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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.
Affiliation
  • Zhu GH; Department of Chemical Engineering and Biotechnology, University of Cambridge, Cambridge CB3 0AS, United Kingdom.
  • Azharuddin M; Department of Biomedical and Clinical Sciences (BKV), Linkoping University, Linköping 58183, Sweden.
  • Pramanik B; Department of Chemistry, Ben Gurion University of the Negev, Be'er Sheva 84105, Israel.
  • Roberg K; Department of Biomedical and Clinical Sciences (BKV), Linkoping University, Linköping 58183, Sweden.
  • Biswas SK; Department of Otorhinolaryngology in Linköping, Anaesthetics, Operations and Specialty Surgery Center, Linköping University Hospital, Region Östergötland, Linköping 58185, Sweden.
  • D'arcy P; AIMP Laboratories, C86 Baishnabghata, Patuli Township, Kolkata 700094, India.
  • Lu M; Department of Biomedical and Clinical Sciences (BKV), Linkoping University, Linköping 58183, Sweden.
  • Kaur A; Department of Chemical Engineering and Biotechnology, University of Cambridge, Cambridge CB3 0AS, United Kingdom.
  • Chen A; Department of Chemical Engineering, Imperial College London, South Kensington Campus, London SW7 2AZ, United Kingdom.
  • Dhara AK; Department of Chemical Engineering and Biotechnology, University of Cambridge, Cambridge CB3 0AS, United Kingdom.
  • Chivu A; Department of Electrical Engineering, National Institute of Technology Durgapur, Durgapur 713209, West Bengal, India.
  • Zhuang Y; Department of Surgical Biotechnology, Division of Surgery and Interventional Science, University College London, London NW3 2PF, United Kingdom.
  • Baker A; Department of Chemical Engineering and Biotechnology, University of Cambridge, Cambridge CB3 0AS, United Kingdom.
  • Liu X; Department of Chemical Engineering and Biotechnology, University of Cambridge, Cambridge CB3 0AS, United Kingdom.
  • Fairen-Jimenez D; Department of Chemical Engineering and Biotechnology, University of Cambridge, Cambridge CB3 0AS, United Kingdom.
  • Mazumder B; Department of Chemical Engineering and Biotechnology, University of Cambridge, Cambridge CB3 0AS, United Kingdom.
  • Chen R; Department of Chemical Engineering and Biotechnology, University of Cambridge, Cambridge CB3 0AS, United Kingdom.
  • Kaminski CF; Department of Chemical Engineering, Imperial College London, South Kensington Campus, London SW7 2AZ, United Kingdom.
  • Kaminski Schierle GS; Department of Chemical Engineering and Biotechnology, University of Cambridge, Cambridge CB3 0AS, United Kingdom.
  • Hinkula J; Department of Chemical Engineering and Biotechnology, University of Cambridge, Cambridge CB3 0AS, United Kingdom.
  • Slater NKH; Department of Biomedical and Clinical Sciences (BKV), Linkoping University, Linköping 58183, Sweden.
  • Patra HK; Department of Chemical Engineering and Biotechnology, University of Cambridge, Cambridge CB3 0AS, United Kingdom.
ACS Appl Mater Interfaces ; 15(14): 17485-17494, 2023 Apr 12.
Article in En | MEDLINE | ID: mdl-36976817
ABSTRACT
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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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Nanostructures / Nanoparticles / Neoplasms Limits: Humans Language: En Journal: ACS Appl Mater Interfaces Journal subject: BIOTECNOLOGIA / ENGENHARIA BIOMEDICA Year: 2023 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Nanostructures / Nanoparticles / Neoplasms Limits: Humans Language: En Journal: ACS Appl Mater Interfaces Journal subject: BIOTECNOLOGIA / ENGENHARIA BIOMEDICA Year: 2023 Document type: Article Affiliation country: