Effects of Alginate Oligosaccharide Mixture on the Bioavailability of Lysozyme as an Antimicrobial Agent

被引:14
作者
Park, Hyun Jung [1 ]
Ahn, Joo-Myung [1 ]
Park, Ra-Mi [1 ]
Lee, Sang-Hee [2 ]
Sekhon, Simranjeet Singh [2 ]
Kim, Sang Yong [3 ]
Wee, Ji-Hyang [4 ]
Kim, Yang-Hoon [2 ]
Min, Jiho [1 ]
机构
[1] Chonbuk Natl Univ, Dept Chem Engn, 664-14 Deokjin Dong, Jeonju 561756, South Korea
[2] Chungbuk Natl Univ, Dept Microbiol, 52 Naesudong Ro, Cheongju 361763, South Korea
[3] Shin Ansan Univ, Dept Food Sci & Biotechnol, 135 Sinansandaehak Ro, Ansan 425792, South Korea
[4] Jeonnam Bioind Fdn, Inst Food Res, Jeonnam 520300, South Korea
基金
新加坡国家研究基金会;
关键词
Alginate Oligosaccharide; Lysozyme; Antimicrobial Activity; CONTROLLED-RELEASE; INTESTINAL DELIVERY; DRUG-DELIVERY; HYDROGELS; POLYMERS; MICROSPHERES;
D O I
10.1166/jnn.2016.10757
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this study, we report an oral drug delivery system without any additional process using pH-sensitive biopolymer, alginate, and alginate oligosaccharide with lysozyme as a model drug. These biopolymers exhibited pH-sensitive characteristics such as shrinking at acidic pH and eroding with dissolution at alkaline pH. The incorporation of lysozyme and biopolymers was performed an artificial intestinal juice (pH 6.8). The immobilization efficiency and lysozyme stability in gastric juice (pH 1.2) has been tested by E. coli antimicrobial activity. The lysozyme without biopolymer immobilization lost similar to 80-90% of antimicrobial activity than that of pure lysozyme. However, the pH-sensitive biopolymer-controlled lysozyme maintained similar antimicrobial activity compared to that of pure lysozyme (50-90% of cell mortality). Therefore, this simple, easy, and rapid system can be effectively and practically applied for pathogen treatment for in vivo oral drug delivery.
引用
收藏
页码:1445 / 1449
页数:5
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