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64 Cards in this Set
- Front
- Back
Chemical that kills microorganisms, but doesn't damage the host. |
Antimicrobial drug |
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Drug made in a lab. |
Synthetic drug |
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Antibacterial. Some are formed naturally from bacteria or mold, like Penicillin. |
Antibiotic |
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The measure of how many organisms one drug targets. |
Spectrum of activity |
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Effects multiple categories of organisms. |
Broad spectrum |
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What is the advantage to broad spectrum antimicrobial drugs? |
Can target multiple organisms if you are not sure what the organism is. |
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What is the disadvantage to broad spectrum antimicrobial drugs? |
Kills normal flora. |
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Antimicrobial drugs that only affect one category of organisms. |
Narrow spectrum |
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What is the advantage of narrow spectrum antimicrobial drugs? |
They do not contribute to drug resistance. |
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What is the disadvantage of narrow spectrum antimicrobial drugs? |
If you don't know what the organism is, you cannot use a specific killer. |
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What are the actions of antimicrobial drugs? (How do they work-5 ways) |
1. Inhibition of cell wall synthesis 2. Inhibition of protein synthesis 3. Injury to plasma membrane 4. Inhibition of nucleic acid synthesis 5. Enzyme inhibition (stops organ growth) |
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Name 4 antibacterial drugs that inhibit cell wall synthesis: |
1. Penicillin 2. Cephalosporins 3. Vancomycin 4. Isomiazid |
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Penicillin nucleus has a: |
B-lactam ring |
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Penicillin is a ___________ spectrum drug. |
Narrow |
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What does penicillinase target? |
B-lactam ring formation |
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What is the prototype of natural penicillin? |
penicillin G |
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Semisynthetic penicillins are ___________ range. |
Broad |
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Cephalosporins is an alternative to ______________ that targets gram _______________. |
Pencillin; negative |
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Vancomycin is a ____________ spectrum that targets Gram ____________ and was designed as a solution to ________________. |
narrow; positive; MSRA |
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Isoniazid is designed to fight _____________ _________ and blocks/interferes with ______________________. |
Mycobacterium tuberculosis; mycolic acid/mycolic acid synthesis |
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Name the four antibacterial drugs that inhibit protein synthesis: |
1. Aminoglycosides 2. Tetracyclins 3. Macrolids 4. Oxazolidinones |
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Aminoglycosides fights Gram __________ organisms and is not used much due to lots of ____________ ___________. |
Negative; side effects |
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Tetracyclins is _____________ spectrum and is used against ___________ and ___________. |
broad; UTI; pneumonia |
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Macrolids are ____________ range. |
Narrow |
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An example of Oxazolidinones is ___________ and it is the latest drug against ____________. |
Zyvox; MSRA |
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What is the only antibiotic that causes injury to plasma membrane? |
Polymyxin B |
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Polymyxin B fights Gram _________ and stops the growth of ________________. It can be found in __________ __________ to treat __________. |
negative; pseudonoma; topical creams; burns |
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What are the two antibacterial drugs that are DNA/RNA inhibitors? |
1. Rifamycins 2. Quinolones and Fluoroquinolones |
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Rifamycins are structurally related to ______________. They inhibit ________ synthesis. They are used to fight _____________. |
macrolids; mRNA; tuberculosis |
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What is a side effect of Rifamycins? |
orange body secretions |
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Quinolones and Fluoroquinolones inhibit: |
DNA replication |
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What are two examples of quinolones/fluoroquinolones? |
nalidixic acid (UTI) and ciproflaxacin (UTI, anthrax) |
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Why is ciproflaxacin not recommended for children or pregnant women? |
It prevents cartilage formation |
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Sulfonomides are _____________ inhibitors. |
Enzyme |
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How are sulfonomides bacteriostatic? |
They prevent folic acid synthesis for bacteria |
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Name 5 antifungal drugs: |
1. Polyenes 2. Azoles 3. Flucytocine 4. Griseofulvin 5. Pentamidine |
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Why are antifungal drugs more challenging? |
Fighting eukaryotic cells. |
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What is an example of polyenes? |
Amphotericin B |
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What does polyenes fight and how do they fight it? |
systemic fungal infections; they interfere with sterols |
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Sterols in humans are called ____________. Sterols in fungi are called ______________. |
cholesterol; ergestron |
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Azoles interfere with ______________ and fight _______________________________. |
sterols; systemic and cutaneous infections |
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Flucytocine interferes with ________________________; has a __________ spectrum; fights ______________ mycosis. |
RNA biosynthesis; narrow; systemic |
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Griseofulvin inhibits ___________ __________. It fights ____________ and _____________ mycoses. |
fungal reproduction; superficial; cutaneous |
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How does pentamidine work? |
It binds to DNA; not sure after that. |
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What does pentamidine fight? |
Pneumocystis carinii |
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Name 7 antiviral drugs: |
1. Acyclovir 2. Ribavirin 3. Zidovudine 4. Relenza/Tamiflu/Amantadine 5. Indinavir 6. Isentress 7. Interferon |
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How does Acyclovir work? |
It mimics DNA to stop DNA replication |
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What is Acyclovir used against? |
genital herpes |
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Ribavirin resembles __________ and increases _________________. |
guanine; mutation rate of RNA virus |
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What does Zidovudine inhibit? |
reverse transcription |
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What is Zidovudine used against? |
HIV |
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How do Relenza, Tamiflu, and Amantadine work? |
They inhibit the enzyme neuraminidase, which is an enzyme that allows budding separation to occur. Once this separation is stopped, the virus can no longer grow/spread. |
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Indinavir is an anti ____________ drug that inhibits ____________. |
HIV; protease |
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Isentress is an ____________ blocker that blocks the integration process of ___________ into host ___________. It is given to people ___________. |
integrase; HIV; chromosome. Already being treated for HIV |
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Interferon have ____________ for ____________ treatment. |
cytokines; hepatitis |
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Name 3 antiprotozoan drugs: |
1. Quinine 2. Quinacrine 3. Metronidazole |
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Quinine is used against: |
malaria |
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Quinacrine is used against: |
Giardiasis |
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Metronidazole is used against: |
protozoa(eukaryotic) and obligate anaerobic bacteria(prokaryotic) |
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Name 3 antihelminth drugs: |
1. Niclosamide 2. Praziquantel 3. Mebebdazole, Pyantel pamoate |
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Niclosamide inhibits __________ production in the presence of O2. It targets _________ and _________. |
ATP; tapeworms; flukes |
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Praziquantel alters __________________ and targets ___________. |
plasma membrane permeability; tapeworms |
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Mebebdazole/Pyantel pamoate inhibits _____________ formation and is used against: |
microtubule; roundworm, pin worm, whip worm |
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How do microorganisms resist drug mechanisms? |
1. Block entry of drug 2. Inactivation by enzymes (ex. penicillinase) 3. Efflux of antibiotic (pump drug out of cell) 4. Alteration of target molecule (ex. change shape of cell) |