Department of Drug Delivery Technology and Science, Pharmaceutical Engineering, Gifu Pharmaceutical University, Gifu, Japan.
Biol Pharm Bull. 2011;34(6):894-7. doi: 10.1248/bpb.34.894.
We examined the feasibility of using submicron-sized liposomes (ssLips) for retinal delivery of hydrophilic compounds, which would also have a wide range of applications. To evaluate the uptake into conjunctival cell line and the intraocular behavior of hydrophilic compound-containing ssLips after eyedrop application, fluorometric investigation was carried out by using a hydrophilic fluorescence probe, 5(6)-carboxyfluorescein (CF). A relatively high amount of CF (>50%) could be incorporated into an internal phase of ssLips by a calcium acetate gradient method. CF being entrapped within the liposomes markedly enhanced both the uptake of CF into conjunctival cells and CF-oriented emission in the retina in mice after eyedrop application, while the free CF did not clear delivery efficiency in both in vitro and in vivo study. In addition, the cellular uptake and luminescence intensity in the retina were higher when a ssLip formulation composed of L-α-distearoyl phosphatidylcholine was applied than when a ssLip formulation composed of egg phosphatidylcholine was applied. Consequently, ssLips of appropriate composition were considered to have good potential to carry hydrophilic compounds into the retina.
我们研究了使用亚微米大小的脂质体(ssLips)来递送至视网膜的亲水性化合物的可行性,这也将有广泛的应用。为了评估滴眼后亲水性化合物包含的 ssLips 进入结膜细胞系和眼内的行为,通过使用亲水性荧光探针 5(6)-羧基荧光素 (CF) 进行荧光研究。通过醋酸钙梯度法,ssLips 的内部相中可以掺入相当大量的 CF (>50%)。CF 被包封在脂质体中,显著增强了滴眼后 CF 进入结膜细胞的摄取和 CF 定向在小鼠视网膜中的发射,而游离 CF 在体外和体内研究中均未提高递送效率。此外,当应用由 L-α-二硬脂酰基磷脂酰胆碱组成的 ssLip 制剂时,细胞摄取和视网膜中的发光强度高于应用由卵磷酯酰胆碱组成的 ssLip 制剂时。因此,具有适当组成的 ssLips 被认为具有将亲水性化合物携带到视网膜的良好潜力。