Novel crosslinking methods to design hydrogels

Research output: Contribution to journalReview articlepeer-review

Abstract

Hydrogels are presently under investigation as matrices for the controlled release of bioactive molecules, in particular pharmaceutical proteins, and for the encapsulation of living cells. For these applications, it is often required that the gels degrade under physiological conditions. This means that the originally three-dimensional structure has to disintegrate preferably in harmless products to ensure a good biocompatibility of the hydrogel. In this overview, different chemical and physical crosslinking methods used for the design of biodegradable hydrogels are summarized and discussed. Chemical crosslinking is a highly versatile method to create hydrogels with good mechanical stability. However, the crosslinking agents used are often toxic compounds, which have been extracted from the gels before they can be applied. Moreover, crosslinking agents can give unwanted reactions with the bioactive substances present in the hydrogel matrix. Such adverse effects are avoided with the use of physically crosslinked gels. © 2002 Elsevier Science B.V. All rights reserved.
Original languageEnglish
Pages (from-to)13-36
Number of pages24
JournalAdvanced Drug Delivery Reviews
Volume54
Issue number1
DOIs
Publication statusPublished - 17 Jan 2002

Keywords

  • Crosslinking
  • Degradation
  • Drug release
  • Hydrogel
  • Tissue engineering
  • aldehyde
  • enzyme
  • functional group
  • M protein
  • macrogol
  • polylactic acid
  • polysaccharide
  • antigen antibody reaction
  • biocompatibility
  • controlled release formulation
  • cross linking
  • crystallization
  • drug activity
  • drug stability
  • hydrogel
  • hydrogen bond
  • irradiation
  • physiology
  • polymerization
  • priority journal
  • protein interaction
  • review

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