4.8 Article

Localized Co-delivery of Doxorubicin, Cisplatin, and Methotrexate by Thermosensitive Hydrogels for Enhanced Osteosarcoma Treatment

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 7, Issue 49, Pages 27040-27048

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.5b09112

Keywords

injectable hydrogels; localized delivery; multidrug co-delivery; synergistic therapy; combination therapy; osteosarcoma treatment

Funding

  1. National Natural Science Foundation of China [21174142, 51273081, 51233004, 51390484, 51321062]
  2. Ministry of Science and Technology of China [2011DFR51090]
  3. Changchun Municipal Science and Technology Bureau Foundation [2012092]

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Localized cancer treatments with combination drugs have recently emerged as crucial approaches for effective Inhibition of tumor growth and reoccurrence. In this study, we present a new strategy for the osteosarcoma treatment by localized co-delivery of multiple drugs, including doxorubicin (DOX), cisplatin (CDDP) and methotraxate (MTX), using thermosensitive PLGA PEG PLGA hydrogels. The release profiles of the drugs from the hydrogels were investigated in vitro. It was found that the multidrug coloaded hydrogels exhibited synergistic effects on cytoto]dcity against osteosarcoma Saos-2 and MG-63 cells in vitro. After a single peritumoral injection of the drug-loaded hydrogels into nude mice bearing human osteosarcoma Saos-2 xenografts, the hydrogels coloaded with DOX, CDDP, and MTX displayed the highest tumor suppression efficacy in vivo for up to 16 days, as well as led to enhanced tumor apoptosis and increased regulation of the expressions of apoptosis-related genes. Moreover, the monitoring on the mice body change and the ex vivo histological analysis of the key organs indicated that the localized treatments caused less systemic toxicity and no obvious damage to the normal organs. Therefore, the approach of localized co-delivery of DOX, CDDP, and MTX by the thermosensitive hydrogels may be a promising approach for enhanced osteosarcoma treatment.

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