1. Academic Validation
  2. MXene-Based Cartilage-Adhesive Microspheres for Photothermal-Controlled Hydrophobic Drug Release and Mesenchymal Stem Cell Delivery in Osteoarthritis

MXene-Based Cartilage-Adhesive Microspheres for Photothermal-Controlled Hydrophobic Drug Release and Mesenchymal Stem Cell Delivery in Osteoarthritis

  • ACS Nano. 2025 Jun 10;19(22):20502-20515. doi: 10.1021/acsnano.4c16918.
Fan Chen 1 Wenzhe Wang 1 Hengxin Zhao 1 Zian Zhang 1 Nanyu Pang 1 Yijie Tang 2 Tian Wang 3 Chang Liu 1 Zhenchao Huang 1 Feiyu Mou 1 Chaoqun Yu 1 Haining Zhang 1
Affiliations

Affiliations

  • 1 Department of Joint Surgery, The Affiliated Hospital of Qingdao University, Qingdao 266000, PR China.
  • 2 Rehabilitation Medicine Department, the First People's Hospital of Yancheng, Yancheng, Jiangsu 224002, PR China.
  • 3 Shandong Key Laboratory of Medical and Health Textile Materials, College of Textiles and Clothing, State Key Laboratory of Bio-Fibers and Eco-Textiles, Research Center for Intelligent and Wearable Technology, Qingdao University, Qingdao 266071, PR China.
Abstract

Intra-articular drug injection is an effective treatment for osteoarthritis (OA). However, the rapid clearance of drugs from the joint cavity results in low drug utilization and suboptimal therapeutic outcomes. This study describes MXene-based cartilage-adhesive microspheres for photothermal-controlled hydrophobic drug release and bone marrow mesenchymal stem cell (BMSC) delivery. Nano cationic amylose (NCA) was obtained by modifying amylose with glycidyltrimethylammonium chloride (GTAC), and hydrophobic drug Kartogenin (KGN) was encapsulated in the hydrophobic helical cavity of NCA through ultrasonic treatment, resulting in nano cationic amylose@KGN complexes (NCA@KGN). HAMA/MXene-NCA@KGN (H/M-NCA@KGN) microspheres were prepared using a microfluidic device. These microspheres exhibited excellent biocompatibility, effectively adhered to the cartilage surface, and carried BMSCs. H/M-NCA@KGN microspheres demonstrated photothermal-controlled release of the hydrophobic drug KGN. Notably, KGN promoted the differentiation of BMSCs into chondrocytes, thereby improving the loss of extracellular matrix in joint cartilage. Additionally, appropriate thermal stimulation induced the expression of heat shock protein 70 (HSP70) in OA chondrocytes, providing a protective effect and delaying the progression of OA. H/M-NCA@KGN microspheres enable controlled hydrophobic drug release and stem cell delivery for potential OA treatment applications.

Keywords

MXene-based materials; cartilage-adhesive microspheres; cationic amylose; osteoarthritis; photothermal-controlled release.

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