Complexation and Protein Binding

Complexation and Protein Binding involve the reversible interaction of a drug with proteins or other molecules, forming complexes that affect the drug’s distribution, activity, and elimination.

Complexation Introduction

  • Complexation is a chemical process where molecules or ions combine to form a stable complex. It typically involves:
  • Central Metal Ion: Usually a metal (e.g., Fe, Cu, Zn) that acts as an electron acceptor.
  • Ligands: Molecules or ions that donate electron pairs to the metal, forming coordinate covalent bonds. Ligands can be small ions (like Cl⁻) or larger molecules (e.g., ethylenediamine).
  • Complexation is key in coordination chemistry, influencing the structure and stability of complexes, which can vary from linear to complex geometries (e.g., octahedral).
  • It plays a significant role in processes like catalysis and metal ion transport in biological systems.
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Protein Binding Introduction

  • Protein binding involves the interaction of drugs or molecules with proteins in biological systems, particularly in the bloodstream.
  • Plasma Proteins: Proteins like albumin bind to various molecules, affecting their availability.
  • Drug Impact: When bound to proteins, drugs are often inactive; only the unbound fraction is pharmacologically active.
  • Pharmacokinetics/Pharmacodynamics: Protein binding influences a drug’s movement, duration, and elimination in the body, impacting its therapeutic effects.

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