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Determination of free formaldehyde in cosmetics products through derivatization with 2,4-DNPH using an optimized and validated HPLC-PDA method

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AbstractFormaldehyde plays a significant role in the global economy due to its unique chemical properties and widespread use in both the medical field and various industrial sectors. However, formaldehyde (HCHO) is classified as a persistent organic pollutant and is known to be harmful. Exposure to formaldehyde, both direct and prolonged, can cause severe health issues and potentially lead to death. It is recognized as a human carcinogen by numerous organizations and can negatively impact the endocrine system, as well as having mutagenic or teratogenic effects. Formaldehyde has been detected in various matrices at levels exceeding those permitted by international health regulatory bodies. Chromatography, particularly high-performance liquid chromatography (HPLC) coupled with detection methods, is an analytical technique frequently used to determine volatile organic molecules, including formaldehyde. This investigation aimed to develop and validate an assay method to identify and quantify formaldehyde in cosmetic products using HPLC-PDA. The chosen isocratic system consisted of a ZORBAX RX-C8 column (250 mm × 4.6 mm; 5 μm) and a mobile phase mixture of acetonitrile and water in a 55:45 (v/v) ratio, with a flow rate of 1.5 mL min−1. Formaldehyde was detected at 353 nm after derivatization with a 0.1N 2,4-dinitrophenylhydrazine solution, with a retention time of approximately 5.0 min and a total run time of 7.0 min for formaldehyde. The method was validated according to ICH Q2 (R1) guidelines. The validation parameters demonstrated high selectivity, precision (RSD <2%), accuracy (mean recovery of 101.3%), linearity (r > 0.995 in the 1,000–2,400 ppm range), and a limit of quantification (LOQ) of 0.1 ppm. The validated analytical method was applied to 35 cosmetic products. None of these products were labeled as containing formaldehyde, although 6 imported products were labeled as containing formaldehyde-releasing preservatives. The results indicated that 88.6% of the samples tested positive for formaldehyde, with free formaldehyde levels ranging from 20 to 981 ppm. All samples contained formaldehyde levels below the 2000 ppm threshold.
Title: Determination of free formaldehyde in cosmetics products through derivatization with 2,4-DNPH using an optimized and validated HPLC-PDA method
Description:
AbstractFormaldehyde plays a significant role in the global economy due to its unique chemical properties and widespread use in both the medical field and various industrial sectors.
However, formaldehyde (HCHO) is classified as a persistent organic pollutant and is known to be harmful.
Exposure to formaldehyde, both direct and prolonged, can cause severe health issues and potentially lead to death.
It is recognized as a human carcinogen by numerous organizations and can negatively impact the endocrine system, as well as having mutagenic or teratogenic effects.
Formaldehyde has been detected in various matrices at levels exceeding those permitted by international health regulatory bodies.
Chromatography, particularly high-performance liquid chromatography (HPLC) coupled with detection methods, is an analytical technique frequently used to determine volatile organic molecules, including formaldehyde.
This investigation aimed to develop and validate an assay method to identify and quantify formaldehyde in cosmetic products using HPLC-PDA.
The chosen isocratic system consisted of a ZORBAX RX-C8 column (250 mm × 4.
6 mm; 5 μm) and a mobile phase mixture of acetonitrile and water in a 55:45 (v/v) ratio, with a flow rate of 1.
5 mL min−1.
Formaldehyde was detected at 353 nm after derivatization with a 0.
1N 2,4-dinitrophenylhydrazine solution, with a retention time of approximately 5.
0 min and a total run time of 7.
0 min for formaldehyde.
The method was validated according to ICH Q2 (R1) guidelines.
The validation parameters demonstrated high selectivity, precision (RSD <2%), accuracy (mean recovery of 101.
3%), linearity (r > 0.
995 in the 1,000–2,400 ppm range), and a limit of quantification (LOQ) of 0.
1 ppm.
The validated analytical method was applied to 35 cosmetic products.
None of these products were labeled as containing formaldehyde, although 6 imported products were labeled as containing formaldehyde-releasing preservatives.
The results indicated that 88.
6% of the samples tested positive for formaldehyde, with free formaldehyde levels ranging from 20 to 981 ppm.
All samples contained formaldehyde levels below the 2000 ppm threshold.

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