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Determining plasma morphine levels using GC-MS after solid phase extraction to monitor drug levels in the postoperative period
Santos, Veronica; López, Karin Jannet Vera; Santos, Luciana Moraes; Yonamine, Mauricio; Carmona, Maria José Carvalho; Santos, Silvia Regina Cavani Jorge.
  • Santos, Veronica; Universidade de São Paulo. School of Pharmaceutical Sciences. São Paulo. BR
  • López, Karin Jannet Vera; Universidade de São Paulo. School of Pharmaceutical Sciences. São Paulo. BR
  • Santos, Luciana Moraes; Universidade de São Paulo. Faculdade de Medicina. Instituto do Coração. São Paulo. BR
  • Yonamine, Mauricio; Universidade de São Paulo. School of Pharmaceutical Sciences. São Paulo. BR
  • Carmona, Maria José Carvalho; Universidade de São Paulo. Faculdade de Medicina. Instituto do Coração. São Paulo. BR
  • Santos, Silvia Regina Cavani Jorge; Universidade de São Paulo. School of Pharmaceutical Sciences. São Paulo. BR
Clinics ; 63(3): 307-314, 2008. graf, tab
Article in English | LILACS | ID: lil-484755
ABSTRACT

OBJECTIVE:

To implement a selective and sensitive analytical method to quantify morphine in small volumes of plasma by gas-liquid chromatography-mass spectrometry (GC-MS), aimed at post-operatively monitoring the drug.

METHOD:

A gas-liquid chromatographic method with mass detection has been developed to determine morphine concentration in plasma after solid phase extraction. Morphine-d3 was used as an internal standard. Only 0.5 mL of plasma is required for the drug solid-phase extraction in the Bond Elut-Certify®, followed by the quantification of morphine derivative by GC-MS using a linear temperature program, a capillary fused silica column, and helium as the carrier and make-up gas. The method was applied to determine morphine content in plasma samples of four patients during the postoperative period of cardiac surgery. Patient-controlled analgesia with morphine was performed by a venous catheter, and a series of venous blood samples were collected. After the oro-After the orotracheal extubation, morphine plasma levels were monitored for up to 36 hours.

RESULTS:

The run time was 16 minutes because morphine and the internal standard were eluted after 8.8 minutes. The GC-MS method had 0.5 -1000 ng/mL linearity range (r²=0.9995), 0.1 ng/mL limit of detection, intraday and interday precision equivalent to 1.9 percent and 6.8 percent, and 0.1 percent and 0.8 percent systematic error (intraday and interday, respectively). The analytical method showed optimal absolute (98 percent) and relative (100.7 percent) recoveries. Morphine dose requirements and plasma levels are discussed.

CONCLUSION:

The analytical gas-liquid chromatography-mass spectrometry method is selective and adequate for morphine measurements in plasma for applications in clinical studies.
Subject(s)

Full text: Available Index: LILACS (Americas) Main subject: Drug Monitoring / Solid Phase Extraction / Analgesics, Opioid / Gas Chromatography-Mass Spectrometry / Morphine Type of study: Diagnostic study / Evaluation studies Limits: Adult / Aged / Female / Humans / Male Language: English Journal: Clinics Journal subject: Medicine Year: 2008 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade de São Paulo/BR

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Full text: Available Index: LILACS (Americas) Main subject: Drug Monitoring / Solid Phase Extraction / Analgesics, Opioid / Gas Chromatography-Mass Spectrometry / Morphine Type of study: Diagnostic study / Evaluation studies Limits: Adult / Aged / Female / Humans / Male Language: English Journal: Clinics Journal subject: Medicine Year: 2008 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade de São Paulo/BR