This study sought to develop a liposomal delivery system of
fasudil--an
investigational drug for the treatment of
pulmonary arterial hypertension (PAH)--that will preferentially accumulate in the PAH lungs. Liposomal
fasudil was prepared by film-hydration method, and the drug was encapsulated by active loading. The
liposome surface was coated with a targeting moiety, CARSKNKDC, a
cyclic peptide; the
liposomes were characterized for size, polydispersity index, zeta potential, and storage and nebulization stability. The in vitro drug release profiles and uptake by TGF-β activated pulmonary arterial smooth muscle cells (PASMC) and alveolar macrophages were evaluated. The pharmacokinetics were monitored in male Sprague-Dawley rats, and the pulmonary hemodynamics were studied in acute and chronic PAH rats. The size, polydispersity index (PDI), and zeta potential of the
liposomes were 206-216 nm, 0.058-0.084, and -20-42.7 mV, respectively. The formulations showed minimal changes in structural integrity when nebulized with a commercial microsprayer. The optimized formulation was stable for >4 weeks when stored at 4 °C.
Fasudil was released in a continuous fashion over 120 h with a cumulative release of 76%.
Peptide-linked
liposomes were taken up at a higher degree by TGF-β activated PASMCs; but alveolar macrophages could not engulf
peptide-coated
liposomes. The formulations did not injure the lungs; the half-life of liposomal
fasudil was 34-fold higher than that of plain
fasudil after
intravenous administration.
Peptide-linked liposomal
fasudil, as opposed to plain
liposomes, reduced the mean pulmonary arterial pressure by 35-40%, without influencing the mean systemic arterial pressure. This study establishes that CAR-conjugated inhalable liposomal
fasudil offers favorable pharmacokinetics and produces pulmonary vasculature specific dilatation.