姜黄素
透明质酸
血管抑制剂
角膜新生血管
新生血管
角膜炎
医学
眼科
纳米颗粒
药理学
材料科学
血管生成
贝伐单抗
纳米技术
外科
癌症研究
化疗
解剖
作者
Qingdong Bao,Yi Zheng,Binfeng Lu,Guangwei Li,Muchen Dong
标识
DOI:10.1080/10667857.2024.2428532
摘要
The facilitation of targeted drug delivery within the ocular region presents a formidable challenge owing to its intricate physiological structure, which confers a biological barrier. This barrier is characterised by short retention times, diminished drug accumulation, and suboptimal bioavailability. To overcome these limitations, this study aimed to develop a hyaluronic acid-based nanoparticulate system encapsulating curcumin (CUR) and ranibizumab (RAN), designated as CUR-RAN@NPs with a uniform distribution of particle size and exhibited the capacity for sustained release of both CUR and RAN. The evaluation of biosafety and biocompatibility using cytotoxicity assays indicated that CUR-RAN@NPs are non-toxic and biologically compatible. Consequently, the CUR-RAN@NPs have promising potential for the advancement of ocular drug delivery systems. Finally, CUR-RAN@NPs demonstrated exceptional antibacterial activity and inhibition of neovascularization, thereby underscoring their therapeutic potential in ophthalmic applications.
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