Surface-mediated nucleic acid delivery by lipoplexes prepared in microwell arrays

Small. 2013 Jul 8;9(13):2358-67. doi: 10.1002/smll.201202258. Epub 2013 Mar 8.

Abstract

Many delivery methods have been developed to improve the therapeutic efficacy and facilitate the clinical translation of nucleic acid-based therapeutics. A facile surface-mediated nucleic acid delivery by lipoplexes is prepared in a microwell array, which combines the advantages of lipoplexes as an efficient carrier system, surface-mediated delivery, and the control of surface topography. Uniform disc-like lipoplexes containing nucleic acids are formed in the microwell array with a diameter of ∼818 nm and thickness of ∼195 nm. The microwell array-mediated delivery of lipoplexes containing FAM-oligodeoxynucleotides is ∼18.6 and ∼10.6 times more efficient than the conventional transfection method in an adherent cell line (A549 non-small cell lung cancer cells) and a suspension cell line (KG-1a acute myelogenous leukemia cells), respectively. MicroRNA-29b is then used as a model nucleic acid to investigate the therapeutic efficacy of lipoplexes delivered by the microwell array. Compared to conventional transfection methods, the effective therapeutic dosage of microRNA-29b is reduced from the microgram level to the nanogram level by lipoplexes prepared in the microwell array. The microwell array is also a very flexible platform. Both nucleic acid therapeutics and imaging reagents are incorporated in lipoplexes and successfully delivered to A549 cells, demonstrating its potential applications in theranostic medicine.

Keywords: lipoplexes; microwell arrays; nuleic acid delivery; theranostic medicine.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Carbocyanines / metabolism
  • Cell Line, Tumor
  • Down-Regulation / genetics
  • Flow Cytometry
  • Gene Transfer Techniques / instrumentation*
  • Humans
  • Inhibitor of Differentiation Protein 1 / genetics
  • Inhibitor of Differentiation Protein 1 / metabolism
  • Lipids / chemistry*
  • MicroRNAs / genetics
  • MicroRNAs / metabolism
  • Microscopy, Fluorescence
  • Nucleic Acids / metabolism*
  • Oligodeoxyribonucleotides / metabolism
  • Quantum Dots
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Surface Properties

Substances

  • Carbocyanines
  • ID1 protein, human
  • Inhibitor of Differentiation Protein 1
  • Lipids
  • MIRN29a microRNA, human
  • MicroRNAs
  • Nucleic Acids
  • Oligodeoxyribonucleotides
  • RNA, Messenger
  • cyanine dye 5