Different mathematical processing of absorption, ratio and derivative spectra for quantification of mixtures containing minor component: An application to the analysis of the recently co-formulated antidiabetic drugs; canagliflozin and metformin

dc.AffiliationOctober University for modern sciences and Arts (MSA)
dc.contributor.authorLotfy H.M.
dc.contributor.authorMohamed D.
dc.contributor.authorElshahed M.S.
dc.contributor.otherPharmaceutical Chemistry Department
dc.contributor.otherFaculty of Pharmaceutical Sciences & Pharmaceutical Industries
dc.contributor.otherFuture University in Egypt
dc.contributor.otherCairo
dc.contributor.other12311
dc.contributor.otherEgypt; Analytical Chemistry Department
dc.contributor.otherFaculty of Pharmacy
dc.contributor.otherHelwan University
dc.contributor.otherEin Helwan
dc.contributor.otherCairo
dc.contributor.other11795
dc.contributor.otherEgypt; Pharmaceutical Analytical Chemistry Department
dc.contributor.otherFaculty of Pharmacy
dc.contributor.otherOctober University for Modern Sciences and Arts11787
dc.contributor.otherEgypt
dc.date.accessioned2020-01-09T20:41:00Z
dc.date.available2020-01-09T20:41:00Z
dc.date.issued2018
dc.descriptionScopus
dc.description.abstractIn the presented work several spectrophotometric methods were performed for the quantification of canagliflozin (CGZ) and metformin hydrochloride (MTF) simultaneously in their binary mixture. Two of these methods; response correlation (RC) and advanced balance point-spectrum subtraction (ABP-SS) were developed and introduced for the first time in this work, where the latter method (ABP-SS) was performed on both the zero order and the first derivative spectra of the drugs. Besides, two recently established methods; advanced amplitude modulation (AAM) and advanced absorbance subtraction (AAS) were also accomplished. All the proposed methods were validated in accordance to the ICH guidelines, where all methods were proved to be accurate and precise. Additionally, the linearity range, limit of detection and limit of quantification were determined and the selectivity was examined through the analysis of laboratory prepared mixtures and the combined dosage form of the drugs. The proposed methods were capable of determining the two drugs in the ratio present in the pharmaceutical formulation CGZ:MTF (1:17) without the requirement of any preliminary separation, further dilution or standard spiking. The results obtained by the proposed methods were in compliance with the reported chromatographic method when compared statistically, proving the absence of any significant difference in accuracy and precision between the proposed and reported methods. � 2017 Elsevier B.V.en_US
dc.description.urihttps://www.scimagojr.com/journalsearch.php?q=24530&tip=sid&clean=0
dc.identifier.doihttps://doi.org/10.1016/j.saa.2017.08.015
dc.identifier.doiPubMed ID 28802856
dc.identifier.issn13861425
dc.identifier.otherhttps://doi.org/10.1016/j.saa.2017.08.015
dc.identifier.otherPubMed ID 28802856
dc.identifier.urihttps://t.ly/1VJrE
dc.language.isoEnglishen_US
dc.publisherElsevier B.V.en_US
dc.relation.ispartofseriesSpectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy
dc.relation.ispartofseries189
dc.subjectAdvanced absorbance subtraction methoden_US
dc.subjectAdvanced amplitude modulation methoden_US
dc.subjectAdvanced balance point using spectrum subtraction methoden_US
dc.subjectCanagliflozinen_US
dc.subjectMetformin hydrochlorideen_US
dc.subjectResponse correlation methoden_US
dc.subjectAmplitude modulationen_US
dc.subjectBinary mixturesen_US
dc.subjectChromatographic analysisen_US
dc.subjectDrug dosageen_US
dc.subjectMixturesen_US
dc.subjectModulationen_US
dc.subjectOptical transfer functionen_US
dc.subjectSpectrophotometryen_US
dc.subjectAdvanced amplitude modulation methoden_US
dc.subjectCanagliflozinen_US
dc.subjectMetformin hydrochloridesen_US
dc.subjectSpectrum subtractionsen_US
dc.subjectSubtraction methoden_US
dc.subjectDrug productsen_US
dc.subjectantidiabetic agenten_US
dc.subjectcanagliflozinen_US
dc.subjectmetforminen_US
dc.subjectchemistryen_US
dc.subjectdrug formulationen_US
dc.subjectlimit of detectionen_US
dc.subjectproceduresen_US
dc.subjectreproducibilityen_US
dc.subjectsolution and solubilityen_US
dc.subjectspectrophotometryen_US
dc.subjecttheoretical modelen_US
dc.subjectCanagliflozinen_US
dc.subjectDrug Compoundingen_US
dc.subjectHypoglycemic Agentsen_US
dc.subjectLimit of Detectionen_US
dc.subjectMetforminen_US
dc.subjectModels, Theoreticalen_US
dc.subjectReproducibility of Resultsen_US
dc.subjectSolutionsen_US
dc.subjectSpectrophotometryen_US
dc.titleDifferent mathematical processing of absorption, ratio and derivative spectra for quantification of mixtures containing minor component: An application to the analysis of the recently co-formulated antidiabetic drugs; canagliflozin and metforminen_US
dc.typeArticleen_US
dcterms.isReferencedByKaur, I., Wakode, S., Singh, H.P., Development and validation of UV spectroscopic method for determination of canagliflozin in bulk and pharmaceutical dosage form (2015) Pharm. Methods, 6, pp. 82-86; Elkinson, S., Scott, L.J., Canagliflozin: first global approval (2013) Drugs, 73, pp. 979-988; Rosiak, M., Grzeszczak, S., Kosior, D.A., Postu?a, M., Emerging treatments in type 2 diabetes: focus on canagliflozin (2014) Ther. Clin. Risk Manag., 10, pp. 683-689; Lajara, R., The potential role of sodium glucose co transporter 2 inhibitors in combination therapy for type 2 diabetes mellitus (2014) Expert. Opin. Pharmacother., 15, pp. 2565-2585; The United States Pharmacopoeia 39, National Formulary 34 (2016), USP Convension Inc. Rockville, Maryland; Sweetman, S.C., Martindale, The Complete Drug Reference (2009), thirty sixth ed. Pharmaceutical Press London; The British Pharmacopoeia, The Stationery Office, Electronic Version, London (2009), pp. 3813-3816; Mubeen, G., Noor, K., Spectrophotometric method for analysis of metformin hydrochloride (2009) Indian J. Pharm. Sci., 71, pp. 100-102; Ashour, S., Kabbani, R., Direct spectrophotometric determination of metformin hydrochloride in pure form and in drug formulations (2003) Anal. Lett., 2, pp. 361-370; Kaur, I., Wakode, S., Singh, H.P., Development and validation of a stability-indicating high performance thin layer chromatography (HPTLC) method for estimation of canagliflozin in bulk and pharmaceutical dosage form (2016) J. Appl. Pharm. Sci., 6, pp. 51-57; Havele, S., S Dhaneshwar estimation of metformin in bulk drug and in formulation by HPTLC (2010) J. Nanosci. Nanotechnol., 102, pp. 1-3; Suma, M., Manasa, K., Rajakumari, C., Lakshmaiah, B., RP-HPLC method development and validation for the estimation of canagliflozin in tablet dosage form (2014) Int. J. Pharm., 5, pp. 1288-1292; Suneetha, A., Sharmila, D., A validated stability indicating RP-HPLC method for estimation of canagliflozin in dosage form (2015) Res. J. Pharm., Biol. Chem. Sci., 6, pp. 1186-1194; Kar, M., Choudhury, P.K., HPLC method for estimation of metformin hydrochloride in formulated microspheres and tablet dosage form (2009) Indian J. Pharm. Sci., 71, pp. 318-320; Chhetri, H.P., Thapa, P., Schepdael, A.V., Simple HPLC-UV method for the quantification of metformin in human plasma with one step protein precipitation (2014) Saudi Pharm. J., 22, pp. 483-487; Muzaffar, I., Nasr, K., Amer, A., Khalid, A., A simple and sensitive high performance liquid chromatography assay with a fluorescence detector for determination of canagliflozin in human plasma (2015) Anal. Methods, 7, pp. 3028-3035; Muzaffar, I., Essam, E., Khalid, A., Yousif, A., Naser, L., Rapid determination of canagliflozin in rat plasma by UHPLC-MS/MS using negative ionization mode to avoid adduct-ions formation (2015) Talanta, 132, pp. 29-36; Kobuchi, S., Yano, K., Ito, Y., Sakaeda, T., A validated LC-MS/MS method for the determination of canagliflozin, a sodium-glucose co-transporter 2 (SGLT-2) inhibitor, in a lower volume of rat plasma: application to pharmacokinetic studies in rats (2016) Biomed. Chromatogr., 30, pp. 549-1555; Heinig, K., Bucheli, F., Fast liquid chromatographic-tandem mass spectrometric (LC-MS-MS) determination of metformin in plasma samples (2004) J. Pharm. Biomed. Anal., 34, pp. 1005-1011; Zhang, W., Han, F., Zhao, H., Lin, Z., Huang, Q., Weng, N., Determination of metformin in rat plasma by HILIC-MS/MS combined with Tecan automation and direct injection (2012) Biomed. Chromatogr., 26, pp. 1163-1169; Ali, I., Aboul-Enein, H.Y., Gupta, V.K., Analysis of metformin dosage formulations by capillary electrophoresis at nanoscale detection (2007) Comb. Chem. High Throughput Screen., 10, pp. 611-615; Songa, J.Z., Chen, H.F., Tian, S.J., Sun, Z.P., Determination of metformin in plasma by capillary electrophoresis using field-amplified sample stacking technique (1998) J. Chromatogr. B Biomed. Sci. Appl., 708, pp. 277-283; Gaware, D., Patil, R.N., Harole, M., A validated stability indicating RP-HPLC method for simultaneous determination of metformin and canagliflozin in pharmaceutical formulation (2015) World J. Pharm. Pharm. Sci., 4, pp. 631-640; Redd, N.P., Chevela, N.T., RP-HPLC method development and validation for simultaneous estimation of metformin and canagliflozin in tablet dosage form (2015) Int. J. Pharm. Sci., 5, pp. 1155-1159; Panigrahy, U.P., Reddy, A.S.K., A novel validated RP-HPLC-DAD for the simultaneous estimation of metformin hydrochloride and canagliflozin in bulk and pharmaceutical tablet dosage form with forced degradation studies (2015) Orient. J. Chem., 31, pp. 1489-1507; Lotfy, H.M., Tawakkol, S.M., Fahmy, N.M., Shehataa, M.A., A comparative study of novel spectrophotometric resolution techniques applied for pharmaceutical mixtures with partially or severely overlapped spectra (2015) Spectrochim. Acta A, 136, pp. 937-952; Lamie, N.T., Yehia, A.M., Development of normalized spectra manipulating spectrophotometric methods for simultaneous determination of dimenhydrinate and cinnarizine binary mixture (2015) Spectrochim. Acta A, 150, pp. 142-150; Lotfy, H.M., Hegazy, M.A., Rezk, M.R., Omran, Y.R., Comparative study of novel versus conventional two-wavelength spectrophotometric methods for analysis of spectrally overlapping binary mixture (2015) Spectrochim. Acta A, 148, pp. 328-337; Lotfy, H.M., Saleh, S.S., Hassan, N.Y., Salem, H., A comparative study of progressive versus successive spectrophotometric resolution techniques applied for pharmaceutical ternary mixtures (2014) Spectrochim. Acta A, 132, pp. 239-248; Erram, S., Tipnis, H., Simple spectrometric analysis of acebutolol hydrochloride and atenolol in combined pharmaceutical dosages with hydrochlorothiazide (1993) Indian Drugs Bombay, 30, p. 462; Lotfy, H.M., Mohamed, D., Mowaka, S., A comparative study of smart spectrophotometric methods for simultaneous determination of sitagliptin phosphate and metformin hydrochloride in their binary mixture (2015) Spectrochim. Acta A, 149, pp. 441-451; Hassan, N.Y., Elgizawy, S.M., Lotfy, H.M., Saleh, S.S., A comparative study of spectrophotometric methods versus chemometric methods, an application on a pharmaceutical binary mixture of ofloxacin and dexamethasone (2013) Int. Res. J. Pure Appl. Chem., 3, pp. 90-110; Lotfy, H.M., Saleh, S.S., Recent development in ultraviolet spectrophotometry through the last decade (2006�2016) (2016) Int J Pharm Pharm Sci, 8 (10), pp. 40-56; (1997) International Conference on Harmonization (ICH), Q2B: Validation of Analytical Procedures: Methodology, 62, US FDA, Federal Register; Wahbi, A.A.M., El-Yazbi, F.A., Barary, M.H., Sabri, S.M., Derivative spectrophotometric analysis of two-component mixtures using a compensation technique (1992) Analyst, 117, pp. 785-789; Erk, N., Analysis of binary mixtures of losartan potassium and hydrochlorothiazide by using high performance liquid chromatography, ratio derivative spectrophotometric and compensation technique (2001) J. Pharm. Biomed. Anal., 24, pp. 603-611; Wahbi, A.A.M., Abdel-Razak, O., Gazy, A.A., Mahgoub, H., Moneeb, M.S., Spectrophotometric determination of omeprazole, lansoprazole and pantoprazole in pharmaceutical formulations (2002) J. Pharm. Biomed. Anal., 30, pp. 1133-1142; Vessman, J., Stefan, R.I., Van Staden, J.F., Danzer, K., Lindner, W., Burns, D.T., Fajgelj, A., M�ller, H., Selectivity in analytical chemistry (IUPAC Recommendations 2001) (2001) Pure Appl. Chem., 73, pp. 1381-1386; Rao, D.R., Rao, M.P., Hussain, J.N., Sumanoja, S.L., Rao, V.R., Method development and validation of forced degradation studies of metformin hydrochloride by using UV spectroscopy (2013) Int. J. Pharm., Chem. Biol. Sci., 3, pp. 546-553; Miller, J.N., Miller, J.C., Statistics and Chemometrics for Analytical Chemistry (2005), fifth ed. Pearson Education Limited England, Harlow
dcterms.sourceScopus

Files

Original bundle

Now showing 1 - 2 of 2
Loading...
Thumbnail Image
Name:
avatar_scholar_256.png
Size:
6.31 KB
Format:
Portable Network Graphics
Description:
Loading...
Thumbnail Image
Name:
spectrochimicaacta_CANA.pdf
Size:
640.05 KB
Format:
Adobe Portable Document Format
Description: