

Positive-Pressure SPE Manifold for Drug Extraction
药物萃取用正压固相萃取装置
- SKU SAE-0001
- Sample Preparation
- CE (to be confirmed)
- ISO 9001 manufacturing (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Format | Cartridge (1–6 mL) and 96-well plate |
|---|---|
| Pressure range | 1–100 psi |
| Positions | 12, 24 or 96 |
| Gas | Nitrogen or clean air |
| Pressure control | Digital regulator |
| Collection format | Tubes or 96-well plate |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ANSI/ASB Standard 036, ISO/IEC 17025, ISO 15189
What is the Positive-Pressure SPE Manifold for Drug Extraction?
A positive-pressure SPE manifold pushes samples and solvents through SPE cartridges or 96-well plates with controlled gas pressure. It gives consistent flow for urine and blood extraction in toxicology laboratories without a full robotic system.
What is the Positive-Pressure SPE Manifold for Drug Extraction?
A positive-pressure SPE manifold pushes samples and solvents through SPE cartridges or 96-well plates with controlled gas pressure. It gives consistent flow for urine and blood extraction in toxicology laboratories without a full robotic system.
Overview
The manifold holds SPE cartridges or a 96-well plate above collection tubes or a plate, and applies regulated nitrogen or air pressure from above, typically 1 to 100 psi. Unlike vacuum manifolds, positive pressure can push viscous samples, such as hemolyzed blood or hydrolyzed urine, through sorbent beds without channeling, and it avoids sample evaporation and cross-contamination between wells. Flow is controlled by pressure setting and time, which improves reproducibility of recovery. Pressure can be adjusted stepwise for load, wash, dry and elute steps. The manifold is used with mixed-mode polymeric sorbents that retain basic, acidic and neutral drugs. It is compact and low cost, but sample loading and solvent addition are manual unless paired with a pipetting system.
How does it work?
Biological samples contain proteins, lipids and salts that interfere with chromatography and mass spectrometry, so drugs must be separated before analysis. Solid-phase extraction passes the sample through a sorbent bed that retains the drug, is washed to remove interferences and releases the drug with an elution solvent. Supported liquid extraction uses a diatomaceous earth support to perform liquid-liquid extraction without emulsions. Hydrolysis with acid, base or enzyme such as beta-glucuronidase releases conjugated drugs. Evaporation with heated nitrogen concentrates extracts, and derivatization may be needed for GC-MS. Hair is decontaminated, pulverized or cut and extracted to release incorporated drug. Automated liquid handlers pipette samples, internal standards and reagents with volume precision near 1 percent. Good preparation improves recovery, reproducibility and instrument uptime.
What are the key features?
- Regulated nitrogen or air pressure from 1 to 100 psi
- Handles viscous samples without channeling
- Cartridge and 96-well plate formats
- Stepwise pressure programs for each SPE stage
- Sealed design limits cross-contamination between wells
What are the technical specifications?
A typical positive-pressure spe manifold for drug extraction configuration offers format of Cartridge (1–6 mL) and 96-well plate, pressure range of 1–100 psi, positions of 12, 24 or 96, gas of Nitrogen or clean air, pressure control of Digital regulator and collection format of Tubes or 96-well plate. Values are indicative of the product class; the exact figures for each configuration are confirmed on the quotation and the calibration documents supplied with the instrument.
Which applications is it used for?
The Positive-Pressure SPE Manifold for Drug Extraction is used in urine drug confirmation extraction, whole blood extraction, oral fluid extraction and method development. Across the wider Sample Preparation class, laboratories also deploy it for urine and blood extraction for toxicology, hair testing preparation and workplace drug testing confirmation.
Which standards and certifications apply?
Relevant standards and methods include ANSI/ASB Standard 036, ISO/IEC 17025, ISO 15189, CLSI C62 and IEC 61010-1. Certification candidates for this model are CE and ISO 9001 manufacturing; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Validate each preparation method for recovery, matrix effects, precision and carryover, and use isotope-labeled internal standards added early. Keep consistent flow rates and drying times in SPE because variation changes recovery. Place evaporators and manifolds in a fume hood or use solvent vapor extraction, and follow biosafety procedures for blood and urine. Clean pipetting channels, needles and manifold ports regularly to avoid cross-contamination. Use calibrated pipettes and balances, verify temperature blocks with an independent thermometer, and document maintenance. For hair, decontamination steps must be defined and controlled. Keep chain-of-custody records and label every tube, plate and vial unambiguously.
How do I select the right Positive-Pressure SPE Manifold for Drug Extraction?
Select a positive-pressure manifold when consistent flow and viscous samples matter and throughput is moderate. For hundreds of samples, choose an automated workstation. In an RFQ, specify positions, pressure range, plate or cartridge format, gas supply and solvent compatibility.
How does it compare with other Sample Preparation variants?
Choose according to sample type, volume and downstream technique. Positive-pressure manifolds suit laboratories running tens of SPE samples with consistent flow, while automated SPE workstations suit hundreds of samples and reduce hands-on time. Nitrogen evaporators are needed whenever eluates must be concentrated or solvents exchanged, and their throughput is set by the number of positions and block temperature range. Hair testing requires a cryogenic or ball-mill pulverizer to achieve reproducible extraction. Liquid handlers add precision and traceability for calibrators, internal standards and dilutions. Check plate formats, such as 96-well, compatibility with consumables, carryover control, solvent resistance and the ability to log operations. Consider operator safety, because organic solvents and biological samples are present.
Full specifications
| Format | Cartridge (1–6 mL) and 96-well plate |
|---|---|
| Pressure range | 1–100 psi |
| Positions | 12, 24 or 96 |
| Gas | Nitrogen or clean air |
| Pressure control | Digital regulator |
| Collection format | Tubes or 96-well plate |
| Material | PTFE, stainless steel, polypropylene |
| Solvent compatibility | Methanol, acetonitrile, ethyl acetate |
| Programmable steps | Load, wash, dry, elute |
| Power supply | 24 V DC / 220 V AC |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Urine drug confirmation extraction
- Whole blood extraction
- Oral fluid extraction
- Method development
Key features
- Regulated nitrogen or air pressure from 1 to 100 psi
- Handles viscous samples without channeling
- Cartridge and 96-well plate formats
- Stepwise pressure programs for each SPE stage
- Sealed design limits cross-contamination between wells
Frequently asked questions about Positive-Pressure SPE Manifold for Drug Extraction
Positive pressure gives consistent, controllable flow for viscous samples and avoids drying or evaporation effects, which improves recovery reproducibility across wells.
A regulated nitrogen or clean dry air line at about 5 to 7 bar inlet pressure is typical. Gas quality affects extract cleanliness, so filtered gas should be used.
Manifolds can be placed on the deck of liquid handlers or used with pipetting robots, but compatibility of plate formats and pressure connections should be checked first.
Biological samples contain proteins, salts and lipids that interfere with chromatography and mass spectrometry. Preparation removes these interferences, concentrates the drug and improves accuracy, sensitivity and instrument life.
Solid-phase extraction passes the sample through a sorbent that retains the drug, washes away interferences and then elutes the drug in a small solvent volume. It gives cleaner extracts than simple protein precipitation.
Many drugs are excreted as glucuronide conjugates. Enzymatic or chemical hydrolysis releases the free drug so that total drug concentration can be measured accurately.
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