2003
DOI: 10.1016/s0099-9598(03)60001-5
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Clinical Studies of Camptothecin and Derivatives

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Cited by 11 publications
(11 citation statements)
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“…However, many side effects were also observed in those assays. For instance, CPT is a water-insoluble (0.551 mg/mL) molecule and has no specific targeting ability towards tumor cells, which causes damage to healthy tissues near the tumor [38]. Additionally, CPT has low tumor penetration ability, which means that only the surface of the tumor tissue can be treated.…”
Section: Camptothecinsmentioning
confidence: 99%
See 1 more Smart Citation
“…However, many side effects were also observed in those assays. For instance, CPT is a water-insoluble (0.551 mg/mL) molecule and has no specific targeting ability towards tumor cells, which causes damage to healthy tissues near the tumor [38]. Additionally, CPT has low tumor penetration ability, which means that only the surface of the tumor tissue can be treated.…”
Section: Camptothecinsmentioning
confidence: 99%
“…Afterwards, the mechanisms of action for CPT were revealed. CPT can selectively combine with the nuclear DNA topoisomerase types I and DNA complexes and then stabilize them to induce the failure re-ligation of DNA, which causes DNA eradication and results in cell apoptosis [38]. Later, many artificial CPT derivatives were designed and synthesized.…”
Section: Camptothecinsmentioning
confidence: 99%
“…The principle of this approach has been shown for camptothecin. The most promising derivatives are 9-[(dimethylamino)methyl]-10-hydroxy camptothecin (topotecan) and 7ethyl-10-[4-(1-piperidino)-1-piperidino] carbonyl oxy camptothecin (irinotecan), which exhibit a much better water solubility than camptothecin [22]. Camptothecin can be found in most parts of C. acuminata, e.g., roots, root barks, fruits, and leaves, but it is especially abundant in seeds.…”
Section: Phytochemistrymentioning
confidence: 99%
“…Carboxylic acid or its sodium salt, even though soluble, has considerably lower antitumor potential as compared to CPT. Furthermore, this ionic form favorably binds to the human serum albumin, lowering the accessible drug concentration [ 45 , 46 ].…”
Section: Introductionmentioning
confidence: 99%