Weinstein J N
Cancer Treat Rep. 1984 Jan;68(1):127-35.
Liposomes, microscopic particles composed of lipid bilayer membranes, can carry water-soluble drugs in their aqueous compartments and lipid soluble drugs in their bilayers. Over the last 10 years, they have been studied more intensively than any other type of drug carrier. The first impulse, as with other pharmaceuticals, has been to inject them iv. However, since they do not leave the vascular system readily except in the sinusoids of liver and spleen, many of the projected applications to nonhematogenous cancers are unlikely to succeed. Nonetheless, the last few years have brought a great increase in sophistication with respect to the physical chemistry, biochemistry, and pharmacology of liposomes. Routes other than the vascular are being explored, and iv injection is being exploited for access to targets within the vascular space. The most likely clinical applications to be successful soon are in parasitology and immunology; practical applications in oncology are distinctly possible, but still speculative.
脂质体是由脂质双分子层膜构成的微观粒子,其水相隔室可携带水溶性药物,双分子层中可携带脂溶性药物。在过去十年中,对脂质体的研究比其他任何类型的药物载体都更为深入。与其他药物一样,最初的想法是通过静脉注射给药。然而,由于脂质体除了在肝脏和脾脏的血窦外不容易离开血管系统,许多针对非血源性癌症的预期应用不太可能成功。尽管如此,在过去几年中,脂质体在物理化学、生物化学和药理学方面的复杂性有了很大提高。正在探索血管外给药途径,静脉注射正被用于进入血管空间内的靶点。最有可能很快取得成功的临床应用是在寄生虫学和免疫学领域;在肿瘤学中的实际应用虽有明显可能,但仍具有推测性。