Simultaneous determination of sulfamethoxazole, trimethoprim and bromhexine in veterinary formulation using high performance liquid chromatography (HPLC)

Patrícia Espinosa Dos Santos, Marcos Serrou do Amaral, Nájla Mohamad Kassab
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Abstract

Aim: To develop and to validate a simple, sensitive and fast method for the simultaneous determination of sulfamethoxazole (SMT), trimethoprim (TMP) and bromhexine (BMX) in veterinary formulation by high performance liquid chromatography according to the guidelines of the Validation and Control Guide for analytical quality of medicines in food products and veterinary medicines, RDC 166/2017 and international guides International Conference on Harmonization and International Association of Official Analytical Chemists. Materials and methods:The separation was performed on a ThermoScientific® C18 AcclaimTM120 analytical column (4.6 × 250 mm, 5 µm), with a flow rate of 0.7 mL min-1 and detection at 245 nm, 265 nm and 271 nm, for BMX, SMT and TMP, respectively. All measurements were performed in methanol: water (84:16 v/v; pH 3.0). The analytical curves were linear (r > 0.9997) in the concentration range of 15.0 to 30.0 μg·mL-1 for SMT, 3.0 to 9.0 μg·mL-1 for TMP and 0.5 to 2.0 μg·mL-1 for BMX. Results: The method proved to be accurate, with coefficients of variation below the maximum limit of 2.0%, robust, without significant influence of the variations used in the analysis, exact (recovery >99%) and selective, in the assessment of interference from adjuvants. Conclusion:Therefore, the developed method proved to be suitable for routine quality control analyzes for the simultaneous determination of SMT, TMP and BMX in pharmaceutical formulations.
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高效液相色谱法同时测定兽药制剂中磺胺甲恶唑、甲氧苄啶和溴甲辛的含量
目的:依据《食品兽药中药品分析质量验证与控制指南》,建立兽药制剂中磺胺甲恶唑(SMT)、甲氧苄啶(TMP)和溴甲辛(BMX)的高效液相色谱同时测定方法并进行验证。RDC 166/2017和国际指南国际协调会议和国际官方分析化学家协会。材料和方法:采用ThermoScientific®C18 accclaimtm120分析柱(4.6 × 250 mm, 5µm),流速为0.7 mL min-1,分别在245 nm、265 nm和271 nm检测BMX、SMT和TMP。所有测量均在甲醇:水(84:16 v/v;pH值3.0)。SMT浓度在15.0 ~ 30.0 μg·mL-1范围内、TMP浓度在3.0 ~ 9.0 μg·mL-1范围内、BMX浓度在0.5 ~ 2.0 μg·mL-1范围内均呈线性关系(r > 0.9997)。结果:该方法准确,变异系数低于2.0%的最大限,鲁棒性好,分析中使用的变异系数无显著影响,在评估佐剂干扰方面具有准确性(回收率>99%)和选择性。结论:该方法可用于制剂中SMT、TMP和BMX的常规质量控制分析。
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