Title:  Formulation of fast-dissolving efavirenz capsules or tablets using super-disintegrants

United States Patent:  6,238,695

Assignee:  DuPont Pharmaceuticals Company (Wilmington, DE)

Filed:  April 6, 1999

The present invention provides improved oral dosage form formulations of efavirenz that are useful in the inhibition of human immunodeficiency virus (HIV), the prevention or treatment of infection by HIV, and in the treatment of the resulting acquired immune deficiency syndrome (AIDS). In particular, the present invention relates to compressed tablets or capsules comprising efavirenz that contain one or more disintegrants that enhance the dissolution rate of the efavirenz in the gastrointestinal tract thereby improving the rate and extent of absorption of efavirenz in the body. The present invention also relates to the process of making such tablets or capsules.

DETAILED DESCRIPTION OF THE INVENTION

The present invention provides improved oral dosage form formulations of efavirenz that are useful in the inhibition of human immunodeficiency virus (HIV), the prevention or treatment of infection by HIV, and in the treatment of the resulting acquired immune deficiency syndrome (AIDS). In particular, the present invention relates to compressed tablets or capsules comprising efavirenz that contain one or more disintegrants that enhance the dissolution rate of the efavirenz in the gastrointestinal tract thereby improving the rate and extent of absorption of efavirenz in the body. The present invention also relates to the process of making such tablets or capsules.

The active ingredient of the formulation of the present invention is the NNRTI efavirenz, which is present in a therapeutically effective amount. Methods for the manufacture of efavirenz are disclosed in U.S. Pat. No. 5,519,021. The disclosure of U.S. Pat. No. 5,519,021 in its entirety is hereby incorporated by reference. Efavirenz is (s)6-chloro-4-(cyclopropylethynyl)-1,4-dihydro-4-(trifluoromethyl)-2H-3,1- benzoxazin-2-one.

In addition to the active ingredient, solid dosage forms contain a number of additional ingredients referred to as excipients. These excipients include among others diluents, binders, lubricants, glidants and disintegrants. Diluents are used to impart bulk to the formulation to make a tablet a practical size for compression. Examples of diluents are lactose and cellulose. Binders are agents used to impart cohesive qualities to the powered material ensuring the tablet will remain intact after compression, as well as improving the free-flowing qualities of the powder. Examples of typical binders are lactose, starch and various sugars. Lubricants have several functions including preventing the adhesion of the tablets to the compression equipment and improving the flow of the granulation prior to compression or encapsulation. Lubricants are in most cases hydrophobic materials. Excessive use of lubricants can result in a formulation with reduced disintegration and/or delayed dissolution of the drug substance. Glidants are substances that improve the flow characteristics of the granulation material. Examples of glidants include talc and colloidal silicon dioxide. Disintegrants are substances or a mixture of substances added to a formulation to facilitate the breakup or disintegration of the solid dosage form after administration. Materials that serve as disintegrants include starches, clays, celluloses, algins, gums and cross-linked polymers. A group of disintegrants referred to as "super-disintegrants" generally are used at a low level in the solid dosage form, typically 1% to 10% by weight relative to the total weight of the dosage unit. Croscarmelose, crospovidone and sodium starch glycolate represent examples of a cross-linked cellulose, a cross-linked polymer and a cross-linked starch, respectively. Sodium starch glycolate swells seven- to twelve-fold in less than 30 seconds effectively disintegrating the granulations that contain it. Granulation refers to a mixing technique by which the overall particle size of a formulation is increased through the permanent aggregation of smaller particles. Wet granulation refers to granulation that is accomplished by wetting the smaller particles so they tack to one another. The newly-formed larger particles remain intact after drying. In dry granulation, larger particles are formed as a result of the compaction of the dry ingredients, followed by milling of this compacted material into suitably sized particles.

An embodiment of the present invention is a formulation and a process for manufacturing tablets or capsules using a high-shear, wet granulation step in which a very high level of a super-disintegrant such as sodium starch glycolate is included, followed by a dry blending step that incorporates additional quantities of super-disintegrant. In the present invention the amount of the super-disintegrant in the wet granulation step of the manufacturing process is preferably in the range of about 20% to about 75% by weight relative to the total dry weight of the materials used in the wet granulation step. More preferably the super-disintegrant component will range from about 20% to about 55% by weight relative to the total dry weight of all of the ingredients in the wet granulation step of the manufacturing process. In general, the range for the HIV reverse transcriptase inhibitor in the wet granulation step can vary from about 25% to about 80% by weight relative to the total dry weight of all of the ingredients in the wet granulation step of the manufacturing process. More preferably the drug substance component will range from about 45% to about 80% by weight relative to the total dry weight of all of the ingredients in the wet granulation step of the manufacturing process. Also included in the wet granulation step is a surfactant such as sodium lauryl sulfate, or another material that improves the wettability of the drug. Preferably the surfactant component will range from about 0.1% to about 5% by weight relative to the total weight of ingredients in the formulation. After the wet granulation step, the material is dried, milled, and dry blended with other ingredients such as diluents, glidants, disintegrants, and lubricants. The result of the dry blending step is then filled into gelatin capsule shells or compressed into tablets. Gelatin capsules may contain the active ingredient and powdered carriers such as lactose, starch, cellulose derivatives, magnesium stearate, stearic acid, and the like. Similar diluents can be used to make compressed tablets. Both capsules and tablets can be manufactured as sustained release products to provide for continuous release of medication over a period of hours. Compressed tablets can be sugar coated or film coated to mask any unpleasant taste and to protect the tablet from the atmosphere, or enteric coated for selective disintegration in the gastrointestinal tract. Technology for the formation of solid dosage forms such as capsules and compressed tablets, that utilize conventional pharmaceutical manufacturing equipment for their purpose, is described in detail in Remington's Pharmaceutical Sciences (Alfonso R. Gennaro ed., ch. 89, 18th ed. 1990).

In one aspect of the present invention, it was discovered that the sodium starch glycolate acts as a highly swellable carrier material onto which the efavirenz adheres during the wet granulation step of the process for the manufacture of tablets or capsules containing efavirenz. Granulation refers to a processing technique by which the overall particle size of a formulation is increased through the permanent aggregation of smaller particles. Wet granulation refers to granulation that is accomplished by wetting the smaller particles so they tack to one another. The newly-formed larger particles remain intact after drying. In the dry blending step of the process for the manufacture of tablets or capsules containing efavirenz, extragranular materials are added to the granulation to impart other improved characteristics such as flow and lubricity. The granulation is evenly blended throughout the mixture.

The adherence of the drug efavirenz substance particles to the hydrated disintegrant sodium starch glycolate is accomplished by intimate mixing in the wet granulation step. In an embodiment of the present invention the quantity of sodium starch glycolate used in the wet granulation step is significantly higher than is typically used. In the present invention the wet granulation preferably contains about 20% to about 75% by weight sodium starch glycolate relative to the total dry weight of the ingredients of the wet granulation step, as opposed to the 1-10% that is used in a typical wet granulation step (Handbook of Pharmaceutical Excipients, Ainley Wade and Paul J. Weller eds., 2d ed. 1994; The Theory and Practice of Industrial Pharmacy, Leon Lachman, Herbert A. Lieberman, and Joseph L. Kanig eds., 3rd ed. 1986; Disintegrating Agents in Hard Gelatin Capsules, John E. Botzolakis and Larry L. Augsburger, Drug Development and Industrial Pharmacy 14(1), 29-41 1988). During the wet granulation, efavirenz drug substance particles are attached to the surface of the sodium starch glycolate particles. When these granules are exposed to the fluid in the gastrointestinal tract following the disintegration of the solid dosage form, the sodium starch glycolate rapidly swells and presents the attached efavirenz drug substance particles to the fluid allowing for rapid dissolution of the efavirenz.

The present invention provides capsule or compressed tablet pharmaceutical dosage forms comprising a therapeutically effective amount of efavirenz and comprising one or more disintegrants in an amount greater than about 10% by weight relative to the total weight of the contents of the capsule or the total weight of the tablet.

The disintegrant used in the present invention is preferably selected from the group comprising modified starches, croscarmelose sodium, carboxymethylcellulose calcium and crospovidone.

The preferred disintegrant in the present invention is a modified starch.

The more preferred disintegrant in the present invention is the modified starch sodium starch glycolate.

In the present invention the capsule formulation contains efavirenz present in an amount from about 5 to about 1000 mg per capsule.

It is preferred in the present invention that the capsule formulation contain from about 5 to about 500 mg of efavirenz per capsule.

It is preferred in the present invention that the capsule formulation contain from about 500 to about 1000 mg of efavirenz per capsule.

It is preferred in the present invention that the capsule formulation contain from about 25 to about 350 mg of efavirenz per capsule.

It is preferred in the present invention that the capsule formulation contain from about 50 to about 200 mg of efavirenz per capsule.

The compressed tablet of the present invention contains efavirenz in an amount from about 5 to about 800 mg per tablet.

The present invention provides for a pharmaceutical dosage form comprising:

(a) a therapeutically effective amount of efavirenz;

(b) a surfactant;

(c) a disintegrant;

(d) a binder;

(e) a diluent;

(f) a lubricant;

(g) a glidant; and

(h) optionally additional pharmaceutically acceptable excipients;

wherein the disintegrant is selected from modified starches, croscarmallose sodium, carboxymethylcellulose calcium and crospovidone and is present in an amount greater than about 10% by weight of the total dry weight of the capsule contents or the compressed tablet.

Another embodiment of the present invention provides a method for manufacturing a solid dosage form comprising the steps of:

(a) wet granulating the efavirenz and the intragranular sodium starch glycolate in a high-shear granulator using an aqueous solution of sodium lauryl sulfate;

(b) drying result of step (a);

(c) milling result of step (b);

(d) dry blending result of step (c) with the extragranular sodium starch glycolate and additional pharmaceutically acceptable excipients; and

(e) encapsulating or compressing into tablets the result of step (d).

As used herein, the following terms and expressions have the indicated meanings. "Sodium starch glycolate" refers to sodium carboxymethyl starch. "Efavirenz" refers to the pharmacologically active ingredient (S)6-chloro-4-(cyclopropylethynyl)-1,4-dihydro-4(trifluoromethyl)-2H-3,1-b enzoxazin-2-one. The process for the synthesis of this compound is described in U.S. Pat. No. 5,519,021, which is hereby incorporated by reference. "Therapeutically effective amount" is intended to mean an amount of a compound sufficient to produce the desired pharmacological effect. "Modified starch" as used herein means any of several water-soluble polymers derived from a starch (corn, potato, tapioca) by acetylation, chlorination, acid hydrolysis, or enzymatic action.

Claim 1 of 18 Claims

What is claimed is:

1. A capsule or a compressed tablet pharmaceutical dosage form comprising a therapeutically effective amount of efavirenz and greater than about 10% by weight of a disintegrant relative to the total dry weight of the pharmaceutical dosage form.

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