KR101953294B1 - An oral solid formulation containing oseltamivir and a process for the preparation thereof - Google Patents

Abstract

The present invention provides an oral solid preparation comprising oseltamivir or a pharmaceutically acceptable salt thereof and an organic acid, and a preparation method thereof.

Description

TECHNICAL FIELD The present invention relates to an oral solid preparation containing oseltamivir and a preparation method thereof,

The present invention relates to a solid preparation comprising oseltamivir or a pharmaceutically acceptable salt thereof and more particularly to a solid preparation comprising oseltamivir or a pharmaceutically acceptable salt thereof and more particularly to a solid preparation comprising oseltamivir or a pharmaceutically acceptable salt thereof, And a method for preparing the same.

Tamiflu, which is commonly used as a therapeutic agent for influenza A (H1N1), referred to as H1N1 or H1N1 influenza, contains oseltamivir phosphate as a main ingredient and is formulated as a suspension or capsule.

However, oseltamivir phosphate has a large content of active ingredients (30 mg, 45 mg, 75 mg) to be contained per capsule when formulated as a capsule. In addition, although oseltamivir phosphate is known to have higher storage stability than oseltamivir free base, it is difficult to control the quality because the desired initial dissolution rate is not easily obtained even if the particle size is controlled to increase the dissolution rate and the deviation of dissolution rate is high .

On the other hand, the free base of oseltamivir is advantageous from the standpoint of the fact that the initial dissolution rate is remarkably excellent and the deviation of the dissolution rate is low. In addition, the oseltamivir free base has a lower molecular weight than oseltamivir phosphate, and the content of the active ingredient to be filled in the capsules is relatively small, so that the productivity for capsule production is higher than that of oseltamivir phosphate.

1. Korean Patent Publication 2008-0097468 2. US patent application publication number 2012/0093738

It is an object of the present invention to provide a pharmaceutical composition containing oseltamivir free base which is more stable than oseltamivir phosphate-containing preparations by increasing the stability of the active ingredient of the preparation containing oseltamivir free base to a higher initial dissolution rate, An oseltamivir free base-containing oral solid preparation capable of securing the stability of the active ingredient at a high level.

Another object of the present invention is to provide a method for preparing an oral solid preparation containing oseltamivir free base.

One aspect of the present invention is

Oseltamivir or a pharmaceutically acceptable salt thereof, and

An oral solid preparation comprising an organic acid is provided.

In another aspect of the present invention,

A granulation step of producing a granule comprising oseltamivir or a pharmaceutically acceptable salt thereof, a diluent, a disintegrant, and a binder;

A granulating step of granulating the granules;

A post-mixing step of mixing the settled granules with a disintegrant and a lubricant; And

Optionally, formulating the mixture obtained by said post-mixing,

Wherein the organic acid is added in the granulation step or the post-mixing step.

The present invention also provides a method for producing the oral solid preparation according to the present invention.

The solid preparation containing the oseltamivir free base according to the present invention has an equivalent stability or higher than that of the oseltamivir phosphate-containing preparation by containing an organic acid as a stabilizer. Therefore, according to the present invention, there is provided an oseltamivir-containing solid preparation having an advantage of being excellent in initial dissolution rate as compared with a conventional tamifluer capsule and having a small elution deviation and being highly effective in producing capsules, Can be provided.

Hereinafter, the present invention will be described in more detail.

All technical terms used in the present invention are used in the sense that they are generally understood by those of ordinary skill in the relevant field of the present invention unless otherwise defined. In addition, preferred methods or samples are described in this specification, but similar or equivalent ones are also included in the scope of the present invention. The contents of all publications referred to in this specification are incorporated herein by reference in their entirety.

One aspect of the present invention is

Oseltamivir or a pharmaceutically acceptable salt thereof, and

An oral solid preparation comprising an organic acid is provided.

In the present specification, the term "organic acid" is generally used as an organic compound showing acidity. Specific examples thereof include carboxylic acid, sulfonic acid, sulfinic acid, sulfamic acid, phenol, enol, thiol, phosphonic acid, phosphoric acid, boronic acid, imidic acid, hydrazinic acid , Hydroxamic acid, hydroxamic acid, and the like (hereinafter referred to as " acidic functional group "

The organic acid may serve as a stabilizer to increase the stability of the active ingredient oseltamivir. The organic acid may be one type or a combination of several kinds of organic acids.

In one embodiment of the present invention, the organic acid is an organic acid having 1 to 5 carbon atoms and includes an organic acid having a carboxylic acid.

The organic acid having a carboxylic acid may be an organic acid having from 1 to 5 carbon atoms and having two carboxylic acid functional groups, for example, malonic acid, succinic acid, tartaric acid, fumaric acid, glutaric acid, But is not limited thereto. Preferably, the organic acid is tartaric acid, fumaric acid, or a combination thereof.

The amount of the organic acid to be stabilized can be determined according to the specific constituents of the organic acid. For example, it may be present in an amount of 0.3 to 6% by weight based on the total amount of the solid preparation, more specifically, 0.5 To 5% by weight of the composition.

The oseltamivir or a pharmaceutically acceptable salt thereof includes oseltamivir free base or oseltamivir phosphate, and may further include any other pharmaceutically acceptable salt.

In one embodiment of the present invention, the active ingredient of the solid preparation is an oseltamivir free base, and the oseltamivir free base has an average particle size (d _(0.9) ) of the lower 90% Particle size, more specifically from 10 [mu] m to 200 [mu] m.

In the present specification, the term "average particle size (d _(0.9) ) of the lower 90% particles" means that when the particle size is measured using a particle size analyzer, Size "

Although oseltamivir free base is known to have low stability compared to oseltamivir phosphate, oseltamivir free base has a higher initial dissolution rate than oseltamivir phosphate due to particle size control and has a small deviation of dissolution rate (Korean Patent Application 2014-0081137). In addition, the oseltamivir free base has a lower molecular weight than oseltamivir phosphate and has a pharmaceutical advantage that the amount of the active ingredient-containing mixture to be filled into capsules when manufactured as capsules is small, so that it can be manufactured with higher productivity.

The oral solid preparation according to the present invention can sufficiently stabilize the oseltamivir free base due to the use of the organic acid (see Test Example 3). Therefore, the oral solid preparation can contain the active ingredient of oseltamivir free base, and can have stability of the active ingredient similar to that of oseltamivir phosphate when it contains oseltamivir phosphate. Therefore, There is an advantage that oseltamivir free basic compound having pharmaceutical superiority in dissolution rate and capsule productivity can be used as an active ingredient.

The oral solid preparations may be any solid suspensions known in the art. In one embodiment of the invention, the oral solid preparation is an oral solid preparation containing granules comprising oseltamivir or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable additive.

The organic acid may be contained in the preparation of the granules. The fact that it can be contained in the preparation of the granules means that it can be added and prepared at any stage of the granule manufacturing process. Specifically, to the mixture containing the active ingredient, the diluent and the disintegrant, Or added after incorporation with the disintegrant and lubricant after granulation, or combinations thereof. In addition, according to a specific method for producing the granule, a person skilled in the art can appropriately select the step of adding the organic acid.

The amount of the organic acid may be determined according to the specific component of the organic acid, for example, in an amount of 0.3 to 6% by weight in the oral solid preparation containing the granule. More specifically, In an amount of 0.5 to 5% by weight. In one embodiment of the present invention, the organic acid is tartaric acid, and the content of tartaric acid in the solid preparation is 0.3 to 6% by weight. In another embodiment of the present invention, the organic acid is fumaric acid, and the content of fumaric acid in the solid preparation is 0.3 to 6 wt% (Test Example 4).

In one embodiment of the present invention, the granules have a water content of 3.5% by weight or less. If the content of water increases, the stability of the active ingredient may deteriorate (see Test Example 5).

The pharmaceutically acceptable excipient may be selected from the group consisting of a diluent, a disintegrant, a binder, a lubricant, and any combination thereof, and in one embodiment includes both a diluent, a disintegrant, a binder, and a lubricant .

The diluent may be any diluent that can be used in the manufacture of the granule and does not affect the action of the active ingredient and may be selected from, for example, pregelatinized starch, mannitol, lactose, microcrystalline cellulose, A diluent selected from the group consisting of, but not limited to,

The disintegrant can be any disintegrant that can be used in the preparation of the granule but does not affect the action of the active ingredient, for example, croscarmellose sodium, crospovidone, glycolic acid starch sodium and low substituted hydroxy Hydroxypropylcellulose, hydroxypropylcellulose, hydroxypropylcellulose, hydroxypropylcellulose, hydroxypropylcellulose, hydroxypropylcellulose, hydroxypropylcellulose, hydroxypropylcellulose, and combinations thereof.

The binder may be any binder that can be used in the manufacture of granules and does not affect the action of the active ingredient. In one embodiment, the binder may be a hydrophilic binder. When the hydrophilic binder is used, the stability of the active ingredient can be further increased. The hydrophilic binder may be selected from the group consisting of, for example, povidone, hydroxypropylcellulose, hydroxypropylmethylcellulose, light silicic anhydride, aluminum silicate, calcium silicate, calcium hydrogen phosphate, calcium carbonate, However, the present invention is not limited thereto. In one embodiment of the invention, the hydrophilic binder is povidone, hydroxypropylcellulose, or a combination thereof.

The solid oral preparation containing the granules may be a granule, a tablet, a capsule, or a dry syrup.

In one embodiment of the present invention, the oral solid preparation is a capsule and comprises oseltamivir free base as an active ingredient. Since the solid preparation contains oseltamivir free base, the molecular weight is lower than that of oseltamivir phosphate, and the amount of the mixture to be filled in the blank capsule is relatively small. Therefore, the solid preparation is preferable because it can have high initial productivity and low dissolution rate as well as being able to be produced with high productivity, while securing the stability of the active ingredient to a conventional commercially available preparation.

In one embodiment of the present invention, the oral solid preparation is a capsule, comprising oseltamivir free base as an active ingredient, and oseltamivir free base has an average particle size (d _{(0.9 ) May} have a particle size of 200 mu m or less, more specifically, a particle size of 10 mu m to 200 mu m.

The capsules of the capsules may be any capsules widely used in the art, for example, gelatin capsules, gelatin-PEG capsules, or HPMC (hydroxypropylmethylcellulose) capsules.

In one embodiment, the capsule is a capsule having a moisture content of 3 to 7% by weight. The capsule may be, but is not limited to, HPMC capsules.

In another aspect of the present invention,

A granulation step of producing a granule comprising oseltamivir or a pharmaceutically acceptable salt thereof, a diluent, a disintegrant, and a binder;

A granulating step of granulating the granules;

A post-mixing step of mixing the settled granules with a disintegrant and a lubricant; And

Optionally, formulating the mixture obtained by said post-mixing,

Wherein the organic acid is added in the granulation step or the post-mixing step.

The present invention also provides a method for producing the oral solid preparation according to the present invention.

The details of the method for producing the solid preparation can be applied to the oral solid preparation according to one aspect of the present invention.

The granule preparation step may be manufactured according to any granule production method known in the art, and may be prepared by a wet granulation method or a dry granulation method.

The wet granulation method may be carried out by granulating a mixture containing oseltamivir or a pharmaceutically acceptable salt thereof, a diluent and a disintegrant in combination with a binding liquid, followed by drying. The organic acid may be added to the mixture, the bonding liquid, or both the mixture and the bonding liquid.

The solvent for preparing the binding solution may be water, ethanol, isopropanol, acetone, or a combination thereof. In addition to the binder, the binding liquid may be prepared by adding to the solvent additional additives commonly used in the pharmaceutical field, for example, a surfactant, a buffer, or a combination thereof. According to one embodiment, the binding solution is prepared by dissolving a hydrophilic binder in ethanol.

The drying process is preferably carried out at a temperature which does not exceed about 60 캜, preferably not more than about 50 캜, more preferably not more than about 40 캜, most preferably not more than 20 For example, by air drying, fluid bed drying, oven drying or microwave drying at a temperature of from < RTI ID = 0.0 > 40 C < / RTI >

The dry granulation method may employ roller compacting or slugging of a mixture comprising oseltamivir or a pharmaceutically acceptable salt thereof and a diluent, a disintegrant, and a binder. In one embodiment of the present invention, a roller pressing method can be used. Specifically, roller pressing refers to a method of manufacturing granules through a method in which powder is passed between two rollers while being compressed at a constant pressure. The roller pressing method can be carried out using a roller compactor. The roller-squeezed mixture may then be further roughened and milled using a fitz-mill, oscillator or the like as needed to obtain granules of suitable size.

In the dry granulation method, the organic acid may be added to a mixture comprising oseltamivir or a pharmaceutically acceptable salt thereof and a diluent, a disintegrant, and a binder.

In the post-mix step of mixing with the disintegrant and glidant, the disintegrant may be any disintegrant used in the manufacture of capsules containing granules, such as, for example, croscarmellose sodium, crospovidone, Hydroxypropylcellulose, hydroxypropylcellulose, hydroxypropylcellulose, hydroxypropylcellulose, hydroxypropylmethylcellulose, hydroxypropylmethylcellulose, hydroxypropylmethylcellulose, hydroxypropylmethylcellulose, hydroxypropylmethylcellulose, In one embodiment, the disintegrant is croscarmellose sodium. The lubricant may be selected from the group consisting of magnesium stearate, talc, sodium stearyl fumarate, and any combination thereof, and in one embodiment the lubricant is a combination of talc and sodium stearyl fumarate. In the subsequent mixing step, the organic acid may be added and mixed.

The formulation may be carried out according to any method known in the art for the formulation of a solid preparation using granules and may be carried out by any known method of formulation into, for example, tablets, capsules, or dry syrups .

Hereinafter, the present invention will be described in detail based on the following examples. However, the following examples are intended to illustrate the present invention, but the scope of the present invention is not limited thereto.

Test Example 1: Forced decomposition test of oseltamivir free base

Oseltamivir (Dongwoo, Korea) 100 mg of free base was precisely weighed, placed in a 100-mL volumetric flask, and dissolved in 10 mL of distilled water. Then, oseltamivir was forcibly decomposed according to the method of forced decomposition experiment using strong acids, weak acids, strong bases and weak bases described below.

1) Control: 10 mL of distilled water was added, and the reaction was allowed to proceed in an oven at 60 ° C. for 2 hours. After cooling to room temperature, 10 mL of distilled water

2) Strong acid: After adding 10 mL of 0.1N HCl, allow the reaction to proceed in an oven at 60 ° C for 2 hours, cool to room temperature, add 10 mL of 0.1N NaOH (neutralize)

3) Mild acid: After adding 10 mL of 0.001N HCl, the reaction was allowed to proceed in an oven at 60 ° C for 2 hours. After cooling to room temperature, 0.001N NaOH 10 mL was added dropwise (neutralized)

4) Strong Base: After adding 10 mL of 0.1N NaOH, allow to stand in an oven at 60 ° C for 2 hours, cool to room temperature, add 10 mL of 0.1N HCl (neutralize)

5) Weak bases: After adding 10 mL of 0.001N NaOH, allow the reaction to proceed in an oven at 60 ° C for 2 hours, cool to room temperature, add 10 mL of 0.001N HCl (neutralize)

Next, each sample obtained in the above-mentioned decomposition experiment was added to an extract (liquid of 245 mL of methanol, 135 mL of acetonitrile and 620 mL of 0.01 N phosphoric acid) to make exactly 100 mL, and the resulting solution was used as a sample solution. The total amount of the suppositories was calculated by measuring the supernatant according to the supernatant analysis method described in the USP 'Oseltamivir phosphate Capsule'. The results are shown in Table 1 below.

[Table 1]

As shown in Table 1, it can be seen that oseltamivir is unstable and decomposed under acidic conditions, relatively stable and neutral to basic pH conditions. That is, it can be confirmed that oseltamivir is most stable at a slightly acidic pH condition.

Test Example 2: Water stability test of oseltamivir free base

The appropriate amount of Oseltamivir (Dongwoo) was added to the HDPE bottle and Petri dish, exposed at 25 ° C and 90% relative humidity for 1 day and 3 days, taken out, 100 mg precisely weighed, placed in a 100 ml volumetric flask, Add the extract (245 mL of methanol, 135 mL of acetonitrile and 620 mL of 0.01N phosphoric acid) to make exactly 100 mL, and use this solution as the sample solution. The total amount of the suppositories was calculated by measuring the supernatant according to the supernatant analysis method described in the USP 'Oseltamivir phosphate Capsule'. The results are shown in Table 2 below.

[Table 2]

As shown in Table 2, it can be seen that oseltamivir is unstable when exposed to moisture.

Example 1: Preparation of oseltamivir granule (1)

After mixing oseltamivir (Dongwoo, Korea), pregelatinized starch, croscarmellose sodium and tartaric acid in the composition as shown in Table 3 below, povidone was combined with 70% ethanol in a binding solution to obtain a water content of 2% by weight Dried and sieved with a 20 mesh sieve to prepare wet granules.

Croscarmellose sodium, talc and sodium stearyl fumarate were added to the prepared granules, followed by mixing to prepare granules.

Example 2: Preparation of oseltamivir granule (2)

Granules were prepared in the same manner as in Example 1 except that fumaric acid was used instead of tartaric acid as a stabilizer.

Example 3: Preparation of oseltamivir granule (3)

After mixing oseltamivir (Dongwoo, Korea), pregelatinized starch and croscarmellose sodium in the composition as shown in Table 3 below, povidone and tartaric acid were combined in a 70% ethanol-soluble binding liquid to obtain a water content of 2 wt% Dried and sieved with a 20 mesh sieve to prepare wet granules.

Croscarmellose sodium, talc, and sodium stearyl fumarate were added to the granules and mixed to prepare oseltamivir granules.

Example 4: Preparation of oseltamivir granule (4)

Granules were prepared by the same composition and method as in Example 3, except that fumaric acid was used instead of tartaric acid as the stabilizer.

Example 5: Preparation of oseltamivir granule (5)

Oseltamivir (Dongwoo, Korea), pregelatinized starch and croscarmellose sodium were mixed in the composition shown in Table 3 below, povidone was combined with a binding solution dissolved in 70% ethanol, and dried to have a moisture content of 2% by weight And sieved with a 20 mesh sieve to prepare wet granules.

Tartaric acid, croscarmellose sodium, talc and sodium stearyl fumarate were added to the granules and mixed to prepare oseltamivir granules.

Example 6: Preparation of oseltamivir granules (6)

Granules were prepared in the same manner as in Example 5 except that fumaric acid was used instead of tartaric acid as a stabilizer.

Comparative Example 1: Preparation of oseltamivir granule (7)

Separating the filling from the commercially available Tamiflu ^® 75 mg capsules to, oseltamivir obtain a granule.

Comparative Example 2: Preparation of oseltamivir granule (8)

Oseltamivir (Dongwoo, Korea), pregelatinized starch and croscarmellose sodium were mixed with the composition as shown in Table 4 below, povidone was combined with a binding solution dissolved in 70% ethanol, and dried to have a moisture content of 2% by weight And sieved with a 20 mesh sieve to prepare wet granules.

Croscarmellose sodium, talc, and sodium stearyl fumarate were added to the granules and mixed to prepare oseltamivir granules.

In the following Tables 3 to 4, the components, contents and processes of Examples and Comparative Examples are shown.

[Table 3]

[Table 4]

Test Example 3: Evaluation of the stability of the granule according to the type of organic acid

The oseltamivir granules obtained in Examples 1 to 6 and Comparative Examples 1 and 2 were taken in an HDPE bottle and allowed to stand for 6 months under accelerated condition at 40 DEG C and 75% relative humidity. Then, the oseltamivir phosphate capsules The contents of the C and the total flexible substances were calculated by measuring the contents of the flexible materials according to the method of analyzing the contents of the flexible materials. The results are shown in Table 5 below.

[Table 5]

From the results shown in Table 5, in Examples 1 to 6 using tartaric acid and fumaric acid as stabilizers in wet granules, the stability was improved to 0.25% or less compared with Comparative Example 2 in which no stabilizer was added, and commercially available oseltamivir phosphate the it can be seen that it is similar to the stability of Tamiflu ^® (Comparative example 1) used.

According to the results, when using an organic acid as a stabilizer than when not in use, and a significant increase in stability, exhibited similar stability and commercially available formulations of Tamiflu ^® (Comparative Example 1). In addition, when organic acid is used as a stabilizer, it can be seen that there is not a large difference in stability depending on the difference in the step of introducing organic acid during the wet granulation process.

Test Example 4: Evaluation of granular stability by amount of organic acid

[Table 6]

An appropriate amount of oseltamivir granules obtained by preparing granules according to the method of Example 5 with the composition shown in Table 6 was placed in an HDPE bottle and allowed to stand for 6 months at an acceleration condition of 40 DEG C and 75% relative humidity. Thereafter, The contents of C and C were calculated by measuring the contents of the substances according to the method of analyzing the contents of Oseltamivir phosphate Capsule. The results are shown in Table 7 below.

[Table 7]

From the results of Table 7, it can be seen that the stability is similar to that of Comparative Example 2 (negative control) when the weight ratio of tartaric acid is 0.25% (Example 11) The stability is deteriorated when the weight ratio of tartaric acid is 7.5%. Considering that the stability of oseltamivir is the most excellent in the slightly acidic pH condition as in the above Test Example 1 and the range of the weight ratio of the organic acid as in Test Example 4 is also important in consideration of the fact that the proportion of the organic acid in the oseltamivir granule It is understood that about 0.3 to 6% by weight is preferable.

Test Example 5: Evaluation of granulometry stability (loss on drying)

After mixing oseltamivir (Dongwoo, Korea), pregelatinized starch and croscarmellose sodium in the composition as shown in Table 8 below, the povidone was combined with a binding solution dissolved in 70% ethanol, The mixture was sieved through a 20 mesh sieve to prepare wet granules. Moisture content was determined by the drying loss test method described in the general test method of KP.

Each of the prepared granules was mixed with tartaric acid, croscarmellose sodium, talc and sodium stearyl fumarate to prepare oseltamivir granules.

[Table 8]

An appropriate amount of oseltamivir granules prepared using the composition of Table 8 was placed in an HDPE bottle and allowed to stand at 60 ° C for 4 weeks. Then, the supernatant was measured according to the supernatant analysis method described in USP's Oseltamivir phosphate Capsule The contents of C and C were calculated. The results are shown in Table 9 below.

[Table 9]

From the results in Table 9, it can be seen that the moisture content of the oseltamivir granules affects the stability. As in Example 16, when the water content of the granules was 4.5% or more, a flexible substance was produced and unstable, and when the water content of the granules was 3.5% or less as in Examples 13 to 15, it was found to be relatively stable.

Test Example 6: Evaluation of release by formulation

75 mg of oseltamivir was taken from the granule of Example 13 and filled in a No. 2 gelatin capsule (Seoheung capsule) to prepare a capsule. Separately, 75 mg of oseltamivir was taken from the granule of Example 13 and tableted by tableting under the condition of about 10 in a rotary tablet machine (Sejong, MRC-18).

The thus obtained 75 mg of granules, capsules, tablets and a control product, Tamiflu ( ^R) , of Example 13 were subjected to a dissolution test under the following test conditions and the average dissolution rate (% by weight) was calculated. The results are shown in Table 10 below.

≪ Dissolution test conditions >

Dissolution test method: Dissolution method 2 of Korea Pharmacopoeia (paddle method)

Eluent: 0.1N-hydrochloric acid solution

Amount of eluate: 900 mL

Effluent temperature: 37.5 DEG C

Paddle speed: 50 rpm

Number of test specimens: 6

Sample collection time: 5 minutes, 10 minutes, 15 minutes and 20 minutes

* [Table 10]

From the results shown in the above Table 10, it was found that oseltamivir dissolution rate in all the formulations was 90% by weight or more in 20 minutes, and the dissolution profile similar to that of the control product tamiflu was shown.

The present invention has been described with reference to the preferred embodiments. It will be understood by those skilled in the art that various changes in form and details may be made therein without departing from the spirit and scope of the invention as defined by the appended claims. Therefore, the above-described embodiments should be considered in an illustrative rather than a restrictive sense. The scope of the present invention is defined by the appended claims rather than by the foregoing description, and all differences within the scope of equivalents thereof should be construed as being included in the present invention.

Claims (10)

Oseltamivir free base, and
1. A solid preparation for oral use comprising tartaric acid in an amount of 1 to 2.8 wt% based on the total amount of the solid preparation,
The oral solid preparation may be prepared by granulating a granule containing oseltamivir free base, a diluent, a disintegrant, and a binder;
A granulating step of granulating the granules;
A post-mixing step of mixing the settled granules with a disintegrant and a lubricant; And
And then formulating the mixture obtained by the subsequent mixing,
Adding tartaric acid in said post-mixing step,
The oseltamivir free base is characterized in that the average particle size (d (0.9)) of the lower 90% of the particles has a particle size of 200 μm or less,
Wherein the oral solid preparation is a granule, a capsule, or a dry syrup. The oral solid preparation according to claim 1, wherein the granules contain 3.5 wt% or less of water delete The oral solid preparation according to claim 1, wherein the binder is a hydrophilic binder. 5. The composition of claim 4 wherein said hydrophilic binder is selected from the group consisting of povidone, hydroxypropylcellulose, hydroxypropylmethylcellulose, light silicic anhydride, aluminum silicate, calcium silicate, calcium hydrogen phosphate, calcium carbonate, A solid formulation for oral use selected as a binder. 2. The oral solid preparation according to claim 1, wherein the oral solid preparation is a capsule and contains an oseltamivir free base as an active ingredient. A granulation step of producing a granule comprising an oseltamivir free base, a diluent, a disintegrant, and a binder;
A granulating step of granulating the granules;
A post-mixing step of mixing the settled granules with a disintegrant and a lubricant; And
And then formulating the mixture obtained by the subsequent mixing,
And adding tartaric acid in said post-mixing step.
A method for producing a solid preparation for oral use according to any one of claims 1, 2, and 4 to 6. The manufacturing method according to claim 7, wherein the granulating step is carried out by a wet granulation method or a dry granulation method. 9. The wet granulation method according to claim 8, wherein the wet granulation method comprises granulating a mixture containing an oseltamivir free base, a diluent, and a disintegrant in combination with a binding liquid containing a binder, and adding an organic acid to the mixture, Is added to the mixture. delete