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 >Application of triple quadrupole tandem mass spectrometry to the bioanalysis of collision-induced dissociation-resistant cyclic peptides - Ultra-sensitive quantification of the somatostatin-analog pasireotide utilizing UHPLC-MS/MS
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Application of triple quadrupole tandem mass spectrometry to the bioanalysis of collision-induced dissociation-resistant cyclic peptides - Ultra-sensitive quantification of the somatostatin-analog pasireotide utilizing UHPLC-MS/MS

机译:三重四杆串联质谱法在抗碰撞诱导的解离抗性环状肽的生物分析中的应用 - 利用UHPLC-MS / MS的生长抑素 - 模拟Pasireotide的超敏定量

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摘要

Cyclic peptides are considered collision-induced dissociation (CID)-resistant due to immobile protons, and the necessity of at least two consecutive dissociation reactions to produce fragments with deviating m/z values. Therefore, the bioanalysis of cyclic peptides by tandem mass spectrometry (MS/MS) poses a major challenge, especially on triple quadrupole (TQ) instruments. One of these peptides is the somato-statin analog pasireotide, a cyclic hexapeptide administered to treat Cushing's disease and acromegaly. To support oral formulation development, sub-therapeutic quantification of pasireotide is highly beneficial. Regardless of the considered CID-resistance, we investigated the CID-characteristics of pasireotide and subsequently developed an ultra-sensitive UHPLC-MS/MS assay with a lower limit of quantification (LLOQ) of 5 pg/mL (4.9 pM) when using 100 mu L of plasma and validated it according to the guidelines of the FDA and EMA. The achieved sensitivity, which is the highest thus far reported, demonstrates that TQ-MS/MS is a feasible approach to sensitive quantification of cyclic peptides despite their CID-resistance. Pasireotide was fast and efficiently extracted by protein depletion via precipitation using acetonitrile. Correlation coefficients > 0.99 were achieved for all calibration curves with linear regression. Inter-run and intra-run accuracy ranged from 89.4 to 99.3 % with corresponding precision of <= 7.5 % in the calibrated range, and from 94.6 to 105.6 % with corresponding precision of <= 14.5 % at the LLOQ. Quantification of 10-fold diluted samples showed an accuracy of 90.8 % and corresponding precision of 4.0 %. The assay was applied to the quantification of pasireotide plasma concentrations after intravenous administration to beagle dogs. (C) 2020 Elsevier B.V. All rights reserved.
机译:由于质子不可移动,环肽被认为具有抗碰撞诱导解离(CID)的能力,并且至少需要两次连续的解离反应才能产生具有不同m/z值的片段。因此,通过串联质谱(MS/MS)对环肽进行生物分析是一个重大挑战,尤其是在三重四极杆(TQ)仪器上。其中一种肽是生长抑素类似物帕西雷肽,一种用于治疗库欣病和肢端肥大症的环六肽。为了支持口服制剂的开发,帕西罗替德的亚治疗定量是非常有益的。无论考虑到哪种抗酸性,我们研究了帕西罗替德的抗酸性特征,随后开发了一种超灵敏的UHPLC-MS/MS分析方法,当使用100μL血浆时,定量下限(LLOQ)为5 pg/mL(4.9 pM),并根据FDA和EMA的指南进行验证。所获得的灵敏度是迄今为止报道的最高灵敏度,表明TQ-MS/MS是一种可行的方法,可以对环肽进行敏感定量,尽管环肽具有抗CID能力。通过乙腈沉淀去除蛋白质,快速有效地提取帕西罗替德。所有线性回归校准曲线的相关系数均大于0.99。批间和批内准确度范围为89.4%至99.3%,在校准范围内的相应精度<=7.5%,在LLOQ下的相应精度<=14.5%,范围为94.6%至105.6%。10倍稀释样品的定量显示准确度为90.8%,相应的精密度为4.0%。该方法用于定量测定比格犬静脉注射帕西罗肽后的血浆浓度。(C) 2020爱思唯尔B.V.版权所有。

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