摘要
Emulsion and polyphase liposome (PL) of ricinoleic acid (RA) and RA containing selenium (Se-RA) were prepared by tween-80 treatment and injection-ultrasonic method. Their antitumor effects were tested in vitro and in vivo. As a result, the emulsion of RA (91 ) and Sc-RA (92) can completely kill the mouse ascites tumor cells of S180 in vitro (500 μg/ml). While. 97% cells of the control group still survive. When tested in vivo, 91 and 92 were injected into mice peritoneally (200 mg/Kg/day) for 7 days, their inhibit rate on S180 are 30. 6% (P<0. 05) and 33. 3% (P<0. 05) respectively. For the PL of RA (113) and Se-RA (114), the inhibit rate are 58% (P< 0.001) and 61.4% (P<0. 001) respectively (400 mg/kg/day). The result of 3H-TdR incorporation experiment indicates that the possible antitumor mechanism of Se-Ra is that it can inhibit the incorporation of 3H- TdR into tumor cells and hense inhibit the DNA synthesis of the tumor cells.
Emulsion and polyphase liposome (PL) of ricinoleic acid (RA) and RA containing selenium (Se-RA) were prepared by tween-80 treatment and injection-ultrasonic method. Their antitumor effects were tested in vitro and in vivo. As a result, the emulsion of RA (91 ) and Sc-RA (92) can completely kill the mouse ascites tumor cells of S180 in vitro (500 μg/ml). While. 97% cells of the control group still survive. When tested in vivo, 91 and 92 were injected into mice peritoneally (200 mg/Kg/day) for 7 days, their inhibit rate on S180 are 30. 6% (P<0. 05) and 33. 3% (P<0. 05) respectively. For the PL of RA (113) and Se-RA (114), the inhibit rate are 58% (P< 0.001) and 61.4% (P<0. 001) respectively (400 mg/kg/day). The result of 3H-TdR incorporation experiment indicates that the possible antitumor mechanism of Se-Ra is that it can inhibit the incorporation of 3H- TdR into tumor cells and hense inhibit the DNA synthesis of the tumor cells.
