Pharmacokinetic and pharmacodynamic evaluation of a novel in situ forming poly(ethylene glycol)-based hydrogel for the controlled delivery of the camptothecins

Anita Lalloo, Piyun Chao, Peidi Hu, Stanley Stein, Patrick J. Sinko

Research output: Contribution to journalArticlepeer-review

71 Scopus citations

Abstract

Inadequate drug delivery, due to problems associated with achieving constant therapeutic blood levels, has hampered the use of anticancer agents of the camptothecin (CPT) class. The objective of the current studies was to develop a depot delivery system for the water-soluble analog of CPT, topotecan (TPT). In this study, a 2-phase drug depot consisting of TPT-loaded liposomes entrapped in a poly(ethylene glycol) hydrogel was designed. Physically entrapped unaltered TPT displayed a rapid release rate from the hydrogel. Controlled release was demonstrated in vitro and in vivo from the 2-phase system with constant blood levels being achieved for several days in rats. Cytotoxicity and antitumor activity were also evaluated in rats inoculated with syngeneic MAT B III breast cancer cells. Rats treated with the liposome-loaded hydrogel displayed significantly longer tumor growth suppression and did not exhibit body weight loss compared to those treated with other delivery modes. These experiments constitute a proof-of-principle of the 2-phase depot concept and its potential value for enhancing safety and efficacy in chemotherapy.

Original languageEnglish (US)
Pages (from-to)333-342
Number of pages10
JournalJournal of Controlled Release
Volume112
Issue number3
DOIs
StatePublished - May 30 2006

All Science Journal Classification (ASJC) codes

  • Pharmaceutical Science

Keywords

  • Camptothecin
  • Controlled release
  • Hydrogel
  • Pharmacokinetics

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