2021
DOI: 10.1021/acsabm.0c01240
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Preparation and In Vitro Cytotoxicity Assessments of Spherical Silica-Encapsulated Liposome Particles for Highly Efficient Drug Carriers

Abstract: This work reports the formation of spherical solid silica-encapsulated liposome particles (SLPs) as functions of the concentration of silica precursor, reaction time, temperature, and volume ratios of solvent, respectively. The solid SLPs are more robust and have better drug-loading-efficiency liquid liposomes in carrier formulations. The liquid-state liposomes are hard to handle and have a lower drug-loading efficiency because they are fragile to external stimuli and have narrow hydrophobic phospholipid bilay… Show more

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Cited by 5 publications
(5 citation statements)
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“…Compared with the blank control group, MOC, 1.25 wt% PA-MOC and 1 wt% SrR/1.25 wt% PA-MOC cells were all more than 70% active. Indicating that the extract of the sample was not cytotoxic to BMSCs (according to ISO 10993-5, cell viability results of 70% or more were considered to be non-cytotoxic [ 24 ]), the sample had good biocompatibility. Compared with MOC and 1.25 wt% PA-MOC, the cell activity value of 1 wt% SrR/1.25 wt% PA-MOC sample group was higher, indicating that the loading of SrR could promote cell proliferation, which may be related to the Sr 2+ contained in SrR.…”
Section: Resultsmentioning
confidence: 99%
“…Compared with the blank control group, MOC, 1.25 wt% PA-MOC and 1 wt% SrR/1.25 wt% PA-MOC cells were all more than 70% active. Indicating that the extract of the sample was not cytotoxic to BMSCs (according to ISO 10993-5, cell viability results of 70% or more were considered to be non-cytotoxic [ 24 ]), the sample had good biocompatibility. Compared with MOC and 1.25 wt% PA-MOC, the cell activity value of 1 wt% SrR/1.25 wt% PA-MOC sample group was higher, indicating that the loading of SrR could promote cell proliferation, which may be related to the Sr 2+ contained in SrR.…”
Section: Resultsmentioning
confidence: 99%
“…Its high surface area and porous structure provide it with superior adsorption properties, and the presence of many hydroxyl groups on its surface promotes enzyme adhesion. 132,133 Moreover, silica can be used in many different forms, such as colloidal silica particles, silica gel matrix, and fumed silica. For instance, immobilized lipase with a functionalized mesoporous SiO 2 retained 96% of the free enzyme activity.…”
Section: Classic Support Materials For Enzyme Immobilizationmentioning
confidence: 99%
“…The mechanical properties of silica shells can be controlled using different silica precursors with varying chemical structures. For instance, triethoxyvinylsilane (TEVS) [ 141 , 142 ] can be used for a soft shell, while Tetraethoxysilane (TEOS) [ 143 ] can be used for a hard one. The deposition of silica on the surfaces of liposomes is structure-dependent on the silanization condition [ 144 ] and influenced by the reaction conditions.…”
Section: Shell Stabilization Strategy Inspired By Biomineralizationmentioning
confidence: 99%
“…The deposition of silica on the surfaces of liposomes is structure-dependent on the silanization condition [ 144 ] and influenced by the reaction conditions. Chang et al [ 142 ] used TEOS through a sol–gel silicide to endow the liposome with a silicon shell ( Figure 6 A). This work reported that the formation of solid silica encapsulated liposomes (SLPs) was related to the TEOS concentration, reaction time, temperature, and solvent volume ratio.…”
Section: Shell Stabilization Strategy Inspired By Biomineralizationmentioning
confidence: 99%
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