| Literature DB >> 34653563 |
Lali Ronsoni Zancan1, Franciele Aline Bruinsmann2, Karine Paese2, Patrick Türck3, Alan Bahr3, Alexsandra Zimmer3, Cristina Campos Carraro3, Paulo Cavalheiro Schenkel3, Adriane Belló-Klein3, Claiton I Schwertz4, David Driemeier4, Adriana Raffin Pohlmann2, Sílvia Stanisçuaski Guterres5.
Abstract
Ambrisentan (AMB) is an orphan drug approved for oral administration that has been developed for the treatment of pulmonary arterial hypertension (PAH), a chronic and progressive pathophysiological state that might result in death if left untreated. Lipid-core nanocapsules (LNCs) are versatile nanoformulations capable of loading lipophilic drugs for topical, vaginal, oral, intravenous, pulmonary, and nasal administration. Our hypothesis was to load AMB into these nanocapsules (LNCamb) and test their effect on slowing or reducing the progression of monocrotaline-induced PAH in a rat model, upon oral administration. LNCamb displayed a unimodal distribution of diameters (around 200 nm), negative zeta potential (-11.5 mV), high encapsulation efficiency (78%), spherical shape, and sustained drug release (50-60% in 24 h). The in vivo pharmacodynamic effect of the LNCamb group was evaluated by observing the echocardiography, hemodynamic, morphometric, and histological data, which showed a significant decrease in PAH in this group, as compared to the control group (AMBsolution). LNCamb showed the benefit of reversing systolic dysfunction and preventing vascular remodeling with greater efficacy than that observed in the control group. The originality and contribution of our work reveal the promising value of this nanoformulation as a novel therapeutic strategy for PAH treatment.Entities:
Keywords: Ambrisentan; In vivo; Lipid-core nanocapsules; Monocrotaline-induced model; Nanotechnology; Pulmonary arterial hypertension
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Year: 2021 PMID: 34653563 DOI: 10.1016/j.ijpharm.2021.121181
Source DB: PubMed Journal: Int J Pharm ISSN: 0378-5173 Impact factor: 5.875