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Chimeric liposomes decorated with P407: an alternative biomaterial for producing stealth nano-therapeutics.
Tsakiri, Maria; Peraki, Aikaterini; Chountoulesi, Maria; Demetzos, Costas.
  • Tsakiri M; Section of Pharmaceutical Technology, Department of Pharmacy, School of Health Sciences, National and Kapodistrian University of Athens, Athens, Greece.
  • Peraki A; Section of Pharmaceutical Technology, Department of Pharmacy, School of Health Sciences, National and Kapodistrian University of Athens, Athens, Greece.
  • Chountoulesi M; Section of Pharmaceutical Technology, Department of Pharmacy, School of Health Sciences, National and Kapodistrian University of Athens, Athens, Greece.
  • Demetzos C; Section of Pharmaceutical Technology, Department of Pharmacy, School of Health Sciences, National and Kapodistrian University of Athens, Athens, Greece.
J Liposome Res ; 32(1): 83-91, 2022 Mar.
Article in English | MEDLINE | ID: covidwho-1550450
ABSTRACT
The aim of the present study is the development and evaluation of the physicochemical properties of chimeric hydrogenated soya phosphatidylcholine (HSPC) and egg phosphatidylcholine (EggPC) liposomes with incorporated triblock copolymer Poloxamer P407 (P407). The physicochemical assay was held in water HPLC-grade and Foetal Bovine Serum (FBS), in order to determine whether these systems can be used as drug or antigen delivery nanosystems. Dynamic and electrophoretic light scattering (DLS/ELS) techniques were used for the measurement of the hydrodynamic diameter, the polydispersity index, and the ζ-potential of the prepared nanosystems. The incorporation of the P407 resulted in a size reduction of all systems. A decrease in the hydrodynamic diameter and polydispersity index were also found as a result of increasing the storage temperature from 4 °C to 25 °C, attributed to P407. The experiments that were carried out in FBS, showed that the addition of P407 improved systems stealth properties. Concluding, we propose P407 as a promising alternative to PEG in the development of lipid nanoparticles with optimized bio- and shelf-stability.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Nanoparticles / Liposomes Type of study: Experimental Studies Language: English Journal: J Liposome Res Journal subject: Biochemistry Year: 2022 Document Type: Article Affiliation country: 08982104.2021.1978486

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Nanoparticles / Liposomes Type of study: Experimental Studies Language: English Journal: J Liposome Res Journal subject: Biochemistry Year: 2022 Document Type: Article Affiliation country: 08982104.2021.1978486