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一种两亲生物降解高分子-聚丙交酯-聚乙二醇嵌段共聚物的研究进展 总被引:4,自引:0,他引:4
PLA-PEG良好的生物相容和降解性能在生物医学领域受到了广泛关注,对其性能和应用已经有了深入的研究。就PLA-PEG这一类两亲生物降解高分子的合成、性能作一简介,并对其在组织工程,药物控释以及靶向载体等方面的应用和前景作一综述和展望。 相似文献
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生物可降解5-氟尿嘧啶载药微球的制备及性能研究 总被引:5,自引:0,他引:5
5-氟尿嘧啶(5-Fu)为水溶性嘧啶类抗代谢药,是治疗实体肿瘤的首选药物.但5-Fu毒性很大,血浆中停留半衰期t1/2仅为10~20min.为了减少氟尿嘧啶的毒副作用并提高药物利用率,可以将其制成聚合物载药微球.聚酯类高分子是较为常用的生物降解型药物载体材料,其中聚乳酸(PLA)及其共聚物具有良好的生物相容性及生物可降解性,常被广泛应用于药物缓释材料, 相似文献
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The role of PEG on the stability in digestive fluids and in vivo fate of PEG-PLA nanoparticles following oral administration 总被引:10,自引:0,他引:10
Tobío M Sánchez A Vila A Soriano I Evora C Vila-Jato JL Alonso MJ 《Colloids and surfaces. B, Biointerfaces》2000,18(3-4):315-323
The aim of the present work was to evaluate if the presence of a polyethylenglycol (PEG) coating around PLA nanoparticles would affect their interaction with biological surfaces, following oral administration to rats. For this purpose, a model antigen, 125I-radiolabeled tetanus toxoid, was encapsulated in PLA and PLA-PEG nanoparticles by a modified water-in-oil-in-water solvent evaporation technique. Firstly, the stability of the nanoparticles in simulated gastrointestinal fluids was evaluated. Results showed an interaction between the nanoparticles and the enzymes of the digestive fluids, this interaction being considerably reduced by the PEG coating around the particles. On the other hand, the PLA forming the nanoparticles was found to be only slightly degraded (9% converted to lactate for PLA nanoparticles and 3% for PLA-PEG nanoparticles) and that the encapsulated tetanus toxoid remained mostly associated to the nanoparticles upon incubation in the digestive fluids for up to 4 h. Finally, the in vivo experiments showed that, after oral administration to rats, the levels of encapsulated radioactive antigen in the blood stream and lymphatics were higher for PLA-PEG nanoparticles than for PLA nanoparticles. In conclusion, the PLA-PEG nanoparticles have a promising future as protein delivery systems for oral administration. 相似文献
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