细胞凋亡
糖尿病性视网膜病变
透明质酸
超氧化物
血管生成
视网膜
化学
生物物理学
渗透(HVAC)
纳米颗粒
免疫系统
药理学
癌症研究
材料科学
医学
内分泌学
生物化学
纳米技术
免疫学
糖尿病
生物
解剖
复合材料
酶
作者
Jingzhi Shao,Jingjing Wan,Fengyan Zhang,Lirong Zhang
标识
DOI:10.1166/jbn.2021.3190
摘要
We developed an effective nanoparticle-biomaterial in alleviating diabetic retinopathy (DR), hyaluronic acid (HA)-CeO 2 , composed mainly of CeO 2 and HA. To demonstrate its anti-DR capacity, retinal cells from a B6/J mouse model were used to compare the efficiency of PEI-CeO 2 and HA-CeO 2 . We investigated the transport performance, histolysis, immune cell infiltration, angiogenesis, and hyperemia induced by the transport system. The structural integrity, microvascular apoptosis, and superoxide and peroxide concentrations in the retina were measured to evaluate the clinical efficacy of CeO 2 . The infiltration efficiency of HA-CeO 2 was higher than that of PEI-CeO 2 . Lower levels of foreign body reaction were evident for HA-CeO 2 with less histolysis, immune cell infiltration, angiogenesis, and hyperemia. The clinical efficacy of HA-CeO 2 in terms of preservation of retinal structure and lowering of microvascular apoptosis and superoxide and peroxide concentrations was superior to those of PEI-CP. HA-CeO 2 was shown to have significant antioxidation and anti-vascular injury capacity in a mouse model, and may be a potential compound nanodrug for DR treatment in the future.
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