PT - JOURNAL ARTICLE AU - Angelique Wolter AU - Christian H. Bucher AU - Sebastian Kurmies AU - Viktoria Schreiner AU - Frank Konietschke AU - Katharina Hohlbaum AU - Robert Klopfleisch AU - Max Löhning AU - Christa Thöne-Reineke AU - Frank Buttgereit AU - Jörg Huwyler AU - Paulin Jirkof AU - Anna E. Rapp AU - Annemarie Lang TI - A Buprenorphine depot formulation provides effective sustained post-surgical analgesia for 72h in mouse femoral fracture models AID - 10.1101/2022.07.05.498859 DP - 2022 Jan 01 TA - bioRxiv PG - 2022.07.05.498859 4099 - http://biorxiv.org/content/early/2022/08/06/2022.07.05.498859.short 4100 - http://biorxiv.org/content/early/2022/08/06/2022.07.05.498859.full AB - Adequate pain management is essential for ethical and scientific reasons in animal experiments and should completely cover the period of expected pain without the need for frequent re-application. However, current depot formulations of Buprenorphine are only available in the USA and have limited duration of action. Recently, a new microparticulate Buprenorphine formulation (BUP-Depot) for sustained release has been developed as an alternative product within Europe. Pharmacokinetics indicate a potential effectiveness for about 72h. Here, we investigated whether the administration of the BUP-Depot ensures continuous and sufficient analgesia in two mouse femoral fracture models and could therefore serve as a potent alternative to the application of Tramadol via drinking water. Both protocols were examined for analgesic effectiveness, side effects on experimental readout, and effects on fracture healing outcomes in male and female C57BL/6N mice. The BUP-Depot provided effective analgesia for 72h, comparable to the effectiveness of Tramadol in drinking water. Fracture healing outcome was not different between analgesic regimes. The availability of a Buprenorphine depot formulation for laboratory animals in Europe would be a beneficial addition for extended pain relief in mice, thereby increasing animal welfare.Competing Interest StatementThe authors have declared no competing interest.