Conclusion: Stearic acid solid lipid nanoparticles might be a novel drug delivery carrier.
结论：硬脂酸纳米粒有可能成为一种新型药物载体。
OBJECTIVE to prepare and optimize the composition of mitoxantrone solid lipid nanoparticles.
目的：制备米托蒽醌固体脂质纳米粒并优化其处方组成。
Methods Monostearin solid lipid nanoparticles was prepared by solvent diffusion method in aqueous system.
方法用水性溶剂扩散法，制备得到甘油单硬脂酸酯固体脂质纳米粒。
Objective To review the new research development of the solid lipid nanoparticles as a drug delivery system.
目的综述固脂纳米粒作为药物释放系统的最新研究进展。
CONCLUSION Oridonin loaded stearic acid solid lipid nanoparticles were produced with stable physical properties.
结论冬凌草甲素可以制成硬脂酸纳米粒，各项物理指标稳定。
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。
Solid lipid nanoparticles is a new drug delivery system, which can enhance the bioavailability of poorly soluble drugs.
固体脂质纳米粒作为一种新型给药系统，可以提高难溶性药物生物利用度。
OBJECTIVE To prepare imiquimod-loaded solid lipid nanoparticles and investigate their properties and transdermal permeation.
目的制备咪喹莫特固体脂质纳米粒，并考察其理化性质及其对透皮的影响。
To introduce the latest research advances on solid lipid nanoparticles by referring to the domestic and international documents.
通过整理和归纳国内外文献，介绍固体脂质纳米粒的最新研究进展。
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。
ABSTRACT: OBJECTIVE To prepare diazepam solid lipid nanoparticles, evaluate the pharmacy characters and study the pharmacokinetics after intranasal administration.
摘要：目的制备地西泮固体脂质纳米粒，评价其制剂学性质，并探讨其经鼻腔给药后的药动学过程。
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。
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。
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