Radiation chemistry of salicylic and methyl substituted salicylic acids: Models for the radiation chemistry of pharmaceutical compounds

被引:13
作者
Ayatollahi, Shakiba [1 ]
Kalnina, Daina [2 ]
Song, Weihua [3 ]
Turks, Mans [2 ]
Cooper, William J. [1 ]
机构
[1] Univ Calif Irvine, Urban Water Res Ctr, Dept Civil & Environm Engn, Irvine, CA 92697 USA
[2] Riga Tech Univ, Fac Mat Sci & Appl Chem, LV-1007 Riga, Latvia
[3] Fudan Univ, Dept Environm Sci, Shanghai, Peoples R China
基金
美国国家科学基金会;
关键词
Pulse radiolysis; Methyl substituted salicylates; Hydroxyl radicals; Hydrated electron; Irradiation; Transient absorption spectra; FREE-RADICAL DESTRUCTION; PULSE-RADIOLYSIS; REDUCTIVE DEGRADATION; ACETYLSALICYLIC-ACID; ADVANCED OXIDATION; RATE CONSTANTS; WATER; SOLUBILITY; REACTIVITY; FATE;
D O I
10.1016/j.radphyschem.2013.06.007
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Salicylic acid and its derivatives are components of many medications and moieties found in numerous pharmaceutical compounds. They have been used as models for various pharmaceutical compounds in pharmacological studies, for the treatment of pharmaceuticals and personal care products (PPCPs), and, reactions with natural organic matter (NOM). In this study, the radiation chemistry of benzoic acid, salicylic acid and four methyl substituted salicylic acids (MSA) is reported. The absolute bimolecular reaction rate constants for hydroxyl radical reaction with benzoic and salicylic acids as well as 3-methyl-, 4-methyl-, 5-methyl-, and 6-methyl-salicylic acid were determined (5.86 +/- 0.54) x 10(9), (1.07 +/- 0.07) x 10(10), (7.48 +/- 0.17) x 10(9), (731 +/- 0.29) x 10(9), (5.47 +/- 025) x 10(9), (6.94 +/- 0.10) x 10(9) (M-1 s(-1)), respectively. The hydrated electron reaction rate constants were measured (3.02 +/- 0.10) x 10(9), (8.98 +/- 027) x 10(9), (5.39 +/- 0.21) x 10(9), (433 +/- 0.17) x 10(9), (4.72 +/- 0.15) x 10(9), (1.42 +/- 0.02) x 10(9) (M-1 s(-1)), respectively. The transient absorption spectra for the six model compounds were examined and their role as model compounds for the radiation chemistry of pharmaceuticals investigated. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:93 / 98
页数:6
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