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Chitosan (CS) is expected to be an ideal gene carrier for its high biosafety. In this work, CS with low molecular weight were prepared through the γ-ray radiation on the acetic acid solution of CS. The CS chains were scissioned under the γ-ray radiation, and the molecular weight (MW) of CS decreased with the absorbed dose. When the absorbed dose was above 30 kGy, the molecular weight of CS decreased about an order of magnitude. The γ-ray-radiation-scissioned CS can e ectively bind with plasmid (pEGFP) through complex coacervation method, forming pEGFP/ γ-ray-radiation-scissioned CS complex particles with a size of 200-300 nm. The complex particles have good stability and little cytotoxicity. The in uitro gene transfection efficiencies of the pEGFP/ γ-ray-radiation-scissioned CS complex particles were investigated by fluorescence microscope and flow cytometry. The results showed that the gene vectors using γ-ray-radiation-scissioned CS as the carrier will possess better gene transfection efficiency than those using natural high-MW CS as the carrier. The higher the absorbed dose, the smaller the MW of CS and the better transfection efficiency of the corresponding gene vector. This work provides a green and simple method on the preparation of CS-based gene vectors with high efficiency and biosafety. 相似文献
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生命体中大部分生物分子都具有手性。生物分子的手性构象与等离激元纳米晶的局域表面等离激元共振(LSPR)通过偶极子-偶极子耦合作用,在其LSPR的位置会诱导出一个新的圆二色吸收光谱,具有这种光学活性的等离激元纳米晶称为手性等离激元纳米晶。手性等离激元纳米晶的光学响应信号的稳定性和可重复性都比较高,广泛应用在生物传感、化学传感、圆偏振器、光催化、癌症治疗等领域。手性等离激元纳米晶的制备技术一直是该领域的研究热点。然而,通过将手性分子直接吸附在等离激元纳米晶表面的方式所诱导的手性光学响应信号非常弱,故本综述聚焦于手性等离激元纳米晶的其他制备技术,包括通过手性分子或者软模板组装技术获得手性等离激元超结构;湿化学法将手性分子嵌入到单个纳米晶当中制备出核-壳型手性等离激元纳米晶,或者将手性分子的手性构象传递到无机纳米材料的结构当中制备出单个螺旋型手性等离激元纳米晶等。基于目前对手性等离激元纳米晶的最新研究进展,对其纳米制备技术作了进一步的总结和展望。 相似文献
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建立水产品和水发食品中甲胺、乙胺、二甲胺和二乙胺的柱前衍生-高效液相色谱同时测定方法。样品经10%三氯乙酸匀浆、离心后,取上清液与9-芴甲氧羰酰氯(FMOC-Cl)在0.10 mol/L四硼酸钠溶液中反应生成具有紫外吸收的衍生产物,然后以C18柱为分离柱、甲醇-水为流动相,流速梯度洗脱分离,以DAD检测器在265nm波长处检测,标准曲线法定量。4种脂肪胺衍生产物在16 min内可完全分离。在0.5~25μg/mL浓度范围内,各物质的质量浓度与色谱峰面积均具有良好线性关系(r>0.999),方法检出限分别为:甲胺0.05 mg/kg、乙胺0.21 mg/kg、二甲胺0.29 mg/kg、二乙胺0.80 mg/kg。方法的加标回收率为88.1%~100.7%,相对标准差均小于5%。方法可用于水产品和水发食品中4种脂肪胺的同时快速测定。 相似文献
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