4.7 Article

Enzyme-responsive multistage vector for drug delivery to tumor tissue

Journal

PHARMACOLOGICAL RESEARCH
Volume 113, Issue -, Pages 92-99

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.phrs.2016.08.024

Keywords

Enzyme-responsive release; Lung metastasis; MMP2; Multistage vector; Porous silicon

Funding

  1. Houston Methodist Research Institute
  2. Ernest Cockrell Jr. Distinguished Endowed Chair
  3. US Department of Defense [W81XWH-09-1-0212]
  4. National Institute of Health [U54CA143837, U54CA151668]
  5. Department of Defense [W81XWH-12-1-0414]
  6. State of Texas CPRIT [RP121071]

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Various nanodelivery systems have been designed to release therapeutic agents upon contact with specific enzymes. However, enzyme-triggered release typically takes place in the tissue interstitium, thereby resulting in the extracellular delivery of drugs. Here, we have designed an enzyme-stimulated multistage vector (ESMSV), which enables stimulus-triggered release of drug-encapsulated nanoparticles from a microparticle. Specifically, polymeric nanoparticles with a surface matrix metalloproteinase-2 (MMP2) peptide substrate were conjugated to the surface of porous silicon microparticles. In the presence of MMP2, the polymeric nanoparticles were released into the tumor interstitium. This platform can be used to attain triggered drug release, while simultaneously facilitating the cellular internalization of drugs. The results indicate that nanoparticle release was MMP2-specific and resulted in improved intracellular uptake of hydrophobic agents in the presence of MMP2. Furthermore, in a mouse model of melanoma lung metastasis, systemic delivery of ESMSVs caused a substantial increase in intracellular accumulation of agents in cancer cells in comparison to delivery with non-stimulus-responsive particles. (C) 2016 Elsevier Ltd. All rights reserved.

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