pH-Responsive Carboxymethylcellulose Nanoparticles for <sup>68</sup>Ga-WBC Labeling in PET Imaging

Carboxymethylcellulose (CMC) is a well-known pharmaceutical polymer, recently gaining attention in the field of nanomedicine, especially as a polyelectrolyte agent for the formation of complexes with oppositely charged macromolecules. Here, we report on the application of pH-sensitive pharmaceutical...

Full description

Bibliographic Details
Main Authors: Anna Maria Piras, Angela Fabiano, Stefania Sartini, Ylenia Zambito, Simona Braccini, Federica Chiellini, Angela G. Cataldi, Francesco Bartoli, Ana de la Fuente, Paola Anna Erba
Format: Article
Language:English
Published: MDPI AG 2019-10-01
Series:Polymers
Subjects:
pet
Online Access:https://www.mdpi.com/2073-4360/11/10/1615
Description
Summary:Carboxymethylcellulose (CMC) is a well-known pharmaceutical polymer, recently gaining attention in the field of nanomedicine, especially as a polyelectrolyte agent for the formation of complexes with oppositely charged macromolecules. Here, we report on the application of pH-sensitive pharmaceutical grade CMC-based nanoparticles (NP) for white blood cells (WBC) PET imaging. In this context and as an alternative to <sup>99m</sup>Tc-HMPAO SPECT labeling, the use of <sup>68</sup>Ga<sup>3+</sup> as PET radionuclide was investigated since, at early time points, it could provide the greater spatial resolution and patient convenience of PET tomography over SPECT clinical practices. Two operator-friendly kit-type formulations were compared, with the intention of radiolabeling within a short time (10 min), under mild conditions (physiological pH, room temperature) and in agreement with the actual clinically applied guidelines. NP were labeled by directly using <sup>68</sup>Ga<sup>3+</sup> eluted in HCL 0.05 N, from hospital suited <sup>68</sup>Ge/<sup>68</sup>Ga generator and in absence of chelator. The first kit type approach involved the application of <sup>68</sup>Ga<sup>3+</sup> as an ionotropic gelation agent for in-situ forming NP. The second kit type approach concerned the re-hydration of a proper freeze-dried injectable NP powder. pH-sensitive NP with 250 nm average diameter and 80% labeling efficacy were obtained. The NP dispersant medium, including a cryoprotective agent, was modulated in order to optimize the Zeta potential value (&#8722;18 mV), minimize the NP interaction with serum proteins and guarantee a physiological environment for WBC during NP incubation. Time-dependent WBC radiolabeling was correlated to NP uptake by using both confocal and FT-IR microscopies. The ready to use lyophilized NP formulation approach appears promising as a straightforward <sup>68</sup>Ga-WBC labeling tool for PET imaging applications.
ISSN:2073-4360