| Literature DB >> 25731143 |
Petr Chytil1, Eva Koziolová2, Olga Janoušková2, Libor Kostka2, Karel Ulbrich2, Tomáš Etrych2.
Abstract
High-molecular-weight star polymer drug nanocarriers intended for the treatment and/or visualisation of solid tumours were synthesised, and their physico-chemical and preliminary in vitro biological properties were determined. The water-soluble star polymer carriers were prepared by the grafting of poly(amido amine) (PAMAM) dendrimers by hetero-telechelic N-(2-hydroxypropyl)methacrylamide (HPMA) copolymers, synthesised by the controlled radical Reversible Addition Fragmentation chain Transfer (RAFT) polymerisation. The well-defined star copolymers with Mw values ranging from 2 · 10(5) to 6 · 10(5) showing a low dispersity (approximately 1.2) were prepared in a high yield. A model anticancer drug, doxorubicin, was bound to the star polymer through a hydrazone bond, enabling the pH-controlled drug release in the target tumour tissue. The activated polymer arm ends of the star copolymer carrier enable a one-point attachment for the targeting ligands and/or a labelling moiety. In this study, the model TAMRA fluorescent dye was used to prove the feasibility of the polymer carrier visualisation by optical imaging in vitro. The tailor-made structure of the star polymer carriers should facilitate the synthesis of targeted polymer-drug conjugates, even polymer theranostics, for simultaneous tumour drug delivery and imaging.Entities:
Keywords: HPMA copolymers; drug delivery systems; pH-controlled release; reversible addition fragmentation chain transfer (RAFT); star copolymers
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Year: 2015 PMID: 25731143 DOI: 10.1002/mabi.201400510
Source DB: PubMed Journal: Macromol Biosci ISSN: 1616-5187 Impact factor: 4.979