TY - JOUR
T1 - Lyophilisation and sterilisation of liposomal vaccines to produce stable and sterile products
AU - Mohammed, Afzal-Ur-Rahman
AU - Bramwell, Vincent W.
AU - Coombes, Allan G.A.
AU - Perrie, Yvonne
PY - 2006/9
Y1 - 2006/9
N2 - The advantages of liposomes as delivery systems for peptide, protein and DNA vaccines is well-recognised, unfortunately their application has been stinted by their instability during storage and their limited shelf-life. Further, sterilisation of these systems has been problematic, with degradation of the liposomes being reported after sterilisation using the various techniques available. Work form our laboratory has investigated techniques that can be applied to particulate liposomal vaccines such that they can be prepared in a freeze-dried and sterile format. In this article, we describe techniques for the lyophilisation, cryoprotection and sterilisation of liposomal vaccines. Applying these methods allows for the retention of both the chemical integrity of the lipids and the key physico-chemical characteristics of the liposomes (e.g., particle size, zeta potential, and dynamic viscosity), thus supporting the enhanced transition of liposomal vaccines from the bench to the clinic. © 2006 Elsevier Inc. All rights reserved.
AB - The advantages of liposomes as delivery systems for peptide, protein and DNA vaccines is well-recognised, unfortunately their application has been stinted by their instability during storage and their limited shelf-life. Further, sterilisation of these systems has been problematic, with degradation of the liposomes being reported after sterilisation using the various techniques available. Work form our laboratory has investigated techniques that can be applied to particulate liposomal vaccines such that they can be prepared in a freeze-dried and sterile format. In this article, we describe techniques for the lyophilisation, cryoprotection and sterilisation of liposomal vaccines. Applying these methods allows for the retention of both the chemical integrity of the lipids and the key physico-chemical characteristics of the liposomes (e.g., particle size, zeta potential, and dynamic viscosity), thus supporting the enhanced transition of liposomal vaccines from the bench to the clinic. © 2006 Elsevier Inc. All rights reserved.
KW - liposomes
KW - freeze-drying
KW - cyroprotectants
KW - lyophilisation
KW - gamma-irradiation
KW - ionizing radiation
KW - sterilisation
UR - http://www.scopus.com/inward/record.url?scp=33748796936&partnerID=8YFLogxK
UR - https://www.sciencedirect.com/science/article/pii/S1046202306001599?via%3Dihub
U2 - 10.1016/j.ymeth.2006.05.025
DO - 10.1016/j.ymeth.2006.05.025
M3 - Article
C2 - 16997711
SN - 1046-2023
VL - 40
SP - 30
EP - 38
JO - Methods
JF - Methods
IS - 1
ER -