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Thermal analysis and FTIR spectral curve-fitting investigation of formation mechanism and stability of indomethacin-saccharin cocrystals via solid-state grinding process.
J Pharm Biomed Anal. 2012 Jul; 66:162-9.JP

Abstract

The cocrystal formation of indomethacin (IMC) and saccharin (SAC) by mechanical cogrinding or thermal treatment was investigated. The formation mechanism and stability of IMC-SAC cocrystal prepared by cogrinding process were explored. Typical IMC-SAC cocrystal was also prepared by solvent evaporation method. All the samples were identified and characterized by using differential scanning calorimetry (DSC) and Fourier transform infrared (FTIR) microspectroscopy with curve-fitting analysis. The physical stability of different IMC-SAC ground mixtures before and after storage for 7 months was examined. The results demonstrate that the stepwise measurements were carried out at specific intervals over a continuous cogrinding process showing a continuous growth in the cocrystal formation between IMC and SAC. The main IR spectral shifts from 3371 to 3,347 cm(-1) and 1693 to 1682 cm(-1) for IMC, as well as from 3094 to 3136 cm(-1) and 1718 to 1735 cm(-1) for SAC suggested that the OH and NH groups in both chemical structures were taken part in a hydrogen bonding, leading to the formation of IMC-SAC cocrystal. A melting at 184 °C for the 30-min IMC-SAC ground mixture was almost the same as the melting at 184 °C for the solvent-evaporated IMC-SAC cocrystal. The 30-min IMC-SAC ground mixture was also confirmed to have similar components and contents to that of the solvent-evaporated IMC-SAC cocrystal by using a curve-fitting analysis from IR spectra. The thermal-induced IMC-SAC cocrystal formation was also found to be dependent on the temperature treated. Different IMC-SAC ground mixtures after storage at 25 °C/40% RH condition for 7 months had an improved tendency of IMC-SAC cocrystallization.

Authors+Show Affiliations

Department of Biotechnology, Yuanpei University, Hsin Chu, Taiwan, ROC.No affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

22497855

Citation

Zhang, Gang-Chun, et al. "Thermal Analysis and FTIR Spectral Curve-fitting Investigation of Formation Mechanism and Stability of Indomethacin-saccharin Cocrystals Via Solid-state Grinding Process." Journal of Pharmaceutical and Biomedical Analysis, vol. 66, 2012, pp. 162-9.
Zhang GC, Lin HL, Lin SY. Thermal analysis and FTIR spectral curve-fitting investigation of formation mechanism and stability of indomethacin-saccharin cocrystals via solid-state grinding process. J Pharm Biomed Anal. 2012;66:162-9.
Zhang, G. C., Lin, H. L., & Lin, S. Y. (2012). Thermal analysis and FTIR spectral curve-fitting investigation of formation mechanism and stability of indomethacin-saccharin cocrystals via solid-state grinding process. Journal of Pharmaceutical and Biomedical Analysis, 66, 162-9. https://doi.org/10.1016/j.jpba.2012.03.039
Zhang GC, Lin HL, Lin SY. Thermal Analysis and FTIR Spectral Curve-fitting Investigation of Formation Mechanism and Stability of Indomethacin-saccharin Cocrystals Via Solid-state Grinding Process. J Pharm Biomed Anal. 2012;66:162-9. PubMed PMID: 22497855.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Thermal analysis and FTIR spectral curve-fitting investigation of formation mechanism and stability of indomethacin-saccharin cocrystals via solid-state grinding process. AU - Zhang,Gang-Chun, AU - Lin,Hong-Liang, AU - Lin,Shan-Yang, Y1 - 2012/03/28/ PY - 2011/12/31/received PY - 2012/03/19/revised PY - 2012/03/19/accepted PY - 2012/4/14/entrez PY - 2012/4/14/pubmed PY - 2012/10/10/medline SP - 162 EP - 9 JF - Journal of pharmaceutical and biomedical analysis JO - J Pharm Biomed Anal VL - 66 N2 - The cocrystal formation of indomethacin (IMC) and saccharin (SAC) by mechanical cogrinding or thermal treatment was investigated. The formation mechanism and stability of IMC-SAC cocrystal prepared by cogrinding process were explored. Typical IMC-SAC cocrystal was also prepared by solvent evaporation method. All the samples were identified and characterized by using differential scanning calorimetry (DSC) and Fourier transform infrared (FTIR) microspectroscopy with curve-fitting analysis. The physical stability of different IMC-SAC ground mixtures before and after storage for 7 months was examined. The results demonstrate that the stepwise measurements were carried out at specific intervals over a continuous cogrinding process showing a continuous growth in the cocrystal formation between IMC and SAC. The main IR spectral shifts from 3371 to 3,347 cm(-1) and 1693 to 1682 cm(-1) for IMC, as well as from 3094 to 3136 cm(-1) and 1718 to 1735 cm(-1) for SAC suggested that the OH and NH groups in both chemical structures were taken part in a hydrogen bonding, leading to the formation of IMC-SAC cocrystal. A melting at 184 °C for the 30-min IMC-SAC ground mixture was almost the same as the melting at 184 °C for the solvent-evaporated IMC-SAC cocrystal. The 30-min IMC-SAC ground mixture was also confirmed to have similar components and contents to that of the solvent-evaporated IMC-SAC cocrystal by using a curve-fitting analysis from IR spectra. The thermal-induced IMC-SAC cocrystal formation was also found to be dependent on the temperature treated. Different IMC-SAC ground mixtures after storage at 25 °C/40% RH condition for 7 months had an improved tendency of IMC-SAC cocrystallization. SN - 1873-264X UR - https://www.unboundmedicine.com/medline/citation/22497855/Thermal_analysis_and_FTIR_spectral_curve_fitting_investigation_of_formation_mechanism_and_stability_of_indomethacin_saccharin_cocrystals_via_solid_state_grinding_process_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0731-7085(12)00162-8 DB - PRIME DP - Unbound Medicine ER -