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- multilamellar liposomes 多室脂质体
- Objective To optimize the prescription of tea tree oil liposomes. 目的优化制备茶树油纳米脂质体的处方。
- Objective To prepare and optimize formulation of ATRA liposomes. 目的通过制备不同配方全反式维甲酸脂质体,对处方进行优化。
- AIM To study the preparation and stability of sinomenine liposomes. 目的:优选青藤碱脂质体的制备方法,并研究其稳定性。
- Hydrostatic Pressure Effects on Transport in Liposomes and Red Cells. 静水压力对脂质体、红细胞运输的影响。
- OBJECTIVE To determine the trap efficiency of liposomes using Sephadex. 目的考察用葡聚糖凝胶法测定脂质体包封率的影响因素。
- OBJECTIVE To optimize the preparation formulation of the taspine liposomes. 目的优化塔斯品碱脂质体的制备处方。
- If there is only one lipid bilayer, they are called unilamellar vesicles; otherwise they are called multilamellar. 只有一个脂双分子层的叫单膜小泡；其余的叫多膜小泡。
- Objective To study the distribution of the surfactant-like multilamellar bodies in the human nose. 目的通过超微结构观察,探讨鼻腔鼻窦粘膜表面活性物质样板层体的分布情况及其临床意义。
- Conclusion The existence of surfactant-like multilamellar bodies in the human lateral nasal wall and maxillary sinus wer... 结论人鼻腔鼻窦粘膜普遍存在表面活性物质样板层体,为急、慢性鼻鼻窦炎的药物治疗提供了形态学依据。
- Results The surfactant-like multilamellar bodies were identified in the epithelium on the lateral wall and maxillary sinus. 结果下鼻甲、中鼻甲、钩突、上颌窦和腺样体粘膜均有表面活性物质样板层体的存在。
- The measuring range of 3 to 6,000 nm covers the size of very small micelles as well as the larger liposomes. 测量范围在3至6000纳米之间，非常小的微胶粒和大微脂粒同样适用。
- Observe the suscitation of podophyllotoxin liposomes chitosan film torabbits' vagina. 三、察鬼臼毒素脂质体壳聚糖涂膜剂对家兔阴道的刺激性。
- The experimental study on in vivo pharmacokinetics of carboplatin liposomes via intralymphatic vessel perfusion. 经淋巴管灌注卡铂脂质体的药代动力学实验研究。
- METHODS the pharmacokinetics of EPC and HEPC sterically stabilized liposomes (EPC-SSL, and HEPC-SSL) were studied by HPLC. 方法用高效液相色谱法研究EPC和HEPC长循环阿霉素脂质体在大鼠体内的药物动力学。
- The results revealed that DPPC:Chol:DCP liposomes could markedly enhance the immunogenicity of the ESS. 结果表明,DPPC:Chol:DCP 脂质体能显著增强ESS的免疫原性。
- The entrapment efficiency in cationic liposomes was in the same range even if the drug loading was increased. 即使填充药量增加，带有阳离子的脂质体的包封率（仍处于相同范围）没有变化。
- OBJECTIVE To prepare Lomustine thermo-sensitive liposomes(CCNU-TSL) and investigate the anti-tumor activity in vitro. 目的制备洛莫司汀热敏脂质体并考察其体外抗肿瘤活性。
- OBJECTIVE:To present the optimum method of the preparation of mitoxantrone liposomes. 目的：优选米托蒽醌脂质体制备工艺。
- Typically, liposomes must be smaller than 200 nm in order to pass through the blood system unobstructed. 微脂粒必须小于200纳米才能没有障碍的穿过血液系统。
