KR20180102730A - Natural coating formulas and composition for coating tablets - Google Patents

Abstract

The present invention relates to a solid formulation coating composition containing gray oyster shell powder and having a proper form to be coated on a solid formulation. Additionally, the present invention relates to a method including a step of coating a solid formulation with the coating composition containing gray oyster shell powder, and a step of drying the coating composition into a film.

Description

NATURAL COATING FORMULAS AND COMPOSITION FOR COATING TABLETS [0002]

The present invention relates to solid formulation coatings.

Film coatings for solid formulations such as tablets in the diet, nutrition and pharmacy markets are common practice in a variety of markets. The purpose of coating the tablets or dragees with a film is to protect the active ingredient, to remove dust for packaging, to improve appearance, to improve swallowing, to extend shelf life, and to reduce unpleasant odors and stains. Typically, the coating formulations comprise a viscous polymer to form a film, an opacifier to inhibit light through the coating film, a plasticizer to improve the dispersibility of the polymer during the coating process, a stability of the coating solution during the coating process Lt; RTI ID = 0.0 > and / or < / RTI > Polymers include natural and synthetic polymers. Examples of natural polymers include starch, seaweed extracts such as cariguanan, plants and fungi. Examples of semi-natural polymers are chemically modified starches, hydroxypropylmethylcellulose (HPMC), hydroxyethylcellulose, and hydroxyethylmethylcellulose. Examples of synthetic polymers include polyvinyl alcohol and polyvinyl alcohol esters. Examples of the milky body include titanium dioxide, zinc oxide, iron oxide and calcium carbonate. Examples of plasticizers include polyethylene glycol, polysorbate, glycerin, heavy chain triglycerides, food oils, low melting point

Lt; RTI ID = 0.0 > triethyl citrate. ≪ / RTI > Examples of colorants include natural and artificial colors. Examples of stabilizers and bulk agents include talc and maltodextrin. Solid formulations, such as tablets, are typically coated in a controlled environment in which the temperature, airflow, pan rotation, tablet bed thickness, and coating solution spray rate are both measured. The coating powder representing the coating formulation is generally mixed with water and then sprayed onto the tablet in the form of droplets. The tablets fall down in the pan under a thermal aeration. Tablet heat

By rolling down under aeration, the coating liquid droplets on the tablet are dried and a film is formed on the surface of the tablet. Many tablets containing nutritional supplements or pharmacologically active cores may contain discoloration and / or dark staining in the early or late stages of the shelf life. The appearance of discoloration and / or dark spots affects tablet quality and consumer acceptability. To minimize discoloration and / or visibility of dark speckles, tablet coating compositions or formulations often contain titanium dioxide. However, the thermal effect of titanium dioxide has recently been questioned.

Methods of using solid formulation coating compositions, solid formulation coatings, and methods of forming coating compositions in solid formulations are described herein. As used herein, solid formulations are tablets, dragees or soft capsules for oral, buccal and sublingual administration, including ingestion, to mammals including humans.

In one embodiment, the solid dosage form coating composition comprises a gray oyster shell powder in a form suitable for being coated in a solid dosage form. Gray oyster shells are natural or non-produced products that have been conventionally used as sources of calcium, for example, cores of calcium refining. In one aspect, the gray oyster shell acts as a light inhibitor or blocker and imparts a dark shade to the coating to inhibit light in core solid formulations (e. G., Core tablets) as well as to mask dark spots. Calcium present in both gray oyster shell powder and white oyster shell powder is a heavy metal element and tends to block light rays. Surprisingly, the natural gray of the gray oyster shell powder is more effective in blocking light than the white oyster shell powder. The improved effect is believed to be derived from gray oyster shell powder which further blocks light rays from white oyster shells; The gray shields against the dark spots and discoloration of the core tablet; The coated tablets have a more natural food appearance. The substantial achievement of tablet appearance is an advantage. Also, the gray oyster shell powder removing titanium dioxide from the coating composition provides an acceptable shielding of dark spots and discoloration. In one embodiment, representative formulations of solid formulation coating compositions comprising gray oyster shell powder also include a cellulose derivative or a cellulosic gel. An example of a cellulosic gel is hydroxypropylmethylcellulose (HPMC) ultra low viscosity (VLV) Hi Prom Melos (TM), available from Dow Chemical Company, Midland, Mich., USA. HPMC VLV is a hydrocracking agent with 27% to 30% methoxyl substituents and 4% to 7.5%

Hydroxypropylmethylcellulose (CAS No. 9004-65-3). Composition details of HPMC VLV were 85-99% hydroxypropyl methylcellulose; 0.5 to 5% sodium chloride (CAS No. 7647-14-5); And 1 to 10% water (CAS No. 7732-18-5). In another embodiment, suitable cellulosic gels include, but are not limited to, those commercially available from Dow Chemical Company

("HPMC 24: 9", containing 24% methoxyl substituent and 9% hydroxypropyl substituent) or Ashland Aqualon Functional Ingredients (Delaware, USA) (HPMC), including BENECEL (trademark) HPMC, which is commercially available from Wilmington, Wear. In a further embodiment, suitable cellulosic gels include hydroxypropylmethylcellulose grades including HPMC VLV and one or more other grades of HPMC (e.g., HPMC VLV: HPMC 80:20, 60:40, 50:50, 40: 60 mixture) in combination with one or more other polymers including, but not limited to, hydroxyethyl cellulose, ethyl cellulose, hydroxypropyl cellulose, povidone, sodium carboxymethyl cellulose, hydrolyzed guar gum, acacia fruit gum or seaweed gum HPMC (e.g., HPMC VLV). In addition to the gray oyster shell powder and the cellulosic gel, in one embodiment, the solid dosage form coating composition comprises natural color such as coffee, cocoa powder, jalapeno, tea leaves, spirulina algae, berry extract, cabbage, And other natural or non-manufactured ingredients. Natural or non-produced sweeteners may also be included. Examples of natural or non-produced sweeteners include, but are not limited to, stevia extract. In one embodiment, the natural spices also included in the coating composition include, but are not limited to, extracts of mint, orange or vanilla fruit. Adding sweeteners and / or flavoring to the coating composition improves the taste of the solid formulation during the mouth. Representative formulations of solid formulation coating compositions are as follows:

In another embodiment, the composition comprises:

The compositions described above provide a natural product coating composition for solid formulations. In one embodiment, all components can be selected to be considered as natural products. The ingredients include cellulosic gel, gray oyster shell powder, natural or non-prepared colorant, flavoring and sweetening agent. The natural coating compositions as described above are useful for the dietary, nutritional and pharmaceutical industries

It is power. In one embodiment, the components of the solid dosage form coating composition are mixed in dry form. The dry formulation is weighed and mixed with purified water in a stainless steel tank to form a solution. The solution typically contains 5 to 30% by weight of solids and 10 to 95% of water. The solution is then pressurized and sprayed onto the core tablet which is rolled in a pan in the form of subdivided droplets. This is done under controlled heated drying conditions. Typical coating conditions are as follows: Rotation speed of coating pan: 2 to 15 times / min; Purification temperature: 20 ° C to 65 ° C; Airflow: 2000 to 6000 cubic feet per minute (cfm). The temperature, the degree of drying, and the airflow are maintained such that once the coating solution droplet contacts the surface of the tablet, it is dried and forms a film on the surface and evaporates any water. In the 20 to 200 minute cycle of the tablet rolling inside the coating pan, a large number of coating solution droplets contact each tablet tablet, thus forming a film on each tablet, including the coating. When the coating process is complete, each tablet is coated with a coating composition. The coating process described above can be carried out as a batch process or as a continuous process. In a batch process, the coating pan is loaded with the desired amount of core tablet, the tablet is coated with the desired amount of coating composition, and then released when coated as a finished product. In a continuous process, the core tablet is continuously loaded into the coating pan, the rolling tablet is coated continuously, and then the tablet is not loaded from the pan. Embodiments of the coating composition are described in the following examples.

 Example 1: Composition for tablet coating with blue film

 Example 2: Composition for tablet coating with green film

Example 3: Composition for tablet coating with magenta film

Example 4: Composition for tablet coating with a beige film

In another embodiment, methods of use are described. Representatively, methods of using solid formulations, such as tablets comprising a coating composition, include pouring the tablet into the mouth of a mammal (e.g., a human) and swallowing the tablet with the aid of a beverage. In another embodiment, the tablet may be intended for oral or sublingual administration. In this case, rather than swallowing the tablet, it will be retained in the mouth of the mammal until the tablet is degraded or dissolved. In the foregoing, for purposes of explanation, numerous specific details are provided to provide a thorough understanding of the embodiments. It will be apparent, however, to one skilled in the art that one or more other embodiments may be practiced without some of these specific details. The specific embodiments described are not intended to be limiting and are intended to be exemplary of the invention. The scope of the invention is not to be determined by the specific embodiments described above, but should be determined only from the following claims. In other instances, well-known structures, devices, and operations have been shown in block diagram form, or without detail, in order to avoid obscuring the understanding of the description. Where considered appropriate, reference numerals or the end portions of reference numerals are repeated in the figures to indicate corresponding or analogous elements which may have arbitrarily similar features. In addition, references throughout the specification to "one embodiment", "one embodiment", "one or more embodiments" or "different embodiments" may refer to specific features, for example, As used herein. Similarly, it is to be understood that in the description, various features are sometimes grouped together in a single embodiment, figure, or description thereof for the purpose of streamlining the disclosure and assisting the understanding of the various aspects of the invention. This disclosure, however, should not be interpreted as reflecting an intention that the invention requires more features than are expressly recited in each claim. Rather, as the following claims reflect, aspects of the invention may be less than all features of the disclosed embodiments. Accordingly, the claims following the Detailed Description are expressly incorporated into the Detailed Description, as each claim is in itself a separate embodiment of the invention.

Claims (22)

A solid dosage form comprising a gray oyster shell powder in a form suitable for being coated on a solid dosage form. The method according to claim 1,
≪ / RTI > further comprising a cellulosic gel. 3. The method of claim 2,
Wherein the cellulose gel comprises hydroxypropyl methylcellulose. 3. The method of claim 2,
Wherein the cellulose gel comprises hydroxypropylmethylcellulose ultra low viscosity. 5. The method of claim 4,
Wherein the cellulosic gel further comprises another class of hydroxypropylmethylcellulose. 3. The method of claim 2,
A solid formulation coating composition, further comprising a non-produced colorant. The method according to claim 6,
Wherein the non-fabricated colorant comprises coffee. 3. The method of claim 2,
A solid dosage form coating composition, further comprising a non-manufactured sweetener. 9. The method of claim 8,
Wherein the sweetener comprises a stevia extract. The method according to claim 1,
Hydroxypropylmethylcellulose;
Fractionated coconut oil; And
A solid formulation coating composition, further comprising a non-produced colorant. 11. The method of claim 10,
≪ / RTI > further comprising a non-prepared sweetener or flavoring. 12. The method of claim 11,
Wherein the sweetener comprises a stevia extract. 11. The method of claim 10,
Wherein the hydroxypropylmethylcellulose comprises hydroxypropylmethylcellulose ultra low viscosity. Coating the solid formulation with a coating composition comprising a gray oyster shell powder; And
And drying the coating composition to a film. 15. The method of claim 14,
Wherein the coating composition comprises a cellulosic gel. 16. The method of claim 15,
Wherein the cellulose gel comprises hydroxypropyl methylcellulose. 16. The method of claim 15,
Wherein the cellulose gel comprises hydroxypropylmethylcellulose ultra low viscosity. 16. The method of claim 15,
Wherein the cellulosic gel comprises a combination of hydroxypropylmethylcellulose ultra low viscosity and another grade of hydroxypropyl methylcellulose. 15. The method of claim 14,
Wherein the coating solution comprises 70-95% water. 15. The method of claim 14,
Wherein the coating composition further comprises a non-produced colorant. 15. The method of claim 14,
Wherein the coating composition further comprises a non-prepared sweetener. 15. The method of claim 14,
Wherein the coating composition comprises water, a solution comprising hydroxypropyl methylcellulose, fractionated coconut oil, a non-prepared colorant and a natural sweetener, stevia extract.