SUSTAINED-RELEASE PHARMACEUTICAL FORMULATION OF FUSED TRICYCLIC ?-AMINO ACID DERIVATIVE AND PREPARATION METHOD THEREFOR

Abstract

Disclosed are a sustained-release pharmaceutical formulation of a fused tricyclic γ-amino acid derivative and a preparation method therefor. The fused tricyclic γ-amino acid derivative is a compound represented by formula (I) or a stereoisomer, a solvate, a prodrug, a metabolite, a pharmaceutically acceptable salt or a eutectic crystal thereof.

##STR00001##

Claims

1. A sustained-release pharmaceutical formulation, characterised in that the sustained-release pharmaceutical formulation comprises: (i) a compound represented by formula (I), or a stereoisomer, a solvate, a prodrug, a metabolite, a pharmaceutically acceptable salt or a eutectic crystal thereof as an active substance, which is 2%-40% by weight; (ii) optionally one or more matrix-forming agents, which is/are 15%-50% by weight; (iii) optionally one or more swelling agents, which is/are 15%-70% by weight; and (iv) optionally one or more gelling agents, which is/are 1%-45% by weight, wherein the structure of formula (I) is as follows: ##STR00010## wherein R.sup.1 and R.sup.4 are combined to form —(CR.sup.9R.sup.9′)n— or —CR.sup.9═CR.sup.9′—; R.sup.1′, R.sup.2, R.sup.3, R.sup.3′, R.sup.4′, R.sup.5, R.sup.5′, R.sup.6, R.sup.9 or R.sup.9′ is each independently selected from H, F, Cl, Br, I, hydroxyl, amino, carboxyl, a carboxylate group, amido, cyano, C.sub.1-6 alkyl, C.sub.1-6 alkoxy, C.sub.1-6 sulphanyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, 3- to 6-membered carbocyclyl or 3- to 6-membered heterocyclyl, wherein the alkyl, alkoxy, sulphanyl, alkenyl, alkynyl, carbocyclyl or heterocyclyl is optionally further substituted with 0-6 groups selected from F, Cl, Br, I, hydroxyl, amino, carboxyl, C.sub.1-6 alkyl, 3- to 6-membered carbocyclyl or 3- to 6-membered heterocyclyl, and the heterocyclyl contains 1-2 heteroatoms selected from N, O or S; and n is selected from 1, 2 or 3.

2. The sustained-release pharmaceutical formulation according to claim 1, characterised in that the pharmaceutically acceptable salt is benzene sulphonate or other salts.

3. The sustained-release pharmaceutical formulation according to claim 1 [[or 2]], characterised in that the active substance is selected from one of the following structures: ##STR00011## ##STR00012## ##STR00013## .

4. The sustained-release pharmaceutical formulation according to claim 3, characterised in that the active substance is 3%-30% by weight.

5. The sustained-release pharmaceutical formulation according to claim 3, characterised in that the matrix-forming agent is selected from polyvinyl acetate, glyceryl behenate, polyvinylpyrrolidone or a polyvinyl acetate-povidone copolymer, or any combination thereof.

6. The sustained-release pharmaceutical formulation according to claim 5, characterised in that the matrix-forming agent is 20%-40% by weight.

7. The sustained-release pharmaceutical formulation according to claim 3, characterised in that the swelling agent comprises water-soluble or water-insoluble polymers and is selected from one of polyvinylpolypyrrolidone, croscarmellose sodium, sodium carboxymethyl starch, low-substituted hydroxypropyl cellulose or polyoxyethylene, or any combination thereof.

8. The sustained-release pharmaceutical formulation according to claim 7, characterised in that the swelling agent is 30%-65% by weight.

9. The sustained-release pharmaceutical formulation according to claim 7, characterised in that the swelling agent is polyoxyethylene which, according to the molecular weights, can be selected from one of N80, N750, 205, N12, 1125, N60K, 301, COAGULANT or 303, or any combination thereof.

10. The sustained-release pharmaceutical formulation according to claim 7, wherein the swelling agent is polyvinylpolypyrrolidone, which is 15%-50% by weight, preferably 25%-40% by weight.

11. The sustained-release pharmaceutical formulation according to claim 7, wherein the swelling agent is a mixture of polyoxyethylene and polyvinylpolypyrrolidone in different proportions, and the polyoxyethylene is 0%-35% by weight, preferably 5%-35% by weight, and most preferably 10%-35% by weight.

12. The sustained-release pharmaceutical formulation according to claim 3, characterised in that the gelling agent can be selected from one of hypromellose, sodium carboxymethyl cellulose, carbomer, xanthan gum, sodium alginate or polyoxyethylene, or any combination thereof.

13. The sustained-release pharmaceutical formulation according to claim 12, characterised in that the gelling agent is hypromellose, which is 5%-45% by weight.

14. The sustained-release pharmaceutical formulation according to claim 12, characterised in that the gelling agent is carbomer, which is 1%-35% by weight,.

15. The sustained-release pharmaceutical formulation according to claim 12, characterised in that the gelling agent is sodium alginate, which is 1%-30% by weight.

16. The sustained-release pharmaceutical formulation according to claim 12, characterised in that the gelling agent is polyoxyethylene, which is 1%-35% by weight,.

17. The sustained-release pharmaceutical formulation according to claim 3, characterised in that the sustained-release pharmaceutical formulation can also contain a filler, wherein the filler can be selected from one of mannitol, Eudragit EPO, microcrystalline cellulose, maltodextrin, silicified microcrystalline cellulose, lactose or silica, or any combination thereof.

18. The sustained-release pharmaceutical formulation according to claim 17, characterised in that the filler is 0%-15% by weight.

19. The sustained-release pharmaceutical formulation according to claim 3, characterised in that the sustained-release pharmaceutical formulation also contains a lubricant selected from one of magnesium stearate, talcum powder, sodium stearyl fumarate or colloidal silica, or any combination thereof.

20. The sustained-release pharmaceutical formulation according to claim 19, characterised in that the lubricant is 0.1%-5% by weight.

21. The sustained-release pharmaceutical formulation according to claim 19, characterised in that the lubricant is magnesium stearate, which is 0.1%-5% by weight.

22. The sustained-release pharmaceutical formulation according to claim 3, characterised in that the sustained-release pharmaceutical formulation is a sustained-release tablet.

23. The sustained-release pharmaceutical formulation according to claim 22, characterised in that the sustained-release tablet can also contain an appropriate excipient, and the excipient can be selected from one of a diluent or a glidant, or any combination thereof.

24. The sustained-release pharmaceutical formulation according to claim 23, characterised in that the diluent is one of microcrystalline cellulose, silicified microcrystalline cellulose, maltodextrin, mannitol or lactose, or any combination thereof, and the glidant is silica.

25. A method for preparing the sustained-release pharmaceutical formulation according to claim 22, the method comprising the following steps: (1) weighing each component according to the formulation, passing the active substance and the adjuvant components except for the lubricant at amounts according to the formulation through a 40-mesh sieve, and mixing same uniformly to obtain mixture 1); (2) passing the lubricant at an amount according to the formulation through a 40-mesh sieve, and then mixing all the materials uniformly to obtain mixture 2); and (3) compressing the mixture 2) into tablets using suitable tabletting equipment to obtain the sustained-release pharmaceutical formulation.

26. A method for treating and/or preventing pain, wherein, the method comprises administering the sustained-release pharmaceutical formulation according to claim 1.

27. The method according to claim 26, wherein the pain includes: post herpetic neuralgia, trigeminal neuralgia, migraine, osteoarthritis- or arthrorheumatism-related pain, lower back pain, sciatica, toothache, pain caused by burns, pain caused by diabetic neuropathy, pain caused by chemotherapy-induced neuropathy, HIV-related neuralgia, AIDS-related neuralgia, cancer-related neuropathic pain or non-neuropathic pain, acute or chronic tension headache, post-operative pain or fibromyalgia, preferably post herpetic neuralgia, pain caused by diabetic neuropathy or fibromyalgia.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0053] FIG. 1. In vitro release profiles of Examples 1-9.

[0054] FIG. 2. In vitro release profiles of Example 10.

DETAILED DESCRIPTION OF EMBODIMENTS

[0055] The technical solutions of the present disclosure will be described in detail below in conjunction with the drawings and examples, but the protection scope of the present disclosure includes but is not limited thereto.

[0056] The compounds required in the examples of the present disclosure can be prepared according to the preparation methods disclosed in the patent applications WO 2018050046 or WO 2020011258.

Example 1

[0057] The formulation is as follows:

TABLE-US-00002 Ingredients Amount (mg) Compound IV 87.79 Kollidon SR 300.21 Polyvinylpolypyrrolidone 360 Polyoxyethylene N80 232 Carbomer 10 Magnesium stearate 10 Total 1000

[0058] The above components were weighed, and compound IV and the excipient components except for magnesium stearate at the amounts according to the formulation were passed through a 40-mesh sieve and then mixed uniformly to obtain mixture 1); magnesium stearate at the amount according to the formulation was passed through a 40-mesh sieve, and then all the materials were uniformly mixed to obtain mixture 2); and the mixture 2) was compressed into tablets using suitable tableting equipment. The release profile of the compressed tablets was determined using 900 ml of hydrochloric acid medium (pH 1.2) or 900 ml of acetate buffer medium (pH 4.5).

Example 2

[0059] The formulation is as follows:

TABLE-US-00003 Ingredients Amount (mg) Compound IV 87.79 Kollidon SR 258.01 Polyvinylpolypyrrolidone 290 Polyoxyethylene N60K 85 Polyoxyethylene N80 110 Carbomer 17 Magnesium stearate 2.2 Total 850

[0060] The above components were weighed, and compound IV and the excipient components except for magnesium stearate at the amounts according to the formulation were passed through a 40-mesh sieve and then mixed uniformly to obtain mixture 1); magnesium stearate at the amount according to the formulation was passed through a 40-mesh sieve, and then all the materials were uniformly mixed to obtain mixture 2); and the mixture 2) was compressed into tablets using suitable tableting equipment. The release profile of the compressed tablets was determined using 900 ml of hydrochloric acid medium (pH 1.2) or 900 ml of acetate buffer medium (pH 4.5).

Example 3

[0061] The formulation is as follows:

TABLE-US-00004 Ingredients Amount (mg) Compound IV 87.79 Kollidon SR 299.71 Polyvinylpolypyrrolidone 360 Polyoxyethylene N60K 100 Polyoxyethylene N12K 130 Carbomer 20 Magnesium stearate 2.5 Total 1000

[0062] The above components were weighed, and compound IV and the excipient components except for magnesium stearate at the amounts according to the formulation were passed through a 40-mesh sieve and then mixed uniformly to obtain mixture 1); magnesium stearate at the amount according to the formulation was passed through a 40-mesh sieve, and then all the materials were uniformly mixed to obtain mixture 2); and the mixture 2) was compressed into tablets using suitable tableting equipment. The release profile of the compressed tablets was determined using 900 ml of hydrochloric acid medium (pH 1.2) or 900 ml of acetate buffer medium (pH 4.5).

Example 4

[0063] The formulation is as follows:

TABLE-US-00005 Ingredients Amount (mg) Compound IV 87.79 Kollidon SR 309.71 Polyvinylpolypyrrolidone 350 Polyoxyethylene N60K 100 Polyoxyethylene N12K 130 Carbomer 20 Magnesium stearate 2.5 Total 1000

[0064] The above components were weighed, and compound IV and the excipient components except for magnesium stearate at the amounts according to the formulation were passed through a 40-mesh sieve and then mixed uniformly to obtain mixture 1); magnesium stearate at the amount according to the formulation was passed through a 40-mesh sieve, and then all the materials were uniformly mixed to obtain mixture 2); and the mixture 2) was compressed into tablets using suitable tableting equipment. The release profile of the compressed tablets was determined using 900 ml of hydrochloric acid medium (pH 1.2) or 900 ml of acetate buffer medium (pH 4.5).

Example 5

[0065] The formulation is as follows:

TABLE-US-00006 Ingredients Amount (mg) Compound IV 87.79 Kollidon SR 300.21 Polyvinylpolypyrrolidone 280 Polyoxyethylene N60K 80 Polyoxyethylene N80 222 Carbomer 20 Magnesium stearate 10 Total 1000

[0066] The above components were weighed, and compound IV and the excipient components except for magnesium stearate at the amounts according to the formulation were passed through a 40-mesh sieve and then mixed uniformly to obtain mixture 1); magnesium stearate at the amount according to the formulation was passed through a 40-mesh sieve, and then all the materials were uniformly mixed to obtain mixture 2); and the mixture 2) was compressed into tablets using suitable tableting equipment. The release profile of the compressed tablets was determined using 900 ml of hydrochloric acid medium (pH 1.2) or 900 ml of acetate buffer medium (pH 4.5).

Example 6

[0067] The formulation is as follows:

TABLE-US-00007 Components Amount (mg) Compound IV 87.79 Kollidon SR 312.21 Polyvinylpolypyrrolidone 340 Sodium carboxymethyl cellulose 150 Xanthan gum 100 Magnesium stearate 10 Total 1000

[0068] The components were weighed according to the formulation, and compound IV and the excipient components except for magnesium stearate at the amounts according to the formulation were passed through a 40-mesh sieve and then mixed uniformly to obtain mixture 1); magnesium stearate at the amount according to the formulation was passed through a 40-mesh sieve, and then all the materials were uniformly mixed to obtain mixture 2); and the mixture 2) was compressed into tablets using suitable tableting equipment. The release profile of the compressed tablets was determined using 900 ml of hydrochloric acid medium (pH 1.2) or 900 ml of acetate buffer medium (pH 4.5).

Example 7

[0069] The formulation is as follows:

TABLE-US-00008 Components Amount (mg) Compound IV 87.79 Kollidon SR 312.21 Polyvinylpolypyrrolidone 340 Xanthan gum 100 Sodium alginate 150 Magnesium stearate 10 Total 1000

[0070] The components were weighed according to the formulation, and compound IV and the excipient components except for magnesium stearate at the amounts according to the formulation were passed through a 40-mesh sieve and then mixed uniformly to obtain mixture 1); magnesium stearate at the amount according to the formulation was passed through a 40-mesh sieve, and then all the materials were uniformly mixed to obtain mixture 2); and the mixture 2) was compressed into tablets using suitable tableting equipment. The release profile of the compressed tablets was determined using 900 ml of hydrochloric acid medium (pH 1.2) or 900 ml of acetate buffer medium (pH 4.5).

Example 8

[0071] The formulation is as follows: (with no swelling agent and gelling agent added)

TABLE-US-00009 Components Amount (mg) Compound IV 87.79 Kollidon SR 185 Glyceryl behenate 70 Mannitol 75 Microcrystalline cellulose 72.21 Magnesium stearate 10 Total 500

[0072] The components were weighed according to the formulation, and compound IV and the excipient components except for magnesium stearate at the amounts according to the formulation were passed through a 40-mesh sieve and then mixed uniformly to obtain mixture 1); magnesium stearate at the amount according to the formulation was passed through a 40-mesh sieve, and then all the materials were uniformly mixed to obtain mixture 2); and the mixture 2) was compressed into tablets using suitable tableting equipment. The release profile of the compressed tablets was determined using 900 ml of hydrochloric acid medium (pH 1.2) or 900 ml of acetate buffer medium (pH 4.5).

Example 9

[0073] The formulation is as follows: (with no matrix-forming agent and swelling agent added)

TABLE-US-00010 Components Amount (mg) Compound IV 87.79 Hypromellose 197.2 Silicified microcrystalline cellulose 122.41 Colloidal silica 4.2 Magnesium stearate 8.4 Total 420

[0074] The components were weighed according to the formulation, and compound IV and the excipient components except for magnesium stearate at the amounts according to the formulation were passed through a 40-mesh sieve and then mixed uniformly to obtain mixture 1); magnesium stearate at the amount according to the formulation was passed through a 40-mesh sieve, and then all the materials were uniformly mixed to obtain mixture 2); and the mixture 2) was compressed into tablets using suitable tableting equipment. The release profile of the compressed tablets was determined using 900 ml of hydrochloric acid medium (pH 1.2) or 900 ml of acetate buffer medium (pH 4.5).

Example 10

[0075] The formulation is as follows: (with no matrix-forming agent and swelling agent added)

TABLE-US-00011 Components Amount (mg) Compound IV 87.79 Hypromellose 120 Mannitol 180 Silicified microcrystalline cellulose 200.21 Magnesium stearate 12 Total 600

[0076] The components were weighed according to the formulation, and compound IV and the excipient components except for magnesium stearate at the amounts according to the formulation were passed through a 40-mesh sieve and then mixed uniformly to obtain mixture 1); magnesium stearate at the amount according to the formulation was passed through a 40-mesh sieve, and then all the materials were uniformly mixed to obtain mixture 2); and the mixture 2) was compressed into tablets using suitable tableting equipment. The release profile of the compressed tablets was determined using 900 ml of hydrochloric acid medium (pH 1.2) or 900 ml of acetate buffer medium (pH 4.5).

Example 11

[0077] The formulation is as follows:

TABLE-US-00012 Components Amount (mg) Compound III 66 Kollidon SR 363 Polyvinylpolypyrrolidone 270.6 Polyoxyethylene N60K 110 Polyoxyethylene N12K 154 Maltodextrin 110 Carbomer 22 Magnesium stearate 4.4 Total 1100

[0078] The components were weighed according to the formulation, and compound III and the excipient components except for magnesium stearate at the amounts according to the formulation were passed through a 40-mesh sieve and then mixed uniformly to obtain mixture 1); magnesium stearate at the amount according to the formulation was passed through a 40-mesh sieve, and then all the materials were uniformly mixed to obtain mixture 2); and the mixture 2) was compressed into tablets using suitable tableting equipment. The release profile of the compressed tablets was determined using 900 ml of hydrochloric acid medium (pH 1.2) or 900 ml of acetate buffer medium (pH 4.5).

Example 12

[0079] The formulation is as follows:

TABLE-US-00013 Components Amount (mg) Compound IV 154.5 Kollidon SR 285.5 Polyvinylpolypyrrolidone 286 Polyoxyethylene N60K 150 Maltodextrin 100 Carbomer 20 Magnesium stearate 4 Total 1000

[0080] The components were weighed according to the formulation, and compound IV and the excipient components except for magnesium stearate at the amounts according to the formulation were passed through a 40-mesh sieve and then mixed uniformly to obtain mixture 1); magnesium stearate at the amount according to the formulation was passed through a 40-mesh sieve, and then all the materials were uniformly mixed to obtain mixture 2); and the mixture 2) was compressed into tablets using suitable tableting equipment, wherein the tablet hardness was controlled within a range of 170-220N. The release profile of the compressed tablets was determined using 900 ml of hydrochloric acid medium (pH 1.2) or 900 ml of acetate buffer medium (pH 4.5).

Example 13

[0081] The formulation is as follows:

TABLE-US-00014 Components Amount (mg) Compound IV 84.3 Kollidon SR 312.7 Polyvinylpolypyrrolidone 350 Polyoxyethylene N60K 100 Polyoxyethylene N12K 130 Carbomer 20 Magnesium stearate 3 Total 1000

[0082] The components were weighed according to the formulation, and compound IV and the excipient components except for magnesium stearate at the amounts according to the formulation were passed through a 40-mesh sieve and then mixed uniformly to obtain mixture 1); magnesium stearate at the amount according to the formulation was passed through a 40-mesh sieve, and then all the materials were uniformly mixed to obtain mixture 2); and the mixture 2) was compressed into tablets using suitable tableting equipment. The release profile of the compressed tablets was determined using 900 ml of hydrochloric acid medium (pH 1.2) or 900 ml of acetate buffer medium (pH 4.5).

Swelling Performance Tests

[0083] Tablets were placed in a dissolution cup, and 900 ml of acetate buffer medium (pH 4.5) was added. The temperature was controlled to 37° C. and the tablets were allowed to be completely immersed in the medium. The tablets were taken out at 0 h, 1 h, 2 h, 4 h, 6 h and 9 h respectively to measure the length (L), width (W) and thickness (H) thereof with a vernier caliper.

TABLE-US-00015 Swelling performance tests of Example 3 and Example 7 Time (h) Example 3 Example 7 L (mm) W (mm) H (mm) L (mm) W (mm) H (mm) Initial value 20.68 10.21 7.90 20.71 10.25 7.96 1 21.70 11.44 9.06. 21.94 11.58 9.22 2 23.41 12.85 10.47 23.36 12.69 10.26 4 24.12 13.72 11.28 24.57 13.59 11.19 6 24.83 14.26 12.05 24.93 14.03 11.87 9 25.66 14.53 12.71 25.48 14.34 12.33

[0084] The results of the swelling performance tests indicated that the drug of the present disclosure can swell to 9 mm or larger in size upon contact with water, and with the large swelling volume, the gastric residence time of the pharmaceutical formulation can be effectively prolonged.

In Vitro Release of Tablets

[0085] 1. According to “Method 2 (Paddle)” in “Dissolution and Drug Release Test” of the “Chinese Pharmacopoeia”, the in vitro release of the self-made product was determined under the dissolution condition of 37° C. and the rotational speed of 50 rpm with the dissolution medium of 900 ml of hydrochloric acid (pH 1.2) or acetate medium (pH 4.5). The results are shown in Table 2.

TABLE-US-00016 In vitro release results of Examples 1-13 Time (h) Examples 1 2 3 4 5 6 7 8 9 10 11 12 13 1 21.1 19.0 28.4 20.4 19.0 13.8 13.0 19.0 18.6 44.8 22.0 14.2 17.5 2 30.3 27.4 40.1 29.6 27.4 21.5 20.3 25.8 27.7 71.3 31.9 22.4 26.5 4 46.7 40.0 54.6 44.3 40.0 33.8 31.5 35.3 40.5 94.0 45.8 35.3 39.3 6 53.9 49.9 63.1 54.3 49.9 43.7 41.8 44.4 51.3 96.2 56.5 45.7 49.3 8 62.4 57.9 71.2 63.6 57.9 51.8 52.5 51.8 59.5 / 64.7 54.5 56.9 12 74.2 70.4 82.4 75.5 70.4 64.9 68.8 66.5 73.1 / 77.2 67.3 68.9 16 82.8 78.8 88.9 84.2 78.8 74.2 79.4 78.6 83.7 / 85.3 78.0 77.0 24 84.6 92.3 97.0 93.7 92.3 86.2 89.3 94.3 96.7 / 90.3 86.7 84.5

[0086] During the in vitro release tests of Examples 1-13, we observed that for Example 8, which had no swelling agent and gelling agent added in the formulations, the tablet had a good sustained-release ability, but remained sunk at the bottom of the cup due to its high density. It is speculated that the tablet cannot float inside human stomach. With regard to Examples 9 and 10, which had no matrix-forming agent and swelling agent added in the formulations, Example 9 had a good sustained-release ability, but remained sunk at the bottom of the cup due to its high density. It is speculated that the tablet cannot float inside human stomach; and Example 10 had an extremely rapid rate of release and hence a poor sustained-release ability.

[0087] The drugs of Examples 1-7 and 11-13 of the present disclosure all can float in the cup, and their sustained-release performances were roughly consistent. 2. In vitro release of the above-mentioned Examples 3 and 10 was investigated using the paddle method at 75 rpm. The comparative data of the release results and the release results of the paddle method at 50 rpm were shown in Table 3.

TABLE-US-00017 Comparison of in vitro release (Paddle, 75 rpm) results of Example 3 and Example 10 Time (h) Example 3 Example 10 50 rpm 75 rpm 50 rpm 75 rpm 1 28.4 34.2 44.8 58.6 2 40.1 46.1 71.3 82.6 4 54.6 58.0 94.0 97.8 6 63.1 67.6 96.2 96.3 8 71.2 73.8 / / 12 82.4 85.1 / / 16 88.9 91.4 / / 24 97.0 99.9 / /

[0088] It can be seen from the comparative test that the release rate of Example 10 was fast-increasing with the increase of the rotational speed, and the release of the drug was substantially finished at 6 hours and the tablet did not have the expected sustained-release ability; and the drug of Example 3 of the present disclosure can show good release consistency under different dynamic conditions and no burst release occurred, ensuring better safety.

[0089] 3. The tablet obtained in Example 3 was subjected to an in vitro dissolution test according to the paddle method (at 50 rpm) of the “Chinese Pharmacopoeia” using acetate buffer (pH 1.2), acetate buffer (pH 4.5) and phosphate buffer (pH 6.8) (all being 900 ml) as the dissolution media respectively while the temperature of the media was controlled to 37° C. The dissolution release results are shown in Table 4.

TABLE-US-00018 Comparison of in vitro release results of Example 3 in different dissolution media Time (h) pH 1.2/50 rpm pH 4.5/50 rpm pH 6.8/50 rpm 1 17.9 18.8 19.3 2 27.4 28.4 27.7 4 40.1 40.6 39.7 6 50.1 50 49.2 8 58.8 58.8 57.1 12 69.9 70.4 69.2 16 77.9 79.9 79.7 20 85.9 85.3 86.5 24 90.4 91.2 92.6

[0090] The comparative in vitro release results of the drug of Example 3 in different dissolution media showed that the drug was not sensitive to changes in the pH environment and can maintain good release consistency in environments with large pH differences.

[0091] The above-mentioned test results showed that, by using the formulation technology of the present disclosure, the drug can swell to 9 mm or larger in size upon contact with water, which effectively prolongs the gastric residence time of the pharmaceutical formulation. At the high-intensity rotational speed (75 rpm), the pharmaceutical formulation prepared with the formulation technology of the present disclosure still maintains good release consistency as compared with the case at the low-intensity rotational speed (50 rpm) and no burst release occurs, ensuring better safety. In addition, the pharmaceutical formulation of the present disclosure is not sensitive to changes in the gastrointestinal pH environment and maintains good release consistency in different in vitro dissolution media, which can effectively reduce individual differences in patients after administration.

[0092] Moreover, by using the formulation technology of the present disclosure, the drug can be slowly released from the formulation, which ensures that the drug has a prolonged in vivo absorption period.

[0093] Although specific embodiments of the present disclosure have been described, those skilled in the art should know that the present disclosure can be changed and modified in many ways without departing from the range and spirit of the present disclosure. Therefore, the present disclosure is intended to cover all these changes and modifications falling within the scope of the attached claims and their equivalents.