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可植入锌离子电池及其代谢产物的成骨-免疫调节双重功能。

Implantable Zinc Ion Battery and Osteogenesis-Immunoregulation Bifunction of Its Catabolite.

机构信息

State Key Laboratory of Crystal Materials, Shandong University Jinan 250100, P. R. China.

Department of Oral and Maxillofacial Surgery, Qilu Hospital of Shandong University.Jinan 250012, P. R. China.

出版信息

ACS Nano. 2024 Aug 13;18(32):21246-21257. doi: 10.1021/acsnano.4c04705. Epub 2024 Jul 31.

Abstract

Biocompatible batteries can power implantable electronic devices and have broad applications in medicine. However, the controlled degradation of implantable batteries, the impact of battery catabolites on surrounding tissues, and wireless charging designs are often overlooked. Here, we designed an implantable zinc ion battery (ZIB) using a gelatin/polycaprolactone-based composite gel electrolyte. The prepared ZIBs deliver a high specific capacity of 244.0 mA h g (0.5C) and long cycling stability of 300 cycles (4C). ZIBs were completely degraded within 8 weeks in rats and 30 days in a phosphate-buffered saline lipase solution, demonstrating good biocompatibility and degradability. ZIBs catabolites induced macrophage M2 polarization and exhibited anti-inflammatory properties, with mRNA levels of the M2 markers Arg-1 and CD206 up-regulated 15.8-fold and 13.4-fold, respectively, compared to the blank control group. Meanwhile, the expressions of two typical osteogenic markers, osteopontin and osteocalcin, were up-regulated by 3.6-fold and 5.6-fold, respectively, demonstrating that designed ZIBs promoted osteogenic differentiation of bone marrow mesenchymal stem cells. Additionally, a wireless energy transmission module was designed using 3D printing technology to realize real-time charging of the ZIB in rats. The designed ZIB is a promising power source for implantable medical electronic devices and also serves as a functional material to accelerate bone repair.

摘要

生物相容性电池可为植入式电子设备供电,在医学领域有广泛的应用。然而,植入式电池的可控降解、电池代谢物对周围组织的影响以及无线充电设计往往被忽视。在这里,我们使用明胶/聚己内酯基复合凝胶电解质设计了一种可植入的锌离子电池(ZIB)。所制备的 ZIB 具有 244.0 mA h g(0.5C)的高比容量和 300 次循环(4C)的长循环稳定性。ZIB 在大鼠体内 8 周内完全降解,在磷酸盐缓冲液脂肪酶溶液中 30 天内降解,表现出良好的生物相容性和可降解性。ZIB 代谢物诱导巨噬细胞 M2 极化并表现出抗炎特性,与空白对照组相比,M2 标志物 Arg-1 和 CD206 的 mRNA 水平分别上调了 15.8 倍和 13.4 倍。同时,两个典型的成骨标志物骨桥蛋白和骨钙素的表达分别上调了 3.6 倍和 5.6 倍,表明设计的 ZIB 促进了骨髓间充质干细胞的成骨分化。此外,还使用 3D 打印技术设计了无线能量传输模块,以实现大鼠体内 ZIB 的实时充电。所设计的 ZIB 是一种有前途的植入式医疗电子设备的电源,也是一种加速骨修复的功能材料。

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