Nanostructure Control of an Antibiotic‐Based Polyion Complex Using a Series of Polycations with Different Side‐Chain Modification Rates
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- Asmariah Ahmad
- Department of Applied Chemistry Faculty of Engineering Kyushu University 744 Moto‐oka, Nishi‐ku Fukuoka 819‐0395 Japan
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- Teruki Nii
- Department of Applied Chemistry Faculty of Engineering Kyushu University 744 Moto‐oka, Nishi‐ku Fukuoka 819‐0395 Japan
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- Takeshi Mori
- Department of Applied Chemistry Faculty of Engineering Kyushu University 744 Moto‐oka, Nishi‐ku Fukuoka 819‐0395 Japan
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- Yoshiki Katayama
- Department of Applied Chemistry Faculty of Engineering Kyushu University 744 Moto‐oka, Nishi‐ku Fukuoka 819‐0395 Japan
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- Masanori Toyofuku
- Faculty of Life and Environmental Sciences University of Tsukuba 1‐1‐1 Tennodai Tsukuba 305‐8572 Japan
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- Akihiro Kishimura
- Department of Applied Chemistry Faculty of Engineering Kyushu University 744 Moto‐oka, Nishi‐ku Fukuoka 819‐0395 Japan
抄録
<jats:title>Abstract</jats:title><jats:p>Developing nanovehicles for delivering antibiotics is a promising approach to overcome the issue of antibiotic resistance. This study aims to utilize a polyion complex (PICs) system for developing novel nanovehicles for polymyxin‐type antibiotics, which are known as last resort drugs. The formation of antibiotic‐based PIC nanostructures is investigated using colistimethate sodium (CMS), an anionic cyclic short peptide, and a series of block catiomers bearing different amounts of guanidinium moieties on their side chains. In addition, only the modified catiomer, and not the unmodified catiomer, self‐assembles with CMS, implying the importance of the guanidine moieties for enhancing the interaction between the catiomer and CMS via the formation of multivalent hydrogen bonding. Moreover, micellar and vesicular PIC nanostructures are selectively formed depending on the ratio of the guanidine residues. Size‐exclusion chromatography reveals that the encapsulation efficiency of CMS is dependent on the guanidinium modification ratio. The antimicrobial activity of the PIC nanostructures is also confirmed, indicating that the complexation of CMS in the PICs and further release from the PICs successfully occurs.</jats:p>
収録刊行物
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- Macromolecular Rapid Communications
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Macromolecular Rapid Communications 43 (19), 2200316-, 2022-06-16
Wiley
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詳細情報 詳細情報について
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- CRID
- 1360580230578349312
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- ISSN
- 15213927
- 10221336
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- データソース種別
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- Crossref
- KAKEN