4.7 Article

Chitosan-alginate BSA-gel-capsules for local chemotherapy against drug-resistant breast cancer

期刊

DRUG DESIGN DEVELOPMENT AND THERAPY
卷 12, 期 -, 页码 921-934

出版社

DOVE MEDICAL PRESS LTD
DOI: 10.2147/DDDT.S158001

关键词

polyelectrolyte capsule; bovine serum albumin; layer-by-layer; pH-responsive; intratumor injection; multidrug resistance

资金

  1. National Natural Science Foundation of China [81402870, 81502800]
  2. Natural Science Foundation of Jiangsu Province [BK20140579]
  3. China Postdoctoral Science Foundation [2015M571696, 2013M540424, 2015T80513]
  4. Jiangsu Province Postdoctoral Science Foundation [1401145C]
  5. Scientific Research Foundation of Jiangsu University [14JDG046]

向作者/读者索取更多资源

Background and object: Polyelectrolyte microcapsule is a promising candidate for multifunctional drug delivery system. However, the lack of reports about animal experiments have greatly slowed down their development for drug delivery. We engineered biodegradable chitosan-alginate polyelectrolyte multilayer capsule filled with bovine serum albumin gel (BSA-gel-capsule). Herein, we demonstrated their applicability for local chemotherapy, a means of treating local or regional malignancies by direct administration of anti-tumor agents to tumor sites. Method: Doxorubicin (DOX) was loaded in BSA-gel-capsules and DOX-resistant cell line (MCF-7/ADR cells) was employed for antitumor studies in vitro. The cytotoxicity, cellular uptake and distribution of DOX from BSA-gel-capsules were studied. Afterwards, MCF-7/ADR xenografts tumor model was established in nude mice. The in vivo antitumor efficacy of DOX-loaded BSA-gel-capsules by intratumor injection was then evaluated. Result: Compared with free DOX, more effective cytotoxicity against MCF-7/ADR cells after treatment with DOX-loaded BSA-gel-capsules was revealed, demonstrating the positive reversal effect on drug-resistance. Thereafter, the more cellular uptake and nucleus distribution of DOX from BSA-gel-capsules in MCF-7/ADR cells provided convincing explanation for the reversal effect. DOX-loaded BSA-gel-capsules displayed remarkably more antitumor efficacy than free DOX in MCF-7/ADR cell-xenografted mice. Finally, the high DOX accumulation and prolonged retention in tumor site after local administration of DOX-loaded BSA-gel-capsules was demonstrated, displaying the unique advantages of BSA-gel-capsules for local chemotherapy. Conclusion: These findings indicate that DOX-loaded BSA-gel-capsules should be considered a potential candidate for the treatment of drug-resistant breast cancer. This paper provides a feasibility for the local chemotherapy of polyelectrolyte microcapsules, which will be a big step towards their application as drug delivery vehicles.

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