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Exploring Tc-Labeled Iron-Binding Glycoprotein Nanoparticles as a Potential Nanoplatform for Sentinel Lymph Node Imaging: Development, Characterization, and Radiolabeling Studies. | LitMetric

AI Article Synopsis

  • Lactoferrin nanoparticles (LF-NPs) are being studied as a new method for drug delivery and imaging, particularly for tracking cancer-related sentinel lymph nodes.
  • The nanoparticles were developed through thermal treatment to achieve a specific size and were characterized for stability, biocompatibility, and safety through various tests.
  • The successful radiolabeling with technetium-99m and subsequent biodistribution studies in rats indicate LF-NPs' potential for effective targeted drug delivery and further biomedical applications.

Article Abstract

Lactoferrin, an iron binding glycoprotein-based nanoparticle, has emerged as a promising platform for drug delivery and imaging. This study presents the potential use of the protein nanocarrier in tracking sentinel lymph nodes for cancer staging. Lactoferrin nanoparticles (LF-NPs) were synthesized using a thermal treatment process and optimized to obtain 60-70 nm particle size with PDI less than 0.2. The NPs were characterized microscopically and spectroscopically, ensuring a comprehensive understanding of their physicochemical properties. The LF-NPs were found to be stable in different pH conditions. Their biocompatibility was confirmed through cytotoxicity assessments on RAW 264.7 cells, and hemolysis assay and in vivo toxicity study reveal their safe profile. Additionally, LF-NPs were successfully radiolabeled with technetium-99m (>90% labeling yield). Cell uptake studies with RAW 264.7 exhibited an uptake of ∼6%. Biodistribution studies in Wistar rats shed light on their in vivo behavior and suitability for targeted drug delivery systems. These findings collectively emphasize the multifaceted utility of LF-NPs, positioning them as a promising platform for diverse biomedical innovations.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11483396PMC
http://dx.doi.org/10.1021/acsomega.4c05991DOI Listing

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