4.6 Article

Nanoprobing the acidification process during intracellular uptake and trafficking

Journal

NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE
Volume 11, Issue 6, Pages 1585-1596

Publisher

ELSEVIER
DOI: 10.1016/j.nano.2015.04.010

Keywords

Nanoparticle; Intracellular trafficking; Acidification; pH responsiveness; Rab-family

Funding

  1. Deutsche Forschungsgemeinschaft (DFG) [SPP 1313, LA1013/13-1, MA 3271/3-1, SFB1066]
  2. Max Planck Graduate Center with the Johannes Gutenberg University Mainz (MPGC)

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Many nanoparticular drug delivery approaches rely on a detailed knowledge of the acidification process during intracellular trafficking of endocytosed nanoparticles (NPs). Therefore we produced a nanoparticular pH sensor composed of the fluorescent pH-sensitive dual wavelength dye carboxy seminaphthorhodafluor-1 (carboxy SNARF-1) coupled to the surface of amino-functionalized polystyrene NPs (SNARF-1-NP). By applying a calibration fit function to confocal laser scanning microscopy (CLSM) images, local pH values were determined. The acidification and ripening process of endo/lysosomal compartments containing nanoparticles was followed over time and was found to progress up to 6 h to reach an equilibrium pH distribution (maximum pH 5.2 [+/- 0.2]). The SNARF-1-NP localization in endo/lysosomal compartments was confirmed by transmission electron microscopy (TEM) and quantitative co-localization analysis with fluorescent endolysosomal marker Rab-proteins by confocal laser scanning microscopy (CLSM). The herein described nanoparticular pH-sensor is a versatile tool to monitor dynamic pH processes inside the endolysosomal compartments. (C) 2015 Elsevier Inc. All rights reserved.

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