Adaptable polymerization platform for therapeutics with tunable biodegradability.


Journal

Acta biomaterialia
ISSN: 1878-7568
Titre abrégé: Acta Biomater
Pays: England
ID NLM: 101233144

Informations de publication

Date de publication:
11 2023
Historique:
received: 13 04 2023
revised: 10 08 2023
accepted: 05 09 2023
medline: 27 10 2023
pubmed: 12 9 2023
entrez: 11 9 2023
Statut: ppublish

Résumé

Biodegradable polymer-based therapeutics have recently become essential drug delivery biomaterials for various bioactive compounds. Biodegradable and biocompatible polymer-based biomaterials fulfill the requirements of these therapeutics because they enable to obtain polymer biomaterials with optimized blood circulation, pharmacokinetics, biodegradability, and renal excretion. Herein, we describe an adaptable polymerization platform employed for the synthesis of long-circulating, stimulus-sensitive and biodegradable biomaterials, therapeutics, or theranostics. Four chain transfer agents (CTA) were designed and successfully synthesized for the reversible addition-fragmentation chain transfer polymerization, allowing the straightforward synthesis of hydrolytically biodegradable structures of block copolymers-based biomaterials. The controlled polymerization using the CTAs enables controlling the half-life of the hydrolytic degradation of polymer precursors in a wide range from 5 h to 21 days. Moreover, the antitumor drug pirarubicin (THP) was successfully conjugated to the polymer biomaterials via a pH-sensitive hydrazone bond for in vitro and in vivo experiments. Polymer conjugates demonstrated superior antitumor efficacy compared to basic linear polymer-based conjugates. Notably, the biodegradable systems, even though those with degradation in the order of hours were selected, increased the half-life of THP in the bloodstream almost two-fold. Indeed, the presented platform design enables the main chain-end specific attachment of targeting ligands or diagnostic molecules. The adaptable polymerization platform design allows tuning of the biodegradability rate, stimuli-sensitive drug bonding, and optimized pharmacokinetics to increase the therapy outcome and system targeting, thus allowing the preparation of targeted or theranostic polymer conjugates. STATEMENT OF SIGNIFICANCE: Biodegradable and biocompatible polymer-based biomaterials are recognized as potential future bioactive nanomedicines. To advance the development of such biomaterials, we developed polymerization platforms utilizing tailored chain transfer agents allowing the straightforward synthesis of hydrolytically degradable polymer biomaterials with tuned biodegradability from hours to several days. The platform allows for the synthesis of long-circulating, stimulus-sensitive and biodegradable biomaterial serving as drug carriers or theranostics. The therapeutic potential was validated by preparation of polymer biomaterials containing pirarubicin, anticancer drug, bound via pH sensitive bond and by showing prolonged blood circulation and increased antitumor activity while keeping the drug side effects low. This work paves the way for future development of biodegradable polymer biomaterials with advanced properties in drug delivery.

Identifiants

pubmed: 37696413
pii: S1742-7061(23)00538-X
doi: 10.1016/j.actbio.2023.09.004
pii:
doi:

Substances chimiques

pirarubicin D58G680W0G
Doxorubicin 80168379AG
Antineoplastic Agents 0
Drug Carriers 0
Polymers 0
Biocompatible Materials 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

417-427

Informations de copyright

Copyright © 2023 The Author(s). Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

M Hrochová (M)

Institute of Macromolecular Chemistry, Czech Academy of Sciences, Prague 16200, Czechia.

L Kotrchová (L)

Institute of Macromolecular Chemistry, Czech Academy of Sciences, Prague 16200, Czechia.

M Frejková (M)

Institute of Macromolecular Chemistry, Czech Academy of Sciences, Prague 16200, Czechia.

R Konefał (R)

Institute of Macromolecular Chemistry, Czech Academy of Sciences, Prague 16200, Czechia.

S Gao (S)

Faculty of Pharmaceutical Sciences, Sojo University, Kumamoto 860-0082, Japan.

J Fang (J)

Faculty of Pharmaceutical Sciences, Sojo University, Kumamoto 860-0082, Japan.

L Kostka (L)

Institute of Macromolecular Chemistry, Czech Academy of Sciences, Prague 16200, Czechia.

T Etrych (T)

Institute of Macromolecular Chemistry, Czech Academy of Sciences, Prague 16200, Czechia. Electronic address: etrych@imc.cas.cz.

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