The morphology of self-assembled lipid-based nanoparticles affects their uptake by cancer cells

Wafa Aresh, Ying Liu, Jessica Sine, Derek Thayer, Anu Puri, Yike Huang, Yong Wang, Mu Ping Nieh

Research output: Contribution to journalArticle

13 Scopus citations

Abstract

The morphology of nanoparticles (NPs) has been presumed to play an important role in cellular uptake and in vivo stability. This report experimentally demonstrates such dependence by using two types of uniform-sized self-assembled lipid-based NPs, namely nanodiscs and nanovesicles, composed of identical lipid composition. The morphology is characterized by small angle neutron scattering, dynamic light scattering and transmission electron microscopy. Both NPs have similar bio-stability in serum and cellular cytotoxicity. However, cellular uptake of the nanodiscs at 37 °C is consistently and significantly higher than that of the vesicles according to the uptake results of several human cancer cell lines, i.e., CCRFCEM, KB, and OVCAR-8, indicating a strong morphological dependence of cellular internalization. Further studies on such morphological dependence using CCRF-CEM reveals that vesicles only use Clathrin- and caveolae-mediated endocytic pathways, while nanodiscs also take the additional routes of macropinocytosis and microtubule-mediated endocytosis.

Original languageEnglish (US)
Pages (from-to)1852-1863
Number of pages12
JournalJournal of Biomedical Nanotechnology
Volume12
Issue number10
DOIs
StatePublished - Oct 1 2016

All Science Journal Classification (ASJC) codes

  • Bioengineering
  • Medicine (miscellaneous)
  • Biomedical Engineering
  • Materials Science(all)
  • Pharmaceutical Science

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