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INNOTEG TF-SPME Thin-Film Solid-Phase Microextraction Device

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Brand INNOTEG
Origin Guangdong, China
Manufacturer Type Authorized Distributor
Product Origin Domestic (China)
Model TF-SPME
Pricing Upon Request

Overview

The INNOTEG TF-SPME (Thin-Film Solid-Phase Microextraction) is a robust, membrane-based microextraction platform engineered for quantitative and semi-quantitative analysis of volatile and semi-volatile organic compounds (VOCs and SVOCs) in complex matrices. Unlike conventional fiber-based SPME, TF-SPME utilizes a planar polymeric film—coated with standardized sorbent chemistries—mounted on a rigid stainless-steel support frame. This architecture eliminates fiber breakage, improves mechanical stability during field deployment, and enables reproducible immersion or headspace exposure under variable environmental conditions. The technique operates on the principle of equilibrium partitioning: analytes migrate from the sample matrix into the thin-film coating based on their distribution coefficients, followed by thermal desorption or solvent elution prior to instrumental analysis—typically coupled with GC-MS, GC-FID, or LC-MS/MS. Designed for green analytical chemistry, TF-SPME eliminates organic solvent consumption during extraction, reduces sample preparation time, and aligns with principles of ISO 17025-compliant method validation workflows.

Key Features

  • Two standardized film dimensions: 20 mm × 4.8 mm and 40 mm × 4.8 mm—optimized for controlled surface-area-to-volume ratios and scalable extraction capacity
  • Three validated sorbent chemistries: Polydimethylsiloxane (PDMS), PDMS/Divinylbenzene (PDMS/DVB), and PDMS/High-Loading Bonded (PDMS/HLB)—covering broad polarity ranges from non-polar PAHs to moderately polar pesticides and polar aldehydes
  • Enhanced phase ratio (surface area/volume) compared to traditional SPME fibers—yielding higher absolute recovery and improved detection limits for trace-level analytes
  • Mechanically reinforced polymer film bonded to corrosion-resistant metal substrate—enabling direct immersion in turbid wastewater, sediment pore water, or high-salinity lake samples without delamination or physical deformation
  • Compatible with standard autosampler trays (e.g., Gerstel MPS, CTC CombiPAL) and thermal desorption units meeting ASTM D7369 and EPA Method 8260D requirements

Sample Compatibility & Compliance

TF-SPME demonstrates proven performance across heterogeneous sample types including aqueous environmental media (wastewater, surface water, groundwater), headspace vapors (indoor air, soil gas), food homogenates (meat extracts, dairy emulsions, fruit juices), botanical volatiles (tobacco leaf headspace, herbal decoction vapors), and biological fluids (urine, saliva, sweat). Extraction efficiency remains stable across pH 2–12 and salinities up to 35 g/L NaCl. The device complies with core principles of green chemistry (Anastas & Warner, 1998) and supports method development aligned with ISO/IEC 17025:2017 for laboratory competence. When integrated into validated workflows, TF-SPME meets data integrity expectations under FDA 21 CFR Part 11 for electronic records and signatures—particularly when paired with audit-trail-enabled chromatography data systems (CDS).

Software & Data Management

While TF-SPME itself is a passive sampling device requiring no embedded electronics or firmware, its implementation is fully supported within industry-standard analytical software environments. Chromatographic data systems (e.g., Thermo Fisher Chromeleon, Agilent OpenLab CDS, Waters Empower) accommodate custom calibration tables for film-specific response factors. Method templates—including equilibration time, agitation parameters, desorption temperature ramps, and internal standard normalization schemes—are programmable and version-controlled. All extraction metadata (batch ID, operator, ambient temperature/humidity, matrix type) can be logged via LIMS integration to ensure full traceability per GLP and GMP documentation standards.

Applications

  • Environmental monitoring: In situ extraction of organochlorine pesticides (e.g., endosulfan), polycyclic aromatic hydrocarbons (PAHs), and chlorinated benzenes from wastewater effluents and lake sediments
  • Food authenticity and quality control: Profiling esters, aldehydes, and terpenes in alcoholic beverages, fermented dairy products, and cured meats
  • Natural product research: Headspace capture of monoterpenes and sesquiterpenes from fresh plant tissues, dried herbs, and tobacco curing barns
  • Clinical toxicology and exposomics: Quantification of volatile metabolites (e.g., isoprene, acetone, alkanes) in human biofluids without derivatization
  • Industrial hygiene: Real-time VOC screening in workplace air using passive diffusion-controlled exposure protocols

FAQ

Can TF-SPME films be reused?
Yes—under controlled cleaning protocols (e.g., 10-min solvent rinse in methanol/acetone followed by thermal conditioning at 250 °C for 15 min), films demonstrate ≥20 extraction cycles with <15% signal drift for mid-polarity analytes.
Is TF-SPME compatible with LC-MS analysis?
Yes—solvent elution (e.g., 100 µL acetonitrile) is recommended for thermally labile or non-volatile compounds; eluates are directly injectable into reversed-phase LC-MS systems.
How does TF-SPME compare to traditional SPME fibers in terms of sensitivity?
Due to its 3–5× greater active surface area and reduced mass-transfer resistance, TF-SPME typically delivers 2–4× lower method detection limits (MDLs) for target VOCs in aqueous matrices.
Does the device require special calibration standards?
No—standard certified reference materials (CRMs) and isotopically labeled internal standards used in conventional SPME or purge-and-trap methods remain fully applicable.
What storage conditions are recommended for unused TF-SPME films?
Store sealed in aluminum foil pouches at 4 °C in low-humidity environments; shelf life exceeds 18 months when unopened.

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