Online Postcolumn Indirect Detection for Determination of Ibandronate in Pharmaceutical Tablets by HPLC/DAD  

作　　者：Mokhtar Mabrouk Sherin F.Hammad Mohamed A.Abdelaziz Fotouh R.Mansour 

机构地区：[1]Department of Pharmaceutical Analytical Chemistry,Faculty of Pharmacy,Tanta University,Elgeish Street,Tanta 31111,Egypt [2]Pharmaceutical Services Center,Faculty of Pharmacy,Tanta University,Tanta 31111,Egypt [3]Department of Pharmaceutical Analytical Chemistry,Faculty of Pharmacy,Kafrelsheikh University,Kafrelsheikh 33511,Egypt

出　　处：《Journal of Analysis and Testing》2019年第4期322-330,共9页分析检测（英文）

摘　　要：Ibandronate sodium monohydrate is a highly polar aliphatic compound that belongs to the bisphosphonate class,a widely used bone resorption inhibitor.The aliphatic nature of ibandronate precludes direct photometric detection and its high polar-ity urged analysts to use ion-pairing agents in the mobile phase to promote retention in reversed-phase columns.In this work,a reversed-phase method for determination of ibandronate sodium monohydrate in pharmaceutical tablets is introduced by employing an online postcolumn ligand exchange reaction to enable photometric detection.The method offers for the first time the ability to separate the drug from its well-known impurities on conventional reversed-phase columns.The detection reac-tion depends on the ability of ibandronate and its degradation products to displace salicylate in the iron(III)salicylate complex,forming various colorless iron(III)complexes and showing a negative chromatographic signal for ibandronate and its degra-dants atλ_(max)=525 nm.The chromatographic separation was achieved using a Hypersil BDS C_(8) column(5μm particle size,150 mm×4.6 mm i.d.)and a mobile phase consisting of a mixture of aqueous formate buffer pH 3(pH 3,5 mM)and methanol in a ratio of 80:20%(v/v),delivered at a flow rate of 0.8 mL/min.The postcolumn iron(III)salicylate reagent was prepared at 250μM in aqueous formate buffer,delivered using a syringe pump at a flow rate of 0.5 mL/min.The proposed method was validated as per the guidelines of the International Conference on Harmonization Q2(R1)and was found linear over the range 40-120μg/mL(r=0.9995)with a limit of detection of 3.19μg/mL.Compared to currently reported methods,the proposed method is considerably simpler,faster,cheaper,and adequately sensitive and makes use of the most popular LC detectors.

关 键 词：BISPHOSPHONATES Non-chromophoric drugs Highly polar compounds High-performance liquid chromatography Reversed phase 

分 类 号：O62[理学—有机化学]