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S. A. Lapidot, J. Kost, K. H. J. Buschow, W. C. Robert, C. F. Merton, I. Bernard, J. K. Edward, M. Subhash and V. Patrick, “Hydrogels,” In: K. H. J. Buschow, et al., Eds., Encyclopedia of Materials: Science and Technology, El- sevier, Oxford, 2001, pp. 3878- 3882.

has been cited by the following article:

• TITLE: Modular Hydrogels for Drug Delivery

  AUTHORS: Susana Simões, Ana Figueiras, Francisco Veiga

  KEYWORDS: Hydrogels; Swelling; Stimuli-Environmental; Controlled Drug Deliver

  JOURNAL NAME: Journal of Biomaterials and Nanobiotechnology, Vol.3 No.2, April 28, 2012

  ABSTRACT: The development of novel drug delivery systems is an essential step toward controlled site-specific administration of therapeutics within the body. It is desirable for delivery vehicles to be introduced into the body through minimally invasive means and, these vehicles should be capable of releasing drug to their intended location at a controlled rate. Furthermore, it is desirable to develop drug delivery systems that are capable of in vivo to suffer degradation and to deliver the drug completely, avoiding the need to surgically remove the vehicle at the end of its useful lifetime. Hydrogels are of particular interest for drug delivery applications due to their ability to address these needs in addition to their good biocompatibility, tunable network structure to control the diffusion of drugs and, tunable affinity for drugs. However, hydrogels are also limited for drug delivery applications due to the often quick elution of drug from their highly swollen polymer matrices as well as the difficulty inherent in the injection of macroscopic hydrogels into the body. This paper presents an overview to the advances in hydrogels based drug delivery. Different types of hydrogels can be used for drug delivery to specific sites in the gastrointestinal tract ranging from the oral cavity to the colon. These novel systems exhibit a range of several peculiar properties which make them attractive as controlled drug release formulations. Moreover, such materials are biocompatible and can be formulated to give controlled, pulsed, and triggered drug release profiles in a variety of tissues.