4.8 Article

Co-delivery of daunomycin and oxaliplatin by biodegradable polymers for safer and more efficacious combination therapy

Journal

JOURNAL OF CONTROLLED RELEASE
Volume 163, Issue 3, Pages 304-314

Publisher

ELSEVIER
DOI: 10.1016/j.jconrel.2012.06.004

Keywords

Combination chemotherapy; Daunorubicin; Drug delivery; Oxaliplatin; Polymer conjugates

Funding

  1. National Natural Science Foundation of China [21004062, 51103148, 20674084]
  2. 100 Talents Program of the Chinese Academy of Sciences [KGCX2-YW-802]
  3. Ministry of Science and Technology of China (973 Project) [2009CB930102]

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An oxaliplatin pro-drug (Oxa(IV)-COOH) with an axial carboxyl group was synthesized and conjugated to biodegradable polymers with pendant hydroxyl groups to prepare polymer-Oxa(IV) conjugates. A hydrophobic anthracycline-based drug, daunorubicin (DRB) was conjugated to similar biodegradable polymers with carboxyl groups to synthesize polymer-DRB conjugates. The two drug conjugates have the similar polymer backbone and are amphiphilic; thus, they can co-assemble into composite micelles. In the composite micelles, the polymer-Oxa(IV) conjugates can release clinically widely used water soluble anticancer drug oxaliplatin (Oxa(II)) upon reduction, while polymer-DRB conjugate is thought to release DRB via acid hydrolysis in the cancer cells. In this way, combination of the hydrophilic platinum drug Oxa(II) and hydrophobic drug DRB can be realized by delivering them in one platform. Moreover, the composite micelles showed reduced systematic toxicity and greater synergistic effect than combination of small molecules of the two anticancer drugs both in vitro and in vivo; thus, this polymer based combination therapy can be useful in future clinic application. (c) 2012 Elsevier B.V. All rights reserved.

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