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抗生物降解的非膨胀性润滑纳米胶体水凝胶

Nonswelling Lubricative Nanocolloidal Hydrogel Resistant to Biodegradation.

作者信息

Ding Tiantian, Ren Chunxia, Meng Liyuan, Han Guoyong, Xue Yao, Song Wenlong, Li Daowei, Sun Hongchen, Yang Bai, Li Yunfeng

机构信息

State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, 2699 Qianjin Street, Changchun, 130012, People's Republic of China.

Jilin Provincial Key Laboratory of Oral Biomedical Engineering, Hospital of Stomatology, Jilin University, Changchun, 130021, People's Republic of China.

出版信息

Nanomicro Lett. 2025 Jul 11;17(1):327. doi: 10.1007/s40820-025-01830-0.

Abstract

Hydrogels derived from biopolymers have numerous applications in bioengineering, drug delivery, wound healing, and wearable devices. Yet, their strong swelling and uncontrollable degradation stimulate the development of hydrogels that overcome these limitations. Here, we report nanocolloidal hydrogels formed from nanoparticles of methacryloyl-modified biopolymers that exhibit resistance to swelling and enzymatic degradation both in vitro and in vivo, along with exhibiting a broad-range of mechanical and lubrication properties, wear resistance and biocompatibility. The nonswelling behavior of nanocolloidal hydrogels takes origin in the resistance to swelling of their hydrophobic regions which are resulted from the nanophase of hydrophobic methacryloyl groups in the interior of the constituent nanoparticles. The developed approach to the preparation of nanocolloidal hydrogel with greatly enhanced properties will have applications in long-term drug delivery and cell culture, soft tissue augmentation, and implantable bioelectronics.

摘要

源自生物聚合物的水凝胶在生物工程、药物递送、伤口愈合和可穿戴设备等领域有众多应用。然而,它们强烈的溶胀和不可控的降解促使人们开发能克服这些局限性的水凝胶。在此,我们报道了由甲基丙烯酰基改性生物聚合物纳米颗粒形成的纳米胶体水凝胶,其在体外和体内均表现出抗溶胀和抗酶降解性能,同时还具有广泛的机械和润滑性能、耐磨性及生物相容性。纳米胶体水凝胶的非溶胀行为源于其疏水区域的抗溶胀性,这是由组成纳米颗粒内部疏水甲基丙烯酰基的纳米相导致的。这种制备性能大幅增强的纳米胶体水凝胶的方法将在长期药物递送和细胞培养、软组织增强以及可植入生物电子学等方面得到应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5b5/12254464/5a52384f5074/40820_2025_1830_Fig1_HTML.jpg

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