Chen Weiyang, Nkosi Thobile A N, Combrinck Sandra, Viljoen Alvaro M, Cartwright-Jones Catherine
Department of Pharmaceutical Sciences, Faculty of Science, Tshwane University of Technology, Private Bag X680, Pretoria 0001, South Africa.
Department of Pharmaceutical Sciences, Faculty of Science, Tshwane University of Technology, Private Bag X680, Pretoria 0001, South Africa; SAMRC Herbal Drugs Research Unit, Faculty of Science, Tshwane University of Technology, Private Bag X680, Pretoria, 0001, South Africa.
J Pharm Biomed Anal. 2016 Sep 5;128:119-125. doi: 10.1016/j.jpba.2016.05.020. Epub 2016 May 12.
Henna (Lawsonia inermis) is applied to stain keratin, present in hair, skin and fingernails, a red-orange or rust colour. Producers of temporary tattoos mix the aromatic amine compound, para-phenylenediamine (PPD) into natural henna to create 'black henna' that rapidly stains the skin black. However, PPD may cause severe delayed hypersensitivity reactions following skin contact. This study proposes a rapid direct-analysis method to detect and identify PPD using an atmospheric solids analysis probe (ASAP) coupled to a Q-ToF mass spectrometer (MS). Since laborious, multistep methods of analysis to determine PPD are undesirable, due to the instability of the compound in solution, a screening method involving no sample preparation steps was developed. Experiments were carried out to optimise the corona current, sample cone voltage, source temperature, and desolvation gas temperature to determine ideal ASAP-Q-ToF-MS analysing conditions. Eleven of the 109 henna samples, originating from various countries, tested positive for PPD when henna products were screened using ASAP-MS, without any form of sample preparation other than grinding. Ultra-performance liquid chromatography electrospray ionisation-mass spectrometry (UPLC-Q-ToF-MS) was subsequently used to confirm the results from ASAP and to determine the concentrations of PPD in henna products. The allergen was detected in the same eleven samples, with concentrations ranging from 0.05-4.21% (w/w). It can be concluded that the sensitivity of the ASAP-MS technique is sufficient (limit of detection=0.025% w/w) to allow screening of henna samples for the presence of PPD. This relatively new technique can be applied to commercial products without extraction, sample treatment or chromatographic separation.
指甲花(散沫花)用于给头发、皮肤和指甲中的角蛋白染成红橙色或铁锈色。临时纹身产品制造商将芳香胺化合物对苯二胺(PPD)混入天然指甲花中制成“黑色指甲花”,可迅速将皮肤染黑。然而,PPD接触皮肤后可能会引起严重的迟发型超敏反应。本研究提出了一种快速直接分析方法,使用常压固体分析探头(ASAP)与四极杆-飞行时间质谱仪(Q-ToF MS)联用检测和鉴定PPD。由于该化合物在溶液中不稳定,繁琐的多步PPD分析方法不可取,因此开发了一种无需样品制备步骤的筛选方法。进行实验以优化电晕电流、样品锥电压、源温度和去溶剂化气体温度,以确定理想的ASAP-Q-ToF-MS分析条件。当使用ASAP-MS对来自不同国家的109份指甲花样品进行筛选时,除研磨外无需任何形式的样品制备,其中11份样品PPD检测呈阳性。随后使用超高效液相色谱电喷雾电离质谱(UPLC-Q-ToF-MS)来确认ASAP的结果,并测定指甲花产品中PPD的浓度。在相同的11份样品中检测到了该过敏原,浓度范围为0.05 - 4.21%(w/w)。可以得出结论,ASAP-MS技术的灵敏度足够高(检测限 = 0.025% w/w),能够筛选指甲花样品中是否存在PPD。这种相对较新的技术可应用于商业产品,无需提取、样品处理或色谱分离。