Beilstein J. Org. Chem.2021,17, 2832–2839, doi:10.3762/bjoc.17.194
inhibitory activity of CPE against E. coli.
Keywords: antibacterial activity; chloramphenicol; cucurbit[8]uril; host–guest interaction; invitrocumulativerelease; stability; Introduction
Chloramphenicol (CPE, Figure 1A) is a broad-spectrum antibiotic resulting from the metabolism of chorismic acid in
artificial intestinal fluid, CPE reached the release end point after 1.67 h, and its invitrocumulativerelease rate was 85.63% (Figure 8B). The release rate of CPE@Q[8] was faster before 2 h, but the release rate was slow after 2 h, and its cumulative release rate was 32.59% after 12 h. The results show
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Graphical Abstract
Figure 1:
The structures of chloramphenicol (A) and cucurbit[n]urils (B).