p-man said:
So how's that codeine master thread going Mr Blonde
It's finally finished! It's just sitting in the mod thread because I'm waiting on the other moderators to read it first. It may actually end being being broken into two parts; one the codeine and CWE mega thread, the other a mega thread for addiction. I'm actually quite impressed with it, I've been working on it hard for the last week and have in-line citations and a bibliography and everything.
footscrazy said:
I find it the most euphoric out of any opiates, I love it. I thank my blessings that I get such an awesome high off the cheapest and most accessible opiate
Oh God me too I love it.... 2000mg plus a small bottle of rikodeine gets me feeling pretty good, I need to take a break though to get my tolerance down.
footscrazy said:
You can snort codeine but it's a lot more of a fuck around - since after a cwe you're left with codeine dissolved in water, you'd have to leave that to evapourate for a day or two, and even then as codeine is a pro drug it needs to go through your liver to become effective anyway. So snorting it doesn't make a whole lot of difference.
I would not even consider snorting as a method of administration. As you said, it has to go through first pass metabolism in the liver to become morphine and take effect and the quickest way to make that happen is to take it orally.
As for the evaporating, you can do it in an oven at a low temperature with the door open. Just be careful as at 80°C the codeine will be destroyed.
L3inad said:
You cant compare the two - not in that sense anyway.
Paracetemol toxicity is to do with glutathione depletion, and cells loosing their protective buffer. Alcohol just has a toxic metabolite. Both are broken down by different enzymes, making any strain on the liver specific to the one substance(and enzyme).
That's not correct; paracetamol's toxic effects on the liver are due to a metabolite as well; N-acetyl-p-benzoquinoneimine (NAPQI). Normally this metabolite is excreted by conjugation with glutathione, as you said, but in an overdose glutathione stores are depleted trying to deal with the amount of NAPQI produced. The cells don't lose their 'protective buffer' so much as NAPQI is a strong oxidizing agent which destroys the protein structure of the cell membranes and then destroys proteins and nucleic acids inside the cell. This leads to hepatic necrosis, that is, death of the liver.
As for the post/s earlier suggesting that ingesting 4 grams at once was fine, take a look at this study:
Aminotransferase Elevations in Healthy Adults Receiving 4 Grams of Acetaminophen Daily
These increased levels of ALT indicate stress on the liver, and that was in participants taking the paracetamol in divided doses throughout the day. Clearly the substance can have a negative effect on the liver at a single dose of 4 grams, and I'm sure I've read a case report on liver damage resulting from a single dose of 4 grams before.