TY - JOUR
T1 - Nicotinamide Adenine Dinucleotide-Loaded Lubricated Hydrogel Microspheres with a Three-Pronged Approach Alleviate Age-Related Osteoarthritis
AU - Lin, Yanpeng
AU - Wu, Hangtian
AU - Wang, Jun
AU - He, Wanling
AU - Hou, Jiahui
AU - Martin, Vidmi Taolam
AU - Zhu, Chencheng
AU - Chen, Yupeng
AU - Zhong, Junyuan
AU - Yu, Bin
AU - Lu, Aiping
AU - Guan, Daogang
AU - Qin, Genggeng
AU - Chen, Weiguo
N1 - This study was supported by the Science and Technology Project of Ganzhou, China (2022-ZD1373, and 2022-RC1349), the Provincial Natural Science Foundation of Guangdong, China ( 2022A1515110904, 2022A1515110221 , 2024A1515011520, and 2024A1515011417), National Key Research and Development Program of China (2022YFC2504305), and the National Natural Science Foundation of China (82171929).
Publisher Copyright:
© 2025 The Authors. Published by American Chemical Society
PY - 2025/5/13
Y1 - 2025/5/13
N2 - Chondrocyte senescence, synovitis, and decreased level of lubrication play pivotal roles in the pathogenesis of age-related osteoarthritis (AROA). However, there are currently no effective therapeutic interventions capable of altering the progression of OA until it reaches advanced stages, necessitating joint replacement. In this study, lubricious and drug-loaded hydrogel microspheres were designed and fabricated by utilizing microfluidic technology for radical polymerization of chondroitin sulfate methacrylate and incorporating nicotinamide adenine dinucleotide (NAD)-loaded liposomes modified with lactoferrin that are positively charged. Mechanical, tribological, and drug release analyses demonstrated enhanced lubrication properties and an extended drug dissemination time for the NAD@NPs@HM microspheres. In vitro assays unveiled the ability of NAD@NPs@HM to counteract chondrocyte senescence. RNA sequencing analysis, untargeted metabolomics analysis, and in vitro experiments on macrophages revealed that NAD@NPs@HM can regulate the metabolic reprogramming of synovial macrophages, promoting their repolarization from the M1 to M2 phenotype, thereby alleviating synovitis. Intra-articular injection of NAD@NPs@HM in aged mice reduced the mechanisms associated with AROA. These results suggest that NAD@NPs@HM may provide extended drug release, improved joint lubrication leading to better gait, and attenuation of AROA pathogenic processes, indicating its potential as a therapeutic approach for AROA.
AB - Chondrocyte senescence, synovitis, and decreased level of lubrication play pivotal roles in the pathogenesis of age-related osteoarthritis (AROA). However, there are currently no effective therapeutic interventions capable of altering the progression of OA until it reaches advanced stages, necessitating joint replacement. In this study, lubricious and drug-loaded hydrogel microspheres were designed and fabricated by utilizing microfluidic technology for radical polymerization of chondroitin sulfate methacrylate and incorporating nicotinamide adenine dinucleotide (NAD)-loaded liposomes modified with lactoferrin that are positively charged. Mechanical, tribological, and drug release analyses demonstrated enhanced lubrication properties and an extended drug dissemination time for the NAD@NPs@HM microspheres. In vitro assays unveiled the ability of NAD@NPs@HM to counteract chondrocyte senescence. RNA sequencing analysis, untargeted metabolomics analysis, and in vitro experiments on macrophages revealed that NAD@NPs@HM can regulate the metabolic reprogramming of synovial macrophages, promoting their repolarization from the M1 to M2 phenotype, thereby alleviating synovitis. Intra-articular injection of NAD@NPs@HM in aged mice reduced the mechanisms associated with AROA. These results suggest that NAD@NPs@HM may provide extended drug release, improved joint lubrication leading to better gait, and attenuation of AROA pathogenic processes, indicating its potential as a therapeutic approach for AROA.
KW - age-related osteoarthritis
KW - cellular senescence
KW - lubrication
KW - macrophage reprogramming
KW - nicotinamide adenine dinucleotide
UR - https://pubs.acs.org/doi/10.1021/acsnano.5c01184
UR - http://www.scopus.com/inward/record.url?scp=105004201129&partnerID=8YFLogxK
U2 - 10.1021/acsnano.5c01184
DO - 10.1021/acsnano.5c01184
M3 - Journal article
C2 - 40315404
SN - 1936-0851
VL - 19
SP - 17606
EP - 17626
JO - ACS Nano
JF - ACS Nano
IS - 18
ER -