• Corpus ID: 1470288

Antitumor efficacy, pharmacokinetics, and biodistribution of NX 211: a low-clearance liposomal formulation of lurtotecan.

@article{Emerson2000AntitumorEP,
  title={Antitumor efficacy, pharmacokinetics, and biodistribution of NX 211: a low-clearance liposomal formulation of lurtotecan.},
  author={David L. Emerson and Raymond A. Bendele and Eric N. Brown and Soong T. Chiang and John Desjardins and Larry Dihel and Stanley C. Gill and Marta Hamilton and J D Leray and Lotus Moon-Mcdermott and K Moynihan and Frank C. Richardson and Blake E. Tomkinson and Michael Joseph Luzzio and David P. Baccanari},
  journal={Clinical cancer research : an official journal of the American Association for Cancer Research},
  year={2000},
  volume={6 7},
  pages={
          2903-12
        }
}
  • D. EmersonR. Bendele D. Baccanari
  • Published 1 July 2000
  • Biology, Chemistry
  • Clinical cancer research : an official journal of the American Association for Cancer Research
Lurtotecan is a clinically active water-soluble camptothecin analogue that has been formulated into a low-clearance unilamellar liposome, NX 211. Comparative studies between free drug and NX 211 have been performed assessing pharmacokinetics in nude mice, tissue distribution in tumor-bearing mice, and antitumor efficacy in xenografts. Compared with lurtotecan, NX 211 demonstrated a significant increase in plasma residence time and a subsequent 1500-fold increase in the plasma area under the… 

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