靶向藥物濃度篩選微流控器件的設(shè)計(jì)與制作

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關(guān)鍵詞：微流控;細(xì)胞微環(huán)境；靶向藥物濃度篩選；平行共培養(yǎng)中圖分類號(hào)：TP394.1;TH691.9 文獻(xiàn)標(biāo)識(shí)碼：Adoi：10.37188/OPE.20253308.1228 CSTR：32169.14.OPE.20253308.1228

Abstract：To screen the concentrations of targeted drugs，a cellco-culture microfluidic device with an integrated concentration gradient generator was designed and fabricated. The principles of concentration gradient generation，theconcentration fields，the velocity fields，and the abilityofcell co-culture within the device were studied. A microchannel model capable of generating a concentration gradient was designed based on the equivalent circuit principle，using a series-paralel structure to integrate the concentration gradient unit with thecellco-culture unit. The velocity and concentration fields were simulated and validated using the laminar flow and masstransfer modules in the finite element simulation software Comsol.The microfluidic device was fabricated using soft ithography techniques，and fluorescein sodium solution and polystyrene suspension with a 1{μm diameter were used to simulate drug concentration distribution. Co-culture of Hela cells and A549 cels was performed within the device，and the growth curves and folate receptor targeting of both celltypes were analyzed. Simulation and experimental results indicate that the designed microfluidic device could generate the desired concentration gradient （5：1： O ratio），with concentration variation within each branch cell culture unit below 0.1% . The velocity distribution in the cell culture unit is uniform，with an average flow velocity of （7.1±0.3）μm/s under an inlet flow rate of 925 μm/s . The growth of both celltypes follows an S-shaped growth curve，and membrane staining experiments demonstrate the successful parallel co-culture of two cell types within the microfluidic device. These findings demonstrate that microfluidic device could simulate the in vivo fluidic environment of cells and provide a technological platform for targeted drug concentration screening and personalized therapy.

Key words： microfluidics；cell microenvironment；targeted drugs concentration screening； parallel coculture

1引言

腫瘤靶向藥物具有靶向性、藥物用量少、全身毒副作用低等特點(diǎn)，是抗癌藥物發(fā)展的一個(gè)重要方向[1-3]。（剩余14386字）