固体脂质纳米粒
生物制药
药品
药代动力学
药理学
药物输送
化学
结合
毒品携带者
纳米颗粒
纳米技术
材料科学
医学
生物技术
生物
数学分析
数学
作者
S. A. Wissing,Oliver Kayser,Rainer Müller
标识
DOI:10.1016/j.addr.2003.12.002
摘要
This review describes the use of nanoparticles based on solid lipids for the parenteral application of drugs. Firstly, different types of nanoparticles based on solid lipids such as “solid lipid nanoparticles” (SLN), “nanostructured lipid carriers” (NLC) and “lipid drug conjugate” (LDC) nanoparticles are introduced and structural differences are pointed out. Different production methods including the suitability for large scale production are described. Stability issues and drug incorporation mechanisms into the particles are discussed. In the second part, the biological activity of parenterally applied SLN and biopharmaceutical aspects such as pharmacokinetic profiles as well as toxicity aspects are reviewed.
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