4.8 Article

Platinum(IV) complex-based two-in-one polyprodrug for a combinatorial chemo-photodynamic therapy

Journal

BIOMATERIALS
Volume 177, Issue -, Pages 67-77

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2018.05.052

Keywords

ROS self-generation; Photoactive prodrug; O-2-independence; Drug-resistance; Polyprodrug; Hypoxia

Funding

  1. National Key Research and Development Plan of China [2016YFA0201500]
  2. National Natural Science Foundation of China [21504053, 21661162001, 21673139, 91527304, 51690151, 51473093]
  3. Innovation Fund from Joint Research Center for Precision Medicine by Shanghai Jiao Tong University & Affiliated Sixth People's Hospital South Campus [IFPM 20168001]
  4. special program for collaborative innovation in Shanghai University of Medicine & Health Sciences [SPCI-17-15-001]

Ask authors/readers for more resources

A combinatorial therapy that utilizes two or more therapeutic modalities is more effective in overcoming the limitations than each individual method used alone. Despite great advances have been achieved, the combination of chemotherapy and photodynamic therapy (PDT) still cannot satisfy the clinic requirements as the antitumor efficacy could be severely affected by tumor-associated hypoxia. Herein, for the first time, we reported a platinum(IV) complex-based polyprodrug that can in situ generate the highly toxic platinum(II) species as chemotherapeutics and simultaneously induce a high level of reactive oxygen species (ROS) in a PDT-like process without the use of photosensitizer and consumption of oxygen. By in situ polymerizing the platinum(IV) complex-based prodrug monomer (PPM) and 2-methacryloyloxy ethyl phosphorylcholine (MPC), nanosized hydrogel-like polyprodrug could be synthesized. Upon being exposed to light, Pt(IV) moieties in this photoactivable polyprodrug were reduced to generate Pt(II) species. At the meantime, a high level of ROS was generated without the presence of endogenous oxygen, which was confirmed by electron spin resonance (ESR) and fluorescence probes. With the unique nanosized architecture and photoresponsive feature, the as-synthesized polyprodrug exhibited the advantages of sustained drug release, long-term circulation, preferable tumor accumulation, and reversing drug resistance by downregulating the expression of multidrug resistance-associated protein 1 (MRP1) in the anticancer treatment. (C) 2018 Elsevier Ltd. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available