Enhancing Quercetin's Potential: A Nanoliposome Delivery System for High Altitude Pulmonary Edema.

PURPOSE: This study aimed to develop quercetin-loaded nanoliposomes (QUL) to improve the oral bioavailability of quercetin (QU). Furthermore, we comprehensively evaluated the potential of QU for preventing high-altitude pulmonary edema (HAPE) and explored its underlying molecular mechanisms.

METHODS

Quercetin nanoliposome was created using thin-film hydration method, which was analyzed for morphology, zeta potential, drug loading, encapsulation efficiency, and release in vitro. A simple, sensitive and accurate LC MS/MS method was developed and validated for the simultaneous quantification of QU and QUL in rat plasma using Carbamazepine as internal standard (IS). The efficacy of QU and QUL in preventing HAPE was demonstrated in vitro and in vivo. Various techniques such as Western blotting, and immunofluorescence were employed to elucidate the associated mechanism.

RESULTS

Transmission electron microscopy proved that the nanoparticles were evenly distributed. The mean particle size (DLS) was determined to be 157.08±1.215 nm, with a polydispersity index (PDI) of 0.204±0.012. After oral administration of QU and QUL, Tmax values were 2.677±1.033h and 1.167±0.408h, respectively. Additionally, the Cmax values were 0.37±0.049ug/mL and 0.585±0.032ug/mL, respectively, suggesting a faster absorption rate and greater absorption content for QUL. QU and QUL improved lung permeability, reduced mortality, and decreased lung water content in a mouse model. Moreover, they significantly inhibited hypoxia-induced hyperproliferation and migration of pulmonary arterial smooth muscle cells (PASMCs). Mechanistic studies indicated that these effects were mediated through the PI3K/AKT/VEGF and ROCK/HIF/TRPC signaling pathways.

CONCLUSION

QU reduces lung water content by modulating the PI3K/AKT/VEGF and ROCK/HIF/TRPC signaling pathways, suggesting its potential for preventing and treating HAPE. Furthermore, quercetin-loaded lipid nanoparticles improve oral bioavailability, thereby enhancing the therapeutic efficacy of quercetin in HAPE management.