Cited by 58Osteoarthritis Treatment and MechanismsCurcumin's Biomedical ApplicationsAdvanced Drug Delivery Systems

Therapeutic potential of hyaluronic acid/chitosan nanoparticles for the delivery of curcuminoid in knee osteoarthritis and an in�vitro evaluation in chondrocytes

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Wang, Jian, Wang, Xiang, Cao, Yun, Huang, Tao, Song, Deng‑Xin, Tao, Hai‑Rong·2018·International Journal of Molecular Medicine

Abstract

Knee osteoarthritis (OA) is the main cause of leg pain in middle‑aged and elderly individuals. Hyaluronic acid (HA), as well as curcuminoid, has been used in the treatment of knee OA. In the present study, HA/chitosan nanoparticles (CNPs) were prepared for the delivery of curcuminoid, in order to investigate whether HA and curcuminoid can act synergistically as a better treatment option. The knee OA model was established by the Hulth method, and a knee OA chondrocyte model was constructed by the co‑induction of interleukin‑1β and tumor necrosis factor (TNF)‑α. The drug loading capacity of HA/CNP for the delivery of curcuminoid was measured by an ultraviolet assay, and the cytotoxicity to chondrocytes was measured by an MTT assay. Collagen II was detected by immunofluorescence, and the expression levels of nuclear factor (NF)‑κB and inflammation‑related genes in cartilage tissue and chondrocytes were detected. Chondrocyte proliferation was determined by an EdU assay, and chondrocyte apoptosis was determined by flow cytometry. The Mankin pathological score of the Outerbridge classification was obtained. The results demonstrated that the optimum drug loading capacity of HA/CNP for the delivery of curcuminoid was 38.44%, with a good sustained release function. HA/CNP treatment resulted in inhibition of the NF‑κB pathway, as well as the expression of matrix metalloproteinase (MMP)‑1 and MMP‑13, but it increased collagen II expression. HA/CNP for the delivery of curcuminoid significantly decreased the Outerbridge classification and Mankin pathological scores to close to normal until the 4th week. Furthermore, it was also observed that all the effects of HA/CNP on the delivery of curcuminoid were more prominent compared with the effects of HA or curcuminoid treatment individually. Taken together, these findings demonstrated that HA/CNP for the delivery of curcuminoid may suppress inflammation and chondrocyte apoptosis in knee OA via repression of the NF‑κB pathway.

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Authors
Wang, J., Wang, X., Cao, Y., Huang, T., Song, D., & Tao, H.
Affiliations
  • Shanghai First People's Hospital (CN)
  • Shanghai Jiao Tong University (CN)
  • Department of Orthopedics, Baoshan Branch of Shanghai First People's Hospital, Shanghai 200940, P.R. China
  • Department of Orthopaedics, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 201999, P.R. China
Venue
International Journal of Molecular Medicine
Published
2018-08-09
Volume
42
Issue
5
Pages
2604-2614
ISSN
  • 1107-3756 (ISSN-L)
  • 1791-244X
OpenAlex
W2886128255
Cited by
58
References
0
Citations by year
2025: 6 · 2024: 10 · 2023: 8 · 2022: 14 · 2021: 9 · 2020: 9 · 2019: 1 · 2017: 1
FWCI
3.96
Type
journal article
Language
en
Open access
Licence
cc-by-nc-nd
Locations
  • International Journal of Molecular Medicine (publishedVersion, cc-by-nc-nd)
  • Europe PMC (PubMed Central) (publishedVersion, other-oa)
  • PubMed Central (publishedVersion, cc-by-nc-nd)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Rheumatology › Osteoarthritis Treatment and Mechanisms
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Medicine › Curcumin's Biomedical Applications
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advanced Drug Delivery Systems
Keywords
knee osteoarthritis, hyaluronic acid, chitosan nanoparticles, curcuminoids, drug delivery, chondrocytes, NF-κB signaling, chondrocyte apoptosis, cartilage inflammation, type II collagen, MMP-1, matrix metalloproteinase-13, drug loading capacity, sustained drug release, IL-1β, TNF-α
MeSH terms
Animals, Curcumin, Flow Cytometry, Fluorescent Antibody Technique, Hyaluronic Acid, Male, Blotting, Western, Rats, Sprague-Dawley, Chondrocytes, Reverse Transcriptase Polymerase Chain Reaction, Osteoarthritis, Knee, Matrix Metalloproteinase 1, Collagen Type II, Chitosan, Rats, Matrix Metalloproteinase 13, Nanoparticles

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