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.

Synthesis and Biodistribution of 99mTc-Labeled PLGA Nanoparticles by Microfluidic Technique / Varani, Michela; Campagna, Giuseppe; Bentivoglio, Valeria; Serafinelli, Matteo; Luisa Martini, Maria; Galli, Filippo; Signore, Alberto. - (2022), pp. 137-149. [10.3390/pharmaceutics13111769].

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

Michela Varani
;
Giuseppe Campagna;Valeria Bentivoglio;Matteo Serafinelli;Filippo Galli;Alberto Signore
2022

Abstract

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.
2022
Nanomedicine Formulations Based on PLGA Nanoparticles for Diagnosis Monitoring and Treatment of Disease. From Bench to Bedside
978-3-0365-4490-8
978-3-0365-4489-2
radiolabeled nanoparticles; poly (lactic-co-glycolic acid) (plga); nuclear medicine; microfluidics
02 Pubblicazione su volume::02a Capitolo o Articolo
Synthesis and Biodistribution of 99mTc-Labeled PLGA Nanoparticles by Microfluidic Technique / Varani, Michela; Campagna, Giuseppe; Bentivoglio, Valeria; Serafinelli, Matteo; Luisa Martini, Maria; Galli, Filippo; Signore, Alberto. - (2022), pp. 137-149. [10.3390/pharmaceutics13111769].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1667830
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