College of Chinese Materia Medica, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China
| Abstract: | In this study, Irinotecan (ICA) was used as a model drug, and MIL-101(Fe) was used as a drug carrier to load ICA, ICA@MIL-100(Fe) complex was prepared by impregnating adsorption method. A high performance liquid chromatography (HPLC) method was established to determine the content of ICA from ICA@MIL-100(Fe) complex. The established method had good linear relationship, precision, repeatability, stability and sample recovery, and the RSD was less than 2%. Molecular simulation was used to further investigate the site and stability of interaction. Experiment results showed that when the concentration of ICA was 1mg/mL, the mass ratio of drug to carrier was 1:1, the adsorption time was 24 h, the drug loading capacity of ICA by MIL-100(Fe) was (8.88±0.03) %. Molecular simulation experiments showed that when ICA was incorporated into the tetrahedron of MIL-101(Fe), the binding between ICA and MIL-100(Fe) revealed the most stable dominant conformation, which supported the feasibility of MIL-101(Fe) used as a new drug carrier loading ICA. |
| Keywords: | Irinotecan; MIL-101(Fe); Drug Loading; Molecular Docking |
| DOI: | 10.57237/j.cse.2023.04.002 |
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