Eyebright – Euphrasiae herba (Euphrasia officinalis L. and Euphrasia rostkoviana Hayne)
|Latin name of the genus:||Euphrasiae herba|
|Latin name of herbal substance:||Euphrasia officinalis l. and euphrasia rostkoviana hayne|
|Botanical name of plant:||Herbalref.com|
|English common name of herbal substance:||Eyebright|
Latin name of the genus: Euphrasiae herba
Botanical name of plant: Euphrasia officinalis L. and Euphrasia rostkoviana Hayne
English common name of herbal substance: Eyebright
This assessment report reviews the scientific data available for Euphrasia officinalis L. and Euphrasia rostkoviana Hayne, herba. The classification of the genus Euprasia differs greatly in the literature and is to some extent contradictory. Some authors consider Euphrasia officinalis L. the same as Euphrasia rostkoviana Hayne whereas others consider E. rostkoviana Hayne as a subspecies of E. officinalis L.1. According to some taxonomists, E. officinalis L. is also called E. stricta Wolff. (Heimans et al. 1983).
However, other sources make a distinction between both species. Euphrasia or eyebright belongs to the botanical family of the Scrophulariaceae.
The following databases were assessed:
–PubMed, until February 2009;
–The Cochrane Library, December 2008;
–OvidMedline, December 2008;
–Embase, December 2008;
Search terms: Euphrasia, Eyebright, Euphrasia and officinalis.
Apart from these sources standard books on phytotherapy were reviewed (see literature references).
1.1. Description of the herbal substance(s), herbal preparation(s) or combinations thereof
The herbal substance described in the Hagers Handbuch der pharmazeutischen Praxis as the dried total herb of Euphrasia officinalis harvested before flowering and dried out under sunlight in a well- ventilated area (Blascheck 1998). In the Deutsche Arzneimittel Codex, DAC, (Anonymous 2003) ‘Augentrostkraut’ is described as: “… aus den zur Blütezeit gesammelten, getrockneten, ganzen oder geschnittenen oberirdischen Teilen verschiedener
According to the information in the DAC, the plant is collected in the flowering status. The species used are confirmed.
Therefore, for the purpose of the establishment of a Community herbal monograph, in the herbal substance definition, flowers are also included in the herb.
Euphrasia is also known under the common names:
Spanish: Ojo brillante
1 Euphrasia officinalis is considered as an ambiguous name (De Langhe et al. 1988) Flora van België, het Groothertogdom Luxembrug,
Euphrasia stricta Host. is a well known European species (2 to 40 cm high), of which the aerial parts are harvested during flowering. Euphrasia stricta (Host.) can be differentiated from Euphrasia officinalis L. by the presence of curved hairs on the tops of the leaves (Schulze & Diepenbrock 1944).
Constituents (Blazics 2008)
–Flavonoids: 0.38%: apigenin, luteolin, kaempferol, rhamnetin, quercetin
–Phenolic acids: caffeic acid and its ester derivatives, chlorogenic acids and coumaric acids
–Hydroxycinnamic derivatives: 1.97%
–Iridoids: aucubin 0.05%
Figure 1: aucubine
Chudnicka (2005) showed that eyebright contains acidic phosphatases and
a)Comminuted herbal substance for tea infusion
b)Tincture 1:5 in ethanol 45% V/V (Barnes 2007)
Combinations of herbal substance(s) and/or herbal preparation(s) including a description of vitamin(s) and/or mineral(s) as ingredients of traditional combination herbal medicinal products assessed, where applicable.
–Infusion: 50% Camomille flower and 50% eyebright herb. Five soupspoons dried herb in 0.25 l freshly boiled water.
–Infusion: 60% eyebright herb, 20% melilot herb and 20% plantain herb. One soupspoon dried herb in a cup of freshly boiled water. After fifteen minutes the infusion is passed through a filtering tissue and applied as an ocular compress.
–Tincture: 50% eyebright tincture, 35% passionflower tincture and 15% belladonna tincture. Twenty drops in 15 ml of water can be taken orally up to four times a day.
1.2. Information about products on the market in the Member States
Regulatory status overview
2 The following preparations could be identified in Belgium (they can be considered as homeopathic preparations without a tradition of at least 30 years):
–Eye drops: 0.045g mother tincture per 100 mL.
–Eye drops in single doses: 0.05g mother tincture per 100 mL.
–Fixed combination with homeopathic preparations
–Euphrasia stillidoses D2: solvent = aqua purificata
MA: Marketing Authorisation TRAD: Traditional Use Registration
Other TRAD: Other national Traditional systems of registration Other: If known, it should be specified or otherwise add ’Not Known’
This regulatory overview is not legally binding and does not necessarily reflect the legal status of the products in the MSs concerned.
1.3. Search and assessment methodology
2. Historical data on medicinal use
2.1. Information on period of medicinal use in the Community
Felter (1922), Felter and Lloyd (1898) as well as Grieve (1931) give an extended historical overview of the traditional use of Euphrasia.
According to Grieve (1931) the name Euphrasia is of Greek origin, derived from Euphrosyne (gladness), the name of one of the three graces who was distinguished for her joy and mirth, and it is thought to have been given the plant from the valuable properties attributed to it as an eye medicine preserving eyesight and so bringing gladness into the life of the sufferer. The same Greek word is also given to the linnet, whence another old tradition says that it was the linnet that first made use of the leaf for clearing the sight of its young and who then passed on the knowledge to mankind, who named the plant in its honour.
Grieve further states that although always known under a name of Greek origin, the herb seems to have been unnoticed by the ancients and no mention of it is made by Dioscorides, Pliny, Galen or even by the Arabian physicians. In the fourteenth century, however, it was supposed to cure ‘all evils of the eye’ and is described as the source of ‘a precious water to clear a man’s sight’. Matthaeus Sylvaticus, a
physician of Mantua, who lived about the year 1329, recommended this plant in disorders of the eyes and Arnoldus Villanovanus, who died in 1313, was the author of a treatise on its virtues, Vini Euphrasiati tantopere celebrati. How long before Euphrasia was in repute for eye diseases it is impossible to say, but in Gordon’s Liticium Medicina, 1305, among the medicines for the eyes, Euphragia is named and is recommended both outwardly in a compound distilled water and inwardly as a syrup. Euphragia is not, however, mentioned in the Schola Salernitana, compiled about 1100.
Grieves states that Euphrasia is used in a European tradition since the fourteenth century. It was supposed to cure ‘all evils of the eye’. Paracelsus also recognised the structure of an eye in the plant. Many literatures of different European countries from the late eighteenth and early nineteenth century refer to eyebright “as a solution for all the eye problems”. Euphrasia is mentioned in standard works such as The British flora medica (Barton and Castle 1837), Reine Arzneimittellehre (Hahnemann 1826), Flora parisiensis (Bulliard 1779), Flora veneta (Naccari 1827), Flora Scotica (Lightfoot 1777) and
Afbeeldingen der artsenygewassen met derselver nederduitsche en latynse beschryvingen (Oskamp 1796).
Felter and Lloyd (1898) report slightly tonic and astringent activity. Quoting the authors, Euphrasia was used with much benefit in the form of infusion or poultice, in catarrhal ophthalmia, also of service in all mucous diseases attended with increased discharges; and in cough, hoarseness, earache, and headache, which have supervened in catarrhal affections. It is said to specifically influence the nasal membranes and lachrymal apparatus. In acute catarrh (fluent coryza), in which there is a profuse watery flow, it is reported to exert its most specific action. It has been attributed great utility to control inflammatory and catarrhal phases of the parts during or following an attack of measles, as it has been thought to avert unpleasant aftereffects, as catarrhal conjunctivitis, nasal catarrh, catarrhal deafness, etc. Catarrhal diseases of the intestinal tract were treated with Euphrasia. Four fluid ounces of the infusion taken every morning upon an empty stomach, and also every night at bedtime is asserted to have been found successful in curing epilepsy.
The Ergänzungsbuch zum Deutschen Arzneibuch included Euphrasia as a rinsing solution prepared as a 2% infusion.
2.2. Information on traditional/current indications and specified substances/preparations
The comminuted herbal substance is mainly used as herbal tea for external ocular application (i.e. conjunctivitis, blepharitis, styes,…). Secondly, the comminuted dried herb is used as an infusion for internal administration in case of common cold and eye problems. Thirdly, herbal preparations can be applied as a nasal ointment against a runny nose. There is only poor clinical evidence as the data available are scarce. Eyebright is listed by the Council of Europe as a natural source of food flavouring (category N3) (Anonymous 2010).
Traditional herbal medicinal product for symptomatic treatment and prevention of conjunctivitis of any etiology (allergic, irritative, infectious) (Barnes 2007; Blascheck 1998; Delfosse 1998; Van Hellemont 1985; Weiss 1999; Wichtl 1994).
Traditional herbal medicinal product for symptomatic treatment of minor ocular diseases; for example blepharitis, eye fatigue, purulent ocular inflammation and styes (Barnes 2007; Blascheck 1998; Delfosse 1998; Van Hellemont 1985; Weiss 1999; Wichtl 1994).
Traditional herbal medicinal product for symptomatic treatment of cold (Delfosse 1998).
Some sources are expressing doubts about the safe ocular use of Euphrasia preparations as their efficacy is undocumented and the hygienic conditions of applying ex tempore made infusions on the eye are not acceptable (Gruenwald et al. 2007; British Herbal Pharmacopoeia 1983).
2.3. Specified strength/posology/route of administration/duration of use for relevant preparations and indications
Liquid preparations used for conjunctivitis and minor ocular affections Application: oral and external use
Homeopathic eye drops (D3=0.1%): one drop 3 times daily (Stoss et al. 2000).
Eye rinse, ocular compress: tea is prepared by pouring freshly boiled water over two to three grams of the dried substance
According to Williamson (2003) the powdered herbal substance in a dose of
Oral use: an infusion of one teaspoon dried herb in 0.5 l freshly boiled water (Weiss 1999).
Liquid preparations in case of common cold Application: oral use
Tincture 1:5 ethanol 45% V/V: 50 drops 3 to 5 times a day (Delfosse 1998; Barnes 2007; Van Hellemont 1985).
Nasal ointment for a runny nose (Van Hellemont 1985) Application: external use
1 application 3 times a day in each nostril.
According to old references, the juice obtained by expression from the plant in the fresh state is sometimes employed, or an infusion in milk, but the simple infusion in water is the more usual form in which it is applied. An infusion of 1 OZ4 of the herb to a pint5 of boiling water should be used and the eyes bathed three or four times a day. When there is much pain, it is considered desirable to use a warm infusion rather more frequently for inflamed eyes till the pain is removed. In ordinary cases, the cold application is found sufficient.
In Iceland, the expressed juice is used for most ailments of the eye, and in Scotland the Highlanders make an infusion of the herb in milk and anoint weak or inflamed eyes with a feather dipped in it (Grieve 1931).
3.1. Overview of available pharmacological data regarding the herbal substance(s), herbal preparation(s) and relevant constituents thereof
Porchezhian et al. (2000) tested the
In the first part of the experiment, there were three groups of rats (fasted overnight): control group (distilled water), test group (600 mg Euphrasia extract per kg, p.o.) and a reference group (phenformin, 600 mg/kg, p.o.). The control group received only the vehicle in which alloxan was dissolved; the other two groups received alloxan.
The administration of alloxan showed a rise in the blood glucose levels as compared to the control group. Three to six hours after oral administration of the aqueous extract of Euphrasia to diabetic rats, the blood glucose level had significantly dropped (P<0.01), while the control group showed no significant reduction of the blood glucose level.
In the second part of the experiment, the effect of Euphrasia on normoglycemic rats was tested. Again there were three groups of rats (fasted overnight): control group (distilled water, test group (600 mg Euphrasia extract per kg, p.o.) and a reference group (phenformin, 600 mg/kg, p.o.). There was no alloxan administered.
Treatment with the extract showed no significant decrease in blood glucose levels in normoglycemic rats (P<0.01).
3.2. Overview of available pharmacokinetic data regarding the herbal substance(s), herbal preparation(s) and relevant constituents thereof
No data available.
3.3. Overview of available toxicological data regarding the herbal substance(s)/herbal preparation(s) and constituents thereof
Porchezhian et al. (2000) investigated the acute toxicity of aqueous eyebright extract on wistar albino rats. 100 grams of
Tests on reproductive toxicity, genotoxicity and carcinogenicity have not been performed.
3.4. Overall conclusions on
In general there is a discrepancy between the traditional use and the
4. Clinical Data
4.1. Clinical Pharmacology
No data available.
4.1.1. Overview of pharmacodynamic data regarding the herbal substance(s)/preparation(s) including data on relevant constituents
No data available.
4.1.2. Overview of pharmacokinetic data regarding the herbal substance(s)/preparation(s) including data on relevant constituents
No data available.
4.2. Clinical Efficacy
4.2.1. Dose response studies
No data available.
4.2.2. Clinical studies (case studies and clinical trials)
Stoss (2000) (also cited by Mills 2005) performed an open prospective cohort trial of a homeopathic fixed combination with an
The recommended dose was one drop
In 81% of the patients, there was complete recovery. Only one case showed a slight worsening of the symptoms. The tolerability of the medication was very good.
No undesirable serious adverse events occurred due to the medication during the entire prospective cohort trial. No conclusion on efficacy and safety of herbal preparations can be drawn from this study.
4.2.3. Clinical studies in special populations (e.g. elderly and children)
Stoffel (2007) performed a pilot project to investigate the effect of local application of eye drops with a Swiss
There were 2 groups: in the control group (20 neonates) the eyes of the neonates were washed every six hours with NaCl 0.9% and in the test group (24 neonates) the eyes were washed every six hours with NaCl 0.9% and additionally one drop of the eye drops was administered. If the doctors considered the treatment after 48 hours as “successfull”, it was not changed. If they considered the treatment as “not successfull”, the treatment changed to
The authors concluded that there was no difference between the control group and the test group and so immediate antibiotic treatment is not always necessary. There were no side effects reported.
The number of subjects was low and there was no appropriate statistical evaluation of the results. No conclusions on efficacy and safety of herbal preparations can be drawn from this study.
4.3. Overall conclusions on clinical pharmacology and efficacy
The two published studies are of limited value. First, the studies do not relate to defined herbal medicinal products/herbal preparations. The open design of the first one is not reliable to confirm whether the therapeutic effect is due to the preparation or to spontaneous healing. The second study
with the neonates is not conclusive due to the limited number of patients and divergent outcomes. No adverse effects were reported, but this finding is also not conclusive because of the
5. Clinical Safety/Pharmacovigilance
5.1. Overview of toxicological/safety data from clinical trials in humans
In the study performed by Stoss (2000) no serious adverse events were reported.
5.2. Patient exposure
No data available.
5.3. Adverse events and serious adverse events and deaths
No data available.
5.4. Laboratory findings
No data available.
5.5. Safety in special populations and situations
No data available.
5.6. Overall conclusions on clinical safety
The clinical studies reported above involved 124 patients. The number is too small to draw any conclusions on clinical safety. As up to now no authorized or registered medicinal preparations are on the market in Europe, no periodic safety update reporting has been established.
6. Overall conclusions
Traditional herbal preparations from Euphrasiae herba are mainly liquid water extracts which are ex tempore made as infusions for application as an ocular impregnated dressing for symptomatic treatment of minor irritation of the eye”. A nasal ointment containing an Euphrasia tincture6 20% as a traditional herbal medicinal product for the relief of local nasal irritation in common cold has also been described.
No adequate data are however available for these preparations concerning their safe use. The quality and safety of ex tempore preparations for ocular use does not correspond to current standards for ocular preparations.
6.1. Risk – benefit analysis
A monograph on Euphrasia officinals L. or Euphrasia rostkoviana Hayne, herba does not exist in the current European Pharmacopoeia. There is no major concern about adulteration with related species as
6 Specifications of the tincture not available.
Euphrasia stricta Wolff. (=E. stricta Host.) can be differentiated from Euphrasia officinalis L. by the presence of curved hairs on the tops of the leaves.
There are no reports about serious adverse events or
Some references provide instructions to make ex tempore preparations as infusions to use on the eye. However, the quality and safety of these preparations cannot be guaranteed.
From the presence of secondary metabolites, an astringent and
An ointment made with Euphrasia tincture has been documented as a traditional herbal medicinal product for the relief of local nasal irritation in common cold. However no information is available about the tincture, safety and plausibility of use.
Based on the