Abstract

Azo dyes, in spite of being additives, are indeed an integral constituent of consumer goods with bio-therapeutic values. The addition of dyes is for consumer compliance which lends a sense of pleasing aesthetics to the consumption ready product, “a kind of placebo effect”. Consequently, imperative need of the hour is felt to quantify such azo dyes due to complications like skin allergic reactions, genotoxicity, and ADHD symptoms leading to carcinogenicity in the long run, by apt analytical technique. In the proposed research, a pivotal USP-HPTLC compliant, validated, digitized method with multiple wavelength detection using TLC silica gel 60 F254 aluminum plates is developed. Mobile phase comprising of n-butanol–isopropanol–25% ammonia (GR grade)–water (65:20:10:5, v/v) has been put to task and subjected to spectro-densitometric scan for their simultaneous screening and quantification. Validation was done as per ICH and US FDA guidelines incorporating the latest 21 CFR approved, digital image CAMAG visionCATS software. The results revealed that the proposed method was highly sensitive with good linear relationship R = 99.999% and RSD of 0.456%. Thus, the method may be employed as standard quality control tool in consumer goods for characterization of azo dyes, which are still in the spectrum of doubt especially given the opaque data that surfaces on their safety profiles.

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