WO1983003757A1

WO1983003757A1 - Dry powder formulations having improved flow and compressibility characteristics, and method for the preparation thereof

Info

Publication number: WO1983003757A1
Application number: PCT/US1983/000587
Authority: WO
Inventors: Harry B. Demopoulos
Original assignee: Individual
Current assignee: Individual
Priority date: 1982-04-22
Filing date: 1983-04-20
Publication date: 1983-11-10
Anticipated expiration: 1984-10-22
Also published as: JPH0516404B2; US4454125A; JPS59500564A; CA1209041A; DE3382047D1; EP0105924A1; EP0105924B1; EP0105924A4

Abstract

Dry, stable, self-lubricating formulations for use as pharmaceuticals or vitamin/mineral supplements, which do not require the inclusion of fillers, lubricants, binders and other conventional excipients, and which exhibit excellent free flowability and compressibility characteristics, are produced by incorporating crystalline ascorbic acid or physiologically acceptable ascorbate salts therein.

Description

DRY POWDER FORMULATIONS HAVING IMPROVED FLOW

AND COMPRESSIBILITY CHARACTERISTICS, AND METHOD FOR THE PREPARATION THEREOF - Technical Field

This invention is directed to dry powder formulations for use as pharmaceuticals or vitamin/mineral supplements which are free of conventional fillers, lubricants and other excipients, and in particular to such compositions 0 which exhibit excellent flow, compressibility and other cha acteristics.

OMP Bac qround Art

In order to utilize modern mass-production technology in the encapsulation of dry powder pharmaceutical and vitamin/mineral supplement formulations it is necessary that such compositions have desirable flow characteristics permitting rapid flow through high speed encapsulators without clumping or aggregation. (Remington's Pharmaceutical Sciences ed. A. Usol Mack Publishing Co., Eaton, Pennsylvania, 1980, 1553-1584.) Moreover, dry pow¬ 0 der formulations to be encapsulated must exhibit a suffi¬ cient degree of compressibility to permit the use of piston-type compressive high speed automatic encapsulators therefor. Good compressibility characteristics are additionally necessary to facilitate the production of 5 relatively high-potency pharmaceutical or vitamin/mineral supplement formulations. Conventionally, the requisite flow and compressibility characteristics are provided in dry powder encapsulatable formulations by the addition of significant proportions, e.g., from about 10 to 85% by _Q weight thereof, of various lubricants such as talc, silica (sand), stearic acid, magnesium stearate or glyceryl mon- ostearate (soaps), Carbowax, and/or other fillers and excipients to impart the necessary physical characteris¬ tics thereto. 5 Dry powder formulations utilized in tableted pharma-

- . ceuticals or vitamin/mineral supplements must have flow and compressibility characteristics similar to those required for encapsulated materials. (Remington's Pharmaceutical Sciences). In addition, tablet formulations typically contain one or more binders to insure cohesion of the tableted formulation; such binders include, for .example, proteins such as gelatin, water-soluble casein derivatives such as sodium caseinate, water-soluble gums such as gum acacia, tragacanth or the like, or water- 5 soluble cellulose derivatives such as methyl cellulose, hydroxyethyl cellulose, sodium carboxy ethyl cellulose, or the like. (Cooper, J. , Tableting research and technol¬ ogy, Journal Pharmaceutical Sciences, J5T:1511-1555, 1972).

OMP Dry powder encapsulated or tableted formulations incorporating such lubricants, fillers, binders and/or other excipients as described hereinabove are disclosed, for example, in Stoyle et al U.S. Patent No. 3,293,132; Dines et al U.S. Patent No. 3,518,345; Cavalli U.S. Patent No. 3,584,114; and Magid U.S. Patent No. 3,740,432. A substantial proportion of the population may exhibit allergic or other acute noxious reactions to var¬ ious of the lubricants, fillers, binders or other exci¬ pients utilized in encapsulated or tableted pharmaceuti¬ cals or vitamin/mineral supplements. This is particularly the case in connection with vitamin supplements, particu¬ larly those containing the water-soluble vitamin C (ascor¬ bic acid) and B-complex vitamins. Ingestion of vitamin C and B-complex vitamin supple¬ ments may be necessary because of poor dietary habits and various environmental stresses (physical, psychological, and secondary due to infection, trauma, ischemia, r.adia- tion, chemical exposure or cigarette or alcohol con- sumption) . It is recognized that the tissue ascorbic acid levels of individuals exposed to many of these stresses are decreased by approximately 50%, increasing suscepti¬ bility to free radical pathologic reactions, disordered functioning of enzymes which require ascorbic acid as a co-factor (e.g., dopamine beta hydroxylase) , abnormal prostaglandin production, or generally altere blood flows through tissue. (De opoulos, H.B., The free radical pathology and the microcirculation in the major central nervous system disorders, Acta Physiologica Scandinavica, Supplement 492;91-119, 1980; and Demopoulos, H.B., The possible role of free radical reactions in carcinogenesis. Journal of Environmental Pathology and Toxicology 3_^:273-303, 1980.) The water-soluble vitamins are thus required in increased amounts in stressful situations. Since, however, such materials have only a relatively short life span and are excreted in the urine, if the stress situation continues over a prolonged period, or is repetitive, it may be necessary to consume water-soluble vitamin supplements 3 to 4 times daily, over prolonged or indefinite periods. In view of the large doses thus consumed, negative reactions to the lubricants, fillers or other excipients in water-soluble vitamin supplements have been widely reported. Thus, side effects noted by many of those on _c- high potency vitamin supplement regimens include heada¬ ches, significant gastro-intestinal distress (perhaps due to the combined irritating actions of the insoluble lubricants and fillers such as talc and silica, coupled with the detergent action of other excipients such as the

X_.Q^* stearate soaps), dizziness, malaise, and a host of aller¬ gic reactions, (Rawlins, M.D. , Adverse reactions to drugs, British Medical Journal 282;974-976, 1981; Bachmann, E., Biochemical effects of gum arabic, gum tra- gacanth, methylcellulose, and carboxymethylcellulose-Na in

IS rat heart and liver, Pharmacology 1_7_: 39-49, 1978; and

Rippere, V., Adverse reactions to drugs, British Medical Journal 282.1401, 1981.

Indeed, some of the noxious reactions appear to have a serious biochemical basis. Bachmann, for example, found

20 that some of the complex carbohydrate excipients can: (1) uncouple oxidative phosphor lation, which will decrease the ability of the cells to produce ATP (adenosinetriphos- phate); and (2) inhibit mixed function oxidases in the endoplasmic reticulum which function to detoxify drugs and

25. to otherwise metabilize them. Such impairments, potentially, are serious and may explain several types of adverse reactions to pharmaceutical and vitamin/mineral " preparations, including malaise, headaches, and gastro-intestinal discomfort.

30 A number of studies have further shown that the use of water-soluble vitamin supplements in high, repetitive doses provides antioxidant functions which are beyond the usual functions of preventing or treating vitamin defi¬ ciency diseases. For example, ascorbic acid may thus pre- -5. vent free radical lipid peroxidation of membrane phospho- lipids (Leung, H.W. , The cooperative interaction between vitamin E and vitamin C in suppression of peroxidation of membrane phospholipids, Bioc i ica et Biophysica Acta, 664:266-272, 1981.) Lipid peroxidation by free radical

SUBSTITUTE SHEET ^OMPI reactions is involved in key steps in carcinogenesis

(Demopoulos, H.B., The possible role of free radical reactions in carcinogenesis. Journal of Environmental Pathology and Toxicology _3_^:273-303, 1980; and Rosen, G.M., ^{β *}5 Spin trapping of the primary radical involved in the acti¬ vation of the carcinogen. Molecular Pharmacology, 1/7:233-238, 1980), as well as in occlusive atherosclerosis in which the synthesis of prostaglandin I₂, a substance which prevents platelet adhesion and aggregation, is 10 blocked (Demopoulos, H.B., The free radical pathology and the microcirculation in the major central nervous system disorders, Acta Physiologica Scandinavica, Supplement 492:91-119, 1980; and Editorial: Prevention of thrombosis. The Lancet, January 15, 1977, p. 127.) 5 Noxious reactions to vitamin preparations which contain allergic or other potentialy toxic additives (e.g., bind¬ ers, fillers, lubricants, and the like) may preclude the use of vitamins at the high doses which are necessary to achieve the antioxidant effects necessary to counteract 0 such peroxidation (see the Rawlins, Bachmann and Rippere papers noted above).

A number of other problems have been particularly noted in connection with conventional dry powder formu¬ lations incorporating vitamin C in the form of finely 5 divided, amorphous ascorbic acid, sodium ascorbate or the like. For example, the flow characteristics of such pro¬ ducts are impaired because of the recognized hygroscopicity of ascorbic acid (see, for example, Pipher U.S. Patent No. 2,846,353, column 4, lines 45-54; and the _Q aforesaid Stoyl et al Patent No. 3,293,132, column 2, lines 21-27). In addition, it has long been known that ascorbic acid is a reducing agent which, upon oxidation (e.g., during storage at elevated temperatures), is sus¬ ceptible to discoloration (see, for example, Magid U.S. Patent No. 3,493,659, column 1, lines 21-23). The reduc¬ ing characteristics of ascorbic acid are of particular concern in multi-vitamin supplements containing various of the B-complex vitamins which may be reduced thereby. For example, vitamin B₁₂ may be readily reduced in the

SUBSTI presence of ascorbic acid to toxic degradation products, which have anti-vitamin B₁₂ activity and, in some instances, may cause pernicious anemia. (Beaven, G.H., The reduction of vitamin B-12, Nature 176:1264-1265, 1955; and Herbert, V., Vitamin B-12, American Journal of Clinical Nutrition =971-972, 1981.)

It has thus been necessary to devise specific formu¬ lations for vitamin supplements incorporating both ascor¬ bic acid and vitamin B._, to preclude degradation thereof. For example, Bouchard et al U.S. Patent No. 2,830,933 discloses such a formulation in which the vitamin B.. _ has been adsorbed on a synthetic ion-exchange resin prior to blending with other multi-vitamin and/or mineral ingredi¬ ents. Vitamin B,₂ has also been marketed in a stable form within an external matrix; the use of such forms may, however, reduce the bioavailability of the vitamin.

It is, accordingly, among the objects of the present invention to provide dry powder formulations for use as ^* pharmaceuticals or vitamin and/or mineral supplements, which formulations have improved flow and compressibility characteristics faciliting encapsulation or tableting in state-of-the-art, high speed production equipment. A fur¬ ther object of the invention is to provide such formula¬ tions which do not require the presence of large quanti- ties, if any, of conventional lubricants, fillers, binders and/or other excipients and which are not, therefore, sub¬ ject to the toxic side effects associated with such addi¬ tives. Yet an additional object is to provide dry powder formulations of the indicated types incorporating ascorbic acid as the principal lubricant and/or binder therein, together with a method for the preparation thereof. These and other objects and advantages of the present invention will be apparent from the following description and the accompanying drawings.

OI.-IPI

VIFO Brief Description of Drawings

In the drawings:

FIG. IA is a photomicrograph, taken with a trans¬ mitted beam in a light microscope at llOx magnification, 5. or a crystalline ascorbic acid material utilized in the dry powder formulations of the present invention. The . crystals are flat, and transparent to the transmitted beam of light;

FIG. IB is a photomicrograph similar to FIG. IA, 10 taken at the same magnification (llOx), but illustrating a , representative dry powder formulation of the invention in a multi-vitamin composition incorporating the crystalline ascorbic acid material of FIG. IA in admixture with var¬ ious powdered B-complex vitamins; 25 FIG. 2A is a scanning electron micrograph, taken at

280 X magnification, of the ascorbic acid crystals of FIG. IA;

FIG. 2B is a scanning electron micrograph similar to FIG. 2A, illustrating the structure of the same ascorbic 20 acid crystals at 510 X magnification;

FIG. 3A is a scanning electron micrograph similar to FIG. 2A, taken at the same magnification (280 X), but illustrating the structure of the dry powder formulation of FIG. IB; 25 FIG. 3B is a scanning electron micrograph similar to

FIG. 3A, illustrating the structure of the same dry powder formulation shown in FIG. 3A, at 510 X magnification; - . FIG. 4A is a scanning electron micrograph similar to " FIG. 2A, taken at 280 X magnification, of finely divided, 30 amorphous ascorbic acid; ι. FIG. 4B is a scanning electron micrograph similar to

FIG. 4A, illustrating the structure of the same finely divided, amorphous ascorbic acid shown in FIG. 4A, at 510 X magnification; 'c FIG. 5A is a scanning electron micrograph similar to

FIG. 4A, taken at the same magnification (280 X), but illustrating the structure of a representative dry powder formulation incorporating finely divided, amorphous ascor¬ bic acid with the various B-complex vitamins; and

f OMPI

SUB^STITUTE SHEE '^P FIG. 5B is a scanning electron micrograph similar to

FIG. 5A, illustrating the structure of the same dry powder formulation shown in FIG. 5A, at 510 X magnification.

Disclosure of the Invention - It has been found that a dry powder formulation suitable for use as a pharmaceutical or vitamin/mineral supplement can be readily and efficiently encapsulated or ⁵ tableted without requiring the addition of any of the con¬ ventional fillers, lubricants, binders or other excipients therein. Such a formulation is produced in accordance with the invention simply by mixing the desired effective ingredients with ascorbic acid crystals or crystalline, 10 physiologically acceptable ascorbate salts, in an amount of at least about 5% by weight of the formulation. The crystalline ascorbic acid material may thus be employed to reduce the proportions of, or totally eliminate, all other additives and excipients from the formulation. ¹⁵ As more fully explained hereinafter, when added to dry powders the crystalline ascorbic acid or ascorbate salt serves as a "dry lubricant" imparting free flowing characteristics to the resulting composition and facil-' itating encapsulation or tableting thereof in state-of- 20 the-art, high speed encapsulators without caking or stick¬ ing. Additionally, the relative fracturability of the crystalline ascorbic acid materials permits the molecular units thereof to be broken up and compositions containing such crystals to be compacted during the encapsulation or 25 ^" tableting operation.

The crystalline ascorbic acid or ascorbate salts uti¬ lized herein may, because of the specific characteristics of their flat, rhomboid and plate-like multi-layer structures, and the pharmacologically acceptable and bene- 30 ficial properties thereof, be utilized as a dry lubricant -_^**-^* in a wide variety of dry powder formulations utilized as pharmaceuticals or vitamin/mineral supplements. As those skilled in the art will appreciate, however, there may be some formulations in which inclusion of the crystalline 5 ascorbic acid materials may not be desirable because of their reducing characteristics and the resulting risk of reductive degradation of particularly unstable materials which may be admixed therewith. In particular, it has been found that stable, self-lubricating, compressible dry powder formulations suitable for either pharmaceutical or vitamin/mineral sup¬ plement use may be provided by admixing the crystalline ascorbic acid materials with any of a wide variety of active agents. Such agents include vitamins such as the B-complex vitamins, e.g., thiamine (B^, riboflavin (B₂, niacin (B.,), pyridoxine (B_g), cyanocobalamin (B-_j-) ' f°lic acid, pantothenic acid, paraminobenzoic acid, inositol, choline, biotin, retinoids, and calciferols; mineral sup¬ plements such as selenium, zinc, calcium, magnesium, manganese, chromium and dolomite; other food supplements such as lecithin, yeast, herbs, plankton or plant fiber; or pharmaceutically active agents such as the barbitu- rates, e.g., secobarbital, the phenothiazine tranquili- zers, e.g., chlorpro azine, antibiotics, e.g., tetra- cycline or penicillin, analgesics, e.g. acetaminophen or aspirin, antiasthmatics, e.g. theophylline, decongestants, e.g., chlorpheniramine or phenylpropanolamine, cardiovas- cular preparation, e.g. , ^"quinidine or digitalis prepara¬ tions; or other compounds such, for example, as beta caro¬ tene, canthaxanthin or the like. Accordingly, it will be understood that the present invention embraces dry powder formulations which may be broadly useful as either vita- min/ ineral supplements or pharmaceuticals, including pre¬ scription drugs and over-the-counter substances, wherein the crystalline ascorbic acid material is utilized to •■» .impart improved flow and compressibility characteristics ' thereto, even apart from its desirable properties as a vitamin.

The crystalline ascorbic acid-containing formulations hereof are particularly useful in connection with the preparation of multi-vitamin compositions containing var¬ ious of the B-complex vitamins, including vitamin B,.-. It has been found that with the exception of vitamin

^B12' ^the B-complex vitamins are adsorbed on the crystal faces of the crystalline ascorbic acid materials, thus forming relatively dense, flat, composite particles. Adsorption of the B-complex vitamins on the relatively

^" massive reducing surface provided by the ascorbic acid crystals protects the B-complex vitamins against oxida-^' tion.

The dense, flat particles thus formed are best illus- 5 trated in FIGS. 1 through 3 of the accompanying drawings, wherein it may be seen that the B-complex vitamins are adsorbed on the broad flat surfaces of the ascorbic acid crystals without forming irregular clumped aggregates. Comparing FIGS. IA and IB for example, adsorption of the 10 B-complex vitamins on the transparent ascorbic acid crys¬ tals of FIG. IA eliminates their transparency (FIG. IB); moreover, it may be seen from FIG. IB that very little of the B-complex is unadsorbed. On the other hand, as illus¬ trated in FIGS. 5A and 5B, the B-complex vitamins tend to ■15 clump with the amorphous ascorbic acid powder; par¬ enthetically, it may be noted that not all of the B- co plex material is visible in FIGS. 5A and 5B, a portion being dislodged and lost during vacuum-evaporation prepa¬ ration of the specimen since it does not have a surface 0 upon which to be adsorbed.

The preferred multi-vitamin formulations of the invention desirably incorporate vitamin B, - in the form of relatively large cyanocobalamin crystals which, notwith¬ standing the recognized susceptibility of vitamin δ, _ to 5 reductive degradation, are not reduced by the crystalline ascorbic acid ingredient thereof. As indicated more fully below, the vitamin B,- I^s protected against reduction because of the size, density, rigid crystalline structure, and surface characteristics of the cyanocobalamin crys- 0 tals, which prevent adherence thereof to the ascorbic acid crystals. Thus, as illustrated in FIGS. 3A and 3.B of the accompanying drawings, the cyanocobalamin crystals do not adhere to the crystalline ascorbic acid materials. Moreover, the adsorbed "coating" of the B-complex vitamins on the crystalline ascorbic acid (see FIGS. IA and IB, and 3A and 3B) additionally serves to shield the crystalline vitamin B^₂ from reduction by the ascorbic acid ingredient of the multi-vitamin formulation. It may thus be seen that, in the preferred water- soluble multi-vitamin formulations of the invention, the crystallographic and physical properties of the ascorbic acid and the several B-complex vitamins not only improve the flow and compressibility characteristics of the compo¬ sition but additionally minimize, if not eliminate, the risk of degradation of the respective constituents and thereby significantly improve the stability thereof.

OMH Best Mode For Carrying Out The Invention

The crystalline ascorbic acid materials referred to herein include both ascorbic acid per se, and the physio¬ logically acceptable cationic ascorbate salts, e.g., sodium ascorbate, calcium ascorbate, and magnesium ascor¬ bate. The crystalline ascorbic acid materials are gen¬ erally rhomboid shaped, plate-like crystals which may have particle sizes passing anywhere from 200 to 10 mesh screens, crystals of medium-fine grade (30-80 mesh) being particularly preferred. The crystals are incorporated in the dry powder formulation in amounts of as little as about 5% to as much as about 90% by weight thereof. In the preferred water-soluble multi-vitamin formulations, the crystalline ascorbic acid materials are desirably incorporated in amounts of from about 30 to 80% thereof.

The crystalline- ascorbic acid materials utilized her¬ ein are commercially available substances which may be produced by the hydrogenation of D-glucose to D-sorbitol, followed by the microbial oxidation to L-sorbose, carboxy- lation to diacetone-2-keto-L-gulonic acid, and conversion to ascorbic acid by heating with hydrogen chloride. The ascorbate salts may of course be produced directly from the acid, if desired.

The structure of the crystalline ascorbic acid mate¬ rials utilized in accordance herewith has been elucidated in the literature (see "The Crystal Structure of L- Ascorbic Acid 'Vitamin C", J.Hvoslef, Acta Chemica Scandinavica, jL8_, No. 3, 1964, pp. 841-842). It has thus been shown by Fourier mapping that crystalline ascorbic acid possesses the following, generally accepted structural formula:

The 5-member ring is substantially planar. The material has a monoclinic crystalline structure, usually in plate-like form with occasional needles, four molecules of the ascorbic acid defining a unit cell. Two unit cells form pairs in pseudo-symmetrical order, whereby the mole¬ cules as well as the unit cells are connected by hydrogen bonding. The resultant planar crystals are thus slidable relative to each other, permitting them to act as a dry lubricant to impart free flowability to powders which otherwise tend to cake, stick or clump during encapsula¬ tion or tableting thereof.

In addition, the individual ascorbic acid (or ascorbate) crystals are readily fracturable due to the lack of extreme density and strength within the individual crystal structures. It is thus possible to break and com¬ pact the individual crystals upon subjecting the dry pow¬ der formulations containing the same to compressive forces during encapsulation or tableting. The dry powder formu¬ lation incorporating the crystalline ascorbic acid mate- rials are thus readily compressible, as well as free flowing.

It is further believed that the crystalline synthetic ascorbic acid materials utilized in accordance with the present invention are more stable than natural ascorbic acid crystals or the amorphous, fine powder ascorbic acid utilized in conventional multi-vitamin formulations. Materials of these latter types have been described as subject to oxidation upon exposure to air and light (see the Merck Index, 8th Edition, 1968, p. 105). The synthe- tic crystalline ascorbic acid utilized in the formulations hereof may, because of the existence of hydrogen bonding in the crystal, be less susceptible to autoxidation to dehydro ascorbic acid and thus exhibit superior stability. It will be understood that the preceding is but one pos- sible explanation of the superior flow, compressibility and stability characteristics of the crystalline ascorbic acid materials incorporated in the dry formulations of the

SU invention. Accordingly, it is intended that the invention not be construed as limited to the proposed structural mechanisms described.

As indicated hereinabove, the preferred dry powder formulations of the invention incorporate the crystalline ascorbic acid materials, in amounts of from about 30 to 80%, in admixture with other water-soluble vitamins, preferably blends with vitamin B,_ and other B-complex vitamins. Particularly preferred multi-vitamin formulations of this type desirably incorporate the following ingredients:

Ingredient Parts By Weight

Crystalline Ascorbic acid material From 400 to 1,600 mgs

(from 30 to 80 mesh)

Calcium pantothenate From 30 to 120 mgs powder

Thiamine hydrochloride From 20 to 80 mgs powder

Pyridoxine From 20 to 80 mgs powder

Niacin From 10 to 40 mgs powder

Riboflavin From 2 to 8 mgs powder

Cyanocobalamin From 100 to 400 micrograms

(approximately 0.1 to 1.0 mm. length, and 0.01 to 0.2 mm. width) _As indicated, it is particularly preferred to utilize vitamin B, ~ in the form of pure, reduction-resistant cyan¬ ocobalamin crystals. The crystals thus utilized in the dry powder formulations hereof are needle-shaped, having a dense, strong lattice structure. (Ric es, E.L., Crystalline vitamin B-12, Science 107:396-397, 1948; Hodgin, D.C., Structure of vitamin B-12. The crystal structure of the hexacarboxylic acid derived from B-12 and the molecular structure of the vitamin, Nature 176:325-328, 1955; and Kamper, M.J. , Some observations on the crystal structure of a chlorine-substituted vitamin B-12, Nature 176:551-553, 1955). They are considerably larger than the crystalline ascorbic acid materials admixed therewith, having surface areas varying from about 2 0.02 to 0.2mm with lengths of from about 0.1 to 1 ram, and widths of from about 0.01 to 0.2mm. These are of 99% purity.

This crystal form exhibits superior resistance to reductive degradation. Such is the case because the many points of inter-molecular bonding in the cyanocabalamin crystal lattice create a dense, tight structure which is highly resistant to reduction (see Rickes, Hodgin and Kamper, above). Moreover, because of the difference in size and shape of the cyanocobalamin and ascorbic acid crystals, and the adsorption of the further B-complex vitamins ^"on the crystalline ascorbic acid materials, the cyanocobalamin is not readily attracted by electrostatic attraction to the ascorbic acid crystals.

The B-complex vitamins, including vitamin B,^ in the form of the above indicated cyanocabalamin crystals, may thus be admixed with the crystalline ascorbic acid mate¬ rials without risk of either reductive degradation of the vitamin B,₂ or oxidative degradation of the other B-complex vitamins. Such is of particular importance in the frequent dosing of largedoses of the multi-vitamins. Hence, while only small proportions of vitamin B, ate normally incorporated in such formulations, when large dose regimens are utilized the possibility exists of the dosing of clinically significant amounts of degraded

OMPI

SUBSTITUTE SHEET vitamin B with the concomitant risk of pernicious -anemia

12

(Beaven, G.H., The reduction of vitamin B-12, Nature 176:1264-1265, 1955; and Herbert, V., Vitamin B-12, American Journal of Clinical Nutrition 3_:971-972, 1981). The dry powder formulations of the invention may be prepared by blending the various constituents thereof in any suitable proportion and manner, dependent on the par¬ ticular constitutents thereof. In forming the preferred water-soluble multi-vitamin formulations incorporating cyanocobalamin and other B complex vitamins, it is pre¬ ferred to prepare the mix as follows: (1) triturate the cyanocobalamin crystals with an aliquot of the calcium pantothenate (5-10% of the total pantothenate to be used) to insure uniform dispersion of the microgram quantities of cyanocobalamin in each capsule; (2) mix all the other materials together without the triturate of cyanocobalamin in order to adsorb the other B-complex vitamins without affecting attraction of the cyanocobalamin to the crys¬ talline ascorbic acid materials; and (3) add the triturate of cyanocobalamin to the mixture.

The following examples are given to further illus¬ trate the invention and are not to be construed in a limiting sense. All parts and percentages given in the examples are by weight, unless otherwise indicated: Example 1 - Flow Characteristics Of A Dry Powder Formulation Of The Invention A mixture of crystalline ascorbic acid and B-complex vitamins containing the following ingredients was pre¬ pared: ascorbic acid crystals (30-80 mesh) 200 grams calcium pantothenate powder 30 grams thiamine hydrochloride powder 10 grams pyridoxine powder 10 grams niacin powder 5 grams riboflavin powder 1 gram cyanocobalamin crystals (99% purity) 50 mg

(0.2 mm - 0.5 mm length, 0.05 mm - 0.1 mm width)

OMP ^y.^*t^~>. WIP The mixture was prepared by (1) triturating the cyan¬ ocobalamin with a 5% aliquot of the calcium pantothenate (1.5 grams); (2) mixing all the other materials together without the triturate of cyanocobalamin; and (3) adding the triturate of cyanocobalamin to the mixture. These steps were performed in sequence to insure the uniform dispersion of the cyanocobalamin and also to adsorb the other B-complex vitamins on the crystalline ascorbic acid prior to adding the cyanocobalamin.

10 In an initial laboratory test, the above mixture flo¬ wed by gravity feed through a vertically positioned glass funnel (90° from the horizontal) having a 10 cm circular opening and a 15 cm stem having a narrow 6-mm. internal diameter, at a rate of 1 kg/min., without clumping, stick-

^■" ing, or caking. The flow rate was 0.9 kg/min. with the funnel inclined at 60° from the horizontal, and 0.6 kg/min. with the funnel inclined at 45° from the horizon¬ tal. On the other hand, a control blend incorporating identical proportions of each of the above materials save

2 for the substitution of an amorphous finely divided ascor¬ bic acid powder was found to stick within the stem, at the point at which the funnel met the stem proper, and could not be fed therethrough at 90°, 60°, or 45° angles from the horizontal. ^ In subsequent tests the preceding mixture was uti¬ lized to fill 0 and 00 size capsules in both manual and antomated two-piece capsule filling equipment. Thus, in a semi-automatic Parke-Davis encapsulator, slightly more than 14,000 size 0 capsules, each containing 720 mg of the 0 mixture, were filled in one hour. The encapsulation rate was close to the maximum machine speed, and the mixture freely flowed without caking, sticking or clumping. In addition, the mixture was compressed into the capsules without difficulty, and the capsules were readily closed, 5 without the addition of any further dry lubricant, filler or excipient. Exa ple 2 - Compressibility Of A Dry Powder Formulation

Of The Invention

A further batch of a dry powder formulation similar to that described in Example 1 was prepared and encapsula¬ ted in size 0 capsules, employing the semi-automatic Parke-Davis encapsulator referred to hereinabove. The dry powder mixture was prepared as described in Example 1.

720 mg. of the formulation was compressed into each size 0 capsule, about 14,000 capsules being filled in a one hour encapsulation run.

Each size 0 capsule thus filled contained approxi¬ mately the following composition: ascorbic acid 570 mg

(30-80 mesh)

calcium pantothenate 80 mg powder

thiamine hydrochloride 27 mg powder

pyridoxine 27 mg powder

niacin 13 mg powder

riboflavin 3 mg powder

cyanocobalamin (99% pure) 150 micrograms crystals

(0.2 mm - 0.5 mm length, 0.05 mm - 0.1 mm width)

TOTAL 720 mg The 720 mg. packing density is to be compared to the normal packing density of 500 g. for similar, conven¬ tional formulations in the same size capsule.. It may be seen that the encapsulated formulation of the invention had a more than 40% greater potency than conventional for¬ mulations encapsulated in the specified capsule size. Example 3 - Comparison of Compressibility Of Dry Powder

Formulations Incorporating Crystalline Ascorbic Acid And Ascorbic Acid Fine Powder

The compressibility of two multi-vitamin mixtures utilized in a hand-filling encapsulation operation was compared. In a first experiment, the following mixture, containing an amorphous ascorbic acid fine powder, was filled: Ascorbic Acid powder 200 grams

Calcium Pantothenate powder 30 grams

Thiamine Hydrochloride powder 10 grams i Pyridoxine powder 10 grams

Niacin powder 5 grams Riboflavin powder 1 gram

Cyanocobalamin (99% pure) crystals 50 mgs (0.2 mm - 0.5 mm length, 0.05 mm - 0.1 mm width) The above mixture was hand filled into size 0 cap- sules at a rate of 80 capsules per hour, each capsule con- - . taining about 482 mg. of the mixture.

In a second experiment, a mixture differing only from the above in that the ascorbic acid ingredient was replaced with an equal quantity of crystalline ascorbic acid (30 - 80 mesh), was similarly hand-filled into size 0 capsules. In this instance, approximately 602.5 mg. of the mixture was encapsulated in each size 0 capsule, and a faster hand filling rate of 110 capsules per hour was obtained. It may be seen from the preceding that use of the formulation of the invention in the hand-filling test resulted in a 25% increase in multi-vitamin potency and a 37.5% increase in encapsulation rate. Example 4 - Comparison of Compressibility of Dry Powder

Formulations Containing Various Vitamins

In a further test, the degree of compressibility of formulations containing the individual B-complex vitamins and either crystalline ascorbic acid (30 - 80 mesh) δr amorphous ascorbic acid fine powder was compared. The following average potencies were obtained in 500 capsule sample escapsulation tests:

0 Vitamin Batch Amount in Amount in Weight Size 0 Size 0 Capsule Capsule with with

Ascorbic Acid Ascorbic 5 Crystals Acid Powder (30-80 mesh) ascorbic ac-id 200 grams 500 mg 400 mg

calcium 15 grams 37.5 mg 30 mg 0 pantothenate powder

thiamine 10 grams 25 mg 20 mg HCL powder

pyridoxine 10 grams 25 mg 20 mg powder

niacin powder 5 grams 12.5 mg 10 mg

riboflavin 1 gram 2.5 mg 2 mg powder

cyanocobalamin 50 mg 125 meg 100 meg ' (99% pure) crystals (0.2 mm - 0.5 mm length, 0.05 mm - 0.1 mm width)

folic acid 50 mg 125 meg 100 meg powder It will be seen from the preceding that the increased compressibility of the crystalline ascorbic acid facil¬ itated the encapsulation of each of the noted B-complex vitamins in 25% greater potencies than when the same mate¬ rials were blended with amorphous ascorbic acid. Example 5 - Comparison of Flow and Compressibility of Tetracy cline Antibiotic Formulations Incorporating Crys¬ talline Ascorbic Acid or Ascorbic Acid Fine Powde Mixtures of crystalline ascorbic acid (30 - 80 mesh), or amorphous ascorbic acid fine powder, with tetracycline were prepared and compared for flow and compressibility characteristics. Flow was determined as in Example 1, in a gravity-feed glass funnel of the same dimensions, whereas compressibility was evaluated in 500 capsule sa - pie hand-filled encapsulation tests. Significantly, the ascorbic acid comprised only 10% of the ^"total mixture, by weight.

Substance Batch Weight tetracycline 230 grams hydrochloride powder

ascorbic acid, crystalline (30 - 80 mesh) 25 grams

The flow rate through the gravity-feed funnel system described in Example 1 was 0.8 kg/min. with the funnel at 90° from the horizontal and 0.4 kg/min. at 45° from the horizontal. On the other hand, a control blend incorporat- ing identical proportions of each of the above materials save for the substitution of an amorphous finely divided ascorbic acid powder was found to stick within the stem at the point at which the funnel met the stem proper, and could not be fed therethrough at 90° or 45° angles with the horizontal.

OMPI in a hand-filling encapsulation using the batches employed in the foregoing flow studies:

Vitamin Batch Weight Amount in Amount in

Size 0 Size 0

Capsule Capsule with with

Ascorbic Ascorbic Acid Acid

Crystals Powder (30-80 mesh) tetracycline 230 grams 570 mg 455 mg hydrochloride powder

ascorbic 25 grams 60 mg 50 mg acid

It will be seen from the preceding that the increased compressibility of the crystalline ascorbic acid facilita¬ ted the encapsulation of the tetracycline hydrochloride in 25% greater potency than when the same material was blended with amorphous ascorbic acid.

Claims

CLAIMS:

1. In a dry powder formulation for use as a pharmaceutical or vitamin/mineral supplement, the improve¬ ment comprising the inclusion of crystalline ascorbic acid or a crystalline physiologically acceptable ascorbate salt in an amount of at least 5% by weight of said formulation as the principal lubricant therein.

2. The dry powder formulation of claim 1, com¬ prising a multi-vitamin composition consisting essentially of materials selected from the group consisting of vita¬ mins and minerals and being substantially free of exci¬ pients other than said crystalline ascorbic acid or crys¬ talline physiologically acceptable ascorbate salt.

3. The dry powder formulation of claim 2, com- prising a multi-vitamin composition consisting essentially of one of more B complex vitamins in admixture with said crystalline ascorbic acid or crystalline physiologically acceptable ascorbate salt.

4. The dry powder formulation of claim 3, wherein said multi-vitamins consist essentially of cyano¬ cobalamin crystals having lengths of from 0.01 to 1 mm, and widths of from 0.01 to 0.2 mm and, adsorbed on said crystalline ascorbic acid or crystalline physiologically acceptable ascorbate salt, one or more other B complex vitamins.

^* - .

5. The dry powder formulations of any of claims 1-4 , wherein the crystalline ascorbic acid or crys¬ talline physiologically acceptable ascorbate salt has an average particle size passing from 200 to 10 mesh , and is incorporated in the formulation in an amount of from 5 to

90% by weight thereof .

6. The dry powder formulation of claim 4 , con¬ sisting essentially of the fol lowing ingredients in the proportions indicated : Parts by Weight

Ascorbic acid From 400 to 1600 parts

Calcium pantothenate From 30 to 120 parts

Thiamine hydrochloride From 20 to 80 parts

Pyridoxine From 20 to 80 parts

Niacin From 10 to 40 parts

Riboflavin From 2 to 8 parts

Cyanocobalamin From 0.1 to 0.4 parts

7. A method for improving the flow and com¬ pressibility characteristics of a dry powder formulation useful as a pharmaceutical or vitamin/mineral supplement, which comprises adding crystalline ascorbic acid or a crystalline physiologically acceptable ascorbate salt to said formulation as the principal lubricant therein, in an amount of at least 5% by weight thereof.

8. The method of claim 7, wherein the dry pow¬ der formulation is a multi-vitamin composition consisting essentially of materials selected from the group con¬ sisting of vitamins and minerals, and wherein the crys¬ talline ascorbic acid. or crystalline inert^ ascorbate salt is the sole material added as an excipient thereto.

9. The method of claim 8, wherein the formula¬ tion is prepared by blending cyanocobalamin crystals

2 having surface areas of from 0.02 to 0.2 mm with ascorbic acid or physiologically acceptable ascorbate salt crystals having an average particle size passing from 200 to 10 mesh, and adsorbing one or more other B complex vitamins on the ascorbic acid or ascorbate salt crystals, the ascorbic acid or ascorbate salt comprising from 5 to 90% by weight of the formulation.

OMPI