3D-Printed Microcubes for Catalase Drug Delivery

过氧化氢酶 药物输送 3d打印 纳米技术 活性氧 药品 细胞毒性 材料科学 化学 氧化应激 生物医学工程 药理学 生物化学 生物 医学 体外
作者
Sungmun Lee,Dong-Wook Lee,Nitul S. Rajput,T. Levato,Aya Shanti,Tae‐Yeon Kim
出处
期刊:ACS omega [American Chemical Society]
卷期号:8 (30): 26775-26781 被引量:3
标识
DOI:10.1021/acsomega.3c00789
摘要

Oxidative stress, i.e., excessive production of reactive oxygen species (ROS), plays an important role in the pathogenesis of inflammatory diseases such as cardiovascular diseases, cancer, and neurodegenerative diseases. Catalase, an antioxidant enzyme, has great therapeutic potential; however, its efficacy is limited by its delivery to target cells or tissues. In order to achieve efficient delivery, consistent drug distribution, and drug activity, small and uniformly sized drug delivery vehicles are needed. Here, three-dimensional (3D) microcubes were printed by Nanoscribe Photonic Professional GT2, a high-resolution 3D printer, and the characteristics of 3D-printed microcubes as drug delivery vehicles for the delivery of catalase were investigated. The size of the 3D-printed microcubes was 800 nm in length of a square and 600 nm in height, which is suitable for targeting macrophages passively. Microcubes were also tunable in shape and size, and high-resolution 3D printing could provide microparticles with little variation in shape and size. Catalase was loaded on 3D-printed microcubes by nonspecific adsorption, and catalase on 3D-printed microcubes (CAT–MC) retained 83.1 ± 1.3% activity of intact catalase. CAT–MC also saved macrophages, RAW 264.7, from the cytotoxicity of H2O2 by 86.4 ± 4.1%. As drug delivery vehicles, 3D-printed microparticles are very promising due to their small and uniform size, which provides consistent drug distribution and drug activity. Therefore, we anticipate numerous applications of 3D-printed microparticles for delivering therapeutic proteins.
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