4.6 Article

The first zwitterionic cocrystal of indomethacin with amino acid showing optimized physicochemical properties as well as accelerated absorption and slowed elimination in vivo

Journal

NEW JOURNAL OF CHEMISTRY
Volume 44, Issue 10, Pages 3930-3939

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c9nj06180k

Keywords

-

Funding

  1. Shandong Province Natural Science Foundation [ZR2019MH098]
  2. Shandong Province Key Research and Development Project [2018GSF118174]
  3. Qingdao People's Livelihood Science and Technology Projects [18-6-1-95-nsh, 19-6-1-37-nsh]
  4. Fundamental Research Funds for the Central Universities [201961027]

Ask authors/readers for more resources

The first zwitterionic cocrystal of indomethacin (INC) with amino acid, INC-PL-H2O, where PL represents l-proline, was prepared and thoroughly characterized by single crystal and powder X-ray diffraction and TGA-DSC and IR analyses. Single crystal X-ray diffraction revealed that there is a two-dimensional hydrogen bonding network with the surfaces being covered by hydrophobic groups in the cocrystal. The relevant pharmaceutical properties including solubility, permeability, and intrinsic dissolution rate in vitro, along with the in vivo pharmacokinetics, were systematically studied. It has been found that the dissolubility and penetrability of INC from the INC-PL-H2O cocrystal were both improved in comparison with pure INC, and the enhanced solubility was comparatively more obvious than its penetrability. These strengthened properties in vitro may mainly be attributed to the advantageous nature of the zwitterionic PL and the cocrystal structure in which INC self-dimers have been broken, and these INC molecules are grafted upon the column type supermolecular motifs constructed from PL molecules. Interestingly, the increased in vitro properties of the cocrystal have converted to satisfactory in vivo pharmacokinetics, showing a shorter peak time and a longer retention time compared with INC per se. These results not only provided an important scientific basis for PL in regulating properties in vitro and in vivo of drugs, but also tapped into its potential as an auxiliary agent to combine with NSAIDs in the treatment of joint diseases.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available