O. Kamstrup et al., THE BIOPERSISTENCE AND PATHOGENICITY OF MAN-MADE VITREOUS FIBERS AFTER SHORT-TERM AND LONG-TERM INHALATION, The Annals of occupational hygiene, 42(3), 1998, pp. 191-199
A summary is given of the biopersistence and pathology after inhalatio
n by rats of two different Man-made Vitreous Fibres, MMVF21 (tradition
al stone wool) and MMVF34 (HT stone wool), and the results are discuss
ed in relation to biopersistence measured after intra-tracheal instill
ation. The results are given from a short-term inhalation biopersisten
ce study, a completed chronic inhalation study, and interim results fr
om an on-going chronic inhalation study. In both the short-term and ch
ronic studies, laboratory rats were exposed by nose-only inhalation to
well-characterised fibre test atmospheres that had been selected to b
e largely rat respirable. The shortterm inhalation study included grou
ps exposed to aerosols targeted at 150 fibres longer than 20 mu m per
cm(3). The exposure duration was 6 hours/day for 5 days, with subseque
nt post-exposure periods lasting up to 12 months. For lung burden anal
yses, interim sacrifices were performed at regular intervals. The ongo
ing chronic study comprises a group of rats exposed to the MMVF34 fibr
e at one exposure level of 30 mg/m(3). The negative control group is f
iltered air. The exposure duration is 6 hours/day, 5 days/week for 2 S
ears, with a subsequent post-exposure period lasting until approximate
ly 20% survival in the test fibre group. Interim sacrifices are perfor
med at months 3, 6, 12, 18 and 24 and biopersistence monitored for rat
s exposed for 3 and 12 months, with subsequent post-exposure periods l
asting 6 months. Effectively the main protocol for the previously cond
ucted chronic study tr as the same, except that there were 3 fibre exp
osure groups (3, 16 and 30 mg/m(3)) and no specific biopersistence sat
ellite groups mere included. For MMVF34, the inhalation tests of diffe
rent duration show a similar biopersistence pattern, while the intra-t
racheal test gives longer elimination half-times especially for long f
ibres. The MMVF34 fibre is considerably less biopersistent than the tr
aditional MMVF21 fibre when comparing the calculated elimination half-
times after short-term inhalation. When comparing the pathology after
3, 6, 12 and 18 months exposure, MMVF34 showed minor histopathological
changes compared to MMVF21. The carcinogenicity and toxicity results
of the chronic study with MMVF21 suggest that this fibre does not pose
a significant health risk to humans and the current results with MMVF
34 indicate that this fibre consequently should pose an even smaller r
isk, if any. (C) 1998 British Occupational Hygiene Society. Published
by Elsevier Science Ltd.