Tumor-targeting multifunctional micelles for imaging and chemotherapy of advanced bladder cancer

被引:1
|
作者
Lin, Tzu-yin [1 ]
Li, Yuan-Pei [2 ]
Zhang, Hongyong [1 ]
Luo, Juntao [3 ]
Goodwin, Neal [4 ]
Gao, Tingjuan [5 ]
White, Ralph de Vere [6 ]
Lam, Kit S. [1 ,2 ]
Pan, Chong-Xian [1 ,6 ,7 ]
机构
[1] Univ Calif Davis, Div Hematol & Oncol, Dept Internal Med, Sch Med, Sacramento, CA 95817 USA
[2] Univ Calif Davis, Dept Biochem & Mol Med, Sch Med, Sacramento, CA 95817 USA
[3] SUNY Upstate Med Univ, Dept Pharmacol, Syracuse, NY 13210 USA
[4] Jackson Lab, Sacramento, CA 95838 USA
[5] Univ Calif Davis, NSF Ctr Biophoton Sci & Technol, Sacramento, CA 95817 USA
[6] Univ Calif Davis, Dept Urol, Ctr Canc, Sacramento, CA 95817 USA
[7] Vet Adm Northern Calif Hlth Care Syst, Mather, CA 95655 USA
关键词
bladder cancer-specific ligand; bladder urothelial carcinoma; diagnostic imaging; nanoparticle; targeted therapy; PEGYLATED-LIPOSOMAL DOXORUBICIN; TRANSITIONAL-CELL CARCINOMA; PACLITAXEL DELIVERY; OVARIAN-CANCER; DRUG-DELIVERY; CREMOPHOR EL; IN-VIVO; NANOPARTICLES; THERAPY; THERAPEUTICS;
D O I
10.2217/NNM.12.150
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aim: This work aimed to determine if the treatment outcomes of bladder cancer could be improved by targeting micelles that are decorated with bladder cancer-specific ligands on the surface and loaded with the chemotherapeutic drug paclitaxel. Materials & methods: Targeting efficacy and specificity was determined with cell lines. An in vivo targeting and anti-tumor efficacy study was conducted in mice carrying patient-derived xenografts. Results & discussion: Targeting micelles were more efficient than nontargeting micelles in delivering the drug load into bladder cancer cells both in vitro and in vivo (p < 0.05). The micelle formulation of paclitaxel was less toxic than free paclitaxel in Cremophor (R) (Sigma, MO, USA) and allowed administration of three-times the maximum tolerated dose without increasing the toxicity. Targeting micelles were more effective than the nontargeting micelles in controlling cancer growth (p = 0.0002) and prolonging overall survival (p = 0.002). Conclusion: Targeting micelles loaded with paclitaxel offer strong potential for clinical applications in treating bladder cancer.
引用
收藏
页码:1239 / 1251
页数:13
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