Issue 46, 2020

One-pot synthesis of acid-degradable polyphosphazene prodrugs for efficient tumor chemotherapy

Abstract

In order to improve the therapeutic efficacy and reduce the side effects of anticancer drugs, stimuli-responsive and biodegradable drug-delivery systems have attracted significant attention in the past three decades. Herein, we report acid-responsive and degradable polyphosphazene nano-prodrugs synthesized via a one-pot cross-linking reaction of 4-hydroxybenzhydrazide-modified doxorubicin (BMD) with hexachlorocyclotriphosphazene (HCCP). The phenol groups in the as-synthesized BMD exhibited a high reactivity towards HCCP and in the presence of a basic catalyst the determined drug loading ratio of the nanoparticles, denoted as HCCP-BMD, was up to 85.64%. Interestingly, the hydrazone bonds in BMD and the skeleton of polyphosphazene tended to break down in acidic environments, and the antitumor active drug DOX was found to be released in an acidic tumor microenvironment (pH ∼ 6.8 for extracellular, and pH ∼ 5.0 for endosomes and lysosomes). The resulting HCCP-BMD prodrug exhibited high cytotoxicity to HeLa cells and could effectively suppress tumor growth, with negligible damage to normal tissues. We therefore believe that this acid- degradable polyphosphazene prodrug may offer great potential in various biomedical fields.

Graphical abstract: One-pot synthesis of acid-degradable polyphosphazene prodrugs for efficient tumor chemotherapy

Associated articles

Supplementary files

Article information

Article type
Paper
Submitted
17 ago 2020
Accepted
24 out 2020
First published
26 out 2020

J. Mater. Chem. B, 2020,8, 10540-10548

One-pot synthesis of acid-degradable polyphosphazene prodrugs for efficient tumor chemotherapy

N. Zhou, N. Zhang, Z. Zhi, X. Jing, D. Liu, Y. Shao, D. Wang and L. Meng, J. Mater. Chem. B, 2020, 8, 10540 DOI: 10.1039/D0TB01992E

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