Treatment for chemical burning using liquid crystalline nanoparticles as an ophthalmic delivery system for pirfenidone

被引:26
|
作者
Silva, Rummenigge Oliveira [1 ]
da Costa, Bruna Lopes [1 ]
da Silva, Flavia Rodrigues [1 ,2 ]
da Silva, Carolina Nunes [1 ]
de Paiva, Mayara Brandao [1 ]
Nunes Dourado, Lays Fernanda [1 ]
Malachias, Angelo [3 ]
de Souza Araujo, Adriano Antunes [4 ]
Nunes, Paula Santos [2 ]
Silva-Cunha, Armando [1 ]
机构
[1] Univ Fed Minas Gerais, Fac Pharm, BR-31270901 Belo Horizonte, MG, Brazil
[2] Univ Fed Sergipe, Grad Program Appl Sci Hlth, BR-49400000 Lagarto, SE, Brazil
[3] Univ Fed Minas Gerais, Exact Sci Inst, Dept Phys, BR-31270901 Belo Horizonte, MG, Brazil
[4] Univ Fed Sergipe, Dept Pharm, BR-49100000 Lagarto, SE, Brazil
基金
巴西圣保罗研究基金会;
关键词
Ocular chemical burns; Pirfenidone; Liquid crystalline nanoparticles; Cornea; Wound healing; DRUG-DELIVERY; OCULAR DELIVERY; GROWTH-FACTORS; PHARMACOKINETICS; STABILITY; PROLIFERATION; SPECTROSCOPY; MESOPHASES; LIPOSOMES; PHASES;
D O I
10.1016/j.ijpharm.2019.118466
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Some recent studies have shown that pirfenidone (PFD) has favorable results in the healing process of the cornea. However, PFD in solution exhibits short half-life after topical application, and in this context, a liquid crystal nanoparticle system containing PFD (PFD-LCNPs) was developed. The nanoparticles were characterized by transmission electron microscopy, atomic force microscopy, small angle X-ray diffraction and polarized light microscopy. The PFD-LCNPs had particle size and zeta potential of 247.3 nm and -33.60 mV (stores at 4 degrees C), respectively, and 257.5 nm and -46.00 mV (stored at 25 degrees C), respectively. The pH of the formulation was 6.9 and the encapsulation efficiency was 35.9%. The in vitro release profiles indicated that PFD sustained release from PFD-LCNPs for up to 12 h. In vitro study of ocular irritation (HET-CAM test) concluded that components of the formulation are well tolerated for ocular administration. Corneal re-epithelialization time after chemical burning was significantly reduced in rabbits treated with PFD-loaded LCNPs when compared to the group treated with a vehicle. In addition, the anti-inflammatory action of pirfenidone was observed by reducing myeloperoxidase activity (MPO) and inflammatory cells in the histology of the tissues of animals treated with PFD-LCNPs. These findings indicated that the PFD-LCNPs might have the potential for effective ocular drug delivery.
引用
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页数:14
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