کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1392437 | 1501133 | 2014 | 8 صفحه PDF | دانلود رایگان |
• Synthesis, cytotoxicity and intestinal permeability of DioxinoCPT analog is presented.
• Permeability value of hexacyclic derivative was 5-fold higher than Topotecan.
• Permeability value of the hexacyclic derivative was slightly higher than CPT.
• DioxinoCPT is a potentially effective candidate for cancer treatment by oral administration.
Oral administration of camptothecin (CPT) derivatives and other antitumoral agents is being actively developed in order to improve the quality of life of patients with cancer. Though several lipophilic derivatives of CPT have shown interesting oral bioavailability in preclinical and clinical studies, only Topotecan has been approved for this route of administration. Semisynthesis, antitumor activity, biological inhibition mechanism, and in situ intestinal permeability of 9, 10-[1,3]-Dioxinocamptothecin (CDiox), an unexplored CPT derivative, have been studied in this paper. The hexacyclic analog was as effective as Topotecan and CPT in different tumor cell lines, showing an expected similar apoptosis cell mechanism and high ability to inhibit DNA synthesis in HeLa, Caco-2, A375 and MDA-MB-231 cell lines. Furthermore, in vitro and in situ pharmacokinetics transport values obtained for CDiox displayed more favorable absorption profile than CPT and Topotecan.
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Journal: European Journal of Medicinal Chemistry - Volume 83, 18 August 2014, Pages 366–373