Analytical Instruments Solutions for Seized Drugs
Brochures and specifications | 2020 | ShimadzuInstrumentation
Forensic analysis of seized drugs is critical to uphold legal standards and ensure reliable evidence in courts. Laboratories must identify a wide variety of sample types—powders, tablets, oils and edibles—with accuracy and traceability. Adherence to SWGDRUG and OSAC guidelines drives the selection of analytical schemes that balance speed, sensitivity and selectivity.
This white paper presents a comprehensive survey of Shimadzu’s analytical solutions for seized drug analysis. It categorizes techniques by their level of selectivity (C, B and A), outlines workflows for screening through confirmation, and demonstrates real-world applications including quantitation limits, isomer separation and legal compliance for hemp and cannabis products.
The workflow spans three levels of selectivity:
Key findings include:
The integrated portfolio supports: legal defensibility through high-selectivity confirmation; accelerated workflows to address case backlogs; minimal sample preparation for rapid screening; and flexible configurations for routine and challenging forensic analyses.
Emerging directions include:
Shimadzu’s suite of analytical instruments addresses the full spectrum of forensic drug analysis needs—from rapid screening to definitive confirmation. Leveraging tailored workflows, reliable software and extensive libraries, laboratories can achieve accurate, reproducible results that meet stringent regulatory and legal requirements.
GC, GC/MSD, HPLC, LC/MS, SFC, LC/SQ
IndustriesPharma & Biopharma
ManufacturerShimadzu
Summary
Importance of the Topic
Forensic analysis of seized drugs is critical to uphold legal standards and ensure reliable evidence in courts. Laboratories must identify a wide variety of sample types—powders, tablets, oils and edibles—with accuracy and traceability. Adherence to SWGDRUG and OSAC guidelines drives the selection of analytical schemes that balance speed, sensitivity and selectivity.
Objectives and Study Overview
This white paper presents a comprehensive survey of Shimadzu’s analytical solutions for seized drug analysis. It categorizes techniques by their level of selectivity (C, B and A), outlines workflows for screening through confirmation, and demonstrates real-world applications including quantitation limits, isomer separation and legal compliance for hemp and cannabis products.
Methodology and Instrumentation
The workflow spans three levels of selectivity:
- Category C (screening): Fluorescence spectroscopy for rapid, low-selectivity detection of fluorescent compounds.
- Category B (preliminary): UV-Vis, GC-FID, LC, SFC to separate and quantify target analytes in complex matrices.
- Category A (confirmation): GC-MS, LC-MS, FTIR-ATR, XRD for high-confidence identification using mass spectra, infrared fingerprints and crystallographic patterns.
Used Instrumentation
- Fluorescence Spectrofluorometer RF-6000 for high-speed 3D scanning and low quantitation limits.
- UV-Vis Spectrophotometer UV-1900i with ultra-fast scan and regulatory-compliant software.
- Gas Chromatograph Nexis GC-2030 with FID and optional VUV detection for isomer differentiation.
- Liquid Chromatograph Nexera-i (LC-2040C 3D) with PDA detector for rapid UHPLC separation of 16 cannabinoids in under 5 minutes.
- Supercritical Fluid Chromatograph Nexera UC for fast chiral and isomeric separations with reduced solvent use.
- GC-MS System GCMS NX Series with autosampler for trace-level confirmation and library matching of drugs (e.g., cocaine on currency).
- LC-MS Single Quadrupole LCMS-2020 for soft ionization, SIM quantitation of ten common seized drugs and in-source CID fragmentation.
- FTIR Spectrophotometer IRSpirit/IRAffinity-1 and SurveyIR™ microscope for ATR fingerprinting of powders and residues.
- X-ray Diffractometers XRD-6100/7000 with OneSight detector for phase identification of crystalline samples.
- Reference libraries: NIST/Wiley GC-MS, SWGDRUG FTIR, KnowItAll IR, designer drug and LC-MSn metabolite libraries.
Main Results and Discussion
Key findings include:
- Fluorescence: Unique emission–excitation profiles enable rapid screening despite limited compound coverage.
- UV-Vis: Calibration curves with r²≈0.99998 demonstrate reliable quantitation down to low mg/L levels.
- GC-FID: Accurate THC/CBD ratios in hemp oil confirm compliance with regulatory THC thresholds.
- SFC: Enhanced resolution of D/L amphetamine isomers and compatibility with MS for increased sensitivity.
- GC-MS: Successful quantitation of cocaine residues on various currencies down to sub-nanogram levels, confirmed by library searches.
- LC-MS: Simultaneous detection and quantitation of ten drugs at μg/mL levels, with characteristic in-source CID spectra.
- FTIR-ATR: Clear spectral fingerprints allow identification of powders, tablets and contaminants without sample preparation.
- XRD: Direct phase matching against PDF-4 Organics database provides unambiguous identification of crystalline APIs.
Benefits and Practical Applications
The integrated portfolio supports: legal defensibility through high-selectivity confirmation; accelerated workflows to address case backlogs; minimal sample preparation for rapid screening; and flexible configurations for routine and challenging forensic analyses.
Future Trends and Opportunities
Emerging directions include:
- High-resolution MS and time-of-flight detectors for expanded screening libraries and greater confidence.
- Automated sample preparation and AI-driven spectral matching to streamline data processing.
- Green analytical approaches using SFC and reduced solvent volumes to lower environmental impact.
- Integration of multimodal data (MS, IR, XRD) into unified platforms for comprehensive substance profiling.
Conclusion
Shimadzu’s suite of analytical instruments addresses the full spectrum of forensic drug analysis needs—from rapid screening to definitive confirmation. Leveraging tailored workflows, reliable software and extensive libraries, laboratories can achieve accurate, reproducible results that meet stringent regulatory and legal requirements.
Content was automatically generated from an orignal PDF document using AI and may contain inaccuracies.
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