Kitamura I, Kochi M, Matsumoto Y, Ueoka R, Kuratsu J, Ushio Y
Department of Neurosurgery, Kumamoto University Medical School, Japan.
Cancer Res. 1996 Sep 1;56(17):3986-92.
1,3-bis(2-chloroethyl)-1-nitrosourea (BCNU), one of the chloroethyl nitrosoureas, is effective against malignant glioma. To develop its use in intrathecal chemotherapy, we encapsulated BCNU in hybrid liposomes composed of dimyristoylphosphatidylcholine and micellar surfactants (Tween 20) and dissolved it in artificial cerebrospinal fluid (lipo-BCNU). We then studied the toxicity of hybrid liposomes and cellular proliferation inhibition of lipo-BCNU in vitro. We found that 3 mM hybrid liposomes did not affect the viability of human endothelial cells and that lipo-BCNU inhibited the proliferation of human glioma cell lines U-105MG, U-251MG, and U-373MG, and rat glioma cell lines C6 and 9L in a concentration-dependent fashion. Wistar rats that were administered lipo-BCNU intracisternally showed no weight loss, neurological symptoms, or histological changes of the brain and spinal cord. A Wistar rat model of meningeal gliomatosis was established by intracisternal inoculation of 0.1 ml cell suspension containing 1 x 10(6) or 5 x 10(6) viable C6 glioma cells. Two days after inoculation, lipo-BCNU (BCNU, 2.5 mg/kg) was administered intracisternally. When 1 x 10(6) glioma cells were inoculated (experiments 1 and 2), the median survival times were 24.5 and 26 days in the control groups and 32 and 45 days in the lipo-BCNU-treated groups. respectively. When 5 x 10(6) glioma cells were inoculated (experiments 3-6), the median survival times were 17-29.5 days in the control groups and 23-44 days in the treated groups, respectively. Significantly prolonged survival was obtained in three of six experimental groups. After the administration of 1 ml lipo-BCNU (BCNU, 4.67 mM) or 1 ml BCNU solubilized with 5% dextrose/water (BCNU, 4.67 mM) into the cisterna magna of dogs, the cisterna magna cerebrospinal fluid was sampled, and the BCNU concentrations were assayed by high-performance liquid chromatography. The half-life of the lipo-BCNU was longer than that of BCNU solubilized with 5% dextrose/water. These results suggest that the intrathecal administration of lipo-BCNU may be possible for the treatment of meningeal gliomatosis.
1,3-双(2-氯乙基)-1-亚硝基脲(卡莫司汀,BCNU)是氯乙基亚硝基脲类药物之一,对恶性胶质瘤有效。为了开发其鞘内化疗的应用,我们将BCNU包裹在由二肉豆蔻酰磷脂酰胆碱和胶束表面活性剂(吐温20)组成的混合脂质体中,并将其溶解在人工脑脊液中(脂质体包裹的BCNU,lipo-BCNU)。然后我们研究了混合脂质体的毒性以及lipo-BCNU在体外对细胞增殖的抑制作用。我们发现3 mM的混合脂质体不影响人内皮细胞的活力,并且lipo-BCNU以浓度依赖性方式抑制人胶质瘤细胞系U-105MG、U-251MG和U-373MG以及大鼠胶质瘤细胞系C6和9L的增殖。经鞘内注射lipo-BCNU的Wistar大鼠未出现体重减轻、神经症状或脑和脊髓的组织学变化。通过向脑池内接种0.1 ml含有1×10⁶或5×10⁶个活C6胶质瘤细胞的细胞悬液建立了Wistar大鼠脑膜胶质瘤病模型。接种后两天,经鞘内注射lipo-BCNU(BCNU,2.5 mg/kg)。当接种1×10⁶个胶质瘤细胞时(实验1和2),对照组的中位生存时间分别为24.5天和26天,lipo-BCNU治疗组分别为32天和45天。当接种5×10⁶个胶质瘤细胞时(实验3 - 6),对照组的中位生存时间分别为17 - 29.5天,治疗组为23 - 44天。六个实验组中有三个组的生存时间显著延长。向犬的脑池内注射1 ml lipo-BCNU(BCNU,4.67 mM)或1 ml用5%葡萄糖/水溶解的BCNU(BCNU,4.67 mM)后,采集脑池脑脊液,并用高效液相色谱法测定BCNU浓度。lipo-BCNU的半衰期比用5%葡萄糖/水溶解的BCNU长。这些结果表明,鞘内注射lipo-BCNU可能可用于治疗脑膜胶质瘤病。