纳米颗粒
生物相容性
材料科学
润滑
石英晶体微天平
Zeta电位
化学工程
吸附
硅酮
纳米技术
复合材料
聚合物
表面电荷
明胶
溶剂
弹性体
硅油
均质化(气候)
电动现象
生物医学工程
粒径
作者
Piaopiao Pan,Konstantina Simou,Yiben Ouyang,Lawrence Shere,Jon A. Preece,Simon W. Jones,Edward T. Davis,Yanling Lan,Zhenqiu Chen,Zhenyu J. Zhang,Qingguo Li
出处
期刊:PLOS ONE
[Public Library of Science]
日期:2026-01-16
卷期号:21 (1): e0327958-e0327958
标识
DOI:10.1371/journal.pone.0327958
摘要
Drug loaded nanoparticles (NPs) were developed as a model intra-articular injection (IAI) formulation to mitigate early stage osteoarthritis (OA). Different types of celecoxib-loaded nanoparticles were prepared by a hybrid method that combines homogenization and solvent evaporation. The hydrodynamic diameter of the nanoparticles prepared were approximately 200 nm (PLLA: 238 ± 19 nm; PCL: 249 ± 28 nm; PLA: 252 ± 18 nm; PMMA: 234 ± 21), and zeta potential were about −40 mV (PLLA: −45.3 ± 2.3 mV; PCL: −38.0 ± 0.9 mV; PLA: −44.4 ± 3.2 mV; PMMA: −45.5 ± 2.7 mV). Our friction data evidences that nanoparticles could improve considerably the lubrication between a stainless steel sphere and a silicone elastomer that were used as model substrates. Quartz Crystal Microbalance (QCM) and Atomic Force Microscope (AFM) measurements were carried out to unravel the lubrication mechanism. The magnitude and amount of NPs adsorbed on the surface determines the effect of lubrication. Drug release experiment suggests that nanoparticles could release up to more than one week, when being compared with free celecoxib. NPs formulation exhibited excellent biocompatibility in cytotoxicity of chondrocytes experiment.
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