TY - JOUR
T1 - Mechanisms and Barriers in Nanomedicine
T2 - Progress in the Field and Future Directions
AU - Anchordoquy, Thomas
AU - Artzi, Natalie
AU - Balyasnikova, Irina V.
AU - Barenholz, Yechezkel
AU - La-Beck, Ninh M.
AU - Brenner, Jacob S.
AU - Chan, Warren C.W.
AU - Decuzzi, Paolo
AU - Exner, Agata A.
AU - Gabizon, Alberto
AU - Godin, Biana
AU - Lai, Samuel K.
AU - Lammers, Twan
AU - Mitchell, Michael J.
AU - Moghimi, S. Moein
AU - Muzykantov, Vladimir R.
AU - Peer, Dan
AU - Nguyen, Juliane
AU - Popovtzer, Rachela
AU - Ricco, Madison
AU - Serkova, Natalie J.
AU - Singh, Ravi
AU - Schroeder, Avi
AU - Schwendeman, Anna A.
AU - Straehla, Joelle P.
AU - Teesalu, Tambet
AU - Tilden, Scott
AU - Simberg, Dmitri
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/6/4
Y1 - 2024/6/4
N2 - In recent years, steady progress has been made in synthesizing and characterizing engineered nanoparticles, resulting in several approved drugs and multiple promising candidates in clinical trials. Regulatory agencies such as the Food and Drug Administration and the European Medicines Agency released important guidance documents facilitating nanoparticle-based drug product development, particularly in the context of liposomes and lipid-based carriers. Even with the progress achieved, it is clear that many barriers must still be overcome to accelerate translation into the clinic. At the recent conference workshop “Mechanisms and Barriers in Nanomedicine” in May 2023 in Colorado, U.S.A., leading experts discussed the formulation, physiological, immunological, regulatory, clinical, and educational barriers. This position paper invites open, unrestricted, nonproprietary discussion among senior faculty, young investigators, and students to trigger ideas and concepts to move the field forward.
AB - In recent years, steady progress has been made in synthesizing and characterizing engineered nanoparticles, resulting in several approved drugs and multiple promising candidates in clinical trials. Regulatory agencies such as the Food and Drug Administration and the European Medicines Agency released important guidance documents facilitating nanoparticle-based drug product development, particularly in the context of liposomes and lipid-based carriers. Even with the progress achieved, it is clear that many barriers must still be overcome to accelerate translation into the clinic. At the recent conference workshop “Mechanisms and Barriers in Nanomedicine” in May 2023 in Colorado, U.S.A., leading experts discussed the formulation, physiological, immunological, regulatory, clinical, and educational barriers. This position paper invites open, unrestricted, nonproprietary discussion among senior faculty, young investigators, and students to trigger ideas and concepts to move the field forward.
KW - barriers
KW - complement
KW - delivery
KW - formulation
KW - inflammation
KW - mRNA
KW - nanomedicine
KW - translation
KW - tumor
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U2 - 10.1021/acsnano.4c00182
DO - 10.1021/acsnano.4c00182
M3 - Review article
C2 - 38767983
AN - SCOPUS:85194029254
SN - 1936-0851
VL - 18
SP - 13983
EP - 13999
JO - ACS Nano
JF - ACS Nano
IS - 22
ER -