The structure of liposomes was observed under the microscope.
显微镜下观察到了脂质体结构。
The liposomes were prepared by the reverse evaporation method.
采用逆向蒸发法自制了甲氨喋呤磁靶向脂质体；
OBJECTIVE: To prepare the liposomes carrier materials lecithin.
目的：制备脂质体载体材料卵磷脂。
The structure and shape of the PST liposomes were also observed.
此外，用扫描电镜观察了PST脂质体的结构与形态。
Tanshinone liposomes were prepared by freeze thawing (FT) method.
采用冻融法制备了丹参酮的脂质体。
Objective: To study the preparing technique of baicalin liposomes.
目的：探讨黄芩苷脂质体的制备工艺。
The control group was only given equivalent liposomes except plasmid.
对照组只给予等量的脂质体，不加入质粒。
Methods the liposomes were prepared by the reverse evaporating method.
方法采用逆相蒸发法制备脂质体。
Lomustine liposomes were prepared by the reversed-phase evaporation method.
采用逆相蒸发法制备洛莫司汀脂质体。
OBJECTIVE: To optimize the prescription and preparation of matrine liposomes.
目的：筛选苦参碱脂质体的最优处方和最佳制备工艺。
Clinical applications can be eye drops, liposomes, ointment and other agents.
临床应用时可采用滴眼液、脂质体、眼膏等制剂。
The influence of AKP and HRP activities after coupling to liposomes was studied.
研究了碱性磷酸酶(akp)和辣根过氧化物酶(HRP)与脂质体偶联后对其活性的影响。
This paper summarizes the progress of research on liposomes for controlled drug release.
综述了药物控释用脂质体的研究进展情况。
Physical stability and envelope rate remains the main problems in preparation of liposomes.
脂质体制备的难点在于改善物理稳定性和提高包封率。
Objective: To determine the content of daunorubicin hydrochloride in its liposomes by HPLC.
目的：测定脂质体中盐酸柔红霉素的含量。
Seed Oil, Dead Sea Mineral Water, Olive Oil, Evening Primrose Oil, Liposomes (Phospholipids).
琉璃苣菜籽油，死海矿物水，橄榄油，晚樱草油，脂质体(磷脂)。
Borage Seed Oil, Dead Sea Mineral Water, Olive Oil, Evening Primrose Oil, Liposomes (Phospholipids).
琉璃苣菜籽油，死海矿物水，橄榄油，晚樱草油，脂质体(磷脂)。
Objective To investigate the preparation method and the transdermal diffusion of flurbiprofen liposomes.
目的研究氟比洛芬脂质体的制备和体外透皮扩散。
METHODS The long circulating mitoxantrone liposomes were prepared by ammonium sulphate gradients method.
方法采用乙醇注入合并硫酸铵梯度法制备米托蒽醌长循环脂质体。
OBJECTIVE The recent progresses of liposomes as a carrier for dermal topical application were introduced.
目的了解脂质体作为皮肤局部给药载体的研究进展。
Objective To investigate the release rate and pharmacodynamics in vitro of of vincristine sulfate liposomes.
目的考察硫酸长春新碱脂质体的体外释放度及其药效。
Results liposomes, especially chitosan coated liposomes enhanced the transcellular transportation of insulin.
结果脂质体，特别是壳聚糖均可以增加胰岛素的通透量。
Thus, the targeted liposomes can specifically deliver the antitumor drugs to gastric cancer cells and kill them.
因此，靶向脂质体可以把包裹的抗癌药物专一地送给胃癌细胞，井杀伤它们。
The coupling condition of different lipid ratio, glutaraldehyde concentration and types of liposomes was probed.
探索了不同比例的脂、不同戊二醛浓度和不同类型脂质体的偶联情况。
The literatures on stability, targetability and modification material of the liposomes are analyzed and discussed.
本文归纳和分析了近期有关脂质体稳定性、靶向性及修饰材料的文献。
In this article, the structural type, preparation and application prospects of polymerized liposomes are reviewed.
本文综述了聚合脂质体的结构类型、制备及应用前景。
Oral albendazole liposomes has shown higher bioavailability and liver targeting in comparison with tablet formulation.
口服阿苯达唑脂质体有较高的生物利用度并有一定的肝脏靶向性。
The results indicated that the content of ADM target liposomes in the tumor tissues was higher apparently than free ADM.
结果表明，靶向脂质体组阿霉素（ADM）在肿瘤组织的含量明显高于游离阿霉素组。
CONCL_ USION: The established method is simple and accurate, which can be used for quality control of matrine liposomes.
结论：本方法操作简便、准确，可用于苦参碱脂质体的质量控制。
CONCL_ USION: The established method is simple and accurate, which can be used for quality control of matrine liposomes.
结论：本方法操作简便、准确，可用于苦参碱脂质体的质量控制。
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