Polymeric nanoparticles and cancer: Lessons learnt from CRLX101

  • Ismael Gritli
  • , Edward Garmey
  • , Scott Eliasof
  • , Andres Tellez
  • , Mark E. Davis
  • , Yen Yun

研究成果: 書貢獻/報告類型章節

7 引文 斯高帕斯(Scopus)

摘要

CRLX101 (formerly IT-101) is a novel cyclodextrin-based polymer that self-assembles into nanoparticles. CRLX101 is covalently conjugated to the hydrophobic topoisomerase 1 (TOP1)-inhibitor camptothecin (CPT) resulting in stabilized structure and increased water solubility. Extensive preclinical studies of CRLX101 demonstrated delayed renal clearance and a prolonged plasma half-life. The nanoparticle passively accumulates in tumour tissue through the enhanced permeability and retention effect and slowly releases active CPT leading to enhanced TOP1 inhibition, potential hypoxia inducible factor-1a (HIF-1a) effect, cancer stem cell targeting, and increased antitumour activity against multiple human tumour xenografts. More than 200 human cancer patients have been treated with CRLX101 in phase I/IIa and phase II clinical trials. In this chapter we explore a wide range of anti-cancer nanotherapeutic strategies to inhibit TOP1, HIF-1a and cancer stem cells. Moreover, we discuss the therapeutic value of combining HIF-1a inhibition with antiangiogenics. Finally, we return to CRLX101 and cover in detail the latest preclinical and clinical evaluations and discuss future directions.
原文英語
主出版物標題Privileged Scaffolds in Medicinal Chemistry
主出版物子標題Design, Synthesis, Evaluation
編輯David Thurston, Martin Braddock
發行者Royal Society of Chemistry
頁面199-232
頁數34
版本51
ISBN(電子)9781782620303, 9781782620693, 9781782627869, 9781782628668, 9781849738033, 9781849738286, 9781849738828, 9781849739474
DOIs
出版狀態已發佈 - 1月 1 2016

出版系列

名字RSC Drug Discovery Series
號碼51
2016-January
ISSN(列印)2041-3203
ISSN(電子)2041-3211

ASJC Scopus subject areas

  • 藥物發現

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