Journal
NANOMEDICINE
Volume 14, Issue 18, Pages 2395-2408Publisher
FUTURE MEDICINE LTD
DOI: 10.2217/nnm-2018-0398
Keywords
anticancer; curcumin; doxorubicin; ethosome; melanoma; transdermal drug delivery
Funding
- National Key Research and Development Program of China [2018YFC1706200, 2018YFB1105602]
- Shanghai Science and Technology Committee Project [18490740400, 17JC1404300]
- National Natural Science Fund of China [81522049, 31571735, 31270007]
- Zhejiang Provincial Ten Thousands Program for Leading Talents of Science and Technology Innovation
- Zhejiang Provincial Program for the Cultivation of High-level Innovative Health Talents
- Dawn Program of Shanghai Education Commission [16SG38]
- Opening project of Zhejiang provincial preponderant and characteristic subject of Key University, Zhejiang Chinese Medical University [ZYAOX2018035]
- Project of Health and Family Planning Commission of Zhejiang province [2018KY831]
- Fundamental Research Funds for the Central Universities [2232019D3-20]
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Multidrug resistance is the main reason for the failure of chemotherapy during the treatment of the tumor. To overcome multidrug resistance, this study attempts to develop a novel transdermal drug-delivery system (TDDS) loading cytotoxic drug and chemosensitizer. Materials & methods: The polyethylenimine-modified ethosomes (Eth(-PEI)) and sodium cholate-modified ethosomes (Eth(-SC)) were firstly fabricated, and then a novel TDDS based on the carriers complex of Eth(-PEI)/Eth(-SC) was prepared by electrostatic interaction and evaluated both in vitro and in vivo. Results: The Eth(-PEI)/Eth(-SC) showed the excellent antitumor effect on treating melanoma, using doxorubicin and curcumin as the cytotoxic drug and chemosensitizer, respectively. Conclusion: The as-prepared TDDS composed of Eth(-PEI)/Eth(-SC) loading multidrug is an effective means for treating melanoma.
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