Thermal decomposition mechanism of piroxicam

被引:0
作者
Cheng-Jie Wu
Jin-Zong You
Xue-Jie Wang
机构
[1] Zhejiang International Studies University,School of Science and Technology
来源
Journal of Thermal Analysis and Calorimetry | 2018年 / 134卷
关键词
Piroxicam (PRX); Thermal decomposition mechanism; TGA–FTIR; Quantum chemistry;
D O I
暂无
中图分类号
学科分类号
摘要
Piroxicam (PRX) is a nonsteroidal anti-inflammatory drug. The thermal decomposition process of PRX was investigated with thermogravimetry and differential scanning calorimetry. The gaseous products generated by thermal decomposition were characterized with thermogravimetric analysis coupled with Fourier transform infrared spectroscopy. The residues of the thermal decomposition at various temperatures were identified with infrared spectroscopy. The molecular bond orders were calculated using an ab initio method from the GAMESS program of quantum chemistry. The mechanism of thermal decomposition for PRX was discussed. The results indicated that the thermal decomposition of PRX is a two-stage process with the initial temperature of 198 °C either in nitrogen or air atmospheres. The thermal decompositions of the first stage in two atmospheres are the same process. The main part of the molecule, including sulfamide, amide, benzene ring and pyridine ring, decompose simultaneously and to form gasifiable small molecules and carbonaceous residue in the first stage. The second stage in nitrogen is a slow thermal pyrolysis process of carbonaceous residue. The forepart of the second stage in air is a slow thermal pyrolysis process as like as in nitrogen, and the later period of the second stage is an oxidation (combustion) reaction process of carbonaceous residue. PRX is stable under ambient temperature and air atmosphere, and it can be preserved for long-term storage under ambient temperature and in air atmosphere.
引用
收藏
页码:2041 / 2048
页数:7
相关论文
共 126 条
[21]  
Ross SG(2012)General atomic and molecular electronic structure system Curr Top Med Chem 12 2013-2033
[22]  
Verbeeck RK(2018)GAMESS as a free quantum-mechanical platform for drug research J Therm Anal Calorim 131 1361-1371
[23]  
Eichstadt LR(2016)Study on the thermal decomposition of famciclovir J Therm Anal Calorim 123 2307-2312
[24]  
Moore GE(2016)Studying the thermal decomposition of carvedilol by coupled TG–FTIR J Mol Liq 223 1311-1332
[25]  
Childress MO(2014)Mixed-ligand complex formation of tenoxicam drug with some transition metal ions in presence of valine: synthesis, characterization, molecular docking, potentiometric and evaluation of the humeral immune response of calves Inorg Chim Acta 409 479-483
[26]  
Kovala-Demertzi D(2010)Arene ruthenium and pentamethylcyclopentadienyl rhodium and iridium complexes containing Spectrochim Acta A. 75 901-907
[27]  
Tita B(undefined), undefined undefined undefined-undefined
[28]  
Stefanescu M(undefined)-chelating ligands derived from piroxicam: synthesis, molecular structure and cytotoxicity undefined undefined undefined-undefined
[29]  
Tita D(undefined)A theoretical and spectroscopic study of conformational structures of piroxicam undefined undefined undefined-undefined
[30]  
Dutta S(undefined)undefined undefined undefined undefined-undefined