Frontiers in Pharmacology (Apr 2024)

Iodine-induced synthetic method and pharmacokinetic study of cis- and trans-crocetin

  • Boshen Li,
  • Boshen Li,
  • Yuxuan Zhang,
  • Yuxuan Zhang,
  • Zhiqiang Yang,
  • Xiaolin Li,
  • Xiaolin Li,
  • Jun Yang,
  • Jun Yang,
  • Kai Luo,
  • Kai Luo,
  • Renjie Wang,
  • Renjie Wang,
  • Chengrong Xiao,
  • Maoxing Li,
  • Maoxing Li,
  • Maoxing Li,
  • Maoxing Li,
  • Yue Gao

DOI
https://doi.org/10.3389/fphar.2024.1364286
Journal volume & issue
Vol. 15

Abstract

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Objective:This experiment aimed to obtain the relatively rare cis-crocetin isomer from natural plants, which predominantly exist in the more stable all-trans configuration. This was achieved through iodine-induced isomerization, followed by purification and structural identification. The study also aimed to compare the pharmacokinetic differences between cis- and trans-crocetin in vivo.Methods:Trans-crocetin of high purity was extracted by hydrolysis from gardenia yellow pigment. Cis-crocetin was then synthesized through an optimized electrophilic addition reaction induced by elemental iodine, and subsequently separated and purified via silica gel column chromatography. Structural identification of cis-crocetin was determined using IR, UV, and NMR techniques. In vivo pharmacokinetic studies were conducted for both cis- and trans-crocetin. In addition to this, we have conducted a comparative study on the in vivo anti-hypoxic activity of trans- and cis-crocetin.Results:Under the selected reaction conditions using DMF as the solvent, with a concentration of 2.5 mg/mL for both trans-crocetin and the iodine solution, and adjusting the illumination time according to the amount of trans-crocetin, the rate of iodine-induced isomerization was the fastest. Cis-crocetin was successfully obtained and, after purification, its structure was identified and found to be consistent with reported data. Cis-crocetin exhibited a faster absorption rate and higher bioavailability, and despite its shorter half-life, it could partially convert to trans-crocetin in the body, thereby extending the duration of the drug’s action within the body to some extent.Conclusion:This study accomplished the successful preparation and structural identification of cis-crocetin. Additionally, through pharmacokinetic studies, it uncovered notable variations in bioavailability between cis- and trans-crocetin. These findings serve as a solid scientific foundation for future functional research and practical applications in this field.

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