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Merck
  • Imaging approach to mechanistic study of nanoparticle interactions with the blood-brain barrier.

Imaging approach to mechanistic study of nanoparticle interactions with the blood-brain barrier.

ACS nano (2014-04-30)
Mattia Bramini, Dong Ye, Anna Hallerbach, Michelle Nic Raghnaill, Anna Salvati, Christoffer Aberg, Kenneth A Dawson
摘要

Understanding nanoparticle interactions with the central nervous system, in particular the blood-brain barrier, is key to advances in therapeutics, as well as assessing the safety of nanoparticles. Challenges in achieving insights have been significant, even for relatively simple models. Here we use a combination of live cell imaging and computational analysis to directly study nanoparticle translocation across a human in vitro blood-brain barrier model. This approach allows us to identify and avoid problems in more conventional inferential in vitro measurements by identifying the catalogue of events of barrier internalization and translocation as they occur. Potentially this approach opens up the window of applicability of in vitro models, thereby enabling in depth mechanistic studies in the future. Model nanoparticles are used to illustrate the method. For those, we find that translocation, though rare, appears to take place. On the other hand, barrier uptake is efficient, and since barrier export is small, there is significant accumulation within the barrier.

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Sigma-Aldrich
DAPI, for nucleic acid staining
Sigma-Aldrich
氢化可的松, BioReagent, suitable for cell culture
Sigma-Aldrich
氢化可的松, γ-irradiated, powder, BioXtra, suitable for cell culture
Sigma-Aldrich
氢化可的松, ≥98% (HPLC)
USP
氢化可的松, United States Pharmacopeia (USP) Reference Standard
Supelco
氢化可的松, Pharmaceutical Secondary Standard; Certified Reference Material
Sigma-Aldrich
氢化可的松, meets USP testing specifications
峰鉴别用氢化可的松, European Pharmacopoeia (EP) Reference Standard
氢化可的松, European Pharmacopoeia (EP) Reference Standard
氢化可的松, British Pharmacopoeia (BP) Assay Standard