CEPI0913 Introduction to Nanotechnology: Drug Delivery Systems

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CEPI0913 Introduction to Nanotechnology

Questions:

  1. Briefly, what (who, when?) are the origins of cell culture methods?
  2. What are some types of cells that are routinely cultured?
  3. List the issues and remedies of basic cell culture.
  4. What are some disadvantages of 2D cell culture?
  5. What are self-assembling peptide structures, and what is their interest for cell culture?
  6. What is meant by cellularizing a nanoscaffold, and what are some means to effect such?

Chapter 7:  “Nanoparticle-Based Drug Delivery”

  1. What is the difference between tumor-specific antigens and tumor-associated antigens?
  2. What is the difference between active targeting and passive targeting of e.g., tumor cells?
  3. What are PLAs and how are they designed for controlled release?
  4. Describe some of the features of penicillin delivered by PACA, including a method to evaluate its effectiveness.
  5. What are some criteria for nanoparticle based drug delivery systems?
  6. What is a Kaplan-Meier survival curve, and what is its use?
  7. What does it mean to derivatize C60 (bucky balls), and what does it enable?
  8. Describe the transfection assay to assess the uptake of C60 into cells.
  9. What is the significance of Figure 7.23?
  10. What are some advantageous features of chitosan for drug delivery?

Chapter 8 “Nanodiagnostics”

  1. How are most nanofluidic channels fabricated? (Note this is different than microfluidics which are made in plastic by machining or laser cutting.)
  2. What type of sensor (DNA, immunoassay, cell, metabolite) is shown in Figure 8.4?
  3. What is a translocation event signal in a nanopore and how is it related to DNA sequencing?
  4. McDevitt’s Oral Cancer Chip took a picture of captured cells from an oral biopsy. What six criteria were cells evaluated to discern cancer or pre-cancer?
  5. What is SERS?, how is it used to detect molecules, and why is it more conducive to multiplexing?
  6. What does in vivo nanodiagnostics accomplish?

Chapter 9 “Government Influence on Nanotechnology

(We’ll skip this chapter.  You can read it at your own leisure, especially if you’re interested in funding.)

Chapter 10: “Future Concepts in Nanomedicine”

  1. What powers a rotaxane motor, how fast does it turn, how long does it last?
  2. How do you make the DNA motor of Tan et al open and close?
  3. What powers J Wang’s nanowire motors? How fast do they go?
  4. Have ‘nano-gears’ been demonstrated? What do you suppose might be some challenges?
  5. What is theranostics?
  6. What are respirocytes?
  7. What are some nano-based therapies for serious kidney disease?
  8. The resolution of conventional microscopy/endoscopy are limited by the wavelength of light used? What is one approach to circumvent this?  Briefly describe.

CEPI0913 Introduction to Nanotechnology

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