China Surfactant Detergent & Cosmetics ›› 2026, Vol. 56 ›› Issue (3): 368-375.doi: 10.3969/j.issn.2097-2806.2026.03.012
• Reviews • Previous Articles Next Articles
Wanping Yu1,2,Li Li2,Haiyan Wang2,*(
),Jianbo Sun1,*(
)
Received:2025-05-07
Revised:2026-03-11
Online:2026-03-22
Published:2026-05-14
Contact:
Haiyan Wang,Jianbo Sun
E-mail:summerwhy163@163.com;1020142420@cpu.edu.cn
CLC Number:
Wanping Yu,Li Li,Haiyan Wang,Jianbo Sun. Current status of analytical detection of Per- and polyfluoroalkyl substances in cosmetics and research progress on the application of molecular network[J].China Surfactant Detergent & Cosmetics, 2026, 56(3): 368-375.
Tab.1
Current regulatory landscape of PFASs in domestic and international jurisdictions"
| 国家/地区 | 法规/政策名称 | 发布机构 | 主要内容 | 实施时间 | 参考文献 |
|---|---|---|---|---|---|
| 欧盟 | 法规 (EU) 2024/2462 | 欧盟委员会 | 新增对化妆品中全氟己酸(PFHxA)、其盐类及相关物质的监管,设定添加限值 | 2024年 | [ |
| 法规 (EU) 2025/40 | 欧盟委员会 | 对食品接触包装的PFAS和氟物质的含量进行限制,每种PFAS不超过25 ppb;PFAS总和不超过250 ppb;PFAS包括聚合物PFAS以氟记不超过50 ppm | 已实施 | [ | |
| 《欧盟持久性有机污染物法规 (EU) 2019/1021》 | 欧盟议会及理事会 | 将PFOS及其衍生物、PFOA及其盐类和相关化合物、PFHxA及其盐类及相关化合物等PFASs纳入禁/限用清单。自2020年7月4日起,开始逐步禁止PFOA及能降解为PFOA的物质在欧盟销售产品中的使用,限量分别为25 ng/g (PFOA)和1 000 ng/g(相关物质) | 逐步实施 | [ | |
| 法规(EC)1907/2006 | 欧盟议会及理事会 | 限制全氟羧酸(C9~C14 PFCAs)及其盐类和相关物质、全氟癸酸(PFDA)及其钠盐和铵盐、全氟丁烷磺酸(PFBS)及其盐等在欧盟市场化学品中的使用 | 持续更新 | [ | |
| 美国 | 《美国有毒物质控制法(TSCA)》 | 美国环境保护署(EPA) | 将7种PFASs自动添加至有毒物质排放报告清单并严格管理其用途、生产、处理及危害信息 | 持续更新 | [ |
| 《美国包装材料中有毒物质控制示范法规》 | 美国各州立法机构 | 禁止在包装材料中检出PFASs | 2021年 | [ | |
| 日本 | 《日本化审法全称化学物质审查及制造管理法》 | 日本经产省、厚生劳动省、环境省 | 将PFOA及其相关化合物列为第一类特定化学物质进行限制,原则上禁止制造、进口和使用,同时也禁止进口含有该类物质的产品 | 已实施 | [ |
| 新西兰 | 化妆品禁用PFASs规定 | 新西兰政府 | 禁止在新西兰进口和制造的化妆品中使用PFASs | 2027年起 | [ |
| 法国 | 《保护公众免受PFAS危害法案》 | 法国国民议会 | 禁止PFASs在在化妆品、服装和鞋类等领域的使用 | 2026年1月1日起 | [ |
Tab.2
Common PFAS congeners"
| 化合物 名称 | 英文名称 | 化学式 | CAS号 |
|---|---|---|---|
| 全氟辛酸 | Perfluorooctanoic acid | C8HF15O2 | 335-67-1 |
| 全氟辛基磺酸 | Perfluorooctanesulfonic acid | C8HF17O3S | 1763-23-1 |
| 全氟丁酸 | Heptafluorobutyric acid | C4HF7O2 | 375-22-4 |
| 全氟丁烷磺酸 | Perfluorobutanesulfonic acid | C4HF9O3S | 375-73-5 |
| 全氟戊酸 | Perfluoropentanoic acid | C5HF9O2 | 2706-90-3 |
| 全氟戊烷磺酸 | Perfluoropentanesulfonic acid | C5HF11O3S | 2706-91-4 |
| 全氟己基磺酸 | Perfluorohexanesulfonic acid | C6HF13O3S | 355-46-4 |
| 全氟庚酸 | Perfluoroheptanoic acid | C7HF13O2 | 375-85-9 |
| 全氟庚基磺酸 | Perfluoroheptanesulfonic acid | C7HF15O3S | 375-92-8 |
| 全氟壬烷磺酸 | Perfluorononanesulfonic acid | C9HF19O3S | 68259-12-1 |
| 全氟壬酸 | Perfluorononanoic acid | C9HF17O2 | 375-95-1 |
| 全氟癸烷磺酸 | Perfluorodecanesulfonic acid | C10HF21O3S | 335-77-3 |
| 全氟十一烷酸 | Perfluoroundecanoic acid | C11HF21O2 | 2058-94-8 |
| 全氟十二烷酸 | Perfluorododecanoic acid | C12HF23O2 | 307-55-1 |
| 全氟十三酸 | Perfluorotridecanoic acid | C13HF25O2 | 72629-94-8 |
| 全氟代十 四酸 | Perfluorotetradecanoic acid | C14HF27O2 | 376-06-7 |
Tab.3
Typical analytical methodologies for PFASs detection in cosmetic matrices"
| 化合物 | 检测方法 | 前处理技术 | 色谱柱 | 质谱模式 | 仪器条件 | 检出限 | 回收率/ % |
|---|---|---|---|---|---|---|---|
| 全氟丙酸、全氟十三酸、全氟十六酸等PFASs[ | LC-MS/MS | 多种盐溶液与有机溶剂分散提取 | C18(3.0 mm×100 mm, 1.8 μm) | ESI- ;MRM模式 | 流动相:A(5 mmol/L乙酸铵水溶液), B(乙腈);柱温:40 ℃;进样量:1 μL | 0.025~0.125 μg/g | 70.8~ 112.0 |
| 全氟萘烷、全氟辛基乙基三乙氧基硅烷等[ | GC-MS | 饱和氯化钠溶液-乙酸乙酯分散提取 | INNOWAX(60 m× 0.25 mm,0.25 μm) | EI ;SIM模式 | 流速1 mL/min;程序升温 | 0.004,0.020和0.003 5 μg/mL | 60.7~ 95.8 |
| PFOS[ | HPLC-MS/MS | 甲醇提取,超声辅助萃取 | C18(100 mm×2.1 mm, 2.7 μm) | ESI-;MRM模式 | 流动相:A(0.1%甲酸水溶液)- B(甲醇);柱温:30 ℃;进样量:5 μL | 0.015 mg/kg | 98.7~ 112.5 |
| 8种挥发性PFASs[ | QuEChERS/GC-Q-TOF/MS | 有机溶剂提取,除水后利用吸附材料组合进行分散固相萃取净化 | DB-5 ms(30 m×250 μm, 0.25 μm) | EI ;SCAN模式 | 载气流速1.5 mL/min;程序升温 | 20~200 μg/kg | 81.4~ 112.0 |
| 9种全氟羧酸和8种全氟磺酸[ | UHPLC-MS/MS | 分散萃取后共沉淀,进行WAX-SPE净化 | C18(100 mm×3 mm, 2.6 mm) | ESI- ;MRM模式 | 流动相:A(含2 mmol/L乙酸铵的水);B(甲醇);进样量:5 μL | 0.09~0.26 ng/g | 70.1~ 114.7 |
Tab.4
Comparative analysis of four analytical methods for PFAS detection"
| 检测方法 | 原理 | 优势 | 局限性 |
|---|---|---|---|
| LC-MS/MS | 基于极性分离与质谱定量,适用于极性大、热不稳定的PFASs | 灵敏度高;选择性好;适用范围广 | 前处理复杂;成本较高 |
| GC-MS | 基于挥发性分离,需衍生化处理提升PFASs挥发性 | 分离效率高;经济性较好 | 适用性受限;灵敏度较低 |
| QuEChERS/GC-Q-TOF/MS | 结合快速样品前处理与高分辨质谱 | 前处理简便;适用于非靶向检测和高通量筛查 | 净化能力有限;分辨率要求高: |
| UHPLC-MS/MS | 通过超高效液相色谱提升分离速度与分辨率,结合质谱实现高灵敏度检测 | 分析速度快;灵敏度优异,合超痕量分析 | 基质干扰显著,前处理复杂;设备成本高 |
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