Exam I Flashcards

1
Q

1st Law of Motion (Law of Intertia)

A

A body in motion tends to stay in motion unless acted on by another force.

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2
Q

2nd Law of Motion (Law of Acceleration)

A

Acceleration of a body is in the direction of and proportional to the force (f), and that acceleration (a) is inversely proportional to the mass (m) of the body.

F = m x a

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3
Q

3rd Law of Motion (Law of Reciprocal Action)

A

For every action, there is an equal and opposite reaction; objects exert opposite forces on one another.

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4
Q

First Law of Thermodynamics

A

Energy cannot be created or destroyed.

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5
Q

Second Law of Thermodynamics

A

Energy moves toward greater entropy or randomness.

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6
Q

Third Law of Thermodynamics

A

Absolute zero (0K or -273.15 C) is void of all energy.

As a system approaches absolute zero, all processes cease, and the entropy of a system approaches minimum value.

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7
Q

Force

A

The amount of energy required to move an object.

Force = mass x acceleration

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8
Q

Pressure

A

Force over an area. Increasing the area in which force is applied results in a lower pressure.

P = f / a

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9
Q

Work

A

Transfer of energy by a force acting on an object as it is displaced.

Work (w) = force (f) x distance (m)

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10
Q

Energy

A

The capacity to do work (potential energy) or the exertion of force (kinetic energy).

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11
Q

Power

A

The rate at which work is done.

Amount of energy transferred or converted per unit time.

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12
Q

Force SI Units

A

Newton = 102 g weight

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13
Q

Pressure SI Units

A

Pascal (Pa) = 102 g / 1 m2

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14
Q

Work SI Units

A

Joule

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15
Q

Energy SI Units

A

Joule

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16
Q

Power SI Units

A

Watts

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17
Q

Radiation

A

Electromagnetic transfer of energy away from a warm body.

Largest contributor to heat loss.

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18
Q

Convection

A

Heat creates air currents. Bodies transfer kinetic energy to air molecules on the surface of the skin. Warmed air molecules rise and colder molecules replace them.

The second largest contributor to heat loss.

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19
Q

Conduction

A

Transfer of heat via contact with a less warm object. Heat exchange from high concentration to low concentration.

Smallest contributor to heat loss.

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20
Q

Evaporation

A

Heat loss includes moisture evaporation from the patient’s skin and exhaled water vapor.

Latent heat evaporation is the amount of energy per unit mass required to convert a liquid into the vapor phase.

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21
Q

Mitigating Radiation in the OR

A

Cover the head, a major contributor to heat loss.

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22
Q

Mitigating Convection in the OR

A

Blankets, forced air warming device, prevent draft.

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23
Q

Mitigating Conduction in the OR

A

Warm OR table, cover the table with blankets.

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24
Q

Mitigating Evaporation in the OR

A

HMEs, only prep areas needed.

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25
Q

Scalar Values

A

Magnitude only.

Possess no motion.

Includes mass, energy, and work.

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26
Q

Vector Values

A

Magnitude and direction.

Expresses motion and is described by force, speed, velocity, acceleration, distance, and displacement.

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27
Q

Accuracy

A

Closeness of a measured value to a standard or known value.

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28
Q

Precision

A

Closeness of two or more measurements to each other.

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29
Q

How can accuracy be improved?

A

Recalibration (ex. zeroing lines).

Maintain consistent experimental conditions.

Control external factors that can introduce variability.

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30
Q

How can precision be improved?

A

Education on the proper use of the device to use the device consistently.

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31
Q

Specific Gravity

A

The ratio of the density of a substance compared to the density of water.

Sg = density of object / density of water

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32
Q

Density

A

The measurement of how tightly a material is packed together.

D = mass / volume

Ex. g/dl

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33
Q

Baricity

A

The ratio of density of LAs compared to CSF.

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34
Q

Hypobaric

A

<0.999

Achieved by mixing LA with sterile water.

Rises to the highest point in the spinal column.

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35
Q

Isobaric

A

1.000

Achieved by mixing LA with NS or CSF.

Remains relatively at the site of injection.

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36
Q

Hyperbaric

A

> 1.0015

Achieved by mixing LA with 5% or 8% dextrose.

Sinks to lowest point in the spinal column.

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37
Q

Ions

A

Atoms that have gained or lost electrons from their natural composition.

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38
Q

Electron

A

Negatively charged subatomic particle.

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39
Q

Anion

A

Gained +1 electron and is negatively charged.

Ex. Cl-

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40
Q

Cation

A

Lost +1 electron and is positively charged.

Ex. Na+

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41
Q

Anion Gap

A

The imbalance of cations and anions

[Na + K] - [Cl + HCO3]

Normal = 8-12 mEq/L (with a normal albumin of 4).

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42
Q

Hydrogen Bonds

A

Hydrogen atom with slight (+) charge is attracted to a (-) atom/molecule.

Needs to be in a polar covalent bond.

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43
Q

Covalent Bonds

A

Share electrons rather than gain or lose them.

Can hold up to triple bonds.

Tends to be bonding between atoms that share similar electronegativity.

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44
Q

Nonpolar Covalent Bonds

A

Equal sharing of electrons.

Strongest bond.

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45
Q

Polar Covalent Bonds

A

Unequal sharing of electrons.

Second-strongest bond.

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46
Q

Ionic Bonds

A

One atom lost 1+ atoms (cations +), and the other atoms gains one or more electrons (anions -).

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47
Q

Functional Groups

A

The portion of the compound that undergoes chemical transformations or reactions.

They can be grouped into several classes with unique physical and chemical properties.

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48
Q

Hydrocarbons

A

A molecule that is made up of solely carbon and hydrogen atoms.

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49
Q

Saturated Hydrocarbon

A

Single bonded carbon chain with all available carbon bonds attached to hydrogen.

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50
Q

Unsaturated Hydrocarbon

A

One or more double or triple bonds between carbon atoms.

51
Q

Alkane

A

Hydrocarbon containing only single-bonded atoms.

52
Q

Ex. of Alkanes

A

Methane
Ethane
Propane

Anesthesia: Halothane (alkane + halogen)

53
Q

Halothane

A

Replace the H atoms with the halogens.

Not explosive, but it causes hepatotoxicity and cardiac depression.

54
Q

Alkene

A

Hydrocarbon with double-bonded carbon.

55
Q

Alkyne

A

Hydrocarbon with a triple-bonded carbon.

56
Q

Cycloalkanes

A

Saturated hydrocarbons in a ring.

Ex. Cyclopropane

57
Q

Arene

A

One or more double bonds in a benzene (hydrocarbons) ring (aromatic hydrocarbons).

58
Q

Groups without carbonyls (Heteroatomic)

A

Ethers
Alcohols
Epoxides

59
Q

Groups with carbonyls (Carbonyl Compounds)

A

Aldehydes
Ketones
Carboxylic acids
Carboxylic acid derivatives (esters)
Acid Anhydrides
Acyl Halides
Amides

60
Q

Alcohols

A

R-OH

Contains a hydroxyl group (-OH)

61
Q

Ex. of Alcohols

A

Cholesterol
Methanol
Ethanol (ethane + alcohol).

62
Q

Ether

A

R-O-R’ or C-O-C

Oxygen single bonded to 2 carbons.

63
Q

Ex. of Ethers

A

Inhalation anesthetics

Diethyl ether = first inhalation anesthetic.

64
Q

Ex. of Halogenated Ethers

A

Isoflurane
Desflurane
Sevoflurane

65
Q

Ester

A

Also called carboxylic ester because it is derived from a carboxylic acid.

A carbon group replaces hydrogen.

-COOC

66
Q

Ex. of Esters

A

LAs containing 1 “i”

Benzocaine
Cocaine
Procaine

67
Q

Carbonyl

A

Carbon double bonded to oxygen (C=O)

68
Q

Carboxyl Group

A

Carbon double bonded to (C=O) bonded to a hydroxyl group (-OH) = (C=O-OH)

Carbonyl + Hydroxyl

69
Q

Carboxylic Acid

A

A compound that contains a carboxyl group (C=O-OH).

Considered a combination of two functional groups.

Ex. alcohol + carbonyl (C=O + -OH)

70
Q

Amines

A

Carbon-nitrogen bonds (called an amino group).

N can be bonded to 1-4 carbons (primary to quaternary).

71
Q

Ex. of Amines

A

Atropine
Glycopyrrolate

72
Q

Amino Acids

A

Amine + carboxylic acid

Molecules contain both amine (carbon to nitrogen bond) and a carboxylic (C=O-OH) functional group.

73
Q

Amides

A

Molecules containing nitrogen atoms connected to a carbonyl group.

Nitrogen + carbonyl group

R-C=O-N-R

74
Q

Ex. of Amides

A

LAs with 2 “i’s”

Lidocaine
Prilocaine
Bupivicaine

75
Q

Ketones

A

Carbonyl group boned to two carbons.

(C-C=O-C)

76
Q

Aldehyde

A

Carbonyl group bonded to a hydrogen.

(C-C=O-H)

77
Q

Thiols

A

Contains a sulfhydryl group (-SH) bonded to a tetrahedral carbon.

78
Q

Disulfide Bonds

A

(-S-S-)

Important in protein folding.

79
Q

Phase 1 Metabolism

A

Metabolic process that introduces or uncovers polar functional groups through oxidation, reduction, and/or hydrolysis.

Typically uses CYP450

Uses enzymes called oxidases to unmask or introduce polar groups on the drug.

80
Q

OIL RIG

A

Oxidation is loss = 1+

Reduction is gain = 1-

Electrons are negatively charged, so the gain of electrons leads to a reduction of charge.

81
Q

Oxidation

A

Loss of electrons = 1+

The ion or molecule that accepts electrons is called the oxidizing agent - by accepting electrons, it oxidizes the other element.

82
Q

Reduction

A

Gain of electrons = 1-

The ion or molecule that donates electrons is called a reducing agent - by giving electrons, it reduces the other element.

83
Q

Hydrolysis

A

Most carbohydrates and triglycerides are metabolized through hydrolysis.

84
Q

Phase II Metabolism

A

Metabolic processes that involve the conjugation of functional groups with endogenous polar molecules.

Ex. Sulfation, glucuronidation, amino acid glutathione.

85
Q

Conjugation

A

Forming glucuronides, sulphuric esters, sulphamates.

Results in the production of compounds that are more ionized and more water soluble than parent compounds.

86
Q

Glycolysis

A

Process of breaking down of glucose into pyruvate (yields 2 ATP).

87
Q

Gluconeogenesis

A

Process of generating glucose from non-carbohydrate sources.

88
Q

Glycogenesis

A

Process of converting glucose molecules into glycogen.

89
Q

Glycogenolysis

A

Process of breaking down glycogen into glucose.

90
Q

Citric Acid Cycle Totals

A

38 ATP
6 CO2
10 NADHs
2 FADH2s

91
Q

Oxidative Phosphorylation

A

It involves the electron transport chain.

1 molecule of glucose = 32 ATP

Requires oxygen.

92
Q

Beta Oxidation

A

Utilization of fats as an energy source.

Yields 129 ATP per fatty acid molecule.

Yields ketones.

93
Q

Urea Cycle

A

A process in the liver that converts toxic ammonia into less harmful urea.

Urea is excreted in the urine.

94
Q

Where does ammonia come from?

A

By-product of amino acid catabolism.

95
Q

Name two parts that make up organic molecules

A

Carbon
Hydrogen

96
Q

Why are functional groups important?

A

They are the compound that undergoes chemical transformations or reactions.

97
Q

3 Types of Steriods

A

Cholesterol
Testosterone
Estrogen

98
Q

Anesthetic agents are considered what kind of ethers?

A

Halogenated ethers

99
Q

4 Categories of Biomolecules

A

Proteins
Lipids
Carbs
Nucleic acids

100
Q

How are carbs classified?

A

Mono-
Di-
Poly-
-Saccharides

101
Q

Cis-Isomer

A

Hydrogen atoms are on the same side of the two carbon atoms.

Double bond creates a bend in fatty acid chains.

Liquids at room temp.

102
Q

Trans-Isomer

A

Hydrogen atoms are on the opposite sides of the two carbon atoms.

Double bond does NOT cause a bend in the fatty acid chain.

Solid at room temp.

103
Q

Most carbs/trigs are metabolized through what type of reaction?

A

Hydrolysis

104
Q

Three ways proteins are denatured?

A

Heat

Acidity

Heavy metal ions

105
Q

RNA

A

Contains ribose as a base.

Has an extra hydroxyl group.

Thymine

Single strand

106
Q

3 Types of RNA

A

Messenger RNA (mRNA)

Ribosomal RNA (rRNA)

Transfer RNA (tRNA)

107
Q

Examples of Carbonyl Groups

A

Amides
Carboxylic acids
Aldehydes
Ketones

108
Q

Nucleotides are made up of what 3 parts?

A

Phosphate group

Nitrogenous base

Pentose sugar

109
Q

What type of molecule is ATP?

A

Nucleic acid

110
Q

DNA

A

Contains deoxyribose as a base.

DNA has uracil

Double-strand

111
Q

Bonds in organic compounds

112
Q

Bonds in inorganic compounds

113
Q

Chiral

A

Cannot be superimposed.

Ex. Hands

114
Q

Achiral

A

Can be superimposed.

Ex. Water bottle

115
Q

Isomers

A

Compounds that contain the same number and types of atoms but differ in how those atoms are arranged in space.

116
Q

Constitutional (Structural) Isomers

A

Same molecular formula but a different connectivity.

Same molecular formula, but different bonding arrangement amon the atoms.

117
Q

Stereoisomers

A

Identical molecular formula and arrangement of atoms; however, they differ in spacial orientation.

Includes: diastereomers and enantiomers

118
Q

Enantiomers

A

Stereoisomers that are mirror images but not superimposable.

If the carbon is attached to two of the same atom, it is achiral and may be superimposable.

Racemic mixtures of drugs, 50% of each enantiomer.

119
Q

Dextrorotatory (d, i)

A

Rotates light in a clockwise direction.

Ex. Dextrose

120
Q

Levorotatory (l, -)

A

Rotates light in a counterclockwise direction.

Ex. Levalbuterol

121
Q

Enantiomer Nomenclature

A

Configured around a stereocenter as R (right-handed; rectus) or S (left-handed; sinister).

Ex. S-Epinphrine + R-Epinephrine

122
Q

Diastonomers

A

Stereoisomers that are NOT superimposable and are NOT mirror images.

Ex. Cis/Trans-isomers

123
Q

3 Components of Amino Acids

A

Amino group

Carboxyl group

Side chain R group