Development and Validation of New High Performance Liquid Chromatography Analytical Technique For Separation of Diclofenac Sodium and Lidocaine Hydrochloride From Ampoule Injection
In the current investigation, a number of chromatographic methods with the accurate, precise and specific criteria have been developed and validated for diclofenac sodium and lidocaine hydrochloride Commitment of their large quantities ampule of pharmaceutical dosage form. The High-Performance Liqui...
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Sulaimani Polytechnic University
2020-06-01
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| Series: | Kurdistan Journal of Applied Research |
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| Online Access: | https://www.kjar.spu.edu.iq/index.php/kjar/article/view/514 |
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| author | Mohammed Ali Salih Dlivan Fattah Aziz Salar Ibrahim Ali |
| author_facet | Mohammed Ali Salih Dlivan Fattah Aziz Salar Ibrahim Ali |
| author_sort | Mohammed Ali Salih |
| collection | DOAJ |
| description | In the current investigation, a number of chromatographic methods with the accurate, precise and specific criteria have been developed and validated for diclofenac sodium and lidocaine hydrochloride Commitment of their large quantities ampule of pharmaceutical dosage form. The High-Performance Liquid Chromatography (HPLC) system was performed at 25 ° C; with appropriate chromatographic isolation accomplished through the use of Waters Symmetry SB-C7 column with a mobile phase containing 0.1 M sodium acetate and methanol (40:60) (v/v). During development the portable stage was delivered at a stream rate of 1 mL/min, the wavelength was adjusted at 254 nm. First of all, the retention times for diclofenac sodium and lidocaine HCl were about 4.1 and 10.8 min accordingly. A performance and technical demonstration of the suggested Revers phase-HPLC method has been numerically challenged with support to process appropriateness, verticality, scales, simplicity, repeatability, sensitivity, stability, discovery and limits of quantification. In addition, the calibration curves for diclofenac sodium active pharmaceutical ingredient (API) with linear regressions > 0,999895 obtained linear in the distances 1870-5600 ?g / mL. Moreover, for determining of lidocaine HCl drug, a range of 500 - 1500 ?g/mL of working standard was used, the result showed for lidocain HCl that a linear curve with correlation coefficients of > 0.99980. Finally, the both drugs were isolated and resolute with selective and stable characteristics by the proposed technique. In the conclusion, successful validation of the HPLC approach has been demonstrated with high precision and accuracy for the assessment of both the mixed dosage form type of both diclofenac sodium and lidocaine HCl.
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| format | Article |
| id | doaj-art-cbe76e54273c4def8485d213cc9e83f1 |
| institution | Kabale University |
| issn | 2411-7684 2411-7706 |
| language | English |
| publishDate | 2020-06-01 |
| publisher | Sulaimani Polytechnic University |
| record_format | Article |
| series | Kurdistan Journal of Applied Research |
| spelling | doaj-art-cbe76e54273c4def8485d213cc9e83f12025-02-11T21:00:46ZengSulaimani Polytechnic UniversityKurdistan Journal of Applied Research2411-76842411-77062020-06-015110.24017/science.2020.1.11514Development and Validation of New High Performance Liquid Chromatography Analytical Technique For Separation of Diclofenac Sodium and Lidocaine Hydrochloride From Ampoule InjectionMohammed Ali Salih0Dlivan Fattah Aziz1Salar Ibrahim Ali2Chemistry Department, College of Science, University of Sulaimani, Sulaimani. IraqCollege of Pharmacy, University of Sulaimani, Sulaimani, IraqNursing Department, Technical College of Health, Sulaimani Polytechnic University, Sulaimani, IraqIn the current investigation, a number of chromatographic methods with the accurate, precise and specific criteria have been developed and validated for diclofenac sodium and lidocaine hydrochloride Commitment of their large quantities ampule of pharmaceutical dosage form. The High-Performance Liquid Chromatography (HPLC) system was performed at 25 ° C; with appropriate chromatographic isolation accomplished through the use of Waters Symmetry SB-C7 column with a mobile phase containing 0.1 M sodium acetate and methanol (40:60) (v/v). During development the portable stage was delivered at a stream rate of 1 mL/min, the wavelength was adjusted at 254 nm. First of all, the retention times for diclofenac sodium and lidocaine HCl were about 4.1 and 10.8 min accordingly. A performance and technical demonstration of the suggested Revers phase-HPLC method has been numerically challenged with support to process appropriateness, verticality, scales, simplicity, repeatability, sensitivity, stability, discovery and limits of quantification. In addition, the calibration curves for diclofenac sodium active pharmaceutical ingredient (API) with linear regressions > 0,999895 obtained linear in the distances 1870-5600 ?g / mL. Moreover, for determining of lidocaine HCl drug, a range of 500 - 1500 ?g/mL of working standard was used, the result showed for lidocain HCl that a linear curve with correlation coefficients of > 0.99980. Finally, the both drugs were isolated and resolute with selective and stable characteristics by the proposed technique. In the conclusion, successful validation of the HPLC approach has been demonstrated with high precision and accuracy for the assessment of both the mixed dosage form type of both diclofenac sodium and lidocaine HCl. https://www.kjar.spu.edu.iq/index.php/kjar/article/view/514Diclofenac sodium, HCl lidocaine, Reverse phase Higher performance chrmomatography, Simultaneous estimation |
| spellingShingle | Mohammed Ali Salih Dlivan Fattah Aziz Salar Ibrahim Ali Development and Validation of New High Performance Liquid Chromatography Analytical Technique For Separation of Diclofenac Sodium and Lidocaine Hydrochloride From Ampoule Injection Kurdistan Journal of Applied Research Diclofenac sodium, HCl lidocaine, Reverse phase Higher performance chrmomatography, Simultaneous estimation |
| title | Development and Validation of New High Performance Liquid Chromatography Analytical Technique For Separation of Diclofenac Sodium and Lidocaine Hydrochloride From Ampoule Injection |
| title_full | Development and Validation of New High Performance Liquid Chromatography Analytical Technique For Separation of Diclofenac Sodium and Lidocaine Hydrochloride From Ampoule Injection |
| title_fullStr | Development and Validation of New High Performance Liquid Chromatography Analytical Technique For Separation of Diclofenac Sodium and Lidocaine Hydrochloride From Ampoule Injection |
| title_full_unstemmed | Development and Validation of New High Performance Liquid Chromatography Analytical Technique For Separation of Diclofenac Sodium and Lidocaine Hydrochloride From Ampoule Injection |
| title_short | Development and Validation of New High Performance Liquid Chromatography Analytical Technique For Separation of Diclofenac Sodium and Lidocaine Hydrochloride From Ampoule Injection |
| title_sort | development and validation of new high performance liquid chromatography analytical technique for separation of diclofenac sodium and lidocaine hydrochloride from ampoule injection |
| topic | Diclofenac sodium, HCl lidocaine, Reverse phase Higher performance chrmomatography, Simultaneous estimation |
| url | https://www.kjar.spu.edu.iq/index.php/kjar/article/view/514 |
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