In vivo degradation of semi-rigid polymeric films made of alginate and polyethylene glycol

Alginate-based biomaterials can form naturally derived polymeric hydrogels with sufficient structural integrity to readily be used in many clinical applications. However, ionically cross-linked alginate gels do not always possess structural properties suitable for application as erodable polymeric films for controlled release of drugs and growth factors. In this study, semi-rigid polymeric films were constructed of sodium alginate and polyethylene glycol (PEG) by means of a rehydration cross-linking technique. The films were assembled by dehydrating a solution of alginate and PEG and cross-linking the alginate during its rehydration with a solution of calcium chloride. The product is a highly dense polymeric network that prevents in vivo cellular infiltration and disassembles primarily by surface erosion. By implanting the PEG-alginate films into the subcutis of rats, the mechanism of polymer degradation was demonstrated to occur via inflammation-mediated erosion of the material rather than by means of cellular infiltration. There were extensive areas of foamy macrophages at the site of the implant, indicating a likely mechanism of removal and disposal of the disassembled PEG and alginate polymer. The eroded fragments of the film that remained after six weeks did not exhibit signs of a cellular infiltrate but rather stayed intact, appearing as small, dense fragments of polymer. Our observations that nearly all the PEG-alginate material was cleared from the implantation site by the sixth postoperative week highlight the potential exploitation of these films as bioresorbable wound dressings with prospective utilization as a drug delivery device. Moreover, the employment of polymeric films made of functionalized PEG, which enables covalent attachment of biological molecules, potentiates their use for growth factor delivery applications.