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“Doses of ≥1,600 mg clodronate produced mean reductions of >40% in U-NTX, S-CTX and U-Ca , all significantly different from placebo (P = 0.0015, 0.001, 0.0036, respectively), after 6 weeks.”
International journal of pharmaceutics • 2001 | View Paper
“Although clodronate is less potent than EDTA in depleting calcium from the intestinal tissue, it significantly increased the paracellular permeability of viable rat jejunum "in vitro" when tested at 15 mM and higher concentrations (the highest therapeutic dose dissolved in 250 ml gives a 22 mM solution of clodronate).”
Calcified Tissue International • 2005 | View Paper
“Free and esterified cholesterol and total Ca++ concentrations in the wall of thoracic aorta were reduced by the greatest dose of clodronate , compared with the groups treated with saline solution or smaller doses of the drug (p < 0.05).”
The Journal of laboratory and clinical medicine • 1994 | View Paper
“The L‐type Ca2+ channel blocking drugs, nicardipine (10 nM) and verapamil (1 μM), reduced the second component of the norepinephrine‐mediated vasoconstriction, but in the presence of clodronate (20 μM) this blocking action was prevented.”