Yan Xingyang, Tan Deng, Yu Lei, Li DanYu, Huang Wei, Huang Weiren, Wu Hongkai
Department of Chemistry, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon 999077, Hong Kong, China.
Department of Biology, Southern University of Science and Technology, Shenzhen 518055, Guangdong, China.
ACS Pharmacol Transl Sci. 2024 Dec 4;7(12):4135-4143. doi: 10.1021/acsptsci.4c00565. eCollection 2024 Dec 13.
Tumor organoids are biological models for studying precision medicine. Microfluidic technology offers significant benefits for high throughput drug screening using tumor organoids. However, the range of concentrations achievable with traditional linear gradient generators in microfluidics is restricted, generating logarithmic drug concentration gradients by adjusting the channel ratio in the chip is confined to single-drug dilution chips, significantly restricting the application of microfluidics in drug screening. Here, we presented a microfluidic chip featuring continuous dilution capabilities, which generates logarithmic stepwise drug concentration gradients. We have devised a "mathematical-circuit-chip" model for designing such chips, and based on this model, we have developed and fabricated a device capable of providing 36 distinct drug concentration conditions for two types of drugs. The chip is composed of two structurally identical yet orthogonally arranged layers, each containing a dilution network capable of forming a 5-fold gradient and a tumor organoid culture module. Drug and culture medium delivery to the open culture chamber array is driven by syringe pumps. We have conducted drug screening experiments on patient-derived tumor organoids. This device facilitates high-throughput drug screening for patient-derived organoids, representing a significant stride toward the realization of precision medicine.
肿瘤类器官是用于研究精准医学的生物学模型。微流控技术为使用肿瘤类器官进行高通量药物筛选提供了显著优势。然而,微流控中传统线性梯度发生器可实现的浓度范围有限,通过调整芯片中的通道比例来生成对数药物浓度梯度仅限于单药稀释芯片,这极大地限制了微流控在药物筛选中的应用。在此,我们展示了一种具有连续稀释能力的微流控芯片,它能生成对数逐步药物浓度梯度。我们设计了一个“数学 - 电路 - 芯片”模型来设计此类芯片,并基于该模型开发并制造了一种能够为两种药物提供36种不同药物浓度条件的装置。该芯片由两个结构相同但正交排列的层组成,每层都包含一个能够形成5倍梯度的稀释网络和一个肿瘤类器官培养模块。药物和培养基输送到开放培养室阵列由注射泵驱动。我们已经对患者来源的肿瘤类器官进行了药物筛选实验。该装置有助于对患者来源的类器官进行高通量药物筛选,代表了向实现精准医学迈出的重要一步。