A Synchronous Fluorescence Spectrofluorometric Method for the Simultaneous Determination of Clonazepam and Paroxetine Hydrochloride in Combined Pharmaceutical Dose Form
Abstract:ÖZAmaç: Yüksek spesifiklikte spektral ayırıcılığı, kolay bulunan çözücülerin kullanımı, ekonomik ve çevre dostu oluşu ve ekstraksiyona gerek duymaması sebebiyle birinci türev senkron spektroflorimetri yönteminin üstün olduğu bulundu. Gereç ve Yöntemler: Bu çalışmada farmasötik preparatlardan klonazepam (CLO) ve paroksetin hidroklorürün (PH) eş zamanlı tayini için basit, hassas ve zamandan tasarruf sağlayan birinci türev senkronize spektroflorimetri yöntemi geliştirilmiştir. Bulgular: CLO, 512.79 nm'deki (PH'ni… Show more
“…Upon addition of CLZ to the probe, the fluorescence intensity of PDNPs is enhanced by blocking the quenching effect of π‐π interactions. A comparison of the analytical figure‐of‐merits of the fabricated method and reported methods has been collected in Table 1 2,4,5,8–11,34–39 . The developed probe provided high sensitivity, low cost, and a simple detection process, among other advantages, compared to previously reported platforms.…”
Section: Resultsmentioning
confidence: 99%
“…A comparison of the analytical figure-of-merits of the fabricated method and reported methods has been collected in Table 1. 2,4,5,[8][9][10][11][34][35][36][37][38][39] The developed probe provided high sensitivity, low cost, and a simple detection process, among other advantages, compared to previously reported platforms. Furthermore, its detection performance was investigated in the quantification of CLZ in patients' plasma samples.…”
Section: Analytical Performance Of the Probementioning
Despite the necessity of the study of therapeutic drug monitoring of clonazepam (CLZ), there are only a few fast detection methods available for determining CLZ in biological media. This study aims to develop a cost‐effective and ratiometric probe for the quantification of CLZ in plasma samples. Fluorescent polydopamine nanoparticles were produced through a self‐polymerization process at a pH of 8.5. Rhodamine B molecules were employed as a fluorescent reference material, emitting stable fluorescence in the visible range. The fabricated probe exhibited a specific detection capability for CLZ. The fluorescence emission of the probe was enhanced in two concentration ranges: from 50 ng/mL to 1.0 μg/mL and from 1.0 to 15.0 μg/mL with a lower limit of quantification of 50 ng/mL, indicating the sensitivity of the probe for detecting CLZ plasma levels. The accuracy of the probe is favorable which could be recommended for CLZ monitoring in the biological media. Furthermore, this probe is highly specific towards CLZ in the presence of various interfering agents which is mainly caused by its ratiometric nature. The developed platform showed high reliability in quantifying CLZ concentrations in patients' plasma samples. Hence, the fabricated probe could be recommended as a reliable method for the routine detection of CLZ in clinical settings.
“…Upon addition of CLZ to the probe, the fluorescence intensity of PDNPs is enhanced by blocking the quenching effect of π‐π interactions. A comparison of the analytical figure‐of‐merits of the fabricated method and reported methods has been collected in Table 1 2,4,5,8–11,34–39 . The developed probe provided high sensitivity, low cost, and a simple detection process, among other advantages, compared to previously reported platforms.…”
Section: Resultsmentioning
confidence: 99%
“…A comparison of the analytical figure-of-merits of the fabricated method and reported methods has been collected in Table 1. 2,4,5,[8][9][10][11][34][35][36][37][38][39] The developed probe provided high sensitivity, low cost, and a simple detection process, among other advantages, compared to previously reported platforms. Furthermore, its detection performance was investigated in the quantification of CLZ in patients' plasma samples.…”
Section: Analytical Performance Of the Probementioning
Despite the necessity of the study of therapeutic drug monitoring of clonazepam (CLZ), there are only a few fast detection methods available for determining CLZ in biological media. This study aims to develop a cost‐effective and ratiometric probe for the quantification of CLZ in plasma samples. Fluorescent polydopamine nanoparticles were produced through a self‐polymerization process at a pH of 8.5. Rhodamine B molecules were employed as a fluorescent reference material, emitting stable fluorescence in the visible range. The fabricated probe exhibited a specific detection capability for CLZ. The fluorescence emission of the probe was enhanced in two concentration ranges: from 50 ng/mL to 1.0 μg/mL and from 1.0 to 15.0 μg/mL with a lower limit of quantification of 50 ng/mL, indicating the sensitivity of the probe for detecting CLZ plasma levels. The accuracy of the probe is favorable which could be recommended for CLZ monitoring in the biological media. Furthermore, this probe is highly specific towards CLZ in the presence of various interfering agents which is mainly caused by its ratiometric nature. The developed platform showed high reliability in quantifying CLZ concentrations in patients' plasma samples. Hence, the fabricated probe could be recommended as a reliable method for the routine detection of CLZ in clinical settings.
“…Clonazepam is a benzodiazepine derivative that is widely used as a treatment for sleep disorders, anxiety, muscle relaxant, sedative, and epileptic seizures. It has side effects such as drowsiness and fatigue when low doses lead to dizziness, mood swings, and memory loss at high concentrations (Gurusamy and Thangadurai, 2019;Degreef et al , 2021;Qriouet et al, 2019) .…”
Section: Introductionmentioning
confidence: 99%
“…Several analytical methods have been reported for assay of CLZM in different samples including diazo coupling spectrophotometric methods (Hajir and Kassim, 2020;Ameen and Al-Badry, 2005), Cloud point extraction (CPE) combined with diazocoupling (Abdullah, 2017;Mahdi and Kadhim, 2020), oxidative coupling (Saddam and Kadhim, 2019;Mahdi and Kadim, 2018), charge transfer (Hadi, 2015;Zankanah and Dikran, 2017;Salem et al, 2002), Prussian blue complex (Fadhel and Khamees, 2018), UV-spectrophotometry (Kakde and Satone, 2009;Karajgi et al , 2016), spectrofluorometric (Patel and Chhalotiya, 2017;Belal et al, 2017;Salem et al, 2004).…”
An easy and sensitive spectrophotometric method has been suggested for the assay of clonazepam (CLZM) as pure form and in its formulation as tablets. The present method based on the reaction of CLZM with alizarin red S reagent (ALRS) via proton transfer reaction to form a colored solution with a maximum absorption at wavelength of 528 nm and the optimal conditions for the reaction were studied. The linearity was within the concentration range from 1 to 30 µg/ml, with an R 2 value (determination coefficient) of 0.9888 and the sensitivity express via the molar absorption of 7.04x10 3 l mol -1 .cm -1 , while Sandell's sensitivity index has been determined and equal to 0.0448 µg/ cm 2 .The percentage of relative standard deviation (RSD%) which express the precision of the method, percentage of relative error (RE%) express the accuracy, the LOD and LOQ also have been estimated. The application of the suggested method to the determination of CLZM in tablet gave satisfactory results.
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