Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Dana Vardeman"'
Publikováno v:
Journal of Pharmacy & Pharmaceutical Sciences, Vol 16, Iss 1 (2013)
Purpose. The aim of this study was to correlate the relationship between the pharmacokinetic behaviors and the toxicity of a new investigational anticancer agent CZ48, a C20-propionate ester of camptothecin (CPT) in mice. Methods. In this study, the
Externí odkaz:
https://doaj.org/article/4d1c3546eca84bbf914a74ff0b9803ed
Autor:
Douglas R. Coil, John Mendoza, Dana Vardeman, Beppino C. Giovanella, Constantine S.A. Markides, Tony Kozielski, Linh H. Luong
Publikováno v:
Oncology Letters
Desmoplastic small round cell tumor (DSRCT) is an extremely rare and aggressive neoplasm, which mainly affects young males and generally presents as a widely disseminated tumor within the peritoneal cavity. Due to the rarity of the tumor, its younger
Publikováno v:
Biomedical Reports. 1:202-206
Crystalline camptothecin-20-O-propionate hydrate (CZ48) is an esterification product from the reaction of natural camptothecin with propionic anhydride. CZ48 has been tested against 29 human tumor lines grown in nude mice as xenografts. Of the tested
Autor:
Beppino C. Giovanella, Xing Liu, Dana Vardeman, A. J. Kozielski, Zhisong Cao, Yang Wang, Chang-Guo Zhan, Albert DeJesus, John Mendoza
Publikováno v:
Anti-Cancer Agents in Medicinal Chemistry. 12:818-828
All chemotherapeutic agents currently in use have a narrow window of therapeutic index of 1 to 1.2. Camptothecin ester compounds are reported to have a wider therapeutic index when being used to treat human xenografts in nude mice. As a continuous ef
Publikováno v:
Open Journal of Medicinal Chemistry. :10-14
Camptothecin-20-propinate (CZ48) and other camptothecin ester derivatives were prepared by the esterification reac-tions of camptothecin or 9-nitrocamptothecin with the corresponding acylating agents such as organic acid anhydride or chloride with co
Publikováno v:
Cancer Research. 69:4742-4749
To find a more effective and less toxic chemotherapeutic agent, we have successfully prepared crystalline camptothecin-20(S)-O-propionate hydrate (CZ48) by reacting camptothecin with propionic anhydride using concentrated sulfuric acid as catalyst. T
Publikováno v:
Journal of Chromatography B. 867:84-89
A simple and sensitive high-performance liquid chromatography (HPLC) assay for the analysis of CZ48, a potent anticancer candidate, and its active metabolite camptothecin (CPT) in mouse plasma was developed and validated. CZ44 was used as an internal
Autor:
John S. Stehlin, Nick Harris, Dana Vardeman, Beppino C. Giovanella, Zhisong Cao, Anthony J. Kozielski
Publikováno v:
Journal of Medicinal Chemistry. 41:31-37
Eleven camptothecin esters, 6a-e and 7a-f, were prepared by straightforward acylation of camptothecins with the corresponding acylating reagents such as organic anhydrides and carboxylic acid chlorides. The in vitro pharmacokinetic determination of l
Publikováno v:
Annals of the New York Academy of Sciences. 803:181-187
Thirty-five human tumors of various histological types xenografted at various sites into nude mice and rats have been used to assess the anticancer activity of camptothecin and derivatives administered by different routes (subcutaneous, intramuscular
Autor:
Dana Vardeman, Albert DeJesus, Janet Early, John Mendoza, A. J. Kozielski, Panayotis Pantazis, Beppino C. Giovanella
Publikováno v:
Leukemia Research. 19:43-55
Human leukemia U-937 cell clones resistant to 9-nitrocamptothecin (9NC) appear after exposure to increase 9NC-concentrations. Drug resistance is irreversible, regardless of whether the 9NC-resistant (U-937/CR150) cells grow in media with or without 9