Development and Validation of Colorimetric and RP- HPLC Methods for the Determination of Formaldehyde in Cosmetics
نویسندگان
چکیده
Aims: To develop and validate two assay methods for the determination of total and free formaldehyde content in cosmetics by Colorimetric and High Performance Liquid Chromatographic (HPLC) methods, respectively. Study Design: Colorimetric and HPLC methods. Place and Duration of Study: Department of Pharmaceutical Technology, Faculty of Pharmacy, University of Dhaka, Dhaka-1000, Bangladesh; between February 2012 and June 2013. Short Research Article Rahman et al.; ACSj, 5(3): 224-237, 2015; Article no.ACSj.2015.022 225 Methodology: In Colorimetric method the quantitation was performed by a UV/Vis spectrophotometer at 410 nm and by HPLC at 345 nm and the methods were linear over the concentration ranges of 4-12 mg/L (R 2 =0.999) and 2-32 mg/L (R 2 =0.999), respectively. Based on 2, 4-dinitrophenylhydrazine (DNPH) derivatization, free formaldehyde was analyzed using a Phenomenex C18 (250 mm × 4.6 mm i. d., 5 μm particle size) column in a binary separation mode with mobile phase consisting of acetonitrile and distilled water (45:55, v/v) and flow rate of 2.0 mL/min. Results: The overall recovery rate of free formaldehyde was (95.33-98.37)±(0.29-1.6)% (RSD). Seventy five cosmetics of local and foreign brands were investigated. None of those products was labeled to contain formaldehyde. 18 products were labeled with specific formaldehyde donors (17 with DMDM hydantoin and 1 with imidazolidinyl urea). 64% of the products were formaldehyde positive among which 54% exceeded 0.05% limit of formaldehyde content for which EU dictates the mandatory formaldehyde donors labeling. The investigated amounts of the total formaldehyde and free formaldehyde were 190-5502 mg/L and 47-604 mg/L, respectively. Conclusion: The methods were found valid as per in terms of suitability, linearity, accuracy, sensitivity, ruggedness, and robustness. The formaldehyde content found in the cosmetics was highly alarming and must be addressed by the authority in an immediate basis.
منابع مشابه
Simultaneous RP-HPLC and UV Spectroscopic Method Development and Validation for Estimation of Ibandronate Sodium in Bulk and Pharmaceutical Dosage Form
The present study describes a simple, accurate, precise and cost effective UV-Vis Spectroscopic and RP-HPLC method for the estimation of Ibandronate sodium (IBN). The determination of Ibandronate sodium (IBN) was performed by both UV and RP-HPLC method using 215 nm as the determination wavelength. The drug was dissolved in NaOH solution (0.1N NaOH) for estimation in UV and in distilled water fo...
متن کاملDevelopment and validation of a fast, simple and specific stability indicating RP-HPLC method for determination of Dexpanthenol in eye gel formulation.
AIn this study a simple and reliable stability-indicating RP-HPLC method was developed and validated for analysis of Dexpanthenol in an artificial tear formulation. The chromatographic separation was performed on a HPLC C18 column (25.0 cm 4.6 mm, 5 m) using a mixture of 0.037 M monobasic potassium phosphate in water (adjusted with 0.1% (v/v) phosphoric acid to a pH of 3.2) and methanol (90:...
متن کاملDevelopment and validation of a fast, simple and specific stability indicating RP-HPLC method for determination of Dexpanthenol in eye gel formulation.
AIn this study a simple and reliable stability-indicating RP-HPLC method was developed and validated for analysis of Dexpanthenol in an artificial tear formulation. The chromatographic separation was performed on a HPLC C18 column (25.0 cm 4.6 mm, 5 m) using a mixture of 0.037 M monobasic potassium phosphate in water (adjusted with 0.1% (v/v) phosphoric acid to a pH of 3.2) and methanol (90:...
متن کاملDevelopment and Validation of RP-HPLC-UV Method for Determination of Diclofenac Sodium Residues on Surfaces for Cleaning Validation
In recent years, cleaning validation has achieved a position of increasing in the pharmaceutical industry. It provides assurance to the cleaning procedure that ensures equipment is consistently cleaned from the product, detergent and microbial residues to an acceptable level to avoid cross-contamination and adulteration of drug product with other active ingredients. The aim of this study was to...
متن کاملRP-HPLC method development and validation for determination of eptifibatide acetate in bulk drug substance and pharmaceutical dosage forms
A new, rapid, economical and isocratic reverse phase high performance liquid chromatography (RP-HPLC) method was developed for the determination of eptifibatide acetate, a small synthetic antiplatelet peptide, in bulk drug substance and pharmaceutical dosage forms. The developed method was validated as per of ICH guidelines. The chromatographic separation was achieved isocratically on C18 colum...
متن کامل