Kreuter J, Wilson C G, Fry J R, Paterson P, Ratcliffe J H
Department of Pharmaceutics, Swiss Federal Institute of Technology ETH, Zurich.
J Microencapsul. 1984 Jul-Sep;1(3):253-7. doi: 10.3109/02652048409049364.
The degradation of polybutylcyanoacrylate (PBC) and polyhexylcyanoacrylate (PHC) nanoparticles, together with their association with and toxicity towards isolated hepatocytes, were determined. Nanoparticles were not taken up by rat hepatocytes at a significant level. The LD50S of PBC and PHC nanoparticles towards hepatocytes were 0.4 mg/2 x 10(6) cells and greater than 1 mg/2 x 10(6) cells respectively. This hepatocyte toxicity cannot be attributed solely to the formaldehyde formed during degradation.
测定了聚氰基丙烯酸丁酯(PBC)和聚氰基丙烯酸己酯(PHC)纳米颗粒的降解情况,以及它们与分离的肝细胞的结合和对肝细胞的毒性。纳米颗粒未被大鼠肝细胞大量摄取。PBC和PHC纳米颗粒对肝细胞的半数致死剂量分别为0.4毫克/2×10⁶个细胞和大于1毫克/2×10⁶个细胞。这种肝细胞毒性不能仅归因于降解过程中形成的甲醛。