4.7 Article

Biodistribution Study of Niosomes in Tumor-Implanted BALB/C Mice Using Scintigraphic Imaging

Journal

FRONTIERS IN PHARMACOLOGY
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fphar.2021.778396

Keywords

biodistribution; nanotechnology; nanocarrier; niosomes; radiolabeling; gamma scintigraphy

Funding

  1. Fundamental Research Grant Scheme (FRGS)
  2. Ministry of Higher Education, Malaysia [FRGS/2/2014/SG05/MUSM/03/3]
  3. Malaysian Palm Oil Board (MPOB)

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The study found that Technetium-99m-labeled niosomes had high radiolabeling efficiency and stability in vivo, with scintigraphic imaging showing radioactivity mainly accumulated in the liver, spleen, and kidneys, indicating higher specificity for the tumor area.
The purpose of this work was to study the biodistribution of niosomes in tumor-implanted BALB/c mice using gamma scintigraphy. Niosomes were first formulated and characterized, then radiolabeled with Technetium-99 m (Tc-99m). The biodistribution of 99mTc-labeled niosomes was evaluated in tumor-bearing mice through intravenous injection and imaged with gamma scintigraphy. The labeled complexes possessed high radiolabeling efficiency (98.08%) and were stable in vitro (>80% after 8 h). Scintigraphic imaging showed negligible accumulation in the stomach and thyroid, indicating minimal leaching of the radiolabel in vivo. Radioactivity was found mainly in the liver, spleen and kidneys. Tumor-to-muscle ratio indicated a higher specificity of the formulation for the tumor area. Overall, the formulated niosomes are stable both in vitro and in vivo, and show preferential tumor accumulation.

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