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- 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。
- Objective: To optimize the formulation of chansu-loaded solid lipid nanoparticles(Cs-SLN). 目的:优化蟾酥固体脂质纳米粒的制备工艺。
- Objective To investigate lyophilization of oridonin-loaded solid lipid nanoparticles(ORI-SLN). 目的 对冬凌草甲素固体脂质纳米粒冻干工艺进行研究。
- OBJECTIVE:To prepare Glaucocalyxin A solid lipid nanoparticles(SLN) and study its physico-chemical property. 目的:制备蓝萼甲素固体脂质纳米粒,并对其理化性质进行研究。
- HPLC method for determination of isotretinoin in solid lipid nanoparticles was established. 建立了HPLC法测定异维A酸固体脂质纳米粒含量。
- OBJECTIVE To review the latest research development of the solid lipid nanoparticles (SLN). 摘要目的综述固体脂质纳米粒的最新研究进展。
- Objective To prepare actarit solid lipid nanoparticles(A-SLN)by solvent emulsification-evaporation method. 目的以乳化蒸发-低温固化法制备阿克他利固体脂质纳米粒。
- 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。
- Solid lipid nanoparticles(SLNs)loading mifepristone were prepared and the properties of SLNs wereinvestigated. 制备并考察了米非司酮固体脂质纳米粒(SLN)。
- Methods The apigenin solid lipid nanoparticles were prepared by melt-emulsification-ultrasound method. 方法 采用热熔超声法制备芹菜素固体脂质纳米粒；
- 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。
- Objective To study the effects of podophyllotoxin solid lipid nanoparticles (POD-SLN) on the proliferation of human epidermal cells in vitro. 目的研究鬼臼毒素固体脂质纳米粒(POD-SLN)对人表皮细胞增殖的影响。
- The lyophilized solid lipid nanoparticles (SLN) loaded with all-trans retinoic acid were prepared using different cryoprotectants. 选用不同辅料作为冻干保护剂,制备维甲酸固体脂质纳米粒冻干品,并考察不同制品的外观、粒径、包封率。
- Objective To prepare apigenin solid lipid nanoparticles, optimize the formulation and investigate characteristics of the particles. 目的 为芹菜素新型制剂的研究和开发提供实验基础。
- The influences of ingredient composition on the physicochemical properties of melatonin solid lipid nanoparticles(SLN)and drug release from SLN were investigated. 考察不同的处方对褪黑素固体脂质纳米粒粒径和包封率等理化性质的影响,并进行其体外释放实验。
- 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. 摘要对固体脂质纳米粒(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。
- Objective To improve the therapeutic efficacy and reduce the adverse effect of podophyllotoxin (PPT) by wrapping it in stearic acid solid lipid nanoparticles. 目的为提高鬼臼毒素(PPT)制剂的疗效,降低毒副作用,以硬脂酸为载体材料制备PPT固体脂质纳米粒。
- Objective To prepare solid lipid nanoparticles containing praziquantel(PZQ-SLN) by ultrasonic technique,and investigate the main factors in the process of preparing PZQ-SLN. 目的采用超声分散法制备吡喹酮固体脂质纳米粒,并考察制备过程中的主要影响因素。
- Solid lipid nanoparticle is a new drug delivery system of nano-range. 固体脂质纳米粒是一种新型的纳米给药系统。
- Objective: To prepare the insulin solid lipid nanoparticles(SLNs), insulin SLNs modified by wheat germ agglutinin(WGA), and to investigate the enhancing effect on insulin absorption through GI tract. 目的:制备胰岛素固体脂质纳米粒(SLNs)、麦胚凝集素(WGA)修饰固体脂质纳米粒(WGA-SLNs),研究其对口服吸收胰岛素的促进作用。
