An anti-ROS/hepatic fibrosis drug delivery system based on salvianolic acid B loaded mesoporous silica nanoparticles

介孔二氧化硅 药物输送 活性氧 细胞毒性 罗丹明B 药品 药理学 纳米颗粒 化学 内吞作用 材料科学 毒品携带者 生物物理学 纳米技术 介孔材料 生物化学 细胞 医学 体外 生物 光催化 催化作用
作者
Qianjun He,Jiamin Zhang,Feng Chen,Limin Guo,Ziyan Zhu,Jianlin Shi
出处
期刊:Biomaterials [Elsevier]
卷期号:31 (30): 7785-7796 被引量:120
标识
DOI:10.1016/j.biomaterials.2010.07.008
摘要

The rhodamine B (RhB) covalently grafted SBA-15-structured mesoporous silica nanoparticles (MSNs-RhB) of high surface area (750 m2 g−1), large pore volume (0.7 cm3 g−1), uniform particle size (about 400 nm) and positively charged surface (29.6 ± 5.0 mV), has been developed as a drug delivery system (SAB@MSNs-RhB) for anti-ROS (reactive oxygen species)/hepatic fibrosis by loading a negatively charged drug salvianolic acid B (SAB). The dosage formulation SAB@MSNs-RhB effectively protected the loaded drug SAB from decomposition. The multi-release experimental results showed that SAB@MSNs-RhB exhibited an outstanding SAB sustained-release property, and relatively high SAB release rates and concentrations in a long term after the consumption of previously released SAB as compared to SAB loaded MSNs (SAB@MSNs) of negatively charged surface (−31.1 ± 2.6 mV). The influences of the drug concentration, incubation time, drug formula and drug carrier on the ROS level, proliferative activity and cytotoxicity of LX-2 cells were evaluated. The results showed that the inhibiting effect of SAB@MSNs-RhB on the ROS level and proliferative activity of LX-2 cells was more remarkable than free SAB in a long term (72 h), and became more intensive with the increase of the sample concentration and the incubation time. SAB@MSNs-RhB enhanced the cellular drug uptake, the drug bioaccessability and efficacy for anti-ROS/hepatic fibrosis via the nanoparticles-mediated endocytosis and the sustained release of the drug. There was no visible cytotoxicity of free SAB, MSNs-RhB and SAB@MSNs-RhB against LX-2 cells in a broad concentration range (0.5–100 μm) and incubation time periods up to 72 h. The blood compatibility of the carrier MSNs-RhB was evaluated by investigating the hemolysis and coagulation behaviors in a broad concentration range (50–500 μg mL−1) under in vitro conditions. The results suggested that MSNs-RhB possessed good blood compatibility.
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