An unionized drug tends to be lipophilic (and hence, would be hydrophobic). Thus, an ionized drug on the other hand would be lipophobic (i.e. the opposite of lipophilic), lipid-hating.
When an atom is ionized, that means that it is sharing one or more electrons with another atom.
When an atom is ionized, that means that it is sharing one or more electrons with another atom.
The process of metabolism transforms lipophilic drugs into more polar(hydrophilic), readily excretable products.
Hcl, it's ph is lower.
because they dissociate more rapidly and donate hydrogen ion for reduction as soon as it is ionized
the more ionized the drug is the less absorption
Drug metabolism is needed is lipophilic drugs cannot be cleared renally. These lipophilic drugs need to be metabolised into more polar products so that they can be excreted in the urine.
The COOH group can be changed to a tetrazole group to increase the drug's lipophilicity. Both groups have a similar pKa value so the ionisation of the molecules should be similar.
an ionized gas consisting of positive ions and free electrons in proportions resulting in more or less no overall electric charge.
When an atom is ionized, that means that it is sharing one or more electrons with another atom.
When an atom is ionized, that means that it is sharing one or more electrons with another atom.
Some trends for drugs in a homologous series include increasing molecular weight and size with an increase in the number of carbon atoms in the chain. This can affect the drug's potency, pharmacokinetics, and metabolic stability. Additionally, there may be trends in solubility, lipophilicity, and protein binding affinity as the alkyl chain length varies.
When an atom is ionized, that means that it is sharing one or more electrons with another atom.
Yes. When substances are lipophilic (hydrophobic), they are usually much more easily retained in fat in the body, reducing its elimination rate. This allows for such substances (such as lipophilic vitamins) to accumulate in the body to toxic levels.
Yes. However, more to the point is that steroid hormones are lipophilic.
Lipophilic viruses require the lipid (fatty) envelope to remain active ("live"*), and the fatty layer can be destroyed by alcohol. Non-lipophilic viruses do not require this fatty envelope, and the protein layer (capsid) is more resistant to alcohol. *Note: viruses are not actually alive, they are only genetic codes with 1 or 2 (lipophilic) protective layers. Biologists call "live" viruses *active* and "dead" viruses *inactive* or *inactivated*.
Phase I: Lipophilic drugs need to become more polar so that they can be excreted in urine. New polar functional groups hence need to be unmasked for added to them. This can happen via oxidation, reduction, or hydrolysis.Phase II: The original drug or drug metabolites gets conjugated to acetate, sulfate, glutathione, or glucuronic acid. They can hence be excreted even more quickly due to their increased polarity.