4.12
Drug binding to proteins depends on various factors, including physicochemical properties, protein concentration, disease states, and the number of binding sites on the protein.
The physicochemical properties of proteins, influenced by the physiological pH, play a significant role in protein-drug binding. Lipoproteins and adipose tissue bind lipophilic drugs, dissolving them in their lipid core.
Protein concentration is a key determinant. Albumin, abundant in plasma, predominantly binds drugs.
Disease states can alter the availability of proteins, and tissue components for binding can change, affecting drug binding.
The number of binding sites on the protein also impacts drug binding. Albumin, with numerous binding sites, has a high binding capacity.
Some drugs, like ketoprofen, flurbiprofen, and tamoxifen can bind to multiple sites on albumin. Indomethacin binds to three distinct sites on albumin.
α1-acid glycoprotein has limited binding capacity due to its low concentration and molecular size.
Drug binding to proteins is a key aspect of pharmacokinetics and can influence a drug's distribution, absorption, and elimination in the body. Several…
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