Ch 14: Lab-on-a-chip Biosensors Flashcards

1
Q

What are the benefits of paper-based lab-on-a-chip devices?

A

They are cost-effective, portable, and allow fluid flow without pumps due to capillary action​

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2
Q

What is PCR, and how is it conducted on lab-on-a-chip devices?

A

PCR amplifies DNA by cycling through denaturation, annealing, and extension. Lab-on-a-chip devices miniaturize this process for faster and more efficient diagnostics

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3
Q

Q: What is a lab-on-a-chip (LOC)?

A

A: A miniaturized device that integrates multiple laboratory processes onto a single chip.

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4
Q

Q: What is photolithography?

A

A: A process using light to transfer patterns onto a substrate for microfabrication.

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5
Q

Q: Why is soft lithography popular in LOC fabrication?

A

A: It is cost-effective, flexible, and compatible with various materials.

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6
Q

Q: How is capillary electrophoresis used in LOCs?

A

A: To separate molecules based on their charge and size.

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7
Q

Q: What is electroosmotic flow (EOF)?

A

A: The movement of liquid in a microchannel induced by an electric field.

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8
Q

Q: What are the strengths of using EOF for fluid delivery?

A

A: Precise flow control and integration with other microfluidic processes.

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9
Q

Q: How does a microfluidic mixer work?

A

A: By combining fluids at the microscale using designs like zig-zag channels or herringbone patterns.

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10
Q

Q: What is PCR, and why is it used in LOCs?

A

A: Polymerase chain reaction, used for amplifying DNA, is miniaturized in LOCs for rapid diagnostics.

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11
Q

Q: What is LAMP, and how does it differ from PCR?

A

A: Loop-mediated isothermal amplification is faster and simpler, as it doesn’t require thermal cycling.

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12
Q

Q: What are the benefits of paper-based LOCs?

A

A: Low cost, easy fabrication, and fluid handling without external pumps.

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13
Q

Q: How are optical fibers used in LOCs?

A

A: For precise light delivery and collection in optical sensing applications.

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14
Q

Q: What is a microfluidic channel?

A

A: A small conduit on a chip used for fluid transport and analysis.

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15
Q

Q: How are microchannels fabricated?

A

A: Using techniques like photolithography, etching, and soft lithography.

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15
Q

Q: What are the advantages of integrating PCR into LOCs?

A

A: Reduced reaction time, sample volume, and contamination risk.

16
Q

Q: What is the role of optical detection in LOCs?

A

A: To analyze fluorescence, absorbance, or scattering signals from the sample.

16
Q

Q: What is isothermal nucleic acid amplification?

A

A: Techniques like LAMP that amplify DNA/RNA at a constant temperature.

17
Q

Q: Why are syringes used in LOCs?

A

A: For precise fluid injection into microfluidic channels.

18
Q

Q: How does LOC enable point-of-care testing?

A

A: By integrating diagnostics into portable, easy-to-use devices.

18
Q

Q: What are common LOC applications?

A

A: Disease diagnosis, drug testing, and environmental monitoring.

19
Q

Q: Why is miniaturization key in LOC development?

A

A: It reduces reagent use, speeds up reactions, and enables portability.

20
Q

Q: Compare photolithography and soft lithography.

A

A: Soft lithography is cheaper and more versatile.

21
Q

Q: What is electroosmotic flow (EOF)?

A

A: Fluid motion induced by an electric field in a microchannel.

22
Q

Q: How do EOF and syringe pumps differ?

A

A: EOF offers precise flow control; pumps deliver higher pressures.

23
Q

Q: Why is a microfluidic mixer important?

A

A: To ensure thorough mixing in small volumes.

24
Q

Q: What are the benefits of paper-based LOCs?

A

A: Low cost, portability, and capillary-driven fluid flow.

25
Q

Q: How is PCR conducted in LOCs?

A

A: By miniaturizing thermal cycling to amplify DNA on a chip.

26
Q

Q: What is LAMP?

A

A: Loop-mediated isothermal amplification, a simpler alternative to PCR.