Biocompatibility and safety of a hybrid core-shell nanoparticulate OP-1 delivery system intramuscularly administered in rats

被引:29
作者
Haidar, Ziyad S. [1 ,2 ,3 ,4 ,5 ,6 ]
Hamdy, Reggie C. [3 ,4 ,5 ,6 ]
Tabrizian, Maryam [1 ,2 ,3 ,4 ]
机构
[1] McGill Univ, Fac Dent, Montreal, PQ H3A 2B4, Canada
[2] McGill Univ, Dept Biomed Engn, Fac Med, Montreal, PQ H3A 2B4, Canada
[3] McGill Univ, Ctr Biorecognit & Biosensors, Montreal, PQ H3A 2B4, Canada
[4] McGill Univ, Ctr Bone & Periodontal Dis Res, Montreal, PQ H3A 2B4, Canada
[5] McGill Univ, Shriners Hosp Children, Montreal, PQ H3A 2B4, Canada
[6] McGill Univ, Div Orthopaed Surg, Montreal Childrens Hosp, Montreal, PQ H3A 2B4, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
Biocompatibility; BMP; Drug delivery; Foreign body response; Haemocompatibility; Nanoparticle; BONE MORPHOGENETIC PROTEINS; DISTRACTION OSTEOGENESIS; TISSUE DISTRIBUTION; OSTEOINDUCTION; LIPOSOMES; EXPRESSION; TOXICITY; ANGIOGENESIS; IMPLANTATION; CIRCULATION;
D O I
10.1016/j.biomaterials.2009.12.034
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
A hybrid, localized and release-controlled delivery system for bone growth factors consisting of a liposomal core incorporated into a shell of alternating layer-by-layer self-assembled natural polyelectrolytes has been formulated. Hydrophilic, monodisperse, spherical and stable cationic nanoparticles (<350 nm) with an extended shelf-life resulted. Cytocompatibility was previously assayed with MC3T3-E1.4 mouse preosteoblasts showing no adverse effects on cell viability. In this study, the in vivo biocompatibility of unloaded and loaded nanoparticles with osteogenic protein-1 or OP-1 was investigated. Young male Wistar rats were injected intramuscularly and monitored over a period of 10 weeks for signs of inflammation and/or adverse reactions. Blood samples (600 mu L/collection) were withdrawn followed by hematological and biochemical analysis. Body weight changes over the treatment period were noted. Major organs were harvested, weighed and examined histologically for any pathological changes. Finally, the injection site was identified and examined immunohistochemically. Overall, all animals showed no obvious toxic health effects, immune responses and/or change in organ functions. This hybrid core-shell nanoparticulate delivery system localizes the effect of the released bioactive load within the site of injection in muscle with no significant tissue distress. Hence, a safe and promising carrier for therapeutic growth factors and possibly other biomolecules is presented. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2746 / 2754
页数:9
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