参 考 文 献
[1] Mc Neish IA, Bell SJ, Lemoine NR. Gene therapy progress and prospects: cancer gene therapy usingtumour suppress or genes. Gen Ther, 2004, 11 (6): 497.
[2] Ho EA,Ramsay E,Ginj M,et al. Characterization of cationic liposome formulations designed to exhibit extended plasma residence times and tumor vasculature targeting properties[J].J Pharm Sci,2010,99(6):2839.
[3] Kim H,Davaa E,Myung C,et al. Enhanced siRNA delivery using cationic liposomes with new polyarginine-conjugated PEG-lipid[J].Int J Pharm,2010,392:141.
[4] Kuesters GM,Campbell RB. Conjugation of bevacizumab to cationicliposomes enhances their tumor-targeting potential[J]. Nanomedicine (Lond),2010,5(2):181.
[5] Pirollo KF, Zon G, Rait A, et al. Tumor-targeting nanoimmunoliposome complex for short interfering RNA delivery[J].Hum Gene Ther,2006,17(1):117.
[6] Wang H,Zhao P,Liang X,et al. Folate-PEG coated cationic modified chitosan -Cholesterol liposomes for tumor-targeted drug delivery[J]. Biomaterials,2010,31(14):4129.
[7] Pirollo KF,Rait A,Zhou Q,et al. Tumor-targeting nanocomplex delivery of novel tumor suppressor RB94 chemosensitizes bladder carcinoma cells in vitro and in vivo[J]. Clin Cancer Res,2008,14(7):2190.
[8] Chunmao Wang, Chao Ding, Minjian Kong, et al. Tumor-targeting magnetic lipoplex delivery of short hairpin RNA suppresses IGF-1R overexpression of lung adenocarcinoma A549 cells in vitro and in vivo[J]. Bioch and Biophy Res Commun,2011(Received).
[9] Azam Bolhassani, Shima Safaiyan, Sima Rafati. Improvement of different vaccine delivery systems for cancer therapy. Molecular Cancer 2011, 10:3.
[10] 孙逊,田聆,聂宇等,阳离子脂质体-DNA复合物与脂质-鱼精蛋白-DNA复合物体外细胞转染率比较[J], 生物医学工程学杂志,2007,24(1):191.
[11] Chen J, Yu H, Chen H, et al. Transfection efficiency and intracellular fate of polycation liposomes combined with protamine[J]. Biomaterials, 2011, 32(5):1412.
[12] Torchilin VP. Cell penetrating peptide-modified pharmaceutical nanocarriers for intracellular drug and gene delivery[J].Biopolymers,2008,90(5):604.
[13] Tseng YL,Liu JJ,Hong RL.Translocation of liposomes into cancer cellsby cell-penetrating peptides penetratin and tat:a kinetic and efficacy study[J]. Mol Pharmacol,2002,62(4):864.
[14] Gupta B,Levchenko TS,Torchilin VP.TAT peptide-modified liposomes provide enhanced gene delivery to intracranial human brain tumor Xenografts in nude mice[J]. Oncol Res,2007,16(8):351.
[15] Zhang C,Tang N,Liu X,et al. siRNA-containing liposomes modified with polyarginine effectively silence the targeted gene[J]. J Control Release, 2006,112(2):229.
[16] Li Qiang,Jin Yi,Cui Fu-de.Study on melanoma vaccine using membrane fusogenic 1iposomes as the vector[J].Chin Pharm J,2003,38(11):851.
[17] 孙瑞琳,金发光,吴道澄等,多聚胺阳离子脂质体转染效率及细胞毒性的评价[J],解放军医学杂志,2006,31(4):327.
[18] Sawant RM,Hurley JP,Salmaso S,et al. “SMART”drug delivery systems:double-targeted pH-responsive pharmaceutical nanocarriers[J]. BioconjugChem,2006,17(4):943.
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