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环孢素A制剂对牛角膜吸收的影响:体外研究。

Effect of cyclosporine A formulations on bovine corneal absorption: ex-vivo study.

作者信息

Le Bourlais C A, Chevanne F, Turlin B, Acar L, Zia H, Sado P A, Needham T E, Leverge R

机构信息

Laboratoire de Pharmacie Galénique, Biopharmacie et Pharmacie Clinique, Faculté de Pharmacie, Université de Rennes I, France.

出版信息

J Microencapsul. 1997 Jul-Aug;14(4):457-67. doi: 10.3109/02652049709033830.

Abstract

The purpose of this study was to evaluate, in an ex-vivo study, the absorption of cyclosporine A on bovine cornea after 24 h contact with various drug delivery systems containing 1% cyclosporine A and in comparison with an olive oil formulation as the reference vehicle for cyclosporine A. The different formulations studied were poly(acrylic acid) polymeric gels in aqueous/non-aqueous solvents, polyisobutylcyanoacrylate nanocapsules, and a combination of both formulations. The histological effects of these formulation on corneal cells after 24 h of contact were also studied. The lowest absorption rate of cyclosporine A was found using olive oil with a percent absorption of 2.52 +/- 1.52% (259 +/- 171 micrograms/g cornea). The three formulations developed for this study, nanocapsules, poly(acrylic acid) polymeric gel and nanocapsules gel showed significantly better absorption of CsA than olive oil, with a mean percent absorption of 5.81 +/- 2.04% (621 +/- 218 micrograms/g cornea), 6.09 +/- 2.93% (651 +/- 313 micrograms cornea) and 7.92 +/- 2.55% (847 +/- 273 micrograms/g cornea) respectively. As we studied the penetration of cyclosporine A into the different layers of the cornea, we observed that for all formulations, CsA remained at the corneal surface and did not penetrate the whole cornea. The histological study showed that olive oil, nanocapsules and poly(acrylic acid) gel in aqueous/non-aqueous solvents show some modifications on the cornea, contrary to the nonocapsules gel which did not indicate any toxic effect. The nanocapsule gel, with the highest percent absorption along with its margin of safety on the cornea, seems to present a new promising drug delivery system for ocular administration.

摘要

本研究的目的是在一项体外研究中,评估含有1%环孢素A的各种药物递送系统与牛角膜接触24小时后环孢素A的吸收情况,并与作为环孢素A参考载体的橄榄油制剂进行比较。所研究的不同制剂包括水相/非水相溶剂中的聚丙烯酸聚合物凝胶、聚异丁基氰基丙烯酸酯纳米胶囊以及两种制剂的组合。还研究了这些制剂在接触24小时后对角膜细胞的组织学影响。使用橄榄油时环孢素A的吸收率最低,吸收百分比为2.52±1.52%(259±171微克/克角膜)。为本研究开发的三种制剂,即纳米胶囊、聚丙烯酸聚合物凝胶和纳米胶囊凝胶,显示出比橄榄油显著更好的环孢素A吸收效果,平均吸收百分比分别为5.81±2.04%(621±218微克/克角膜)、6.09±2.93%(651±313微克角膜)和7.92±2.55%(847±273微克/克角膜)。当我们研究环孢素A渗透到角膜不同层时,我们观察到对于所有制剂,环孢素A都留在角膜表面,没有穿透整个角膜。组织学研究表明,橄榄油、纳米胶囊和水相/非水相溶剂中的聚丙烯酸凝胶对角膜有一些改变,而纳米胶囊凝胶未显示出任何毒性作用。纳米胶囊凝胶具有最高的吸收百分比以及在角膜上的安全边际,似乎是一种新的有前景的眼部给药药物递送系统。

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