摘要
目的探究N-琥珀酰壳聚糖(NSCS)对牛血红蛋白(BHb)和正常肝细胞(HL-7702)的毒性。方法在模拟人体生理条件下,以BHb为研究对象,采用紫外-可见分光光度法、荧光光谱法和同步荧光光谱法结合,探究NSCS对BHb的毒性;同时以HL-7702为研究对象,利用四甲基偶氮唑蓝(MTT)法考察NSCS对HL-7702的细胞毒性。结果紫外-可见分光光度法和MTT法结果表明,NSCS的毒性较弱,且取代度对NSCS毒性的影响较小。荧光光谱显示,NSCS可以猝灭BHb的内源性荧光,且猝灭作用随取代度的增大略有增强。其猝灭机制主要为动态猝灭,二者间作用力主要为静电作用力和疏水作用力。同步荧光光谱显示,NSCS对BHb的构象基本无影响。结论 NSCS对BHb和HL-7702细胞的毒性均较弱。
OBJECTIVE To investigate the toxicity of N-succinyl-chitosan （NSCS） to bovine hemoglobin （BHb） and human liver cells （HL-7702）. METHODS BHb was used as a research object and the toxic effect of NSCS was investigated by UV-Vis absorption spectroscopy, fluorescence spectroscopy and synchrotron spectroscopy under the simulative human physiological condition. At the same time, human HL-7702 cells was used as a research object and methyl thiazolyl tetrazolium （MTT） assay was employed to examine the cytotoxicity of NSCS. RESULTS The results of UV-Vis absorption spectroscopy and MTT showed that the toxicity of NSCS was weak, and substitution degree had little effect on it. The result of fluorescence spectroscopy demonstrated that the intrinsic fluorescence of BHb was quenched by NSCS and the quenching effect slightly increased with the increase of substitution degree. The quenching mechanism was mainly dynamic quenching, and the major driving forces were hydrophobic and electrostatic force. CONCLUSION The result of synchronous fluorescence spectroscopy reveals that NSCS has almost no influence on the conformation of BHb. The toxicity of NSCS to BHb and HL-7702 is weak.
出处
《中国药学杂志》
CAS
CSCD
北大核心
2018年第3期193-198,共6页
Chinese Pharmaceutical Journal
基金
山西省自然科学基金资助项目(2015011012)
山西医科大学大学生创新创业校级项目资助(20170707)
