Week 5 - Penicillin Flashcards
1
Q
What year where the first antibiotics developed?
A
- Salvarsan (1911)
- Prontisil (1935)
2
Q
How sulfonamides effected antibiotics?
A
- Proved fatal infections such as pneumonia can be managed by drugs
- Fostered improvements in microbiology facilities
3
Q
Sulfa drugs and their issues
A
- Narrow spectrum of action
- Problems with drug resistance
- Toxicity
4
Q
The penicillin mould (milestones)
A
- 1870 Pasteur’s germ theory
- 1871 Penicillin found to stop bacterial growth
- Curative properties of penicillin soaked dressings.
- 1928 Fleming took 2 weeks off and accidentally discovered it when he returned to no bacteria growth
- 1940 great success in animal trials
- 1941 first human trials
- 1942 Saved millitary infection in WWII
- 1945 Dorothy Hodgkin solved B- lactan ring problem
- 1957 first successful synthesis of penicillin
5
Q
Howard Florey
A
- Fixed instability and extraction issues
6
Q
Antibiotics Now?
A
- Face a huge problem with drug resistance and the rise of super bugs.
7
Q
AIDS and following infections
A
- Auto-immune deficiency syndrome
- Pnemonia
- Tuberculosis
- AIDS dementia
- Lymphomas
- Kaposis Sarcoma
8
Q
Retroviruses
A
- use reverse transcription
- converts RNA into DNA within infected cells
- integrates with host genome
- contain few genes so few targets for antvirals
- e.g. HIV
9
Q
Anti-Metabolite drugs
A
- anti metabolite drugs aimed to starve the tumor slowing growth
- Mercaptopurine
- 1950
- effective anticancer drug
- Zipovudine
- 1964
- ineffective against leukemia
- 1984, strong anti-HIV activity seen in HIV- infected
T-cells. However
10
Q
25 Drugs in 25 Years
A
- RTI’s -> Reverse Transcriptase Inhibitors
- PI’s -> Protease Inhibitors
- INI’s -> intergrase inhibitors
- FI’s -> Fusion Inhibitors
11
Q
Dr Ho?
A
- Cocktail therapy combination of many antiviral drugs in an attempt to overwhelm the illness. Effective against drug resistance
- HAART Highly Active Anti-Retroviral Therapy
12
Q
Short comings of Cocktail therapy
A
- rise of resistance lead to reduced effectiveness, cross resistance, increased mortality. This all lead to more toxic, expensive and complex alternatives