Journal
JOURNAL OF PHARMACY AND PHARMACOLOGY
Volume 67, Issue 5, Pages 640-650Publisher
WILEY
DOI: 10.1111/jphp.12362
Keywords
apoptosis; cell injection; cell therapies; NIH 3T3; viability
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Funding
- University of Nottingham International Office scholarship
- Misr El-Kheir Foundation
- UK Regenerative Medicine Platform Hub for Acellular Technologies
- MRC [MR/K026682/1] Funding Source: UKRI
- Medical Research Council [MR/K026682/1] Funding Source: researchfish
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ObjectivesThis study focuses on the effect of the injection administration process on a range of cell characteristics. MethodsEffects of different ejection rates, needle sizes and cell suspension densities were assessed in terms of viability, membrane integrity, apoptosis and senescence of NIH 3T3 fibroblasts. For ratiometric measurements, a multiplex assay was used to verify cell viability, cytotoxicity and apoptosis independent of cell number. Co-delivery with alginate hydrogels and viscosity-modifying excipients was also assessed. Key findingsEjections at 150l/min resulted in the highest percentage of dose being delivered as viable cells among ejection rates tested. The difference in proportions of apoptotic cells became apparent 48h after ejection, with proportions being higher in samples ejected at slower rates. Co-delivery with alginate hydrogels demonstrated a protective action on the cell payload. ConclusionsThis study demonstrates the importance of careful consideration of administration protocols required for successful delivery of cell suspensions, according to their nature and cellular responses post-ejection.
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