BULBUS SCILLÆ.

_Radix Scillæ_; _Squill_; F. _Bulbe ou squames de Scille_, _Ognon

marin_; G. _Meerzwiebel_.

=Botanical Origin=—_Urginea maritima_ Baker[2582] (_Scilla maritima_

L., _Urginea Scilla_ Steinheil). It is found generally in the regions

bordering the Mediterranean, as in Southern France, Italy, Dalmatia,

Greece, Asia Minor, Syria, North Africa and the Mediterranean islands.

In Sicily, where it grows most abundantly, Urginea ascends to

elevations of 3000 feet. It is also very common throughout the South of

Spain, where it is by no means confined to the coast; it occurs also in

Portugal. In the Riviera of Genoa the peasants like to see it growing

under the fig trees.

Two varieties of squill, termed respectively _white_ and _red_,

are distinguished by druggists. In the first, the bulb-scales are

colourless; in the second they are of a roseate hue. No other

difference in the plants can be pointed out, nor have the two varieties

distinct areas of growth.

=History=—Squill is one of the most ancient of medicines. Epimenides,

a Greek who lived in the 30th Olympiad, is said to have made much use

of it, from which circumstance it came to be called _Epimenidea_[2583].

It is also mentioned by Theophrastus, and was probably well known

to all the ancient Greek physicians. Pliny was not only acquainted

with it, but had noticed its two varieties. Dioscorides describes the

method of making vinegar of squills; and a similar preparation, as well

as compounds of squill with honey, were administered by the Arabian

physicians, and still remain in use. The medical school of Salerno

preferred the red variety of the drug, which on the whole is not

frequently met with in mediæval literature.

[2581] By R. V. Tuson, London, 1869.

[2582] _Journ. of Linn. Soc._, Bot., xiii. (1872) 221.—The genus

_Urginea_ has flat, discoid seeds, while in _Scilla_ proper they are

triquetrous. The name _Urginea_ was given in allusion to the Algerian

tribe Ben _Urgin_, near Bona, where Steinheil (1834) examined this

plant.

[2583] Haller, _Bibliotheca botanica_, i. 12.

=Description=—The bulb of squill is pear-shaped, and of the size of

a man’s fist or larger, often weighing more than four pounds. It

has the usual structure of a tunicated bulb; its outer scales are

reddish-brown, dry, scarious, and marked with parallel veins. The inner

are fleshy and juicy, colourless or of a pale rose tint, thick towards

the middle, very thin and delicate at the edges, smooth and shining on

the surface. The fresh bulb has a mucilaginous, bitter, acrid taste,

but not much odour.

For medicinal use, squill is mostly imported ready dried. The bulbs are

collected in the month of August, at which period they are leafless,

freed from their dry outer scales, cut transversely into thin slices,

and dried in the sun. Thus prepared, the drug appears in the form of

narrow, flattish or four-sided curved strips, 1 to 2 inches long, and ⅜

to ⅝ of an inch wide, flexible, translucent, of a pale dull yellowish

colour, or when derived from the red variety, of a decided roseate

hue. When thoroughly dried, they become brittle and pulverizable, but

readily absorb water to the extent of about 11 per cent. Powdered

squill by the absorption of water from the air, readily cakes together

into a hard mass.

=Microscopic Structure=—The officinal portion of the plant being simply

modified leaves, has the histological characters proper to many of

those organs. The tissue is made up of polyhedral cells, covered on

both sides of the scales by an epidermis provided with stomata. It

is traversed by numerous vascular bundles, and also exhibits smaller

bundles of laticiferous vessels. If thin slices of squill be moistened

with dilute alcohol, most of the parenchymatous cells are seen to be

loaded with _mucilage_, which contracts into a jelly on the addition of

alcohol. In the interior of this jelly, crystalline particles are met

with consisting of oxalate of calcium. This salt is largely deposited

in cells, forming either bundles of needle-shaped crystals, or large

solitary square prisms, frequently a millimetre long. In either case

they are enveloped by the mucilaginous matter already mentioned.

Oxalate of calcium as occurring in other plants has been shown in many

instances to originate in the midst of mucilaginous matter. The fact is

remarkably evident in _Scilla_, especially when examined in polarized

light.

On shaking thin slices of the bulb with water, the crystals are

deposited in sufficient quantity to become visible to the naked eye,

though their weight is actually very small. Direct estimation of the

oxalic acid (by titration with chamæleon solution) gave us only 3·07

per cent. of C₂CaO₄,3H₂O from white squill dried at 100° C., which

moreover yielded only 2 to 5 per cent. of ash. It is these extremely

sharp brittle crystals which occasion the itching and redness, and

sometimes even vesication, which result from rubbing a slice of fresh

squill on the skin. These effects, which have long been known, were

attributed to a volatile acrid principle, until their true cause was

recognized by Schroff.[2584]

[2584] We have found that the slimy juice of the leaves of _Agapanthus

umbellatus_ Hérit., which is very rich in spicular crystals, also

occasions when rubbed on the skin both itching and redness, lasting for

several hours.

The mucilage also contains albuminous matters, hence the orange colour

it assumes on addition of iodine. The vascular bundles are accompanied

by some rows of longitudinally extended cells, containing a small

number of starch granules. In the red squill the colouring matter is

contained in many of the parenchymatous cells, others being entirely

devoid of it. It turns blackish-green if a persalt of iron be added.

=Chemical Composition=—The most abundant among the constituents of

squill are mucilaginous and saccharine matters. Mucilage may be

precipitated by means of neutral and basic acetate of lead, yet there

remains in solution another substance of the same class, called

_Sinistrin_. It was discovered in 1879 by Schmiedeberg, who obtained it

by mixing the powder of squill, either red or white, with a solution of

basic acetate of lead in slight excess. The gummy matters thus forming

insoluble lead compounds being removed, the liquid is deprived of the

lead and mixed with slaked lime. An insoluble compound of sinistrin

and calcium separates and yields the former on decomposing the well

washed precipitate with carbonic acid. The small amount of calcium

remaining in the filtrate is to be removed by adding cautiously to the

warm solution the small quantity just required of oxalic acid. Lastly,

sinistrin is thrown down by alcohol. It is a white amorphous powder, on

exposure to air soon forming transparent brittle lumps. The composition

of sinistrin is that of dextrin = C₆H₁₀O₅, both these substances being

very closely allied, yet the aqueous solution of sinistrin deviates the

plane of polarization to the left. The rotatory power appears not to be

much influenced by the concentration or the temperature of the solution

of sinistrin.

An alkaline solution of tartrate of copper is not acted upon by

sinistrin. It is transformed into sugar by boiling it for half an hour

with water containing 1 per cent. of sulphuric acid. The sugar thus

produced is stated by Schmiedeberg to consist of lævulose[2585] and

another sugar, which in all probability, when perfectly pure, must

prove devoid of rotatory power.

The name sinistrin[2586] has also been applied to a mucilaginous matter

extracted from barley (see Hordeum decorticatum); it remains to be

proved that the latter is identical with the sinistrin of squill.

We have obtained a considerable amount of an uncrystallizable levogyre

sugar by exhausting squill with dilute alcohol.[2587] Alcohol added to

an aqueous infusion of squill causes the separation of the mucilage,

together with albuminoid matter. If the alcohol is evaporated and

a solution of tannic acid is added, the latter will combine with

the _bitter principle_ of squill, which has not yet been isolated,

although several chemists have devoted to it their investigations,

and applied to it the names of _Scillitin_ or _Skuleïn_. Schroff, to

whom we are indebted for a valuable monograph on Squill,[2588] infers

from his physiological experiments the presence of a non-volatile

acrid principle (_Skulein?_), together with scillitin, which latter he

supposes to be a glucoside.

Merck of Darmstadt has isolated _Scillipicrin_, soluble in water;

_Scillitoxin_, likewise a bitter principle, insoluble in water, but

readily dissolving in alcohol; and _Scillin_, a crystalline substance,

abundantly soluble in boiling ether. The physiological action of these

substances and of _Scillaïn_ has been examined (1878) by Moeller, and

by Jarmersted (1879); that of scillitoxin and scillaïn was found to be

analogous to that of Digitalis.

[2585] This is the name applied to the lævogyrate uncrystallizable

glucose produced, together with crystallizable dextro-glucose, by

decomposing cane-sugar by means of dilute acids.

[2586] In 1834 first proposed, by Marquart, for inulin.

[2587] In Greece they have even attempted to manufacture alcohol by

fermenting and distilling squill bulbs.—Heldreich, _Nutzpflanzen

Griechenlands_, 1862. 7.

[2588] Reprinted from the _Zeitschrift der Gesellschaft der Aerzte zu

Wien_, No. 42 (1864). Abstracted also in Canstatt’s _Jahresbericht_

1864. 19, and 1865. 238.

=Commerce=—Dried squill, usually packed in casks, is imported into

England from Malta.

=Use=—Commonly employed as a diuretic and expectorant.

=Substitutes=—There are several plants of which the bulbs are used in

the place of the officinal squill, but which, owing to the abundance

and low price of the latter, never appear in the European market.

1. _Urginea altissima_ Baker (_Ornithogalum altissimum_ L.), a South

African species, very closely related to the common squill, and having,

as it would appear, exactly the same properties.[2589]

2. _U. indica_ Kth. (_Scilla indica_ Roxb.), a widely diffused plant,

occurring in Northern India, the Coromandel Coast, Abyssinia, Nubia,

and Senegambia. It is known by the same Arabic and Persian names as _U.

maritima_, and its bulb is used for similar purposes. But according to

Moodeen Sheriff[2590] it is a poor substitute for the latter, having

little or no action when it is old and large.

3. _Scilla indica_ Baker[2591] (non Roxb.), (_Ledebouria hyacinthina_

Roth), native of India and Abyssinia, has a bulb which is often

confused in the Indian bazaars with the preceding, but is easily

distinguishable when entire by being _scaly_ (not tunicated); it is

said to be a better representative of the European squill.[2592]

4. _Drimia ciliaris_ Jacq., a plant of the Cape of Good Hope, of the

order _Liliaceæ_. Its bulb much resembles the officinal squill, but has

a juice so irritating if it comes in contact with the skin, that the

plant is called by the colonists _Jeukbol_, i.e. _Itch-bulb_. It is

used medicinally as an emetic, expectorant, and diuretic.[2593]

5. _Crinum asiaticum_ var. _toxicarium_ Herbert (_C. toxicarium_

Roxb.), a large plant, with handsome white flowers and noble foliage,

cultivated in Indian gardens, and also found wild in low humid spots

in various parts of India and the Moluccas, and on the sea-coast of

Ceylon. The bulb has been admitted to the _Pharmacopœia of India_

(1868), chiefly on the recommendation of O’Shaughnessy, who considers

it a valuable emetic. We have not been able to examine a specimen,

and cannot learn that the drug has been the subject of any chemical

investigation.

[2589] Pappe, _Floræ Medicæ Capensis Prodromus_, ed. 2, 1857. 41.

[2590] _Supplement to the Pharmacopœia of India_, Madras, 1869. 250.

[2591] Saunders, _Refugium Botanicum_, iii. (1870) appendix, p. 12.

[2592] _Suppl. to the Pharm. of India_, 250.

[2593] Pappe, _op. cit._ 42.

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