Development and validation of RP-HPLC method for quantification of trace levels of topical corticosteroids in ambiphilic cream

Author:

Ivković Branka1,Crevar Milkica1ORCID,Cvetanović Anka2,Ubavkić Katarina3,Marković Bojan1

Affiliation:

1. Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Belgrade, Vojvode Stepe 450, Belgrade, Serbia

2. PrimeVigilance d.o.o., Đorđa Stanojevića br. 14, Belgrade, Serbia

3. Apoteka Privatna Praksa Iris SM 2015, Pop Lukina br. 1, Belgrade, Serbia

Abstract

AbstractCorticosteroids are anti-inflammatory and immunosuppressant drugs. Topical corticosteroids formulations (ointments, creams, gels) are used in the treatment of different types of dermatitis and urticaria. Considering their therapeutic and whitening effects, they are frequently used for counterfeiting of cosmetic products. Corticosteroids can cause different local and systemic side effects. HPLC method is often chosen for their analysis, because it is selective, sensitive, precise, simple and fast.The aim of this study was optimization and validation of RP-HPLC method with UV detection for determination of trace levels of corticosteroids in ambiphilic creams. This method is used for qualitative and quantitative analysis of evaluated corticosteroids.Mometasone furoate, hydrocortisone acetate, fluocinonide, fluocinolone acetonide, betamethasone, betamethasone dipropionate and triamcinolone acetonide were evaluated. Separation was performed on Inertsil® ODS-3V 250 × 4.6 mm, 5 μm chromatographic column. Mobile phase was mixture of acetonitrile and water 50:50 (v/v) with gradient elution and flow rate 1 mL min−1. Column temperature was held on 40 °C and UV detection was performed at 240 nm.Selectivity, linearity, accuracy, precision and limit of quantification (LOQ) were evaluated. Method is selective because ambiphilic cream base peaks and corticosteroids peaks were not overlapping. Linearity was confirmed since correlation coefficient was 1 for all compounds. Accuracy and precision were evaluated for hydrocortisone acetate and betamethasone dipropionate. Determined Recovery values were in range of 70–130%. Both RSD values (21.46% and 9.59%) were lower than 30%. Method is highly sensitive since LOQ concentrations were in ng mL−1 range.All evaluated parameters of validation were in accordance with regulatory requirements. Validated RP-HPLC method can be used for qualitative and quantitative analysis of selected corticosteroids in ambiphilic creams.

Publisher

Akademiai Kiado Zrt.

Subject

General Chemistry

Reference16 articles.

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4. Studies on the stability of corticosteroids: degradation of clobetasol propionate, desonide and hydrocortisone in topical formulations by HPLC and UPLC-MS/MS;Hotha, K. K.r,2020

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