Reprint

EPR Effect-Based Tumor Targeted Nanomedicine

Edited by
October 2022
290 pages
  • ISBN978-3-0365-5428-0 (Hardback)
  • ISBN978-3-0365-5427-3 (PDF)

This is a Reprint of the Special Issue EPR Effect-Based Tumor Targeted Nanomedicine that was published in

Medicine & Pharmacology
Public Health & Healthcare
Summary

I am honored to undertake the work for Guest Editor for this Special Issue of EPR Effect-Based Tumor Targeted Nanomedicine for the Journal of Personalized Medicine. It has already been 35 years since we published the concept of the EPR effect for the first time. The discovery of the new concept of EPR effect gave an impetus effect of growth momentum in nanomedicine, and numerous works are focused on tumor delivery, although the initial idea was based on vascular permeability in infection-induced inflamed tissue, where we discovered bradykinin in the key mediator of vascular permeability.I know, however, there are pros and cons to EPR effect. Cons stem either from a poor understanding of EPR effect, or somehow a biased view of the EPR effect, or from the tumor models being used, particularly in the clinical settings where vascular blood flow is so frequently obstructed. I hope scientists in the clinic, or basic researchers working on the tumor drug delivery, will join the forum of this Special Issue and express their data and opinions.The scope of this issue includes an in-depth understanding of the EPR effect, and issues associated with tumor microenvironment and also further exploitation of EPR effect in human cancer. In addition, new strategies for enhancement of the EPR effect using nanomedicine will be welcome, which is as important as the EPR effect itself. These papers cover not only cancer therapy, but also imaging techniques using nanofluorescent agents, including photodynamic therapy for inflammation, and boron neutron capture therapy.

Format
  • Hardback
License and Copyright
© 2022 by the authors; CC BY-NC-ND license
Keywords
extracellular matrix; drug delivery; tumor; cancer; targeting; cancer; reactive oxygen species; antioxidant; self-assembling drug; HPMA copolymers; EPR effect; drug delivery; controlled release; nanomedicines; nanoparticles; tumor vascular regulation; EPR effect; angiogenesis; blood perfusion; vascular permeability; EPR effect; tumor targeting; photodynamic; hyaluronan; zinc protoporphyrin; EPR effect; enhanced permeability and retention effect; nanomedicines; cancer therapy; drug delivery; nanotechnology; tumor-selective drug delivery; photodynamic therapy; boron neutron capture therapy; isosorbide dinitrate; sildenafil citrate; EPR effect; EPR-effect enhancers; heterogeneity of the EPR effect; nitric oxide donors; tumor blood flow; TNBC; dasatinib; poly(styrene-co-maleic acid) micelles; nanoformulation; metabolism; EPR; nanomedicine; targeted therapy; solid cancer; microenvironment; hypoxia; cancer therapy; DDS; anaerobic bacteria; Bifidobacterium; bacterial therapy; iDPS; EPR; EPR-based therapy; passive targeting; heterogeneity; solid-tumor; EPR-imaging techniques; sildenafil; phosphodiesterase 5 inhibitors; drug repurposing; cancer; chemoadjuvant; EPR effect; nanomedicine; drug delivery; arterial infusion; canine cancer; particle beam therapy; proton beam therapy; carbon-ion beam therapy; boron neutron capture therapy; combination therapy; drug delivery; iNaD; siRNA; microRNA; calcium phosphate; PEG blending; cancer treatment; n/a

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