Incorporation and effects of mesoporous SiO2-CaO nanospheres loaded with ipriflavone on osteoblast/osteoclast cocultures

被引:26
作者
Casarrubios, Laura [1 ]
Gomez-Cerezo, Natividad [2 ,3 ]
Jose Feito, Maria [1 ]
Vallet-Regi, Maria [2 ,3 ]
Arcos, Daniel [2 ,3 ]
Teresa Portoles, Maria [1 ]
机构
[1] Univ Complutense Madrid, Fac Ciencias Quim, Dept Bioquim & Biol Mol, Inst Invest Sanitaria,Hosp Clin San Carlos,IdISSC, E-28040 Madrid, Spain
[2] Univ Complutense Madrid, Fac Farm, Dept Quim Ciencias Farmaceut, Inst Invest Sanitaria,Hosp 12 Octubre I 12, Plaza Raman y Cajal S-N, E-28040 Madrid, Spain
[3] CIBER BBN, CIBER Bioingn Biomat & Nanomed, Madrid, Spain
基金
欧洲研究理事会;
关键词
Mesoporous bioactive glasses; Nanospheres; Osteoblasts; Osteoclasts; Ipriflavone; OSTEOCLAST DIFFERENTIATION; CALCIUM PHOSPHATES; BONE-RESORPTION; ROLES; OSTEOBLASTS; MODULATION;
D O I
10.1016/j.ejpb.2018.10.019
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Mesoporous nanospheres in the system SiO2-CaO (NanoMBGs) with a hollow core surrounded by a radial arrangement of mesopores were characterized, labeled with FITC (FITC-NanoMBGs) and loaded with ipriflavone (NanoMBG-IPs) in order to evaluate their incorporation and their effects on both osteoblasts and osteoclasts simultaneously and maintaining the communication with each other in coculture. The influence of these nanospheres on macrophage polarization towards pro-inflammatory Ml or reparative M2 phenotypes was also evaluated in basal and stimulated conditions through the expression of CD80 (as M1 marker) and CD206 (as M2 marker) by flow cytometry and confocal microscopy. NanoMBGs did not induce the macrophage polarization towards the Ml pro-inflammatory phenotype, favoring the M2 reparative phenotype and increasing the macrophage response capability against stimuli as LPS and IL-4. NanoMBG-IPs induced a significant decrease of osteoclast proliferation and resorption activity after 7 days in coculture with osteoblasts, without affecting osteoblast proliferation and viability. Drug release test demonstrated that only a fraction of the payload is released by diffusion, whereas the rest of the drug remains within the hollow core after 7 days, thus ensuring the local long-term pharmacological treatment beyond the initial fast IP release. All these data ensure an appropriate immune response to these nanospheres and the potential application of NanoMBG-IPs as local drug delivery system in osteoporotic patients.
引用
收藏
页码:258 / 268
页数:11
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