A Novel HPLC Method for Simultaneous Determination of Methyl, Ethyl, n-propyl, Isopropyl, n-butyl, Isobutyl and Benzyl Paraben in Pharmaceuticals and Cosmetics

被引:4
|
作者
Ozcan, Saniye [1 ,2 ]
Levent, Serkan [2 ,3 ]
Can, Nafiz Oncu [1 ,2 ]
Kozanli, Murat [1 ]
机构
[1] Anadolu Univ, Fac Pharm, Dept Analyt Chem, TR-26470 Eskisehir, Turkey
[2] Anadolu Univ, Fac Pharm, Doping & Narcot Cpds Anal Lab, TR-26470 Eskisehir, Turkey
[3] Anadolu Univ, Fac Pharm, Dept Pharmaceut Chem, TR-26470 Eskisehir, Turkey
关键词
Core-shell column; cosmetic product; isomer separation; LC-DAD; pharmaceutical product; P-hydroxybenzoic acid derivatives; ASSISTED EMULSIFICATION MICROEXTRACTION; LIQUID-LIQUID MICROEXTRACTION; SOLID-PHASE DISPERSION; ENDOCRINE DISRUPTORS; SAMPLE PREPARATION; SAFETY ASSESSMENT; HUMAN EXPOSURE; CHROMATOGRAPHY; PRESERVATIVES; PRODUCTS;
D O I
10.2174/1386207323999200728121657
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Introduction: The alkyl esters of p-hydroxybenzoic acid at the C-4 position, "the parabens," including methyl, ethyl, propyl, and butyl, are widely used as antimicrobial preservatives in foods, cosmetics, and pharmaceuticals. Official regulations on the use of these compounds make their analysis essential for the estimation of their exposure. Methods: On this basis, the presented study was realized to develop a simple, selective and cheap high-performance liquid chromatographic method for the quantitative determination of methylparaben, ethylparaben (EP), n-propyl paraben (NPP), isopropyl paraben (IPP), n-butyl paraben (NBP), isobutyl paraben (IBP) and benzyl paraben (BP) in pharmaceuticals and cosmetic products. Results: The chromatographic separation of the analytes was achieved under flow rate gradient elution conditions using a C18-bonded core-shell silica particle column (2.6 mu m particle size, 150 x 3.0 mm from Phenomenex Co.). The samples were injected into the system as aliquots of 1.0 mu L, and the compounds were detected by using a photodiode array detector set at 254 nm wavelength. With this technique, seven paraben derivatives can be determined in the concentration range of 250-2000 ng/mL. The recovery of the method is in the range of 99.95-13.84%, and the RSD is at a maximum value of 3.95%. Conclusion: The proposed method was fully validated and successfully applied to different pharmaceutical and cosmetic samples (n=16), including syrups, suspensions, oral sprays, gels, etc. At least one paraben derivative was detected in six samples and was determined quantitatively. The maximum amount of a paraben derivative found in the analyzed samples was 321.7 ng/mL, which was MP. To the best of our knowledge, this is the first LC method, which is applicable both on pharmaceutical and cosmetic samples.
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页码:352 / 365
页数:14
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