Bioengineered chondrocyte membrane-camouflaged anti-ferroptotic drug-loaded liposomes: A highly effective cartilage-targeted drug delivery system for osteoarthritis treatment

被引:1
|
作者
Cao, Siyang [1 ,2 ,3 ]
Wei, Yihao [1 ,2 ,4 ,5 ,7 ]
Qian, Junyu [1 ,2 ,3 ]
Yue, Yaohang [1 ,2 ,3 ]
Xiong, Ao [1 ,2 ,3 ]
Udduttula, Anjaneyulu [6 ]
Chen, Yingqi [1 ,2 ,3 ]
Zhao, Jiawei [5 ,7 ]
Liu, Peng [1 ,2 ,3 ]
Zeng, Hui [1 ,2 ,3 ]
机构
[1] Peking Univ, Shenzhen Hosp, Natl & Local Joint Engn Res Ctr Orthopaed Biomat, Shenzhen, Guangdong, Peoples R China
[2] Peking Univ, Shenzhen Hosp, Shenzhen Key Lab Orthopaed Dis & Biomat Res, Shenzhen, Guangdong, Peoples R China
[3] Peking Univ, Shenzhen Hosp, Dept Bone & Joint Surg, Shenzhen, Guangdong, Peoples R China
[4] Hong Kong Polytech Univ, Dept Rehabil Sci, Hong Kong, Peoples R China
[5] Chinese Acad Sci, Shenzhen Inst Adv Technol, Fac Pharmaceut Sci, Shenzhen, Guangdong, Peoples R China
[6] Vellore Inst Technol, Ctr Biomat Cellular & Mol Theranost, Vellore, Tamil Nadu, India
[7] Shenzhen Univ Adv Technol, Fac Pharmaceut Sci, Shenzhen, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Bioengineered chondrocyte membrane; Biomimetic liposomes; Ferroptosis; Osteoarthritis; CELL; NANOPARTICLES; CHARGE;
D O I
10.1016/j.cej.2024.155619
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Osteoarthritis (OA) is a chronic degenerative joint disorder that severely impacts patients' quality of life. Despite various drug treatment strategies, achieving effective therapeutic outcomes remains challenging due to the joint's unique structure, which results in rapid drug clearance through synovial fluid and the dense, avascular cartilage matrix. To address this issue, we developed an innovative nanoplatform utilizing biomimetic cell membrane-coating technology. This bioengineered chondrocyte membrane-camouflaged, anti-ferroptotic, drug- loaded system enhances cartilage penetration, prolongs drug retention, and provides targeted therapy. As a nanovehicle, it targets chondrocytes through membrane fusion, allowing rapid penetration and mitigating OA progression. In vitro experiments show that this nanocarrier alleviates iron homeostasis imbalance and suppresses lipid peroxidation, helping ameliorate metabolic disorders in chondrocytes and addressing multiple pathological processes triggered by ferroptosis. In vivo results further suggest that this "Trojan Horse" strategy extends drug retention in joints and improves therapeutic efficacy. This study presents a potential universal nanoplatform comprising bioengineered chondrocyte membrane-coated liposomes for highly effective cartilage-targeted drug delivery in OA treatment.
引用
收藏
页数:15
相关论文
共 5 条
  • [1] Anti-platelet Drug-loaded Targeted Technologies for the Effective Treatment of Atherothrombosis
    Muruganantham, Selvakumar
    Krishnaswami, Venkateshwaran
    Alagarsamy, Shanmugarathinam
    Kandasamy, Ruckmani
    CURRENT DRUG TARGETS, 2021, 22 (04) : 387 - 408
  • [2] Red blood cell membrane-camouflaged prednisolone acetate-loaded PLGA nanoparticles for kidney-targeted drug delivery
    Yang, Jing
    Zhang, Rongtao
    Wang, Fangliang
    Shang, Jinlu
    Wu, Siqiong
    Ding, Qian
    Yang, Liuxuan
    Fan, Qingze
    Ye, Yun
    Zhou, Meiling
    JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY, 2023, 86
  • [3] An intelligent responsive macrophage cell membrane-camouflaged mesoporous silicon nanorod drug delivery system for precise targeted therapy of tumors
    Minghua Li
    Xiaolong Gao
    Chao Lin
    Aijun Shen
    Jing Luo
    Qiongqiong Ji
    Jiaqi Wu
    Peijun Wang
    Journal of Nanobiotechnology, 19
  • [4] An intelligent responsive macrophage cell membrane-camouflaged mesoporous silicon nanorod drug delivery system for precise targeted therapy of tumors
    Li, Minghua
    Gao, Xiaolong
    Lin, Chao
    Shen, Aijun
    Luo, Jing
    Ji, Qiongqiong
    Wu, Jiaqi
    Wang, Peijun
    JOURNAL OF NANOBIOTECHNOLOGY, 2021, 19 (01)
  • [5] Panobinostat-loaded folate targeted liposomes as a promising drug delivery system for treatment of canine B-cell lymphoma
    Andre, Ana S.
    Dias, Joana N. R.
    Aguiar, Sandra I.
    Leonardo, Ana
    Nogueira, Sara
    Amaral, Joana D.
    Fernandes, Celia
    Gano, Lurdes
    Correia, Joao D. G.
    Cavaco, Marco
    Neves, Vera
    Correia, Jorge
    Castanho, Miguel
    Rodrigues, Cecilia M. P.
    Gaspar, Maria Manuela
    Tavares, Luis
    Aires-da-Silva, Frederico
    FRONTIERS IN VETERINARY SCIENCE, 2023, 10