SILYMARIN
HAZARDTEXT ®
Information to help in the initial response for evaluating chemical incidents
-IDENTIFICATION
SYNONYMS
IDENTIFIERS
65666-07-1(Silymarin) 22888-70-6(Silibinin)
USES/FORMS/SOURCES
ORAL: Milk thistle (silymarin) has been used as a hepatoprotectant and as a supportive treatment of toxic liver damage by chemicals. In addition, it has been used to treat Amanita phalloides mushroom poisoning, jaundice, chronic inflammatory liver diseases, hepatic cirrhosis, hepatitis and fatty infiltration by alcohol and industrial chemical, loss of appetite, dyspeptic and gallbladder complaints, hangover, diseases of the spleen, prostate cancer, pleurisy, malaria, depression, uterine complaints, stimulating breast milk flow, and stimulating menstrual flow (Arteel et al, 2003; Flora et al, 1998; Anon, 1997; Leng-Peschlow, 1996). Milk thistle may have a role as a renoprotective agent against such therapy as cisplatin and aminoglycosides that can induce nephrotoxicity (Dashti-Khavidaki et al, 2012). PARENTERAL: Milk thistle (Silymarin) has been used as an antidote for Amanita phalloides mushroom poisoning (Madaus Inc., 2009; Hruby et al, 1983). Actual absorption of silymarin from the gastrointestinal tract is thought to be about 23% to 47%. Silymarin is best administered parenterally for maximum absorption (Anon, 1997; Tyler , 1994). In a study of 60 patients with severe Amanita mushroom poisoning who were given 20 mg/kg of silybin (syn. silibinin) IV, no patients died (Vogel, 1981). Death rates for this type of mushroom poisoning vary widely but may reach up to 40% or 50%. Hruby et al reported on a total of 18 cases of poisoning by Amanita phalloides that were treated by combined chemotherapy. After attempted primary elimination, all patients received silibinin (16 intravenously, 2 orally). All patients survived except one, who received a massive dose of toxin with suicidal intent. Using severe liver damage as a marker, silibinin given within 48 hours of mushroom ingestion appeared to be an effective prophylactic measure. The earlier the silibinin was given, the more benign the subsequent clinical course of mushroom poisoning. A dose of 20 to 50 mg/kg/day, given within the first 48 hours, may have helped prevent severe liver damage (Hruby et al, 1983; Hruby et al, 1983a). Silymarin (syn. silibinin) and high-dose penicillin G were used to treat a 7-year-old girl with severe Amanita phalloides poisoning (prothrombin-time less than 10% and hepatic coma). The child responded favorably to the treatment (Rambousek et al, 1993).
FOOD USES: In Europe, the de-spined leaves have been used in fresh salads and as a spinach substitute. The pealed and soaked young stalks have been eaten like asparagus. In addition, the flower-heads were eaten like those of the artichoke. Milk thistle seeds (fruit) were used as a coffee substitute (Anon, 1997; Awang, 1993). AMANITA PHALLOIDES MUSHROOM POISONING: The hepatoprotective and antagonist effects of silibinin against amatoxins have been confirmed in experimental models. Silibinin is thought to inhibit the penetration of the amatoxins into liver cells (Jahn et al, 1980; Faulstich et al, 1980a; Floersheim, 1987). The efficacy of silibinin is difficult to evaluate because it is often combined with other therapies, such as penicillin, ascorbic acid, and hemodialysis(Lheureux et al, 1992), however the results appear to be positive in the treatment of mushroom poisoning.
PARENTERAL Silibinin is not available as a licensed drug in the US. It is widely available, under a variety of trade names, in Europe and South America. Silibinin (silybin) ampules for intravenous use are available (Legalon(R)SIL (Madaus AG, Germany): CLINICAL TRIAL: An open-label, multicenter, clinical trial (start date: February 2010; anticipated end date December, 2015), sponsored by Madaus Inc, (a division of Madaus GmbH, Cologne, Germany), is evaluating the safety and efficacy of intravenous silibinin (Legalon(R) SIL) for treating patients with amatoxin mushroom poisoning diagnosed by history, GI symptoms, elevated liver enzymes, and/or diagnostic assay. Patients will be treated with 5 mg/kg loading dose of silibinin followed by 20 mg/kg/day via continuous infusion. Treatment will be discontinued when coagulopathy has resolved, and when liver enzyme concentrations have significantly improved. Patients will be monitored for 7 to 14 days after the end of silibinin therapy with follow up lab studies. For more information on this clinical trial, check the following website: http://clinicaltrials.gov/ct2/show/NCT00915681 (Madaus Inc., 2009). To obtain silibinin, a 24-hour hotline is available for physicians: 866-520-4412 (Madaus Inc., 2009).
ORAL In the US, milk thistle extracts, tablets, capsules or tincture containing 70% to 80% silymarin, are available as commercial preparations (Thisilyn (Nature's Way)) (Javed et al, 2011; Anon, 1997).
HERBAL TEA
-CLINICAL EFFECTS
GENERAL CLINICAL EFFECTS
- USES: ANTIDOTE: Silybum marianum (also known as milk thistle) has been used intravenously (Legalon(R) SIL) as an antidote for Amanita phalloides mushroom poisoning. It is available in the US based on compassionate use under an FDA sanctioned Open Treatment IND. ORAL THERAPY: As an herbal supplement it is widely used for its hepatoprotective effect and has been used in the treatment of toxic liver damage (ie, commonly prescribed for cirrhosis and viral hepatitis). FOOD: The de-spined leaves, the young stalks of the plant and the flower-heads have all been used as a food source.
- PHARMACOLOGY: Silybum marainum is part of the family Asteraceae. Silymarin is a lipohilic extract and the active part of the plant. It has been suggested that it acts as an antiinflammatory. Extracts of the plant usually contain 70% to 80% silymarin and contain 3 isomers of flavonolignans (ie, silybin, silydianin and silychristin) and 2 flavonoids (taxifolin and quercetin) and the remaining portion (20% to 30%) is made up of polyphenolic compounds.
- EPIDEMIOLOGY: Exposure is not common. Serious toxicity has not been reported.
ADVERSE EFFECTS: Silymarin is usually well tolerated. ORAL: Nausea, diarrhea, dyspepsia, flatulence, abdominal bloating, fullness or pain, and anorexia have been reported. Urticaria and allergic reactions to silymarin may occur. INFREQUENT: Pruritus, headache, exanthema, malaise, asthenia and vertigo may develop. Intermittent episodes of sweating, nausea and vomiting, colicky abdominal pain, diarrhea, weakness, and collapse occurred in a woman following daily administration of milk thistle capsules for 2 months. INTRAVENOUS: No serious adverse reactions have been reported with intravenous therapy. Flushing has been reported during infusion; effects have been mild.
- Editor's Note: An ERG guide with information appropriate to this material does not exist.
-FIRST AID
FIRST AID AND PREHOSPITAL TREATMENT
-RANGE OF TOXICITY
MAXIMUM TOLERATED EXPOSURE
Most clinical trials have used daily oral dosages of 420 to 480 mg silymarin, divided into 2 or 3 doses daily (Rainone, 2005). Silipide doses up to 360 mg (silybin equivalent) 3 times a day for 3 weeks have been given to normal volunteers without toxic effects (Marena & Lampertico, 1991).
- Carcinogenicity Ratings for CAS65666-07-1 :
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): Not Listed EPA (U.S. Environmental Protection Agency, 2011): Not Listed IARC (International Agency for Research on Cancer (IARC), 2016; International Agency for Research on Cancer, 2015; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2010; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2010a; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2008; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2007; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2006; IARC, 2004): Not Listed NIOSH (National Institute for Occupational Safety and Health, 2007): Not Listed MAK (DFG, 2002): Not Listed NTP (U.S. Department of Health and Human Services, Public Health Service, National Toxicology Project ): Not Listed
- Carcinogenicity Ratings for CAS22888-70-6 :
ACGIH (American Conference of Governmental Industrial Hygienists, 2010): Not Listed EPA (U.S. Environmental Protection Agency, 2011): Not Listed IARC (International Agency for Research on Cancer (IARC), 2016; International Agency for Research on Cancer, 2015; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2010; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2010a; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2008; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2007; IARC Working Group on the Evaluation of Carcinogenic Risks to Humans, 2006; IARC, 2004): Not Listed NIOSH (National Institute for Occupational Safety and Health, 2007): Not Listed MAK (DFG, 2002): Not Listed NTP (U.S. Department of Health and Human Services, Public Health Service, National Toxicology Project ): Not Listed
TOXICITY AND RISK ASSESSMENT VALUES
- EPA Risk Assessment Values for CAS65666-07-1 (U.S. Environmental Protection Agency, 2011):
- EPA Risk Assessment Values for CAS22888-70-6 (U.S. Environmental Protection Agency, 2011):
LD50- (INTRAPERITONEAL)DOG: LD50- (INTRAPERITONEAL)MOUSE: LD50- (INTRAPERITONEAL)RABBIT: LD50- (INTRAPERITONEAL)RAT:
-STANDARDS AND LABELS
WORKPLACE STANDARDS
- ACGIH TLV Values for CAS65666-07-1 (American Conference of Governmental Industrial Hygienists, 2010):
- ACGIH TLV Values for CAS22888-70-6 (American Conference of Governmental Industrial Hygienists, 2010):
- AIHA WEEL Values for CAS65666-07-1 (AIHA, 2006):
- AIHA WEEL Values for CAS22888-70-6 (AIHA, 2006):
- NIOSH REL and IDLH Values for CAS65666-07-1 (National Institute for Occupational Safety and Health, 2007):
- NIOSH REL and IDLH Values for CAS22888-70-6 (National Institute for Occupational Safety and Health, 2007):
- OSHA PEL Values for CAS65666-07-1 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA PEL Values for CAS22888-70-6 (U.S. Occupational Safety, and Health Administration (OSHA), 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS65666-07-1 (U.S. Occupational Safety and Health Administration, 2010):
- OSHA List of Highly Hazardous Chemicals, Toxics, and Reactives for CAS22888-70-6 (U.S. Occupational Safety and Health Administration, 2010):
ENVIRONMENTAL STANDARDS
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS65666-07-1 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities for CAS22888-70-6 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS65666-07-1 (U.S. Environmental Protection Agency, 2010):
- EPA CERCLA, Hazardous Substances and Reportable Quantities, Radionuclides for CAS22888-70-6 (U.S. Environmental Protection Agency, 2010):
- EPA RCRA Hazardous Waste Number for CAS65666-07-1 (U.S. Environmental Protection Agency, 2010b):
- EPA RCRA Hazardous Waste Number for CAS22888-70-6 (U.S. Environmental Protection Agency, 2010b):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS65666-07-1 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Extremely Hazardous Substance List for CAS22888-70-6 (U.S. Environmental Protection Agency, 2010):
- EPA SARA Title III, Community Right-to-Know for CAS65666-07-1 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
- EPA SARA Title III, Community Right-to-Know for CAS22888-70-6 (40 CFR 372.65, 2006; 40 CFR 372.28, 2006):
- DOT List of Marine Pollutants for CAS65666-07-1 (49 CFR 172.101 - App. B, 2005):
- DOT List of Marine Pollutants for CAS22888-70-6 (49 CFR 172.101 - App. B, 2005):
- EPA TSCA Inventory for CAS65666-07-1 (EPA, 2005):
- EPA TSCA Inventory for CAS22888-70-6 (EPA, 2005):
LABELS
- NFPA Hazard Ratings for CAS65666-07-1 (NFPA, 2002):
- NFPA Hazard Ratings for CAS22888-70-6 (NFPA, 2002):
-PERSONAL PROTECTION
SUMMARY
- Editor's Note: An ERG guide with information appropriate to this material does not exist.
PROTECTIVE CLOTHING
- CHEMICAL PROTECTIVE CLOTHING. Search results for CAS 65666-07-1.
- CHEMICAL PROTECTIVE CLOTHING. Search results for CAS 22888-70-6.
-PHYSICAL HAZARDS
FIRE HAZARD
- FLAMMABILITY CLASSIFICATION
- NFPA Flammability Rating for CAS65666-07-1 (NFPA, 2002):
- NFPA Flammability Rating for CAS22888-70-6 (NFPA, 2002):
- FIRE CONTROL/EXTINGUISHING AGENTS
- Editor's Note: An ERG guide with information appropriate to this material does not exist.
- NFPA Extinguishing Methods for CAS65666-07-1 (NFPA, 2002):
- NFPA Extinguishing Methods for CAS22888-70-6 (NFPA, 2002):
EVACUATION PROCEDURES
- Editor's Note: An ERG guide with information appropriate to this material does not exist.
- AIHA ERPG Values for CAS65666-07-1 (AIHA, 2006):
- AIHA ERPG Values for CAS22888-70-6 (AIHA, 2006):
- DOE TEEL Values for CAS65666-07-1 (U.S. Department of Energy, Office of Emergency Management, 2010):
- DOE TEEL Values for CAS22888-70-6 (U.S. Department of Energy, Office of Emergency Management, 2010):
- AEGL Values for CAS65666-07-1 (National Research Council, 2010; National Research Council, 2009; National Research Council, 2008; National Research Council, 2007; NRC, 2001; NRC, 2002; NRC, 2003; NRC, 2004; NRC, 2004; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; 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62 FR 58840, 1997; 65 FR 14186, 2000; 65 FR 39264, 2000; 65 FR 77866, 2000; 66 FR 21940, 2001; 67 FR 7164, 2002; 68 FR 42710, 2003; 69 FR 54144, 2004):
- AEGL Values for CAS22888-70-6 (National Research Council, 2010; National Research Council, 2009; National Research Council, 2008; National Research Council, 2007; NRC, 2001; NRC, 2002; NRC, 2003; NRC, 2004; NRC, 2004; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; United States Environmental Protection Agency Office of Pollution Prevention and Toxics, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; 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National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2008; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2007; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2005; National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances, 2006; 62 FR 58840, 1997; 65 FR 14186, 2000; 65 FR 39264, 2000; 65 FR 77866, 2000; 66 FR 21940, 2001; 67 FR 7164, 2002; 68 FR 42710, 2003; 69 FR 54144, 2004):
- NIOSH IDLH Values for CAS65666-07-1 (National Institute for Occupational Safety and Health, 2007):
- NIOSH IDLH Values for CAS22888-70-6 (National Institute for Occupational Safety and Health, 2007):
CONTAINMENT/WASTE TREATMENT OPTIONS
-PHYSICAL/CHEMICAL PROPERTIES
-REFERENCES
GENERAL BIBLIOGRAPHY- 40 CFR 372.28: Environmental Protection Agency - Toxic Chemical Release Reporting, Community Right-To-Know, Lower thresholds for chemicals of special concern. National Archives and Records Administration (NARA) and the Government Printing Office (GPO). Washington, DC. Final rules current as of Apr 3, 2006.
- 40 CFR 372.65: Environmental Protection Agency - Toxic Chemical Release Reporting, Community Right-To-Know, Chemicals and Chemical Categories to which this part applies. National Archives and Records Association (NARA) and the Government Printing Office (GPO), Washington, DC. Final rules current as of Apr 3, 2006.
- 49 CFR 172.101 - App. B: Department of Transportation - Table of Hazardous Materials, Appendix B: List of Marine Pollutants. National Archives and Records Administration (NARA) and the Government Printing Office (GPO), Washington, DC. Final rules current as of Aug 29, 2005.
- 62 FR 58840: Notice of the National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances - Proposed AEGL Values, Environmental Protection Agency, NAC/AEGL Committee. National Archives and Records Administration (NARA) and the Government Publishing Office (GPO), Washington, DC, 1997.
- 65 FR 14186: Notice of the National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances - Proposed AEGL Values, Environmental Protection Agency, NAC/AEGL Committee. National Archives and Records Administration (NARA) and the Government Publishing Office (GPO), Washington, DC, 2000.
- 65 FR 39264: Notice of the National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances - Proposed AEGL Values, Environmental Protection Agency, NAC/AEGL Committee. National Archives and Records Administration (NARA) and the Government Publishing Office (GPO), Washington, DC, 2000.
- 65 FR 77866: Notice of the National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances - Proposed AEGL Values, Environmental Protection Agency, NAC/AEGL Committee. National Archives and Records Administration (NARA) and the Government Publishing Office (GPO), Washington, DC, 2000.
- 66 FR 21940: Notice of the National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances - Proposed AEGL Values, Environmental Protection Agency, NAC/AEGL Committee. National Archives and Records Administration (NARA) and the Government Publishing Office (GPO), Washington, DC, 2001.
- 67 FR 7164: Notice of the National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances - Proposed AEGL Values, Environmental Protection Agency, NAC/AEGL Committee. National Archives and Records Administration (NARA) and the Government Publishing Office (GPO), Washington, DC, 2002.
- 68 FR 42710: Notice of the National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances - Proposed AEGL Values, Environmental Protection Agency, NAC/AEGL Committee. National Archives and Records Administration (NARA) and the Government Publishing Office (GPO), Washington, DC, 2003.
- 69 FR 54144: Notice of the National Advisory Committee for Acute Exposure Guideline Levels for Hazardous Substances - Proposed AEGL Values, Environmental Protection Agency, NAC/AEGL Committee. National Archives and Records Administration (NARA) and the Government Publishing Office (GPO), Washington, DC, 2004.
- AIHA: 2006 Emergency Response Planning Guidelines and Workplace Environmental Exposure Level Guides Handbook, American Industrial Hygiene Association, Fairfax, VA, 2006.
- Alaspaa AO, Kuisma MJ, Hoppu K, et al: Out-of-hospital administration of activated charcoal by emergency medical services. Ann Emerg Med 2005; 45:207-12.
- American Conference of Governmental Industrial Hygienists : ACGIH 2010 Threshold Limit Values (TLVs(R)) for Chemical Substances and Physical Agents and Biological Exposure Indices (BEIs(R)), American Conference of Governmental Industrial Hygienists, Cincinnati, OH, 2010.
- Anon: An adverse reaction to the herbal medication milk thistle (silybum marianum). MJA 1999; 170:218-219.
- Anon: Milk thistle. The Review of Natural Products(R)., Facts and Comparisons, a Wolters Kluwer Company, St Louis, Missouri, US, 1997, pp 1-6.
- Arteel G, Marsano L, Mendez C, et al: Advances in alcoholic liver disease. Best Pract Res Clin Gastroenterol 2003; 17(4):625-647.
- Awang D: Herbal Medicine: Milk thistle. Can Pharm J 1993; 126(8):403-404, 422.
- Barzaghi N, Crema F, & Gatti G: Pharmacokinetic studies on IdB 1016, a silybin-phosphatidylcholine complex, in healthy human subjects. Eur J Drug Metab Pharmacokinet 1990; 15:333-338.
- Chyka PA, Seger D, Krenzelok EP, et al: Position paper: Single-dose activated charcoal. Clin Toxicol (Phila) 2005; 43(2):61-87.
- Comoglio A, Leonarduzzi G, Carini R, et al: Studies on the antioxidant and free radical scavenging properties of IdB 1016 a new flavanolignan complex. Free Radic Res Commun 1990; 11:109-115.
- Conti M, Porzio A, & Malandrino S: Activity of silipide against ethanol-induced liver damage in rats. Planta Med 1991; 57(suppl 2):A115-A116.
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