Screening Drugs in Saliva

May 20, 2013

E-Separation Solutions

E-Separation Solutions-05-23-2013, Volume 0, Issue 0

A team of scientists from Stockholm University in Sweden has developed a method for screening and determining drugs in human saliva using microextraction by packed sorbent (MEPS) and liquid chromatography tandem mass spectrometry (LC?MS?MS).1

A team of scientists from Stockholm University in Sweden has developed a method for screening and determining drugs in human saliva using microextraction by packed sorbent (MEPS) and liquid chromatography tandem mass spectrometry (LC–MS–MS).1

Traditionally, blood, plasma, and urine are used in drug studies in clinical and preclinical settings. Saliva, on the other hand, offers a non-invasive alternative to these traditional options. A range of drugs and their metabolites can be found in different concentrations in saliva.

MEPS is a miniaturized sample preparation technique invented by lead author of the study, Mohamed Abdel-Rehim, and has been used to extract a wide range of drugs. In this study, published in Biomedical Chromatography, the team used lidocaine, a common local anesthetic, as the drug they extracted from saliva. A sample of 500 mg lidocaine salve was applied topically to the skin and saliva samples were collected at 0, 1, 1.5, 2, 3, and 4 h. The samples were then passed through the MEPS sorbent and analysed by LC–MS–MS.

The team was able to collect an exact volume of saliva at each attempt and high throughput was achieved. When the results were compared with those obtained from plasma, they were found to be similar. The only difference was that the concentration levels were lower in saliva than plasma. The method was also cost-effective because the MEPS sorbent could be used more than 50 times before it was disposed of.

It was concluded that the study was suitable for automation and the small sample collections makes it ideal to obtain samples from children.

Reference

1. A. Abdel-Rehim and M. Abdel-Rehim, Biomedical Chromatography doi: 10.1002/bmc.2925 (2013).