Evolution of macromolecular complexity in drug delivery systems

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作者
Ashok Kakkar
Giovanni Traverso
Omid C. Farokhzad
Ralph Weissleder
Robert Langer
机构
[1] Koch Institute for Integrative Cancer Research,Harvard
[2] Massachusetts Institute of Technology,MIT Division of Health Sciences, Department of Chemical Engineering
[3] McGill University,Department of Chemistry
[4] Brigham and Women's Hospital,Division of Gastroenterology
[5] Harvard Medical School,Center for Nanomedicine and Department of Anesthesiology
[6] Brigham and Women's Hospital,undefined
[7] Harvard Medical School,undefined
[8] Center for Systems Biology,undefined
[9] Massachusetts General Hospital,undefined
[10] Harvard Medical School,undefined
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摘要
Designing therapeutics is a process with many challenges. Even if the first hurdle — designing a drug that modulates the action of a particular biological target in vitro — is overcome, selective delivery to that target in vivo presents a major barrier. Side-effects can, in many cases, result from the need to use higher doses without targeted delivery. However, the established use of macromolecules to encapsulate or conjugate drugs can provide improved delivery, and stands to enable better therapeutic outcomes. In this Review, we discuss how drug delivery approaches have evolved alongside our ability to prepare increasingly complex macromolecular architectures. We examine how this increased complexity has overcome the challenges of drug delivery and discuss its potential for fulfilling unmet needs in nanomedicine.
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