2015
DOI: 10.1038/nprot.2015.054
|View full text |Cite
|
Sign up to set email alerts
|

Construction of a liposome dialyzer for the preparation of high-value, small-volume liposome formulations

Abstract: The liposome dialyzer is a small-volume equilibrium dialysis device, built from commercially available materials, that is designed for rapid exchange of small volumes of an extraliposomal reagent pool against a liposome preparation. The dialyzer is prepared by modification of commercially available dialysis cartridges and consists of a reactor with two 300 µL chambers and a 1.56 cm 2 dialysis surface area. The dialyzer is prepared in three stages: 1) disassembly of dialysis cartridges to obtain required parts;… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
9
0

Year Published

2017
2017
2024
2024

Publication Types

Select...
10

Relationship

1
9

Authors

Journals

citations
Cited by 15 publications
(9 citation statements)
references
References 22 publications
0
9
0
Order By: Relevance
“…A large volume of O-solution is required, and the required long time (hours) restricts this purification method to those solutes that are not massively released from GVs in the allotted time, otherwise the intravesicle solute concentration would also decrease. Recently, the use of home-modified small-volume commercial dialysis cassettes for exchanging the solution outside vesicles has been reported [ 26 ]. This method is particularly useful when high-cost solutions must be exchanged with vesicle suspensions.…”
Section: Discussionmentioning
confidence: 99%
“…A large volume of O-solution is required, and the required long time (hours) restricts this purification method to those solutes that are not massively released from GVs in the allotted time, otherwise the intravesicle solute concentration would also decrease. Recently, the use of home-modified small-volume commercial dialysis cassettes for exchanging the solution outside vesicles has been reported [ 26 ]. This method is particularly useful when high-cost solutions must be exchanged with vesicle suspensions.…”
Section: Discussionmentioning
confidence: 99%
“…Liposomes are lipid bi-layer with outer hydrophobic and center hydrophilic compartments (Adamala et al, 2015). These nano-sized active molecules entangled between the hydrophobic membrane and hydrophilic position (Fig.…”
Section: Nanoparticles Formulationmentioning
confidence: 99%
“…Start the timer and keep the reaction sample tumbling all the time. (Optional) For continuous fresh monomer feeding, transfer 300 µL of reaction solution to one chamber of a lab constructed small-volume liposome dialyzer 11 and put 300 µL feeding solution in the other chamber. The feeding solution should contain all the ingredients at the same concentration as in the reaction solution, except for replacing RNA containing vesicles with empty vesicles.…”
Section: Protocolmentioning
confidence: 99%