Exam 2 Flashcards

1
Q

Calcium (Phosphate/Sulfate) is a main component of _____

A

PHOSPHATE!

Bone

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2
Q

Integrins are

A

intracellular transmembrane proteins that Govern signals and cell growth, FACILITATE FOCAL ADHESIONS

NOT Differentiation

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3
Q

Endothelial cells in the _______ layer of a blood vessel experience shear stress as blood flows through the vessel

A

Tunica INTIMA contains endothelial cells

Tunica Media = Muscle cells

Tunica Adventitia contains fibrous collagen

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4
Q

Bioactive materials act to elicit

A

specific biological responses at the tissue/material interface in attempts to enhance bond formation

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5
Q

Osteoinductivity is the ability of a material to:

A

encourage osteoCLAST attachment and migration

Osteoconductivity = OsteoBLAST

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6
Q

The 3D structure of a protein can influence the function of the protein

A

True

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7
Q

Hydrogel swelling can be activated by

A

pH, temperature or electric field

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8
Q

Surface topography (roughness) of a biomaterial can influence

A

cell attachment

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9
Q

Secondary Ion Mass spectroscopy allows analysis of surface based on

A

mass + charge ratio
or mass + ion composition
or mass and functional groups

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10
Q

Experimental data has shown that fluid flow over osteoblasts can

A

align actin filaments

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11
Q

Complements are (Intracellular/proteins in the bloodstream) that are capable of activating the immune system

A

PROTEINS IN THE BLOODSTEAM

not intracellular

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12
Q

Surface modification at the nanolevel is a

A

top down approach

Surface mod = top down

Bottom up is when the whole thing is nano

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13
Q

Size of imprint in photolithography depends on

A

The wavelength of the beam

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14
Q

The pattern of focal adhesions is dictated by

A

nanoscale surface features

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15
Q

Nanocrystalline hydroxyapatite enhances

A

bone growth in vivo

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16
Q

When testing the release of drug from a degradable polymer, temperature IS important because

A

It influences rate of diffusion and degradation and thus drug delivery

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17
Q

Growth factors affect:

A

Cell growth, proliferation, AND DIFFERENTIATION

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18
Q

Experimental data discussed has shown that dynamic loading:

A

HAS an effect on the rate of bone repair (Wolff’s law)

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19
Q

Nanoscale material surfaces can cause

A

altered protein adsorption

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20
Q

In general, it is advisable to obey the hierarchical structure of tissue when designing a tissue engineering scaffold

A

True

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21
Q

Contact angle measurement is a way of directly determining strength of adhesion between a cell + substrate

A

False! It is to determine the hydrophilicity or hydrophobicity of a material

and it is SURFACE characterization

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22
Q

Experimental data has shown that all drugs are delivered at the (Same/different) rate when incorporated into (CPP:SA) polymers

A

Different

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23
Q

Actin expression (can/cannot) be influenced by the physical forces associated with fluid flow

A

CAN

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24
Q

The (Yield/Ultimate) stress is indicative of the max load a material can sustain prior to failure

A

ULTIMATE

Yield stress is point between elastic/plastic

Elastic modulus is

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25
Nanotechnology encompasses:
Any material with at least 1D below 1um in measure, any material between 1-100 nm in length, any material between 1-1000 nm in length ALL of the ABOVE
26
Which of the following is not a type of cell-matrix adhesion: A. Microtubule B. Fibrillar adhesion C. 3D matrix adhesion D. Focal adhesion
A. Microtubule it is in the cytoskeleton not the matrix at all
27
Which characterization method involves analysis of construct's pore structure
Mercury Porosimetry Not SEM or FTIR spec
28
Top-down approach of nanoscale biomaterials development:
Modification of structures larger than nano | NOT Nanotubes
29
Bottom up approach of nanoscale development:
Involves formation of structures originating at the nanoscale size level AND the nanotubes one - unless there's no answer with both, in that case select "involves formation of structures that originate at nanoscale level"
30
Altering the ratio of CPP:SA can influence what
Influence rate of degradation of the polymer AND Influence rate of Drug delivery But it does NOT control rate of biocompatibility of the polymer Careful, it's B and C if it's about rate of delivery/degradation, but NOT if it is about biocompatibility!
31
T/F : Cytoskeleton's only function is to provide strength to the cell
THIS IS FALSE! It also allows for structure and transport of molecules for signaling and sensing
32
Cytoskeleton composed of:
Composed of 3 different proteins: Actin microfilaments, Intermediate filaments, and microtubules
33
Where are actin microfilaments found?
Mostly just below the plasma membrane **Might be the one that's false though, do process of elimination, and look out for the word "ONLY"
34
ECM is communicated to the nucleus via the cytoskeleton (T/F)
True
35
Which statement is true about the body and bone
Body responds to weightlessness by DECREASING bone formation due to the LACK of mechanical forces applied to the skeletal system Watch out, this may change on the exam ---
36
Which statement is true about the body and bone Scenario 2 - Flexible/inflexible vessel
When designing a synthetic vessel, you need a FLEXIBLE compliant structure to minimize smooth muscle cell proliferation at the anastamosis between the native vessel and synthetic vessel
37
T/F: Foreign body giant cells are indicative of a non-inflammatory response
False It IS an inflammatory response
38
Which statements are true about inflammation:
Neovascularization is part of the wound healing process Newly formed vessels are part of granulation tissue Simple implantation of biomaterial constitutes a would and therefore initiates the wound healing response All true!
39
Which 3 intracellular components contribute to the mechanical integrity
Microtubules Actin microfilaments Intermediate filaments Integrins are cell-ECM attachments
40
Which method of surface analysis provides a unique fingerprint
X-ray diffraction | Also FTIR
41
What is NOT a function of the ECM
Provide energy for intracellular protein production is NOT a function of the ECM
42
Functions of the ECM
Facilitate cell-cell communication Store and release important molecules Aid in cell attachment
43
Which method is not related to surface analysis
Gel permeation chromatography
44
Which methods are for surface analysis
FTIR Xray photoelectron spec Secondary ion mass spec
45
Tissue response to inert materials involves
Thin fibrous capsule formation NOT: foreign body giant cells/inflammation Slow healing
46
3 complications associated with biomaterials
1. Biodegradation effects in body (toxicity) 2. Calcification 3. Inflammation, reduction in blood flow and pain
47
2 Reasons why in vivo testing is important
1. See the negative effects of material on the body in controlled realistic conditions 2. See if the desired effect is achieved in controlled realistic conditions
48
2 Mechanisms through which nanotubes can be used as drug delivery vehicles
1. Filling the hollow nanotube w/ drug | 2. Attach drug to surface of nanotube
49
Advantages of nanotubes vs. other strategies
Carbon Nanotubes are good conductors and have good mechanical properties (strong). Also, they are permeable to cell membrane and can reach destinations that other materials cannot.
50
What 2 parameters control the nanofiber dimensions during the process of electrospinning and how does manipulating these alter the nanofibers produced?
The NEEDLE GAUGE can affect the size of nanofibers formed - smaller/narrower needles = LARGER nanofibers, and vice versa. -- CAREFUL - small needles = larger fibers Increasing the CONCENTRATION OF MATERIAL in the solvent will INCREASE the diameter of the nanofiber formed.
51
What is focal adhesion and what is role in transmitting extracellular signals to the intracellular environment?
Focal adhesions are made of integrins and cadherins and allows for the transmission of signals to the cell from the ECM. Integrins produce FA complexes, and adherins/cadherins anchor FAs to the actin cytoskeleton. MHC-I involves focal adhesion proteins for INTRACELLULAR interactions while MHC-II involves focal adhesion proteins with EXTRACELLULAR interactions.
52
2 Advantages of nanoparticles for drug delivery
1. Nanoparticles have more similar size to biomolecules 2. The produce no immune response since they can pass through the cell membrane 3. They can make dosing more manageable and target specific areas (like low pH areas for cancer cells.)
53
What is rationale for using nanofibers as scaffolds for tissue engineering?
Nanofibers can be created using electrospinning or reverse self-assembly. Nanofibers increase surface area to allow for increase in CELL PROLIFERATION, CELL ADHESION, and PROTEIN ADSORPTION.
54
3 Characterization techniques, surface or bulk- and what they inform on
1. Mercury porosimetry - bulk - uses mercury to determine the pore structure of material 2. FTIR - Surface - samples functional groups on the outside surface - can determine what type of sterilization to do 3. Contact angle goniometry - surface - determine the hydrophilicity of a substance. Low angle = hydrophilic
55
2 Advantages to delivering peptides from a biomaterial rather than proteins?
1. Peptides do not have an exact form - more adaptable to the body. Proteins have a set structure and cannot adapt as well. 2. Peptides more readily received by the cell membrane and produce no immune response. Peptides allow for smoother delivery with less immune response.
56
Surface (Smoothness/roughness) promotes faster blood coagulation
ROUGHNESS
57
3 different in vitro cell proliferation assays
1. Colormetric assays 2. Dead cell assays 3. Cytometer
58
2 reasons why in vitro testing is important
1. Parameters like temperature or acidity can be controlled | 2. Cell proliferation and adhesion can be tested before a live specimen is used.
59
3 Mechanisms by which nanostructured surfaces modulate cell functions
1. Surface roughness can alter protein adsorption + promote blood coagulation 2. High surface area/volume ratio, improves cellular uptake 3. Very small size, can permeate the cell membrane and have targeted delivery of active ingredient
60
5 different types of innate immune systems What do they mean? Option 1 is the immune responses -->
1. Minimal response - thin collagenous membrane, response to PTFE and ceramics 2. Chemically induced acute - absorbable sutures + thermoset resins 3. Physically induced - particulates of PMMA or nylon 4. Chromic severe inflam. - degradable materials w/ toxins or metal particulates 5. Necrotic response = premature death of cells - bone cement or surgical additives -
61
5 different types of immune systems Ask what they mean, cells or responses? option 2 - types of cells
1. Natural killer cells - detect low levels of MHC I 2. Mast cells - Release histamine + heparin 3. Neutrophils - inhibit growth of pathogens 4. Foreign body giant cell - collection of fused macrophages - Chronic inflammation/large foreign bodies 5. Macrophages - Phagocytize pathogens 6?. Eosinophils - release granules like neutrophils