v. injection of CTT2-SL liposome or Caelyx. A2780 xenografts (n = 6) were collected at 2, 6, 24, 48, 72, and 96 hours after CTT2-liposome or Caelyx injection, and their doxorubicin content … CTT2-SL liposomal

antitumor efficacy data following i.v. bolus injections of CTT2-SL liposome, Caelyx, doxorubicin, and buffer in A2780 xenografts is shown in Figure 8. Live mice exhibiting tumor sizes exceeding 1000mm3 were sacrificed, including those at days 15 and 24 following i.v. administration of buffer or doxorubicin, respectively. Importantly, 80% of Inhibitors,research,lifescience,medical mice treated with CTT-SL liposomes and 50% treated with Caelyx were alive at 24 days following initiation of treatment. Treatment with CTT2-SL liposomes was therefore found to increase mean survival times of mice by 38% from 27.9 to 38.6 days. Figure 8 Kaplan-Meier plot of the survival of tumor bearing mice. Mice were treated Inhibitors,research,lifescience,medical with doxorubicin (9mg/kg), administered either as CTT2-SL liposome or Caelyx. Controls were injected with doxorubicin (9mg/kg) or saline dilution

buffer. Injections … Mouse body weights were monitored throughout Inhibitors,research,lifescience,medical the study period (Figure 9). Each doxorubicin regimen (CTT2-SL liposome, Caelyx, and Doxorubicin) induced a slight weight decrease with a maximum loss of about 10% at day 9. However, one week later, body weights returned to initial levels. Figure 9 Mouse body weight changes in each treatment group during the first 32 days of the trial. Mice were treated with 9mg/kg doxorubicin (calculated

Inhibitors,research,lifescience,medical doxorubicin equivalents) or saline dilution buffer at day 0, 3 and 6. All values are expressed as … Given the overall improved survival found following Inhibitors,research,lifescience,medical treatment of A2780 xenografts with CTT2-SL liposomes, studies were extended to assess treatment www.selleckchem.com/products/Trichostatin-A.html response in OV-90 xenograft models. As seen in Figure 10, despite the lower doses of CTT2-SL liposomes administered, efficient targeting, along with rising selleck kinase inhibitor Concentrations of doxorubicin was measured using this serous ovarian model (Figure 10(b)) over a 6-hr time interval relative to the untargeted formulation. Figure 10 Concentrations of doxorubicin in (a) serum and (b) OV-90 xenografts in mice treated with CTT2-SL liposome and Caelyx at 0.5 and 6 hours. Data are represented as a mean of 5 mice ± SD. Dacomitinib Additional serum and tumor uptake measurements conducted with CTT2-SL DSPE-PEG3400 liposomes are shown in Figure 11. Initial serum doxorubicin concentrations were found to be lower for CTT2-SL-DSPE-PEG3400 liposomes than for untargeted liposomes (i.e., PEG-liposomes), but the overall kinetic profile of the two liposomal formulations was essentially equivalent over time. Figure 11(b)demonstrates time-dependent changes in the total amount of doxorubicin found in tumor tissue.