Drug formulation and nanomedicine approaches to targeting lymphatic cancer metastases

被引:13
|
作者
Wang, Lili [1 ]
Subasic, Christopher [1 ]
Minchin, Rodney F. [1 ]
Kaminskas, Lisa M. [1 ]
机构
[1] Univ Queensland, Sch Biomed Sci, Fac Med, St Lucia, Qld 4072, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
cancer metastasis; drug delivery; formulation; lymphatic; nanomedicine; PEGylation; pharmacokinetics; poly(ethylene glycol); prodrugs; SOLID LIPID NANOPARTICLES; CONJUGATED PEGYLATED DENDRIMERS; PEG CHAIN-LENGTH; BREAST-CANCER; IN-VITRO; INTRATUMORAL LYMPHANGIOGENESIS; TUMOR LYMPHANGIOGENESIS; CHEMOTHERAPEUTIC DRUGS; POLYMERIC MICELLES; MANNOSE RECEPTOR;
D O I
10.2217/nnm-2018-0478
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
Lymphatic metastasis plays an important role in cancer progression and prognosis. However, conventional small-molecule chemotherapy drugs inefficiently access the lymphatic system, making the effective eradication of lymphatic metastases difficult without dose-limiting toxicity. Various formulation and nanomedicine-based approaches can be used to significantly enhance the trafficking of small-molecule, peptide and protein drugs toward the lymphatic system to enhance drug exposure at sites of lymphatic cancer growth. However, a number of obstacles exist in translating improved lymphatic exposure into improved chemotherapeutic outcomes. This review highlights the opportunities and challenges inherent in employing formulation and nanomedicinal approaches to improve chemotherapeutic drug activity within the lymphatic system and, importantly, at sites of lymphatic cancer metastasis.
引用
收藏
页码:1605 / 1621
页数:17
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