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Supramolecular prodrugs based on host-guest interactions

Journal

CHEMICAL SOCIETY REVIEWS
Volume 49, Issue 8, Pages 2303-2315

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c9cs00622b

Keywords

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Funding

  1. National Science Foundation of China (NSFC) [51873090, 31961143004]
  2. National Institutes of Health [RO1 GM103790]
  3. Robert A. Welch Foundation [F-0018]
  4. China Scholarship Council [201806200072]

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Classic prodrug strategies rely on covalent modification of active drugs to provide systems with superior pharmacokinetic properties than the parent drug and facilitate administration. Supramolecular chemistry is providing a new approach to developing prodrug-like systems, wherein the characteristics of a drug are modified in a beneficial manner by creating host-guest complexes that then permit the stimulus-induced release of the active species in a controlled manner. These complexes are termed supramolecular prodrugs. In this review, we outline the concept of supramolecular drugs via host-guest chemistry and detail progress made in the area. This summary is designed to highlight the many advantages of supramolecular prodrugs, including ease-of-preparation, molecular-level protection, sensitive response to bio-stimuli, traceless release, and adaptability to different drugs. Limitations of the approach and opportunities for future growth are also detailed.

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