Sustained-release preparation containing hydrochlorothiazide and preparation method thereof
A technology of sustained-release preparations and hydrochlorothiazide, which is applied to medical preparations containing active ingredients, medical preparations with non-active ingredients, and pharmaceutical formulas, etc. It can solve the problems of short duration of drug effects, easy to forget to take or miss doses, and blood drug concentration. Low-level problems, to achieve stable blood drug concentration in the body, reduce the number of administrations, and reduce the effects of toxic and side effects
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Embodiment 1
[0026] The following is the amount used in 1000 pieces
[0027] a. Hydrochlorothiazide immediate-release small tablets
[0028] Component Amount (g)
[0029] Hydrochlorothiazide 6
[0030] Microcrystalline Cellulose 10
[0031] Lactose 12.95
[0032] Crospovidone 0.9
[0033] Magnesium stearate 0.15
[0034] b. Hydrochlorothiazide extended-release small tablets
[0035] Component Amount (g)
[0036] Hydrochlorothiazide 31.5
[0037] Hydroxypropyl methylcellulose 12.5
[0038] Kabob 2
[0039] Lactose 8.725
[0040] Magnesium stearate 0.275
[0041] The preparation process is as follows:
[0042] The raw and auxiliary materials are crushed and sieved, mixed according to the above prescription amount, and then mixed with the lubricant. Squeeze them into small pieces, mix them and pour them into capsules.
Embodiment 2
[0044] The consumption of present embodiment is the amount used by 1000
[0045] a. Hydrochlorothiazide immediate-release small tablets
[0046] Component Amount (g)
[0047] Hydrochlorothiazide 6
[0048] Microcrystalline Cellulose 10
[0049] Lactose 12.95
[0050] Crospovidone 0.9
[0051] Magnesium stearate 0.15
[0052] b. Hydrochlorothiazide extended-release small tablets
[0053] Component Amount (g)
[0054] Hydrochlorothiazide 31.5
[0055] Hydroxypropyl methylcellulose K100 10.2
[0056] Kabob 9.6
[0057] Lactose 19.2
[0058] Magnesium stearate 0.3
[0059] The preparation method is the same as in Example 1.
Embodiment 3
[0061] The consumption of present embodiment is the amount used by 1000
[0062] a. Hydrochlorothiazide immediate-release small tablets
[0063] Component Amount (g)
[0064]Hydrochlorothiazide 6
[0065] Microcrystalline Cellulose 10
[0066] Lactose 12.95
[0067] Crospovidone 0.9
[0068] Magnesium stearate 0.15
[0069] b. Hydrochlorothiazide extended-release small tablets
[0070] Component Amount (g)
[0071] Hydrochlorothiazide 31.5
[0072] Hydroxypropyl methylcellulose K15 7.8
[0073] Carbopol 1.2
[0074] Lactose 19.2
[0075] Magnesium stearate 0.3
[0076] The preparation method is the same as in Example 1.
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