目的：制备脂质体载体材料卵磷脂。
OBJECTIVE: To prepare the liposomes carrier materials lecithin.
本发明提供一种脂质体载体，其包裹有较高水平的含针对胃泌素和促性腺素释放激素免疫原的水溶性物质。
The invention provides liposomal vehicles for encapsulating relatively high levels of water-soluble substances including immunogens directed against gastrin and gonadotropin releasing hormone.
脂质体作为药物载体的研究，已取得了重大进展。
Great achievement has been acquired by research of liposome as medicament carrier.
结论：脂质体是抗肿瘤药物的理想载体，在抗肿瘤治疗中有广泛的应用前景。
Conclusion: Liposome is an ideal carrier of antitumor drugs. It has extensive prospect in antitumor therapy.
脂质体作为溶栓药物载体，经RGDS修饰后，具有较好的靶向性抗血栓作用。
The results show liposomes as the carrier of medicine has better target anti-thrombus effect after RGDS modifies it.
按载体分类综述了近年来的脂质体、微球、纳米粒、乳剂等几类中药靶向给药系统的研究进展。
Recent advances of research on TODDSs of CMM classified according to carriers, such as liposomes, microspheres, nanocapsules, and emulsions are reviewed.
结论脂质体可以作为酶和抗原的载体，检测血清中的抗体。
Conclusion Liposome may serve as a carrier of enzyme and antigen detecting antibody in sera.
近年来，许多阳离子脂质体、阳离子多肽及阳离子聚合物被用作非病毒类的基因输送载体。
In recent years, many kinds of cationic lipids, oligopeptides and polymers have been developed as non-viral gene delivery materials.
目的了解脂质体作为皮肤局部给药载体的研究进展。
OBJECTIVE The recent progresses of liposomes as a carrier for dermal topical application were introduced.
结论：长循环脂质体是长春新碱的理想载体。
Conclusions: Long-circulating liposome is a good drug delivery system for vincristine.
非病毒基因载体主要有脂质体、人工合成聚合物载体、天然聚合物载体、局部基因释放载体等。
Nonviral gene carriers include liposomes, synthetic polymeric vectors, natural polymeric vectors, local gene delivery vectors and so on.
在经皮给药系统中，脂质体是一种极具前途的给药载体。
It was suggested that liposome is a promising carrier for trans dermal drug delivery system.
结论：脂质体作为维生素d2皮肤局部给药的载体，能够提高对皮肤的穿透力。
CONCLUSIONS Liposomes can be used as a carrier of vitamin D2 in topical application that increase the permeability through the rat skin.
脂质体作为药物载体，其化学组成和物理结构与载药性能密切相关。
Ljposomes as a drug delivery system, the ability of earring drugs is related to the chemical composition and physical structure of liposomes.
脂质体是一类具有特殊性质的磷脂，近几年已开始被广泛用作多种药物的载体。
The liposome, as a class of phospholipid with outstanding nature has been used in drug carrier system in last years.
本文筛选脂质体作为药物载体进行初步研究。
This text selected liposome as drug carrier to carry on primary study.
目的：综述热敏脂质体的原理和它作为靶向药物载体的应用。
OBJECTIVE: The principle of thermosensitive liposomes and its application as drug target carriers are reviewed.
本发明公开了一种叶酸受体靶向脂质体药物载体及其制备方法和应用。
The present invention discloses one kind of folic acid acceptor targeting liposome as medicine carrier and its preparation process and application.
脂质体作为药物载体，由于其具有靶向性、可降低药物毒性等优点而备受关注。
As a new kind of drug carries, liposomes have been widely studied for their benefits of selectivity and low toxicity.
以脂蛋白和载脂蛋白为主要成分构成的脂质体已成为运载抗病毒和抗肿瘤药物受体的靶向性载体。
The liposome made up of apolipoproteins and phospholipid has became a potential carrier for anti-tumor and anti-virus drugs.
目前在药物靶向性给药系统中，脂质体是最成熟和最先进的药物载体之一。
Among several drug delivery systems, liposomal encapsulated anticancer agents represent an advanced and versatile technology.
研究人员评价将c6-神经酰胺填入分子大小的泡沫中，称其为神经酰胺脂质体（cerasomes）作为一种抗肿瘤药物载体。
Researchers evaluated the use of molecular-sized bubbles filled with C6-ceramide, called cerasomes, as an anti-cancer agent.
脂质体包裹疫苗后兼有佐剂和载体的功能。
Liposome encapsulating with vaccine has the function of adjuvant and Cartier.
结论载药脂质体凝胶剂可显著促进药物经皮吸收，为经皮吸收药物的理想载体。
CONCLUSION Liposomal gel has the ability to enhance LDH transcutaneous permeation. It is effective vehicle for transdermal therapeutic drugs.
一种脂质体的制备方法，涉及药物载体和化妆品载体的制备。
The invention provides a method for preparing a liposome, and relates to preparation of a drug carrier and a cosmetic carrier.
脂质体由于具有高度安全性、生物相容性、广泛的载药性等特点，是极具研发前景的靶向、缓释药物载体。
Liposomes are promising drug targeting and controlled release systems, because of their good safety, biocompatibility and drug loading capability.
脂质体由于具有高度安全性、生物相容性、广泛的载药性等特点，是极具研发前景的靶向、缓释药物载体。
Liposomes are promising drug targeting and controlled release systems, because of their good safety, biocompatibility and drug loading capability.
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