WHO monographs on selected medicinal plants - travolekar.ru

WHO monographs on selected medicinal plants - travolekar.ru WHO monographs on selected medicinal plants - travolekar.ru

20.01.2015 Views

ong>WHOong> ong>monographsong> on selected medicinal plants Foreign organic matter Not more than 5% (3). Total ash Not more than 3% (3). Acid-insoluble ash Not more than 1.5% (3). Water-soluble extractive To be established in accordance with national requirements. Loss on drying Not more than 12% (10). Swelling value Not less than 4.5 determined on the powdered drug (1). Pesticide residues The recommended maximum limit of aldrin and dieldrin is not more than 0.05 mg/kg (1). For other pesticides, see the European pharmacopoeia (1) and the ong>WHOong> guidelines on assessing quality of herbal medicines with reference to contaminants and residues (9) and pesticide residues (11). Heavy metals For maximum limits and analysis of heavy metals, consult the ong>WHOong> guidelines on assessing quality of herbal medicines with reference to contaminants and residues (9). Radioactive residues Where applicable, consult the ong>WHOong> guidelines on assessing quality of herbal medicines with reference to contaminants and residues (9). Chemical assays To be established in accordance with national requirements. Major chemical constituents Contains water-soluble polysaccharides (50%), primarily lichenin, a linear cellulose-like polymer of -D-glucose units, and isolichenin, an -Dglucose polymer. Two glucans, lichenan and isolichenan, have been isolated from the lichen Cetraria islandica (12), as well as galactomannans (5). Major secondary metabolites include the lichen acids (depsidones), 142

Lichen Islandicus fumarprotocetraric acid, protolichestearic acid and cetraric acids (5, 13). A biologically active aliphatic -lactone, (+)-protolichesterinic acid has also been reported (14). The structures of fumarprotocetraric acid, cetraric acid and (+)-protolichesterinic acid are presented below. CHO H 3 C CHO H 3 C HO CO 2 H HO O O OH O O H 3 C H 3 C O O O Cetraric acid CH 3 Fumarprotocetraric acid CO 2 H OH O O CO 2 H H 3 C (+)-Protolichesterinic acid O H O H CO 2 H CH 2 Medicinal uses Uses supported by clinical data Used orally as a demulcent to treat inflammation and dryness of the pharyngeal mucosa (15, 16). Uses described in pharmacopoeias and well established documents Used orally for treatment of loss of appetite and nausea (3, 17). Uses described in traditional medicine Used to treat asthma, cramps, bronchitis, cough, diabetes, exhaustion, gastric disturbances, immune depletion, migraine, nausea in pregnancy and wounds. Also used as an emergency food source, an emollient and a galactagogue (4, 18–20). Pharmacology Experimental pharmacology Antimicrobial and antiviral activities An aqueous extract of the thalli and protolichesterinic acid were screened for in vitro activity against Mycobacterium aurum, a nonpathogenic organism with a similar sensitivity profile to M. tuberculosis. Protolichesterinic acid had a minimum inhibitory concentration (MIC) of 125.0 μg/ml (21). An aqueous extract of the thalli was screened for in vitro activity against Helicobacter pylori. (+)-Protolichesterinic acid was identified as 143

Lichen Islandicus<br />

fumarprotocetraric acid, protolichestearic acid and cetraric acids (5, 13).<br />

A biologically active aliphatic -lact<strong>on</strong>e, (+)-protolichesterinic acid has<br />

also been reported (14). The st<strong>ru</strong>ctures of fumarprotocetraric acid, cetraric<br />

acid and (+)-protolichesterinic acid are presented below.<br />

CHO H 3 C<br />

CHO H 3 C<br />

HO<br />

CO 2 H<br />

HO<br />

O<br />

O<br />

OH<br />

O<br />

O<br />

H 3 C<br />

H 3 C<br />

O<br />

O<br />

O<br />

Cetraric acid CH 3 Fumarprotocetraric acid<br />

CO 2 H<br />

OH<br />

O<br />

O<br />

CO 2 H<br />

H 3 C<br />

(+)-Protolichesterinic acid<br />

O<br />

H<br />

O<br />

H<br />

CO 2 H<br />

CH 2<br />

Medicinal uses<br />

Uses supported by clinical data<br />

Used orally as a demulcent to treat inflammati<strong>on</strong> and dryness of the pharyngeal<br />

mucosa (15, 16).<br />

Uses described in pharmacopoeias and well established documents<br />

Used orally for treatment of loss of appetite and nausea (3, 17).<br />

Uses described in traditi<strong>on</strong>al medicine<br />

Used to treat asthma, cramps, br<strong>on</strong>chitis, cough, diabetes, exhausti<strong>on</strong>,<br />

gastric disturbances, immune depleti<strong>on</strong>, migraine, nausea in pregnancy<br />

and wounds. Also used as an emergency food source, an emollient and a<br />

galactagogue (4, 18–20).<br />

Pharmacology<br />

Experimental pharmacology<br />

Antimicrobial and antiviral activities<br />

An aqueous extract of the thalli and protolichesterinic acid were screened<br />

for in vitro activity against Mycobacterium au<strong>ru</strong>m, a n<strong>on</strong>pathogenic organism<br />

with a similar sensitivity profile to M. tuberculosis. Protolichesterinic<br />

acid had a minimum inhibitory c<strong>on</strong>centrati<strong>on</strong> (MIC) of 125.0 μg/ml<br />

(21). An aqueous extract of the thalli was screened for in vitro activity<br />

against Helicobacter pylori. (+)-Protolichesterinic acid was identified as<br />

143

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