Chuang Yu-Lun, Fang Hsu-Wei, Ajitsaria Aditya, Chen Ko-Hua, Su Chen-Ying, Liu Guei-Sheung, Tseng Ching-Li
Graduate Institute of Biomedical Materials and Tissue Engineering, College of Biomedical Engineering, Taipei Medical University, Taipei 11031, Taiwan.
Department of Chemical Engineering and Biotechnology, National Taipei University of Technology, Taipei 10608, Taiwan.
Pharmaceutics. 2019 Nov 28;11(12):635. doi: 10.3390/pharmaceutics11120635.
Cornea is the transparent layer in front of the eye that does not contain blood vessels. Among eye diseases, corneal neovascularization (NV) is one of the major causes of vision loss, since it can also lead to blindness. An herbal extraction containing flavonoid, kaempferol (KA), with antiangiogenic effect was chosen as a candidate drug for inhibited vessel formation. The use of nanomedicine has led to higher drug bioavailability and slow release of the drug as an effective therapeutic formulation in ocular drug delivery. In this study, we prepared gelatin nanoparticles (GNP) with kaempferol encapsulation (GNP-KA) for corneal NV treatment by topical delivery, i.e., eye drops. We found that GNP with/without KA loading was in the size of 85-150 nm, and its zeta potential was around 22-26 mV. The KA entrapment rate of GNP-KA was around 90-98%, and the loading rate was about 4.6%. The TEM results clearly indicated the GNP-KA NPs to be round spheres. The test involved the adoption of human umbilical vein endothelial cells (HUVECs) for coculture with these nanoparticles. From WST-8 assay, and cell migration examinations, it was evident that GNP-KA had the capacity to inhibit the cell viability and function of HUVECs. The results from tests such as ocular vessels observation, hematoxylin & eosin (H&E) stain, and metalloproteinases (MMP)/vascular endothelial growth factor (VEGF) quantification revealed the mice's eyes with corneal NV treated by eye drops containing GNP-KA once daily for 7 days had better therapeutic effects with less vessels in-growths in the cornea, compared to the KA solution group by reducing the production of MMP and VEGF in the cornea. Therefore, we expected to achieve a comfortable treatment with a simple method using nanomedicine (GNP-KA) as ophthalmological agent delivered as eye drops.
角膜是眼睛前部不含血管的透明层。在眼部疾病中,角膜新生血管形成(NV)是导致视力丧失的主要原因之一,因为它也可能导致失明。一种含有具有抗血管生成作用的黄酮类化合物山奈酚(KA)的草药提取物被选为抑制血管形成的候选药物。纳米药物的使用导致了更高的药物生物利用度以及药物的缓释,作为眼部药物递送中的一种有效治疗制剂。在本研究中,我们制备了包封有山奈酚的明胶纳米颗粒(GNP-KA),用于通过局部给药即滴眼剂来治疗角膜NV。我们发现,负载或未负载KA的GNP尺寸为85-150nm,其zeta电位约为22-26mV。GNP-KA的KA包封率约为90-98%,负载率约为4.6%。透射电子显微镜(TEM)结果清楚地表明GNP-KA纳米颗粒为圆球形状。该试验采用人脐静脉内皮细胞(HUVECs)与这些纳米颗粒共培养。从WST-8测定和细胞迁移检查中可以明显看出,GNP-KA具有抑制HUVECs细胞活力和功能的能力。眼部血管观察、苏木精和伊红(H&E)染色以及金属蛋白酶(MMP)/血管内皮生长因子(VEGF)定量等测试结果显示,与KA溶液组相比,每天滴眼一次含GNP-KA的滴眼剂治疗7天的角膜NV小鼠眼睛具有更好的治疗效果,角膜内血管生长较少,这是通过减少角膜中MMP和VEGF的产生实现的。因此,我们期望通过使用纳米药物(GNP-KA)作为滴眼剂形式的眼科药物,以一种简单的方法实现舒适的治疗。