Microfluidic generation of therapeutically relevant polycaprolactone (PCL) microparticles: computational and experimental approaches
| dc.contributor.author | Forigua, Alejandro | |
| dc.contributor.author | Dalili, Arash | |
| dc.contributor.author | Kirsch, Rebecca | |
| dc.contributor.author | Willerth, Stephanie M. | |
| dc.contributor.author | Elvira, Katherine S. | |
| dc.date.accessioned | 2024-11-04T19:11:07Z | |
| dc.date.available | 2024-11-04T19:11:07Z | |
| dc.date.issued | 2022 | |
| dc.description.abstract | Drug releasing microparticles play an important role in drug delivery as they can be used for site specific delivery as well as control over the release time of therapeutics. The use of microfluidic technologies for the fabrication of these particles is of increasing interest since they provide enhanced control over microparticle size and size distribution compared to bulk production methods. However, the use of microfluidic platforms in the production of drug releasing microparticles with therapeutically relevant cargo still requires optimization depending on their application, and the effect of the addition of cargo on the production process is still unexplored. Here we show the formation of therapeutically relevant (in terms of size and dose of cargo) polycaprolactone (PCL) microparticles using a microfluidic platform and analyze the effect of the addition of cargo in the microparticle size and size distribution. This microfluidic platform was designed with the aid of computational fluid dynamic simulations, allowing us to construct a polydimethylsiloxane (PDMS) microfluidic device capable of making microparticles in the range of 15 to 35 μm with low coefficient of variation (CV) both with and without cargo by varying the flow rate ratios of the phases used during droplet generation. Our data show the effect of the addition of cargo on the droplet and microparticle sizes and monodispersity. Our fabrication method allows the formation of spherical microparticles, optimal for biomedical applications. In addition, our microfluidic platform can maintain the generation of monodisperse droplets (with an average size of 52.5 μm) over extended periods of time, suggesting it has the capacity to be used for scaled-up production of PCL microparticles. This microfluidic device is a robust and reliable method for the fabrication of PCL microparticles with cargo, which can potentially be loaded with other relevant therapeutic molecules for biomedical applications. | |
| dc.description.reviewstatus | Reviewed | |
| dc.description.scholarlevel | Faculty | |
| dc.description.sponsorship | Dr. Willerth receives funding from the Canada Research Chairs program and the Canadian Institutes for Health Research. Dr. Elvira receives funding from the Canada Research Chairs program and the Michael Smith Foundation for Health Research Scholar program in partnership with the Pacific Alzheimer Research Foundation. This research was partially funded by using Innovate BC’s Ignite program. | |
| dc.identifier.citation | Forigua, A., Dalili, A., Kirsch, R., Willerth, S. M., & Elvira, K. S. (2022). Microfluidic generation of therapeutically relevant polycaprolactone (PCL) microparticles: computational and experimental approaches. ACS Applied Polymer Materials, 4(10), 7004–7013. https://doi.org/10.1021/acsapm.2c00943 | |
| dc.identifier.uri | https://doi.org/10.1021/acsapm.2c00943 | |
| dc.identifier.uri | https://hdl.handle.net/1828/20728 | |
| dc.language.iso | en | |
| dc.publisher | ACS Applied Polymer Materials | |
| dc.subject | Centre for Advanced Materials and Related Technology (CAMTEC) | |
| dc.subject.department | Department of Chemistry | |
| dc.subject.department | Department of Mechanical Engineering | |
| dc.subject.department | Division of Medical Sciences | |
| dc.subject.department | School of Medical Sciences | |
| dc.title | Microfluidic generation of therapeutically relevant polycaprolactone (PCL) microparticles: computational and experimental approaches | |
| dc.type | Postprint |