This tag refers to how the body interacts with drugs such as how the body absorbs, distributes, metabolises and excretes (these four aspects of pharmacokinetics are often abbreviated ADME) said drugs.

learn more… | top users | synonyms

2
votes
0answers
18 views

Protein-Bound Drugs in Kwashiorkor

Kwashiorkor is characterised by decreased serum protein (including serum albumin) due to poor dietary protein intake. What is the effect of this lowered serum protein on highly-protein-bound drugs? ...
5
votes
1answer
43 views

How does food intake affect medicine? Why pill instructions recommends taking them before (after) meal?

Even simple vitamins seem to have this in the instruction. Why is is so? Is there some simple model of how do pills interact with food? Does it depend on the food type? (What about drinks?) Should ...
1
vote
0answers
27 views

negatively charged albumin as major carrier of acidic/negative charged drugs in blood

I reading that orsomucoid (alpha-1-acid glycoprotein) is the major carrier of positively charged (basic) drugs in the blood, while albumin carries negatively charged (acidic) and drugs with neutral ...
1
vote
1answer
41 views

Anesthetics, specifically inhaled anesthetics

I have had a look at previous inhaled anesthetics and many of them appear to be fluorocarbons. What could be the mechanism behind fluorine's anesthetic properties? Is it the specific bonding pattern ...
7
votes
1answer
277 views

Does THC excretion increase if urine volume increases?

In regards to the body metabolizing and excreting THC: if urination is increased as a result of drinking lots of fluids, does that mean that more THC is leaving the body? To rephrase the question, is ...
0
votes
0answers
21 views

Why is drug clearance not affected by blood flow in case of low extraction ratios?

Background information: 1) Variation of organ blood flow: a) for drugs with low extraction ratio (<0.3): the venous drug concentration is virtually identical to the arterial concentration ...
1
vote
1answer
21 views

What is the most common way of administering loop diuretics and what is their time course of action?

I am reviewing some material on loop diuretics, and I am curious to know how these drugs are administered. Also, I am interested in knowing their time course of action once they are administered into ...
5
votes
2answers
191 views

Why do different pain killers have different effects on people?

I've noticed some pain killers working great for me, while other having no effect. Works for me Aspirin APC † Naproxen Doesn't work for me Paracetamol Diclofenac Tramadol I doubt there ...
0
votes
0answers
31 views

Thermochemistry of gabapentin

So I am taking a new class at my institution called Theoretic Nuclear Thermochemical Pharmacology, (I know big name, it's an elective from a real pioneering fronteirsman in our department :P) and I am ...
3
votes
1answer
43 views

Drugs metabolism and detection

If someone is taking treatment for a psychiatric disorder, for example diazepine, would traces of the metabolized drug show in their sweat or saliva? Would it be chemically detectable?Any links to ...
1
vote
1answer
243 views

Pharmacokinetics: why do certain drugs follow zero-order kinetics?

I understand that alcohol and phenytoin are two examples of drugs that follow zero-order kinetics. Why do these two particular drugs follow zero-order kinetics as opposed to first-order kinetics?
3
votes
1answer
79 views

Pharmacology Half Life Calculation

I'm really stuck on this question. I'm being asked to find the half life of a drug. The Vd is 50L/kg. The clearance is 0.1 L/hr/kg. The patient weighs 70 kg. Equation is: T1/2 (halflife) = 0.693 * ...
1
vote
1answer
713 views

What is the physiological difference between snorting/swallowing cocaine

I know that mucosa inside the nose absorbs cocaine molecules when snorting cocaine, but what difference is there compared to swallowing? Also more cocaine administration equals more cocaine molecules ...
1
vote
0answers
108 views

Why can't sodium butyrate be delivered orally in humans and other mammals?

I think I know why -- bioavailability problems but since I have no firm evidence to support this theory I thought I would ask the biology stackexchange community for their input. I'd like some firm ...