G
Göran Karlsson
Researcher at University of Florence
Publications - 10
Citations - 1092
Göran Karlsson is an academic researcher from University of Florence. The author has contributed to research in topics: Liposome & Vesicle. The author has an hindex of 10, co-authored 10 publications receiving 1048 citations. Previous affiliations of Göran Karlsson include University of Bayreuth & University of British Columbia.
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Journal ArticleDOI
A New Double-Responsive Block Copolymer Synthesized via RAFT Polymerization: Poly(N-isopropylacrylamide)-block-poly(acrylic acid)
Christine Schilli,Mingfu Zhang,Ezio Rizzardo,San H. Thang,Y. K. Chong,Katarina Edwards,Göran Karlsson,Axel H. E. Müller +7 more
TL;DR: In this article, double-responsive block copolymers in solution were investigated by dynamic light scattering, temperature-sweep NMR, cryogenic transmission electron microscopy, and IR spectroscopy.
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Self-Assembly of β-Cyclodextrin in Water. Part 1: Cryo-TEM and Dynamic and Static Light Scattering
TL;DR: A critical aggregation concentration between 2 and 3 mM was determined by using dynamic (DLS) and static (SLS) light scattering to investigate the presence of β-cyclodextrin aggregates in water.
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Morphological changes induced by phospholipase C and by sphingomyelinase on large unilamellar vesicles: a cryo-transmission electron microscopy study of liposome fusion.
TL;DR: The fact that the same honeycomb intermediate can lead to vesicle fusion or to a cubic phase is taken in support of the hypothesis according to which a highly curved lipid structure ("stalk") would act as a structural intermediate in membrane fusion.
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Synthesis, liposomal preparation, and in vitro toxicity of two novel dodecaborate cluster lipids for boron neutron capture therapy.
Eugen Justus,Doaa Awad,Michaela C. Hohnholt,Tanja Schaffran,Katarina Edwards,Göran Karlsson,Luminita Damian,Detlef Gabel +7 more
TL;DR: The zeta-potential measurements indicate that both B- 6-14- and B-6-16-containing vesicles are negatively charged, with the most negative potential described of any liposome so far.
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Substantial increases in idarubicin plasma concentration by liposome encapsulation mediates improved antitumor activity.
Nancy Dos Santos,Dawn Waterhouse,Dana Masin,Paul Tardi,Göran Karlsson,Katarina Edwards,Marcel B. Bally,Marcel B. Bally +7 more
TL;DR: Assessment of the attributes of a liposome formulation required to significantly increase the plasma levels of idarubicin and whether increases in the circulation longevity of the drug mediate improved antitumor activity are established, and effectiveness studies demonstrated that neither the free nor liposomal formulation of IDA was therapeutically active.