2017
DOI: 10.1002/bio.3292
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Utility of Hantzsch reaction for development of highly sensitive spectrofluorimetric method for determination of alfuzosin and terazosin in bulk, dosage forms and human plasma

Abstract: A highly sensitive, cheap, simple and accurate spectrofluorimetric method has been developed and validated for the determination of alfuzosin hydrochloride and terazosin hydrochloride in their pharmaceutical dosage forms and in human plasma. The developed method is based on the reaction of the primary amine moiety in the studied drugs with acetylacetone and formaldehyde according to the Hantzsch reaction, producing yellow fluorescent products that can be measured spectrofluorimetrically at 480 nm after excitat… Show more

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Cited by 26 publications
(7 citation statements)
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“…Into a centrifuge tube, 1.0 mL of human plasma was spiked with adequate amount of MOD solution. then furtherly 1 mL of methanol were added as protein precipitating agent [ 22 , 23 ]. The mixture was vortexed for 30 s and then completed to 10 mL.…”
Section: Methodsmentioning
confidence: 99%
“…Into a centrifuge tube, 1.0 mL of human plasma was spiked with adequate amount of MOD solution. then furtherly 1 mL of methanol were added as protein precipitating agent [ 22 , 23 ]. The mixture was vortexed for 30 s and then completed to 10 mL.…”
Section: Methodsmentioning
confidence: 99%
“…Acetonitrile was added (2 mL) as a protein precipitating agent. [10][11][12] The resultant supernatant solution was completed to 10 mL with distilled water and then centrifugation at 4000 rpm for 20 min. Furthermore, 2 mL of the supernatant was used to provide the final concentration range (40-500 ng mL −1 ) in the general procedure.…”
Section: Figurementioning
confidence: 99%
“…The Hantzsch reaction is widely used for both spectrophotometric and spectrofluorimetric analysis of drugs. [25][26][27][28] The developed method was dependent on the interaction between aliphatic primary amino groups found in heptaminol and ethyl acetoacetate and formaldehyde, giving a yellow coloured and fluorescent dihydropyridine derivative that showed a maximum fluorescence at 416 nm (excitation at 350 nm) (Figures 2 and 3).…”
Section: Resultsmentioning
confidence: 99%