Topics in Anti-Cancer Research

Volume: 2

Indexed in: Accepted Book Citation Index, Science (BKCI-S), Chemical Abstracts, BIOSIS Previews, EBSCO, Ulrich's Periodicals Directory.

This is the second volume of the Patent eBook Series titled Topics in Anti-Cancer Research. The eBook includes updated chapters on topics relevant to contemporary cancer research published in the ...
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Chemotherapy of Nano-Sized Camptothecin-Derived Drugs

Pp. 495-521 (27)

Nguyen-Van Cuong, Chi-Hui Guo and Ming-Fa Hsieh


DNA topoisomerase is one of drug targets in cancer therapy. Camptothecin is a plant alkaloid derived from the Chinese tree Camptotheca acuminate. It has been demonstrated that the plant alkaloid camptothecin (CPT) and its analogs caused DNA damage by specifically targeting DNA topoisomerase, effectively devastating a broad spectrum of tumors. Although the anti-tumor activities of CPT and its analogs have been intensively studied for nearly fifty years, recent advances in drug delivery systems of CPT have considerably improved this drug’s efficiency and prevented drug resistance. However, CPT and its analogs showed extremely low water solubility, inactivation of carboxylate salt, undesired interaction with human serum albumin and short half-life, therefore, the development of new and effective CPT-derived products is ongoing. In this chapter, we will summarize the current status of CPT-derived anticancer drugs in literatures, patents and highlight their clinical application.


Aminocamptothecin, anti-tumor efficacy, belotecan, bioavailability, Camptothecin, cancer, clinical trial, drug delivery system, irinotecan, liposomal camptothecin, micelles, nanomedicine, nanoparticles, 9-nitrocamptothecin, pharmaceutical dosage form, pharmacokinetics, poly(ethylene glyclol), polymeric therapeutics, serum stability, topoisomerase I inhibitor, topotecan, water solubility.


Department of Biomedical Engineering, Chung Yuan Christian University, 200, Chung Pei Rd., Chung Li, Taiwan 32023, R.O.C.