CAPILLARY ELECTROPHORESIS WITH ELECTROKINETIC INJECTION SIMPLIFIES THE DISSOLUTION TESTING OF AMOXICILLIN CAPSULES

REFERENCES

• Azarmi , S. ; Roac , W. ; Löbenberg , R. Current Perspectives in Dissolution Testing of Conventional and Novel Dosage Forms . Inter. J. Pharm. 2007 , 328 ( 1 ), 12 – 21 .
   PubMed Web of Science ®Google Scholar
• British Pharmacopeia . Her Majesty's Stationery Office : London , UK , 2007 , A295 .
   Google Scholar
• United States Pharmacopoeia USP30-NF25. The United States Pharmacopeia Convention Inc., Rockville, MD, 2007 .
   Google Scholar
• U.S. Department of Health and Human Services FDA (US FDA). Guidance for Industry: Immediate Release Solid Oral Dosage Forms Scale-Up and Post-Approval Changes: Chemistry, Manufacturing, and Controls, in vitro Dissolution Testing, and in vivo Bioequivalence Documentation. U.S. Department of Health and Human Services FDA: Silver Spring, MD, USA, 1995.
   Google Scholar
• U.S. Department of Health and Human Services FDA (US FDA). Guidance for Industry SUPAC-MR: Modified Release Solid Oral Dosage Forms Scale-Up and Postapproval Changes: Chemistry, Manufacturing, and Controls; In Vitro Dissolution Testing and In Vivo Bioequivalence Documentation. U.S. Department of Health and Human Services FDA: Silver Spring, MD, USA, 1997.
   Google Scholar
• U.S. Department of Health and Human Services FDA (US FDA). Bioavailability and Bioequivalence Studies for Orally Administered Drug Products- General Considerations. U.S. Department of Health and Human Services FDA: Silver Spring, MD, USA, 2003.
   Google Scholar
• U.S. Department of Health and Human Services FDA (US FDA). Guidance for Industry: Waiver of In Vivo Bioavailability and Bioequivalence Studies for Immediate-Release Solid Oral Dosage Forms Based on a Biopharmaceutics Classification System. U.S. Department of Health and Human Services FDA: Silver Spring, MD, USA, 2000.
   Google Scholar
• Tapia-Albarran , M. ; Villafuerte-Robles , L. Assay of Amoxicillin Sustained Release from Matrix Tablets Containing Different Proportions of Carbopol 971P NF . Inter. J. Pharm. 2004 , 273 ( 1–2 ), 121 – 127 .
   PubMedGoogle Scholar
• Tokumura , T. ; Machida , Y. UV Absorption Method Should Not Be Applied for Determining Amoxicillin in Acidic Dissolution Test Medium. Inter. J. Pharm. 2001, 228 (1–2), 1–4.
   Google Scholar
• Hidaka , S. ; Tokumura , T. ; Tomono , K. ; Zasshi , Y. Effect of Beta-Cyclodextrin on the Degradation Rate of Amoxicillin in Acidic Solution . J. Pharm. Soc. Japan. 2010 , 130 ( 6 ), 889 – 893 .
   Google Scholar
• Prakash , K. ; Raju , P. N. ; Kumari , K. S. Spectrophotometric Estimation of Amoxicillin Trihydrate in Bulk and Pharmaceutical Dosage Form . E-J. Chem. 2008 , 5 , 1114 – 1116 .
   Google Scholar
• Nagaralli , B. S. ; Seetharamappa , J. ; Melwanki , M. B. Sensitive Spectrophotometric Methods for the Determination of Amoxicillin, Ciprofloxacin and Piroxicam in Pure and Pharmaceutical Formulation . J. Pharm. Biomed. Anal. 2002 , 29 ( 5 ), 859 – 864 .
   Google Scholar
• Saleh , G. A. Two Selective Spectrophotometric Methods for the Determination of Amoxicillin and Cefadroxil . Analyst 1996 , 121 ( 5 ), 641 – 645 .
   Web of Science ®Google Scholar
• Amin , A. S. ; Elansary , A. L. ; Issa , Y. M. Colorimetric Determination of Amoxicillin in Pure Form and in Pharmaceutical Preparations . Talanta 1994 , 41 ( 5 ), 691 – 694 .
   Google Scholar
• Devani , M. B. ; Patel , I. T. ; Patel , T. M. Spectrophotometric Determination of Amoxicillin and Its Dosage Forms . J. Pharm. Biomed. Anal. 1992 , 10 ( 5 ), 355 – 358 .
   Google Scholar
• Li , Q. M. ; Yang , Z. J. Study of Spectrophotometric Determination of Amoxicillin Using Sodium 1,2-Naphthoquinone-4-sulfonate as the Chemical Derivative Chromogenic Reagent . Anal. Lett. 2006 , 39 ( 4 ), 763 – 775 .
   Web of Science ®Google Scholar
• Tsou , T. L. ; Wu , J. R. ; Young , C. D. ; Wang , T. M. Simultaneous Determination of Amoxicillin and Clavulanic Acid in Pharmaceutical Products by HPLC with Beta-Cyclodextrin . J. Pharm. Biomed. Anal. 1997 , 15 ( 8 ), 1197 – 1205 .
   Google Scholar
• Abdelmoety , E. M. ; Abounassif , M. A. ; Gadkariem , E. A. ; Khattab , N. A. Simultaneous Determination of Amoxicillin and Dicloxacillin in Capsules by Potentiometric Titrimetry and High Performance Liquid Chromatography . Talanta 1993 , 40 ( 6 ), 811 – 817 .
   Google Scholar
• Elwalily , A. F. M. ; Elanwar , F. ; Eid , M. A. ; Awaad , H. High-Performance Liquid Chromatographic and Derivative Ultraviolet Spectrophotometric Determination of Amoxicillin and Dicloxacillin Mixtures in Capsules . Analyst 1992 , 117 ( 6 ), 981 – 984 .
   Google Scholar
• Srisom , P. ; Liawruangrath , B. ; Liawruangrath , S. Micellar Liquid Chromatographic Determination of Penicillins in Pharmaceuticals . Chromatographia 2007 , 65 ( 11–12 ), 687 – 693 .
   Google Scholar
• Li , Y. M. ; Van Schepdael , A. ; Zhu , Y. ; Roets , E. ; Hoogmartens , J. Development and Validation of Amoxicillin Determination by Micellar Electrokinetic Capillary Chromatography . J. Chromatogry A 1998 , 812 ( 1–2 ), 227 – 236 .
   Web of Science ®Google Scholar
• Chadha , R. ; Kashid , N. ; Jain , D. V. S. Kinetic Studies of the Degradation of an Aminopenicillin Antibiotic (Amoxicillin Trihydrate) in Aqueous Solution Using Heat Conduction Microcalorimetry . J. Pharm. Pharmacol. 2003 , 55 ( 11 ), 1495 – 1503 .
   Google Scholar
• Bello , M. S. ; Capelli , L. ; Righetti , P. G. Dependence of the Electroosmotic Mobility on the Applied Electric-Field and Its Reproducibility in Capillary Electrophoresis . J. Chromatogr. A 1994 , 684 ( 2 ), 311 – 322 .
   Google Scholar
• Berli , C. L. A. ; Piaggio , M. V. ; Deiber , J. A. Modeling the Zeta Potential of Silica Capillaries in Relation to the Background Electrolyte Composition . Electrophoresis 2003 , 24 ( 10 ), 1587 – 1595 .
   Google Scholar
• Jandik , P. ; Bonn , G. Capillary Electrophoresis of Small Molecules and Ions . VCH Publishers Inc. : New York , 1993 .
   Google Scholar
• International Conference on Harmonization (ICH). International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use: Validation of Analytical Procedures Q2(R1), 1994, incorporated 2007 .
   Google Scholar
• Shah , V. P. ; Tsong , Y. ; Sathe , P. In Vitro Dissolution Profile Comparison- Statistics and Analysis of the Similarity Factor, f2 . Pharm. Res. 1998 , 15 ( 6 ), 889 – 896 .
   PubMed Web of Science ®Google Scholar