Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Levodopa/benserazide orally disintegrating tablet

The technology of oral disintegrating tablet and dopasehydrazine is applied in the directions of drug combination, active ingredient of amide, nervous system diseases, etc., which can solve the problems of difficulty in taking the whole tablet, inconvenience and inconvenience for patients, and achieves refreshing taste, Easy to take, reasonable formula

Inactive Publication Date: 2010-08-11
QINGDAO UNIV OF SCI & TECH
View PDF3 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, many people with Parkinson's disease or Parkinson's syndrome find it difficult to take whole tablets, and the regular tablet form is inconvenient
Injections require medical staff to inject, and it is inconvenient for patients to use at home

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0036] The orally disintegrating tablet of dopaserazide comprises a main drug and auxiliary materials, and is characterized in that it is formulated according to the following mass percentages: 30% of the main drug levodopa, 7.5% of the main drug benserazide, and 62.5% of auxiliary materials.

[0037] Levodopa 75g (30.00%)

[0038] Benserazide 18.75g (7.50%)

[0039] Microcrystalline Cellulose 40g (16.00%)

[0040] Mannitol 67g (26.80%)

[0041] Low-substituted hydroxypropyl cellulose 3g (1.20%)

[0042] Lactose 19.25g (7.70%)

[0043] Anhydrous Citric Acid 2g (0.80%)

[0044] Cross-linked polyvinylpyrrolidone 20g (8.00%)

[0045] Cyclamate 1.5g (0.60%)

[0046] Menthol 1.5g (0.60%)

[0047] Micronized silica gel 1g (0.40%)

[0048] Magnesium Stearate 1g (0.40%)

[0049]

[0050] A total of 1000 tablets were produced

[0051] Among them, lactose and mannitol are fillers, microcrystalline cellulose, cross-linked...

Embodiment 2

[0059] The orally disintegrating tablet of dopaserazide comprises a main drug and auxiliary materials, and is characterized in that it is prepared according to the following mass percentages: 20% of the main drug levodopa, 5% of the main drug benserazide, and 75% of auxiliary materials.

[0060] Levodopa 50 20.00%

[0061] Benserazide 12.5g (5.00%)

[0062] Microcrystalline Cellulose 90g (36.00%)

[0063] Mannitol 5g (2.00%)

[0064] Low Substituted Hydroxypropyl Cellulose 15g (6.00%)

[0065] Lactose 66g (26.40%)

[0066] Anhydrous citric acid 1g (0.40%)

[0067] Cross-linked polyvinylpyrrolidone 2g (0.80%)

[0068] Cyclamate 1g (0.40%)

[0069] Menthol 1g (0.40%)

[0070] Micronized silica gel 5g (2.00%)

[0071] Magnesium Stearate 1.5g (0.60%)

[0072]

[0073] A total of 1000 tablets were produced

[0074] The preparation method of the dopaserazide orally disintegrating tablet of the present invention is the same a...

Embodiment 3

[0078] The orally disintegrating tablet of dopaserazide comprises a main drug and auxiliary materials, and is characterized in that it is prepared according to the following mass percentages: 20% of the main drug levodopa, 5% of the main drug benserazide, and 75% of auxiliary materials.

[0079] Levodopa 50g (20.00%)

[0080] Benserazide 12.5g (5.00%)

[0081] Microcrystalline Cellulose 90g (36.00%)

[0082] Mannitol 5g (2.00%)

[0083] Low Substituted Hydroxypropyl Cellulose 15g (6.00%)

[0084] Lactose 66g (26.40%)

[0085] Anhydrous citric acid 1g (0.40%)

[0086] Cross-linked polyvinylpyrrolidone 2g (0.80%)

[0087] Cyclamate 1g (0.40%)

[0088] Menthol 1g (0.40%)

[0089] Micronized silica gel 5g (2.00%)

[0090] Magnesium Stearate 1.5g (0.60%)

[0091]

[0092] A total of 1000 tablets were produced

[0093] The preparation method of the dopaserazide orally disintegrating tablet of the present invention i...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention discloses a levodopa / benserazide orally disintegrating tablet and a preparation method thereof. The tablet comprises the main drugs including levodopa and benserazide and the auxiliary materials including microcrystalline cellulose, mannitol, lactose, crospolyvinylpyrrolidone, low-substituted hydroxypropyl cellulose, sodium cyclamate, menthol, aerosol and magnesium stearate. The tablet of the invention can effectively treat the Parkinson disease or Parkinsonism syndrome, is convenient to take, good in mouthfeel, quick in disintegration, fast in absorption and high in bioavailability and provides convenience for the Parkinson disease or Parkinsonism syndrome patients who have difficulty in taking the whole tablet or feel inconvenient to take the tablet.

Description

1. Technical field [0001] The invention relates to an oral compound pharmaceutical preparation for treating Parkinson's disease or Parkinson's syndrome, in particular to an orally disintegrating tablet of dopasrazide which can be disintegrated and released quickly, has good taste and is convenient to take. 2. Background technology [0002] Dopaserazide orally disintegrating tablets are compound preparations. Dopamine deficiency in the basal ganglia of patients with Parkinson's disease or Parkinson's syndrome. Unlike dopamine, levodopa can cross the blood-brain barrier and enter the central nervous system. As a direct metabolic precursor of dopamine, it makes dopamine replacement therapy feasible. However, levodopa is rapidly decarboxylated outside the brain and transformed into dopamine, which leads to a large amount of waste of levodopa and frequent occurrence of adverse reactions. Therefore, it would be beneficial to inhibit the extracerebral decarboxylation of levodopa....

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): A61K31/198A61K9/20A61K47/38A61P25/16A61K31/16
Inventor 刘均洪张媛媛王繁业吴汝林孙岩
Owner QINGDAO UNIV OF SCI & TECH
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com