Amelioration of Endotoxin-Induced Uveitis in Rabbit by Topical Administration of Tacrolimus Proglycosome Nano-Vesicles

被引:18
|
作者
Garg, Vaidehi [1 ]
Nirmal, Jayabalan [3 ]
Riadi, Yassine [4 ]
Kesharwani, Prashant [1 ]
Kohli, Kanchan [1 ]
Jain, Gaurav Kumar [2 ]
机构
[1] Jamia Hamdard, Dept Pharmaceut, Sch Pharmaceut Educ & Res, New Delhi 110062, India
[2] Delhi Pharmaceut Sci & Res Univ, Dept Pharmaceut, New Delhi 110017, India
[3] BITS, Translat Pharmaceut Res Lab, Dept Pharm, Hyderabad 500078, India
[4] Prince Sattam Bin Abdulaziz Univ, Coll Pharm, Dept Pharmaceut Chem, Al Kharj 11942, Saudi Arabia
关键词
Tacrolimus; Proglycosomes; Uveitis; Nanoformulation; Ocular delivery; OCULAR DELIVERY;
D O I
10.1016/j.xphs.2020.10.060
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
This work was aimed to improve the efficacy of tacrolimus in the treatment of endotoxin-induced uveitis (EIU) using propylene glycol modified lipid vesicles termed as proglycosome nano-vesicles (PNVs). PNVs were prepared by modified film hydration method. Experimental uveitis in rabbit eye was induced by an intravitreal injection of 20 mu L of the endotoxin solution containing 100 ng of lipopolysaccharide endotoxin. In vivo efficacy of PNVs was determined by studying clinical symptoms of uveitis using slit lamp examination and by quantitatively measuring levels of tumor necrosis factor-alpha, interleukin-6, leukocytes and total proteins in aqueous humor, 24 h after intravitreal injection of endotoxin. Comparison was made with healthy, untreated and tacrolimus solution treated eyes. PNVs developed were nano-sized, deformable and showed sustained release of tacrolimus over period of 12 h. In vivo results indicated statistically significant difference between the effects of PNVs in the treatment of EIU compared to tacrolimus. PNV treatment not only subsides clinical symptoms of uveitis but also prevented breakdown of blood aqueous barrier. Tacrolimus loaded PNVs are potential new topical treatment for uveitis. (c) 2020 American Pharmacists Association (R). Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:871 / 875
页数:5
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