Journal
COMPOSITES PART B-ENGINEERING
Volume 237, Issue -, Pages -Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.compositesb.2022.109855
Keywords
Functional cell membranes; CuS nanoparticle; Photothermal therapy; Targeted delivery; Osteoarthritis
Funding
- National Key R&D Program of China [2018YFC2001500]
- National Natural Science Foundation of China [82172098, 82001968]
- Shanghai Pujiang Program [20PJ1403800]
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This study presents a new type of nanoparticle for treating osteoarthritis, which achieves targeted delivery and anti-inflammatory treatment through cell membrane modification and photothermal responsive drug release. It exhibits significant therapeutic efficacy for osteoarthritis in vivo.
Osteoarthritis (OA), as a chronic degenerative joint disorder, has seriously affected the life quality of patients. Despite lots of drug treatment strategies that have been studied, the therapeutic effect is still unsatisfactory due to the lack of prolonged circulation life and targeted delivery ability. Recently, functional cell membranes modified nanoparticles have been explored to achieve high-efficiency drug delivery. Herein, neutrophilerythrocyte hybrid membranes-coated dexamethasone sodium phosphate (Dexp)-loaded hollow copper sulfide nanoparticles (D-CuS@NR NPs) were fabricated for OA treatment. Generally, we achieved the synergistic treatment of mild-heating, prolonged circulation, and targeted delivery in this system. In particular, this biomimetic nanoparticle showed significant cytocompatibility and anti-inflammatory ability in vitro due to cell membrane coating and photothermal responsive drug release under NIR irradiation. Importantly, in vivo explorations revealed that D-CuS@NR NPs combined with photothermal treatment obtained an excellent therapy effect for preventing the OA process. Hence, this novel hybrid membranes-coated CuS NPs showed significant therapeutic efficacy by local warming and targeted drug delivery, which might become a promising drug delivery vehicle for improving the therapeutic effect of OA.
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