the nature of interaction depends on whether they are lipophilic or hydrophilic. if both are hydorphilic ionic interaction, both lipophilic hydrogen bonding. ionic if lipophilic-hydrophilic.
the nature of interaction depends on whether they are lipophilic or hydrophilic. if both are hydorphilic ionic interaction, both lipophilic hydrogen bonding. ionic if lipophilic-hydrophilic.
She bought a hydrophilic shampoo that is designed to attract and retain moisture in her hair.
Yes. However, more to the point is that steroid hormones are lipophilic.
Palmolive dish soap works by breaking down grease and food particles on dishes, making them easier to wash away. Its formula contains surfactants that help to lift and remove dirt and grime, leaving dishes clean and shiny.
Drugs which are administered percutaneously, sublingually, or have to cross the blood brain barrier have to be lipophilic.
Yes. Xenon is lipophilic and exhibits affinity for cavities in macromolecular interiors. Xenon's lipophilic behavior has been shown from its partition with long-chain hydrocarbons and from its in vitro and in vivo partition with fatty tissue.
Yup. They sure are.
The drug reservoir consists of particles homogeneously dispersed in a hydrophilic or lipophilic polymer matrix. This matrix is then placed on to of a medicated disk. This is then stuck onto an occlusive baseplate. An adhesive polymer then surrounds this system to create a strip of adhesive rim.
Lipophilic means having an affinity for or the ability to dissolve in fats, oils, and other nonpolar solvents. Lipophilic substances tend to accumulate in fatty tissues and cell membranes.
Not all nonpolar molecules are lipophilic, but most lipophilic molecules tend to be nonpolar. Lipophilic molecules are attracted to fats and oils, so they typically do not mix well with water. Nonpolar molecules lack a significant difference in electronegativity and, as a result, do not easily dissolve in water.
An ionized drug is generally less lipophilic than its non-ionized form. This is because ionization usually results in the drug having a greater affinity for water rather than lipid-based environments.