Ueno Y, Futagawa H, Takagi Y, Ueno A, Mizushima Y
Institute of DDS, Jikei University School of Medicine, 3-25-8, Nishi-shinbashi, Minato-ku, Tokyo 105-8461, Japan.
J Control Release. 2005 Mar 2;103(1):93-8. doi: 10.1016/j.jconrel.2004.11.015. Epub 2004 Dec 15.
We devised a simple method for incorporating drugs into solid calcium carbonate nanoparticles (nano-CaCO3). The size of nano-CaCO3 was controlled by mixing speed. Washing the nanoparticles released little incorporated drug but much drug that was adsorbed on the surface. In an in vitro releasing test, granulocyte colony-stimulating factor incorporated in nano-CaCO3 was chemically stable and released very slowly. Subcutaneous injection of nano-CaCO3 incorporating betamethasone phosphate (BP) resulted in a smaller initial increase in plasma concentration and a subsequent sustained release in compared with betamethasone phosphate solution. Nano-CaCO3 may be useful to deliver hydrophilic drugs and bioactive proteins.
我们设计了一种将药物掺入固体碳酸钙纳米颗粒(纳米碳酸钙)的简单方法。纳米碳酸钙的尺寸通过混合速度来控制。洗涤纳米颗粒时,掺入的药物释放很少,但吸附在表面的药物释放较多。在体外释放试验中,掺入纳米碳酸钙的粒细胞集落刺激因子化学性质稳定,释放非常缓慢。与磷酸倍他米松溶液相比,皮下注射掺入磷酸倍他米松(BP)的纳米碳酸钙导致血浆浓度的初始升高较小,随后持续释放。纳米碳酸钙可能有助于递送亲水性药物和生物活性蛋白。