Hopkins S C, Buice R G, Matheny R, Soloway M S
Cancer. 1984 May 15;53(10):2063-8. doi: 10.1002/1097-0142(19840515)53:10<2063::aid-cncr2820531010>3.0.co;2-5.
Although intravesical mitomycin C (MMC) is effective in the treatment of superficial bladder cancer, its expense is a major factor limiting its use. These authors have analyzed the antitumor activity and stability of MMC following 2-hour intravesical instillation in consideration of recycling the drug or using a smaller dose over a longer retention time. The first voided urine samples from 11 patients who received 40 mg MMC intravesically were measured for MMC content by high performance liquid chromatography (HPLC). An average of 50% of the parent drug was recovered. MMC from the urine samples inhibited the growth of a transplantable murine transitional cell carcinoma as effectively as stock drug. Moreover, MMC is relatively stable in human urine at body temperature. These findings suggest that recovery and reuse of the intravesically administered drug is possible and if sterility and appropriate concentrations can be established for the initial and subsequent doses, the drug may be able to be recycled.
尽管膀胱内灌注丝裂霉素C(MMC)在浅表性膀胱癌的治疗中有效,但其费用是限制其使用的一个主要因素。考虑到药物的循环利用或在更长的保留时间内使用较小剂量,这些作者分析了在膀胱内灌注2小时后MMC的抗肿瘤活性和稳定性。通过高效液相色谱法(HPLC)对11例膀胱内接受40mg MMC患者的首次晨尿样本进行MMC含量测定。平均回收了50%的母体药物。尿液样本中的MMC对可移植性小鼠移行细胞癌生长的抑制效果与原液药物相同。此外,MMC在体温下于人体尿液中相对稳定。这些发现表明膀胱内给药药物的回收和再利用是可能的,并且如果能够为初始剂量和后续剂量确定无菌性和合适的浓度,该药物或许能够被循环使用。