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淋巴癌化疗:通过纳米结构脂质载体递送阿霉素-吉西他滨前药和长春新碱。

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

作者信息

Ni Shuqin, Qiu Lei, Zhang Guodong, Zhou Haiyan, Han Yong

机构信息

Department of Internal Medicine Oncology, Shandong Cancer Hospital Affiliated to Shandong University, Shandong Academy of Medical Science, Ji'nan, Shandong, People's Republic of China.

出版信息

Int J Nanomedicine. 2017 Feb 27;12:1565-1576. doi: 10.2147/IJN.S120685. eCollection 2017.

Abstract

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.

摘要

目的

放疗和化疗是B细胞淋巴瘤最常见的治疗方法。阿霉素(DOX)、吉西他滨(GEM)和长春新碱(VCR)是常用的抗淋巴瘤化疗药物。本研究的目的是构建一种新型药物递送系统,用于将这三种药物联合递送至淋巴瘤。

材料与方法

合成DOX-GEM前药。制备了含有DOX-GEM前药和VCR的新型纳米结构脂质载体(NLCs),并通过对淋巴癌动物模型进行体内治疗来用于治疗B细胞淋巴瘤。在治疗过程中还评估了纳米药物的全身毒性。

结果

与单药负载的NLCs和药物溶液相比,负载DOX-GEM前药和VCR的NLCs(DOX-GEM VCR NLCs)在B细胞淋巴瘤细胞和淋巴瘤动物异种移植模型中表现出最高的抗肿瘤效果。

结论

可以得出结论,由于该系统具有稳定的载药能力、诱人的抗癌治疗效果以及在人伯基特淋巴瘤细胞系和荷瘤小鼠模型中降低的毒性,因此能够实现最高的抗肿瘤效果。所得的DOX-GEM VCR NLCs可能是一种有效的抗淋巴癌药物,可进一步开发用于治疗其他肿瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c7a/5338998/e3f7702b1205/ijn-12-1565Fig1.jpg

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