4.8 Article

Nerve Growth Factor-Targeted Molecular Theranostics Based on Molybdenum Disulfide Nanosheet-Coated Gold Nanorods (MoS2-AuNR) for Osteoarthritis Pain

Journal

ACS NANO
Volume 15, Issue 7, Pages 11711-11723

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.1c02454

Keywords

molybdenum disulfide; gold nanorods; osteoarthritis; nerve growth factor; theranostics; pain relief

Funding

  1. Health and Medical Research Fund Scheme [01150087, 16172691]
  2. Research Grants Council of Hong Kong ECS [PolyU 251008/18M]
  3. GRF [PolyU 151061/20M, 152169/17E]
  4. National Natural Science Foundation of China (NSFC) [31771077]
  5. Hong Kong Polytechnic University Project of Strategic Importance [ZE1E, ZE2C]
  6. NFSC/RGC schemes [N_PolyU520/20]

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The study introduced a novel theranostic nanoprobe targeting osteoarthritis pain, utilizing photoacoustic imaging and photothermal therapy to localize and treat the source of pain. The research found that the nanoprobes could accurately target OA knees and effectively alleviate pain and abnormal behavior in a mouse model.
Osteoarthritis (OA) is a leading cause of chronic pain in the elderly worldwide. Yet current diagnosis and therapy for OA pain are subjective and nonspecific with significant adverse effects. Here, we introduced a theranostic nanoprobe based on molybdenum disulfide nanosheet-coated gold nanorods (MoS2-AuNR) targeting never growth factor (NGF), a key player in pain sensation, for photoacoustic pain imaging and near-infrared (NIR) imaging-guided photothermal analgesic therapy. MoS2 coating significantly improved the photoacoustic and photothermal performance of AuNR. Functionalization of MoS2-AuNR nanoprobes by conjugating with NGF antibody enabled active targeting on painful OA knees in a surgical OA murine model. We observed that our functional nanoprobes accumulated in the OA knee rather than the contralateral intact one, and the amount was correlated with the severity of mechanical allodynia in our mouse model. Under imaging guidance, NIR-excited photothermal therapy could mitigate mechanical allodynia and walking imbalance behavior for both subacute and chronic stages of OA in a preclinical setting. This molecular theranostic approach enabled us to specifically localize the source of OA pain and efficiently block peripheral pain transmission.

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