Design and development of novel cyclosporine A lipid nanoparticle formulations appropriate for oral delivery

  1. Guada ., Melissa
unter der Leitung von:
  1. María José Blanco Prieto Doktormutter
  2. María del Carmen Dios Vieitez Doktorvater/Doktormutter

Universität der Verteidigung: Universidad de Navarra

Fecha de defensa: 16 von Februar von 2016

Gericht:
  1. Ángel Concheiro Nine Präsident/in
  2. Azucena Aldaz Pastor Sekretärin
  3. Ana Isabel Torres Suárez Vocal
  4. Julen Oyarzabal Santamarina Vocal
  5. Antonio José Leitâo das Neves Almeida Vocal
Fachbereiche:
  1. (FFN) Ciencias Farmacéuticas

Art: Dissertation

Teseo: 121639 DIALNET lock_openDadun editor

Zusammenfassung

Cyclosporine A (CsA) is a well-known immunosuppressive agent that gained considerable importance in transplant medicine in the late 1970s due to its selective and reversible inhibition of T-lymphocytes. While CsA has been widely used to prevent graft rejection in patients undergoing organ transplant it was also used to treat several systemic and local autoimmune disorders. Currently, the neuro- and cardio-protective effects of CsA (CiCloMulsion®; NeuroSTAT®) are being tested in phase II and III trials respectively and NeuroSTAT® received orphan drug status from US FDA and Europe in 2010. The reformulation strategies focused on developing Cremophor® EL free formulations and address variable bioavailability and toxicity issues of CsA. This review is an attempt to highlight the progress made so far and the room available for further improvements to realize the maximum benefits of CsA.