Development of Resorbable Phosphate-Based Glass Microspheres as MRI Contrast Media Agents

Author:

Molinar-Díaz Jesús12ORCID,Arjuna Andi13,Abrehart Nichola4ORCID,McLellan Alison5,Harris Roy6,Islam Md Towhidul1ORCID,Alzaidi Ahlam7ORCID,Bradley Chris R.8ORCID,Gidman Charlotte5,Prior Malcolm J. W.8,Titman Jeremy5,Blockley Nicholas P.7,Harvey Peter58,Marciani Luca4ORCID,Ahmed Ifty1ORCID

Affiliation:

1. Advanced Materials Research Group, Faculty of Engineering, University of Nottingham, Nottingham NG7 2RD, UK

2. Composites Research Group, Faculty of Engineering, University of Nottingham, Nottingham NG7 2GX, UK

3. Faculty of Pharmacy, Hasanuddin University, Makassar 90245, Indonesia

4. Nottingham Digestive Diseases Centre, Translational Medical Sciences, School of Medicine, University of Nottingham, Nottingham NG7 2UH, UK

5. School of Chemistry, University of Nottingham, Nottingham NG7 2RD, UK

6. Research Design Service East Midlands, Queen’s Medical Centre, Nottingham NG7 2UH, UK

7. School of Life Sciences, University of Nottingham Medical School, Queen’s Medical Centre, Nottingham NG7 2UH, UK

8. Sir Peter Mansfield Imaging Centre, School of Medicine, University of Nottingham, Nottingham NG7 2QX, UK

Abstract

In this research, resorbable phosphate-based glass (PBG) compositions were developed using varying modifier oxides including iron (Fe2O3), copper (CuO), and manganese (MnO2), and then processed via a rapid single-stage flame spheroidisation process to manufacture dense (i.e., solid) and highly porous microspheres. Solid (63–200 µm) and porous (100–200 µm) microspheres were produced and characterised via SEM, XRD, and EDX to investigate their surface topography, structural properties, and elemental distribution. Complementary NMR investigations revealed the formation of Q2, Q1, and Q0 phosphate species within the porous and solid microspheres, and degradation studies performed to evaluate mass loss, particle size, and pH changes over 28 days showed no significant differences among the microspheres (63–71 µm) investigated. The microspheres produced were then investigated using clinical (1.5 T) and preclinical (7 T) MRI systems to determine the R1 and R2 relaxation rates. Among the compositions investigated, manganese-based porous and solid microspheres revealed enhanced levels of R2 (9.7–10.5 s−1 for 1.5 T; 17.1–18.9 s−1 for 7 T) and R1 (3.4–3.9 s−1 for 1.5 T; 2.2–2.3 s−1 for 7 T) when compared to the copper and iron-based microsphere samples. This was suggested to be due to paramagnetic ions present in the Mn-based microspheres. It is also suggested that the porosity in the resorbable PBG porous microspheres could be further explored for loading with drugs or other biologics. This would further advance these materials as MRI theranostic agents and generate new opportunities for MRI contrast-enhancement oral-delivery applications.

Funder

National Institute for Health Research (NIHR) Nottingham Biomedical Research Centre

Engineering and Physical Sciences Research Council

Academy of Medical Sciences Springboard Award

Publisher

MDPI AG

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