Tumor-selective delivery of macromolecular drugs via the EPR effect: background and future prospects.
By H. Maeda. Bioconjugate chemistry, 2010
979 citations recorded by the source corpus.
Subfields: Biomedical Engineering, Molecular Biology, Physiology
View Paper: https://www.semanticscholar.org/paper/4955111f08636c2de0d99c087d63c17d2f3a05a9
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Biomedical Engineering
In Molecular Biology
- Anil Sood
- Gabriel Lopez-Berestein
- Peter L. Choyke
- O. Farokhzad
- Hisataka Kobayashi
- W. Choi
- Linlin Wang
- George A. Calin
In Physiology
Citations in the corpus
- Improving Conventional Enhanced Permeability and Retention (EPR) Effects; What Is the Appropriate Target? (2013, background): “(12) Most nano-sized agents accumulate within tumors due to the EPR effect and then release their therapeutic payloads.”
- Insight into nanoparticle cellular uptake and intracellular targeting (2014, positive): “The groundbreaking discovery of the EPR effect [13,14] associated with the tumor because of the abnormal and leaky microvasculature has emerged as the foundation for the passively targeted first generation of nanomedicines preferentially accumulating in tumor tissue [15, 16].”
- RNA interference in the clinic: challenges and future directions (2010, background): “Another important factor for increased capillary leak is the enhanced permeability and retention (EPR) effect, which can be exploited and enhanced for improved nanoparticle deliver”