Tang Juan, Ding You-Chao, Fei Xiao-Qing, Wu Bin, Qian Zhi-Juan, Chen Shan-Dan, Li Bai
Industrial Products Testing Center, Nanjing Customs, Nanjing 210019, China.
Nanjing Jinjian Inspection Co., Ltd., Nanjing 210019, China.
Se Pu. 2024 Aug;42(8):783-791. doi: 10.3724/SP.J.1123.2023.10013.
Quaternary ammonium salt bactericides are broad-spectrum bactericides often used in oral care products because of their high antibacterial efficacy, strong penetration, and low toxicity. However, the excessive use of quaternary ammonium salt bactericides may cause contact dermatitis, scalding poisoning, and even death. Existing methods to determine quaternary ammonium salt bactericides are unable to meet current requirements owing to the lack of determination components. Therefore, establishing a simple and accurate method for the simultaneous detection of more quaternary ammonium salt bactericides is necessary. In this study, a method that couples sample pretreatment with high performance liquid chromatography-evaporative light-scattering detection (HPLC-ELSD) was developed for the simultaneous determination of quaternary ammonium salt bactericides in oral care products, including dodecyltrimethylammonium chloride, dodecyldimethylbenzylammonium chloride, benzethonium chloride, tetradecyl trimethyl ammonium chloride, tetradecyldimethylbenzylammonium chloride, -hexadecyltrimethylammonium chloride, benzyldimethylhexadecylammonium chloride, trimethylstearylammonium chloride, stearyldimethylbenzylammonium chloride, and docosyltrimethylammonium chloride. Some of these bactericides do not absorb ultraviolet light, so a universal evaporative light-scattering detector was used owing to testing cost and stability concerns. The paste samples contained thickening agents, which are highly soluble in water but insoluble in organic solvents; these agents can seriously affect the results of sample pretreatment and damage the chromatographic column. Hence, sample dehydration was necessary. In this study, four dehydration methods were compared. Anhydrous sodium sulfate (NaSO) was selected, and the amount of NaSO was optimized. Based on the solubility of the 10 target compounds and extraction efficiency, three extraction solvents were compared, and ethanol was selected. Ultrasonic extraction was the primary extraction process used in this study. The effects of different ultrasonication times, temperatures, and powers on the extraction recoveries were also investigated. Ultimately, the optimized conditions were as follows: extraction of the dehydrated paste and powder samples using ethanol at room temperature (25 ℃) for 20 min under 100 W ultrasound power, and dilution of the liquid sample with ethanol. After extraction, the samples were separated on an Acclaim Surfactant column (150 mm×4.6 mm, 5 μm) with 50 mmol/L ammonium acetate aqueous solution (pH=5.5) (A) and acetonitrile (B) as mobile phases. The gradient elution program were as follows: 0-5.0 min, 75%A-35%A, 5.0-15.0 min, 35%A-20%A, 15.0-20.0 min, 20%A, 20.0-21.0 min, 20%A-75%A, 21.0-25.0 min, 75%A. An external standard method was used for quantitative determination. The 10 compounds were analyzed within 25 min. Linear equations, correlation coefficients, and linear ranges were obtained by analyzing a series of mixed standard working solutions. The limits of detection (LODs, =3) and quantification (LOQs, =10) of the 10 components were determined. Stearyldimethylbenzylammonium chloride and docosyltrimethylammonium chloride showed good linear relationships in the range of 10-200 mg/L, while the other compounds demonstrated good linear relationships in the range of 5-100 mg/L. In all cases, correlation coefficients () of no less than 0.9992 were obtained. The LODs and LOQs were in the range of 1.42-3.31 mg/L and 4.25-9.94 mg/L, respectively. Ten analytes were spiked in blank matrices, such as toothpaste (paste), mouthwash (liquid), and dentifrice powder (powder) at three levels, and the recoveries and precisions were calculated. The average recoveries were 87.9%-103.1%, and the corresponding relative standard deviations (RSDs) did not exceed 5.5% (=6). The developed method was used to detect 109 oral care products. Benzyldimethylhexadecylammonium chloride and stearyldimethylbenzylammonium chloride revealed high detection rates. Moreover, the amount of stearyldimethylbenzylammonium chloride in one toothpaste sample exceeded regulatory requirements. Given its advantages of good precision and accuracy, the developed method is suitable for the quantitative analysis of the 10 aforementioned compounds in typical oral care products. The study findings can serve as a reference for the quality and safety monitoring of oral care products.
季铵盐类杀菌剂是一类广谱杀菌剂,因其具有高效抗菌、强渗透力和低毒性等特点,常用于口腔护理产品中。然而,过度使用季铵盐类杀菌剂可能会导致接触性皮炎、烫伤中毒甚至死亡。由于现有测定季铵盐类杀菌剂的方法缺乏测定成分,无法满足当前需求。因此,建立一种简单、准确的同时检测多种季铵盐类杀菌剂的方法很有必要。在本研究中,开发了一种将样品预处理与高效液相色谱 - 蒸发光散射检测(HPLC - ELSD)相结合的方法,用于同时测定口腔护理产品中的季铵盐类杀菌剂,包括十二烷基三甲基氯化铵、十二烷基二甲基苄基氯化铵、苄索氯铵、十四烷基三甲基氯化铵、十四烷基二甲基苄基氯化铵、十六烷基三甲基氯化铵、苄基二甲基十六烷基氯化铵、三甲基硬脂酰氯化铵、硬脂酰二甲基苄基氯化铵和二十二烷基三甲基氯化铵。其中一些杀菌剂不吸收紫外光,出于测试成本和稳定性的考虑,使用了通用的蒸发光散射检测器。膏状样品中含有增稠剂,这些增稠剂易溶于水但不溶于有机溶剂,会严重影响样品预处理结果并损坏色谱柱。因此,样品脱水是必要的。在本研究中,比较了四种脱水方法,选择了无水硫酸钠(Na₂SO₄)并对其用量进行了优化。基于10种目标化合物的溶解度和萃取效率,比较了三种萃取溶剂,选择了乙醇。本研究主要采用超声萃取法。还研究了不同超声时间、温度和功率对萃取回收率的影响。最终,优化条件如下:在室温(25℃)下,使用乙醇对脱水后的膏状和粉末样品进行超声萃取,超声功率为100W,萃取20min,液体样品用乙醇稀释。萃取后,样品在Acclaim Surfactant柱(150mm×4.6mm,5μm)上进行分离,以50mmol/L醋酸铵水溶液(pH = 5.5)(A)和乙腈(B)作为流动相。梯度洗脱程序如下:0 - 5.0min,75%A - 35%A;5.0 - 15.0min,35%A - 20%A;15.0 - 20.0min,20%A;20.0 - 21.0min,20%A - 75%A;21.0 - 25.0min,75%A。采用外标法进行定量测定。10种化合物在25min内完成分析。通过分析一系列混合标准工作溶液获得线性方程、相关系数和线性范围。测定了10种成分的检测限(LODs,n = 3)和定量限(LOQs,n = 10)。硬脂酰二甲基苄基氯化铵和二十二烷基三甲基氯化铵在10 - 200mg/L范围内呈现良好的线性关系,而其他化合物在5 - 100mg/L范围内呈现良好的线性关系。在所有情况下,相关系数(r)均不小于0.9992。检测限和定量限分别在1.42 - 3.31mg/L和4.25 - 9.94mg/L范围内。将10种分析物以三个水平添加到空白基质中,如牙膏(膏状)、漱口水(液体)和牙膏粉(粉末)中,计算回收率和精密度。平均回收率为87.9% - 103.1%,相应的相对标准偏差(RSDs)不超过5.5%(n = 6)。所开发的方法用于检测109种口腔护理产品。苄基二甲基十六烷基氯化铵和硬脂酰二甲基苄基氯化铵的检出率较高。此外,一个牙膏样品中的硬脂酰二甲基苄基氯化铵含量超过了监管要求。所开发的方法具有良好的精密度和准确性,适用于典型口腔护理产品中上述10种化合物的定量分析。研究结果可为口腔护理产品的质量和安全监测提供参考。