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Nanoparticle-mediated co-delivery of chemotherapeutic agent and siRNA for combination cancer therapy

期刊

EXPERT OPINION ON DRUG DELIVERY
卷 14, 期 1, 页码 65-73

出版社

TAYLOR & FRANCIS LTD
DOI: 10.1080/17425247.2016.1205583

关键词

Co-delivery; chemical drug; siRNA; nanoparticle; combination therapy; cancer

资金

  1. Department of Veterans Affairs [BX002526]
  2. National Institutes of Health of Diabetes and Digestive and Kidney [RO1-DK-071594]
  3. National Natural Science Foundation of China [51503172, 81571807]
  4. Fundamental Research Funds for the Central Universities [SWU114086, XDJK2015C067]
  5. Scientific Research Foundation for the Returned Overseas Chinese Scholars (State Education Ministry)

向作者/读者索取更多资源

Introduction: Cancer is the leading cause of death worldwide. Current cancer treatments in the clinic mainly include chemotherapy, radiotherapy and surgery, with chemotherapy being the most common. Areas covered: Cancer treatments based on the single 'magic-bullet' concept are often associated with limited therapeutic efficacy, unwanted adverse effects, and drug resistance. The combination of multiple drugs is a promising strategy for effective cancer treatment due to the synergistic or additive effects. Small interfering RNA (siRNA) has the ability to knock down the expression of carcinogenic genes or drug efflux transporter genes, paving the way for cancer treatment. Treatment with both a chemotherapeutic agent and siRNA based on nanoparticle (NP)-mediated co-delivery is a promising approach for combination cancer therapy. Expert opinion: The combination of chemotherapeutic agents and siRNAs for cancer treatment offers the potential to enhance therapeutic efficacy, decrease side effects, and overcome drug resistance. Co-delivery of chemical drug and siRNA in the same NP would be much more effective in cancer therapy than application of chemical agent or siRNA alone. With the development of material science, NPs have come to be the most widely used platform for co-delivery of chemotherapeutic drugs and siRNAs.

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