Boltia Shereen A, Soudi Aya T, Elzanfaly Eman S, Zaazaa Hala E
Cairo University, Faculty of Pharmacy, Analytical Chemistry Department, Kasr ElAini St., Cairo, Egypt.
J AOAC Int. 2019 May 1;102(3):794-800. doi: 10.5740/jaoacint.18-0217. Epub 2018 Nov 16.
Traditional methods for Lomefloxacin hydrochloride (LOM) determination involve pretreatment steps, which extend analysis time and use hazardous chemicals. The ability to provide a rapid route without sample pretreatment for quantitative determination of compounds via a low-cost instrument is a challenging task. In this work, a simple potentiometric method was developed to determine the antibacterial LOM via in-house fabricated ion selective electrodes. Different sensors were fabricated using a poly vinyl chloride-based membrane, potassium tetrakis(4-chlorophenyl) borate as a cation exchanger, and 2-Nitrophenyl octyl ether as a plasticizer (sensor 1). To increase the selectivity of sensor 1, a selective molecular recognition component 2-hydroxypropyl-β-cyclodextrin was used as ionophore (sensor 2). The proposed method was validated according to International Union of Pure and Applied Chemistry recommendations, in which the proposed sensors show a linear dynamic range from 1 × 10 to 1 × 10 mol/L, with Nernstian slopes of 55.829 and 58.229 mV/decade for sensors 1 and 2, respectively. It was applied to determine LOM in bulk powder, in different dosage forms, and in plasma with no sample pretreatment. Also, the suggested method can be used as a green, in-line bench top real-time analyzer for in-process monitoring of LOM release from its tablets, under U.S. Food and Drug Administration dissolution regulations, with clear discrimination from common excipients. Results obtained by the proposed potentiometric method were compared with those obtained by a reported HPLC method. The proposed method is considered as a perfect alternative to traditional reported methods for LOM determination.
传统的盐酸洛美沙星(LOM)测定方法需要预处理步骤,这延长了分析时间并使用了危险化学品。通过低成本仪器提供一种无需样品预处理即可对化合物进行定量测定的快速方法是一项具有挑战性的任务。在这项工作中,开发了一种简单的电位法,通过自制的离子选择性电极来测定抗菌药物洛美沙星。使用基于聚氯乙烯的膜、四(4-氯苯基)硼酸钾作为阳离子交换剂和2-硝基苯基辛基醚作为增塑剂制备了不同的传感器(传感器1)。为了提高传感器1的选择性,使用了选择性分子识别成分2-羟丙基-β-环糊精作为离子载体(传感器2)。所提出的方法根据国际纯粹与应用化学联合会的建议进行了验证,其中所提出的传感器显示出线性动态范围为1×10至1×10 mol/L,传感器1和传感器2的能斯特斜率分别为55.829和58.229 mV/十年。该方法无需样品预处理即可用于测定散装粉末、不同剂型和血浆中的洛美沙星。此外,根据美国食品药品监督管理局的溶出度规定,所建议的方法可作为一种绿色的在线台式实时分析仪,用于监测洛美沙星片剂的溶出过程,并且能够与常见辅料进行清晰区分。将所提出的电位法获得的结果与报道的高效液相色谱法获得的结果进行了比较。所提出的方法被认为是传统报道的洛美沙星测定方法的完美替代方法。