Dimethyl Sulfoxide (DMSO) is widely used for drug delivery and in biology as a cryoprotectant because of its ability to dissolve drugs and biomolecules and due to its membrane permeating properties. Despite its extensive use, it is still unclear how this solvent affects the membrane structure and whether its effect is strongly dependent on membrane lipid composition. We employed vesicles of different complexity, from the simplest membrane model (DOPC) up to more complex ones (polar lipid extract of yeast and E. coli) in physiological conditions and under osmotic stress. A wide range of DMSO content was studied, from 0 % to 40 %, using dynamic light scattering, small-angle neutron and X-ray scattering techniques. Our results show that vesicles in PBS maintain their integrity and structure up to 20 % DMSO, but only at higher DMSO concentrations ( 40 %) a drastic alteration of vesicle structure will occur. The main effect of DMSO appears to be a reduction in inter-membrane distances, linked to dehydration, and therefore an increase in stacking of membranes. We also demonstrated that DMSO’s effects on lipid vesicles generated in PBS are dependent on lipid composition, with more complex multi-component membranes, such as lipid polar extracts, demonstrating a higher resilience towards dehydration. Our findings highlight the importance of defining a DMSO threshold concentration that would allow stable and defined vesicle formation for any given lipid composition.

Concentration-dependent effect of DMSO on lipid vesicle structure under physiological conditions / A. Piccinini, A. Murmuliuk, G. Gilliard, G. Manna, V. Rondelli, A. Winter, S. Prévost. - In: COLLOIDS AND SURFACES. A, PHYSICOCHEMICAL AND ENGINEERING ASPECTS. - ISSN 0927-7757. - 739:(2026 Jun), pp. 140014.1-140014.9. [10.1016/j.colsurfa.2026.140014]

Concentration-dependent effect of DMSO on lipid vesicle structure under physiological conditions

A. Piccinini
Primo
;
G. Gilliard;V. Rondelli;
2026

Abstract

Dimethyl Sulfoxide (DMSO) is widely used for drug delivery and in biology as a cryoprotectant because of its ability to dissolve drugs and biomolecules and due to its membrane permeating properties. Despite its extensive use, it is still unclear how this solvent affects the membrane structure and whether its effect is strongly dependent on membrane lipid composition. We employed vesicles of different complexity, from the simplest membrane model (DOPC) up to more complex ones (polar lipid extract of yeast and E. coli) in physiological conditions and under osmotic stress. A wide range of DMSO content was studied, from 0 % to 40 %, using dynamic light scattering, small-angle neutron and X-ray scattering techniques. Our results show that vesicles in PBS maintain their integrity and structure up to 20 % DMSO, but only at higher DMSO concentrations ( 40 %) a drastic alteration of vesicle structure will occur. The main effect of DMSO appears to be a reduction in inter-membrane distances, linked to dehydration, and therefore an increase in stacking of membranes. We also demonstrated that DMSO’s effects on lipid vesicles generated in PBS are dependent on lipid composition, with more complex multi-component membranes, such as lipid polar extracts, demonstrating a higher resilience towards dehydration. Our findings highlight the importance of defining a DMSO threshold concentration that would allow stable and defined vesicle formation for any given lipid composition.
Small-Angle Neutron and X-ray Scattering (SANS-SAXS); Dynamic Light Scattering (DLS); DMSO Dimethyl Sulfoxide; Lipid vesiclesSolvent exchange; PBS
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giu-2026
24-feb-2026
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1224364
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