产物为5 ng / g。血浆中洛沙平和阿莫沙平的LLOQs为1 ng / ml,血浆中四种羟基化代谢物的LLOQs为2 ng / ml,CSF中所有分析物的LLOQs为10 ng / ml。所开发的方法被应用于口服低剂量洛沙平治疗大鼠的药代动力学研究。服用洛沙平后四个小时,在所检查的十个大脑区域中发现高水平的7-羟基洛沙平(68-124 ng / g),而在大脑和血浆中仅检测到痕量的洛沙平(<5 ng / g) (<3 ng / ml)。该方法为洛沙平及其代谢物的处置进行临床前和临床研究提供了有用的工具,这将有助于阐明它们在神经治疗学中的作用。

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