acute inhalation toxicity

Acute inhalation toxicity

Acute inhalation toxicity results from the adverse effects caused by substances after a single, uninterrupted inhalation exposure over a short period of 24 hours or less.

Fixed-duration exposure of four hours is generally recommended for testing, but shorter or longer exposure times may be appropriate to meet specific objectives. Vivotecnia’s inhalation team will advise you on the recommended exposure depending on the substance and the objectives that are established for the study.

Acute inhalation toxicity testing provides information on a test item’s hazardous properties and permits its classification according to the globally harmonized system of classification and labelling of chemicals (GHS). In principle, the test is not intended to calculate a precise LC50 but does give a valuable indication to determine defined exposure ranges where lethality is expected, as death of a proportion of the animals is still the principal endpoint for the acute toxicity studies. As such, acute inhalation toxicity testing will permit an informed judgment to be made regarding the test item’s assignment to one of a series of toxicity classes defined by fixed LC50 cut-off values.

Vivotecnia’s inhalation toxicology facilities are authorized to carry out experimental animal exposure studies under good laboratory practices. To learn more about our inhalation facilities, please click here

  • Flow-past chambers can accommodate up to 56 animals and eight sampling points
  • Facilities equipped with 12 inhalation chambers
  • Separate control room
  • Different concentrations
  • Gravimetric and analytic monitoring
  • Vapor, liquid or dust inhalation
  • Rodents
en blanco
Our team and Experience
Vivotecnia employs some of the most experienced and talented minds in the industry who work closely with our clients, always flexible and responsive to find solutions and satisfy your needs. Our scientific team has extensive experience and widely varied backgrounds in multiple disciplines and is fully committed to your nonclinical development program. Their years of experience with complex general toxicology studies and their ability to respond to unexpected issues mean that you will obtain robust and regulatory compliant data, keeping you on-track and progressing with your registration process.


    For more information or a formal quotation, please send us a message and we will contact you as soon as possible.