کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1242803 1495788 2016 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Impedimetric quantification of cells encapsulated in hydrogel cultured in a paper-based microchamber
ترجمه فارسی عنوان
کوانتیزاسیون نامتقارن سلولها که در هیدروژل کپسوله شده و در یک میکروسکوپ کاغذی ساخته شده است
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آنالیزی یا شیمی تجزیه
چکیده انگلیسی


• Cells were successfully seeded and proliferated in paper-based 3D environment.
• Paper-based cell culture was incorporated with impedance measurement.
• Electrical characteristics of cells/hydrogel construct has been investigated.
• Impedimetric quantification of paper-based cell culture has been demonstrated.

Recently, 3D cell culture technique was proposed to provide a more physiologically-meaningful environment for cell-based assays. With the development of microfluidics technology, cellular response can be quantified by impedance measurement technique in a real-time and non-invasive manner. However, handling of these microfluidic systems requires a trained engineering personnel and the operation is not compatible to traditional biological research laboratories. In this work, we incorporated the impedance measurement technique to paper-based 3D cell culture model and demonstrated non-invasive quantification of cells encapsulated in hydrogel during the culture course. A cellulose filter paper was patterned with an array of circular microchambers. Cells were encapsulated in hydrogel and loaded to the microchambers for culturing cells in 3D environment. At the preset schedule during the culture course, the paper was placed on a glass substrate with measurement electrodes for the impedance measurement. Cells in each microchamber was represented by impedance magnitude and cell proliferation could be studied over time. Also, conventional bio-assay was performed to further confirm the feasibility of the impedimetric quantification of cells encapsulated in hydrogel cultured in the paper-based microchamber. This technique provides a convenient, fast, and non-invasive approach to monitor cells cultured in 3D environment. It has potential to be developed for routine 3D cell culture protocol in biological research laboratories.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Talanta - Volume 147, 15 January 2016, Pages 628–633
نویسندگان
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