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100 μL of saliva was added to three cotton swabs (forensiX) and three viscose swabs (Sarstedt), and the swabs were dried in a cabinet dryer (not in a tube) at 56°C for 2 hours.
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On each evaluation, consistency of faeces was categorized into one of six categories; No faeces present (the rectal swab was dry and clean), watery, liquid, creamy, firm or solid (solid bulbs on the rectal swab).
Swabs were air dried and sealed in zip lock pouches for transport to the laboratory.
The skin was dried with cotton swabs, which were scintillation counted separately.
The swab is placed in a tube and is dried by different drying mechanisms and at different rates.
There were fewer AIV positive samples when swabs were transported dry; these differences were statistically significant at day 3 PI with VI.
Swabs were stored dry, in 7H9 medium containing PANTA (7H9) or in the antibiotics free Amies medium (VWR International); the latter two being semi-solid transport media.
Nasal swabs were taken with dry cotton swabs from enrolled children from September to December, 2005 and immediately placed in the sterile culture tube.
Thereafter the swabs were placed in dry cryovial tubes.
Nasal swabs were placed in dry tubes and stored at 4°C until being sent to CIRMF, once a week, for analysis.
However, the nurse who questions why there were dry swabs is 'fixing and reporting'.
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CEO of Professional Science Editing for Scientists @ prosciediting.com