4.7 Article

Zoledronic Acid-Loaded Hybrid Hyaluronic Acid/Polyethylene Glycol/Nano-Hydroxyapatite Nanoparticle: Novel Fabrication and Safety Verification

Journal

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fbioe.2021.629928

Keywords

hybrid; nanoparticle; drug release; cytotoxicity; immune response; zoledronic acid

Funding

  1. Natural Science Foundation of Hunan Province [2017JJ3109]
  2. Project of Changsha Science and Technology Bureau [kq1706042]
  3. Project of Hunan Provincial Health Commission's Scientific Research Program [B20180718]
  4. Hunan Cancer Hospital Climb Plan

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The study developed an organic-inorganic hybrid nanoparticle as a carrier for zoledronic acid, achieving high drug loading efficiency, sustained drug release, and good biocompatibility. In vitro and in vivo experiments showed low cytotoxicity and acceptable immune response under low-dose nanoparticle treatment, suggesting its potential application for future osteosarcoma therapeutic strategies.
Osteosarcoma is a malignant tumor that often occurs in adolescents and children. Zoledronic acid, a new-generation bisphosphonate, has been widely used as an antitumor drug to inhibit bone metastasis. However, the rapid renal elimination results in low effective concentrations. Meanwhile, high-dose intravenous zoledronic acid administration leads to severe side effects. The present study fabricated an organic-inorganic hybrid nanoparticle as the carrier of zoledronic acid. The rod-like nanoparticle, which had 150-nm length and 40-nm cross-sectional diameter, consisted of a hyaluronic acid/polyethylene glycol (HA-PEG) polymer shell and a nano-hydroxyapatite (nHA) core, with zoledronic acid molecules loading on the surface of nHA and clearance of HA-PEG shell. The nanoparticle was characterized by microscopic analysis, in vitro release study, cytotoxicity analysis, and in vivo immune response examination. Results showed that the compact and stable structure could achieve high drug loading efficiency, sustained drug release, and great biocompatibility. In vitro and in vivo experiments revealed the low cytotoxicity and acceptable immune response under low-dose nanoparticle treatment, indicating its potential application for future osteosarcoma therapeutic strategies.

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