The development of the solid lipid nanoparticles (SLN) as a pharmaceutical carrier is reviewed. It is suggested that the SLN has broad prospects in the pharmaceutical field.
对固体脂质纳米粒(SLN)作为药物载体的最新研究进展进行了综述，指出SLN在药学领域的广阔发展前景。
To observe the analgesic effect and lumbar cerebrospinal fluid and serum kinetics of single dose solid lipid nanoparticles morphine(SLN-M) after epidural administration in rats.
观察并探讨硬脂酸纳米吗啡（SLN-M）单次注入大鼠硬膜外腔后的镇痛效应及用药后的药代动力学特点。
Solid lipid nanoparticles (SLN) are nanoparticles generally made from solid lipids by high pressure homogenization.
固体脂质纳米粒通常是由固体脂质材料经高压乳匀法制备而成。
OBJECTIVE To investigate the pharmacy characters and pharmacokinetic processes of the prepared apigenin loaded solid lipid nanoparticles (AP-SLN).
目的本研究对所制得的芹菜素固体脂质纳米粒的制剂学性质和药动学进行研究。
OBJECTIVE To investigate the pharmacy characters and pharmacokinetic processes of the prepared apigenin loaded solid lipid nanoparticles (AP-SLN).
目的本研究对所制得的芹菜素固体脂质纳米粒的制剂学性质和药动学进行研究。
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