Literature DB >> 16934429

Thermal behavior and thermal decarboxylation of 10-hydroxycamptothecin in the solid state.

Shun-Li Wang1, Shan-Yang Lin, Tzu-Feng Hsieh, Shun-An Chan.   

Abstract

In order to investigate the thermal-related properties and thermal stability of 10-hydroxycamptothecin (10-HCPT) in the solid state, differential scanning calorimetry (DSC), thermogravimetric analysis (TGA) and Fourier transform infrared (FT-IR) microspectroscopy were used. A novel combination of FT-IR microspectroscopy with thermal analyzer was applied simultaneously to monitor the dehydration and rehydration processes of the 10-HCPT sample. The thermal-induced decomposition of the 10-HCPT sample was also determined by using electrospray-ion trap mass spectrometry (ES-ITMS). The results indicated that the 10-HCPT sample used in this study was a monohydrate in structure, this form that can dehydrate to an anhydrate form if the temperature goes beyond 90 degrees C. The 10-HCPT anhydrate was first suggested to have two polymorphs, in which the form I might transform to form II when the 110 degrees C-preheated sample was cooled to 30 degrees C. The polymorphic transformation temperature was shown within 90-120 degrees C with 10.46 kcal/mol of enthalpy. The peak at 1723 cm(-1) found in the IR spectrum of 10-HCPT monohydrate might correspond to the hydrogen-bonded CO stretching vibration of lactone, which shifted to 1750 cm(-1) assigned to a free CO group of lactone after the destruction of hydrogen bonding via dehydration. This suggests that monohydrate seems to interact intramolecularly with 10-HCPT by hydrogen bonding. However, the rehydration process of the 10-HCPT anhydrate might cause it to return to being a monohydrate, depending on the storage condition. In addition, the thermal-induced decarboxylation of the solid-state 10-HCPT when the temperature is beyond 226 degrees C was proven by the appearance of a new IR peak at 1701 cm(-1) and one major mass spectral peak at m/z 321. This unique IR spectral peak at 1701 cm(-1) was due to the conjugated carbonyl group in the degraded product of 10-HCPT. The m/z 321 assigned to the decarboxylation of 10-HCPT was equal to the molecular weight loss of 44 from mass spectra; which was consistent with the weight loss of 11.9% (molecular weight of 43.3) from TGA curve of 10-HCPT anhydrate.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16934429     DOI: 10.1016/j.jpba.2006.07.023

Source DB:  PubMed          Journal:  J Pharm Biomed Anal        ISSN: 0731-7085            Impact factor:   3.935


  5 in total

1.  Preparation and physicochemical properties of 10-hydroxycamptothecin (HCPT) nanoparticles by supercritical antisolvent (SAS) process.

Authors:  Xiuhua Zhao; Yuangang Zu; Ru Jiang; Ying Wang; Yong Li; Qingyong Li; Dongmei Zhao; Baishi Zu; Baoyou Zhang; Zhiqiang Sun; Xiaonan Zhang
Journal:  Int J Mol Sci       Date:  2011-04-20       Impact factor: 5.923

2.  Upregulation of NOXA by 10-Hydroxycamptothecin plays a key role in inducing fibroblasts apoptosis and reducing epidural fibrosis.

Authors:  Jihang Dai; Yu Sun; Lianqi Yan; Jingcheng Wang; Xiaolei Li; Jun He
Journal:  PeerJ       Date:  2017-01-12       Impact factor: 2.984

3.  10‑Hydroxycamptothecin induces apoptosis in human fibroblasts by regulating miRNA‑23b‑3p expression.

Authors:  Lingrong Zeng; Yu Sun; Xiaolei Li; Jingcheng Wang; Lianqi Yan
Journal:  Mol Med Rep       Date:  2019-02-01       Impact factor: 2.952

4.  Non-isothermal dehydration kinetic study of aspartame hemihydrate using DSC, TGA and DSC-FTIR microspectroscopy.

Authors:  Wei-Hsien Hsieh; Wen-Ting Cheng; Ling-Chun Chen; Shan-Yang Lin
Journal:  Asian J Pharm Sci       Date:  2017-12-08       Impact factor: 6.598

5.  The role of activating transcription factor 6 in hydroxycamptothecin-induced fibroblast autophagy and apoptosis.

Authors:  Jin Tao; Hui Chen; Xiaolei Li; Jingcheng Wang
Journal:  J Orthop Surg Res       Date:  2021-01-04       Impact factor: 2.359

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.