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Functional Bone-mimetic Scaffolds of Bicontinuous, Thermoresponsive L_3-phase Silica/Hydroxyapatite Nanocomposites

机译:双连续,热响应L_3相二氧化硅/羟基磷灰石纳米复合材料的功能仿骨支架。

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摘要

This work presents the highly controlled drug delivery system free from the burst release at an initial stage and equipped with the capability of long term drug release. The nanoporous drug releasing reservoir was combined with porous body resembling cancellous bone. The materials were prepared by the integration of synthesized inorganic hydroxyapatite (HA) and the hybrid gels of bicontinuous sponge-phased L3 silicate and thermo-responsive poly(N-isopropylacrylamide) (L3-PNIPAm gels). The materials were designed to have the three dimensionally interconnected heterogeneous porosity of macro- and mesoporosity, in which the HA has the macroporosity of 150 μm to be impregnated the drug into the pores and the L3-PNIPAm gels have mesoporosity of 5 nm to regulate the temperature sensitive drug-release through the pore channels and polymeric network, respectively. Consequently, this bone-mimetic system gave the highly long term drug release over the 60 days without the burst release. The release rate could be controlled with the change of the HA and PNIPAm composition ratios. The structural characterization was achieved by TEM, SEM, XRD, Micro-Raman spectroscopy, BET, and the direct contact cytotoxicity test was also described.
机译:这项工作提出了一个高度受控的药物输送系统,该系统在初始阶段没有爆发释放,并且具有长期药物释放的能力。将纳米多孔药物释放储库与类似于松质骨的多孔体结合。该材料是通过合成的无机羟基磷灰石(HA)以及双连续海绵相L3硅酸盐与热响应性聚(N-异丙基丙烯酰胺)(L3-PNIPAm凝胶)的混合凝胶的整合而制备的。这些材料被设计为具有大孔和中孔的三维互连异质性孔隙,其中HA具有150μm的大孔,可将药物浸渍到孔中,L3-PNIPAm凝胶具有5 nm的中孔,以调节药物的渗透性。温度敏感型药物分别通过孔通道和聚合物网络释放。因此,这种仿骨系统在60天内提供了高度长期的药物释放而没有突释。释放速率可以通过HA和PNIPAm组成比的变化来控制。通过TEM,SEM,XRD,Micro-Raman光谱法,BET进行结构表征,并描述了直接接触细胞毒性试验。

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