Norman M E, Williams P, Illum L
Department of Pharmaceutical Sciences, University of Nottingham, University Park, UK.
J Biomed Mater Res. 1993 Jul;27(7):861-6. doi: 10.1002/jbm.820270704.
A diffusion chamber implanted intraperitoneally in the rabbit was employed as an in vivo model to evaluate the interaction of peritoneal proteins with block copolymer (poloxamer and poloxamine)-coated polystyrene microspheres (PS). Using a desorption technique followed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, six proteins of 94, 86, 66, 53, 40, and 20 kDa were desorbed from the carrier systems after incubation with peritoneal fluid in vitro. The 40- and 20-kDa proteins dominated the protein profile. A similar pattern was observed when proteins were desorbed from PS microspheres removed after 24-h implantation in chambers in the peritoneal cavity, although the protein profile was dominated by the 94- and 53-kDa proteins. In general, coating of PS with block copolymers reduced the amount of protein bound to the microspheres in vitro and in vivo but did not change the types of proteins bound.
将植入兔腹腔的扩散室用作体内模型,以评估腹膜蛋白与嵌段共聚物(泊洛沙姆和泊洛沙明)包被的聚苯乙烯微球(PS)之间的相互作用。采用解吸技术,随后进行十二烷基硫酸钠-聚丙烯酰胺凝胶电泳,在体外与腹膜液孵育后,从载体系统中解吸出了分子量分别为94、86、66、53、40和20 kDa的六种蛋白质。40 kDa和20 kDa的蛋白质在蛋白质图谱中占主导地位。当从腹腔内扩散室中植入24小时后取出的PS微球上解吸出蛋白质时,观察到了类似的模式,尽管蛋白质图谱中以94 kDa和53 kDa的蛋白质为主。一般来说,用嵌段共聚物包被PS在体外和体内均减少了与微球结合的蛋白质量,但并未改变所结合蛋白质的类型。