Acetaminophen Interactions with Phospholipid Vesicles Induced Changes in Morphology and Lipid Dynamics
Judith U. De Mel, Sudipta Gupta, Sydney Harmon, Laura Stingaciu, Eric, W. Roth, Miriam Siebenbuerger, Markus Bleuel, Gerald J. Schneider

TL;DR
This study investigates how acetaminophen interacts with phospholipid vesicles, revealing that it alters vesicle morphology and decreases membrane rigidity, which may influence its biological effects.
Contribution
The paper provides novel insights into the effects of acetaminophen on pure lipid membranes, combining multiple biophysical techniques to analyze structural and dynamic changes.
Findings
Acetaminophen reduces membrane rigidity.
It causes vesicle shape irregularities.
Lipid tail motion is significantly affected.
Abstract
Acetaminophen (APAP) or Paracetamol, despite its wide and common use for pain and fever symptoms, shows a variety of side effects, toxic effects, and overdose effects. The most common form of toxic effects of APAP is in the liver where phosphatidylcholine is the major component of the cell membrane with additional associated functionalities. Although this is the case, the effects of APAP on pure phospholipid membranes have been largely ignored. Here, we used DOPC, a commonly found phospholipid in mammalian cell membranes to synthesize large unilamellar vesicles to investigate how the incorporation of APAP changes pure lipid vesicle structure, morphology, and fluidity at different concentrations. We used a combination of dynamic light scattering (DLS), small-angle neutron and X-ray scattering (SANS, SAXS), cryo TEM for structural characterization, and neutron spin-echo (NSE) spectroscopy…
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