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©The Author(s) 2020.
World J Gastroenterol. Aug 21, 2020; 26(31): 4589-4606
Published online Aug 21, 2020. doi: 10.3748/wjg.v26.i31.4589
Published online Aug 21, 2020. doi: 10.3748/wjg.v26.i31.4589
Figure 3 Antitumor activity of different drug-loaded nanofilms against human cholangiocarcinoma cells in vitro.
A: Effects of different concentrations of prototype gemcitabine and cisplatin on the growth of EGI-1 cells; B: Inhibition of EGI-1 cells caused by different drug-loaded nanofilms with different drug-loading ratios for 30 d; C: Inhibition of EGI-1 cells caused by drug-released media from 10% drug-loaded nanofilms every other week for 30 d; D: Effects of 10% drug-loaded nanofilms on the (a) viability (magnification × 100); (b) migration (×100); (c) and invasion (×200) of EGI-1 cells; (d) statistical analysis of the proportion of living and dead cells coincubated with different drug-released media; (e) quantitative analysis of the wound closer area following coincubation with different drug-released media; and (f) quantification of migrated cells coincubated with different drug-released media. aP < 0.05, bP < 0.01, cP < 0.001 vs control (n = 6 mice per group). CIS: Cisplatin; GEM: Gemcitabine; PI: Propidium iodide; PLCL: Poly- L-lactide-caprolactone; PLCL-CIS: PLCL nanofilm loaded with CIS; PLCL-GEM: PLCL nanofilm loaded with GEM; PLCL-GC: PLCL nanofilm loaded with both GEM and CIS.
- Citation: Xiao JB, Weng JY, Hu YY, Deng GL, Wan XJ. Feasibility and efficacy evaluation of metallic biliary stents eluting gemcitabine and cisplatin for extrahepatic cholangiocarcinoma. World J Gastroenterol 2020; 26(31): 4589-4606
- URL: https://www.wjgnet.com/1007-9327/full/v26/i31/4589.htm
- DOI: https://dx.doi.org/10.3748/wjg.v26.i31.4589