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Procuring Virus Transport Medium for the Lab: 6 Critical Specs You Must Check

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Have you ever had to scramble because tubes suddenly leaked during centrifugation?
Or traced an entire run of invalid results back to a batch that was never really sterile?
For lab managers and purchasing officers, VTM is not just another line item—it is the front end of every assay.
Saving a few cents per tube can cost thousands in re-tests, contamination clean-ups and lost time.
Huachenyang, a manufacturer that builds tubes to real-world lab specs, shares the six metrics you should scrutinise before any purchase.


  1. Sterility – the first firewall against contamination
    Why it matters
    Any residual bacteria or fungi will co-amplify in PCR or overgrow in cell culture, giving false positives or masking the target virus.

How to check
Demand a SAL 10⁻⁶ certificate tested to YY/T 1859-2022 (or equivalent). The report must state method, incubation times and pass/fail for each lot.

Huachenyang practice

  • Produced in an ISO 8 (100 000-grade) clean room.
  • Every lot sterility-checked by third-party lab; COA shipped with goods and archived for five years.

  1. Seal integrity – zero-leak for transport and spin
    Why it matters
    A tube that weeps in transit ruins samples, contaminates neighbours and creates a biosafety incident.

How to check
Ask for data from a –40 kPa vacuum hold (10 min) and an inverted 24 h shake test. A dual seal (medical-grade septum + threaded cap) is the safest architecture.

Huachenyang practice

  • 100 % inline –40 kPa leak test; reject rate <0.01 %.
  • Dual-seal design rated for 15 000 × g and –80 °C storage.

  1. Medium chemistry – matched to your assay
    Why it matters
    PCR needs rapid inactivation and RNA/DNA protection; viral culture needs live virus and zero antimicrobials. Mix them up and you waste reagents and time.

How to check
Read the formulation sheet. For molecular work verify ≥48 h nucleic-acid stability at ambient temperature; for culture confirm antibiotic-free and isotonic.

Huachenyang practice
Two validated formulas:

  • Molecular grade: guanidine-based, 72 h RNA stability (Ct shift ≤0.5).
  • Culture grade: protein-rich, antibiotic-free, ISO 10993-5 cytotoxicity passed.

  1. Tube material – survive lab extremes without leachables
    Why it matters
    Cheap resins can shatter at –80 °C or release plasticisers that inhibit PCR.

How to check
Specify medical-grade PP, list working limits (e.g. –86 °C to 121 °C) and ask for extractables data if you do sensitive amplification.

Huachenyang practice

  • Virgin medical PP, USP Class VI certified.
  • Verified for 15 000 × g centrifugation and 121 °C autoclaving; no measurable PCR inhibition (ΔCt <0.2 vs control).

  1. Swab compatibility – guarantee complete elution
    Why it matters
    A narrow neck or short stopper prevents the swab head from reaching the medium, slashing analytical sensitivity.

How to check
Confirm internal diameter ≥8 mm and working volume ≥3 mL. Look for a built-in break point that lets the swab sit below the liquid line while still allowing clean cap closure.

Huachenyang practice

  • 8 mm bore, 3 mL and 5 mL volumes.
  • Precision break point 80 mm from tip; validated for nylon-flocked and rayon swabs.

  1. Lot-to-lot consistency – keep your data comparable
    Why it matters
    Variation in pH, ionic strength or tube dimensions introduces run-to-run noise that no amount of QC can fix afterwards.

How to check
Ask for side-by-side COAs from three consecutive lots; key specs (pH, sterility, seal) should fall within tight ranges. A vendor with full batch-tracking software can email the PDF in minutes.

Huachenyang practice

  • MES system logs every batch; pH held to ±0.1, osmolality ±5 %.
  • Retained samples stored for 12 months for accelerated ageing studies.

Put it all together
A cheap tube that fails any one of the six checks is the most expensive mistake you can make.
Use the list above as your technical RFQ template and demand written proof for every claim.

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