[1] Ma J, Cai Z L, Wei H L, et al. The anti-tumor effect of aspirin:what we know and what we expect[J]. Biomed Pharmacother, 2017, 95:656-661. [2] 姜艳,韩国防. 有机化学实验[M].2版.北京:化学工业出版社, 2010:71-73. [3] Pavia D L, Lampman G M, Kriz G S, et al. Organic laboratory techniques[M]. 2nd ed. USA:Brooks/Cole-Thomson Learning, 2005:55-57. [4] 林沛和,李承范.乙酸钠催化合成阿司匹林[J]. 河北化工, 2006,29(4):19-20. [5] 唐宝华,肖凤娟,张筠.碳酸钠催化微波合成阿司匹林的方法探索[J]. 河北化工, 2006,29(6):24-25. [6] 隆金桥,凌绍明. 柠檬酸催化合成阿司匹林[J].云南化工, 2008,35(5):20-22. [7] 隆金桥,周秀龙,黄阿琨.草酸催化合成阿司匹林的研究[J].百色学院学报,2007, 20(6):76-78. [8] Abdelrahman M M. Selective spectrophotometric methods for determination of ternary mixture with overlapping spectra:a comparative study[J]. Spectrochim Acta A Mol Biomol Spectrosc, 2014, 124:389-396. [9] El-Yazbi F A, Hammud H H, Assi S A. Derivative-ratio spectrophotometric method for the determination of ternary mixture of aspirin, paracetamol and salicylic acid[J]. Spectrochim Acta A Mol Biomol Spectrosc, 2007, 68(2):275-278. [10] 邵建群,徐艳霞,唐静成, 等. 紫外二阶导数光谱法监测柠檬酸催化合成乙酰水杨酸[J].首都医科大学学报,2015,36(5):757-760. [11] 曾泳淮. 分析化学(仪器分析部分)[M]. 3版. 北京:高等教育出版社, 2010:96-99. [12] Ojeda C B, Rojas F S. Recent applications in derivative ultraviolet/visible absorption spectrophotometry:2009-2011 a review[J]. Microchem J, 2013, 106:1-16. [13] 王祎,张鸿.糖化白蛋白与阿司匹林抵抗的关系[J].中国脑血管病杂志,2017,14(9):491-495. [14] 项天庆, 吕亚林,余兰,等.口服阿司匹林患者不停药牙种植手术出血情况的临床观察[J].首都医科大学学报,2016,37(3):270-274. [15] 苗鹏, 关琳,邢承忠.服用阿司匹林对结直肠癌患者生存获益的Meta分析与系统评价[J].中国医科大学,2015,44(6):528-532,537. |