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[链霉素和双氢链霉素脂质体制剂的制备]

[Production of liposomal preparations of streptomycin and dihydrostreptomycin].

作者信息

Vladimirskiĭ M A, Ladygina G A, Tentsova A I, Petiushenko R M, Griazmova N S

出版信息

Antibiotiki. 1984 Mar;29(3):163-6.

PMID:6203483
Abstract

The effect of the conditions of the formation of liposomal preparations of streptomycin and dihydrostreptomycin on incorporation of the antibiotics into the liposomes was studied. The liposomes were obtained with the detergent (cholate) method modified by the authors. The modification implies preliminary application of a 20 per cent antibiotic buffer solution on columns for gel filtration of a mixed mycellar antibiotic solution (20 per cent). The volume ratio of the preliminary applied buffer solution and the mixed mycellar solution is higher than 4:1. The new procedure is simple, readily reproduced, providing formation of the liposomal preparations characterized by high levels of the antibiotic incorporation (about 300 micrograms per 1 mg of lecithin). The preparations are stable with regard to the antibiotic release. The liposomes do not aggregate on storage for a long period (more than 6 months). The liposomal preparations thus formed may be useful as intravenous dosage forms of the antibiotics.

摘要

研究了链霉素和双氢链霉素脂质体制剂的形成条件对抗生素掺入脂质体的影响。脂质体是用作者改进的去污剂(胆酸盐)法制备的。改进之处在于,在对混合胶束抗生素溶液(20%)进行凝胶过滤的柱上预先应用20%的抗生素缓冲溶液。预先应用的缓冲溶液与混合胶束溶液的体积比高于4:1。新方法简单,易于重复,可形成具有高抗生素掺入水平(每1毫克卵磷脂约300微克)的脂质体制剂。这些制剂在抗生素释放方面很稳定。脂质体在长期储存(超过6个月)时不会聚集。如此形成的脂质体制剂可用作抗生素的静脉剂型。

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