Egea M A, Gamisans F, Valero J, Garcia M E, Garcia M L
Department of Pharmacy, Faculty of Pharmacy, University of Barcelona, Spain.
Farmaco. 1994 Mar;49(3):211-7.
The entrapment of cisplatin into biodegradable colloidal systems (polyalkylcyanoacrylates) was studied. Nanoparticles were characterized in terms of relevant parameters for organ distribution in vivo, such as particle diameter and particle size distribution, determined by correlation photon spectroscopy and transmission electron microscopy. Association efficiency was also evaluated by Plasma Emission Spectrophotometry. The ability of surfactants (sodium lauryl sulphate and poloxamer 188), and dextrans of various molecular weights, to improve the binding of the drug to polyalkylcyanoacrylates was also studied. The dextran content in nanoparticles, as determined by polarimetry, increases with the molecular weight of the polysaccharide. The highest value of association efficiency of cisplatin to nanoparticles was obtained in the presence of dextran 70 with sodium lauryl sulphate (0.08%) as stabiliser.
研究了顺铂在可生物降解胶体系统(聚烷基氰基丙烯酸酯)中的包封情况。通过相关光子光谱法和透射电子显微镜确定了纳米颗粒的粒径和粒径分布等体内器官分布相关参数。还通过等离子体发射分光光度法评估了缔合效率。此外,研究了表面活性剂(十二烷基硫酸钠和泊洛沙姆188)以及不同分子量的葡聚糖提高药物与聚烷基氰基丙烯酸酯结合的能力。通过旋光法测定,纳米颗粒中的葡聚糖含量随多糖分子量的增加而增加。在以十二烷基硫酸钠(0.08%)作为稳定剂的葡聚糖70存在下,顺铂与纳米颗粒的缔合效率达到最高值。