1.ApplicationNumber: US-5572460-A
1.PublishNumber: US-3063906-A
2.Date Publish: 19621113
3.Inventor: HECKEL HERMAN C. N.
JR. ROBERT T. JEFFERSON,

4.Inventor Harmonized: HECKEL HERMAN C N()
JEFFERSON JR ROBERT T()

5.Country: US
6.Claims:

7.Description:
(en)3 063 906 BENZYL DEXTRAlQ-AMPHETAMINE AND METHOD or MAKING SAME Herman C. N. Heckel, Oxford, and Robert T. Jefferson,
This invention relates to a method of improving the release rate of drugs, and more particularly with respect to the utilization of benzyl dextran free of benzyl alcohol in the preparation of sustained release pharmaceutical products.
An object of the invention is to provide a method of preparing benzyl dextran compositions with amphetamine or its salts which exhibit an improved release rate of the drug.
A further object is to provide a medicinal drug product of the character described which can be taken orally, for example in the form of a pill or capsule, and which releases the drug slowly over a 24 hour period whereby only one pill or capsule of the drug need be taken each day to obtain the desired treatment.
In accordance with the present invention, it has been discovered unexpectedly that the presence of benzyl alcohol in benzyl dextran compositions with amphetamine adversely affects the rate of release of drugs contained in the same; for example, the rate of release of amphetamine hydrochloride in the presence of benzyl alcohol is lowered to such an extent that it becomes much too low for practical purposes.
When the physiological action of the drugs is required over a long period of time it is convenient to take an amount suflicient for 8, 12 or 24 hours in one dose. This can only be done through use of a slow release product. Otherwise, to keep the drug at the desired level of physiological activity, one would have to take doses at frequent intervals. The present invention eliminates the need of frequent doses.
Benzyl dextran is normally prepared by reaction of dextran with benzyl chloride in the presence of sodium hydroxide, and a considerable amount of benzyl alcohol is formed. Further, since benzyl alcohol is a solvent, for benzyl dextran, it is very difficult to remove.
The presence of benzyl alcohol in the resinous benzyl dextran mass also lowers the softening point of the resinous mass to a marked extent. For instance, when benzyl alcohol is present in amounts greater than about 5% by weight of the powdered resin, the same is no longer free flowing but cakes. This results in rendering the resin unsuitable for most purposes.
To remove benzyl alcohol from benzyl dextran resin, the latter must be thoroughly washed with water and water-methanol solution mixtures. A preferred method comprises steam distilling the reaction mixture containing benzyl dextran, excess benzyl chloride and benzyl alcohol. This removes the benzyl alcohol along with the excess benzyl chloride.
An added procedure for removing excess benzyl alcohol involves adding methanol to the dried benzyl to form a soft paste or gel. This paste or gel is then washed with excess methanol to free it of benzyl alcohol. The
tates ate t benzyl resin paste is insoluble in excess methanol thus making it possible to use methanol to wash out the benzyl alcohol.
In conventional drugs of the prior art which are compounded for oral administration, the same are absorbed rapidly in the stomach and intestinal tract and thus produce a relatively high concentration of the drug in the blood stream in a short period of time. This rapid release and absorption into the blood stream of the drug is undesirable except in special cases. The rapid release and the building up of a high concentration of the drug often produces undesirable physiological and pharmacological reactions, and the desired efiects of the drug are not produced.
He present invention makes it possible to overcome this difficulty and provides an improved pharamaceutical drug product which, when taken orally, slowly liberates the drug in the stomach and intestinal tract for absorption into the blood stream. This rate is controlled whereby the drug remains effective over a relatively long period of time, and the undesirable abnormal physiological reactions, such as usually produced when the drug is rapidly released and absorbed into the blood stream, are eliminated. Also, it makes possible the use of one treatment to cover 8, 12, 24 or 36 hours.
In accordance with the present invention amphetamine, which has been used internally heretofore, as a stimulant, is combined with benzyl dextran. It is essential that the benzyl dextran be substantially free of benzyl alcohol to provide a benzyl dextran amphetamine preparation which exhibits the desirable drug-releasing properties described. Amphetamine hydrochloride is combined with benzyl dextran employing methanol or the like medium which will cause benzyl dextran to dissolve or swell forming a gel or paste and which at the same time is a solvent for the drug. The resultant homogeneous mass of amphetamine hydrochloride, methanol, and benzyl dextran is evaporated in vacuo and the dried mass ground to the desired mesh size. The resultant product when extracted for 1 hour employing simulated gastric juice, followed by extraction up to 24 hours with simulated intestinal juice, is found to give up its amphetamine content quite slowly. Thus a physiologically active level of amphetamine is maintained in the body for an extended period of 8 to 36 hours with a single medication. The benzyl alcohol content of the benzyl dextran is critical both with respect to the rate of release and extent of the release of the drug and also the free-flowing characteristics property of the prepared granules. Where benzyl alcohol is present in amounts of 4-5% or greater the amphetamine is released only to about 50% of its content in the resin whereas under similar conditions a henzyl alcohol-free resin will give up to of its amphetamine content after a combined extraction of 12 to '24 hours in simulated gastric and intestinal juices.
BENZYL DEXTRAN PREPARATION Benzyl dextran, depending upon the extent of benzylation, varies in solubility from a water-soluble to a highly water-insoluble polymer. Such water-insoluble benzyl dextran is the product with which the present invention is concerned. With a degree of substitution of 0.5 to 1,0 the polymer is soluble in benzyl alcohol but insoluble in most of the common organic solvents. Saturation of ton and washing operations are extremely important.
benzyl dextran powder with methanol, ethanol, dioxane, dioxalane and chloroform will cause softening and formation of a gel or paste which is insoluble in excess solvent. The procedure for synthesizing benzyl dextran is as follows.
Example 1 liquid was poured off. The separated mass was washed three or four times with water, then combined with a 50% aqueous sodium hydroxide solution (480 g. NaOH) as before. The mixture was heated, and at 80 C. benzyl chloride (6 moles) was added slowly with constant stirring.
After refluxing for one hour another 6 moles of benzyl chloride was added, and refluxing was continued for one hour more. The reactants were allowed to cool, then 2 N hydrochloric acid (1000 ml.) was added carefully to neutrality (pH 6 to 7).
The product was washed several times with cold water. It was then washed with several volumes of methanol, and
this was followed by a final washing with water, or the reaction mass after neutralization was steam distilled to remove the excess benzyl chloride and benzyl alcohol. The product was dried at 85 C. under vacuum and crushed to particles which could pass through a 40 mesh sieve.
The native dextran used is preferably one having an average molecular structural repeating alpha-1,6 linkage to non-alpha 1,6 linkages ratio between 2:1 and 30:1 a solubility or dispersibility in water such as to yield colloidally stable aqueous solutions.
A suitable dextran is produced enzymatically in the presence of bacteria, for example by inoculating a nutrient medium containing sucrose, particular nitrogenous compounds and certain inorganic salts with an appropriate microorganism, such as those of the Leuconostoc mesen- -teroides and L. dextranicum types and incubating the culture at the temperature most favorable to the growth of the particular microorganism. The dextran also may be produced enzymatically, in the substantial absence of bacteria, by cultivating an appropriate microorganism, for example, Leuconoszoc mesenteroicles B-512 to obtain a dextran-producing enzyme, separating the enzyme from the medium in which it is produced, and introducing the enzyme into a medium in which dextran is produced by action of the enzyme.
In the preparation of the benzyl dextran, the acidifica- Unless all of the benzyl alcohol and/or benzyl chloride is washed from the product it is not free flowing at room temperature. The presence of benzyl alcohol also affects the rate of release of amphetamine salts compounded with the resin, greatly slowing the release to values much too small for the desired effectiveness. Benzyl dextrans containing or more benzyl alcohol have softening points ranging from 53 to 87 C. as determined by the Ring and Ball method, and the slow release amphetamine products prepared from these benzyl dextrans have been found to release less than 50% amphetamine in extraction completely as possible by vacuum distillation, taking care to avoid degradation. A number of slow release products were prepared by this method, and tested. Negligible amounts of amphetamine were extracted to periods up to 8 hours. In addition to poor extraction, it was very difficult to obtain these products in granular form. These benzyl dextran amphetamine products had softening points which were so low that chilling was required in order to break them into small granules for testing. Consequently, shelf life was only a matter of hours. As soon as the granule warmed to room temperature they flowed into a single agglomerate.
Benzyl dextran amphetamine preparations which were prepared as above without regard to the presence of benzyl alcohol showed a low release rate of amphetamine, and did not aproach the desired rate of approximately 35% to 50% release of the drug over a four hour period. Such products as were prepared from pure benzyl dextran released the amphetamine at a much greater rate, approximating the desired rate.
TESTING METHOD FOR RELEASE OF DRUG The rate of extraction of amphetamine from a slow release product was measured by placing a sample (1.25 g.) of granules in simulated gastric fluid 1 (100 ml.) at 37 C. The resulting suspension was agitated on a mechanical shaker for definite time intervals then the undissolved granules were removed by filtration. These were then immediately transferred to fresh gastric fluid, or to simulated intestinal fluid (100 ml.) for an additional extraction period. The filtrates were analyzed for nitrogen content by the Kjeldahl method, and the percent amphetamine extracted in a given time interval from the slow release product was calculated.
Illustrative examples of preparations of slow release products for pure benzyl dextran are as follows.
Example 1 Same as Example 1, using half the amount of amphetamine sulfate and dissolving it directly in the alcohol suspension (no water).
Example 3 Same as Example 1, using less methanol (5 ml. total) and a ratio of 8.5 parts benzyl dextran to 1.5 parts amphetamine sulfate (no water used).
Example 4 Dextroamphetamine (0.53 g.) was added to methanol (10 ml.) and the solution was mixed into benzyl dextran (10.0 g., 40 mesh) adding it in small amounts. The soft mass was dried at 60 C. under vacuum and the dry cake was crushed to 20+40 mesh granules.
Example 5 Small amounts of dioxalane were mixed into benzyl dextran 10.0 g., '40 mesh) until a total of 10 ml. was added. The paste was heated to C. and the amphetamine sulfate (1.3 g.) was added. The soft mass was dried at 60 C. under vacuum, and the dry cake was crushed to 10-1-20 mesh granules.
1 Preparation described in The United States Pharmacopeia, 15th revision, p. 1094 (1955).
3 Preparation described in The United States Pharmacopeia, 15th revision. p. 1095 (1955).
Method of Analysis described in The United States Pharmacopeia, 15th revision, p. 909 (1955).
The extraction data obtained from tests made with the products of Examples 1 through are given in Table I.
5 TABLE IL-AMPHETAMINE EXTRACTED FROM SLOW RELEASE PRODUCTS CONTAINING BENZYL ALCOHOL TO MODIFY THE RELEASE RATE [All samples are composed of +20 mesh granules] TABLE I.AMPHETAMINE EXTRAOTED FROM SLOW RELEASE PRODUCTS PREPARED WITH PURE BENZYL DEXTRAN Amphetamine 10 Amphet- Benzyl Amphetamine extracextraction in amine alcohol tion in simulated gassimulated Amphetamine Amphetamine Product tested in added tric fluid (percent) intestinal extraction in extraction in product (perfluid (percent) Size of Amphetsimulated simulated intestl- (pen cent) 7 Producted granules aminein gastric fluid nal fluid (percent) ent) tested (mesh) roduct (percent) 5min 1 hr. 1.5 hrs 1 hr. 2hrs.
' percent) v 1hr. 1.5hrs. 1hr. 2hrs. 2hrs. Example6 86 8.5 35.8 9.8 8.6 Example 7 11.2 6.2 25.4 7.6 6.6 Example 8"..- 8. 6 8.4 33.6 3.5 Example 1 +40 7.7 15.2 13.0 5.8 Example 9.-. 8.1 4.2 26.5 28.1 4.8 Example 2 20 +40 4.0 22.0 11.2 Example 10.--- 10 8 8.1 5.0 8.1 8.1 10.8 Example 3 -20 +40 9.9 18.4 17.4 Example4- -20 +40 4.5 16.7 12.5 0 Example 5 -10 +20 3.1 17.3 11.4 4.6
lThe samples tested were extracted in simulated gastric fluid for a Th test results h h b l l h l i ff ti ,h v'h d t td ii ddi rfo rl s l timi mtgrvil d hg,zfrlfd imii- 1n reducing the rate of release of the drug. Benzyl l anglexmcted iffi a infiestigalflum i gt g alcohol, however, tends to reduce the softening point of 11183.0 (3 omme (2 eemacmn (ml was am We the benzyl dextran and thus the product is not as free flowing as when benzyl alcohol is not present.
A modified method was employed to remove benzyl alcohol and traces of benzyl chloride from the refined benzyl dextran. This involved the thorough mixing of Benzyl alcohol when P the benzyl dextran methanol with benzyl dextran to the extent that a separate causes a loweflng of the extractlon Tate- A number of phase of methanol is present, the excess of methanol thus l release Products were P p fmm P benzyl extracting the benzyl mcohol and benzyl chloride. The dextran and amphetamine sulfate, or hydrochlonde, to methanol with the dissolved benzyl alcohol and benzyl which there was added fixed amounts of benzyl alcohol chloride was then drained from the benzyl dextran. in each. The methods of preparation of these slow After the extraction was repeated four or five times, release Products am given below, amphetamine hydrochloride (14.1 g. per 100 g. benzyl dextran) Was added to the plastic or gel consisting mass. E p 6 The resultant amphetamine resin mass was then dried Small amounts of methanol were mlxed into benzyl f 60 under vacuum and the dry product was crushed lnto l0 to +20 mesh and 20 to +40 mesh granules. dextran (10.0 g., 60 mesh) untll a total of 10 ml. was
d d B 1 l h 1 1O 39 dd d f n W d Thls procedure was used to refine the benzyl dextran ad e enzy a co o 1-2 m a l 0 o t prior to the addition of amphetamine hydrochloride in y amphetamlnf Sulfate e resu'tmg pas e the preparation of a large batch of slow release material. was dried at 60 C. under vacuum, and the product was Representative Samples of the 10440 mesh granules crushed to 10/2 m hgr and the 2040 mesh granules of this slow release Example 7 product were then subjected to extraction in gastric fluid for five minute and one and one-half hour intervals, and
The same as Example 6, us ir 1g 0.72 ml benzyl alcohol n. in the in estin l fluid r ne r, two h u and 3 amphetamine lf t and eight hour intervals. The extraction data are given in Table III. Example 8 Same as Example 6, using only 9 ml. of methanol A LEI 'I B II.-AMPHE'IAMINE EXTRACTED FR 1 SL W and addlng 1.0 ml. benzyl alcohol and 1.3 g. amphetamine RELEASE AMPHETAMINEBENZYL gx g sulfate. UCI 10% AMPHETAMINE LEVEL) x m l 9 Size 1of nrtnphetaminglertlgc- Amplllleltatrniine extratfition in granu es, ion in sun ae s' f t d,
Benzyl dextran (20.0 g., mesh) and amphetamlne mesh gastric fluid, percent 0:1 1: a e m 'esbma m per sulfate (2.45 g., 60 mesh) were blended together (dry) 60 then small amounts of methanol were mixed into the 5mm ZhPS- Shrepowders until a total of 18 ml. was added. Benzyl 10 alcohol (0.95 ml.) was added, and the paste was dried i28 fig gig as at 60 C. under vacuum. The dry product was crushed to l0/ 20 mesh granules.
Example 10 The use of amphetamme sulfate in the benzyl dextran Benzyl dextran (10.0 g., -40 mesh) and amphetamine slow release combination requires that the level of the hydrochloride (1.3 g.) were blended dry. A solution drug in the resin be rather low. The sulfate is insoluble of benzyl alcohol (0.96 ml.) in methanol (10. ml.) was in the resin at the desired level of 10% 'free base and mixed into the dry powders adding it in small amounts. during the first hour of extraction the percent drug ex- The paste was dried at 80 C. under vacuum. The tracted is too high. product was crushed into 10+20 mesh granules. The rate of sulfate extracted can be decreased by addi- The rate of extraction of amphetamine in each example tion of benzyl alcohol but this causes the product to become tacky and thus lose its free flowing quality. The total amount of drug extracted is greatly reduced by the addition of the benzyl alcohol and this is also objectionable. The benzyl alcohol content of the benzyl dextran should be considerably less than by weight of the benzyl dextran, and preferably not higher than 1% The rate of release of the amphetamine sulfate can also be decreased by lowering the amount of the drug in the benzyl dextran, but this is objectionable from the standpoint of capsule or pill size required for the average dosage.
Amphetamine hydrochloride is much more desirable than the sulfate because it appears to be more soluble in the benzyl dextran and also in the methanol-benzyl dextran paste used in the preparation. Using the hydrochloride it is possible to prepare a mix giving the desired rate of release and yet carrying a content of amphetamine, calculated as the free base. i This is the minimum desired level for convenience of capsule size.
It has also been observed that the rate of release is controlled by the amphetamine level in the product and also by the particle size which preferably should be within the range of l040 mesh. The rate of release of the drug as heretofore shown is greatly affected by the benzyl alcohol content. In the preparation of benzyl dext-ran a considerable quantity of benzyl alcohol is formed as a byproduct, the removal of which is very difficult.
Various medicament drugs may be combined with benzyl dextran to form a time delay pharmaceutical product. For example, chlorpheniramine maleate (Chlor- Trimeton Maleate), l-phenylephrine hydrochloride, methamphetamine, phenylpropanolamine, homotropine, methacopolarnine, pyrilamine, codeine, dextromethorphan, and various water-soluble medicament salts such as amphetamine sulfate, racemic amphetamine sulfate as well as antihistamines and barbiturates. Inert fillers may be added in suitable amounts as desired, e.g., terra alba, starch and the like, and such as is commonly added in the formulation of tablets of the product.
Various changes and substitutions may be made by those skilled in the art to obtain the advantages and achieve the results of this invention and it is understood such changes and variations are within the scope of the foregoing except as stricted in the claims.
What is claimed is:
l. A pharmaceutical product providing a gradual release of medicament over a long period of time, and which comprises an amphetamine medicament disposed in benzyl dextran, said product being free of benzyl alcohol.
2. A pharmaceutical product providing a gradual release of medicament over a long period of time, and which comprises an amphetamine medicament dispersed in benzyl dextran, said medicament comprising amphetamine and benzyl dextran, said benzyl dextran being free of benzyl alcohol.
3. A pharmaceutical product providing a gradual release of medicament over a long period of time, and which comprises an amphetamine medicament dispersed in benzyl dext-ran, said medicament comprising an amphetamine salt and benzyl dextran and which product is free of benzyl alcohol.
4. A pharmaceutical product providing a gradual release of medicament over a long period of time, and which comprises an amphetamine medicament dispersed in benzyl dextran, said medicament comprising amphetamine sulfate and benzyl dextran which is free of benzyl alcohol, and said product being in the form of solid particles of a particle size between 20 and +40 mesh.
5. A pharmaceutical product providing a gradual release of medicament over a long period of time, and which comprises an amphetamine medicament dispersed in benzyl dextran, said medicament comprising amphetamine hydrochloride and benzyl dextran which is free of benzyl alcohol, and said product being in the form of solid particles of a particle size between --20 and +40 mesh.
6. A pharmaceutical product providing a gradual release of medicament over a long period of time, and which comprises an amphetamine medicament dispersed in benzyl dextran, said medicament comprising amphetamine sulfate and benzyl dextran which is free of benzyl alcohol, and said product being in the form of solid particles of a particle size between 10 and +20 mesh.
7. A pharmaceutical product which comprises benzyl dextran amphetamine preparation characterized by a controlled release of the amphetamine in the body over an extended period of time, said preparation being free of benzyl alcohol.
8. In a method of regulating the release of an amphetamine in the body from an amphetamine dispersed in benzyl dextran free of benzyl alcohol, the improvement which consists in removing by steam distillation any benzyl alcohol present with the benzyl dextran before dispersing the amphetamine in the said benzyl dextran.
9. In a method of effecting the controlled release of an amphetamine from compositions comprising an amphetamine dispersed in benzyl dextran produced by reacting a benzyl halide with dextran, the improvement which consists of removing by distillation the excess benzyl alcohol and excess benzyl halide from the said benzyl dextran before dispersing the said amphetamine in the benzyl dextran.
References Cited in the file of this patent UNITED STATES PATENTS 2,536,168 Goggin Ian. 5, 1951 2,609,368 Gaver Sept. 2, 1952 2,749,274 Buckwalter June 5, 1956 2,811,516 Novak Oct. 29, 1957 2,856,398 Novak Oct. 14, 1958 2,885,393 Herb May 5, 1959 2,902,408 Bouman etal Sept. 1, 1959 OTHER REFERENCES Whistler et 21.: Industrial Gums, Polysaccharides, and Their Derivatives, pages l14 and 531-563, Library of Congress copyright Date Aug. 4, 1959, published by Anademic Press, N.Y., N.Y.