The inorganic platinum compound cisplatin (CP) in Oncoplatin, an anticancer
drug, as the test chemical and cyclophosphamide (CY) in Endoxan, another a
nticancer drug, as the positive control, were tested for their cytogenetic
toxicity in bone marrow cells of Swiss mice. The end points selected were m
itotic metaphase chromosomal aberration and mitotic index study at 24-hour
post-treatment and micronucleus test at 30-hour post-treatment after a sing
le intraperitoneal exposure. The doses of the chemicals tested were CP 2, 3
and 5 mg/kg and CY 40 mg/kg b.w, of mice. Each of the doses of CP induced
a significant number of chromosomal aberrations, mostly chromatid breaks an
d fragments and a significant number of micronuclei, The mitotic index stud
y indicated CP as nonmitotoxic. The female mice were found more sensitive t
o each of the doses of CP than the males by showing more chromosomal aberra
tions, a higher number of micronuclei and comparatively less percentages of
dividing cells. CP was thus found to be highly clastogenic in bone marrow
cells of Swiss mice.