Article ; Online: High throughput microfluidics-based synthesis of PEGylated liposomes for precise size control and efficient drug encapsulation.
Colloids and surfaces. B, Biointerfaces
2024 Volume 238, Page(s) 113926
Abstract: The low scalability and reproducibility of existing synthesis methods have hindered the translation of liposome nanoparticles as carriers for targeted drug delivery from conventional laboratory techniques to mass production. To this end, in this study, ... ...
| Abstract | The low scalability and reproducibility of existing synthesis methods have hindered the translation of liposome nanoparticles as carriers for targeted drug delivery from conventional laboratory techniques to mass production. To this end, in this study, we present a high-throughput microfluidics-based approach for the synthesis of PEGylated liposomes with a primary focus on achieving precise size control and efficient encapsulation of hydrophobic drug molecules. In this platform, liposomes were self-assembled through a controllable mixing of lipids (EYPC, cholesterol, and DSPE-PEG 2000) dissolved in ethanol and an aqueous solution. The key parameters, including the chip design, total flow rate, flow rate ratio, lipid concentrations, as well as variations in buffer (HEPES and NaCl) and solvent composition (commercial and reagent-grade ethanol) were explored in detail. Through comprehensive parametric studies, we gained valuable insights into the influence of these variables on the size distribution of liposomes and succeeded in producing highly reproducible liposomes ranging from approximately 60 nm (corresponding to small unilamellar vesicles) to 150 nm (representing large unilamellar vesicles), all while maintaining a polydispersity index (PDI) of less than 0.2. To assess the encapsulation efficiency of hydrophobic drug molecules, Nile red (NR) was employed as a surrogate. We meticulously examined the impact of NR concentration on the drug encapsulation process, resulting in up to 74% drug encapsulation efficiency within the PEGylated liposomes. This research offers crucial advances in liposome synthesis and drug delivery, providing a high-throughput, controllable method for PEGylated liposomes with potential in pharmaceutical and biomedical fields. |
|---|---|
| Language | English |
| Publishing date | 2024-04-22 |
| Publishing country | Netherlands |
| Document type | Journal Article |
| ZDB-ID | 1500523-9 |
| ISSN | 1873-4367 ; 0927-7765 |
| ISSN (online) | 1873-4367 |
| ISSN | 0927-7765 |
| DOI | 10.1016/j.colsurfb.2024.113926 |
| Database | MEDical Literature Analysis and Retrieval System OnLINE |
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