Pharmacokinetic Properties of DNA Aptamers with Base Modifications

Nucleic Acid Ther. 2017 Dec;27(6):345-353. doi: 10.1089/nat.2017.0683. Epub 2017 Sep 29.

Abstract

The addition of novel side chains at the 5-position of uracil is an effective means to increase chemical diversity of aptamers and hence the success rate for discovery of high-affinity ligands to protein targets. Such modifications also increase nuclease resistance, which is useful in a range of applications, especially for therapeutics. In this study, we assess the impact of these side chains on plasma pharmacokinetics of modified aptamers conjugated to a 40 kDa polyethylene glycol. We show that clearance from plasma depends on relative hydrophobicity: side chains with a negative cLogP (more hydrophilic) result in slower plasma clearance compared with side chains with a positive cLogP (more hydrophobic). We show that clearance increases with the number of side chains in sequences of ≥28 synthons, but this effect is dramatically diminished in shorter sequences. These results serve as a guide for the design of new therapeutic aptamers with diversity-enhancing side chains.

Keywords: aptamer pharmacokinetics; modified nucleotides; plasma clearance; side chains.

MeSH terms

  • Animals
  • Aptamers, Nucleotide / administration & dosage
  • Aptamers, Nucleotide / blood
  • Aptamers, Nucleotide / chemistry*
  • Aptamers, Nucleotide / pharmacokinetics*
  • Base Sequence
  • Drug Design
  • Hydrophobic and Hydrophilic Interactions
  • Ligands
  • Linear Models
  • Male
  • Polyethylene Glycols / chemistry*
  • Polyethylene Glycols / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • SELEX Aptamer Technique / methods
  • Statistics, Nonparametric
  • Uracil / chemistry*
  • Uracil / metabolism

Substances

  • Aptamers, Nucleotide
  • Ligands
  • Polyethylene Glycols
  • Uracil