TY - JOUR
T1 - Formation and purification of tailored liposomes for drug delivery using a module-based micro continuous-flow system
AU - Dimov, Nikolay
AU - Kastner, Elisabeth
AU - Hussain, Maryam Tabassum
AU - Perrie, Yvonne
AU - Szita, Nicolas
PY - 2017/12/1
Y1 - 2017/12/1
N2 - Liposomes are lipid based bilayer vesicles that can encapsulate, deliver and release low-soluble drugs and small molecules to a specific target site in the body and they are currently exploited in several nanomedicine formulations. However, their development and application is still limited by expensive and time-consuming process development and production methods. Therefore, to exploit these systems more effectively and support the rapid translation of new liposomal nanomedicines from bench to bedside, new cost-effective and scalable production methods are much needed. Here we present a continuous process flow system for the preparation, modification and purification of liposomes which offers lab-on-chip scale production. The system was evaluated for a range of small vesicles (below 300 nm) varying in lipid composition, size and charge. This system offers effective and rapid nanomedicine purification with high lipid recovery (>98%) combined with effective removal of non-entrapped drug (propofol >95% reduction of non-entrapped drug present) or protein (ovalbumin >90% reduction of OVA present) and organic solvent (ethanol >95% reduction) in less than 4 minutes. Within this manuscript, we outline a new set-up that offer the key advantages of using this bench-top, rapid, process development tool are the flexible operating conditions, interchangeable membranes and scalable high-throughput yields, thereby offering simultaneous manufacturing and purification of nanoparticles with tailored surface attributes.
AB - Liposomes are lipid based bilayer vesicles that can encapsulate, deliver and release low-soluble drugs and small molecules to a specific target site in the body and they are currently exploited in several nanomedicine formulations. However, their development and application is still limited by expensive and time-consuming process development and production methods. Therefore, to exploit these systems more effectively and support the rapid translation of new liposomal nanomedicines from bench to bedside, new cost-effective and scalable production methods are much needed. Here we present a continuous process flow system for the preparation, modification and purification of liposomes which offers lab-on-chip scale production. The system was evaluated for a range of small vesicles (below 300 nm) varying in lipid composition, size and charge. This system offers effective and rapid nanomedicine purification with high lipid recovery (>98%) combined with effective removal of non-entrapped drug (propofol >95% reduction of non-entrapped drug present) or protein (ovalbumin >90% reduction of OVA present) and organic solvent (ethanol >95% reduction) in less than 4 minutes. Within this manuscript, we outline a new set-up that offer the key advantages of using this bench-top, rapid, process development tool are the flexible operating conditions, interchangeable membranes and scalable high-throughput yields, thereby offering simultaneous manufacturing and purification of nanoparticles with tailored surface attributes.
KW - liposomes
KW - microfluidics
KW - continuous-flow
KW - drug delivery
UR - http://www.scopus.com/inward/record.url?scp=85029832199&partnerID=8YFLogxK
U2 - 10.1038/s41598-017-11533-1
DO - 10.1038/s41598-017-11533-1
M3 - Article
AN - SCOPUS:85029832199
SN - 2045-2322
VL - 7
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 12045
ER -