One of the raw forms of graphite is activated charcoal which has an extensive surface area allowing for the adsorption of a wide range of chemicals. It possesses the strongest physical adsorption forces of the available materials, as well as the largest volume of adsorbing porosity. Activated charcoal acts as an adsorbent, collecting and storing substances in the gastrointestinal tract, reducing or blocking absorption in the bloodstream. The ingested toxins interact with charcoal by recycling toxins in the intestinal cavity. In cases where the drug has not been absorbed from the abdominal system, it is recirculated through the liver and intestines or by means of passive diffusion or active secretion. The article aims to review the most recent advances in the use of the activated charcoal, including the dose, how charcoal acts in the body, the mechanism of action, administration, contraindications, as well as the impact of various factors on the adsorption process. In addition, we also discussed numerous medical applications of activated charcoal.
Objective:The aim of the present study is to evaluate the ability of activated charcoal in adsorbing overdosage of gliclazide drug, and to study the effects of pH, concentration and time on this process. Methods:To evaluate the effect of pH, concentration and time; 50 ml of the drug solution (100 mg/L) were allowed to stand with the activated charcoal for 1 h at pH of 1.5, 4, 7, and 9 for pH study. 50 ml of the drug solution concentrations of 25, 50, 75, and 100 (mg/L) were allowed to stand with 1 g activated charcoal for 1 h for concentration study. 50 mg of the drug solution (100 mg/L) were allowed to stand with the activated charcoal for 15, 30, 45, and 60 min for time study. The concentrations of the adsorbed drug were determined spectrophotometrically. Results:The adsorption of the gliclazide drug on activated charcoal was found to be pH, concentration, and time-dependent. The amounts of the drug adsorbed were 3, 0.75, 0.6, and 0.5 mg/g for pHs 1.5, 4, 7, and 9, respectively, for pH study. For concentration study, the amounts adsorbed were 0.15, 0.22, 0.33, and 0.58 mg/g for concentrations 25, 50, 75, and 100 mg/L, respectively. For time study, the amounts were 0.3, 0.4, 0.51, and 0.65 mg/g for reaction times 15, 30, 45, and 60 min, respectively. Conclusion:The best adsorption circumstances of gliclazide drug on activated charcoal that were found; acidic pH, a high concentration of the drug and longtime of contact.
The adsorption of the water-soluble tetra(p-sulphophenyl)porphyrin (TPPS) compound on Fe(II), Fe(III), Cu(II), Co(II), Ni(II), Zn(II), Cd(II), Sn(IV) and UO22+ metal ion-exchanged montmorillonite (MMT) facilitated the formation of the SAT metal-TPPS MMT complexes of these cations (where SAT indicates sitting atop, ie the metal is above the porphyrin plane and is bound to external ligands in this case the MMT surface). All the resulting powder samples have a brown-orange colour due to the presence of the metal-TPPS-MMT complexes of these cations. Heating the solid powder samples caused demetallation and changed the colour of the powder from brown-orange colour of the metal-TPPS-MMT complex to the green colour of the diacid porphyrin on the clay. When such samples were exposed to the open atmosphere where they could absorb water vapour, the brown-orange colour appeared again due to the remetallation. The cation remained in the vicinity of the TPPS molecule upon demetallation, which makes the metallation-demetallation process reversible. The TPPS has been found to be adsorbed only on the external surface, and can be intercalated using sodium ions in solution with the compound to open the clay lattice. The reactions were monitored using visible absorption spectra, diffuse reflectance spectra, Mössbauer spectroscopy and X-ray diffraction.
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