Ultra-high-performance liquid chromatography-tandem mass spectrometry measurement of climbazole deposition from hair care products onto artificial skin and human scalp

被引:8
作者
Chen, Guoqiang [1 ,2 ]
Hoptroff, Michael [1 ]
Fei, Xiaoqing [1 ]
Su, Ya [1 ]
Janssen, Hans-Gerd [2 ,3 ]
机构
[1] Unilever R&D Shanghai, Linkong Econ Dev Zone, Shanghai 200335, Peoples R China
[2] Univ Amsterdam, Analyt Chem Grp, Vant Hoff Inst Mol Sci, NL-1098 XH Amsterdam, Netherlands
[3] Unilever Res Labs, NL-3130 AC Vlaardingen, Netherlands
关键词
Climbazole; Deposition; Human scalp; Artificial skin; UHPLC; MS/MS; IONIZATION; BIOCIDES; MATRICES; LINE; MS;
D O I
10.1016/j.chroma.2013.08.032
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A sensitive and specific ultra-high-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) method was developed and validated for the measurement of climbazole deposition from hair care products onto artificial skin and human scalp. Deuterated climbazole was used as the internal standard. Atmospheric pressure chemical ionization (APCI) in positive mode was applied for the detection of climbazole. For quantification, multiple reaction monitoring (MRM) transition 293.0 > 69.0 was monitored for climbazole, and MRM transition 296.0 > 225.1 for the deuterated climbazole. The linear range ran from 4 to 2000 ng mL(-1). The limit of detection (LOD) and the limit of quantification (LOQ) were 1 ng mL(-1) and 4 ng mL(-1), respectively, which enabled quantification of climbazole on artificial skin and human scalp at ppb level (corresponding to 16 ng cm(-2)). For the sampling of climbazole from human scalp the buffer scrub method using a surfactant-modified phosphate buffered saline (PBS) solution was selected based on a performance comparison of tape stripping, the buffer scrub method and solvent extraction in in vitro studies. Using this method, climbazole deposition in in vitro and in vivo studies was successfully quantified. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:155 / 158
页数:4
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