DEVELOPMENT AND VALIDATION OF ANALYTICAL SPECTROPHOTOMETRIC AND RP-HPLC METHODS FOR THE SIMULTANEOUS ESTIMATION OF HYDROQUINONE, HYDROCORTISONE AND TRETINOIN TERNARY MIXTURE IN TOPICAL FORMULATION
DOI:
https://doi.org/10.22159/ijpps.2019v11i11.35188Keywords:
Hydroquinone, Hydrocortisone, Tretinoin, Ternary mixture, Spectrophotometry and RP-HPLCAbstract
Objective: Development and validation of spectrophotometric and RP-HPLC methods for the simultaneous determination of Hydroquinone (HQ), Hydrocortisone (HC) and Tretinoin (TRT) ternary combination in pharmaceutical preparation.
Methods: The proposed spectrophotometric method was able to determine TRT directly from its absorption spectrum at 362 nm, however, HQ and HC from their first derivative spectra at 284 nm and 252 nm, respectively, without any separation step. The RP-HPLC method was developed using a C18 Sunfire© waters column with a mobile phase composed of acetonitrile: phosphate buffer (adjusted to pH 6.1 using ortho-phosphoric acid) in the ratio of 30:70 %, v/v, respectively at a flow rate of 0.8 ml/min. Quantification was based on measuring peak areas at 260 nm.
Results: The spectrophotometric method was able to selectively quantify each of HQ, HC and TRT in the ranges of 10-50 µg/ml, 2-10 µg/ml and 0.5-5 µg/ml, respectively. The RP-HPLC method was able to produce well-resolved peaks after 3.0, 8.2 and 20.2 min, in the ranges of 2-10 µg/ml, 0.1-1 µg/ml and 0.05-2 µg/ml, for HQ, HC and TRT, respectively. The obtained A, D1 or peak areas values plotted against the concentration of each of the three components showed linear response in the stated ranges. Both methods were validated in terms of linearity, LOD, LOQ, precision, accuracy and selectivity.
Conclusion: Both developed proposed methods were applied for the determination of the active ingredients in the pharmaceutical formulation and the common excipients did not interfere in the analysis. The RP-HPLC method proved to be more sensitive when compared to the applied spectrophotometric method. However, the applied spectrophotometric methods, considered as green analytical chemistry, is a simple, time-saving method that requires minimal use of a hazardous solvent.
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References
https://www.forhers.com/blog/hydroquinone-for-melasma-does-it-work. [Last accessed on 05 Jul 2019]
https://www.aocd.org/page/Hydroquinone. [Last accessed on 05 Jul 2019].
https://pubchem.ncbi.nlm.nih.gov/compound/hydrocortisone. [Last accessed on 05 Jul 2019].
https://pubchem.ncbi.nlm.nih.gov/compound/retinol. [Last accessed on 05 Jul 2019].
Kaur S, Kaur T, Kaur G, Verma SV. Development and validation of UV-spectrophotometric method for estimation of hydroquinone in bulk marketed cream and prepared NLC formulation. Int J Appl Pharm 2017;9:102.
Jogarami R, Jain P, Sharma S. Validated UV spectrophotometric method development for simultaneous estimation of tazarotene and hydroquinone in gel preparation. JPR 2012;5:2273–5.
Kaur S, Kaur T, Kaur G, Verma S. Development and validation of a UV-spectrophotometric method for estimation of hydroquinone in bulk marketed cream and prepared NLC formulation. Int J Appl Pharm 2017;9:102–8.
Garcia PL, Santoro MIRM, Singh AK, Kedor Hackmann ERM. Determination of optimum wavelength and derivative order in spectrophotometry for quantitation of hydroquinone in creams. Braz. J Pharm Sci 2007;43:397–404.
Htet AM, Thin EE, Saw MM, Win S. Chemical analysis of hydroquinone and retinoic acid contents in facial whitening creams. Afr J Plant Sci 2016;11:89–90.
Lin YH, Yang YH, Wu SM. Experimental design and capillary electrophoresis for the simultaneous analysis of arbutin, kojic acid and hydroquinone in cosmetics. J Pharm Biomed Anal 2007;44:279–82.
Abbas SS, Elghobashy MR, Bebawy LI, Shokry RF. Stability-indicating chromatographic determination of hydroquinone in combination with tretinoin and fluocinolone acetonide in pharmaceutical formulations with a photodegradation kinetic study. RSC Adv 2015;5:43178–94.
Elghobashy MR, Bebawy LI, Shokry RF, Abbas SS. Successive ratio subtraction coupled with constant multiplication spectrophotometric method for determination of hydroquinone in a complex mixture with its degradation products, tretinoin and methylparaben. Spectrochim Acta A 2016;157:16–123.
Zanwar As, Sen Db, Sen Ak, Seth Ak. Simultaneous estimation of mometasone furoate and formoterol fumarate by HPLC method in rotacaps. Int J Pharm Pharm Sci 2019;11:12–6.
Sheliya K, Shah K, Kapupara P. Development and validation of analytical method for simultaneous estimation of mometasone furoate, hydroquinone and retinoic acid in the topical formulation by RP-HPLC. J Chem Pharm Res 2014;6:934–40.
Zayed MA, Abdel Basset MH. Spectrophotometric micro determination of tretinoin, isotretinoinusing iodine and tazarotene micro determination via reaction with rose-bengal reagent. Egypt J Chem 2018;61:143-53.
Rahmayuni E, Harmita H, Suryadi H. Development and validation method for simultaneous analysis of retinoic acid, hydroquinone and corticosteroid in cream formula by high-performance liquid chromatography. J Appl Pharm 2018;8:87-92.
Maggadani B, Harmita H, Harahap Y, Hutabalian H. Simultaneous identification and quantification of hydroquinone, tretinoin and betamethasone in cosmetic products by isocratic reversed-phase high-performance liquid chromatography. Int J Appl Pharm 2019;11:181-5.
ICH Harmonized Tripartite guideline, Validation of Analytical Procedures text and methodology Q2 (R1) current step 4 version, parent guideline dated 27 November (Complementary guideline on Methodology. Geneva; 1996. p. 1-13.
JN Mileer JCM. Statistics and chemometrics for analytical chemistry. 5th ed. London, Pearson Prentice Hall; 2005.
FDA Center for Drug Evaluation Research (CDER), Reviewer Guidance: Validation of Chromatographic Methods, Washington, USA; 1994.
ICH, International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use, Validation of analytical procedures: Text and Methodology Q2 (R1); 2005.