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Osteoarthritis is characterized by lubrication failure of the articular cartilage and severe inflammation of the joint capsule. Lubricating mesoporous silica nanoparticles (MSNs) have been developed for the treatment of osteoarthritis based on enhanced lubrication and local drug delivery. However, MSNs are difficult to degrade in vivo in a short time, resulting in potential toxic effect due to bioaccumulation. In this study, biodegradable MSNs (bMSNs) were prepared through an oil-water biphase stratification method, and modified with poly(2-methacryloyloxyethyl phosphocholine) (PMPC) to synthesize lubricating drug-loaded nanoparticles (bMSNs-NH2@PMPC) by photopolymerization. The in vitro degradation test demonstrated that the bMSNs and bMSNs-NH2@PMPC almost degraded within 7 days. The tribiological test showed that the lubrication property of the bMSNs-NH2@PMPC was greatly improved, with a reduction of 50% in the friction coefficient (COF) compared with the bMSNs. It was attributed to hydration lubrication mechanism by which a tenacious hydration layer is formed surrounding the zwitterionic headgroups (N+(CH3)3 and PO4- ) in PMPC polyelectrolyte polymer. Additionally, the bMSNs-NH2@PMPC maintained excellent lubrication property under degradation and achieved sustained drug release behavior compared with the bMSNs. In summary, the biodegradable bMSNs-NH2@PMPC developed in this study with the properties of enhanced lubrication and drug delivery may be a promising approach for osteoarthritis therapy.


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Biodegradable lubricating mesoporous silica nanoparticles for osteoarthritis therapy

Show Author's information Li WAN1,2,Yi WANG1,Xiaolong TAN1Yulong SUN1Jing LUO3Hongyu ZHANG1( )
State Key Laboratory of Tribology, Department of Mechanical Engineering, Tsinghua University, Beijing 100084, China
College of Mining, Guizhou University, Guiyang 550025, China
Beijing Research Institute of Automation for Machinery Industry Co., Ltd., Beijing 100120, China

† These authors contributed equally to this work.

Abstract

Osteoarthritis is characterized by lubrication failure of the articular cartilage and severe inflammation of the joint capsule. Lubricating mesoporous silica nanoparticles (MSNs) have been developed for the treatment of osteoarthritis based on enhanced lubrication and local drug delivery. However, MSNs are difficult to degrade in vivo in a short time, resulting in potential toxic effect due to bioaccumulation. In this study, biodegradable MSNs (bMSNs) were prepared through an oil-water biphase stratification method, and modified with poly(2-methacryloyloxyethyl phosphocholine) (PMPC) to synthesize lubricating drug-loaded nanoparticles (bMSNs-NH2@PMPC) by photopolymerization. The in vitro degradation test demonstrated that the bMSNs and bMSNs-NH2@PMPC almost degraded within 7 days. The tribiological test showed that the lubrication property of the bMSNs-NH2@PMPC was greatly improved, with a reduction of 50% in the friction coefficient (COF) compared with the bMSNs. It was attributed to hydration lubrication mechanism by which a tenacious hydration layer is formed surrounding the zwitterionic headgroups (N+(CH3)3 and PO4- ) in PMPC polyelectrolyte polymer. Additionally, the bMSNs-NH2@PMPC maintained excellent lubrication property under degradation and achieved sustained drug release behavior compared with the bMSNs. In summary, the biodegradable bMSNs-NH2@PMPC developed in this study with the properties of enhanced lubrication and drug delivery may be a promising approach for osteoarthritis therapy.

Keywords: lubrication, drug delivery, osteoarthritis, biodegradable, mesoporous silica nanoparticles

References(32)

[1]
Jin Z M, Dowson D. Bio-friction. Friction 1(2): 100-113 (2013)
[2]
Glyn-Jones S, Palmer A J R, Agricola R, Price A J, Vincent T L, Weinans H, Carr A J. Osteoarthritis. Lancet 386(3991): 376-387 (2015)
[3]
Halilaj E, Le Y, Hicks J L, Hastie T J, Delp S L. Modeling and predicting osteoarthritis progression: Data from the osteoarthritis initiative. Osteoart Cartil 26(12): 1643-1650 (2018)
[4]
Wimmer M A, Birken L, Sellenschloh K, Schneider E. Damage due to rolling in total knee replacement-the influence of tractive force. Friction 1(2): 178-185 (2013)
[5]
Ji X L, Zhang H Y. Current strategies for the treatment of early stage osteoarthritis. Front Mech Eng 5: 57 (2019)
[6]
Choi Y J, Kim S O, Sim J H, Hahm K D. Postoperative anemia is associated with acute kidney injury in patients undergoing total hip replacement arthroplasty: A retrospective study. Anesth Analg 122(6): 1923-1928 (2016)
[7]
Podmore B, Hutchings A, Konan S, van der Meulen J. The agreement between chronic diseases reported by patients and derived from administrative data in patients undergoing joint arthroplasty. BMC Med Res Methodol 19(1): 87 (2019)
[8]
Ji X L, Yan Y F, Sun T, Zhang Q, Wang Y X, Zhang M, Zhang H Y, Zhao X. Glucosamine sulphate-loaded distearoyl phosphocholine liposomes for osteoarthritis treatment: Combination of sustained drug release and improved lubrication. Biomater Sci 7(7): 2716-2728 (2019)
[9]
Zheng Y W, Yang J L, Liang J, Xu X Y, Cui W G, Deng L F, Zhang H Y. Bioinspired hyaluronic acid/phosphorylcholine polymer with enhanced lubrication and anti-inflammation. Biomacromolecules 20(11): 4135-4142 (2019)
[10]
Liu G Q, Cai M R, Zhou F, Liu W M. Charged polymer brushes-grafted hollow silica nanoparticles as a novel promising material for simultaneous joint lubrication and treatment. J Phys Chem B 118(18): 4920-4931 (2014)
[11]
Yan Y F, Sun T, Zhang H B, Ji X L, Sun Y L, Zhao X, Deng L F, Qi J, Cui W G, Santos H A, et al. Euryale ferox seed-inspired superlubricated nanoparticles for treatment of osteoarthritis. Adv Funct Mater 29(4): 1807559 (2019)
[12]
Tan X L, Sun Y L, Sun T, Zhang H Y. Mechanised lubricating silica nanoparticles for on-command cargo release on simulated surfaces of joint cavities. Chem Commun 55(18): 2593-2596 (2019)
[13]
Shao D, Lu M M, Zhao Y W, Zhang F, Tan Y F, Zheng X, Pan Y, Xiao X A, Wang Z, Dong W F, et al. The shape effect of magnetic mesoporous silica nanoparticles on endocytosis, biocompatibility and biodistribution. Acta Biomater 49: 531-540 (2017)
[14]
Wei Y C, Quan L, Zhou C, Zhan Q Q. Factors relating to the biodistribution & clearance of nanoparticles & their effects on in vivo application. Nanomedicine 13(12): 1495-1512 (2018)
[15]
Pohaku Mitchell K K, Liberman A, Kummel A C, Trogler W C. Iron (III)-doped, silica nanoshells: A biodegradable form of silica. J Am Chem Soc 134(34): 13997-14003 (2012)
[16]
Kim I Y, Joachim E, Choi H, Kim K. Toxicity of silica nanoparticles depends on size, dose, and cell type. Nanomed Nanotechnol Biol Med 11(16): 1407-1416 (2015)
[17]
Fu C H, Liu T L, Li L L, Liu H Y, Chen D, Tang F Q. The absorption, distribution, excretion and toxicity of mesoporous silica nanoparticles in mice following different exposure routes. Biomaterials 34(10): 2565-2575 (2013)
[18]
Goel S, Chen F, Luan S J, Valdovinos H F, Shi S X, Graves S A, Ai F R, Barnhart T E, Theuer C P, Cai W B. Engineering intrinsically zirconium-89 radiolabeled self-destructing mesoporous silica nanostructures for in vivo biodistribution and tumor targeting studies. Adv Sci 3(11): 1600122 (2016)
[19]
Du X, Li X Y, Xiong L, Zhang X J, Kleitz F, Qiao S Z. Mesoporous silica nanoparticles with organo-bridged silsesquioxane framework as innovative platforms for bioimaging and therapeutic agent delivery. Biomaterials 91: 90-127 (2016)
[20]
Shao D, Li M Q, Wang Z, Zheng X, Lao Y H, Chang Z M, Zhang F, Lu M M, Yue J, Hu H Z, et al. Bioinspired diselenide-bridged mesoporous silica nanoparticles for dual- responsive protein delivery. Adv Mater 30(29): 1801198 (2018)
[21]
Li H M, Guo H L, Lei C, Liu L, Xu L Q, Feng Y P, Ke J, Fang W, Song H, Xu C, et al. Nanotherapy in joints: Increasing endogenous hyaluronan production by delivering hyaluronan synthase 2. Adv Mater 31(46): 1904535 (2019)
[22]
Wang Z, Zhang F, Shao D, Chang Z M, Wang L, Hu H Z, Zheng X, Li X Z, Chen F M, Tu Z X, et al. Janus nanobullets combine photodynamic therapy and magnetic hyperthermia to potentiate synergetic anti-metastatic immunotherapy. Adv Sci 6(22): 1901690 (2019)
[23]
Huh S, Wiench J W, Yoo J C, Pruski M, Lin V S Y. Organic functionalization and morphology control of mesoporous silicas via a co-condensation synthesis method. Chem Mat 15(22): 4247-4256 (2003)
[24]
Shen D K, Yang J P, Li X M, Zhou L, Zhang R Y, Li W, Chen L, Wang R, Zhang F, Zhao D Y. Biphase stratification approach to three-dimensional dendritic biodegradable mesoporous silica nanospheres. Nano Lett 14(2): 923-932 (2014)
[25]
Liu S Z, Zhang Q, Han Y, Sun Y L, Zhang Y F, Zhang H Y. Bioinspired surface functionalization of titanium alloy for enhanced lubrication and bacterial resistance. Langmuir 35(40): 13189-13195 (2019)
[26]
Zhang H Y, Zhang S H, Luo J B, Liu Y H, Qian S H, Liang F H, Huang Y L. Investigation of protein adsorption mechanism and biotribological properties at simulated stem-cement interface. J Tribol 135(3): 032301 (2013)
[27]
Sundaram H, Voigts B, Beer K, Meland M. Comparison of the rheological properties of viscosity and elasticity in two categories of soft tissue fillers: Calcium hydroxylapatite and hyaluronic acid. Dermatol Surg 36(S3): 1859-1865 (2010)
[28]
Klein J. Hydration lubrication. Friction 1(1): 1-23 (2013)
[29]
Wang Y X, Sun Y L, Gu Y H, Zhang H Y. Articular cartilage-inspired surface functionalization for enhanced lubrication. Adv Mater Interfaces 6(12): 1900180 (2019)
[30]
Murakami T, Yarimitsu S, Nakashima K, Sawae Y, Sakai N. Influence of synovia constituents on tribological behaviors of articular cartilage. Friction 1(2): 150-162 (2013)
[31]
Klein J. Repair or replacement-a joint perspective. Science 323(5910): 47-48 (2009)
[32]
Han Y, Liu S Z, Sun Y L, Gu Y H, Zhang H Y. Bioinspired surface functionalization of titanium for enhanced lubrication and sustained drug release. Langmuir 35(20): 6735-6741 (2019)
Publication history
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Publication history

Received: 22 January 2020
Revised: 12 March 2020
Accepted: 27 March 2020
Published: 22 May 2020
Issue date: January 2022

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© The author(s) 2020

Acknowledgements

This study was financially supported by National Natural Science Foundation of China (51675296), Tsinghua University-Peking Union Medical College Hospital Initiative Scientific Research Program (20191080593), Tsinghua University Initiative Scientific Research Program (20197050026), Foshan-Tsinghua Innovation Special Fund (FTISF), Research Fund of State Key Laboratory of Tribology, Tsinghua University, China (SKLT2020C11), and Ng Teng Fong Charitable Foundation (202-276-132-13).

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