A combination of isocratic and gradient elution modes in HPLC with the aid of time-overlapping process for rapid determination of methyldopa in human urine

dc.AffiliationOctober University for modern sciences and Arts (MSA)
dc.contributor.authorEmara S.
dc.contributor.authorMasujima T.
dc.contributor.authorZarad W.
dc.contributor.authorKamal M.
dc.contributor.authorFouad M.
dc.contributor.authorEl-Bagary R.
dc.contributor.otherDepartment of Pharmaceutical Chemistry
dc.contributor.otherFaculty of Pharmacy
dc.contributor.otherMisr International University
dc.contributor.otherKm 28 Ismailia Road
dc.contributor.otherIsmailia
dc.contributor.otherCairo
dc.contributor.other41522
dc.contributor.otherEgypt; P.I. Lab. Single Cell MS
dc.contributor.otherRIKEN Quantitative Biology Center
dc.contributor.otherSuita
dc.contributor.otherOsaka
dc.contributor.otherJapan; Department of Pharmaceutical Analytical Chemistry
dc.contributor.otherFaculty of Pharmacy
dc.contributor.otherModern Sciences and Arts University
dc.contributor.otherCairo
dc.contributor.otherEgypt; Department of Pharmaceutical Chemistry
dc.contributor.otherFaculty of Pharmacy
dc.contributor.otherCairo University
dc.contributor.otherCairo
dc.contributor.otherEgypt
dc.date.accessioned2020-01-09T20:42:03Z
dc.date.available2020-01-09T20:42:03Z
dc.date.issued2015
dc.descriptionScopus
dc.description.abstractA new rapid time-overlapping high-performance liquid chromatography method using coupled-column double-injection technique with fluorescence detection has been developed and validated to determine methyldopa (MTD) in human urine. The method was based on injecting a new sample onto the second column before finalizing the cleanup and the re-equilibration of the first column for the former sample. A combination of isocratic and gradient elution was employed according to a pre-set program. At the beginning, isocratic step of acetate buffer solution (0.1 M, pH 2.4) was set until 7 min. Subsequently, a gradient elution step using acetate buffer (0.1 M, pH 2.4) as mobile phase A and acetonitrile as mobile phase B was employed. After the end of each gradient step, the column was re-equilibrated with 4 mL of the starting isocratic elution system before the next analysis. The overall cycle time was 7 min per each sample. The calibration curve was linear over the concentration range of 0.1-40 ?g/mL MTD. The overall mean recoveries were in the range of 98.29-101.39%. The applicability of the method was successfully evaluated by monitoring the incremental urinary excretion of MTD in human urine over 12 hr after a single oral administration of 250 mg. � 2015 Taylor & Francis Group, LLC.en_US
dc.description.urihttps://www.scimagojr.com/journalsearch.php?q=24640&tip=sid&clean=0
dc.identifier.doihttps://doi.org/10.1080/10826076.2014.896813
dc.identifier.doiPubMed ID :
dc.identifier.issn10826076
dc.identifier.otherhttps://doi.org/10.1080/10826076.2014.896813
dc.identifier.otherPubMed ID :
dc.identifier.urihttps://t.ly/BXOwp
dc.language.isoEnglishen_US
dc.publisherTaylor and Francis Inc.en_US
dc.relation.ispartofseriesJournal of Liquid Chromatography and Related Technologies
dc.relation.ispartofseries38
dc.subjectOctober University for Modern Sciences and Arts
dc.subjectجامعة أكتوبر للعلوم الحديثة والآداب
dc.subjectUniversity of Modern Sciences and Arts
dc.subjectMSA University
dc.subjectcoupled-columnen_US
dc.subjectdouble injectionen_US
dc.subjectfluorescence detectionen_US
dc.subjectHPLCen_US
dc.subjectmethyldopaen_US
dc.subjectmixed elution modesen_US
dc.subjectCoupled-columnen_US
dc.subjectElution modesen_US
dc.subjectFluorescence detectionen_US
dc.subjectHPLCen_US
dc.subjectMethyldopaen_US
dc.subjectacetic aciden_US
dc.subjectacetonitrileen_US
dc.subjectbufferen_US
dc.subjectmethyldopaen_US
dc.subjectArticleen_US
dc.subjectcalibrationen_US
dc.subjectelutionen_US
dc.subjectfluorescenceen_US
dc.subjecthigh performance liquid chromatographyen_US
dc.subjecthumanen_US
dc.subjectpHen_US
dc.subjectquality controlen_US
dc.subjecttimeen_US
dc.subjecturinalysisen_US
dc.subjecturinary excretionen_US
dc.subjectvalidation studyen_US
dc.titleA combination of isocratic and gradient elution modes in HPLC with the aid of time-overlapping process for rapid determination of methyldopa in human urineen_US
dc.typeArticleen_US
dcterms.isReferencedByBenowitz, N.L., (2004) Basic and Clinical Pharmacology, p. 166. , 9th ed.; Katzung, B. G., Ed.; The McGraw-Hill Companies: New York; (2000) The United States Pharmacopoeial Convention, , The United States Pharmacopoeia, 24th ed. Rockville, MD; Salem, F.B., Spectrophotometric and fluorimetric determination of catecholamines (1993) Anal. Lett, 26 (2), pp. 281-294; Ribeiro, P.R.S., Pezza, L., Pezza, H.R., Spectrophotometric determination of methyldopa in pharmaceutical formulation (2005) Ecl� Tica Qu�mi, 30 (3), pp. 23-28; Alexey, E.P., Anastasia, V.D., Svetlana, V.M., Tatiana, N.S., A peroxidase-based method for the determination of dopamine, adrenaline, and a-methyldopa in the presence of thyroid hormones in pharmaceutical forms (2011) Talanta, 84 (3), pp. 710-716; Athanasiou-Malaki, E.M., Koupparis, M.A., Indirect potentiometric determination of a-amino acids with a copper-selective electrode and determination of dopa and methyldopa in pharmaceutical preparations (1984) Anal. Chim. Acta, 161, pp. 349-353; Martens, J., Guenther, K., Schickedanz, M., Resolution of optical isomers by thin-layer chromatography: Enantiomeric purity of methyldopa (1986) Archiv. Pharm, 319 (6), pp. 572-574; Watson, J.R., Lawrence, R.C., Specific quantitative gas-liquid chromatographic analysis of methyldopa and some foreign related amino acids in raw material and commercial tablets (1975) J. Chromatogr. A, 103 (1), pp. 63-70; Rosa, M.V.C., Jose, M.S.M., Jose, R.T.L., Guillermo, R.R., Analysis of pharmaceutical preparations containing catecholamines by micellar liquid chromatography with spectrophotometric detection (1995) Analyst, 120 (6), pp. 1767-1772; R�na, K., Ary, K., Gach�lyi, B., Klebovich, I., Determination of a-methyldopa in human plasma by validated high-performance liquid chromatography with fluorescence detection (1996) J. Chromatogr. A, 730 (1-2), pp. 125-131; Li, S.F., Wu, H.L., Yu, Y.J., Li, Y.N., Nie, J.F., Fu, H.Y., Yu, R.Q., Quantitative analysis of levodopa carbidopa and methyldopa in human plasma samples using HPLC-DAD combined with second-order calibration based on alternating trilinear decomposition algorithm (2010) Talanta, 81 (3), pp. 805-812; Bahrami, G., Kiani, A., Mirzaeei, S., A rapid high performance liquid chromatographic determination of methyldopa in human serum with fluorescence detection and alumina extraction: Application to a bioequivalence study (2006) J. Chromatogr. B, 832 (2), pp. 197-201; Ze?evi?, M., �ivanovi?, L.J., Agatonovic-Kustrin, S., Minic, D., The use of a response surface methodology on HPLC analysis of methyldopa, amiloride and hydrochlorothiazide in tablets (2001) J. Pharm. Biomed. Anal, 24 (5-6), pp. 1019-1025; Muzzi, C., Bertocci, E., Terzuoli, L., Porcelli, B., Ciari, I., Pagani, R., Guerranti, R., Simultaneous determination of serum concentrations of levodopa, dopamine, 3-o-methyldopa and a-methyldopa by HPLC (2008) Biomed. Pharmacother, 62 (4), pp. 253-258; Lucarelli, C., Betto, P., Ricciarello, G., Grossi, G., High- performance liquid chromatographic determination of L-3 3,4- dihydroxyphenyl)-2-methylalanine (a-methyldopa) in human urine and plasma (1991) J. Chromatogr. A, 541 (1-2), pp. 285-296; Kochak, G.M., Mason, W.D., Determination of free methyldopa in plasma by high-pressure liquid chromatography and electrochemical detection (1980) J. Pharm. Sci, 69 (8), pp. 897-900; Mell, L.D., Gustafson, A.B., Urinary free methyldopa determined by reversed-phase high-performance liquid chromatography (1978) Clin. Chem, 24 (1), pp. 23-26; Metwally, M., Stability-indicating high-performance liquid chromatographic assay for a-methyldopa in sustained-release capsules (1991) J. Chromatogr. A, 549 (1-2), pp. 221-228; Ehrenstr�m, F., Johansson, P., A method for very rapid determinations of catechols using ion-pairing reverse phase hplc with electrochemical detection: Effects of l-dopa treatment on the catechol content in various rat brain structures (1985) Life Sci, 36 (9), pp. 867-879; Causon, R.C., Carruthers, M.E., Measurement of catecholamines in biological fluids by high-performance liquid chromatography: A comparison of fluorimetric with electrochemical detection (1982) J. Chromatogr. B, 229 (2), pp. 301-309; Cooper, M.J., �dea, R.F., Mirkin, B.L., Determination of methyldopa and metabolites in human serum by high- performance liquid chromatography with electrochemical detection (1979) J. Chromatogr. B, 162 (4), pp. 601-604; Munion, G.L., Seaton, J.F., Harrison, T.S., HPLC for urinary catecholamines and metanephrines with alpha-methyldopa (1983) J. Surg. Res, 35 (6), pp. 507-514; Kochak, G.M., Mason, W.D., A simplified method of determining free methyldopa in urine (1981) Anal. Lett, 14 (6), pp. 439-449; Ribeiro, P.R., Neto, J.A., Pezza, L., Pezza, H.R., Flow-injection spectrophotometric determination of methyldopa in pharmaceutical formulations (2005) Talanta, 67 (1), pp. 240-244; Ali, S.A., Sami, M.A., Cyclic voltametric study of alpha- methyldopa at carbon paste electrode (2005) Pak. J. Pharm. Sci, 18 (1), pp. 6-17; Talebpour, Z., Haghgoo, S., Shamsipur, M., 1H nuclear magnetic resonance spectroscopy analysis for simultaneous determination of levodopa carbidopa and methyldopa in human serum and pharmaceutical formulations (2004) Anal. Chim. Acta, 506 (1), pp. 97-104; Matthieu, T., Debora, C.D.V.B., Jose, A.R.R., Kinetic method for the determination of a-methyldopa in pharmaceutical preparations: Analytical procedure and reaction mechanism considerations (2006) Anal. Lett, 39 (2), pp. 327-339; Stewart, J.T., Lo, H.C., Mason, W.D., Determination of methyldopa in pharmaceutical dosage forms and biological fluids based on oxidation at the tubular carbon electrode (1974) J. Pharm. Sci, 63 (6), pp. 954-955; Ballantine, J., Woolfson, A.D., Determination of catecholamines in pharmaceutical preparations by differential pulse polarography at the glassy carbon electrode (1979) Int. J. Pharm, 3 (4-5), pp. 239-246; Salmanipour, A., Taher, M.A., Beitollahi, H., Voltammetric behavior of a multi-walled carbon nanotube modified electrode- ferrocene electrocatalyst system as a sensor for determination of methyldopa in the presence of folic acid (2012) Anal. Methods, 4 (9), pp. 2982-2988; Shahrokhian, S., Rastgar, S., Electrodeposition of pt-ru nanoparticles on multi-walled carbon nanotubes: Application in sensitive voltammetric determination of methyldopa (2011) Electrochim. Acta, 58, pp. 125-133; Gholivand, M.B., Amiri, M., Preparation of polypyrrole=nuclear fast red films on gold electrode and its application on the electrocatalytic determination of methyl-dopa and ascorbic acid (2009) Electroanalysis, 21 (22), pp. 2461-2467; Gholivand, M.B., Amiri, M., Highly sensitive and selective determination methyldopa in the presence of ascorbic acid using oppy=ty=au modified electrode (2013) J. Electroanal. Chem, 694, pp. 56-60; Rezaei, B., Askarpour, N., Ensafi, A.A., Adsorptive stripping voltammetry determination of methyldopa on the surface of a carboxylated multiwall carbon nanotubes modified glassy carbon electrode in biological and pharmaceutical samples (2013) Colloids Surf. B, 109, pp. 253-258; Oliveira, C.H., Barrientos-Astigarraga, R.E., Sucupira, M., Graudenz, G.S., Muscar�, M.N., De, N.G., Quantification of methyldopa in human plasma by high-performance liquid chromatography-electrospray tandem mass spectrometry application to a bioequivalence study (2002) J. Chromatogr. B, 768 (2), pp. 341-348; (2005) Validation of Analytical Procedures: Text and Methodology, , Guideline ICH Q2 R1 The International Conference on Harmonization: London
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:
MethyldopainUrinemyPaper.pdf
Size:
520.35 KB
Format:
Adobe Portable Document Format
Description: