文化大學機構典藏 CCUR:Item 987654321/20898
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    Please use this identifier to cite or link to this item: https://irlib.pccu.edu.tw/handle/987654321/20898


    Title: Comparison in purity and antitumor effect of brand and generic paclitaxel against human ovarian cancer cells by an in vitro experimental model
    Authors: Wang, KL (Wang, Kung-Liahng)
    Yang, YC (Yang, Yuh-Cheng)
    Lai, JCY (Lai, Jerry Cheng-Yen)
    Tsai, TH (Tsai, Tung-Hu)
    Lin, CP (Lin, Chin-Ping)
    Wu, YT (Wu, Yu-Tse)
    Chen, YY (Chen, Yu-Yawn)
    Wang, SC (Wang, Shen-Chuan)
    Chen, YJ (Chen, Yu-Jen)
    Contributors: 運教所
    Keywords: Brand
    generic
    interchangeability
    paclitaxel
    taxol
    Date: 2010-10
    Issue Date: 2011-12-09 10:20:35 (UTC+8)
    Abstract: Context: The purity and the therapeutic effectiveness of the generic paclitaxel have not yet been examined and compared to the original brand form. Objective: This study aimed to compare the in vitro purity and biological effects of original brand form (Taxol) and a generic drug of paclitaxel. Materials and Methods: Purity was determined by high-performance liquid chromatography analysis, cell viability by 3-(4,5-dimethylthiazol- 2-yl)-2,5-diphenyl-tetrazolium bromide assay, cell proliferation by clonogenic assay, morphology by Liu's staining, and cell cycle distribution by DNA histogram. Results: Taxol and generic paclitaxel shared similar high-performance liquid chromatography profiles with a major peak at the same retention time and ultraviolet spectrum. Generic paclitaxel inhibited the cell viability to an extent greater than Taxol. By assessing the IC(50), generic paclitaxel also exhibited a greater inhibitory activity on clonogenicity of human ovarian adenocarcinoma SKOV-3 cells. Although both generic paclitaxel and Taxol arrested SKOV-3 and ES-2 cells at G2/M phase with concurrent development of hypoploid and polyploid cells, Taxol treatment exhibited markedly less extent of these changes. Observation of cellular morphology revealed a greater amount of mitotic catastrophe-like and apoptotic cells in generic paclitaxel-treated cells than Taxol-treated cells. Discussion and Conclusion: The results suggest that generic paclitaxel may possess a greater cell death inducing capacity and clonogenicity inhibitory activity against ovarian cancer cells than the original brand Taxol of the same purity. We conclude that this experimental model for assessing the difference between generic and brand name drugs might be considered as a reference while determining their interchangeability and could be easily established in a hospital-based laboratory.
    Appears in Collections:[Graduate Institute of Sport Coaching Science ] journal articles

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