Skip to main content
Elsevier - PMC COVID-19 Collection logoLink to Elsevier - PMC COVID-19 Collection
. 2007 Sep 4;1:743–752. doi: 10.1016/S1572-4352(05)01025-1

Chapter 11.6 Clays and Clay Minerals as Drugs

MT Droy-Lefaix a, F Tateo b
PMCID: PMC7185446  PMID: 32362802

Publisher Summary

This chapter discusses the applications of clays and clay materials as drugs. Clay minerals are efficient against several aggressors that cause major disorders of the gut. These beneficial effects of clay minerals (on the gastrointestinal mucosa) are associated with two mechanisms of action: (1) adsorption of the aggressors or their toxic secretions and (2) modification of the thickness and rheological properties of the adherent mucus, reinforcing the natural defenses of the gastrointestinal mucosa. At the surface of the gut, a mucus gel adheres to the epithelial cells of the mucosa. This adherent mucus is dynamic, being continuously secreted by the calceiform cells and regularly eroded by environmental aggressors present in the gut lumen. The mucus gel is largely composed of glycoprotein polymers, lipids, and proteins linked together by covalent bonds. It acts as a physical barrier protecting the mucosa against penetration by extraneous molecules and mechanical injury. By maintaining a pH gradient and competing with the epithelial surface for microorganisms, the mucus gel also acts as a chemical barrier.


Clay therapy is based on the ability of clays and clay minerals to adsorb and retain harmful and toxic substances. The beneficial effects of these materials to human health, notably in the treatment of gastrointestinal disorders, were recognized. Indeed, the eating of clay (‘geophagy’) was practiced since antiquity in all parts of the world. Among the variety of clays and clay minerals that were used by primitive tribes are bentonite, kaolinite, montmorillonite, smectite, and ‘pascalite’ (a Ca2+-montmorillonite from Wyoming, USA) (Eaton and Eaton, 1995).

Examination of the diets of certain tribes in the high Andes of South America and central Africa, and those of Australian aborigines, showed that these people use clay to avoid getting stomach-ache, dysentery, and food infections. Indeed, the Quetchus Indians of South America used to dip their potatoes into an aqueous suspension of clay, immediately before eating, in order to prevent the build-up of acidity in the stomach. This dietetic procedure is still being followed by some tribes of American Indians. A similar practice was traditionally carried out on board ships where sailors used clays not only to adsorb odours and moisture but also to treat dysentery, burns, boils, sore mouths, and other internal and external disorders.

Although recent research confirmed that clays and clay minerals possess general curative properties, it is the treatment of disorders that remains the focus of attention. By adsorbing ‘aggressors’ (infectious factors) of the gastrointestinal mucosa barrier, these materials can serve as both prophylactic and therapeutic agents.

11.6.1. Interactions of Clay Minerals with Gastrointestinal Mucus

At the surface of the gut, a mucus gel adheres to the epithelial cells of the mucosa. This adherent mucus is dynamic, being continuously secreted by the caliciform cells and regularly eroded by environmental ‘aggressors’ present in the gut lumen.

The mucus gel is largely composed of glycoprotein polymers, lipids, and proteins, linked together by covalent bonds. As such, it acts as a physical barrier protecting the mucosa against penetration by extraneous molecules and mechanical injury. By maintaining a pH gradient and competing with the epithelial surface for microorganisms, the mucus gel also acts as a chemical barrier.

Thus, a weakening of the mucus gel barrier may be at the origin of disorders such as gastritis and colitis (Droy-Lefaix, 1987). Short-term treatment with clay minerals, such as smectites (Moré et al., 1987) and attapulgite (Moré et al., 1992) increases the thickness of the adherent mucus. This may be ascribed to interactions of mineral particles with mucus components (Leonard et al., 1994) by which the gastrointestinal glycoproteins are modified, and their polymerization is enhanced (Droy-Lefaix et al., 1986). Similarly, aluminium (hydr)oxides (e.g., boehmite) can reduce mucus degradation (Bouyssou et al., 1990). The beneficial effects of minerals are also associated with improvements in the rheological properties of the mucus gel, such as spinability. This reflects the increased extent of polymerization, and the improvement in quality, of the adherent mucus (Droy-Lefaix et al., 1985). Changes in the physico-chemical properties of the mucus, induced by the action of clay minerals, were confirmed by electron paramagnetic resonance and fluorescence spectroscopy. The results indicate that clay mineral ingestion decreases mucus solubility. At the same time, the viscosity and hydrophobicity of the mucus increases, enhancing its adhesion to epithelial cells.

11.6.2. Clay Minerals, Mucosal Barrier, and Gastrointestinal ‘Aggressors’

By acting directly on the mucus gel, clays and clay minerals exert a stabilizing effect on the mucosal barrier (Gwozdzinski et al., 1997), providing protection against different ‘aggressors’ of the gastrointestinal mucosa.

Pepsin, a substance necessary for digestion, is a typical ‘aggressor’. Experiments with rats showed that if pepsin secretion at the surface of the gastric mucosa is strongly increased (due to pathological disregulation), the adherent mucus layer is progressively disrupted. At the same time haemorrhagic mucosal lesions appear, and significant bleeding occurs in the lumen as well as localized ulceration in an otherwise intact epithelium. By binding to the mucus components, smectite can completely inhibit the damage induced by pepsin (Leonard et al., 1994).

Samson et al. (1995), for example, showed that patients with ulcerative colitis show a six-fold greater mean total faecal proteinase activity (expressed in mmol terminal NH2/min/g dry weight of faeces) than the control. Smectite totally inhibits this enzyme activity. The effects of smectite on mucus proteolysis are assessed using a model of mucolytic activity, assayed by the release of degraded colonic mucin from the adherent mucus gel of freshly prepared pig colonic bags in vitro. Similarly, trypsin (2 mg/mL) releases three times more soluble mucin per bag than the control. Smectite (100 mg/mL) inhibits trypsin activity, causing the level of degraded mucin to fall below the normal value. This is ascribed to the interaction of smectite with the adherent mucus layer, and the binding of trypsin to the mineral (Samson et al., 1995).

Clay minerals can also provide protection against attack by bile acids that cause gastrointestinal ulceration. In rats, oral administration of sodium glycodeoxycholate or sodium taurocholate induces severe erosion of the jejunal mucosa. After treatment with smectite (which interacts closely with the mucus glycoproteins) the severity of surface erosion is greatly diminished (Fioramonti et al., 1990), while the rheological properties of the adherent mucus gel are maintained within normal limits (Droy-Lefaix et al., 1985).

Because of their strong bioadhesive properties, clay minerals also afford protection of the colon against damage from reactive oxygen species. Oxygenated free radicals, released by infiltration of white cells into the colonic mucosa barrier, are very unstable. Their presence can induce severe erosion of the colonic mucosa, leading to mucolysis. By maintaining the solution viscosity of the colonic mucin, and inhibiting the hypersecretion of mucus, smectite can prevent the onset of mucolysis (Pearson et al., 1996; Knight et al., 1998).

In many digestive diseases, the intestinal barrier is weakened by the release of pro-inflammatory cytokines, induced by abnormal activation of the epithelial cells and the underlying immune system. These cytokines include a tumour necrosis factor–α (TNF-α) and an interferon-γ factor (INF-γ). When intestinal cells (line HT 29-19 A) are incubated with TNF-α and INF-γ, intestinal function (assessed in Ussing chambers by measuring ionic conductance, apicobasal fluxes of 14C-mannitol, and intact horseradish peroxidase) is altered, and the tight junction between cells is disrupted. In the presence of smectite (100 mg/mL) the values of these parameters are similar to those of the control (Mahraoui et al., 1997).

The cytoprotective effects of clay minerals can also account for their ability to prevent damage of the gastrointestinal mucosa caused by such ‘aggressors’ as ethanol and anti-inflammatory drugs. Ethanol, directly administered into the stomach, gives rise to severe gastric ulcerations and macroscopic necrosis of the gastric mucosa. These deleterious effects are accompanied by a decrease in the gastric transmural potential difference which serves as a criterion of the functional integrity of the mucosa (Fioramonti et al., 1990). Erosion of the mucus layer leads to a significant alteration of rheological properties (Droy-Lefaix et al., 1992; Slitine-Bonet et al., 1994). Smectite treatment for two days can significantly counteract the harmful effect of ethanol, reducing the irritative index (Fioramonti et al., 1990).

Clay minerals also provide protection against the action of anti-inflammatory drugs. For example, the oral administration of aspirin (2 g) to pigs, and phenylbutazone (200 mg/kg) to rats, decreases the gastric potential difference, and induces severe ulceration due to mucus alteration (Fioramonti et al., 1990; Droy-Lefaix et al., 1992). The extent of lesion and mucus degradation is significantly reduced after treatment with smectite. In humans the symptoms of gastropathies, induced by non-steroid anti-inflammatory drugs, can be successfully treated by ingestion of smectite (Peignot et al., 1997).

11.6.3. Adsorptive Properties of Clays and Clay Minerals

The adsorptive properties of clay minerals provide the basis for the therapeutic uses of clays.

A. Toxins

Clays can adsorb a variety of toxic substances, such as strychnine (Droy-Lefaix, 1986), mycotoxins (e.g., T2 toxin) (Fioramonti et al., 1987b), aflatoxin (Schell et al., 1993), enterotoxins (Brouillard and Rateau, 1989), and toxins produced by Vibrio cholerae, Escherichia coli (Fioramonti et al., 1987b), and Yersinia pseudotuberculosis (Carnoy et al., 2000).

By doing so, clays can provide active protection against disturbances during gastrointestinal transit. In mice, for example, gastric emptying and small intestinal transit are significantly accelerated after oral administration (1 mg/kg for 4 days) of T2 toxin. However, if the toxin is incubated with smectite for 24 h beforehand, no increase in the rate of gastric emptying and small intestinal transit occurs (Fioramonti et al., 1987a).

In conscious dogs, intraduodenal administration of cholera toxin (200 mg) affects gastrointestinal transit, and disrupts the migrating motor complexes (MMCs) of the stomach and jejunum. According to the duration of treatment (at a dose of 100 mg/kg/day), smectite can effectively counteract the effects of cholera toxin (Fioramonti et al., 1987b).

Smectite can also adsorb the enterotoxin of Clostridium difficile (Martirosian et al., 1998). In rats, this toxin causes intestinal permeability to increase through hypersecretion of colonic water. Both these conditions can be alleviated by treatment with 51Cr-EDTA in the presence of smectite (Fioramonti et al., 1994).

E. coli toxin is an infectious agent causing diarrhoea. Heat-stable toxin (ST) from E. coli, directly administered to New Zealand rabbits, induces a significant increase in intestinal permeability (as estimated by Evans Blue) and severe damage to ileal loops (as revealed by scanning electron microscopy). The presence of smectite in the ileal loops has a protective effect (Pons et al., 1997).

Similar results are obtained with the enterotoxin of Bacteroides fragilis administered to HT/29 C1 cells (human colon adenocarcinoma cell line). Prior incubation of this toxin with smectite suppresses its toxic effects (Martirosian et al., 1998).

B. Pesticides

Because of their high adsorptive capacity, clay minerals can also protect the digestive mucosa against pesticide damage. Diquat, a widely used non-selective desiccant herbicide, induces erosion of intestinal mucosa and fluid hypersecretion. In rats that were given diquat, treatment with smectite (500 mg/kg for 2 weeks) brings about a normalization of mucus rheological properties and intestinal permeability, as indicated by urine analysis using 51Cr-EDTA (Theodorou et al., 1995). Similarly, montmorillonite and bentonite are good adsorbents, and may be recommended for the treatment of pesticide poisoning (Meredith and Vale, 1987).

C. Microorganisms

Clay minerals are efficient drugs for treating disorders of the gastrointestinal mucosa, induced by microorganisms. Kaolinite and montmorillonite are capable of adsorbing viruses (Lipson and Stotzky, 1984). As such, these minerals can induce rapid recovery when administered to children suffering from gastroenteritis. Similarly, the strong adsorptive power of smectite lies behind its ability to aggregate bacteria, such as strains of E. coli with the plasmid P, carrying a virulence factor in the form of an external protein CS 31A (Girardeau, 1987).

In the stomach, Helicobacter pylori is associated with gastritis and gastroduodenal ulcers. This bacterium is also one of the most important ethiopathogenic factors causing peptic ulcer. Smectite, on HeLa cells infected by H. pylori isolated from human biopsies, significantly reduces adhesion of the bacteria to the surface of epithelial cells (Bonneville et al., 1990). This is why smectite is effective in treating the symptoms of people with non-ulcer dyspepsia who are infected by H. pylori (De Korwin et al., 1993).

In the intestine, smectite is effective against diarrhoea as shown by clinical data for new-born calves with neonatal gastroenteritis. Faeces analysis reveals the presence of rotavirus in 41.3% of the animals as well as that of E. coli K99, coronavirus, and Salmonella. Recovery is observed in 72% of calves after 2.8 and 2.2 days of receiving 250 and 500 mg/kg smectite, respectively, and after 4.2 days in calves which do not receive smectite. After 4 days of treatment, the consistency of the faeces is significantly better in calves receiving smectite than in the control animals (Espinasse et al., 1987).

D. Gas

Clay minerals can serve as gas adsorbents in patients with symptoms of flatulence and abdominal distension. Thus, smectite can reduce the amount of hydrogen emitted during colonic fermentation (Frexinos et al., 1986; Arbeille et al., 1991).

E. Alimentary Allergy

Food allergy is also responsible for disturbances in colonic transit, water absorption, and intestinal permeability. Guinea pigs that were sensitized by β-lactoglobulin from cow milk show colonic transit acceleration, a colonic hypersecretory response, a strong increase in intestinal permeability, and a decrease in faecal dry matter. These effects are not observed in animals that were treated with smectite. Clays can inhibit anaphylaxia probably by controlling the release of mediators at the origin of the degranulation of the mast cells (Theodorou et al., 1994).

11.6.4. Clay Minerals and Clinical Applications

Being good adsorbents and mucostabilizers, clay minerals are efficacious against several aggressive agents causing severe intestinal disorders. Acute gastroenteritis is a major cause of morbidity and mortality among children worldwide (Madkour et al., 1993). By adsorbing viruses, bacteria, and other digestive irritants, clay minerals can shorten the course of acute diarrhoea, and reduce the occurrence of prolonged diarrhoea. Furthermore, these minerals do not interfere with the electrolyte balance, and are well tolerated by patients (Buttron, 1987; DuPont et al., 1990; Bauer and Hirschbrunn, 1992; Charritat et al., 1992; Dupont et al., 1992; Vivatvakin et al., 1992; Lexomboon et al., 1994; Karas, 1996; Milocco et al., 1999; Guarino et al., 2001; Narkeviciute et al., 2002).

Clay minerals also provide protection against diarrhoeas induced by antibiotics treatments (Benhamou et al., 1995), alleviate chronic diarrhoeas induced by chemotherapy and radiation (Hornbrink et al., 1995; Ippolite, 1998; Santantonio et al., 2000), enteral nutrition (Perrotin et al., 1990), and HIV infection (Phanuphak et al., 1992; Mastroianni et al., 1998).

Clay minerals are promising drugs in the treatment of irritable bowel syndrome (IBS), a rather frequent disease in adults with a complex pathogenic mechanism. By enhancing the thickness of the mucus barrier, both colon movement function and faeces consistency are restored, and the symptoms of IBS are alleviated (Opriu et al., 1996; Secondulfo et al., 2002). In parallel, clay minerals have a positive effect on flatulence and abdominal distension (Lukas and Lukas, 2000).

11.6.5. Conclusions

Clay minerals protect and are efficient against several ‘aggressors’ that cause major disorders of the gut. These beneficial effects of clay minerals (on the gastrointestinal mucosa) are associated with two mechanisms of action: (1) adsorption of the ‘aggressors’ or their toxic secretions and (2) modification of the thickness and rheological properties of the adherent mucus, reinforcing the natural defenses of the gastrointestinal mucosa.

References

  1. Arbeille, P.H., Schillio, Y., Bidard, S., 1991. Value of using a gas reductor (Diosmectite) for the preparation of patients prior to the echography of the epigastric area. Gastroenterology 100, Abstract 347.
  2. Bauer C., Hirschbrunn P. Treatment of acute diarrhea in infants. Der Kinderartz. 1992;5:878–884. [Google Scholar]
  3. Benhamou, P.H., Berlier, P., Longue, J., Dupont, C., 1995. Intestinal manifestation during antibiotics treatments in children: a prospective study. Gastroenterology 108, Abstract 273.
  4. Bonneville, F., Moyen, E.N., Droy-Lefaix, M.T., Fauchère, J.L., 1990. In vitro effect of smectite on Campylobacter pylori adhesion upon epithelial cells. Gastroentérologie Clinique et Biologique 14, Abstract 123.
  5. Bouyssou, T., Biosa, S., Cochat, C., Goudey, V., Doubovetzky, M., Poiret, M., 1990. Protective effect of an aluminium hydroxide, boehmite, on rat gastric mucus. Gastroenterology 98, Abstract 25.
  6. Brouillard M.Y., Rateau J.G. Adsorption potency of 2 clays, smectite and kaolin on bacterial endotoxin. In vitro study in cell culture and on the intestine of newborn mice. Gastroentérologie Clinique et Biologique. 1989;13:18–24. [PubMed] [Google Scholar]
  7. Buttron O. Treatment of chronic functional diarrheas. Therapiewoche. 1987;37:2723–2726. [Google Scholar]
  8. Carnoy, C., Muller Alouf, H., Mullet, C., Droy-Lefaix, M.T., Simonet, M., 2000. Oral infection of mice with superantigenic toxic producing Yersinia pseudotuberculosis. Effect of diosmectite. International Journal of Medical Microbiology 290 (30), Abstract 83.
  9. Charritat J.L., Corbineau D., Guth S., Meunier M., Perrin P., Pflieger H. Therapeutic evaluation of Mormoiron attapulgite in acute diarrheas of infants and children. A multicenter study in controlled liberal practice versus placebo in 113 patients. Annales de Pédiatrie (Paris) 1992;39:326–332. [PubMed] [Google Scholar]
  10. De Korwin, J.D., Forestia, B., Plique, O., 1993. Symptomatic improvement of patients with non ulcer dyspepsia and Helicobacter pylori after treatment with diosmectite. Randomized double-blind study versus placebo. Acta Gastroenterologica Belgica 56, Abstract 149.
  11. Droy-Lefaix M.T. Adsorption properties of clays. In Precepta Medica, Digestive Disease Week. 1986;4:42–44. [Google Scholar]
  12. Droy-Lefaix M.T. Intestinal mucosa barrier and smectite. Revue de Médecine Vétérinaire. 1987;138:411–421. [Google Scholar]
  13. Droy-Lefaix, M.T., Drouet, Y., Schatz, B., 1985. Sodium glycodeoxycholate and spinability of gastrointestinal mucosa: protective effect of smectite. Digestive Disease Week 5, Abstract 1369.
  14. Droy-Lefaix, M.T., Plique, O., Géraud, G., Drouet, Y., 1992. Protective effect of diosmectite on the decrease of the adherent mucus gel thickness induced by phenylbutazone on rat stomach. Hellenic Journal of Gastroenterology 5 (70), Abstract 279.
  15. Droy-Lefaix, M.T., Schatz, B., Drouet, Y., 1986. Importance of viscoelasticity in the study of the adherent mucus gel. Digestive Disease Science 31, Abstract 1401.
  16. Dupont C., Moreno J.L., Barau E., Bargaoui K., Thian E., Plique O. Effect of diosmectite on intestinal permeability changes in acute diarrhea: a double blind placebo-controlled trial. Journal of Pediatric Gastroenterology and Nutrition. 1992;14:413–419. doi: 10.1097/00005176-199205000-00007. [DOI] [PubMed] [Google Scholar]
  17. DuPont H.L., Ericsson C.D., DuPont M.W., Cruz Luna A., Mattewson J.J. A randomized, open-label comparison of loperamide and attapulgite in the symptomatic treatment of acute diarrhea. American Journal of Medicine. 1990;20:20–23. doi: 10.1016/0002-9343(90)90271-e. [DOI] [PubMed] [Google Scholar]
  18. Eaton, J.R., Eaton, T.M., 1995. Bentonite: Public Research Project: An Educational Compilation of Related Commentaries and Articles. http://www.eytonsearth.org/bentonite.html.
  19. Espinasse J., Navetat H., Droy-Lefaix M.T., Roger C. Treatment and prevention of diarrhea in young calves by a cytoprotector agent of intestinal mucus barrier: smectite. Bulletin de la Société Vétérinaire Pratique de France. 1987;71:4–13. [Google Scholar]
  20. Fioramonti J., Bouaouiche F., Droy-Lefaix M.T., Plique O., Corthier G., Bueno L. Diosmectite treatment delays colonic water secretion and reduces increase in intestinal permeability by Clostridium difficile toxins in rats. Gut. 1994;35(Suppl 4):A31–A32. [Google Scholar]
  21. Fioramonti J., Droy-Lefaix M.T., Bueno L. Changes in gastric-intestinal motility induced by cholera toxin and experimental osmotic diarrhoea in dogs: effects of treatment with an argillaceous compound. Digestion. 1987;36:230–237. doi: 10.1159/000199423. [DOI] [PubMed] [Google Scholar]
  22. Fioramonti J., Fargeas M.J., Bueno L. Action of T-2 toxin on gastrointestinal transit in mice: protective effect of an argillaceous compound. Toxicology Letters. 1987;36:227–232. doi: 10.1016/0378-4274(87)90190-1. [DOI] [PubMed] [Google Scholar]
  23. Fioramonti J., Navetat H., Droy-Lefaix M.T., Moré J., Bueno L. Antidiarrheal properties of clay minerals: pharmacological and clinical studies. In: Simon F., Lees P., Semjen G., editors. Veterinary Pharmacology, Toxicology and Therapy in Food Producing Animals. Proceedings of the 4th Congress of Pharmacology and Toxicology, Budapest, 1988. University of Veterinary Science; Budapest: 1990. pp. 245–251. [Google Scholar]
  24. Frexinos J., Suduca J.M., Schatz B. Smectite and colic fermentation. Semaine des Hôpitaux de Paris. 1986;62:2025–2028. [Google Scholar]
  25. Girardeau, J.P., 1987. Escherichia coli smectite aggregation. Acta Gastroenterologica Belgica 50, Abstract 85.
  26. Guarino A., Bisceglia M., Castellucci G., Lacono G., Bruzzess E., Musetta A., Greco L. Smectite in the treatment of acute diarrhea: a nationwide randomized controlled study of the Italian Society of Pediatric Gastroenterology and Hepatology (SIGEP) in collaboration with primary care pediatricians. SOGEP study groups for smectite in acute diarrhea. Journal of Pediatric Gastroenterology and Nutrition. 2001;32:71–75. doi: 10.1097/00005176-200101000-00019. [DOI] [PubMed] [Google Scholar]
  27. Gwozdzinski, K., Jedrzejewska, A., Janocka, M., Droy-Lefaix, M.T., 1997. Effect of diosmectite on the physico-chemical properties of gastric mucus in vivo and in vitro. Gastroenterology 12, Abstract 136.
  28. Hornbrink J., Voss A.C., Fröhlich D., Glatzel M., Krauns A., Glaser F.A. Therapy trends in the prevention of radiation induced diarrhea after pelvic and abdominal irradiation. Results of a tricenter study. Strahlentherapie und Onkologie. 1995;174:49–53. [PubMed] [Google Scholar]
  29. Ippolite C. Antidiarrheal agents for the management of treatment related diarrhea in cancer patients. American Journal of Health System Pharmacy. 1998;55:1573–1580. doi: 10.1093/ajhp/55.15.1573. [DOI] [PubMed] [Google Scholar]
  30. Karas J. Smecta and its place in the treatment of acute rotavirus gastroenteritis of neonates. Cesko-Slovenska Pediatrie. 1996;55:85–90. [Google Scholar]
  31. Knight, J., Pearson, J.P., Droy-Lefaix, M.T., Allen, A., 1998. Could the discontinuous and structurally weaker colonic mucus gel in ulcerative colitis be a result of free radical damage? Digestive Disease Week, 99th Annual Meeting of AGA, New Orleans, LA.
  32. Leonard A.J., Droy-Lefaix M.T., Allen A. Pepsin hydrolysis of the adherent mucus barrier and subsequent gastric mucosal damage in the rat: effect of diosmectite and 16,16 dimethyl prostaglandin E2. Gastroentérologie Clinique et Biologique. 1994;8:609–616. [PubMed] [Google Scholar]
  33. Lexomboon U., Harikul S., Lortholary O. Control randomized study of rehydration with dioctahedral smectite in ambulatory Thai infants with acute diarrhea. Southeast Asian Journal of Tropical Medicine and Public Health. 1994;25:157–162. [PubMed] [Google Scholar]
  34. Lipson S.M., Stotzky G. Effect of proteins on reovirus adsorption to clay minerals. Applied Environmental Microbiology. 1984;8:525–530. doi: 10.1128/aem.48.3.525-530.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Lukas K., Lukas M. Dioctahedral smectite in the treatment of irritable colon. Prakticky Lekar. 2000;80:27–29. [Google Scholar]
  36. Madkour A.A., Madina E.M.H., El Azzouni O.E.Z., Amor M.A., El Waliti T.M.K., Abbass T. Smectite in acute diarrhea in children: a double-blind study placebo-controlled clinical trial. Journal of Pediatric Gastroenterology and Nutrition. 1993;17:176–181. doi: 10.1097/00005176-199308000-00008. [DOI] [PubMed] [Google Scholar]
  37. Mahraoui L., Heyman M., Plique O., Droy-Lefaix M.T., Desjeux J.F. Apical effect of diosmectite on damage to the intestinal barrier induced by basal tumour necrosis factor- alpha. Gut. 1997;40:339–343. doi: 10.1136/gut.40.3.339. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Martirosian G., Rouyan G., Zalewski T., Meisel Mikolajczyk F. Dioctahedral smectite neutralization activity of Clostridium difficile and Bacteroides fragilis toxins in vitro. Acta Microbiologica Polonica. 1998;47:171–183. [PubMed] [Google Scholar]
  39. Mastroianni A., Canallieri C., Coronado O., Manfred R., Chiodo F., Pignatari S. Smectite in AIDS-associated chronic idiopathic diarrheas. Minerva Gastroenterologica et Dietologica. 1998;44:231–234. [PubMed] [Google Scholar]
  40. Meredith T.J., Vale J.A. Treatment of paraquat poisoning in man. Methods to prevent absorption. Human Toxicology. 1987;6:49–55. doi: 10.1177/096032718700600108. [DOI] [PubMed] [Google Scholar]
  41. Milocco C., Bolis A., Rizzo V., Suprani T., Cerasoli G., Marani M., Pocecco M. Evaluation of diosmectite in acute diarrhea in children. Pediatria Medica e Chirurgica. 1999;21:129–133. [PubMed] [Google Scholar]
  42. Moré J., Benazet F., Fioramonti J., Droy-Lefaix M.T. Effects of treatment with smectite on gastric and intestinal glycoproteins in the rat: a histochemical study. Histochemical Journal. 1987;19:665–670. doi: 10.1007/BF01676173. [DOI] [PubMed] [Google Scholar]
  43. Moré J., Fioramonti J., Bueno L. Changes in gastrointestinal mucins caused by attapulgite. Experimental study. Gastroentérologie Clinique et Biologique. 1992;16:988–993. [PubMed] [Google Scholar]
  44. Narkeviciute J., Rudzeviciene O., Leviniere G., Mociskiene K., Eidukevicius R. Management of Lithuanian children's acute diarrheas with gastrolit solution and dioctahedral smectite. European Journal of Gastroenterology and Hepatology. 2002;14:419–424. doi: 10.1097/00042737-200204000-00015. [DOI] [PubMed] [Google Scholar]
  45. Opriu, A.L., Diculescu, M., Lov, A., Calin, S., Dumitrescu, A., Calin, G., Manuc, M., Pitigoi, D., 1996. Enterocyte covering agent versus intestinal motility inhibition in the irritable bowel. Gut 9, Abstract 34.
  46. Pearson, J.P., Ayre, D., Droy-lefaix, M.T., Allen, A., 1996. Mucolysis of the colonic mucus barrier by oxygen free radicals: implication for ulcerative colitis. Gastroenterology 110, Abstract 988.
  47. Peignot J.F., Giral P., Plique O. A multicentric, double-blind, placebo controlled study of the efficacy of diosmectite in the treatment of secondary stomach pain due to administration of non steroid antiinflammatory agents. Médecine et Chirurgie Digestive. 1997;26:233–241. [Google Scholar]
  48. Perrotin, D., Legras, A., Boulain, T., Ginies, G., 1990. Diarrhea under parenteral nutrition in reanimation. Prevention study using an adsorbent drug. In: Réanimation et Appareil digestif. Société de Réanimation de Langue française, Paris, pp. 49–53.
  49. Phanuphak P., Hanvanick M., Lortholary O. Smectite in HIV-associated diarrheas: a preliminary study. Journal of Acquired Immune Deficiency Syndrome. 1992;5:954–955. [PubMed] [Google Scholar]
  50. Pons, L., Droy-Lefaix, M.T., Leguere, N., Guillemain, J., 1997. Protective effects of diosmectite from alterations of mucosal permeability and morphology of rabbit ileal loops induced by Escherichia coli enterotoxin. Gastroenterology 112, Abstract 395.
  51. Samson, H.J., Pearson, J.P., Srivastava, E.D., Droy-Lefaix, M.T., Allen, A., 1995. Increased serine-dependent proteinases in ulcerative colitis: mucolysis and inhibition by diosmectite. Gastroenterology 108, Abstract 909.
  52. Santantonio M., Colella M., Fiorica F., Aratisali S., Stefanelli A., Falchi A.M. Diosmectite (diosmectal) prevention antidiarrheic therapy in patients submitted to pelvic radiation. Minerva Gastroenterologica et Dietologica. 2000;46:225–230. [PubMed] [Google Scholar]
  53. Schell T., Lindemann M.D., Kornegay E.T., Blodgett D.L., Doerr J.A. Effectiveness of different types of clay for reducing the detrimental effects of aflatoxin-contaminated diets on performance and serum profiles of weanling pigs. Journal of Animal Science. 1993;71:1226–1231. doi: 10.2527/1993.7151226x. [DOI] [PubMed] [Google Scholar]
  54. Secondulfo M., Mennella R., Fenderico C. Ruolo dei fattori psicologi nei pazienti affeitti da sindrome dell’intestino irritabile. Internista. 2002;10:169–173. [Google Scholar]
  55. Slitine-Bonet, F., Vatier, J., Droy-Lefaix, M.T., 1994. Structural study of rat's gastric adherent mucus: protective effect of diosmectite from alcohol injury. Gut 35, Abstract 210.
  56. Theodorou, V., Chrestian, B., Fioramonti, J., Droy-Lefaix, M.T., Bueno, L., 1995. Diosmectite treatment prevents intestinal permeability and mucus alterations induced by ingestion of a pesticide in rats. Gut 37, Abstract 148.
  57. Theodorou V., Fioramonti J., Droy-Lefaix M.T., Plique O., Bueno L. Protective action of diosmectite treatment on digestive disturbances induced by intestinal anaphylaxis in the guinea pig. Alimentary Pharmacology and Therapeutics. 1994;8:295–299. doi: 10.1111/j.1365-2036.1994.tb00291.x. [DOI] [PubMed] [Google Scholar]
  58. Vivatvakin B., Jongpipatvanich S., Harikul S., Eksaengri P., Lortholary O. Control study of oral rehydration solution (ORS)+dioctahedral smectite in hospitalized Thai infants with acute secretory diarrhea. Southeast Asian Journal of Tropical Medicine and Public Health. 1992;23:414–419. [PubMed] [Google Scholar]

Articles from Developments in Clay Science are provided here courtesy of Elsevier

RESOURCES