Bosanquet A G
Cancer Chemother Pharmacol. 1985;14(2):83-95. doi: 10.1007/BF00434343.
In vitro drug sensitivity of tumour biopsies is currently being determined using a variety of methods. For these chemosensitivity assays many drugs are required at short notice, and this in turn means that the drugs must generally be stored in solution. There are, however, a number of potential problems associated with dissolving and storing drugs for in vitro use, which include (a) drug adsorption; (b) effects of freezing; (c) drug stability under the normal conditions of dilution and setting up of an in vitro assay; and (d) insolubility of drugs in normal saline (NS) or phosphate-buffered saline (PBS). These problems are considered in general, and some recommendations for use of solutions of drugs in in vitro assays are suggested. The nitrosoureas and alkylating agents are also investigated in greater detail in this respect. The nitrosoureas are found to be very labile in PBS at pH 7, with 5% degradation (t0.95) occurring in 10-50 min at room temperature. These values are increased about 10-fold on refrigeration and about 5- to 10-fold on reduction of the pH of the medium to pH 4-5. At pH 7 and room temperature, t0.95 is observed in under 1 h with the alkylating agents nitrogen mustard, chlorambucil, melphalan, 2,5-diaziridinyl-3,6-bis(2-hydroxyethylamino)-1,4-benzoquinone (BZQ), dibromodulcitol, dibromomannitol, treosulphan, and procarbazine. Of the other alkylating agents, 4-hydroperoxycylophosphamide (sometimes used in vitro in place of cyclophosphamide), busulphan, dianhydrogalactitol, aziridinylbenzoquinone (AZQ), and dacarbazine have a t0.95 of between 2 and 24 h, while ifosfamide and pentamethylmelamine are both stable in aqueous solution for greater than 7 days. About half the drugs studied in detail have been stored frozen in solution for in vitro use, although very little is known about their stability under these conditions.
目前正在使用多种方法来测定肿瘤活检组织的体外药物敏感性。对于这些化学敏感性测定,需要在短时间内获得多种药物,这反过来意味着这些药物通常必须以溶液形式储存。然而,将药物溶解和储存用于体外实验存在一些潜在问题,包括:(a)药物吸附;(b)冷冻的影响;(c)在体外实验稀释和准备的正常条件下药物的稳定性;以及(d)药物在生理盐水(NS)或磷酸盐缓冲盐水(PBS)中的不溶性。本文对这些问题进行了总体讨论,并针对体外实验中药物溶液的使用提出了一些建议。同时,还对亚硝基脲类和烷化剂在这方面进行了更详细的研究。结果发现,亚硝基脲类在pH 7的PBS中非常不稳定,在室温下10 - 50分钟内会发生5%的降解(t0.95)。在冷藏条件下,这些值会增加约10倍,而将培养基pH值降至4 - 5时,降解速度会加快约5至10倍。在pH 7和室温下,烷化剂氮芥、苯丁酸氮芥、美法仑、2,5 - 二氮杂环丁烷基 - 3,6 - 双(2 - 羟乙氨基)- 1,4 - 苯醌(BZQ)、二溴卫矛醇、二溴甘露醇、苏消安和丙卡巴肼的t0.95在1小时以内。其他烷化剂中,4 - 氢过氧环磷酰胺(有时在体外实验中用于替代环磷酰胺)、白消安、二去水半乳糖醇、氮杂环丁基苯醌(AZQ)和达卡巴嗪的t0.95在2至24小时之间,而异环磷酰胺和六甲蜜胺在水溶液中均稳定超过7天。尽管对于在这些条件下的稳定性了解甚少,但约一半详细研究的药物已以冷冻溶液形式储存用于体外实验。