4.8 Review

Self-assembling materials for therapeutic delivery

期刊

ACTA BIOMATERIALIA
卷 5, 期 3, 页码 817-831

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.actbio.2008.09.018

关键词

Self-assembly; Parenteral delivery; Peptide hydrogel; Block copolymer

资金

  1. National Institutes of Health Grant (NIDCR) [R01-DE016386-01]
  2. NATIONAL CANCER INSTITUTE [ZIABC011313] Funding Source: NIH RePORTER
  3. NATIONAL INSTITUTE OF DENTAL &CRANIOFACIAL RESEARCH [R01DE016386] Funding Source: NIH RePORTER

向作者/读者索取更多资源

A growing number of medications must be administered through parenteral delivery, i.e., intravenous, intramuscular, or subcutaneous injection, to ensure effectiveness of the therapeutic. For some therapeutics, the use of delivery vehicles in conjunction with this delivery mechanism can improve drug efficacy and patient compliance. Macromolecular self-assembly has been exploited recently to engineer materials for the encapsulation and controlled delivery of therapeutics. Self-assembled materials offer the advantages of conventional crosslinked materials normally used for release, but also provide the ability to tailor specific bulk material properties, such as release profiles, at the molecular level via monomer design. As a result, the design of materials from the bottom up approach has generated a variety of supramolecular devices for biomedical applications. This review provides an overview of self-assembling molecules, their resultant structures, and their use in therapeutic delivery. It highlights the current progress in the design of polymer- and peptide-based self-assembled materials. (c) 2008 Acta Materialia. Inc. Published by Elsevier Ltd. All rights reserved.

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