TY - JOUR
T1 - Pilot-scale production of expansile nanoparticles
T2 - Practical methods for clinical scale-up
AU - Colby, Aaron H.
AU - Liu, Rong
AU - Doyle, Robert P.
AU - Merting, Alyssa
AU - Zhang, Heng
AU - Savage, Natasha
AU - Chu, Ngoc Quynh
AU - Hollister, Beth A.
AU - McCulloch, William
AU - Burdette, Joanna E.
AU - Pearce, Cedric J.
AU - Liu, Kebin
AU - Oberlies, Nicholas H.
AU - Colson, Yolonda L.
AU - Grinstaff, Mark W.
N1 - Funding Information:
The authors acknowledge funding support from the NIH Small Business Innovation Research (SBIR) Program, including: R43 CA189215, R43 CA213538, and R44 CA189215. The authors would also like to acknowledge additional funding sources, including: R01 CA227433, R01 CA232056, R43 CA250780 and the Thoracic Surgery Foundation (NQC). Lastly, the authors would like to thank Christopher Jones, Bauer LeSavage and Nicholas Hall for their work in piloting the LV1 studies.
Publisher Copyright:
© 2021 The Author(s)
PY - 2021/9/10
Y1 - 2021/9/10
N2 - One of the foremost challenges in translating nanoparticle technologies to the clinic is the requirement to produce materials on a large-scale. Scaling nanoparticle production methods is often non-trivial, and the success of these endeavors is frequently governed by whether or not an intermediate level of production, i.e., “pilot-scale” production, can be achieved. Pilot-scale production at the one-liter scale serves as a proof-of-concept that large-scale production will be possible. Here, we describe the pilot-scale production of the expansile nanoparticle (eNP) technology including verification of activity and efficacy following scaleup. We describe the challenges of sonication-based emulsification procedures and how these were overcome by use of a Microfluidizer technology. We also describe the problem-solving process that led to pre-polymerization of the nanoparticle polymer—a fundamental change from the lab-scale and previously published methods. Furthermore, we demonstrate good control over particle diameter, polydispersity and drug loading and the ability to sterilize the particles via filtration using this method. To facilitate long-term storage of these larger quantities of particles, we investigated six lyoprotectants and determined that sucrose is the most compatible with the current system. Lastly, we demonstrate that these changes to the manufacturing method do not adversely affect the swelling functionality of the particles, their highly specific localization to tumors, their non-toxicity in vivo or their efficacy in treating established intraperitoneal mesothelioma xenografts.
AB - One of the foremost challenges in translating nanoparticle technologies to the clinic is the requirement to produce materials on a large-scale. Scaling nanoparticle production methods is often non-trivial, and the success of these endeavors is frequently governed by whether or not an intermediate level of production, i.e., “pilot-scale” production, can be achieved. Pilot-scale production at the one-liter scale serves as a proof-of-concept that large-scale production will be possible. Here, we describe the pilot-scale production of the expansile nanoparticle (eNP) technology including verification of activity and efficacy following scaleup. We describe the challenges of sonication-based emulsification procedures and how these were overcome by use of a Microfluidizer technology. We also describe the problem-solving process that led to pre-polymerization of the nanoparticle polymer—a fundamental change from the lab-scale and previously published methods. Furthermore, we demonstrate good control over particle diameter, polydispersity and drug loading and the ability to sterilize the particles via filtration using this method. To facilitate long-term storage of these larger quantities of particles, we investigated six lyoprotectants and determined that sucrose is the most compatible with the current system. Lastly, we demonstrate that these changes to the manufacturing method do not adversely affect the swelling functionality of the particles, their highly specific localization to tumors, their non-toxicity in vivo or their efficacy in treating established intraperitoneal mesothelioma xenografts.
KW - Clinical translation
KW - Expansile nanoparticle
KW - Microfluidizer
KW - Pilot-scale production
KW - Scale-up
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U2 - 10.1016/j.jconrel.2021.07.012
DO - 10.1016/j.jconrel.2021.07.012
M3 - Article
C2 - 34280414
AN - SCOPUS:85110655953
SN - 0168-3659
VL - 337
SP - 144
EP - 154
JO - Journal of Controlled Release
JF - Journal of Controlled Release
ER -