Muller Aline L H, Oliveira Jussiane S S, Mello Paola A, Muller Edson I, Flores Erico M M
Departamento de Química, Universidade Federal de Santa Maria, 97105-900 Santa Maria, RS, Brazil.
Departamento de Química, Universidade Federal de Santa Maria, 97105-900 Santa Maria, RS, Brazil.
Talanta. 2015 May;136:161-9. doi: 10.1016/j.talanta.2014.12.023. Epub 2014 Dec 29.
In this work a method for active pharmaceutical ingredients (APIs) digestion using the single reaction chamber (SRC-UltraWave™) system was proposed following the new recommendations of United States Pharmacopeia (USP). Levodope (LEVO), primaquine diphosphate (PRIM), propranolol hydrochloride (PROP) and sulfamethoxazole (SULF) were used to evaluate the digestion efficiency of the proposed method. A comparison of digestion efficiency was performed by measuring the carbon content and residual acidity in digests obtained using SRC and in digests obtained using conventional microwave-assisted digestion system (Multiwave(TM)). Three digestion solutions (concentrated HNO3, aqua regia or inverse aqua regia) were evaluated for digestion of APIs. The determination of Cd, Ir, Mn, Mo, Ni, Os, Pb, Pd, Pt, Rh, Ru was performed using inductively coupled plasma mass spectrometry (ICP-MS) in standard mode. Dynamic reaction cell (DRC) mode was used for the determination of (51)V, (52)Cr, (53)Cr, (63)Cu and (65)Cu in order to solve polyatomic ion interferences. Arsenic and Hg were determined using chemical vapor generation coupled to ICP-MS (FI-CVG-ICP-MS). Masses of 500mg of APIs were efficiently digested in a SRC-UltraWave™ system using only HNO3 and allowing a carbon content lower than 250mg L(-1) in final digests. Inverse aqua regia was suitable for digestion of sample masses up to 250mg allowing the determination of Ir, Pd, Pt, Rh and Ru. By using HNO3 or inverse aqua regia, suitable recoveries were obtained (between 91 and 109%) for all analytes (exception for Os). Limits of quantification were in agreement with USP requirements and they ranged from 0.001 to 0.015µg g(-1) for all elemental impurities (exception for Os). The proposed method was suitable for elemental impurities determination in APIs and it can be used in routine analysis for quality control in pharmaceutical industries.
本研究根据美国药典(USP)的新建议,提出了一种使用单反应腔(SRC-UltraWave™)系统消化活性药物成分(API)的方法。使用左旋多巴(LEVO)、磷酸伯氨喹(PRIM)、盐酸普萘洛尔(PROP)和磺胺甲恶唑(SULF)来评估该方法的消化效率。通过测量使用SRC获得的消化液以及使用传统微波辅助消化系统(Multiwave(TM))获得的消化液中的碳含量和残留酸度,对消化效率进行了比较。评估了三种消化液(浓硝酸、王水或逆王水)对API的消化效果。使用电感耦合等离子体质谱(ICP-MS)的标准模式测定镉、铱、锰、钼、镍、锇、铅、钯、铂、铑、钌。为了解决多原子离子干扰问题,使用动态反应池(DRC)模式测定钒(51V)、铬(52Cr、53Cr)、铜(63Cu、65Cu)。使用化学蒸气发生-电感耦合等离子体质谱联用(FI-CVG-ICP-MS)测定砷和汞。在SRC-UltraWave™系统中仅使用硝酸,500mg的API能够被有效消化,最终消化液中的碳含量低于250mg L(-1)。逆王水适用于消化质量高达250mg的样品,可用于测定铱、钯、铂、铑和钌。使用硝酸或逆王水时,所有分析物(锇除外)的回收率都很合适(在91%至109%之间)。定量限符合USP要求,所有元素杂质(锇除外)的定量限范围为0.001至0.015µg g(-1)。所提出的方法适用于API中元素杂质的测定,可用于制药行业质量控制的常规分析。