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用于噬菌体递送的容器创建途径。

The Pathways to Create Containers for Bacteriophage Delivery.

作者信息

Musin Egor V, Kim Aleksandr L, Dubrovskii Alexey V, Ariskina Elena V, Kudryashova Ekaterina B, Tikhonenko Sergey A

机构信息

Institute of Theoretical and Experimental Biophysics, Russian Academy of Science, Institutskaya St., 3, 142290 Puschino, Moscow Region, Russia.

All-Russian Collection of Microorganisms (VKM), G. K. Skryabin Institute of Biochemistry and Physiology of Microorganisms, Federal Research Center, Pushchino Scientific Center for Biological Research of the Russian Academy of Sciences, Prospect Nauki 5, 142290 Pushchino, Moscow Region, Russia.

出版信息

Polymers (Basel). 2022 Feb 4;14(3):613. doi: 10.3390/polym14030613.

Abstract

Antimicrobial resistance is a global public health threat. One of the possible ways to solve this problem is phage therapy, but the instability of bacteriophages hinders the development of this approach. A bacteriophage delivery system that stabilizes the phage is one of the possible solutions to this problem. This study is dedicated to exploring methods to create encapsulated forms of bacteriophages for delivery. We studied the effect of proteolytic enzymes on the destruction of the polyelectrolyte microcapsule shell and revealed that protease from was able to destroy the membrane of the microcapsule (dextran sulfate/polyarginine) ((DS/PArg)). In addition, the protease decreased the activity of the bacteriophage in the second hour of incubation, and the phage lost activity after 16 h. It was found that a medium with pH 9.02 did not affect the survival of the bacteriophage or . The bacteriophages were encapsulated into polyelectrolyte microcapsules (DS/PArg). It was established that it is impossible to use microcapsules as a means of delivering bacteriophages since the bacteriophages are inactivated. When bacteriophages were included inside a CaCO core, it was demonstrated that the phage retained activity before and after the dissolution of the CaCO particle. From the results of this study, we recommend using CaCO microparticles as a container for bacteriophage delivery through the acidic stomach barrier.

摘要

抗菌耐药性是全球公共卫生威胁。解决这一问题的一种可能方法是噬菌体疗法,但噬菌体的不稳定性阻碍了该方法的发展。一种能使噬菌体稳定的噬菌体递送系统是解决这一问题的可能方案之一。本研究致力于探索制备用于递送的噬菌体包囊形式的方法。我们研究了蛋白水解酶对聚电解质微胶囊壳破坏的影响,发现来自[具体来源未提及]的蛋白酶能够破坏微胶囊(硫酸葡聚糖/聚精氨酸)((DS/PArg))的膜。此外,蛋白酶在孵育的第二个小时降低了噬菌体的活性,且噬菌体在16小时后失去活性。发现pH 9.02的培养基不影响噬菌体或[具体内容未提及]的存活。噬菌体被包封在聚电解质微胶囊(DS/PArg)中。已确定由于噬菌体失活,不可能将微胶囊用作递送噬菌体的手段。当噬菌体包含在碳酸钙核心内时,证明在碳酸钙颗粒溶解之前和之后噬菌体都保持活性。从本研究结果来看,我们建议使用碳酸钙微粒作为通过酸性胃屏障递送噬菌体的载体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bb2/8840248/d846b0dbeb97/polymers-14-00613-g001.jpg

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