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Journal of Liquid Chromatography & Related Technologies Volume 38, 2015 - Issue 10
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Original Articles

Stability Indicating High Performance Thin Layer Chromatographic Method for the Determination of Tramadol Hydrochloride in Pharmaceutical Formulation

Bhagyashree R. DhumalSharad Pawar College of Pharmacy, Hingna Road, Wanadongari, Nagpur, IndiaCorrespondence[email protected]
,
Kishore P. BhusariSharad Pawar College of Pharmacy, Hingna Road, Wanadongari, Nagpur, India
,
Arjun PatraInstitute of Pharmaceutical Sciences, Guru Ghasidas University (A Central University), Bilaspur, India
,
Suresh TharejaInstitute of Pharmaceutical Sciences, Guru Ghasidas University (A Central University), Bilaspur, India
&
Nishant S. JainInstitute of Pharmaceutical Sciences, Guru Ghasidas University (A Central University), Bilaspur, India
Pages 1088-1093 | Published online: 29 Apr 2015

References

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  • Yeh, G. C.; Sheu, M. T.; Yen, C. L.; Wang, Y. W.; Liu, C. H.; Ho, H. O. High-performance Liquid Chromatographic Method for Determination of Tramadol in Human Plasma, J. Chromatogr. B 2000, 723 (1–2), 247–253.
  • Gambaro, V.; Benvenuti, C.; De Ferrari, L.; Dell’ Acqua, L.; Farè, F. Validation of a GC/MS Method for the Determination of Tramadol in Human Plasma After Intravenous Bolus, J. Farmaco. 2003, 58 (9), 947–950.
  • Desai, P.; Captain, A.; Kamdar, S. Development and Validation of HPTLC Method for Estimation of Tramadol HCl in Bulk and in Capsule Dosage Form. Intl. J. Pharm. Tech. Res. July-Sept 2012, 4 (3), 1261–1265.
  • Kamble, R. M.; Singh, S. G. Stability-indicating RP-HPLC Method for Analysis of Paracetamol and Tramadol in a Pharmaceutical Dosage Form. E-J. Chem. 2012, 9 (3), 1347–1356.
  • Binnor, A. K.; Mukkanti, K.; Suryanarayana, M. V.; Roy, S. B. Stability-indicating UPLC Method for Tramadol HCl Impurities in the Tramadol Injection After Dilution by Infusion Fluids (5% Dextrose and 0.9% Sodium Chloride). Sci. Pharm. 2013, 14;81 (4), 1003–1015.
  • Makhija, S. N.; Vavia, P. R. Stability Indicating HPTLC Method for the Simultaneous Determination of Pseudoephedrine and Cetirizine in Pharmaceutical Formulations. J. Pharm. Biomed. Anal. 2001, 25 (3–4), 663–667.
  • International Conference on Harmonization (ICH). Validation of Analytical Procedures: Text and Methodology Q2 (R1). IFPMA: Geneva, 2005.
  • International Conference on Harmonization (ICH). Stability Testing of New Drug Substances and Products Q1A (R2). IFPMA: Geneva, 2003.
  • Proceedings of the International Conference on Harmonization. Geneva: 1996. Nov, ICH (Q1B), Harmonized Tripartite Guideline, Stability testing: Photostability Testing of New Drug Substances and Products.
  • United State Pharmacopeia, Interim Revision Announcement Official, March 1, 2013; 1–2 pp.

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