Mechanism of liposome formation by microfluidic mixing: the concept based on lipid bilayer fragments vesiculation
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15110%2F18%3A73591347" target="_blank" >RIV/61989592:15110/18:73591347 - isvavai.cz</a>
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Mechanism of liposome formation by microfluidic mixing: the concept based on lipid bilayer fragments vesiculation
Original language description
Liposomes are known for their biocompatible and encapsulation properties and are the most successful drug-carrier system approved by FDA. Recently new preparation technique based on nanofluidic mixing has been demonstrated a using microfluidic platform with characteristic mixing profile. The instrument NanoAssemblrTM (Precission Nanosystems, Canada) was used to prepare nanoliposomes containing metallochelating lipid 18:0 PE DTPA (Gd) to improve contrast in cryoTEM and resolve individual parts of membrane layers by cryoTEM. The size distribution was analyzed by DLS (Zetasizer Nano ZSP, Malvern Instruments, UK) and NTA (NanoSight NS500, Malvern Instruments, UK), liposomeswere (114±0.3) nm in diameter with low polydispersity 0.04±0.02. By NMR (Bruker-BioSpec 94/30 USR, Bruker, GE) measurement, the use of our Gd-liposomes as theranostic has been proven. Relaxivity was much higher, around 40 mM−1·s−1 compared to common contrast agent for MRI. Using ICP-OES (ULTIMA 2, Horiba Jobin Yvon, FR) analytical measurement, the precise concentration of gadolinium was terminated to (9.30±1.49) mg·l−1. This concentration is suitable for potential in vivoexperiments. Liposomes can be usedas targeted diagnostic agents and will contain encapsulated APIs for therapeutic use. An important observation was the detection of lipid membrane fragments in liposomes. This work also experimentally describes the concept of liposome formulation from a lipid bilayer fragments. This new concept of was proven by modern analytical methods including cryotransmission electron microscopy technique,which allows us to observe single liposomes containing fragment and also double liposomes prior to conversion.
Czech name
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Czech description
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Classification
Type
D - Article in proceedings
CEP classification
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OECD FORD branch
10610 - Biophysics
Result continuities
Project
<a href="/en/project/NV15-32198A" target="_blank" >NV15-32198A: Construction of recombinant mimotopes for induction of neutralizing antibodies against HIV-1 gp120 glycoprotein using high-affinity binders approach</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2018
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Article name in the collection
11th International Conference Drug Delivery Systems Nanotechnology for Healthcare: Progress in Recombinant Vaccines, Molecular Adjuvants, Modern Drug Delivery Systems and Cell Therapy
ISBN
978-80-907074-6-7
ISSN
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e-ISSN
neuvedeno
Number of pages
9
Pages from-to
89-97
Publisher name
nakladatelství Machovský
Place of publication
Olomouc
Event location
Telč
Event date
Jun 5, 2018
Type of event by nationality
WRD - Celosvětová akce
UT code for WoS article
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