To investigate the possible bioactive species from cinnabar after oral administration, which is the fundamental of biological effects of cinnabar.
Under mimetic intestinal and gastric conditions, the chemical components dissolved from cinnabar were analyzed by infrared spectroscopy (IR) and Raman spectroscopy. Furthermore, binding of mercuric species of cinnabar extractions to human serum protein (HSA) was characterized and their intestinal permeability was determined using the Caco-2 cell monolayer. The cytotoxicity of cinnabar extractions was assessed on human kidney-2 (HK-2) cell.
Major dissolved species included mercuric polysulfide (i.e. HgS2(OH)− and Hg3S2Cl2). The apparent permeability coefficient (Papp) of mercuric polysulfides was (1.6 ± 0.3) × 10−6 cm/s, which is slightly lower than that of mercuric chloride (HgCl2). Unlike HgCl2, mercuric polysulfides exhibited two tightly binding sites to HSA and had little effect on viability of HK-2 cells.
Mercuric polysulfides, as the major dissolved components, may serve as the active species of cinnabar exhibiting pharmacological and/or toxicological effects.