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      Synthesis and Biodistribution of 99mTc-Labeled PLGA Nanoparticles by Microfluidic Technique.

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          Abstract

          The aim of present study was to develop radiolabeled NPs to overcome the limitations of fluorescence with theranostic potential. Synthesis of PLGA-NPs loaded with technetium-99m was based on a Dean-Vortex-Bifurcation Mixer (DVBM) using an innovative microfluidic technique with high batch-to-batch reproducibility and tailored-made size of NPs. Eighteen different formulations were tested and characterized for particle size, zeta potential, polydispersity index, labeling efficiency, and in vitro stability. Overall, physical characterization by dynamic light scattering (DLS) showed an increase in particle size after radiolabeling probably due to the incorporation of the isotope into the PLGA-NPs shell. NPs of 60 nm (obtained by 5:1 PVA:PLGA ratio and 15 mL/min TFR with 99mTc included in PVA) had high labeling efficiency (94.20 ± 5.83%) and >80% stability after 24 h and showed optimal biodistribution in BALB/c mice. In conclusion, we confirmed the possibility of radiolabeling NPs with 99mTc using the microfluidics and provide best formulation for tumor targeting studies.

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          Author and article information

          Journal
          Pharmaceutics
          Pharmaceutics
          MDPI AG
          1999-4923
          1999-4923
          Oct 22 2021
          : 13
          : 11
          Affiliations
          [1 ] Nuclear Medicine Unit, Department of Medical-Surgical Sciences and of Translational Medicine, Faculty of Medicine and Psychology, "Sapienza" University of Rome, 00161 Rome, Italy.
          Article
          pharmaceutics13111769
          10.3390/pharmaceutics13111769
          8621482
          34834184
          795bedbe-7604-4d47-88a8-5c77b2e4e854
          History

          radiolabeled nanoparticles,microfluidics,nuclear medicine,poly (lactic-co-glycolic acid) (PLGA)

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