Cited by 17Molecular Sensors and Ion DetectionOsteoarthritis Treatment and MechanismsLuminescence and Fluorescent Materials

Cartilage-targeting fluorophores for early detection of arthritis in the NIR-II window

Open access
Kang, Homan, Park, Seung Hun, Ozmen, Guliz Ersoy, Hur, Won, Dinh, Jason, Wang, Haoran, Nguyen, Vy, Ahn, Sung +6 more·2025·Chem

Abstract

Early diagnosis is crucial for the effective treatment of rheumatoid arthritis because continuing inflammation can lead to irreversible joint damage. However, current diagnostic methods lack tissue-specific guidelines to monitor the progressive course of degenerative joint diseases. Here, we demonstrate that cartilage-targeting fluorophores (CARFs) exhibit a remarkable cartilage-specific affinity and offer advanced imaging capabilities in the near-infrared II (NIR-II) window, characterized by minimal tissue scattering and negligible autofluorescence. CARFs show little to no toxicity, both in vitro (up to 100 μM) and in vivo (3 μmol/kg via intravenous injection), suggesting clinical potential. Furthermore, CARFs in the NIR-II window enable the precise visualization of cartilage lining, serving as a reliable diagnostic indicator for the early detection of arthritis in preclinical mouse models. CARFs are NIR fluorescence-emitting targeted contrast agents for prognostic imaging of joint tissue, with the potential to revolutionize applications in tissue engineering, joint surgery, and drug development for inflammatory diseases.

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Crossref · 10.1016/j.chempr.2025.102481

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  • Targeted molecular design overcomes the nonspecific accumulation and low selectivity that limit the in vivo performance of NIR-II cyanine fluorophores.

    “Targeted molecular design represents a pivotal approach to overcoming the nonspecific accumulation and low selectivity that limit the in vivo performance of NIR-II cyanine fluorophores103.”

    From Organic small-molecule NIR-II fluorophores for tumor phototheranostics (2026) · cites this paper as [103]

    The Discussion (page not provided) identifies lack of effective targeting as a limitation of existing dyes for arthritis imaging and describes a targeting strategy to address it. The Results (page not provided) report selective cartilage targeting and reduced background signal with the designed NIR-II fluorophore. The paper does not establish nonspecific accumulation and low selectivity as limitations of NIR-II cyanine fluorophores generally, so the claim extends beyond its findings. (LLM, conf=0.82)

    Experimental — accuracy not yet measured

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Authors
Kang, H., Park, S. H., Ozmen, G. E., Hur, W., Dinh, J., Wang, H., Nguyen, V., Ahn, S., Yamashita, A., Stiles, W. R., Kashiwagi, S., Bao, K., Henary, M., & Choi, H. S.
Affiliations
  • Harvard University (US)
  • Georgia State University (US)
Corresponding author
  • Henary, Maged
  • Choi, Hak Soo
Venue
Chem
Publisher
Elsevier BV
Published
2025-08
Volume
11
Issue
8
Pages
102481
ISSN
2451-9294 (ISSN-L)
OpenAlex
W4408366255
Cited by
17
References
48
Citations by year
2026: 17
FWCI
2.12
Type
journal article
Language
en
Open access
Locations
  • Chem (acceptedVersion)
  • SSRN Electronic Journal (acceptedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health National Cancer Institute (R01CA280968)
  • Korea Ministry of Health and Welfare (RS-2024-00436472)
  • National Institutes of Health
  • Korea Health Industry Development Institute
  • Korea Ministry of Science and ICT (RS-2024-00466887)
Topics
  • Physical Sciences › Chemistry › Spectroscopy › Molecular Sensors and Ion Detection
  • Health Sciences › Medicine › Rheumatology › Osteoarthritis Treatment and Mechanisms
  • Physical Sciences › Materials Science › Materials Chemistry › Luminescence and Fluorescent Materials
Keywords
rheumatoid arthritis, early diagnosis, near-infrared fluorescence imaging, contrast media, autofluorescence, toxicity, joint degeneration, preclinical mouse models

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