4.7 Article

Microfluidic Generation of Therapeutically Relevant Polycaprolactone (PCL) Microparticles: Computational and Experimental Approaches

Journal

ACS APPLIED POLYMER MATERIALS
Volume 4, Issue 10, Pages 7004-7013

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsapm.2c00943

Keywords

microparticles; drug release; droplets; polycaprolactone; microfluidics

Funding

  1. Canada Research Chairs program
  2. Canadian Institutes for Health Research
  3. Michael Smith Foundation for Health Research Scholar program
  4. Pacific Alzheimer Research Foundation
  5. Innovate BC's Ignite program

Ask authors/readers for more resources

Drug releasing microparticles are important for precise drug delivery. Microfluidic technologies offer better control over microparticle size and distribution compared to bulk production methods. This study demonstrates the formation of polycaprolactone (PCL) microparticles with therapeutically relevant cargo using a microfluidic platform, and investigates the effect of cargo on microparticle size and distribution.
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 mu m 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 mu m) 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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available