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Martin Schäffler

Publications -  16
Citations -  1853

Martin Schäffler is an academic researcher. The author has contributed to research in topics: Blood proteins & Nanoparticle. The author has an hindex of 14, co-authored 16 publications receiving 1539 citations.

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Particle size-dependent and surface charge-dependent biodistribution of gold nanoparticles after intravenous administration.

TL;DR: The alterations of accumulation in the various organs and tissues, depending on GNP size and surface charge, are mediated by dynamic protein binding and exchange, which will improve drug delivery and dose estimates used in risk assessment.
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Size and surface charge of gold nanoparticles determine absorption across intestinal barriers and accumulation in secondary target organs after oral administration

TL;DR: The highest accumulation in secondary organs was mostly found for 1.4 nm particles; the negatively charged particles were accumulated mostly more than positively charged particles, and 18 nm particles show a higher accumulation in brain and heart compared to other sized particles.
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Air-Blood-Barrier Translocation of Tracheally Instilled Gold Nanoparticles Inversely Depends on Particle Size

TL;DR: The study shows that translocation across the ABB and accumulation and retention in secondary organs and tissues are two distinct processes, both depending specifically on particle characteristics such as SSA and surface charge.
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Quantitative biokinetics of titanium dioxide nanoparticles after oral application in rats: Part 2

TL;DR: Since chronic, oral uptake of TiO2 particles by consumers has continuously increased in the past decades, the possibility of chronic accumulation of such biopersistent nanoparticles in secondary organs and the skeleton raises questions about the responsiveness of their defense capacities, and whether these could be leading to adverse health effects in the population at large.
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Blood protein coating of gold nanoparticles as potential tool for organ targeting.

TL;DR: This study clearly suggests that stable conjugation of AuNP with albumin and apoE prior to intravenous administration increases specificity and efficiency of NP in diseased target-organs thus suggesting a potential role in nanomedicine and nanopharmacology.