Automated Extraction of a Drugs of Abuse Panel from Human Urine Using Biotage Extrahera LV-200 and Microelution SPE Prior to UPLC-MS/MS Analysis
Applications | 2021 | BiotageInstrumentation
The reliable detection of a broad spectrum of drugs of abuse in urine is critical in clinical toxicology, forensic investigations and workplace testing. Automated microelution SPE coupled with UHPLC-MS/MS improves sample throughput, reduces solvent consumption and minimizes variability, addressing key challenges in high-volume laboratories.
This study aimed to develop and validate an automated extraction workflow for a multi-class panel of illicit and prescription drugs in hydrolyzed human urine. It compared manual and automated processing using mixed-mode strong cation exchange microelution plates on the Biotage Extrahera LV-200, evaluating recovery, precision, linearity and limits of quantitation.
One-milliliter urine samples were spiked with deuterated internal standards and hydrolyzed with β-glucuronidase at 60 °C for 2 h. Samples were diluted in ammonium acetate buffer (pH 5) and loaded onto 2 mg mixed-mode SCX microelution plates. The SPE protocol included conditioning (methanol), equilibration (4 % phosphoric acid), sequential washes (phosphoric acid and 50:50 water/methanol) and elution with dichloromethane/methanol/ammonium hydroxide (78:20:2). Eluates were evaporated, reconstituted in water/methanol (90:10, 0.1 % formic acid) and analyzed by UHPLC-MS/MS.
Both workflows produced mean recoveries above 60 % with RSDs below 5 % (n=7) across more than 30 analytes. Calibration curves spanning 1–1000 pg/mL achieved R² > 0.999. Lower limits of quantitation ranged from 1 to 250 pg/mL. Automated extraction of 96 samples required approximately 25 minutes (excluding hydrolysis and evaporation), matching or exceeding the performance of manual SPE in reproducibility and throughput.
Emerging advancements may include further SPE miniaturization, direct on-line coupling to LC-MS systems, expanded target lists for novel psychoactive substances and AI-driven workflow optimization. Green chemistry approaches and integrated robotic platforms will continue to enhance efficiency and sustainability.
The automated mixed-mode SCX microelution SPE method implemented on the Biotage Extrahera LV-200 delivers consistent, high-throughput extraction of a comprehensive drugs of abuse panel in urine, with excellent recoveries, precision and sensitivity, streamlining laboratory operations.
Sample Preparation, LC/MS, LC/MS/MS, LC/QQQ
IndustriesForensics
ManufacturerBiotage
Summary
Significance of the Topic
The reliable detection of a broad spectrum of drugs of abuse in urine is critical in clinical toxicology, forensic investigations and workplace testing. Automated microelution SPE coupled with UHPLC-MS/MS improves sample throughput, reduces solvent consumption and minimizes variability, addressing key challenges in high-volume laboratories.
Objectives and Overview
This study aimed to develop and validate an automated extraction workflow for a multi-class panel of illicit and prescription drugs in hydrolyzed human urine. It compared manual and automated processing using mixed-mode strong cation exchange microelution plates on the Biotage Extrahera LV-200, evaluating recovery, precision, linearity and limits of quantitation.
Methodology
One-milliliter urine samples were spiked with deuterated internal standards and hydrolyzed with β-glucuronidase at 60 °C for 2 h. Samples were diluted in ammonium acetate buffer (pH 5) and loaded onto 2 mg mixed-mode SCX microelution plates. The SPE protocol included conditioning (methanol), equilibration (4 % phosphoric acid), sequential washes (phosphoric acid and 50:50 water/methanol) and elution with dichloromethane/methanol/ammonium hydroxide (78:20:2). Eluates were evaporated, reconstituted in water/methanol (90:10, 0.1 % formic acid) and analyzed by UHPLC-MS/MS.
Instrumentation
- Automated SPE: Biotage Extrahera LV-200
- Manual SPE: Biotage PRESSURE+ 96 manifold
- Evaporation: Biotage SPE Dry concentrator
- UHPLC: Shimadzu Nexera with Restek Raptor Biphenyl column (100 × 2.1 mm, 2.7 µm)
- MS/MS: Shimadzu 8060 Triple Quadrupole with ESI
Results and Discussion
Both workflows produced mean recoveries above 60 % with RSDs below 5 % (n=7) across more than 30 analytes. Calibration curves spanning 1–1000 pg/mL achieved R² > 0.999. Lower limits of quantitation ranged from 1 to 250 pg/mL. Automated extraction of 96 samples required approximately 25 minutes (excluding hydrolysis and evaporation), matching or exceeding the performance of manual SPE in reproducibility and throughput.
Benefits and Practical Applications
- High sample throughput with low solvent and consumable usage
- Robust, reproducible extraction for diverse drug panels
- Reduced hands-on time and operator variability
- Scalable solution for routine clinical, forensic and QA/QC laboratories
Future Trends and Possibilities
Emerging advancements may include further SPE miniaturization, direct on-line coupling to LC-MS systems, expanded target lists for novel psychoactive substances and AI-driven workflow optimization. Green chemistry approaches and integrated robotic platforms will continue to enhance efficiency and sustainability.
Conclusion
The automated mixed-mode SCX microelution SPE method implemented on the Biotage Extrahera LV-200 delivers consistent, high-throughput extraction of a comprehensive drugs of abuse panel in urine, with excellent recoveries, precision and sensitivity, streamlining laboratory operations.
References
- Biotage AB. Automated Extraction of Drugs of Abuse from Urine Using Biotage Extrahera LV-200 and Microelution SPE Prior to UPLC-MS/MS Analysis. Application Note AN964; 2021.
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