The potential of Corona Charged Aerosol Detector for investigation of telmisartan: B-cyclodextrin inclusion complexes

Q4 Pharmacology, Toxicology and Pharmaceutics Arhiv za Farmaciju Pub Date : 2019-01-01 DOI:10.5937/arhfarm1901001m
Nevena Maljurić, Jelena Golubović, Biljana Otašević, Jovana Krmar, M. Zečević, A. Protić
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Abstract

Cyclodextrins (CDs) are widely used in pharmaceutical analysis due to its biodegradability and eco-friendly character. The particular structure of CDs, characterized by hydrophobic cavity, enables the formation of inclusion complexes with variety of organic compounds. As structures lacking chromophores, CDs could not be detected by Photodiode Array (PDA) detector and Corona Charged Aerosol Detector (CAD) was introduced as the most appropriate detector for the formed complexes. The aim of the study was to investigate the degree of complexation between telmisartan, used as a model substance, and β-CD. Moreover, the effect of different β-CD concentrations (5-15 mM) and pH of the aqueous part of mobile phase (3-7) on the degree of complexation was also assessed. The intensity of the formed complex appeared to be the highest when 15 mM β-CD was used for the complexation. Also, it was noticed that the increase in peak areas with an increasing β-CD concentration was more evident at pH 7 in comparison with the same trend at lower pH values. The reproducibility of the measurement was confirmed by low relative standard deviation (RSD) of peak areas within five measurements. These findings support the use of HPLC-CAD methods for studying the process of inclusion complexes formation.
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电晕带电气溶胶检测器用于研究替米沙坦:b -环糊精包合物的潜力
环糊精具有生物可降解性和生态友好性,在药物分析中得到了广泛的应用。CDs具有疏水空腔的特殊结构,可与多种有机化合物形成包合物。由于缺乏发色团的结构,CDs无法通过光电二极管阵列(PDA)检测器检测到,因此引入了电晕带电气溶胶检测器(CAD)作为最合适的检测器来检测形成的配合物。该研究的目的是研究替米沙坦(作为模型物质)与β-CD之间的络合程度。此外,还考察了不同的β-CD浓度(5 ~ 15 mM)和流动相水相pH(3 ~ 7)对络合度的影响。用15mm β-CD络合时,形成的络合物强度最高。在pH为7时,随着β-CD浓度的增加,峰面积的增加更为明显,而在较低的pH值下,这一趋势也更为明显。在5次测量中,峰面积的相对标准偏差(RSD)较低,证实了测量的重复性。这些发现支持使用HPLC-CAD方法来研究包合物形成过程。
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来源期刊
Arhiv za Farmaciju
Arhiv za Farmaciju Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
自引率
0.00%
发文量
19
审稿时长
12 weeks
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