Pharmacokinetics in mice of four oligomer-conjugated polymers for amplification targeting

Cancer Biother Radiopharm. 2003 Dec;18(6):941-7. doi: 10.1089/108497803322702905.


For use in amplification targeting, an oligomer-conjugated polymer must display adaptable chemistry, minimal steric hindrance, low toxicity, and favorable pharmacokinetics. In particular, the polymer must remain in circulation sufficiently long to permit target localization.

Objectives: To evaluate their properties for amplification targeting, the biodistribution in normal mice was determined for four polymers conjugated with multiple copies of a phosphorodiamidate morpholino (MORF) oligomer.

Methods: An amine-derivatized 25-mer MORF oligomer was radiolabeled with 99mTc. Three polymers of succinylated polylysine (PL) with initial weight average molecular weights (Mw) of 30, 100, and 200 KDa, and one poly (methyl vinyl ether-alt-maleic acid) (PA) with initial Mw of 45 KDa polymer, were each conjugated with an amine derivatized 25-mer complementary MORF (i.e., cMORF). The average number of attached cMORF groups on each polymer molecule (i.e., gpm) was estimated by a high performance liquid chromatography (HPLC) shift assay after the addition of trace 99mTc-MORF to the unpurified polymer, while the average number of accessible cMORF on each polymer was determined by adding radiolabeled MORF at increasing concentrations to the purified cMORF polymer solution until saturation. After purification, each polymer was radiolabeled by incubation with trace 99mTc-MORF. The biodistribution was then established in normal CD1 mice at a constant dosage of 2-4 micrograms of cMORF.

Results: The gpm varied from about 12 on 30 KDa PL to 40 on 45 KDa PA. The biodistribution results show that the pharmacokinetics of the radiolabel is a function of both the type of polymer as well as its gpm. Of the four polymers, the 30 KDa PL showed the most favorable pharmacokinetic profile, with the lowest liver accumulation and the highest blood values compared to the remaining three polymers.

Conclusion: The biodistribution of the four polymers showed characteristic differences, with one polymer (30 KDa PL) showing the most favorable properties for amplification targeting.

Publication types

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

MeSH terms

  • Animals
  • Chromatography, High Pressure Liquid
  • Drug Delivery Systems / methods*
  • Drug Evaluation, Preclinical / methods
  • Injections, Intravenous
  • Mice
  • Morpholines / administration & dosage
  • Morpholines / chemical synthesis
  • Morpholines / pharmacokinetics*
  • Morpholinos
  • Nucleic Acid Amplification Techniques
  • Polymers / administration & dosage
  • Polymers / chemical synthesis
  • Polymers / pharmacokinetics*
  • Radiopharmaceuticals
  • Technetium
  • Tissue Distribution / drug effects


  • Morpholines
  • Morpholinos
  • Polymers
  • Radiopharmaceuticals
  • Technetium