Copolymer networks of poly(methacrylic acid) (PMAA) and poly(ethylene glycol) (PEG) exhibit large changes in their swelling behavior over a narrow pH range due to the reversible formation/dissociation of interpolymer complexes between the polymer chains. Intepolymer complexation occurs in copolymer gels of PMAA and PEG due to hydrogen bonding between protonated acid groups and the ether groups of the PEG. Because of their nature, these gels have been identified for use as delivery vehicles for macromolecular drugs. In this work, solid-state, nuclear magnetic resonance nuclear Overhauser enhancement (NOE) experiments were performed to detect the molecular level complexation between PMAA and deuterated PEG in copolymer blends and crosslinked networks. For gels swollen in acidic media at room temperature or at 37 degrees C, strong enhancements were detected in the C-13 resonance of the PEG carbons. The NOE was generated due to energy transfer between the rapidly rotating methyl group protons and the deuterated PEG carbons. The presence of the NOE was indicative of close packing of the polymer chains and was evidence of the presence of the intermacromolecular complexes. In basic solutions, no NOE was detected in the PEG, as the complexes were dissociated and the chains were separated in space.