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Determination of cocaine adulterants in human urine by dispersive liquid-liquid microextraction and high-performance liquid chromatography.
da Silva, Pedro Rafael; Sena, Laís Cristina Santana; Silva, Rubens Pedro Lorena; de Santana, Danielle Cristine Almeida Silva; de Santana, Fernando José Malagueño.
Afiliación
  • da Silva PR; Pharmaceutical Science Department, Federal University of Pernambuco, Prof. Artur de Sá S/N; Cidade Universitária, Recife, PE, 50740-521, Brazil.
  • Sena LCS; Laboratory of Forensic Toxicology, Criminalistics Institute, Secretary of Social Defense of Pernambuco, Marquês de Pombal 455, Santo Antônio, Recife, PE, 50100-170, Brazil.
  • Silva RPL; Pharmaceutical Science Department, Federal University of Pernambuco, Prof. Artur de Sá S/N; Cidade Universitária, Recife, PE, 50740-521, Brazil.
  • de Santana DCAS; Pharmaceutical Science Department, Federal University of Pernambuco, Prof. Artur de Sá S/N; Cidade Universitária, Recife, PE, 50740-521, Brazil.
  • de Santana FJM; Pharmaceutical Science Department, Federal University of Pernambuco, Prof. Artur de Sá S/N; Cidade Universitária, Recife, PE, 50740-521, Brazil. fmalagueno@hotmail.com.
Anal Bioanal Chem ; 411(16): 3447-3461, 2019 Jun.
Article en En | MEDLINE | ID: mdl-31123783
This study aimed to determine simultaneously five major street cocaine adulterants (caffeine, lidocaine, phenacetin, diltiazem, and hydroxyzine) in human urine by dispersive liquid-liquid microextraction (DLLME) and high-performance liquid chromatography. The chromatographic separation was obtained in gradient elution mode using methanol:water plus trifluoroacetic acid 0.15% (v/v) (pH = 1.9) at 1 mL min-1 as mobile phase, at 25 °C, detection at 235 nm, and analysis time of 20 min. The effect of major DLLME operating parameters on extraction efficiency was explored using the multifactorial experimental design approach. The optimum extraction condition was set as 4 mL human urine sample alkalized with 0.5 M sodium phosphate buffer (pH 12), NaCl (15%, m/v), 300 µL acetonitrile (dispersive solvent), and 800 µL chloroform (extraction solvent). Linear response (r2 ≥ 0.99) was obtained in the range of 180-1500 ng mL-1 with suitable selectivity, quantification limit (180 ng mL-1), mean recoveries (33.43-76.63%), and showing relative standard deviation and error (within and between-day assays) ≤15%. The analytes were stable after a freeze-thaw cycle and a short-term room temperature stability test. This method was successfully applied in real samples of cocaine users, suggesting that our study may contribute to the appropriate treatment of cocaine dependence or with the cases of cocaine acute intoxication.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Drogas Ilícitas / Cromatografía Líquida de Alta Presión / Cocaína / Microextracción en Fase Líquida Idioma: En Revista: Anal Bioanal Chem Año: 2019 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Drogas Ilícitas / Cromatografía Líquida de Alta Presión / Cocaína / Microextracción en Fase Líquida Idioma: En Revista: Anal Bioanal Chem Año: 2019 Tipo del documento: Article