School of Materials Engineering, Purdue University, West Lafayette, IN 47907, United States; Birck Nanotechnology Center, Purdue University, West Lafayette, IN 47907, United States.
Birck Nanotechnology Center, Purdue University, West Lafayette, IN 47907, United States; Department of Agricultural and Biological Engineering, Purdue University, West Lafayette, IN 47907, United States.
Acta Biomater. 2022 Dec;154:83-96. doi: 10.1016/j.actbio.2022.09.050. Epub 2022 Sep 24.
The gastrointestinal (GI) tract, particularly the colon region, holds a highly diverse microbial community that plays an important role in the metabolism, physiology, nutrition, and immune function of the host body. Accumulating evidence has revealed that alteration in these microbial communities is the pivotal step in developing various metabolic diseases, including obesity, inflammatory bowel disease (IBD), and colorectal cancer. However, there is still a lack of clear understanding of the interrelationship between microbiota and diet as well as the effectiveness of chemoprevention strategies, including pre and probiotic agents in modifying the colonic microbiota and preventing digestive diseases. Existing methods for assessing these microbiota-diet interactions are often based on samples collected from the feces or endoscopy techniques which are incapable of providing information on spatial variations of the gut microbiota or are considered invasive procedures. To address this need, here we have developed an electronic-free smart capsule that enables site-specific sampling of the gut microbiome within the proximal colon region of the GI tract. The 3D printed device houses a superabsorbent hydrogel bonded onto a flexible polydimethylsiloxane (PDMS) disk that serves as a milieu to collect the fluid in the gut lumen and its microbiome by rapid swelling and providing the necessary mechanical actuation to close the capsule after the sampling is completed. The targeted colonic sampling is achieved by coating the sampling aperture on the capsule with a double-layer pH-sensitive enteric coating, which delays fluid in the lumen from entering the capsule until it reaches the proximal colon of the GI tract. To identify the appropriate pH-responsive double-layer coating and processing condition, a series of systematic dissolution characterizations in different pH conditions that mimicked the GI tract was conducted. The effective targeted microbial sampling performance and preservation of the smart capsule with the optimized design were validated using both realistic in vitro GI tract models with mixed bacteria cultures and in vivo with pigs as an animal model. The results from 16s rRNA and WideSeq analysis in both in vitro and in vivo studies showed that the bacterial population sampled within the retrieved capsule closely matched the bacterial population within the targeted sampling region (proximal colon). Herein, it is envisioned that such smart sampling capsule technology will provide new avenues for gastroenterological research and clinical applications, including diet-host-microbiome relationships, focused on human GI function and health. STATEMENT OF SIGNIFICANCE: The colonic microbiota plays a major role in the etiology of numerous diseases. Extensive efforts have been conducted to monitor the gut microbiome using sequencing technologies based on samples collected from feces or mucosal biopsies that are typically obtained by colonoscopy. Despite the simplicity of fecal sampling procedures, they are incapable of preserving spatial and temporal information about the bacteria through the gastrointestinal (GI) tract. In contrast, colonoscopy is an invasive and impractical approach to frequently assess the effect of dietary and therapeutic intake on the microbiome and their impact on the health of the patient. Here, we developed a non-invasive capsule that enables targeted sampling from the ascending colon, thereby providing crucial information for disease prediction and monitoring.
胃肠道(GI),特别是结肠区域,拥有高度多样化的微生物群落,这些微生物群落对宿主身体的代谢、生理、营养和免疫功能起着重要作用。越来越多的证据表明,这些微生物群落的改变是发展各种代谢疾病的关键步骤,包括肥胖、炎症性肠病(IBD)和结直肠癌。然而,人们仍然缺乏对微生物群与饮食之间的相互关系以及化学预防策略(包括前体和益生菌制剂)在改变结肠微生物群和预防消化疾病方面的有效性的明确认识。现有的评估这些微生物群-饮食相互作用的方法通常基于从粪便或内窥镜技术收集的样本,这些方法无法提供关于肠道微生物群的空间变化的信息,或者被认为是侵入性的程序。为了满足这一需求,我们开发了一种无电子智能胶囊,可以在胃肠道的近端结肠区域进行特定部位的肠道微生物组取样。这种 3D 打印设备内部有一个超吸水性水凝胶,固定在一个柔性聚二甲基硅氧烷(PDMS)圆盘上,圆盘充当一个环境,通过快速膨胀收集肠道腔液及其微生物组,并在取样完成后提供必要的机械致动来关闭胶囊。通过在胶囊的取样孔上涂覆双层 pH 敏感的肠溶包衣来实现靶向结肠取样,该包衣层延迟了腔液进入胶囊的时间,直到它到达胃肠道的近端结肠。为了确定合适的 pH 响应双层包衣和处理条件,在不同的 pH 条件下进行了一系列系统的溶解特性研究,这些条件模拟了胃肠道。通过使用混合细菌培养的真实体外胃肠道模型和猪作为动物模型,对具有优化设计的智能胶囊的有效靶向微生物取样性能和保存能力进行了验证。在体外和体内研究的 16s rRNA 和 WideSeq 分析结果表明,从回收胶囊中取样的细菌种群与靶向取样区域(近端结肠)内的细菌种群非常匹配。在此,我们设想这种智能取样胶囊技术将为胃肠病学研究和临床应用提供新的途径,包括饮食-宿主-微生物群关系,侧重于人类胃肠道功能和健康。意义声明:结肠微生物群在许多疾病的发病机制中起着主要作用。人们已经进行了广泛的努力,使用基于从粪便或粘膜活检中收集的样本的测序技术来监测肠道微生物组,这些样本通常通过结肠镜检查获得。尽管粪便取样程序简单,但它们无法通过胃肠道(GI)保留有关细菌的空间和时间信息。相比之下,结肠镜检查是一种侵入性的和不切实际的方法,无法频繁评估饮食和治疗摄入对微生物组及其对患者健康影响的影响。在这里,我们开发了一种非侵入性的胶囊,可以从升结肠进行靶向取样,从而为疾病预测和监测提供重要信息。