Selenium is an essential trace element for human with the antitumor properties. In the present study, the peptidoglycan (PG) derived from Lactobacillus acidophilus was modified by selenylation with the HNO3-Na2SeO3 method. Reaction temperature, reaction duration and the selenide content were optimized according to orthogonal design of three-factors. In addition, the molecular structure of selenizing peptidoglycan (Se-PG) was determined by infrared spectroscopy analysis. Furthermore, the antitumor activity of Se-PG was also investigated in HT-29 cells. The results showed that Se-PG exerted a greater antitumor activity than non-modified PG in a dose-dependent manner. These findings indicated that selenylation modification can enhance the antitumor activity of PG, and Se-PG could achieve its potential in antitumor activity.
Keywords: 5-Fluorouracil (PubChem CID:3385); Antitumor activity; Fluorescein isothiocyanate (PubChem CID: 18730); HT-29 cells; Peptidoglycan; Peptidoglycan (PubChem CID:3035036); Propidium iodide (PubChem CID: 104981); Selenylation modification; Trichloroacetic acid (PubChem CID: 6421).
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