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Feasibility of Coacervate-Like Nanostructure for Instant Drug Nanoformulation

[Image: see text] Despite the enormous advancements in nanomedicine research, a limited number of nanoformulations are available on the market, and few have been translated to clinics. An easily scalable, sustainable, and cost-effective manufacturing strategy and long-term stability for storage are...

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Autores principales: Zhu, Geyunjian H., Azharuddin, Mohammad, Pramanik, Bapan, Roberg, Karin, Biswas, Sujoy Kumar, D’arcy, Padraig, Lu, Meng, Kaur, Apanpreet, Chen, Alexander, Dhara, Ashis Kumar, Chivu, Alexandru, Zhuang, Yunhui, Baker, Andrew, Liu, Xiewen, Fairen-Jimenez, David, Mazumder, Bismoy, Chen, Rongjun, Kaminski, Clemens F., Kaminski Schierle, Gabriele S., Hinkula, Jorma, Slater, Nigel K. H., Patra, Hirak K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10103128/
https://www.ncbi.nlm.nih.gov/pubmed/36976817
http://dx.doi.org/10.1021/acsami.2c21586
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author Zhu, Geyunjian H.
Azharuddin, Mohammad
Pramanik, Bapan
Roberg, Karin
Biswas, Sujoy Kumar
D’arcy, Padraig
Lu, Meng
Kaur, Apanpreet
Chen, Alexander
Dhara, Ashis Kumar
Chivu, Alexandru
Zhuang, Yunhui
Baker, Andrew
Liu, Xiewen
Fairen-Jimenez, David
Mazumder, Bismoy
Chen, Rongjun
Kaminski, Clemens F.
Kaminski Schierle, Gabriele S.
Hinkula, Jorma
Slater, Nigel K. H.
Patra, Hirak K.
author_facet Zhu, Geyunjian H.
Azharuddin, Mohammad
Pramanik, Bapan
Roberg, Karin
Biswas, Sujoy Kumar
D’arcy, Padraig
Lu, Meng
Kaur, Apanpreet
Chen, Alexander
Dhara, Ashis Kumar
Chivu, Alexandru
Zhuang, Yunhui
Baker, Andrew
Liu, Xiewen
Fairen-Jimenez, David
Mazumder, Bismoy
Chen, Rongjun
Kaminski, Clemens F.
Kaminski Schierle, Gabriele S.
Hinkula, Jorma
Slater, Nigel K. H.
Patra, Hirak K.
author_sort Zhu, Geyunjian H.
collection PubMed
description [Image: see text] Despite the enormous advancements in nanomedicine research, a limited number of nanoformulations are available on the market, and few have been translated to clinics. An easily scalable, sustainable, and cost-effective manufacturing strategy and long-term stability for storage are crucial for successful translation. Here, we report a system and method to instantly formulate NF achieved with a nanoscale polyelectrolyte coacervate-like system, consisting of anionic pseudopeptide poly(l-lysine isophthalamide) derivatives, polyethylenimine, and doxorubicin (Dox) via simple “mix-and-go” addition of precursor solutions in seconds. The coacervate-like nanosystem shows enhanced intracellular delivery of Dox to patient-derived multidrug-resistant (MDR) cells in 3D tumor spheroids. The results demonstrate the feasibility of an instant drug formulation using a coacervate-like nanosystem. We envisage that this technique can be widely utilized in the nanomedicine field to bypass the special requirement of large-scale production and elongated shelf life of nanomaterials.
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spelling pubmed-101031282023-04-15 Feasibility of Coacervate-Like Nanostructure for Instant Drug Nanoformulation Zhu, Geyunjian H. Azharuddin, Mohammad Pramanik, Bapan Roberg, Karin Biswas, Sujoy Kumar D’arcy, Padraig Lu, Meng Kaur, Apanpreet Chen, Alexander Dhara, Ashis Kumar Chivu, Alexandru Zhuang, Yunhui Baker, Andrew Liu, Xiewen Fairen-Jimenez, David Mazumder, Bismoy Chen, Rongjun Kaminski, Clemens F. Kaminski Schierle, Gabriele S. Hinkula, Jorma Slater, Nigel K. H. Patra, Hirak K. ACS Appl Mater Interfaces [Image: see text] Despite the enormous advancements in nanomedicine research, a limited number of nanoformulations are available on the market, and few have been translated to clinics. An easily scalable, sustainable, and cost-effective manufacturing strategy and long-term stability for storage are crucial for successful translation. Here, we report a system and method to instantly formulate NF achieved with a nanoscale polyelectrolyte coacervate-like system, consisting of anionic pseudopeptide poly(l-lysine isophthalamide) derivatives, polyethylenimine, and doxorubicin (Dox) via simple “mix-and-go” addition of precursor solutions in seconds. The coacervate-like nanosystem shows enhanced intracellular delivery of Dox to patient-derived multidrug-resistant (MDR) cells in 3D tumor spheroids. The results demonstrate the feasibility of an instant drug formulation using a coacervate-like nanosystem. We envisage that this technique can be widely utilized in the nanomedicine field to bypass the special requirement of large-scale production and elongated shelf life of nanomaterials. American Chemical Society 2023-03-28 /pmc/articles/PMC10103128/ /pubmed/36976817 http://dx.doi.org/10.1021/acsami.2c21586 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Zhu, Geyunjian H.
Azharuddin, Mohammad
Pramanik, Bapan
Roberg, Karin
Biswas, Sujoy Kumar
D’arcy, Padraig
Lu, Meng
Kaur, Apanpreet
Chen, Alexander
Dhara, Ashis Kumar
Chivu, Alexandru
Zhuang, Yunhui
Baker, Andrew
Liu, Xiewen
Fairen-Jimenez, David
Mazumder, Bismoy
Chen, Rongjun
Kaminski, Clemens F.
Kaminski Schierle, Gabriele S.
Hinkula, Jorma
Slater, Nigel K. H.
Patra, Hirak K.
Feasibility of Coacervate-Like Nanostructure for Instant Drug Nanoformulation
title Feasibility of Coacervate-Like Nanostructure for Instant Drug Nanoformulation
title_full Feasibility of Coacervate-Like Nanostructure for Instant Drug Nanoformulation
title_fullStr Feasibility of Coacervate-Like Nanostructure for Instant Drug Nanoformulation
title_full_unstemmed Feasibility of Coacervate-Like Nanostructure for Instant Drug Nanoformulation
title_short Feasibility of Coacervate-Like Nanostructure for Instant Drug Nanoformulation
title_sort feasibility of coacervate-like nanostructure for instant drug nanoformulation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10103128/
https://www.ncbi.nlm.nih.gov/pubmed/36976817
http://dx.doi.org/10.1021/acsami.2c21586
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