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将柯克斯托尔QV600 LLI微流控系统适配用于通过质谱成像和液相色谱-串联质谱法研究胃肠道吸收。

Adaptation of the Kirkstall QV600 LLI Microfluidics System for the Study of Gastrointestinal Absorption by Mass Spectrometry Imaging and LC-MS/MS.

作者信息

Spencer Chloe E, Rumbelow Stephen, Mellor Steve, Duckett Catherine J, Clench Malcolm R

机构信息

Centre for Mass Spectrometry Imaging, Biomolecular Sciences Research Centre, Sheffield Hallam University, Howard Street, Sheffield S1 1WB, UK.

CRODA Inc. (B88), New Castle, DE 19720, USA.

出版信息

Pharmaceutics. 2022 Feb 5;14(2):364. doi: 10.3390/pharmaceutics14020364.

Abstract

Absorption studies on oral drugs can be difficult due to the challenge of replicating the complex structure and environment of the GI tract. Drug absorption studies can be conducted using in vivo and ex vivo animal tissue or animal-free techniques. These studies typically involve the use of Caco-2 cells. However, Caco-2 cells do not incorporate all the cell types found in intestinal tissue and lack P450 metabolizing enzymes. The QV600 LLI system is a microfluidics system designed for use with cell culture. Here, it has been adapted to house appropriate sections of ex vivo porcine tissue to act as a system that models the duodenum section of the small intestine. A pH regulated solution of Atorvastatin was flowed over the apical layer of the GI tissue and a nutrient solution flowed over the basal layer of the tissue to maintain tissue viability. The tissue samples were snap-frozen, cryosectioned, and imaged using MALDI Mass Spectrometry Imaging (MSI). A proof-of-concept study on the effect of excipients on absorption was conducted. Different concentrations of the solubilizing agent were added to the donor circuit of the QV600 LLI. The amount of Atorvastatin in the acceptor circuit was determined to study the effect of the excipient on the amount of drug that had permeated through the tissue. Using these data, Papp, pig values were calculated and compared with the literature.

摘要

由于难以复制胃肠道复杂的结构和环境,口服药物的吸收研究可能会很困难。药物吸收研究可以使用体内和体外动物组织或无动物技术来进行。这些研究通常涉及使用Caco-2细胞。然而,Caco-2细胞并未包含肠道组织中所有的细胞类型,并且缺乏P450代谢酶。QV600 LLI系统是一种设计用于细胞培养的微流控系统。在此,它经过改造以容纳合适的离体猪组织切片,作为模拟小肠十二指肠段的系统。将pH调节的阿托伐他汀溶液流过胃肠道组织的顶层,同时将营养液流过组织的底层以维持组织活力。将组织样本速冻、冷冻切片,并使用基质辅助激光解吸电离质谱成像(MALDI MSI)进行成像。开展了一项关于辅料对吸收影响的概念验证研究。将不同浓度的增溶剂添加到QV600 LLI的供体回路中。测定受体回路中阿托伐他汀的量,以研究辅料对透过组织的药物量的影响。利用这些数据,计算出猪的表观渗透系数(Papp)值,并与文献进行比较。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea3d/8878338/18c70db97dcf/pharmaceutics-14-00364-g001.jpg

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