Department of Radiology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
Mol Pharm. 2010 Aug 2;7(4):993-1006. doi: 10.1021/mp100104x.
The physicochemical characteristics, in vitro properties, and in vivo toxicity and efficacy of a third generation triazine dendrimer bearing approximately nine 2 kDa polyethylene glycol chains and twelve ester linked paclitaxel groups are reported. The hydrodynamic diameter of the neutral construct varies slightly with aqueous solvent ranging from 15.6 to 19.4 nm. Mass spectrometry and light scattering suggest radically different molecular weights with the former approximately 40 kDa mass consistent with expectation, and the latter 400 kDa mass consistent with a decameric structure and the observed hydrodynamic radii. HPLC can be used to assess purity as well as paclitaxel release, which is insignificant in organic solvents or aqueous solutions at neutral and low pH. Paclitaxel release occurs in vitro in human, rat, and mouse plasma and is nonlinear, ranging from 7 to 20% cumulative release over a 48 h incubation period. The construct is 2-3 orders of magnitude less toxic than Taxol by weight in human hepatocarcinoma (Hep G2), porcine renal proximal tubule (LLC-PK1), and human colon carcinoma (LS174T) cells, but shows similar cytotoxicity to Abraxane in LS174T cells. Both Taxol and the construct appear to induce caspase 3-dependent apoptosis. The construct shows a low level of endotoxin, is not hemolytic and does not induce platelet aggregation in vitro, but does appear to reduce collagen-induced platelet aggregation in vitro. Furthermore, the dendrimer formulation slightly activates the complement system in vitro due most likely to the presence of trace amounts (<1%) of free paclitaxel. An animal study provided insight into the maximum tolerated dose (MTD) wherein 10, 25, 50, and 100 mg of paclitaxel/kg of construct or Abraxane were administered once per week for three consecutive weeks to non tumor bearing athymic nude mice. The construct showed in vivo toxicity comparable to that of Abraxane. Both formulations were found to be nontoxic at the administered doses, and the dendrimer had an acute MTD greater than the highest dose administered. In a prostate tumor model (PC-3-h-luc), efficacy was observed over 70 days with an arrest of tumor growth and lack of luciferase activity observed in the twice treated cohort.
本文报道了第三代三嗪树枝状大分子的理化特性、体外性质、体内毒性和疗效,该分子带有大约 9 个 2 kDa 的聚乙二醇链和 12 个酯键连接的紫杉醇基团。中性构建物的水动力直径在不同的水溶剂中略有变化,范围从 15.6 到 19.4nm。质谱和光散射表明分子量有显著差异,前者约为 40 kDa,与预期一致,后者为 400 kDa,与十聚体结构和观察到的水动力半径一致。高效液相色谱法(HPLC)可用于评估纯度以及紫杉醇的释放,在有机溶剂或中性和低 pH 值的水溶液中,紫杉醇的释放微不足道。在人、大鼠和小鼠血浆中,该构建物在体外的紫杉醇释放是非线性的,在 48 小时孵育期间,累积释放率为 7%至 20%。与紫杉醇相比,该构建物的重量在人肝癌(Hep G2)、猪肾近端小管(LLC-PK1)和人结肠癌细胞(LS174T)中低 2-3 个数量级,但在 LS174T 细胞中与 Abraxane 的细胞毒性相似。紫杉醇和该构建物似乎都诱导 caspase 3 依赖性细胞凋亡。该构建物的内毒素水平较低,无溶血作用,体外不会引起血小板聚集,但似乎会降低胶原诱导的血小板聚集。此外,由于痕量(<1%)游离紫杉醇的存在,该树枝状大分子制剂在体外轻度激活补体系统。一项动物研究提供了关于最大耐受剂量(MTD)的见解,其中每周一次连续三周给非肿瘤荷瘤裸鼠注射 10、25、50 和 100mg/kg 的紫杉醇/构建物或 Abraxane。该构建物显示出与 Abraxane 相当的体内毒性。在给予的剂量下,两种制剂均无毒性,树枝状大分子的急性 MTD 大于给予的最高剂量。在前列腺肿瘤模型(PC-3-h-luc)中,在 70 天的观察期内观察到疗效,两次治疗组的肿瘤生长停止且无荧光素酶活性。