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Dual Organic Modifier, Solid Core Technology and Quality by Design Based Tripartite Synergistic Model for Development and Validation of Stability Indicating Method by Reverse Phase-High Performance Liquid Chromatography for Assay and Impurities of Etoricoxib Tablets
被引:0
|作者:
Kolla, S. B.
[2
]
Vallabhaneni, M. R.
[1
]
Puttagunta, S. B.
[3
]
Chakka, V. V. S. M.
[2
]
机构:
[1] Technol & Res Univ, Vignans Fdn Sci, Dept Chem, Guntur 522213, Andhra Pradesh, India
[2] GVK Biosci Private Ltd, Dept Analyt Res & Dev, Hyderabad 500076, Telangana, India
[3] Jawaharlal Nehru Technol Univ Kakinada, Vignan Coll Pharm, Dept Pharm, Guntur 522213, Andhra Pradesh, India
关键词:
Design of experiments;
solid core technology;
dual organic modifier;
assay and impurities method;
impurity profile swap;
etoricoxib;
stability indicating;
high performance liquid chromatography;
SHELL PARTICLES;
SELECTIVITY;
SEPARATION;
SOLVENT;
D O I:
10.36468/pharmaceutical-sciences.964
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Tripartite synergistic model of solid core technology, dual organic modifiers and combined mixture design was implemented to achieve combined assay and related substances method by reverse phase-high performance liquid chromatography with short run time, enhanced sensitivity and improved resolution between multiple impurity peaks. pH of mobile phase, ternary mobile phase composition and high performance liquid chromatography column temperature are experimented as variable parameters. Acetonitrile and isopropyl alcohol mixture was experimented as dual organic modifier. Special focus was given to detailed methodology of dealing with elution order changes by assigning negative sign for resolution. Separation of etoricoxib and related impurities was evaluated as a case study to prove this concept. The method was developed with Ascentis (R) Express C-18, 150x4.6 mm, 2.7 mu column. Mobile phase comprised of buffer (0.1 % v/v ortho phosphoric acid, pH 3.6), acetonitrile and isopropyl alcohol (65.3:29:5.7 v/v) with a flow rate of 1.0 ml/min and ultraviolet detection at 285 nm. Forced degradation studies revealed that the method was stability indicating, suitable for both assay and impurities of drug product. The recoveries for impurities and assay were found to be in the range of 94.0 %-111.0 % and 97.9 %-101.8 %, respectively. Linearity was established for impurities and assay in the range of 0.25-2.0 mu g/ml and 125-750 mu g/ml, respectively. The method was validated as per international conference on harmonisation guidelines. The method can be successfully employed for determination of assay and impurities of etoricoxib in bulk drugs and formulations.
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页码:683 / 702
页数:20
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