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Insoluble carrier to the horseshoe crab blood cell membrane-derived antimicrobial peptides and ligand

机译:crab血细胞膜来源的抗菌肽和配体的不溶性载体

摘要

PURPOSE:To obtain the subject insoluble carrier, having a high removal efficiency for pyrogens consisting of bacterial, fungal substances, etc., and useful for purifying pharmaceuticals for injection, etc., by binding an antimicrobial peptide derived from horsecrab corpuscular membranes as a ligand to a carrier, such as agarose. CONSTITUTION:A carrier, such as agarose, is washed and then suspended in water. Sodium hydroxide and epichlorohydrin are added thereto and reaction is carried out while stirring the resultant mixture for 2hr to epoxidize the carrier. An aqueous solution of hexamethylenediamine is subsequently added and reacted therewith to provide an aminohexylated carrier, which is then suspended in a phosphoric acid buffer solution (pH7.0). Glutaraldehyde is subsequently added and reacted therewith. An antimicrobial peptide (e.g. tachyplesin I) derived from horsecrab corpuscular membranes is then added and reacted with the resultant reaction product and sodium borohydride is added to the obtained suspension. Reduction is subsequently carried out to afford the objective insoluble carrier.
机译:目的:通过结合源自马蹄小体细胞膜的抗菌肽作为配体,获得目标不溶性载体,该载体对由细菌,真菌物质等组成的热原具有较高的去除效率,可用于纯化注射用药物等载体,例如琼脂糖。组成:将诸如琼脂糖之类的载体洗净,然后悬浮在水中。向其中加入氢氧化钠和表氯醇,并在搅拌所得混合物2小时的同时进行反应以使载体环氧化。随后加入六亚甲基二胺的水溶液并与其反应以提供氨基己基化的载体,然后将其悬浮在磷酸缓冲溶液(pH7.0)中。随后加入戊二醛并与之反应。然后加入源自马蹄小体膜的抗微生物肽(例如速凝肽I),并使之与所得反应产物反应,并向所得悬浮液中加入硼氢化钠。随后进行还原以提供目标不溶性载体。

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