Itraconazole is a third generation azol, a fungicide which acts by inhibiting ergerosterol synthesis in the fungal cell membrane, and thereby disturbing fungal regeneration. It has proven to be less toxic, to have a broader spectrum of activity and to be more potent than its predecessor ketoconazole. Itraconazole is only available in therapheutics approved for human use. Pharmacokinetic studies has been performed in humans, dogs, cats and laboratory animals. Although itraconazole has been used tentatively with good effect against fungal infections in horses, no Pharmacokinetic studies have yet been done.

The retrospective part of this study evaluates the susceptibility patterns of bacteria isolated from blood in critically ill foals in Sweden. The most commonly obtained bacteria were Actinobacillus spp. (38 %) and Escherichia coli (27 %). Trimethoprim-sulphonamide (TMS) had good efficacy against most gram negative bacteria with the exception of Klebsiella spp. Among 17 Escherichia coli isolates 94 % were susceptible to trimethoprim-sulphonamide whereas all 24 isolates of Actinobacillus spp.

Clopidogrel is an antiplatelet substance that prevents blood coagulation in the arteries. It is an inactive pro drug that becomes activated after first-pass metabolism by the liver. The active metabolite of clopidogrel is 2-oxoclopidogrel, which is unstable therefore Pharmacokinetic data is obtained by measuring the inactive metabolite clopidogrel acid in plasma. Clopidogrel is taken orally in tablet form. The aim of this project was to develop a LC-MS/MS method for quantification of clopidogrel and its metabolite in plasma. The method has been developed by optimizing the sample preparation.

In this study the opioid buprenorphine was given to 8 clinically healthy goats. The Pharmacokinetics and behavioral effects were studied. Injections of buprenorphine, 0.02 mg/kg body weight was given both intramuscularly (i.m.) and intravenously (i.v.) with a cross over design. The results showed a short half-life of the drug in the plasma, 65.9 ± 17.4 min (mean ± SD), after i.v. injection.

Benzodiazepines are drugs used to treat insomnia and anxiety. This group of drugs should be prescribed with the duty of care to the elderly because of it´s negative effects. Life expectancy is increasing because of the progress of drug development. Aging brings physical and psychological changes leading to changes in Pharmacokinetic and pharmacodynamic features. Drug treatment is becoming increasingly widespread and contributes to the increasing number of interactions and complications for the elderly.

There is a need for correct and adequate pain assessment in horses. Methadone is used in pain management in horses but the full Pharmacokinetic picture of methadone is not yet known. The aim of this pilot study was to develop a behaviour protocol and suggest a reliable recording method for use in a larger research project with an aim to potentially correlate behaviours to concentration of methadone in blood. In this study two coldblooded trotters were given methadone intravenously with doses of 0.1 mg/kg for horse 1 and 0.2 mg/kg for horse 2. The horses were videotaped pre and post methadone administration.

St. John?s wort extract is composed of a large number of components, about 150, but the most studied and interesting substance are hyperforin and hypericin. The herb is very popular and it is known for its pharmacological efficacy in numerous disorders. It is used for treatment of mild to moderated depression as an alternative to synthetic antidepressants.

Opioidplåster avsedda för humant bruk används idag även för smärtlindring av djur eftersom det inte finns några registrerade veterinärmediciniska opioidplåster. För humant bruk finns plåster innehållande fentanyl och buprenorfin. Syftet med litteraturstudien var att granska studier i farmakokinetik och dynamik för att undersöka den vetenskapliga grunden för användningen av opioidplåster till djurslagen hund, katt och häst. Plåster kan vara ett sätt att administrera läkemedel transdermalt till den systemiska cirkulationen. Avsikten med plåster är att uppnå jämna koncentrationer i plasma (steady state) som varar under den tid som plåstret finns på plats, vanligen 72 h för människa. Vid användningen av fentanylplåster uppnåddes steady state hos människa efter 14 h.

Tramadol är en centralt verkande opioid vars smärtlindrande effekt främst anses bero av två mekanismer. Dels en svag affinitet för ?-receptorn men även en inhiberande effekt på återupptaget av och en stimulerande effekt på den cellulära frisättningen av serotonin och noradrenalin. Till strukturen liknar tramadol kodein och morfin men affiniteten för ?-receptorn är 10 gånger lägre jämfört med kodein och 6000 gånger lägre jämfört med morfin.