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IMMUNOLOGICAL AGGLUTINATION REAGENT AND IMMUNITY ANALYSIS METHOD

机译:免疫凝集试剂和免疫分析方法

摘要

PROBLEM TO BE SOLVED: To provide an immunization agglutination reagent for measuring the amount of agglutination having sufficiently high sensitivity in practical use and physicochemical stability, which is not found in conventional liposome agglutination reagent and an immunity analysis method using the immunization agglutination reagent. ;SOLUTION: As the carrier of immunological agglutination reagent, the liposome, on which osmotic pressure is loaded by the substitution of the external water phase of the liposome with the aqueous solution having the osmotic pressure higher than the osmotic pressure of the hydration aqueous solution when the liposome is prepared by 120mOsm or more, is used. In details, the osmotic pressure of the hydration aqueous solution is made to be 0.5-30mOsm, the first substitution is performed so that the difference of the osmotic pressures of the hydration aqueous solution and the first substituted aqueous solution becomes 320mOsm or more and the small particle diameter and the high turbidity of the liposome are achieved. When the undesirable effect is observed after the first substitution, it is recommendable that the second substitution is performed with the second substitution aqueous solution having a osmotic pressure of 700mOsm or less.;COPYRIGHT: (C)1997,JPO
机译:解决的问题:提供一种用于测量凝集量的免疫凝集剂,其在实际使用中具有足够的敏感性和理化稳定性,这是常规脂质体凝集剂所没有的,并且提供了使用该免疫凝集剂的免疫分析方法。 ;解决方案:作为免疫凝集剂的载体,当脂质体的外部水相被具有比水合水溶液的渗透压高的渗透压的水溶液替代时,通过脂质体的外部水相替代而在其上加载渗透压的脂质体使用120mOsm以上制备的脂质体。具体而言,使水合水溶液的渗透压为0.5〜30mOsm,进行第一置换,使水合水溶液与第一被取代水溶液的渗透压之差为320mOsm以上且小。获得了脂质体的粒径和高浊度。当第一次置换后观察到不良影响时,建议使用渗透压为700mOsm或更低的第二次置换水溶液进行第二次置换。;版权:(C)1997,JPO

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