Zaazaa, H. E., E. S. Elzanfaly, H. A. M. Essam, and Y. F. Bassuoni, "Ion Selective Electrode Approach for In-line Determination of Benzydamine Hydrochloride in Different Matrices of Pharmaceutical Industry", analytical & Bioanalytical Electrochemistry, vol. 9, issue 1, pp. 65-79, 2017.
Elzanfaly, E. S., Y. F. Bassuoni, H. A. M. Essam, and H. E. Zaazaa, "on Selective Membrane Electrodes for Determination of Cetrimide in Pure form and in Pharmaceutical Formulations", Analytical & Bioanalytical Electrochemistry, vol. 7, issue 4, pp. 401-414, 2015. my_cetrimide_paper_final_journal_2015_74_401-414.pdf
Abdel-Moety, E. M., A. M. Badawey, H. A. M. Essam, and F. A. M. Alamine, "Stability-Indicating Methods for the Determination of Gemifloxacin in Presence of its Acid Degradation Product(s)", International Journal of Drug Development and Research, vol. 7, issue 2, pp. 1-8, 2015. stabilityindicating-methods-for-the-determination-of-gemifloxacin-inpresence-of-its-acid-degradation-products.pdf
Essam, H. A. M., and M. K. Abd-El Rahman, "Smart manipulation of ratio spectra for resolving a pharmaceutical mixture of Methocarbamol and Paracetamol.", Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, vol. 141, pp. 1-9, 2015 Apr 15. Abstractheba_and_khaled_spectro_paper_2015.pdf

Two smart, specific, accurate and precise spectrophotometric methods manipulating ratio spectra are developed for simultaneous determination of Methocarbamol (METH) and Paracetamol (PAR) in their combined pharmaceutical formulation without preliminary separation. Method A, is an extended ratio subtraction one (EXRSM) coupled with ratio subtraction method (RSM), which depends on subtraction of the plateau values from the ratio spectrum. Method B is a ratio difference spectrophotometric one (RDM) which measures the difference in amplitudes of ratio spectra between 278 and 286 nm for METH and 247 and 260 nm for PAR. The calibration curves are linear over the concentration range of 10-100 μg mL(-1) and 2-20 μg mL(-1) for METH and PAR, respectively. The specificity of the developed methods was investigated by analyzing different laboratory prepared mixtures of the two drugs. Both methods were applied successfully for the determination of the selected drugs in their combined dosage form. Furthermore, validation was performed according to ICH guidelines; accuracy, precision and repeatability are found to be within the acceptable limits. Statistical studies showed that both methods can be competitively applied in quality control laboratories.

Hegazy, M. A., S. S. Abbas, H. E. Zaazaa, and H. A. M. Essam, "Conventional univariate versus multivariate spectrophotometric assisted techniques for simultaneous determination of perindopril arginin and amlodipine besylate in presence of their degradation products.", Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, vol. 150, pp. 940-8, 2015 Nov 5. Abstractdr_hala_2.pdf

The resolving power of spectrophotometric assisted mathematical techniques were demonstrated for the simultaneous determination of perindopril arginin (PER) and amlodipine besylate (AML) in presence of their degradation products. The conventional univariate methods include the absorptivity factor method (AFM) and absorption correction method (ACM), which were able to determine the two drugs, simultaneously, but not in the presence of their degradation products. In both methods, amlodipine was determined directly at 360 nm in the concentration range of 8-28 μg mL(-1), on the other hand perindopril was determined by AFM at 222.2 nm and by ACM at 208 nm in the concentration range of 10-70 μg mL(-1). Moreover, the applied multivariate calibration methods were able for the determination of perindopril and amlodipine in presence of their degradation products using concentration residuals augmented classical least squares (CRACLS) and partial least squares (PLS). The proposed multivariate methods were applied to 19 synthetic samples in the concentration ranges of 60-100 μg mL(-1) perindopril and 20-40 μg mL(-1) amlodipine. Commercially available tablet formulations were successfully analysed using the developed methods without interference from other dosage form additives except PLS model, which failed to determine both drugs in their pharmaceutical dosage form.

Abbas, S. S., 1 halaand E. ZaaZaa, hebat allah m. essam, and G. mohammed El-bardicy, "Stability-Indicating Determination of Rebamipide in the Presence of its Acid Degradation Products", j aoac int, vol. 97, issue 1, pp. 78-85, 2014. s10-11426-abbas.pdf
E.Zaazaa, H., S. S.Abbas, H. A. M. Essam*, and M. G. El-Bardicy, "Validated Chromatographic Methods for Determination of Perindopril and Amlodipine in Pharmaceutical Formulation in the Presence of their Degradation Products", Journal of Chromatographic Science , vol. 51, pp. 533-543, 2013. 533.full_.pdf
Abbas, S. S., H. A. M. Essam, and M. G. El-Bardicy, "Spectrophotometric and TLC-densitometric determination of dantrolene sodium in presence of its acid degradates", Annaallyyttiiccaall CHEMIISSTRY an indian journal, vol. 12, issue 1, pp. 26-31, 2013. dantrolene_paper.pdf