1. Academic Validation
  2. Strategic Assessment of Boron-Enriched Carbon Dots/Naproxen: Diagnostic, Toxicity, and In Vivo Therapeutic Evaluation

Strategic Assessment of Boron-Enriched Carbon Dots/Naproxen: Diagnostic, Toxicity, and In Vivo Therapeutic Evaluation

  • Mol Pharm. 2024 Jan 13. doi: 10.1021/acs.molpharmaceut.3c00919.
Aswandi Wibrianto 1 2 3 Febrianti S D Putri 1 Ummi K Nisa 1 Nila Mahyahani 1 Siti F A Sugito 1 2 Andika P Wardana 1 Satya C W Sakti 1 2 Jia-Yaw Chang 3 Mochamad Z Fahmi 1 2
Affiliations

Affiliations

  • 1 Department of Chemistry, University Airlangga, Surabaya 60115, Indonesia.
  • 2 Supra Modification Nano-Micro Engineering Research Group, Universitas Airlangga, Surabaya 60115, Indonesia.
  • 3 Department of Chemical Engineering, National Taiwan University of Science and Technology, Taipei, 106335, Taiwan Republic of China.
Abstract

Cancer is a significant global public health concern, ranking as the leading cause of mortality worldwide. This study thoroughly explores boron-doped carbon dots (B-CDs) through a simple/rapid microwave-assisted approach and their versatile applications in Cancer therapy. The result was highly uniform particles with an average diameter of approximately 4 nm. B-CDs exhibited notable properties, including strong fluorescence with a quantum yield of 33%. Colloid stability tests revealed their robustness within a pH range of 6-12, NaCl concentrations up to 0.5 M, and temperatures ranging from 30 to 60 °C. The study also delved into the kinetics of naproxen release from B-CDs as a drug delivery system. The loading efficacy of naproxen exceeded 55.56%. Under varying pH conditions, the release of naproxen from B-CDs conformed to the Peppas-Sahlin model, demonstrating the potential of Naproxen-loaded CDs for Cancer drug delivery. In vitro cytotoxicity assessments, conducted using the CCK-8 Assay and flow cytometry, consistently indicated low toxicity with average cell viability exceeding 80%. An in vivo toxicity test on female mice administered 20 mg/kg of B-CDs for 31 days revealed reversible histological changes in the liver and kidneys, while the pancreas remained unaffected. Importantly, B-CDs did not impact the mice's physical behavior, body weight, or survival. In vivo experiments targeting benzo(a)pyrene-induced fibrosarcoma demonstrated the efficacy of B-CDs as naproxen carriers in the treatment of Cancer. This in vivo study provides a thorough comprehension of B-CDs synthesis and toxicity and their potential applications in Cancer therapy and drug delivery systems.

Keywords

boron-doped carbon dots; drug delivery; in vivo; naproxen; toxicity.

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