Rapid-release fructose diphosphate sodium tablet and preparation method thereof
A sodium diphosphate tablet and sodium fructose diphosphate technology, which is applied in the field of solid oral preparations, can solve the problems of whether the active ingredients can be released in time and completely, and achieve the effects of improving reliability and effectiveness, rapid release, and simple preparation
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Embodiment 1
[0039] prescription:
[0040] Sodium fructose diphosphate 300mg
[0041] Calcium hydrogen phosphate 200mg
[0042] Croscarmell Starch Sodium 70mg
[0043] Poloxamer 188 40mg
[0044] Micronized silica gel 20mg
[0045] Preparation: Grind the above excipients and pass through a 60-mesh sieve; fully mix sodium fructose diphosphate and poloxamer 188, sieve and mix with calcium hydrogen phosphate and cross-linked sodium carboxymethyl starch, and prepare by dry granulation Granules, including pressing into large tablets, then crushing, passing through a 14-mesh sieve for granulation, adding micro-powder silica gel to press into tablets, and then obtain.
Embodiment 2
[0047] prescription:
[0048] Sodium fructose diphosphate 300mg
[0049] Compressible starch 200mg
[0050] Low-substituted hypromellose 70mg
[0051] Sodium Lauryl Sulfate 40mg
[0052] Micronized silica gel 20mg
[0053] Preparation: Grind the above-mentioned auxiliary materials and pass through a 60-mesh sieve; fully mix sodium fructose diphosphate and sodium dodecylsulfonate, sieve and mix with compressible starch and low-substituted hypromellose, add micropowder silica gel to press Slices, ready to serve.
Embodiment 3
[0055] prescription:
[0056] Sodium fructose diphosphate 300mg
[0057] Lactose 200mg
[0058] Cross-linked polyvinylpyrrolidone 70mg
[0059] Sodium Alginate 40mg
[0060] Micronized silica gel 20mg
[0061] Preparation: Grind the above-mentioned auxiliary materials and pass through a 60-mesh sieve; fully mix sodium fructose diphosphate and sodium alginate, sieve and mix with lactose and cross-linked polyvinylpyrrolidone, add micronized silica gel to press into tablets, and obtain the product.
[0062] Implement effect test;
[0063] The tablet prepared by above-mentioned comparative example and embodiment is carried out dissolution test respectively, and the results are as follows:
[0064]
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