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一种用于制备用于基于细胞筛选的控释小分子微阵列多份拷贝的简单方法。

A simple method for producing multiple copies of controlled release small molecule microarrays for cell-based screening.

作者信息

Fujita Satoshi, Onuki-Nagasaki Reiko, Ikuta Kenjiro, Hara Yusuke

机构信息

Biomedical Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Ikeda, Osaka, Japan.

出版信息

Biofabrication. 2016 Dec 5;9(1):011001. doi: 10.1088/1758-5090/9/1/011001.

Abstract

Traditional drug discovery involves the screening of lead compounds from a chemical library by using cell-based high throughput screening (HTS) procedures. This has created a demand for the development of cell-based microarray chips for HTS of compounds. Although several cell-based microarray devices and procedures for screening of chemical libraries have been reported, each has limitations in terms of simplicity, speed, and cost. Here, we sought to make a simple method for producing multiple copies of microarray chips for the controlled release of small molecules during cell-based screening. Arrays of polytetrafluoroethylene microchannels were set in poly(dimethylsiloxane) and were formed in a metal mold. Subsequently, a biodegradable polymer, PLGAs, with chemical compounds was injected into each channel, and the array was sliced perpendicular to the channels to create multiple copies of the microarray chip. After seeding the cells on the microarray chip, we were able to successfully control the diffusion of small molecules and locally introduce the compounds into cells. The described method enables the production of multiple copies of the chip by using an easy, rapid, and inexpensive array fabrication without any specialized devices. Moreover, screening using the microarray chip minimizes the consumption of cells and chemicals. Both the biodegradable material and compound injected into each channel can be individually tuned for optimized performance. Therefore, we expect that this method will be useful for developing cell-based HTS assays for small chemical compounds to find drug candidates.

摘要

传统的药物发现涉及通过基于细胞的高通量筛选(HTS)程序从化学文库中筛选先导化合物。这就产生了对用于化合物高通量筛选的基于细胞的微阵列芯片的开发需求。尽管已经报道了几种用于筛选化学文库的基于细胞的微阵列装置和程序,但每种在简单性、速度和成本方面都有局限性。在此,我们试图开发一种简单的方法来生产微阵列芯片的多个副本,以便在基于细胞的筛选过程中实现小分子的可控释放。将聚四氟乙烯微通道阵列设置在聚二甲基硅氧烷中,并在金属模具中形成。随后,将含有化合物的可生物降解聚合物聚乳酸 - 羟基乙酸共聚物(PLGAs)注入每个通道,并将阵列垂直于通道切片以创建微阵列芯片的多个副本。在微阵列芯片上接种细胞后,我们能够成功控制小分子的扩散并将化合物局部引入细胞。所描述的方法能够通过使用简单、快速且廉价的阵列制造方法来生产芯片的多个副本,而无需任何专门的设备。此外,使用微阵列芯片进行筛选可将细胞和化学物质的消耗降至最低。注入每个通道的可生物降解材料和化合物都可以单独调整以实现优化性能。因此,我们预计这种方法将有助于开发用于小型化学化合物的基于细胞的高通量筛选测定法,以寻找候选药物。

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