Chinese Journal of Tissue Engineering Research ›› 2017, Vol. 21 ›› Issue (2): 260-267.doi: 10.3969/j.issn.2095-4344.2017.02.018
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Received:
2016-12-09
Online:
2017-01-18
Published:
2017-02-27
Contact:
Zhang Jie, M.D., Lecturer, Pharmaceutical Research Institute of Heilongjiang Province, Jiamusi University, Jiamusi 154007, Heilongjiang Province, China; Department of Neurology, First Affiliated Hospital of Harbin Medical University, Harbin 150081, Heilongjiang Province, China
Zhang Yu, Master, Professor, Pharmaceutical Research Institute of Heilongjiang Province, Jiamusi University, Jiamusi 154007, Heilongjiang Province, China
About author:
Liu Jun-xi, Studying for master’s degree, Pharmaceutical Research Institute of Heilongjiang Province, Jiamusi University, Jiamusi 154007, Heilongjiang Province, China
Supported by:
the National Natural Science Foundation of China, No. 81601616; the Post Doctoral Foundation of Heilongjiang Province, No. LBH-Z15164; the Natural Science Foundation of Heilongjiang Province, No. H2016086; the Scientific and Technologic Innovation Program for the Graduates of Jiamusi University, No. LM2015-091; the Scientific Innovation Group of Jiamusi University, No. CXTD-2013-05
CLC Number:
Liu Jun-xi, Zhang Jie, Zhang Yu, Zhao Yue, Wan Guo-jing, Li Guo-zhong.
2.2 复合物中间体 2.2.1 FA-CS偶合物 壳聚糖的红外光谱中在3 345 cm-1附近存在较宽的一段吸收峰,这是由于壳聚糖中O-H和N-H的伸缩振动叠加造成的,在2 920 cm-1 和2 864 cm-1 处出现的是C-H伸缩振动吸收峰,在1 655 cm-1和1 597 cm-1吸收峰分别是C-N伸缩振动和氨基(-NH2)的特征峰(图3a)。叶酸的红外光谱中在3 547 cm-1处出现叶酸中羟基(O-H)的吸收峰,在3 419 cm-1和3 321 cm-1处吸收峰是由叶酸中氨基、-NH的伸缩振动引起的(图3c)。FA-CS偶合物红外光谱中在3 436 cm-1附近只有一个吸收峰,为仲酰胺的特征峰,这是由于壳聚糖上的氨基基团与叶酸上的羧基基团(-COOH)发生静电自组装所致;在2 923 cm-1和2 868 cm-1 出现了壳聚糖中C-H伸缩振动吸收峰;在1 655 cm-1和 1 597 cm-1处的吸收峰明显减弱,在1 597 cm-1 处的N-H变形振动峰移动到了高频的1 628 cm-1[35],这是由于FA-CS偶合物中壳聚糖氨基被叶酸部分取代(图3b)。"
2.2.3 静电自组装产物(FA-CNTs)负载紫杉醇 由图3b,7a可知,静电自组装产物FA-CNTs在3 438 cm-1处出现了FA-CS中仲酰胺的特征峰;在1 740 cm-1处出现了一个小峰,此为酯键上的C=O伸缩振动峰;在1 630 cm-1处为羧基的C=O伸缩振动,这是由于FA-CS在1 628 cm-1处的N-H变形振动峰所致。这说明已成功将FA-CS静电自组装至碳纳米管上。 紫杉醇的红外光谱中,在3 500 cm-1附近的O-H伸缩振动吸收峰与N-H伸缩振动峰重叠;在2 942 cm-1处为苯环上的C-H伸缩振动峰,在1 734 cm-1和1 713 cm-1处出现特征吸收峰为酮羰基C=O的2个裂分峰,在1 645 cm-1处为酰胺基的羰基峰,在1 500 cm-1附近为苯环的骨架振动所产生的吸收峰;在1 380 cm-1处为甲基产生的C-H面内弯曲振动, 1 248 cm-1处为C-N键伸缩振动,在1 067 cm-1、 1 110 cm-1处为仲醇和叔醇中的C-O伸缩振动产生的吸收峰;在900-690 cm-1处为苯环C-H的面外弯曲振动所产生的吸收峰,其中715 cm-1为紫杉醇单取代苯的特征峰(图7c)。 复合物FA-CNTs-PTX在3 438 cm-1处的一个单峰,是图7(a)FA-CNTs中仲酰胺的特征峰,在2 921 cm-1苯环上的C-H伸缩振动峰;在1 372 cm-1处为紫杉醇甲基产生的C-H面内弯曲振动吸收峰,在1 241 cm-1处为紫杉醇的C-N键伸缩振动吸收峰,在1 067 cm-1处为紫杉醇的叔醇中的C-O伸缩振动吸收峰;在713 cm-1为紫杉醇单取代苯的特征峰产生的吸收峰(图7b)。这些说明已成功将紫杉醇负载到FA-CNTs上。 综上可知,成功得到复合物FA-CNTs-PTX。 2.3 复合FA-CNTs-PTX的微泡的制备结果"
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