Chapter 12- Drugs Flashcards
1
Q
Penicillin Group
A
An antibacterial drug that targets the cell wall. -Natural penicillin can be obtained through microbial fermentation -Consist of three parts: a thiazolidine ring, a beta-lactam ring, and a variable side chain
2
Q
Cephalosporin Group
A
- Majority of all antibiotics administered 2. Isolated from mold Cephalosporium acremonium 3. Contains beta-lactam ring 4. Broad spectrum of subgroups 5. Resistant to most penicillinases 6. Cause fewer allergic reactions than penicillins 7. Four generations of cephalosporins exist based on their antibacterial activity
3
Q
Bacitracin
A
- Drug that targets cell wall 2. Produced by a strain of Bacillus subtilus 3. Used in triple antibiotics
4
Q
Isoniazid
A
- Drug that targets cell wall 2. Used in treatment of active tuburculosis 3. Generally used in combination with two or three other drugs 4. Helps to prevent resistance
5
Q
Vancomycin
A
- Drug that targets cell wall 2. Narrow spectrum 3. Effective in treating staph infections that are penicillin and methacillin resistant
6
Q
Fosfomycin trimethamine
A
- Drug that targets cell wall 2. Alternate treatment for UTI caused by enteric bacteria
7
Q
Tetracycline Antibiotics
A
- Bind to ribosomes and block protein synthesis 2. Broad-spectrum 3. Gram positive and negative rods and cocci 4. Mycoplasmas, rickettsias, and spirochetes 5. Doxycycline and minocycline used for STD’s, lyme disease, typhus, cholera, acne, etc
8
Q
Chloramphenicol
A
- Broad spectrum and unique nitrobenzene structure 2. Blocks peptide bond formation and protein synthesis. Synthesized through chemical processes. 3. Very toxic to human cells so restricted use
9
Q
Erythromycin
A
- Large lactone ring with sugars attached 2. Broad spectrum 3. Low toxicity 4. Blocks protein synthesis by attaching to the ribosome 4. Used for mycoplasma pneumonia, chlamydia, pertussis, diptheria
10
Q
Clindamycin
A
- Broad spectrum 2. Derived from lincomycin 3. Causes adverse reactions in the GI tract so limited use
11
Q
Synercid
A
- Combined antibiotic from the streptogramin group 2. Effective against staph enterococcus species and streptococcus 3. Binds to sites on the 50Sribosome inhibiting translation
12
Q
Oxazolidones
A
- Inhibit the initiation of protein synthesis 2. NOT found in nature 3. Hoping that drug resistance among bacteria will be slow to develop 4. Used to treat infections caused by TWO of the MOST DIFFICULT clinical pathogens: MRSA and VRE
13
Q
Sulfonamide
A
- Antibacterial drug that targets folic acid synthesis 2. Sulfa drugs 3. Very first modern antimicrobial drug 4. Synthetic 5. Treats shigellosis, acute UTI, and certain protozoan infections
14
Q
Trimethoprim
A
- Antibacterial drug that targets folic acid synthesis 2. Inhibits the enzyme step immediately following the step inhibited by sulfonamides in synthesis of folic acid 3. Often given in combination with sulfamethoxazole 4. One of the primary treatments for pneumocystis jiroveci pneumonia in aids pts
15
Q
Sulfones
A
- Antibacterial drug that targets folic acid synthesis 2. Chemically related to sulfonamides 3. Lack their broad-spectrum effects 4. Key drugs in treating leprosy