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BLEOMYCIN-INDUCED PULMONARY FIBROSIS MODEL

DISEASE AREA IPF THERAPEUTIC AREAS


IPF MODEL

The Bleomycin (BLM) induced pulmonary fibrosis model is our standard IPF model,
widely used in pharmacology and fundamental research. For the BLM model there
are four types of administration route: subcutaneous, intraperitoneal, tail
intravenous and intratracheal, each route with their own pathological features
and imaging. The disease IPF is defined as injury confined to the lungs. Since
subcutaneous, intraperitoneal and tail vein routes of administration cause
systemic injury and deviate from the clinical definition of IPF, SMC utilizes
the Microsprayer to perform intratracheal administration of bleomycin (Figure
1). By administering bleomycin via Microsprayer, it can be evenly exposed to the
lungs and thus, develops a reproducible and uniform pathology. In prevention
studies we often recommend dexamethasone as a positive control. However, for
therapeutic targeting studies we recommend using a positive control such as
Nintedanib. To date, we have extensive experience in evaluating various
categories of test substances such as small molecules, nucleic acids and
antibodies.

 



Figure 1. A Microsprayer can evenly expose lungs to the drugs.
The picture shows the distribution of pigment Evans Blue.

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