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浸浆制备过程中载体微结构及涂膜工艺参数对膜厚度的影响 被引量:4
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作者 丁晓斌 范益群 徐南平 《化工学报》 EI CAS CSCD 北大核心 2006年第11期2739-2744,共6页
以“浸浆”成型法制备α-Al2O3陶瓷膜过程为研究对象,提出以载体的纯水渗透性能关联载体的微结构参数来预测载体对膜厚度的总体影响的方法·实验考察了涂膜工艺参数(浸浆时间和流动速度)以及载体纯水渗透性能对膜厚度的影响·... 以“浸浆”成型法制备α-Al2O3陶瓷膜过程为研究对象,提出以载体的纯水渗透性能关联载体的微结构参数来预测载体对膜厚度的总体影响的方法·实验考察了涂膜工艺参数(浸浆时间和流动速度)以及载体纯水渗透性能对膜厚度的影响·结果表明:浸浆时间越长,所形成的膜层厚度越厚且膜厚度与浸浆时间的1/2次方呈正比·而当载体孔道被完全充满后,膜厚度随着时间延长而下降;在制膜液进入载体和脱离载体过程中,膜厚度首先随着制膜液的流动速度的2/3次方线性增长,当流动速度超过一定值后,膜厚度不再变化;载体的渗透性能越优越,越有利于膜厚的形成,且膜厚度与载体的纯水渗透通量呈线性关系. 展开更多
关键词 膜厚 流动速度 浸浆时间 载体微结构 浸浆法
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Composite core-shell microparticles from microfluidics for synergistic drug delivery 被引量:10
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作者 李艳娜 燕丹 +6 位作者 付繁繁 刘羽霄 张彬 王洁 商珞然 顾忠泽 赵远锦 《Science China Materials》 SCIE EI CSCD 2017年第6期543-553,共11页
Microparticles have a demonstrated value for drug delivery systems. The attempts to develop this tech- nology focus on the generation of featured microparticles for improving the function of the systems. Here, we pres... Microparticles have a demonstrated value for drug delivery systems. The attempts to develop this tech- nology focus on the generation of featured microparticles for improving the function of the systems. Here, we present a new type of microparticles with gelatin methacrylate (GelMa) cores and poly(L-lactide-co-glycolide) (PLGA) shells for syn- ergistic and sustained drug delivery applications. The mi- croparticles were fabricated by using GelMa aqueous solu- tion and PLGA oil solution as the raw materials of the mi- croflnidic double emulsion templates, in which hydrophilic and hydrophobic actives, such as doxorubicin hydrochloride (DOX, hydrophilic) and camptothecine (CPT, hydrophobic), could be loaded respectively. As the inner cores were poly- merized in the microfluidics when the double emulsions were formed, the hydrophilic actives could be trapped in the cores with high efficiency, and the rupture or fusion of the cores could be avoided during the solidification of the micropar- ticle shells with other actives. The size and component of the microparticles can be easily and precisely adjusted by ma- nipulating the flow solutions during the microfluidic emulsi- fication. Because of the solid structure of the resultant mi- croparticles, the encapsulated actives were released from the delivery systems only with the degradation of the biopolymer layers, and thus the burst release of the actives was avoided. These features of the microparticles make them ideal for drug delivery applications. 展开更多
关键词 microfluidic EMULSION micropartide drug delivery biomaterial
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Microfluidic generation of Buddha beads-like microcarriers for cell culture 被引量:4
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作者 王洁 邹旻含 +4 位作者 孙灵钰 程瑶 商珞然 付繁繁 赵远锦 《Science China Materials》 SCIE EI CSCD 2017年第9期857-865,共9页
The fabrication of functional microcarriers capable of achieving in vivo-like three-dimensional cell culture is important for many tissue engineering applications. Here,inspired by the structure of Buddha beads, which... The fabrication of functional microcarriers capable of achieving in vivo-like three-dimensional cell culture is important for many tissue engineering applications. Here,inspired by the structure of Buddha beads, which are generally composed of moveable beads strung on a rope, we present novel cell microcarriers with controllable macropores and heterogeneous microstructures by using a capillary array microfluidic technology. Microfibers with a string of moveable and releasable microcarriers could be achieved by an immediate gelation reaction of sodium alginate spinning and subsequent polymerization of cell-dispersed gelatin methacrylate emulsification. The sizes of the microcarriers and their inner macropores could be well tailored by adjusting the flow rates of the microfluidic phases; this was of great importance in guaranteeing a sufficient supply of nutrients during cell culture. In addition, by infusing multiple cell-dispersed pregel solutions into the capillaries, the microcarriers with spatially heterogeneous cell encapsulations for mimicking physiological structures and functions could also be achieved. 展开更多
关键词 microfluidics MICROCARRIER cell culture MICROFIBER EMULSION
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