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Preparation of Chitosan/Poly(L-Lactide) Porous Composite Scaffolds
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作者 CHEN Pin NIU Xu-feng +4 位作者 she zhen-ding ZHOU Gang TAN Rong-wei WANG Jiang-xue FAN Yu-bo 《Chinese Journal of Biomedical Engineering(English Edition)》 2012年第2期67-72,共6页
This research investigates the formation of chitosan/poly (L-lactide) (CS/PLLA) porous composite scaffold using a novel emulsion freeze-drying technique. First, an oil in-water (O/W) emulsification system was us... This research investigates the formation of chitosan/poly (L-lactide) (CS/PLLA) porous composite scaffold using a novel emulsion freeze-drying technique. First, an oil in-water (O/W) emulsification system was used in the presence of surfactant Tween-80, in which CS solution was used as the water phase and PLLA solution was used as the oil phase. The emulsion was observed by inverted microscope (× 200). The emulsion droplet was spherical and uniform in size. FT-IR analysis revealed that there were hydrogen bonding interactions between CS and PLLA components. The microstructure and physical properties of the scaffolds were also analyzed. The SEM results showed that composite scaffolds formed well interconnected pore structure and homogenous distribution of CS and PLLA. When the content of PLLA reached 50%, the porosity of CS/PLLA composite scaffolds were between 83 %-91% and density in the range of 0.047 to 0.11 g/era3. The porosity showed a slight decrease and the density increased with the increase of PLLA dose. The compressive strength increased from 0.32 to 0.43 MPa, while the compressive modulus increased from 1.99 to 3.91 MPa as the PLLA contents increased from 10% to 50%. 展开更多
关键词 BIOMATERIALS ehitosan poly(L-laeticle) emulsion composite
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静态顶空气相色谱法测定脱细胞基质类产品中有机溶剂残留量 被引量:2
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作者 李丽花 朱勇军 +3 位作者 康文亭 钟梅玲 佘振定 谭荣伟 《中国医疗器械信息》 2020年第13期17-20,共4页
开发了一种快速准确检测脱细胞基质类产品中有机溶剂残留的顶空气相色方法,即先将脱细胞基质类待测样品在密闭的顶空瓶中用1mol/L硫酸在75°C下完成酸解,然后再用静态顶空气相色谱法检测其中的有机溶剂残留量,并对该检测方法进行系... 开发了一种快速准确检测脱细胞基质类产品中有机溶剂残留的顶空气相色方法,即先将脱细胞基质类待测样品在密闭的顶空瓶中用1mol/L硫酸在75°C下完成酸解,然后再用静态顶空气相色谱法检测其中的有机溶剂残留量,并对该检测方法进行系统的方法学验证。结果表明,正己烷与丙酮分离度良好,正己烷和丙酮分别在0.5~100μg/5mL与5.0~1000μg/5mL浓度范围内呈良好的线性关系,线性相关系数(R2)分别为0.9997和0.9995,定量限分别为0.5μg/5mL与4.0μg/5mL,回收率为93.9%~102.01%,相对标准偏差(RSD)为1.55%~2.89%。该方法灵敏度高,重现性好,适用于脱细胞基质类医疗器械产品中有机溶剂残留的检测分析。 展开更多
关键词 脱细胞基质 有机溶剂残留 顶空气相色谱法
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