Exam Microsystems and nanotechnologies Flashcards

1
Q

Top-down micro and nano fabrication technologies involve several sequential cycles of what unit operations?

A

Unit operations:

  1. Deposition
  2. Lithorgaphy
  3. Etching
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2
Q

What are MEMS?

A

MEMS are microelectromechanical systems

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3
Q

Why is MEMS important and needed?

A

The MEMS add mechanical functionalities to micro fabricated devices

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4
Q

Name one important difference in microfluidics compared to fluid in macro scale!

A
  1. In microfluidics we have large surface-to-valume ratios

2. In microfluidics we have laminar flow

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5
Q

Name some potential disadvantages of Lab-on-chip systems for bio sensing with respect to standard laboratory procedures

A

One potential disadvantage is the difficulty to mix different reactant fluids

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6
Q

Name one application involving the use of top-down microfabricated devices in neuroengineering

A

Microelectrode arrays

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7
Q

Name some standard multi electrode array neural probes (MEA)!

A
  1. Utah probes

2. Michigan probes

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8
Q

Name some facts about MEA (Multielectrode arrays)!

A
  1. MEAs can reach up to 1000 recording sites in an area of the order of 1cm2
  2. the MEAs can stimulate fibers at different depths of the neural tissues
  3. MEA can be used both for recording and stimulation
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9
Q

Name one application and some characteristics for the Microfluidic lab-on-chip device!

A
  1. The lab-on-chip device can function as platforms for neuron culture and manipulation
  2. Microfluidic lab-on-chip can integrate micro electrodes for electrophysiology studies of single neurons
  3. Microfluidic lab-on-chip can allow co-culture of different types of neural cells and other cells
  4. Microfluidic lab-on-chip can allow spatially controlled growth of neuritis
  5. Microfluidic lab-on-chip CAN’T be integrated with brainslices from test animals
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10
Q

What is the main motivation for the use of lab-on-chips to function as platforms for neuron culture and manipulation?

A

The main motivation is the ability to control the microenvironment surrounding neuronal cells

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11
Q

What particle size should the nanoparticle be for a long lifetime and be able to reach their destination (the brain)?

A

The particle size should be of the order of 50 nm

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12
Q

In what scale is top-down micro and nanofabriation pattern materials in?

A

20 nm

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13
Q

Name some advantages of Lab-on-chip systems with respect to standard laboratory procedures!

A
  1. portability
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14
Q

What device is cell cultures performed in microfluidic chips?

A

Cell-chips

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15
Q

Name some unique capabilities of cell-chips!

A
  1. precise control of cellular microenvironment
  2. ability to integrate on-chip techniques for analysis if biochemical reactions in cell
  3. ability to fractionate heterogenous cell populations
  4. you CAN’T produce large number of cells
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16
Q

Name one application involving bottom-up technology in neuroengineering!

A

nanoparticles for drug delivery across the blood-brain barrier

17
Q

Name the main advantage with multi electrode arrays (MEA) with respect to conventional single electrodes ot tetrodes!

A
  1. Multielectrode arrays provide large number of electrodes separated by small distances
18
Q

Why has nanotheranostics been considered for therapy of brain diseases?

A

Nanoparticles can be functionalized to cross the blood brain barrier and assist image-guided therapy