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Physiochemical properties blood

The fate of a drag in vivo is dictated by a variety of physiochemical properties, including size, lipophilicity, and charge. These properties determine how a drag is absorbed into the blood, distributed throughout the body, metabolized, and eventually eliminated. While movement of a drug molecule can occur through simple diffusion, there are many transporter proteins expressed on cell membranes to assist... [Pg.41]

There are several physiochemical properties of the toxicant that can influence its distribution. These include lipid solubility, pKa, and molecular weight, all of which were described earlier in this chapter (Section 6.4) and will not be described here. For many toxicants, distribution from the blood to tissues is by simple diffusion down a concentration gradient, and the absorption principles described earlier also apply here. The concentration gradient will be influenced by the partition coefficient or rather the ratio of toxicant concentrations in blood and tissue. Tissue mass and blood flow will also have a significant effect on distribution. For example, a large muscle mass can result in increased distribution to muscle, while limited blood flow to fat or bone tissue can limit distribution. The ratio of blood flow to tissue mass is also a useful indicator of how well the tissue is perfused. The well perfused tissues include liver,... [Pg.97]


See other pages where Physiochemical properties blood is mentioned: [Pg.453]    [Pg.550]    [Pg.37]    [Pg.267]    [Pg.3959]    [Pg.247]    [Pg.91]    [Pg.16]    [Pg.157]    [Pg.182]    [Pg.197]    [Pg.396]    [Pg.147]    [Pg.59]    [Pg.457]    [Pg.119]    [Pg.189]   
See also in sourсe #XX -- [ Pg.115 ]

See also in sourсe #XX -- [ Pg.115 ]




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Physiochemical properties

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