Biological Evaluation of Polyester Dendrimer: Poly(ethylene oxide) “Bow-Tie” Hybrids with Tunable Molecular Weight and Architecture
- 9 February 2005
- journal article
- research article
- Published by American Chemical Society (ACS) in Molecular Pharmaceutics
- Vol. 2 (2) , 129-138
- https://doi.org/10.1021/mp049886u
Abstract
High molecular weight (MW) polymers have shown promise in terms of improving the properties and the efficacy of low MW therapeutics. However, new systems that are highly biocompatible, are biodegradable, have well-defined MW, and have multiple functional groups for drug attachment are still needed. The biological evaluation of a library of eight polyester dendrimer−poly(ethylene oxide) (PEO) bow-tie hybrids is described here. The group of evaluated polymers was designed to include a range of MWs (from 20000 to 160000) and architectures with the number of PEO arms ranging from two to eight. In vitro experiments revealed that the polymers were nontoxic to cells and were degraded to lower MW species at pH 7.4 and pH 5.0. Biodistribution studies with 125I-radiolabeled polymers showed that the high MW carriers (>40000) exhibited long circulation half-lives. Comparison of the renal clearances for the four-arm versus eight-arm polymers indicated that the more branched polymers were excreted more slowly into the urine, a result attributed to their decreased flexibility. Due to their essentially linear architecture that does not provide for good isolation of the iodinated phenolic moieties, the polymers with “two arms” were rapidly taken up by the liver. The biodistributions of two long-circulating high MW polymers in mice bearing subcutaneous B16F10 tumors were evaluated, and high levels of tumor accumulation were observed. These new carriers are therefore promising for applications in drug delivery and are also useful for improving our understanding of the effect of polymer architecture on pharmacokinetic properties. Keywords: Drug delivery; polymer; dendrimer; tumor; biodistribution; biodegradableKeywords
This publication has 28 references indexed in Scilit:
- Pharmacokinetic and biodistribution properties of poly(ethylene glycol)–protein conjugatesAdvanced Drug Delivery Reviews, 2003
- HPMA copolymer–anticancer drug conjugates: design, activity, and mechanism of actionEuropean Journal of Pharmaceutics and Biopharmaceutics, 2000
- A biodegradable multiblock co-polymer derived from an α,ω-bis(methylamino)peptide and an α,ω-bis(oxiranylmethyl)poly(ethylene glycol)Journal of Controlled Release, 2000
- Effects of L-2-oxothiazolidine-4-carboxylate on the cytotoxic activity and toxicity of cyclophosphamide in mice bearing B16F10 melanoma liver metastasesMelanoma Research, 2000
- Polymeric drugs based on conjugates of synthetic and natural macromoleculesJournal of Controlled Release, 2000
- Prolongation of the serum half-life period of superoxide dismutase by poly(ethylene glycol) modificationJournal of Controlled Release, 1997
- Pharmacokinetic evaluation of polymeric carriersAdvanced Drug Delivery Reviews, 1996
- Distribution and Tissue Uptake of Poly(ethylene glycol) with Different Molecular Weights after Intravenous Administration to MiceJournal of Pharmaceutical Sciences, 1994
- Conjugates of anticancer agents and polymers: advantages of macromolecular therapeutics in vivoBioconjugate Chemistry, 1992
- Glomerular permeability of macromolecules. Effect of molecular configuration on the fractional clearance of uncharged dextran and neutral horseradish peroxidase in the rat.Journal of Clinical Investigation, 1979