Departamento de Farmácia, Universidade Federal do Paraná, Av. Lothário Meissner, 632, 80210-170 Curitiba, PR, Brazil; Polícia Científica do Paraná, Instituto de Criminalística, Av. Visconde de Guarapuava, 2652, 80010-100 Curitiba, PR, Brazil.
Departamento de Farmácia, Universidade Federal do Paraná, Av. Lothário Meissner, 632, 80210-170 Curitiba, PR, Brazil.
Forensic Sci Int. 2014 Feb;235:32-9. doi: 10.1016/j.forsciint.2013.11.013. Epub 2013 Dec 19.
Here, an HPLC-DAD method was developed and validated for simultaneous determination of cocaine, two cocaine degradation products (benzoylecgonine and benzoic acid), and the main adulterants found in products based on cocaine (caffeine, lidocaine, phenacetin, benzocaine and diltiazem). The new method was developed and validated using an XBridge C18 4.6mm×250mm, 5μm particle size column maintained at 60°C. The mobile phase consisted of a gradient of acetonitrile and ammonium formate 0.05M - pH 3.1, eluted at 1.0mL/min. The volume of injection was 10μL and the DAD detector was set at 274nm. Method validation assays demonstrated suitable sensitivity, selectivity, linearity, precision and accuracy. For selectivity assay, a MS detection system could be directly adapted to the method without the need of any change in the chromatographic conditions. The robustness study indicated that the flow rate, temperature and pH of the mobile phase are critical parameters and should not be changed considering the conditions herein determined. The new method was then successfully applied for determining cocaine, benzoylecgonine, benzoic acid, caffeine, lidocaine, phenacetin, benzocaine and diltiazem in 115 samples, seized in Brazil (2007-2012), which consisted of cocaine paste, cocaine base and salt cocaine samples. This study revealed cocaine contents that ranged from undetectable to 97.2%, with 97 samples presenting at least one of the degradation products or adulterants here evaluated. All of the studied degradation products and adulterants were observed among the seized samples, justifying the application of the method, which can be used as a screening and quantification tool in forensic analysis.
这里,开发并验证了一种 HPLC-DAD 方法,用于同时测定可卡因、两种可卡因降解产物(苯甲酰爱康宁和苯甲酸),以及在基于可卡因的产品中发现的主要杂质(咖啡因、利多卡因、非那西汀、苯佐卡因和地尔硫䓬)。新方法使用 XBridge C18 4.6mm×250mm,5μm 粒径柱,在 60°C 下进行开发和验证。流动相由乙腈和 0.05M 甲酸铵组成的梯度洗脱,流速为 1.0mL/min。进样量为 10μL,DAD 检测器设置为 274nm。方法验证试验表明该方法具有良好的灵敏度、选择性、线性、精密度和准确度。对于选择性试验,可以直接将 MS 检测系统应用于该方法,而无需对色谱条件进行任何更改。稳健性研究表明,流动相的流速、温度和 pH 值是关键参数,在考虑本文确定的条件下不应改变。该新方法随后成功应用于测定巴西(2007-2012 年)缴获的 115 个可卡因糊剂、可卡因碱和盐可卡因样品中的可卡因、苯甲酰爱康宁、苯甲酸、咖啡因、利多卡因、非那西汀、苯佐卡因和地尔硫䓬。该研究揭示了可卡因含量从不可检测到 97.2%不等,97 个样品至少含有一种本文评估的降解产物或杂质。在所研究的降解产物和杂质都在缴获的样品中观察到,这证明了该方法的应用,该方法可以作为法医分析中的筛查和定量工具。