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    • 3. 发明授权
    • Lignocellulosic and cellulosic beads for use in affinity and
immunoaffinity chromatography of high molecular weight proteins
    • 木质纤维素和纤维素珠,用于高分子量蛋白质的亲和力和免疫亲和层析
    • US5328603A
    • 1994-07-12
    • US932710
    • 1992-08-19
    • William H. VelanderJeffrey A. KasterWolfgang G. Glasser
    • William H. VelanderJeffrey A. KasterWolfgang G. Glasser
    • B01J20/291B01J20/32B01D15/08
    • B01J20/291B01J20/3212B01J20/3219B01J20/3227B01J20/3274B01J20/3287B01J20/3293B01J2220/54
    • Improved cellulosic beads for use as supports in bioaffinity chromatography are produced by dissolution of cellulose in a chaotropic cellulose solvent, formation of the dissolved cellulose into droplets, and immersion of the droplets into a non-solvent capable of solvent interchange with the cellulose solvent to form generally spherical porous cellulose beads of narrow particle size distribution. The beads formed are preferably made with cellulose having a degree of polymerization between 100 and 200, and the resulting beads when saturated with water without drying contain between 1% and 7% cellulose by weight and have a particle size of at least about 0.3 mm. The beads can be activated by a suitable activation method, and specific bioaffinity ligands are bound to the active sites in the beads. The beads reacted ligands, the beads then used in bioaffinity chromatography to isolate specific bioaffinity molecules having molecular weights between 5,000 and 500,000 from complex solutions. The beads are particularly useful in bioaffinity chromatography of antibodies, therapeutic proteins, enzymes, and other high molecular weight proteins. The cellulose beads have similar properties to agarose beads used in the prior art for bioaffinity chromatography of high molecular weight proteins, but the cellulosic beads of the present invention have much greater mechanical strength and resist crushing under higher column flow rates without chemical cross linking are much cheaper to produce than prior art agarose and dextran beads.
    • 用于生物亲和层析中的支持物的改进的纤维素珠粒通过将纤维素溶解在离液纤维素溶剂中,将溶解的纤维素形成液滴并将液滴浸入能够与纤维素溶剂进行溶剂交换的非溶剂中来形成 通常球形的多孔纤维素颗粒粒径分布窄。 形成的珠粒优选由聚合度在100和200之间的纤维素制成,并且当用水饱和而不干燥时所得的珠粒含有1重量%至7重量%的纤维素,并且具有至少约0.3毫米的粒度。 珠子可以通过合适的活化方法活化,并且特定的生物亲和配体结合到珠粒中的活性位点。 珠粒反应配体,然后将珠粒用于生物亲和层析中以从复杂溶液中分离具有5,000至500,000的分子量的特异性生物亲和分子。 珠粒在抗体,治疗蛋白质,酶和其他高分子量蛋白质的生物亲和层析中特别有用。 纤维素珠具有与现有技术中用于高分子量蛋白质的生物亲和层析的琼脂糖珠相似的性质,但是本发明的纤维素珠具有更大的机械强度并且在更高的柱流速下抵抗破碎而没有化学交联是多 比现有技术的琼脂糖和葡聚糖珠更便宜。
    • 6. 发明授权
    • Chemical modification of shaped hydrogels in non-aqueous medium
    • 非水介质中形状水凝胶的化学改性
    • US5530111A
    • 1996-06-25
    • US296171
    • 1994-08-29
    • Wolfgang G. GlasserCharles E. FrazierGamini Samaranayake
    • Wolfgang G. GlasserCharles E. FrazierGamini Samaranayake
    • C08B3/00C08B3/14C08B5/00C08B7/00C08B11/00C08B13/00
    • C08B3/00C08B3/14
    • A method is described for the chemical modification of pre-shaped hydrogels in non-aqueous medium. The conditions permit the reaction of highly expanded, porous hydrogel particles, such as spherical beads, using pseudo homogeneous reaction conditions in the absence of water. The method involves a three step procedure in which the porous gels are solvent exchanged int a water-free solvent (step 1) with minimal change in gel dimension and porosity; followed by reaction under non-aqueous condition (step 2); and followed by solvent exchange into water (step 3). Many different types of reactions requiring non-aqueous conditions may be carried out using these conditions. The method has particularly been demonstrated for crosslinking fluorinating beads, and for esterifying beads in a reaction involving multifunctional free carboxylic acids in the presence of dicyclohexylcarbodiimide (DCC).
    • 描述了一种用于非水介质中预形状水凝胶的化学改性的方法。 该条件允许在不存在水的情况下使用假均匀反应条件使高度膨胀的多孔水凝胶颗粒如球形珠的反应。 该方法涉及三步法,其中多孔凝胶在无水溶剂(步骤1)中溶剂交换,凝胶尺寸和孔隙率变化最小; 然后在非水条件下反应(步骤2); 然后进行与水的溶剂交换(步骤3)。 可以使用这些条件进行需要非水性条件的许多不同类型的反应。 特别是在二环己基碳化二亚胺(DCC)的存在下,涉及氟化珠的交联以及涉及多官能游离羧酸的反应中的酯化珠粒的方法。