Free Quote
With the advent of microfluidic technology, methods of cell culture are meeting a technological revolution. A variety of unique advantages of microfluidic chips provides cell culture more possibilities. As a professional microfluidic chip development services provider, Creative Biolabs also keeps our eyes on microfluidic chip-based cell culture. With an advanced technology platform and rich experience, we are confident in providing high-quality microfluidic chip development services for cell culture.
There is an immediate need to develop reliable tissue models for pre-clinical research. It costs $2.5 billion and 10-15 years on average to bring a drug to market. To decrease drug development costs, it is critical to improving pre-clinical screenings' predictive power for excluding ineffective/toxic candidates as early as possible. Currently, the typical workflow in pre-clinical tests is to screen drug candidates on statically cultured cells followed by animal (e.g., rodent) experiments. However, both models have inherent limitations. In this context, microfluidic technologies-based cell culture is born as a new platform in a more physiologically relevant manner. Microfluidics is devices with mm-scale fluidic channels for controlled flow in small volumes (mL). These cell-laden microfluidic devices are often referred to as organs-on-a-chip. This technology can overcome the limitations of both static cell cultures and animal studies.
Advantages of Microfluidics-based Cell Culture Platform |
|
Microfluidics is a technique to handle small volumes, such as nanoliters to femtoliters, and it has been demonstrated to be a very powerful tool for single cell culture. Different from bottles or flasks, which typically handle milliliter to liter volumes, microfluidic systems can scale down the volume by many orders of magnitude to the nanoliter or below the nanoliter scale. This makes high-throughput single cell culture possible. In addition, microfluidic systems with different operation mechanisms can also manipulate biological and chemical components, which enables the manipulation of the microenvironment for cell growth. Furthermore, microfluidic systems are also capable of splitting cultured cells for downstream analysis with multiple tools.
Fig. 1 Microfluidic cell culture.1,3
Digital microfluidics (DMF) is, at heart, a technique that is used to manipulate droplets of liquid, so it is well suited for cells that grow while suspended in THE liquid culture medium. Hence, no modification is required to manipulate suspended mammalian cells and other microorganisms that are commonly cultured in suspension (e.g., bacteria, algae, yeast). Cells suspended inside droplets may be further sorted or manipulated by the use of electrical, optical, or magnetic forces.
With years of experience focusing on the field of microfluidic chip development, Creative Biolabs has accumulated extensive experience from step-by-step practice. During this long period of exploration and growth, we have gradually optimized our technology platform and organized a staff of excellent experts specialized in microfluidic and cell culture. We are dedicated to supporting cell culture services by developing high-quality microfluidic chips. If you are looking for a novel method to tackle your difficulties in cell culture, please don’t hesitate to contact us for more information.
The findings discussed in the articles related to cell culture on microfluidic chips are presented.
1. Detecting cell-secreted growth factors in microfluidic devices using bead-based biosensors
Fig. 2 A microsystem for the cultivation of hepatocytes and for the detection of secreted growth factors.2,3
Kyung Jin Son and colleagues detail a combined microsystem that features a microfluidic chip along with fluorescent bead-based tests aimed at identifying hepatocyte growth factor (HGF) and transforming growth factor (TGF)-β1 released by primary hepatocytes.2,3 The main characteristic of the device is a slender hydrogel barrier that divides the cell culture chamber from the sensing chamber. This arrangement enables the sensing beads to be positioned near the cells while remaining in a separate chamber. The structure of this device facilitates the injection of sensing beads without interfering with adjacent cells, allowing for localized detection of crucial secreted factors on-chip.
References
For Research Use Only. Not For Clinical Use.