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首页> 外文期刊>Spectrochimica acta, Part A. Molecular and biomolecular spectroscopy >Spectrophotometric and spectrofluorimetric methods for determination of certain biologically active phenolic drugs in their bulk powders and different pharmaceutical formulations
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Spectrophotometric and spectrofluorimetric methods for determination of certain biologically active phenolic drugs in their bulk powders and different pharmaceutical formulations

机译:分光光度法和光谱氟化物方法,用于测定散装粉末和不同药物制剂中某些生物活性酚醛药物

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AbstractTwo simple and sensitive spectrophotometric and spectrofluorimetric methods for the determination of terbutaline sulfate, fenoterol hydrobromide, etilefrine hydrochloride, isoxsuprine hydrochloride, ethamsylate, doxycycline hyclate have been developed. Both methods were based on the oxidation of the cited drugs with cerium (IV) in acid medium. The spectrophotometric method was based on measurement of the absorbance difference (ΔA), which represents the excess cerium (IV), at 317nm for each drug. On the other hand, the spectrofluorimetric method was based on measurement of the fluorescent of the produced cerium (III) at emission wavelength 354nm (λexcitation=255nm) for the concentrations studied for each drug. For both methods, the variables affecting the reactions were carefully investigated and the conditions were optimized. Linear relationships were found between either ΔA or the fluorescent of the produced cerium (III) values and the concentration of the studied drugs in a general concentration range of 2.0–24.0μgmL?1, 20.0–24.0ngmL?1with good correlation coefficients in the following range 0.9990–0.9999, 0.9990–0.9993 for spectrophotometric and spectrofluorimetric methods respectively. The limits of detection and quantitation of spectrophotometric method were found in general concentration range 0.190–0.787 and 0.634–2.624μgmL?1respectively. For spectrofluorimetric method, the limits of detection and quantitation were found in general concentration range 4.77–9.52 and 15.91–31.74ngmL?1respectively. The stoichiometr
机译:<![CDATA [ 抽象 两个简单的和敏感的分光光度和用于测定荧光分析方法硫酸特布他林,氢溴酸非诺特罗,依替福林,盐酸异舒普林盐酸盐,酚磺乙胺化学,多西环素已经被开发。这两种方法都是基于引药的在酸介质中的铈(IV)的氧化。分光光度法是基于吸光度差(ΔA),它代表了过量铈(IV),在317nm为每种药物的测量。在另一方面中,荧光光谱法在发射波长354nm基于荧光的产生的铈(III)的测量(λ激发 = 255nm)为研究每种药物浓度。对于这两种方法,影响了反应变量进行了认真调查和条件进行了优化。发现任一ΔA或荧光所产生的铈(III)的值和所研究的药物在2.0-24.0μgmL的一般浓度范围的浓度之间的线性关系 1 ,20.0-24.0ngmL 1 分别在以下的范围0.9990-0.9999,0.9990-0.9993光度法和荧光光度法方法良好的相关性系数。分别为: 1?检测和分光光度法定量限一般浓度范围0.190-0.787和0.634-2.624μgmL被发现了。分别为: 1?对于荧光光度法方法中,通常的浓度范围4.77-9.52和15.91-31.74ngmL发现检测和定量的极限。该stoichiometr

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