Unit 2 Topic 4Aii Medicine and Drugs Flashcards

1
Q

How do bacteria reprodue

A

binary fission (asexual reproduction in bacteria)
- bacteria splits in half
- under ideal condition, bacteria can split into two cells every 20 mins

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2
Q

How are bacteria used in experiments

A

cultured in experiments to investigate potential medciein

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3
Q

Define culture

A

large number of certain microorganism grown under desirably controlled lab conditions for scientific investigations

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4
Q

What are bacteria survival and reproduction conditions

A
  1. nutrients (glucose for respiration, amino acids for protein synthesis)
  2. oxygen / no oxygen (those respiring aerobically, no oxygen for those anaerobic)
  3. optimum temperature and pH (enzymes controlling metabolic processes to function optimally)
  4. water (hydrolysis reactions, solvent)
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5
Q

What are the precautions of culturing bacteria in experiments

A
  1. risk of arising a pathogenic mutant strain from completely harmless microorganisms
  2. risk of contamination of culture by pathogenic microorganisms from the environment
  3. risk of contamination of culture from microorganism from air or skin into the culture
  4. risk of contamination to the envrionment from the culture
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6
Q

What is antimicrobial

A

substances that kill microbes (bacteria, prevent growth of microbes)

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7
Q

Plants and its antimicrobial properties

A
  • evolved and developed range of chemical defences against microbes which invade and cause disease (antiseptic compounds, antibiotics)
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8
Q

What are the uses of plant’s antimicrobial properties

A
  1. exploited to develop new drugs to treat bacterial and fungal diseases
  2. produce plant extract containing antimicrobial chemicals to test its effect on growth of bacteria
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9
Q

Cotton’s antimicrobial properties

A

produce gossypol
- antiseptic that kills bacteria attacking cotton seeds

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10
Q

Willow bark’s antimicrobial properties

A

salicylic acid
- used as a cosmetic BHA
- chemically engineered into acetylsalicylic acid (aspirin) for painkilling
- Salicylic acid was extracted and purified and use for pain relief -> led to the development of aspirin in the form of a small white tablet

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11
Q

Cinchona tree’s antimicrobial properties

A

Example: Quinine sourced from the cinchona tree, used to prevent and treat malaria, allowing loggers and developers to work in the Amazon Basin

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12
Q

Example of mold’s antimicrobial properties

A

Example: Penicillin developed from mold, used in killing bacteria. Penicillin breaks down the cell wall (beta-lactam ring) of bacteria, killing the bacteria.

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13
Q

What is antibiotics

A

Alter the metabolic pathways of bacteria ( just one type ) -> antibiotics can also directly kill bacteria
* Only treats bacterial infections but not viral infections

Virus are not living, parasitic and they replicate within a host cell

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14
Q

Advantages of the antimicrobial properties of plants

A

1.Enable humans to be more successful at treating diseases, increasing life expectancy

2.Ensuring exact and reliable dosage of medication
- By allowing the production of medication with a known concentration of the active ingredient
- the levels of chemicals in any part of a plant varies with the age of the plant, season, time…

3.Allow analysis of chemical structure of active ingredients, enabling scientists to create synthetic versions
- Reducing the need to remove large amounts of plant material from environment
- Modifications carried out in the lab to make the active ingredient more effective

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15
Q

What is William Withering and digitalis soup

A
  • Found that foxgloves contained active ingredient (digitalis glycosides) for treatment of dropsy ( swelling of tissues by accumulation of fluid ) and heart failure
  • Found that foxgloves are poisonous to humans, hence made different concentrations of digitalis -> digitalis soup
  • Experimented on patients and found the most effective concentration that treats the patient without poison
  • Creating the drug digoxin
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16
Q

How does digoxin work

A
  • Causing the heart muscles to contract quickly and forcefully/ slowing heartbeat/ decreasing the size of the heart to increase the heart output
  • Patient produces large quantities of urine as kidneys recovered to remove excess fluid and their heartbeat became stronger and more regular
17
Q

Limitations of William Withering’s development

A
  1. did not purify and identify ingredients in this test (randomly mix concentration and feed to patients)
  2. no pre-clinical trials
  3. small sample size
  4. did not test on healthy people first
  5. no use of placebo / double-blind trials
  6. not ethical: many side effects, patients almost died
18
Q

What are factors to be considered in drug testing

A
  1. effective (cure prevents relievs)
  2. safe (non-toxic, benefits > harm, no unacceptable side effects)
  3. stable (stored under normal conditions)
  4. easily taken into and removed(
19
Q

Drug research

A
  1. Potential models of the drugs modeled using computers (Fit new structures into the active site of enzymes/ receptors that are important in disease processes)
  2. Patent gives the inventor the right to be the only one to produce and sell their invention for the next 20 years
  3. Drug is tested on human cell/ tissue culture/ whole organs in a lab
20
Q

What should be done for drug development

A
  • Design a suitable delivery system for the drug (ie. nasal spray, oral tablet, liquid medicine)
  • The drug has to be stable such that there is no risk of it breaking down to form something toxic or inactive before it works
  • Drugs are tested on animals to see if the drugs get into the cells easily, if they are chemically changed, excreted safely
21
Q

Phases of clinical trials

A

phase 1: testing on small number of healthy volunteers
phase 2: testing on slightly larger group of volunteers suffering from the target disease (100-500)
phase 3: testing on an even larger group of volunteer patients

22
Q

(past paper) Three-phase testing can be used to check for the safety and effectiveness of these chemicals. Describe the roles of phase 1 and phase 2. (3)

A
  • to test for side effects
  • to determine safe / minimum dosage / concentration
  • to determine if it is more effective than existing treatments
23
Q

What are the purposes and aims for each phase of clinical trials

A

phase 1
- side effects, correct dosage
phase 2
- double-blind trial with a placebo
- see how drug affects the disease in real patients
phase 3
- double-blind trial with a placebo
- effectiveness and safety of the new drug
- identify any unexpected adverse side effects

24
Q

What is placebo

A

One group receives the drug and the other group receives a placebo, which looks identical but contains no active ingredient

  • patients are not tol which group they are in
  • compare with treatment group to prevent false result in the effectiveness of drugs due to placebo
25
What is double-blind trial
- Neither the patients nor doctors know which patient is receiving the drug/ placebo - Reduces and avoids bias/ reducing the effect the attitude of either doctor/ patient may have on the result
26
What are the limitations of clinical trials
Difficult to obtain a complete set of results because many patients stop taking the medicine for various reasons, some don’t take it regularly.
27
What is peer review
- Review methodology and results of drug by other scientists to ensure testing is well designed and the results are accurate and significant - In similar research/ repeated research - Collect data/ compare whether evidence is similar or not - Support or reject the findings of the researcher.
28
What are the challenges of animal testing
- expensive - time consuming - ethical debates
29
What are the substitues of animal testing and its limitation
- Animals are replaced by tissue cultures and computer models whenever possible - Computer models and tests on cell/tissue cultures are not sufficient to move drug testing on people without animal testing - Hence animal testing must be carried out first (by law) - Test used are refined to cause minimum distress to the animals - More rats/ mice are used because they are less emotive
30
Why do tests on rats/mice are more valid
- their genetic-makeup of the strains is well known - they are small, easy to keep in humane conditions