Bone is chemically built up as a mineralized matrix which comprises co
llagen and a small amount of noncollagenous proteins. This paper point
s out some useful methods to evaluate the bone composition. Deminerali
zing extraction of bone powder with EDTA allows the determination of m
atrix size and degree of extractability. These parameters vary with bo
ne type, anatomical site of the bone, disease, species, and drug treat
ment. The study of bone particles in situ can be done by separation of
bone powder according to their density. A shift of the bone particles
to higher density fractions reflects an increased amount of older, mo
re mineralized osteons in the bone with its consequences on the mechan
ical competence of the bone. Quantity and quality of bone matrix miner
alization are related to bone cell activity which can be studied indir
ectly by further exploration of the composition of the bone matrix. Ma
ny noncollagenous proteins are buried in the extracellular bone matrix
from where they can be released when bone is resorbed. These proteins
can then act on bone cells in an autocrine or paracrine manner. Alter
ed concentrations of noncollagenous proteins in bone matrix are descri
bed in three pathological conditions associated with changes in other
bone properties: osteoarthritis, osteopenia, and osteogenesis imperfec
ta. The functional significance and origin of these changes will have
to be subjected to further study.