Abstract

To extend the platform of clinically utilised chemoembolic agents based on ion-exchange systems to support the delivery of anionic drugs, a series of PVA-based beads was produced with different levels of (3-acrylamidopropyl)trimethylammonium chloride (APTA) in their formulation. The beads were characterised to confirm composition and the effect of formulation variation on physical properties was assessed. Suspension polymerisation was shown to successfully produce uniformly spherical copolymer beads with APTA content up to 60 wt%. Equilibrium water content and resistance to compression both increased with increasing APTA content in the formulation. Confocal laser scanning microscopy was used with model drugs to demonstrate that by increasing APTA content, compounds between the molecular weight range 70–250 kDa could permeate the microsphere structures. Interaction with anionic drugs was modelled using multivalent dyes. Dyes with multi-binding sites had increased interaction with the polymer, slowing the release and also demonstrating a reduced rate of elution from beads with higher charge density. The model drug release studies demonstrate that these systems can be engineered for different potential anionic drugs for local therapeutic delivery in the clinic.

Highlights

  • Ion-exchange is the interchange of ions in a liquid phase with counter ions of a solid ionic polymer and is commonly utilised in drug delivery systems as a method of loading and subsequently controlling the release of a charged drug [1]

  • To extend the platform of clinically utilised chemoembolic agents based on ion-exchange systems to support the delivery of anionic drugs, a series of PVAbased beads was produced with different levels of (3acrylamidopropyl)trimethylammonium chloride (APTA) in their formulation

  • Confocal laser scanning microscopy was used with model drugs to demonstrate that by increasing APTA content, compounds between the molecular weight range 70–250 kDa could permeate the microsphere structures

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Summary

Introduction

Ion-exchange is the interchange of ions in a liquid phase with counter ions of a solid ionic polymer (resin) and is commonly utilised in drug delivery systems as a method of loading and subsequently controlling the release of a charged drug [1]. We have previously reported on the development of a commercial drug delivery embolisation system known as DC BeadTM which is a cationic exchange system formed by the copolymerisation of a modified polyvinyl alcohol (PVA) macromer and an acrylamido sulfonate monomer [3,4,5,6]. In this system ion-exchange occurs between the sulfonate moieties of the copolymer and the protonated primary amine of drugs such as doxorubicin hydrochloride salt. The beads are loaded by immersion in an aqueous drug solution and have demonstrated greater than 90 % loading efficiency of doxorubicin [6] in which the drug is stable for at least 14 days when refrigerated [7]

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