Anti-Cancer Composition for Delivering 5-Fluorouracil to Cancer Tissues

This invention relates to compositions for delivering 5-fluorouracil to a cancer sensitive to 5-fluorouracil in a warm-blooded animal.

Anti-cancer compositions comprising a compound having a 5-fluorouracil as its skeleton and serving as the active component thereof have both merits and demerits. For example, 5-fluorouracil, although highly effective, has high toxicity and marked side effects. Accordingly, when administered, the compound produces a therapeutic effect and, at the same time, inevitably gives side effects. Further 1-(2-tetrahydrofuryl)-5-fluorouracil, which has relatively lower toxicity and reduced side effects, is said to be slightly inferior in its anti-cancer effect. In view of these situations, it has been expected to develop more advantageous 5-fluorouracils.

Compounds containing 5-fluorouracil as the skeleton thereof are thought to exhibit an anti-cancer effect when converted to 5-fluorouracil in the living body. It appears that they generally fail to give a high anti-cancer effect because the resulting 5-fluorouracil is promptly metabolized and thereby inactivated. Accordingly it is desired that the 5-fluorouracil in the living body be prevented from inactivation by some expedient, preferably in such a manner that the 5-fluorouracil present in the cancer tissues will remain active, whereas the 5-fluorouracil present in the normal tissues can be inactivated.

An object of this invention is to provide an anti-cancer composition for delivering 5-fluorouracil to cancer tissues of cancer sensitive to 5-fluorouracil in warm-blooded animals, comprising a pharmaceutically effective amount of a 5-fluorouracil derivative and an effective amount of uracil, wherein about 0.5 to about 10 moles of uracil is used per mole of the 5-fluorouracil derivative.

This invention provides anti-cancer compositions for delivering 5-fluorouracil to cancer tissues of cancer sensitive to 5-fluorouracil in warm-blooded animals, said composition comprising a pharmaceutically effective amount of at least one 5-fluorouracil (a) and an effective amount of uracil (b), the 5-fluorouracil (a) being 1-(2-tetrahydrofuryl)-5-fluorouracil.

Although uracil (b) itself has no anti-cancer effect whatever, the use of the 5-fluorouracil (a) in combination therewith according to this invention produces a greatly enhanced anti-cancer effect, by delivering 5-Fu to cancer tissue, resulting in a therapeutic index of about 1.6 to 4.1 times that of the 5-fluorouracil alone. With the composition of this invention administered, cancer tissues have exceedingly increased 5-fluorouracil concentration, whereas the other tissues, such as the blood serum, will exhibit little or no increase in the concentration of 5-fluorouracil. This shows that the present composition by delivering 5-Fu to cancer tissue is an ideal therapeutic agent for cancers.

The compound 1-(2-tetrahydrofuryl)-5-fluorouracil is disclosed in Japanese published examined patent application No. 10510/1974.

When the 5-fluorouracil (a) is administered in combination with uracil (b) according to this invention, the 5-fluorouracil (a) is converted into 5-fluorouracil and consequently the 5-fluorouracil concentration remarkably increases in cancer tissues.

The amount of uracil (b) to be used relative to the 5-fluorouracil (a) for the preparation of the anti-cancer compositions according to this invention is dependent on the kind of the 5-fluorouracil used. Generally about 0.02 to about 10 mols, preferably about 0.05 to 5 mols, more preferably about 0.1 to 2 mols, of uracil (b) is used per mol of the 5-fluorouracil (a).

Compositions of the present invention deliver 5-Fu to cancer tissue, and the 5-Fu is useful for the treatment of cancers in warm-blooded animals.

According to this invention, the 5-fluorouracil (a) and uracil (b) can be administered to warm-blooded animals individually in separate doses but are given preferably at the same time in the form of a single preparation. The anti-cancer compositions of this invention can be administered in the desired form of preparation in accordance with the therapy contemplated. They are provided for example as tablets, capsules and granules for oral administration or as parenteral solutions and suppositories for non-oral administration. These preparations can be formulated with use of carriers already known in the art.

Examples of useful carriers for making oral preparations are lactose, sucrose, starch, talc, magnesium stearate, crystalline cellulose, methyl cellulose, hydroxypropyl cellulose, hydroxypropylmethyl cellulose, carboxymethyl cellulose, glycerin, sodium alginate, gum arabic, etc. The amount of the 5-fluorouracil (a) in oral preparations may preferably be 10 to 200 mg per dosage unit. Carriers suitable for parenteral preparations are, for example, water, physiological saline solution, etc. which can be used with tris(hydroxymethyl)aminomethane, sodium carbonate, sodium hydroxide or the like serving as a solubilizer or pH adjusting agent. The parenteral preparations contain preferably 50 to 1000 mg of the 5-fluorouracil (a) per dosage unit. Suitable carriers for preparing suppositories are for example cacao butter, Witepsol-W35 (fat, trade mark of Dynamit Nobel A.G. of Germany). The suppositories may contain preferably 250 to 1000 mg of the 5-fluorouracil (a) per piece.

The results of biological applications and basic efficacy tests show that the preferred dose of the present anti-cancer compositions, although dependent on the kind of 5-fluorouracil, is usually about 0.5 to about 150 mg/kg, preferably about 0.5 to about 50 mg/kg calculated as the quantity of 5-fluorouracil. These values are in terms of the quantity per kilogram of the body weight of the warm-blooded animal per day.

Given below are examples of anti-cancer compositions prepared according to this invention.

An encapsulated preparation is formulated from the above ingredients.

A parenteral solution is prepared from the above ingredients.

Suppositories are prepared from the above ingredients.

A granular preparation is formulated from the above ingredients.

A parenteral solution is prepared from the above ingredients.

Anti-cancer compositions of this invention are tested in cancer-bearing rats to determine the concentrations of 5-fluorouracil in the blood as well as in cancer tissues and to determine anti-cancer effects.

Ascites cells (5.times.10.sup.6) of AH-130 are subcutaneously transplanted in the armpit portion of male rats of Donryu strain weighing about 200 g. Seven days thereafter, the rats with cancer cells weighing at least 2 g are used, five rats in each group.

An anti-cancer composition comprising a 5-fluorouracil (a) alone or in combination with uracil (b) in the proportion(s) listed in Table 1 is suspended in a 5% solution of gum arabic immediately before use, and the suspension is orally given to the animal at the listed dose. Two, four and eight hours after the administration, the blood serum and cancer tissue homogenate are collected, each of which is acidified with hydrochloric acid and extracted with chloroform. The resulting aqueous layer is examined for antibiotic activity according to the thin-cup method (Media Circle, Vol. 92, p. 259, 1967) with use of Staphylococcus aureus 209P strain. The results are given in Table 1 in terms of 5-fluorouracil concentration.

Ascites cells (5.times.10.sup.6) of AH-130, are subcutaneously transplanted in the armpit of male Donryu rats weighing about 200 g (ten rats in each group). An anti-cancer composition comprising a 5-fluorouracil (a) alone or in combination with uracil (b) in the proportion(s) listed in Table 2 is suspended in a 5% solution of gum arabic immediately before use. Twenty-four hours after the transplantation and during the following seven consecutive days and suspension is orally given to the animal once every day at the dose listed in Table 2. On the 10th day after the transplantation, the tumor is removed from the body and weighed to calculate the average weight (T) of the tumors in the group to which the composition has been given and the corresponding weight (C) in the control group to determine the ratio T/C. The results are listed in Table 2.

The anti-cancer effect (T/C) achieved by the oral administration of 1 m. mol/kg of uracil (b) alone is 0.96.

Tables 1 and 2 reveal the following. When the 5-fluorouracil (a) is used conjointly with uracil (b), the 5-fluorouracil concentration remains almost at the same level in the blood but greatly increases in the cancer tissues and that the use of uracil (b) with any 5-fluorouracil (a) gives an increased anti-cancer effect. These results show that 5-fluorouracils (a), if convertible to 5-fluorouracil in the living body and when used in combination with uracil (b), afford high anti-cancer effects synergically enhanced by the conjoint use of uracil (b).

(5) The anti-cancer compositions of this invention are tested in mice by the following methods to determine acute toxicity, anti-cancer effect and therapeutic index.

Male mice of ICR strain weighing 22.+-.1 g are used, 5 mice in each group. A 5-fluorouracil (a) and uracil (b) in the proportions listed in Table 4 are suspended in a 5% solution of gum arabic to prepare a suspension, which is forcibly orally administered to each mouse through a tube at a dose of 1 ml/100 g. Over the following period of three weeks the mice are checked every day for poisoning, body weight and mortality. The LD.sub.50 is determined according to the up-and-down method 3 weeks after the administration. The results are given in Table 4.

Tissues of sarcoma 180, 2.times.10.sup.6, are subcutaneously transplanted in the back of male mice of ICR strain (6 mice in each group). A 5-fluorouracil (a) and uracil (b) in the proportions listed in Table 4 are suspended in a 5% solution of gum arabic to prepare a suspension. Twenty-four hours after the transplantation and during the following seven consecutive days the suspension is orally given to the animal once every day. On the 10th day after the transplantation, the tumor is removed from the body and weighed to calculate the average weight (T) of the tumors in the group to which the composition has been given and the corresponding weight (C) in the control group to determine the ratio T/C. The effective dose (ED.sub.50) for achieving 50% cancer inhibition is determined from the dose-response curve involving the dose and effect (T/C). The results are given in Table 4.

The LD.sub.50 and ED.sub.50 values obtained above are used to determine the therapeutic index (LD.sub.50 /ED.sub.50). The results are also listed in Table 4.