Microfluidic-assisted nanoprecipitation of (PEGylated) poly (D,L-lactic acid-co-caprolactone): Effect of macromolecular and microfluidic parameters on particle size and paclitaxel encapsulation

التفاصيل البيبلوغرافية
العنوان: Microfluidic-assisted nanoprecipitation of (PEGylated) poly (D,L-lactic acid-co-caprolactone): Effect of macromolecular and microfluidic parameters on particle size and paclitaxel encapsulation
المؤلفون: Kevin Treacher, Katie Barker, Marianne Ashford, Enrique Lallana, Roberto Donno, Nicola Tirelli, Davide Magrì, M. Jayne Lawrence, Zahid Nazir
المصدر: Lallana-Ozores, E, Donno, R, Magri, D, Barker, K, Nazir, Z, Treacher, K, Lawrence, M, Ashford, M & Tirelli, N 2018, ' Microfluidic-assisted nanoprecipitation of (PEGylated) poly (D,L-lactic acid-co-caprolactone): Effect of macromolecular and microfluidic parameters on particle size and paclitaxel encapsulation ', International Journal of Pharmaceutics, vol. 548, no. 1, pp. 530-539 . https://doi.org/10.1016/j.ijpharm.2018.07.031
سنة النشر: 2018
مصطلحات موضوعية: Materials science, Paclitaxel, Drug Compounding, Polyesters, Microfluidics, Pharmaceutical Science, Micromixer, Nanoparticle, 02 engineering and technology, 010402 general chemistry, 01 natural sciences, Polyethylene Glycols, chemistry.chemical_compound, Copolymer, Chemical Precipitation, Particle Size, chemistry.chemical_classification, Polymer, 021001 nanoscience & nanotechnology, Antineoplastic Agents, Phytogenic, 0104 chemical sciences, Polyester, chemistry, Chemical engineering, Polymerization, Nanoparticles, Particle size, 0210 nano-technology, Caprolactone
الوصف: In this work we evaluate the effect of polymer composition and architecture of (PEGylated) polyesters on particle size and paclitaxel (PTX) loading for particles manufactured via microfluidic-assisted, continuous-flow nanoprecipitation using two microfluidic chips with different geometries and mixing principles. We have prepared poly ( d , l -lactic acid-co-caprolactone) (PLCL) from ring-opening polymerization (ROP) of LA and CL mixtures and different (macro) initiators (namely, 1-dodecanol, a MeO-PEG-OH, and a 4-armed star PEG-OH), rendering polyesters that vary in monomer composition (i.e. LA/CL ratios) and architecture (i.e. linear vs 4-armed star). Continuous-flow nanoprecipitation was assayed using two microfluidic chips: a cross-flow chip with a X-shaped mixing junction (2D laminar flow focusing) and a micromixer featuring a Y-shaped mixing junction and a split and recombine path (2D laminar flow focusing convinced with stream lamination for faster mixing). Nanoparticle formulations were produced with Z-average sizes in the range of 30–160 nm, although size selectivity could be seen for different polymer/chip combinations; for instance, smaller particles were obtained with Y-shaped micromixer (30–120 nm), specially for the PEGylated polyesters (30–50 nm), whereas the cross-flow chip systematically produced larger particles (80–160 nm). Loading of the anti-cancer drug paclitaxel (PTX) was also heavily influenced not only by the nature of the polyester, but also by the geometry of the microfluidic chip; higher drug loadings were obtained with the cross-flow reactor and the star block copolymers. Finally, decreasing the LA/CL ratio generally had a positive effect on drug loading.
وصف الملف: application/vnd.openxmlformats-officedocument.wordprocessingml.document
اللغة: English
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2d7a33e0ed9ade37a40cae67c49cccb
https://doi.org/10.1016/j.ijpharm.2018.07.031
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....e2d7a33e0ed9ade37a40cae67c49cccb
قاعدة البيانات: OpenAIRE