Lymph cancer chemotherapy: delivery of doxorubicin-gemcitabine prodrug and vincristine by nanostructured lipid carriers

被引:29
|
作者
Ni, Shuqin [1 ]
Qiu, Lei [1 ]
Zhang, Guodong [1 ]
Zhou, Haiyan [1 ]
Han, Yong [1 ]
机构
[1] Shandong Univ, Shandong Canc Hosp, Shandong Acad Med Sci, Dept Internal Med Oncol, 440 Jiyan Rd, Jinan 250117, Shandong, Peoples R China
来源
关键词
combination chemotherapy; B-cell lymphoma; prodrug; nanostructured lipid carriers; drug delivery; NON-HODGKINS-LYMPHOMA; OVERCOME MULTIDRUG-RESISTANCE; B-CELL LYMPHOMA; DRUG-DELIVERY; CO-DELIVERY; HEPATOCELLULAR-CARCINOMA; TARGETED DELIVERY; NANOPARTICLES SLN; BREAST-CANCER; LIPOSOMES;
D O I
10.2147/IJN.S120685
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Purpose: Radiation and chemotherapy are the most common course of treatment for B-cell lymphoma. Doxorubicin (DOX), gemcitabine (GEM), and vincristine (VCR) are the commonly used antilymphoma chemotherapeutic drugs. The aim of this study is to construct a novel drug delivery system for the combination delivery of the three drugs on lymphoma. Materials and methods: DOX-GEM prodrug was synthesized. Novel nanostructured lipid carriers (NLCs) containing DOX-GEM prodrug and VCR were prepared and used to treat B-cell lymphoma through in vivo treatment to a lymph cancer animal model. The systemic toxicity of the nanomedicine was also evaluated during the treatment. Results: DOX-GEM prodrug and VCR-loaded NLCs (DOX-GEM VCR NLCs) exhibited the highest antitumor effect in B-cell lymphoma cells and lymphoma animal xenografts when compared with the single drug-loaded NLCs and the drug solutions. Conclusion: It could be concluded that the highest antitumor effect can be achieved by the system due to the stable drug-loading capacity, attractive anticancer therapeutic effects, and reduced toxicities in human Burkitt's lymphoma cell line and mice-bearing cancer model. The resulting DOX-GEM VCR NLCs could be an efficient antilymph cancer agent and could be developed further for the treatment of other tumors.
引用
收藏
页码:1565 / 1575
页数:11
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