A microfluidic design to provide a stable and uniform in vitro microenvironment for cell culture inspired by the redundancy characteristic of leaf areoles
Abstract:The leaf venation is considered to be an optimal transportation system with the mesophyll cells being divided by minor veins into small regions named areoles. The transpiration of water in different regions of a leaf fluctuates over time making the transportation of water in veins fluctuate as well. However, because of the existence of multiple paths provided by the leaf venation network and the pits on the walls of the vessels, the pressure field and nutrient concentration in the areoles that the mesophyll ce… Show more
“…Thus considerable attention has been directed toward engineering vascular system on chips inspired by the natural complex vascular networks, through which animals and plants efficiently transport fluids and cells over a long distance. [ 19,20 ] Progress has been made to establish a set of biomimetic design principles to achieve physiologic blood flow within an artificial vascular network. [ 21 ] Murray's law, originally obtained from the study of mammalian cardiovascular systems describing the optimum conditions of the branching hierarchical structures of blood vessels, has been broadly utilized to design artificial vascular microfluidic networks.…”
In article number 2000546, Jiankang He, Xin Zhao, and co‐workers report a human‐on‐leaf#x02010;chip system with biomimetic multiscale vasculature systems connecting vascularized organs, mimicking the complex in vivo architectures of the human cardiovascular system. The native organ‐to‐organ crosstalk is well recapitulated, implicating a strong potential for harnessing the leaf chip for circulatory‐related studies such as metastasis.
“…Thus considerable attention has been directed toward engineering vascular system on chips inspired by the natural complex vascular networks, through which animals and plants efficiently transport fluids and cells over a long distance. [ 19,20 ] Progress has been made to establish a set of biomimetic design principles to achieve physiologic blood flow within an artificial vascular network. [ 21 ] Murray's law, originally obtained from the study of mammalian cardiovascular systems describing the optimum conditions of the branching hierarchical structures of blood vessels, has been broadly utilized to design artificial vascular microfluidic networks.…”
In article number 2000546, Jiankang He, Xin Zhao, and co‐workers report a human‐on‐leaf#x02010;chip system with biomimetic multiscale vasculature systems connecting vascularized organs, mimicking the complex in vivo architectures of the human cardiovascular system. The native organ‐to‐organ crosstalk is well recapitulated, implicating a strong potential for harnessing the leaf chip for circulatory‐related studies such as metastasis.
“…To culture two cell lines paralleled, an axisymmetric structure of the microfluidic chip is designed (as shown in In previous works, the existence of multiple flow paths around the cell culture chamber has been demonstrated to be useful for constructing a uniform and stable flow fields inside the chamber [35,36]. In this work, microgaps around the cell culture chamber has also been designed (as shown in Fig.…”
Section: Design Of the Microfluidic Devicementioning
confidence: 99%
“…The A549 cells and Hela cells (Cell Bank of the Chinese Academy of Sciences, Shanghai, China) are cultured simultaneously in the same microfluidic chip. The device is sterilized and coated with fibronectin according to previous works [35,36]. Before introducing the cells, the microchannels are filled with culture medium containing 89% DMEM, 10% FBS and 1% PS (Gibco, USA) to remove the surplus proteins and gas.…”
Nanoparticles are attractive in medicine because their surfaces can be chemically modified for targeting specific disease cells, especially for cancer. Providing an in-vivo like platform is crucial to evaluate the biological behaviours of nanoparticles. This paper presents a microfluidic device that could culture two cell lines in parallel in in-vivo like fluidic microenvironments and be used for testing the tumor targeting of folic acidcholesterolchitosan (FACC) nanoparticles. The uniformity and uniformity of flow fields inside the cell culture units are investigated using the finite element method and particle tracking technology. Hela and A549 cells are cultured in the microfluidic chip under continuous media supplementation, mimicking the fluid microenvironment in vivo. Cell introducing processes are presented by the flow behaviours of inks with different colours. The two cell lines are identified by detecting folate receptors on the cellular membranes. The growth curves of the two cell lines are measured. The two cell lines cultured paralleled inside the microfluidic device are treated with FITC-FACC to investigate the targeting of FACC. The tumor targeting of FACC are also detected by in vivo imaging of Hela cells growth in nude mice models. The results indicate that the microfluidic device could provide a dynamic, uniform and stable fluidic microenvironment to test the tumor targeting of FACC nanoparticles.
“…The microfluidics-based methods have been widely used for the diagnosis of different diseases, while most of the microfluidic devices are still in the laboratory stage [8]. An important reason for this commercial failure is the disadvantages of the traditional materials used in these devices [9,10], such as polydimethylsiloxane (PDMS), polymethyl methacrylate (PMMA), and polypropylene (PP). For instance, although PDMS-based microfluidic chips have the advantages of miniaturization, integration, and automation, these devices cannot be preserved for a long time [11], and the operation process is complex [8].…”
Bladder cancer is the fourth most common cancer in men, and it is becoming a prevalent malignancy. Most of the regular clinical examinations are prompt evaluations with cystoscopy, renal function testing, which require high‐precision instrument, well‐trained operators, and high cost. In this study, a microfluidic paper‐based analytical device (μPAD) was fabricated to detect nuclear matrix protein 22 (NMP22) and bladder cancer antigen (BTA) from the urine samples. Urine samples were collected from 11 bladder cancer patients and 10 well‐beings as experiment and control groups, respectively, to verify the working efficiency of μPAD. A remarkable checkout efficiency of up to 90.91% was found from the results. Meanwhile, this method is feasible for home‐based self‐detection from urine samples within 10 min for the total process, which provides a new way for quick, economical, and convenient tumor diagnosis, prognosis evaluation, and drug response.
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