TY - JOUR
T1 - High‐Throughput Miniaturized Screening of Nanoparticle Formation via Inkjet Printing
AU - Styliari, Ioanna Danai
AU - Conte, Claudia
AU - Pearce, Amanda
AU - Huesler, Amanda
AU - Cavanagh, Robert
AU - Limo, Marion
AU - Gordhan, Dipak
AU - Nieto-Orellana, Alejandro
AU - Suksiriworapong, Jiraphong
AU - Couturaud, Benoit
AU - Williams, Phil
AU - Hook, Andrew
AU - Alexander, Morgan R.
AU - Garnett, Martin
AU - Alexander, Cameron
AU - Burley, Jonathan
AU - Taresco, Vincenzo
N1 - This is the peer reviewed version of the following article:Ioanna D. Styliari, et al, ‘High‐Throughput Miniaturized Screening of Nanoparticle Formation via Inkjet Printing’, Macromolecular Materials and Engineering, (2018), which has been published in final form at https://doi.org/10.1002/mame.201800146.
Under embargo until 27 May 2019.
This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.
PY - 2018/8/1
Y1 - 2018/8/1
N2 - The self‐assembly of specific polymers into well‐defined nanoparticles (NPs) is of great interest to the pharmaceutical industry as the resultant materials can act as drug delivery vehicles. In this work, a high‐throughput method to screen the ability of polymers to self‐assemble into NPs using a picoliter inkjet printer is presented. By dispensing polymer solutions in dimethyl sulfoxide (DMSO) from the printer into the wells of a 96‐well plate, containing water as an antisolvent, 50 suspensions are screened for nanoparticle formation rapidly using only nanoliters to microliters. A variety of polymer classes are used and in situ characterization of the submicroliter nanosuspensions shows that the particle size distributions match those of nanoparticles made from bulk suspensions. Dispensing organic polymer solutions into well plates via the printer is thus shown to be a reproducible and fast method for screening nanoparticle formation which uses two to three orders of magnitude less material than conventional techniques. Finally, a pilot study for a high‐throughput pipeline of nanoparticle production, physical property characterization, and cytocompatibility demonstrates the feasibility of the printing approach for screening of nanodrug delivery formulations. Nanoparticles are produced in the well plates, characterized for size and evaluated for effects on metabolic activity of lung cancer cells.
AB - The self‐assembly of specific polymers into well‐defined nanoparticles (NPs) is of great interest to the pharmaceutical industry as the resultant materials can act as drug delivery vehicles. In this work, a high‐throughput method to screen the ability of polymers to self‐assemble into NPs using a picoliter inkjet printer is presented. By dispensing polymer solutions in dimethyl sulfoxide (DMSO) from the printer into the wells of a 96‐well plate, containing water as an antisolvent, 50 suspensions are screened for nanoparticle formation rapidly using only nanoliters to microliters. A variety of polymer classes are used and in situ characterization of the submicroliter nanosuspensions shows that the particle size distributions match those of nanoparticles made from bulk suspensions. Dispensing organic polymer solutions into well plates via the printer is thus shown to be a reproducible and fast method for screening nanoparticle formation which uses two to three orders of magnitude less material than conventional techniques. Finally, a pilot study for a high‐throughput pipeline of nanoparticle production, physical property characterization, and cytocompatibility demonstrates the feasibility of the printing approach for screening of nanodrug delivery formulations. Nanoparticles are produced in the well plates, characterized for size and evaluated for effects on metabolic activity of lung cancer cells.
KW - high-throughput-miniaturized screening
KW - inkjet printers
KW - nanoparticles
KW - self-assembling
UR - http://www.scopus.com/inward/record.url?scp=85047661012&partnerID=8YFLogxK
U2 - 10.1002/mame.201800146
DO - 10.1002/mame.201800146
M3 - Article
SN - 1438-7492
VL - 303
JO - Macromolecular Materials and Engineering
JF - Macromolecular Materials and Engineering
IS - 8
M1 - 1800146
ER -