Characterization of Liposome-based Nanomaterials

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Provided by European Commission, Joint Research Centre

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Dataset information

Country of origin
Updated
Created
2020.12.01
Available languages
English
Keywords
innterleukin, particle size distribution, endotoxin, inflammation, cytokines, Limulus Amoebocyte Lisate (LAL), nanomedicine, nanomaterial, physicochemical characterization, liposome, safety assessment
Quality scoring

Dataset description

In order to provide guidelines to design and perform a robust and reliable physical-chemical characterization of liposome-based nanomaterials, and to support method development with a specific focus on their inflammation-inducing potential the following data have been produced: - Physical-chemical characterization - Interference test - Liposome Cytotoxicity - Effects of Liposomes on Complement Activation - Inflammatory response Out of eight differently functionalized liposomes selected as "case-studies", three passed the physical-chemical characterization ( in terms of size-distribution, homogeneity and stability) and the screening for bacterial contamination (sterility and apyrogenicity). Although all three were non-cytotoxic when tested in vitro, they showed a different capacity to activate human blood cells. HSPC/CHOL-coated liposomes elicited the production of several inflammation-related cytokines, while DPPC/CHOL- or DSPC/CHOL-functionalized liposomes did not.
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