Strategies to improve the EPR effect: A mechanistic perspective and clinical translation
Abstract
Many efforts have been made to achieve targeted delivery of anticancer drugs to enhance their efficacy and to reduce their adverse effects. These efforts include the development of nanomedicines as they can selectively penetrate through tumor blood vessels through the enhanced permeability and retention (EPR) effect. The EPR effect was first proposed by Maeda and co-workers in 1986, and since then various types of nanoparticles have been developed to take advantage of the phenomenon with regards to drug delivery. However, the EPR effect has been found to be highly variable and thus unreliable due to the complex tumor microenvironment. Various physical and pharmacological strategies have been explored to overcome this challenge. Here, we review key advances and emerging concepts of such EPR-enhancing strategies. Furthermore, we analyze 723 clinical trials of nanoparticles with EPR enhancers and discuss their clinical translation.
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Inhibitory effects of angiotensin-converting enzyme mediate release of bradykinins through kinin receptors.
“The inhibitory effects of this enzyme mediate the release of bradykinins, a major player of KKS through kinin receptors [106].”
From Approaches to Improve EPR-Based Drug Delivery for Cancer Therapy and Diagnosis (2023) · cites this paper as [106]
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References 264 · Cited by 330
- Authors
- Ikeda-Imafuku, M., Wang, L. L.-W., Rodrigues, D., Shaha, S., Zhao, Z., & Mitragotri, S.
- Affiliations
- Harvard University (US)
- University of Illinois Chicago (US)
- Corresponding author
- Zhao, Zongmin
- Mitragotri, Samir
- Venue
- Journal of Controlled Release
- Publisher
- Elsevier BV
- Published
- 2022-05
- Volume
- 345
- Pages
- 512-536
- ISSN
- 0168-3659 (ISSN-L)
- OpenAlex
- W4220660335
- Cited by
- 330
- References
- 264
- Citations by year
- 2026: 72 · 2025: 106 · 2024: 90 · 2023: 50 · 2022: 12
- FWCI
- 16.06
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- Journal of Controlled Release (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
- Health Sciences › Medicine › Oncology › Drug Transport and Resistance Mechanisms
- Physical Sciences › Engineering › Biomedical Engineering › Nanoplatforms for cancer theranostics
- Keywords
- enhanced permeability and retention effect, tumor vasculature, tumor microenvironment, nanoparticle drug delivery, nanomedicine, targeted drug delivery, anticancer drug delivery, clinical translation
- MeSH terms
- Antineoplastic Agents, Humans, Neoplasms, Permeability, Drug Delivery Systems, Nanomedicine, Nanoparticles, Tumor Microenvironment
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