Hydroxyapatite nano and microparticles: Correlation of particle properties with cytotoxicity and biostability

被引:315
作者
Motskin, M. [1 ]
Wright, D. M. [1 ]
Muller, K. [1 ]
Kyle, N. [2 ]
Gard, T. G. [2 ]
Porter, A. E. [3 ]
Skepper, J. N. [1 ]
机构
[1] Sch Biol Sci, Dept Physiol Dev & Neurosci, Multi Imaging Ctr, Cambridge CB2 3DY, England
[2] Cambridge Biostabil Ltd, Unit 184, Cambridge CB4 0GA, England
[3] Univ London Imperial Coll Sci Technol & Med, Dept Mat, Fac Engn, London SW7 2AZ, England
关键词
Hydroxyapatite; Nanoparticles; Cytotoxicity; Slow release; Vaccine delivery; Transfection; CALCIUM-PHOSPHATE NANOPARTICLES; GENE DELIVERY; RELEASE; TRANSFECTION; MACROPHAGES; PROTEIN; CELLS; MECHANISM; APOPTOSIS; TOXICITY;
D O I
10.1016/j.biomaterials.2009.02.044
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Synthetic colloid and gel hydroxyapatite (HA) nanoparticles (NPs) were spray dried to form microparticles (MPs). These are intended for use as slow release vaccine vectors. The physico-chemical properties of gel and colloid NPs and MPs were compared to those of HA obtained commercially. Their cytotoxicity to human monocytes'-derived macrophages (HMMs) was assessed in vitro using a range of techniques. These included the MTT assay, LDH leakage and a confocal based live-dead cell assay. Cytotoxicity differed significantly between preparations, with the suspended gel preparation being the most toxic (31-500 mu g/ml). Other preparations were also toxic but only at higher concentrations (>250 mu g/ml). Transmission electron microscopy (TEM) and stereology showed variable cellular uptake and subsequent dissolution of the various forms of HA. We have demonstrated that HA particle toxicity varied considerably and that it was related to their physico-chemical properties. Cell death correlated strongly with particle load. The intracellular dissolution of particles as a function of time in HMM suggests that increased cytoplasmic calcium load is likely to be the cause of cell death. Some HA NPs eluded the phagocytic pathway and a few were even seen to enter the nuclei through nuclear pores. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3307 / 3317
页数:11
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