Nuclear magnetic resonance (NMR) is a powerful technique
with applications
ranging from small molecule structure elucidation to metabolomics
studies of living organisms. Typically, solution-state NMR requires
a homogeneous liquid, and the whole sample is analyzed as a single
entity. While adequate for homogeneous samples, such an approach is
limited if the composition varies as would be the case in samples
that are naturally heterogeneous or layered. In complex samples such
as living organisms, magnetic susceptibility distortions lead to broad 1H line shapes, and thus, the additional spectral dispersion
afforded by 2D heteronuclear experiments is often required for metabolite
discrimination. Here, a novel, slice-selective 2D, 1H–13C heteronuclear single quantum coherence (HSQC) sequence
was developed that exclusively employs shaped pulses such that only
spins in the desired volume are perturbed. In turn, this permits multiple
volumes in the tube to be studied during a single relaxation delay,
increasing sensitivity and throughput. The approach is first demonstrated
on standards and then used to isolate specific sample/sensor elements
from a microcoil array and finally study slices within a living earthworm,
allowing metabolite changes to be discerned with feeding. Overall,
slice-selective NMR is demonstrated to have significant potential
for the study of layered and other inhomogeneous samples of varying
complexity. In particular, its ability to select subelements is an
important step toward developing microcoil receive-only arrays to
study environmental toxicity in tiny eggs, cells, and neonates, whereas
localization in larger living species could help better correlate
toxin-induced biochemical responses to the physical localities or
organs involved.