Preparation and application of esmolol sustained release tablets
A technology of sustained-release tablets and sustained-release materials, applied in the new field of drugs, can solve problems such as adverse reactions, and achieve the effects of small toxic and side effects, long action time, and stable blood drug concentration.
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specific Embodiment approach
[0052] Specific embodiments are as follows, but do not limit the present invention in any way.
Embodiment 1
[0055] Esmolol 300g
[0056] Ethyl cellulose 50g
[0057] Diethyl phthalate 10g
[0058] Lactose 150g
[0060] 95% ethanol appropriate amount
[0061] Preparation process: dissolve ethyl cellulose and diethyl phthalate with 95% ethanol, add esmolol while stirring to dissolve completely, wave off ethanol, add lactose and talcum powder in the prescribed amount, mix well, press Slices, ready to serve.
Embodiment 2
[0063] Esmolol 300g
[0064] Ethylcellulose 15g
[0065] Stearic acid 25g
[0066] Diethylphthalate 2g
[0068] Microcrystalline Cellulose 200g
[0069] 95% ethanol appropriate amount
[0070] Preparation process: dissolve ethyl cellulose, diethyl phthalate and stearic acid with 95% ethanol, add esmolol while stirring to dissolve completely, evaporate ethanol, add microcrystalline cellulose and Talcum powder, mixed evenly, compressed into tablets, ready to be prepared.
[0071] Prescription C:
[0072] Esmolol 300g
[0073] Ethyl cellulose 20g
[0074] Eudragit RS100 25g
[0075] Macrogol 6000 10g
[0076] Talc powder 15g
[0077] Microcrystalline Cellulose 250g
[0078] 95% ethanol appropriate amount
[0079] Preparation process: Dissolve ethyl cellulose, Eudragit RS100 and polyethylene glycol 6000 with 95% ethanol, add esmolol while stirring to dissolve completely, evaporate ethanol, add microcrystalline cellulose and talcum powder in th...
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