体内
生物利用度
缺铁性贫血
化学
益生菌
自愈水凝胶
贫血
口服
缺铁
细菌
微生物学
药理学
医学
生物
内科学
生物技术
有机化学
遗传学
作者
Poonam Sagar,Vishal Singh,Ritika Gupta,Sunaina Kaul,Shikha Sharma,Simranjit Kaur,Rupam Kumar Bhunia,Kanthi Kiran Kondepudi,Nitin Kumar Singhal
出处
期刊:ACS applied bio materials
[American Chemical Society]
日期:2021-09-28
卷期号:4 (10): 7467-7484
被引量:11
标识
DOI:10.1021/acsabm.1c00720
摘要
Iron deficiency anemia (IDA) is the most common nutritional disorder worldwide nearly affecting two billion people. The efficacies of conventional oral iron supplements are mixed, intravenous iron administration acquaintances with finite but crucial risks. Usually, only 5–20% iron is absorbed in the duodenum while the remaining fraction reaches the colon, affecting the gut microbes and can significantly impact intestinal inflammatory responses. Therefore, administration of gut bacterial modulators such as probiotics, prebiotics, and any other dietary molecules that can stimulate healthy gut bacteria can enhance iron absorption without any adverse side effects. In this study, we have prepared an iron supplement to avoid the side effects of conventional oral iron supplements. The formulation includes co-encapsulation of iron with anti-inflammatory probiotic bacteria within alginate/starch hydrogels (B + I-Dex (H)), which has been demonstrated to be efficient in mitigating IDA in vivo. As intestinal pH increases, the pore size of hydrogel increases due to ionic interactions and thus releases the encapsulated bacteria and iron. The field emission scanning electron microscopy (FESEM) analysis confirmed the porous structure of hydrogel beads, and in vitro release studies showed a sustained release of iron and bacteria at intestinal pH. The hydrogel was found to be nontoxic and biocompatible in Caco2 cell lines. The formulation showed efficient in vitro and in vivo iron bioavailability in Fe depletion–repletion studies. B + I-Dex (H) was observed to generate less inflammatory response than FeSO4 or nonencapsulated iron dextran (I-Dex) in vivo. We entrust that this duly functional hydrogel formulation could be further utilized or modified for the development of oral therapeutics for IDA.
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