Coupling of Physical and Chromatographic Separation for Analyzing Cream Containing Miconazole, Mometasone Furoate and Gentamicin Sulphate

Author:

Tawakkol Shereen Mostafa12,Fayez Yasmin Mohammed34,Fahmy Nesma Mahmoud12ORCID,Lotfy Hayam Mahmoud56,Shehata Mostafa Abdel-Atty34

Affiliation:

1. Pharmaceutical Chemistry Department , Faculty of Pharmacy, , Banks complex, 4th industrial zone, 6th October City, Giza governorate 12451 , Egypt

2. Ahram Canadian University , Faculty of Pharmacy, , Banks complex, 4th industrial zone, 6th October City, Giza governorate 12451 , Egypt

3. Analytical Chemistry Department , Faculty of Pharmacy, , Al kasr Al Aini St, Cairo governorate 11562 , Egypt

4. Cairo University , Faculty of Pharmacy, , Al kasr Al Aini St, Cairo governorate 11562 , Egypt

5. Pharmaceutical Chemistry Department , Faculty of Pharmacy, , Cairo, End of 90's St, Cairo governorate 11835 , Egypt

6. Future University in Egypt , Faculty of Pharmacy, , Cairo, End of 90's St, Cairo governorate 11835 , Egypt

Abstract

Abstract High-performance liquid chromatographic method was developed, validated and applied for miconazole, mometasone and gentamicin in Momenta® cream. Physical separation was applied using two extraction procedures due to different solubility of the three components. First, a methanolic extract of the cream contained miconazole and mometasone was chromatographed on ODS-3 Inertsil C18 column (150 × 4.6, 5 μm) using acetonitrile: water (80:20, v/v) as a mobile phase, flow rate 1.5 mL·min−1, scanned at 230 nm, showing tR 2.817 and 6.808 min for mometasone and miconazole, respectively. Second, an aqueous extract of the cream containing gentamicin was derivatized with o-phthalaldehyde in order to enhance the gentamicin UV detection and subjected to ion pairing chromatography on Inertsil ODS-3 C18 column (150 × 4.6, 5 μm), using methanol: 0.025 M heptane sulphonic acid: glacial acetic acid (75:20:5, by volume) as a mobile phase, flow rate 0.8 mL·min−1, scanned at 330 nm where the three active gentamicin isomers were separated at tR 11.7, 15.6 and 18.3 min. Suitability of this method for quantitative estimation of the drugs was proved by validation according to ICH guidelines. The method was selective, precise and accurate so could be used for analysis of cream formulation in QC labs.

Publisher

Oxford University Press (OUP)

Subject

General Medicine,Analytical Chemistry

Reference37 articles.

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2. Development and Validation of an Extractive Spectrophotometric Method for Miconazole Nitrate Assay in Pharmaceutical Formulations;J Anal Methods Chem,2018

3. Analysis of miconazole and econazole in pharmaceutical formulations by derivative UV spectroscopy and liquid chromatography (HPLC)*;Cavrini;Journal of Pharmaceutical & Biomedical Analysis,1989

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