Ive had a good look through the course book and I have to say that i'm very impressed.
For a short course the OU have gone to a lot of trouble to produce a really nice book thats easy to follow.
The book is 167 pages long and is divided into 10 chapters as follows:-
1. What's behind it all?
A gentle introduction to the course, including an overview of drug development and testing as well how chemists name structures. It includes a brief foray into the modelling kit (more on this later) as well as atomic structure and some bonding theory.
Nothing too taxing. In fact a lot of the information I found I could recall from my earlier study, which is a good sign. One revelation is that sulphur is now called sulfur!! This happened in 1992 so im amazed that I always knew is as sulphur.
2. Ouch - that hurts!
This chapter briefly covers why we feel pain before moving onto that wonder drug, aspirin and how it works. There is more modelling activities using the kit as well as some additional chemistry involving functional groups, esterification and isomerisation.
Another revision chapter for me, at least from the chemistry side of things. I found the aspirin story fascinating and hope that the rest of the course is of this quality.
3. Enzymes - nature's facilitators.
Chapter 3 covers how enzymes are used as biological catalysts to speed up reactions and what they are mad of. it also covers intramolecular and intermolecular attractive forces including London forces (which I knew as
van der Waals forces).
An interesting chapter covering a topic ive not had much experience of in the past. The section on attractive forces was revision but the rest was new.
4. The Incas, Coca-Cola and a trip to the dentist.
This chapter introduces local anaesthetics to the mix. It starts with coca leaves and the Incas, passing through Coca-Cola and cocaine before arriving at the modern local anaesthetics used in dentistry. Along the way we are introduced to cyclic bonding arrangements and the importance of distance between certain atoms in determining how active they are.
There is not a great deal of additional chemistry introduced in this chapter but a lot of fascinating biology. The modelling kit is becoming more useful as we progress into more complicated molecules, especially in demonstrating how two different molecules can be biologically similar. The section on how local anaesthetics work was much more interesting than I thought it would be.
5. General anaesthetics.
A logical progression from local anaesthetics, this is quite a short chapter covering four general anaesthetics (nitrous oxide, chloroform, ether and halothane). There is also a section on Curare and how molecules derived from its structure are used during operations as muscle relaxants.
The main thing to take away from this chapter is how the polarity of a molecule affects its ability to be used in the human body. General anaesthetics work on the brain so they must pass the blood - brain barrier and as the brain is a non-polar medium (unlike the blood) these molecules must be exhibit some form on non-polar behaviour but to dissolve in blood the molecule must also have some polarity.
I will cover chapters 6 - 10 in a later post...