2015
DOI: 10.1186/s40543-015-0045-6
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Selective spectrofluorimetric method for the determination of perindopril erbumine in bulk and tablets through derivatization with dansyl chloride

Abstract: Background: Perindopril erbumine is an antihypertensive, which belongs to the category of angiotensin-converting enzyme inhibitors (ACE inhibitors) that inhibit the conversion of angiotensin I to angiotensin II. Methods: A new, selective, and sensitive spectrofluorimetric method was developed for the determination of perindopril erbumine based on the reaction with dansyl chloride in alkaline medium to give a highly fluorescent derivative which was measured at 496 nm after excitation at 340 nm in dichloromethan… Show more

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Cited by 13 publications
(10 citation statements)
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“…As a luminous derivatizing reagent for amino-containing compounds, o -phthalaldehyde in conjunction with a mercapto molecule, such as β-mercaptoethanol, is commonly used. Several medicinal molecules have been identified using this method [ 36 , 37 , 38 , 39 , 40 ]. In the presence of β-mercaptoethanol in a borate buffer, ARP and CLZ reacted with benzene-1,2-dicarboxaldehyde to generate a strongly fluorescent compound with maximal fluorescence at 450 nm following excitation at 340 nm ( Figure 1 ).…”
Section: Resultsmentioning
confidence: 99%
“…As a luminous derivatizing reagent for amino-containing compounds, o -phthalaldehyde in conjunction with a mercapto molecule, such as β-mercaptoethanol, is commonly used. Several medicinal molecules have been identified using this method [ 36 , 37 , 38 , 39 , 40 ]. In the presence of β-mercaptoethanol in a borate buffer, ARP and CLZ reacted with benzene-1,2-dicarboxaldehyde to generate a strongly fluorescent compound with maximal fluorescence at 450 nm following excitation at 340 nm ( Figure 1 ).…”
Section: Resultsmentioning
confidence: 99%
“…Perindopril (PER) is an antihypertensive nonsulfhydryl angiotensin‐converting enzyme (ACE) inhibitor that is used to treat hypertension and stable coronary artery disease with the nomenclature of (2 S ,3 aS ,7 aS )‐1‐[(2 S )‐2‐[[(2 S )‐1‐ethoxy‐1‐oxopentan‐2‐yl]amino]propanoyl]‐2,3,3 a ,4,5,6,7,7 a ‐octahydroindole‐2‐carboxylic acid (Figure 1b). For determining PER alone or in combination, various analytical procedures have been published including spectrophotometry [3, 4, 7, 8, 43–45], spectrofluorimetry [46–49], and chromatographic approaches including TLC [30], LC–MS/MS [31] and HPLC [4, 34–36, 39, 50, 51].…”
Section: Introductionmentioning
confidence: 99%
“…The approach was simple, sensitive, and validated according to International Council on Harmonization (ICH) guidelines. The proposed method had higher sensitivity than many of the previously reported methods [19, 20, 23, 25, 28, 46–49]. In addition, some of the reported methods required elevated temperature, were time consuming, and were carried out in the presence of concentrated acids [28, 49].…”
Section: Introductionmentioning
confidence: 99%
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“…1-b). For determination of PER alone or in combination, a variety of analytical techniques have been reported including spectrophotometric techniques (El-Bagary et al 2016;Hegazy et al 2015;Karadurmuş et al 2018;Magdy et al 2018;Rahman et al 2017;Saad et al 2016;Siridevi et al 2019), spectrofluorimetric techniques (Al-Haj Sakur et al 2015Fael and Sakur 2015a, b;Sakur et al 2015) and chromatographic techniques including TLC-densitometry (Patel et al 2020a, b), LC-MS/MS (Rezk and Badr 2020) and HPLC (Duraisamy and Jaganathan 2017;Hassan et al 2020;Hemdan et al 2018;Karadurmuş et al 2018;Naik et al 2020;Patel et al 2020a, b;Saleh et al 2020).…”
Section: Introductionmentioning
confidence: 99%