用简单灵敏的分光光度法测定药品中的特比萘芬盐酸盐抗真菌药

Q4 Pharmacology, Toxicology and Pharmaceutics Ankara Universitesi Eczacilik Fakultesi Dergisi Pub Date : 2024-07-14 DOI:10.33483/jfpau.1348367
N. Qarah, Ezzouhra El-maaıden, K. Basavaiah
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引用次数: 0

摘要

目的利用高锰酸钾(PP)和 2-(1,3-二氧代-2,3-二氢-1H-茚-2-基)喹啉-6,8-二磺酸钠(DSOQ),开发并验证了两种高灵敏、准确、廉价且简单的分光光度法,用于测定纯药和片剂中的抗真菌药物盐酸特比萘芬(TBH):本研究以赛比芬和特比萘芬 250 毫克片剂为药品,以高锰酸钾 KMnO4 和 2-(1,3-二氧代-2,3-二氢-1H-茚-2-基)喹啉-6,8-二磺酸钠水溶液为试剂,使用配备 1 厘米匹配石英池的 DR 3900 分光光度计测量吸光度:测定了盐酸特比萘芬与高锰酸盐和 2-(1,3-二氧代-2,3-二氢-1H-茚-2-基)喹啉-6,8-二磺酸钠在酸性介质中的反应量。两种情况下的有色反应产物分别在 540 纳米和 440 纳米的最大吸收波长处测定。每次测定中测得的吸光度都与 TBH 浓度有关。对不同的实验和检测条件进行了仔细、精确的研究和优化。两种检测方法的验证也是按照国际协调会议(ICH)的现行指南进行的。PP 和 DSOQ 方法在 1-15 µg/ml 和 1-18 µg/ml 浓度范围内分别符合比尔定律(相关系数分别为 0.9983 和 0.9989)。PP 方法的摩尔吸收率、检出限和定量限(LOD 和 LOQ)值分别为(1.38×104 升/摩尔厘米、0.92 和 2.78 微克/毫升),DSOQ 方法的摩尔吸收率、检出限和定量限(LOD 和 LOQ)值分别为(1.73×104 升/摩尔厘米、0.09 和 0.27 微克/毫升)。这两种检测方法被成功地应用于商品片剂中 TBH 的测定,结果可靠且令人满意,因此建议的检测方法可应用于制药实验室的质量控制。
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SIMPLE AND SENSITIVE SPECTROPHOTOMETRIC ASSAYS FOR THE DETERMINATION OF TERBINAFINE HCL ANTIFUNGAL DRUG IN PHARMACEUTICALS
Objective: Two highly sensitive, accurate, inexpensive, and simple spectrophotometric assays were developed and validated for the determination of an anti-fungal drug, Terbinafine HCl (TBH), in pure drug and tablets using potassium permanganate (PP) and disodium 2-(1,3-dioxo-2,3-dihydro-1H-inden-2-yl)quinoline-6,8-disulfonate (DSOQ). Material and Method: In the present study, Sebifin and Terbiforce 250 mg tablets were used as pharmaceuticals, potassium permanganate KMnO4 and disodium 2-(1,3-dioxo-2,3-dihydro-1H-inden-2-yl)quinoline-6,8-disulfonate in water were used as reagents, and DR 3900 spectrophotometer equipped with 1cm matched quartz cells was used for absorbance measurements. Result and Discussion: The amount of terbinafine hydrochloride reacting with permanganate and disodium 2-(1,3-dioxo-2,3-dihydro-1H-inden-2-yl)quinoline-6,8-disulfonate in an acidic medium has been determined. The colored reaction products in both cases were measured at the maximum absorptions of 540 nm and 440 nm, respectively. The absorbance measured in each assay as a function of TBH concentration was related to TBH concentrations. Different experimental and variable conditions of assays were done carefully, accurately studied, and optimized. The validation of two assays also was done by following the current guidelines of the International Conference on Harmonization (ICH). Beer’s law for the two methods is obeyed over the concentration ranges 1-15 µg/ml (Correlation coefficient = 0.9983) and 1-18 µg/ml (Correlation coefficient = 0.9989) for methods PP and DSOQ, respectively. Molar absorptivity, limits of detection, and quantification (LOD & LOQ) values were (1.38×104 l/ mol cm, 0.92 & 2.78 µg/ml) for PP assay, and (1.73×104 l/ mol cm, 0.09 & 0.27 µg/ml) for DSOQ assay, respectively. The two assays were successfully applied for the determination of TBH in commercial tablets with reliable and satisfactory results, and hence the proposed assays can be applied in pharmaceutical laboratories of quality control.
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来源期刊
Ankara Universitesi Eczacilik Fakultesi Dergisi
Ankara Universitesi Eczacilik Fakultesi Dergisi Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
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0.80
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