Chen Haiyan, Gu Yueqing, Hub Yuzhu, Qian Zhiyu
Department of Biomedical Engineering, School of Life Science and Technology, China Pharmaceutical University, Shennong Road, Nanjing 210009, PR China.
PDA J Pharm Sci Technol. 2007 Jul-Aug;61(4):303-13.
Monodispersed poly (N-isopropylacrylamide) (PNIPA) nanoparticles and their derivative poly (N-isopropylacrylamide-co-acrylic acid) (PNIPA-co-AA) nanoparticles were successfully synthesized. Regulation of the size and the lower critical solution temperature (LCST) of the hydrogel nanoparticles was intensively studied. The results showed that the diameters and LCST of the particles can be arbitrarily manipulated according to different application designs. The relationship between the size of the particles and the amount of surfactant were quantitatively disclosed. It was found that the LCST of PNIPA-co-AA nanoparticles ranging from 35-45 degrees C correlated with the molar fraction of acrylic acid which was copolymerized with NIPA. The pH sensitivity of PNIPA-co-AA nanoparticles was displayed by the transmittance transition of their aqueous solution in various pH conditions. Furthermore, the anti-cancer drug 5-fluorouracil (5-Fu) was first loaded into both PNIPA and PNIPA-co-AA hydrogel nanoparticles with an entrapment efficiency larger than 4%. In vitro release of 5-Fu from PNIPA-co-AA nanoparticle hydrogels was shown to be pH- and temperature-dependent, which demonstrated that the PNIPA-co-AA nanoparticles have great potential in the design of controlled drug delivery systems.
成功合成了单分散聚(N-异丙基丙烯酰胺)(PNIPA)纳米颗粒及其衍生物聚(N-异丙基丙烯酰胺-共-丙烯酸)(PNIPA-co-AA)纳米颗粒。深入研究了水凝胶纳米颗粒尺寸和低临界溶液温度(LCST)的调控。结果表明,根据不同的应用设计,颗粒的直径和LCST可以任意调控。定量揭示了颗粒尺寸与表面活性剂用量之间的关系。发现PNIPA-co-AA纳米颗粒的LCST在35-45℃范围内与与NIPA共聚的丙烯酸的摩尔分数相关。PNIPA-co-AA纳米颗粒的pH敏感性通过其水溶液在不同pH条件下的透光率转变得以体现。此外,抗癌药物5-氟尿嘧啶(5-Fu)首次被负载到PNIPA和PNIPA-co-AA水凝胶纳米颗粒中,包封率大于4%。5-Fu从PNIPA-co-AA纳米颗粒水凝胶中的体外释放显示出pH和温度依赖性,这表明PNIPA-co-AA纳米颗粒在可控药物递送系统设计中具有巨大潜力。