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白血病细胞的体外化学敏感性测试:一种半自动比色测定法的开发

In vitro chemosensitivity testing of leukemic cells: development of a semiautomated colorimetric assay.

作者信息

Bernabei P A, Santini V, Silvestro L, Dal Pozzo O, Bezzini R, Viano I, Gattei V, Saccardi R, Rossi Ferrini P

机构信息

U.O. di Ematologia, USL 10/D-Università degli Studi di Firenze, Italy.

出版信息

Hematol Oncol. 1989 May-Jun;7(3):243-53. doi: 10.1002/hon.2900070307.

Abstract

A rapid chemosensitivity assay was developed, employing the human continuous leukemic cell lines HL 60, K 562, FLG 29.1. This automated colorimetric assay is based on the characteristic of viable, metabolically active cells to cleave p-iodonitrotetrazolium violet (INT) into a red formazan derivative, whose optical density is readable at 492 nm by an automated microtiter-plate reader photometer. A linear relationship was found between the viable cell number and the optical density of INT cleaved by the cellular samples. Dead cells did not reduce INT and did not interfere with the formazan derivative generation and the photometric reading. Leukemic cell lines were also tested for INT formazan derivative generation after exposure to antileukemic drugs at various concentrations, representative of plasma levels obtainable in vivo. A dose-dependent inhibition was detected, with different sensitivity patterns, related both to the drugs and to the different cell lines. A significant correlation between the viable cell number and the amount of tetrazolium salt cleaved was also demonstrated after drug exposure. INT assay allows the processing of a great number of samples and gives the opportunity to screen several drugs, saving time and yielding fully reliable results.

摘要

开发了一种快速化学敏感性测定法,采用人连续白血病细胞系HL 60、K 562、FLG 29.1。这种自动比色测定法基于有活力的、代谢活跃的细胞将对碘硝基四氮唑蓝(INT)裂解为红色甲臜衍生物的特性,其光密度可通过自动酶标仪在492nm处读取。发现活细胞数量与细胞样品裂解的INT光密度之间存在线性关系。死细胞不会还原INT,也不会干扰甲臜衍生物的生成和光度读数。白血病细胞系在暴露于代表体内可获得的血浆水平的各种浓度的抗白血病药物后,也进行了INT甲臜衍生物生成的测试。检测到剂量依赖性抑制,具有不同的敏感性模式,这与药物和不同的细胞系有关。药物暴露后,活细胞数量与裂解的四氮唑盐量之间也显示出显著相关性。INT测定法允许处理大量样品,并有机会筛选多种药物,节省时间并产生完全可靠的结果。

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