Marco Scarzello
University of Groningen
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Publication
Featured researches published by Marco Scarzello.
Journal of Molecular Medicine | 2006
Luc Wasungu; Marco Scarzello; Gooitzen M. van Dam; Grietje Molema; Anno Wagenaar; Jan B. F. N. Engberts; Dick Hoekstra
In this study, the in vitro and in vivo transfection capacity of novel pH-sensitive sugar-based gemini surfactants was investigated. In an aqueous environment at physiological pH, these compounds form bilayer vesicles, but they undergo a lamellar-to-micellar phase transition in the endosomal pH range as a consequence of an increased protonation state. In the same way, lipoplexes made with these amphiphiles exhibit a lamellar morphology at physiological pH and a non-lamellar phase at acidic pH. In this study, we confirm that the gemini surfactants are able to form complexes with plasmid DNA at physiological pH and are able to transfect efficiently CHO cells in vitro. Out of the five compounds tested here, two of these amphiphiles, GS1 and GS2, led to 70% of transfected cells with a good cell survival. These two compounds were tested further for in vivo applications. Because of their lamellar organisation, these lipoplexes exhibited a good colloidal stability in salt and in serum at physiological pH compatible with a prolonged stability in vivo. Indeed, when injected intravenously to mice, these stable lipoplexes apparently did not substantially accumulate, as inferred from the observation that transfection of the lungs was not detectable, as examined by in vivo bioluminescence. This potential of avoiding ‘preliminary capture’ in the lungs may, thus, be further exploited in developing devices for specific targeting of gemini lipoplexes.
14th European Microscopy Congress 1–5 September 2008, Aachen, Germany | 2008
Marc C. A. Stuart; Marco Scarzello; Jaap E. Klijn; E.J. Boekema; Jan B. F. N. Engberts
Amphiphilic molecules possess parts which are distinctively hydrophobic and other parts which are distinctively hydrophilic. This ambivalence lies at the basis of the intriguing properties of these molecules, selected by nature as the building-blocks of architectures essential for life. Amphiphile self-assembly can lead to a variety of structures, differing in shape and size, depending on the molecular structure of the amphiphile and on the solution conditions such as temperature, ionic strength and pH. A relatively new and particularly interesting class of amphiphilic molecules, the gemini surfactants (GS), is obtained by connecting two single-tailed surfactants via a spacer at the level of the headgroups. The sugar-based gemini surfactant consists of several unique structural elements by which self-assembly properties can be made to fit the desired properties. The tertiary amino moieties in the headgroup can be protonated depending on the solution pH. The reduced sugars can be varied in length and stereochemistry. The spacer is either hydrophobic or hydrophilic and can be varied in length and the hydrophobic alkyl chain can be varied in length and degree of saturation. Most gemini surfactants form vesicles around neutral pH and exhibit a phase change towards micelles upon decreasing the pH, figure 1. When the nitrogens are protonated the cross-sectional headgroup area increases which gives the molecule a cone-shape appearance. The pH at which the phase changes from lamellar to micellar is dependent on the spacer length [1]. The shorter the spacer the more difficult it is to protonate both nitrogens which gives a lower pH of transition. At high pH the vesicles become neutral which leads to a decreased colloidal stability and the vesicles aggregated.
Biochimica et Biophysica Acta | 2006
Luc Wasungu; Marc C. A. Stuart; Marco Scarzello; Jan B. F. N. Engberts; Dick Hoekstra
Langmuir | 2006
Marco Scarzello; Jaap E. Klijn; Anno Wagenaar; Marc C. A. Stuart; Ron Hulst; Jan B. F. N. Engberts
Biophysical Journal | 2005
Marco Scarzello; Vladimir Chupin; Anno Wagenaar; Marc C. A. Stuart; Jan B. F. N. Engberts; Ron Hulst
Journal of the American Chemical Society | 2005
Marco Scarzello; J. Smisterova; Anno Wagenaar; Marc C. A. Stuart; Dick Hoekstra; Jan B. F. N. Engberts; Ron Hulst
Journal of Physical Chemistry B | 2006
Jaap E. Klijn; Marc C. A. Stuart; Marco Scarzello; and Anno Wagenaar; Jan B. F. N. Engberts
Journal of Physical Chemistry B | 2007
Jaap E. Klijn; Marc C. A. Stuart; Marco Scarzello; and Anno Wagenaar; Jan B. F. N. Engberts
Organic and Biomolecular Chemistry | 2006
Jaap E. Klijn; Marco Scarzello; Marc C. A. Stuart; Jan B. F. N. Engberts
Archive | 2008
Marco Scarzello; Marc C. A. Stuart; Jaap E. Klijn; Anno Wagenaar; Jan B. F. N. Engberts