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Granules comprising cefprozil lipidosome and preparation method thereof

A technology of cefprozil and acrylic ester, which is applied in the field of medicine, can solve the problems of poor solubility, stability and bioavailability of preparations, and low encapsulation efficiency of cefprozil submicroemulsion, so as to avoid peak and valley phenomena and improve bioavailability degree, storage stability

Inactive Publication Date: 2011-01-26
王丽燕
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0013] Chinese patent CN101700232A discloses a cefprozil submicron emulsion solid preparation and its new application, which is characterized in that it is composed of cefprozil, egg yolk lecithin, poloxamer 188 and sodium deoxycholate, and the prepared cefprozil sub Microemulsion encapsulation efficiency is low
[0014] Chinese patent CN101032489A discloses a kind of cefprozil dispersible tablet and preparation method thereof, described dispersible tablet is to adopt simple cefprozil crude drug without any modification to make, and the solubility, stability and bioavailability of the obtained preparation are average. poor

Method used

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  • Granules comprising cefprozil lipidosome and preparation method thereof
  • Granules comprising cefprozil lipidosome and preparation method thereof
  • Granules comprising cefprozil lipidosome and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0070] Embodiment 1: the preparation of cefprozil liposome

[0071] Name of raw material

Dose 1 (mg)

Dose 2 (mg)

Dose 3 (mg)

cefprozil

62.50

125.00

250.00

Hydrogenated Soy Lecithin

156.25

312.50

625.00

egg yolk lecithin

156.25

312.50

625.00

cholesterol

312.50

625.00

1250.00

Vitamin E

50.00

100.00

200.00

total

737.50

1475.00

2950.00

[0072] Preparation:

[0073] (A) Dissolve hydrogenated soybean lecithin, egg yolk lecithin, cholesterol and vitamin E in an appropriate amount of absolute ethanol according to the prescription amount, mix evenly, filter, evaporate and remove absolute ethanol on a rotary evaporator to obtain a phospholipid film, and vacuum reduce Press dry. The amount of dehydrated alcohol used is 30 times of the amount of cefprozil.

[0074] (B) Weigh the prescribed amount of cefprozil...

Embodiment 2

[0079] Embodiment 2: the preparation of cefprozil liposome

[0080] Name of raw material

Dose 1 (mg)

Dose 2 (mg)

Dose 3 (mg)

[0081] cefprozil

62.50

125.00

250.00

Hydrogenated Soy Lecithin

243.75

487.50

975.00

egg yolk lecithin

243.75

487.50

975.00

cholesterol

487.50

975.00

1950.00

Vitamin E

50.00

100.00

200.00

total

1087.50

2175.00

4350.00

[0082] Preparation:

[0083] (A) Dissolve hydrogenated soybean lecithin, egg yolk lecithin, cholesterol and vitamin E in an appropriate amount of absolute ethanol according to the prescription amount, mix evenly, filter, evaporate and remove absolute ethanol on a rotary evaporator to obtain a phospholipid film, and vacuum reduce Press dry. The amount of dehydrated alcohol used is 30 times of the amount of cefprozil.

[0084] (B) Weigh the prescribed...

Embodiment 3

[0089] Embodiment 3: the preparation of cefprozil liposome

[0090] Name of raw material

Dose 1 (mg)

Dose 2 (mg)

Dose 3 (mg)

cefprozil

62.50

125.00

250.00

Hydrogenated Soy Lecithin

312.50

625.00

1250.00

egg yolk lecithin

312.50

625.00

1250.00

cholesterol

625.00

1250.00

2500.00

Vitamin E

50.00

100.00

200.00

[0091] total

1362.50

2725.00

5450.00

[0092] Preparation:

[0093] (A) Dissolve hydrogenated soybean lecithin, egg yolk lecithin, cholesterol and vitamin E in an appropriate amount of absolute ethanol according to the prescription amount, mix evenly, filter, evaporate and remove absolute ethanol on a rotary evaporator to obtain a phospholipid film, and vacuum reduce Press dry. The amount of dehydrated alcohol used is 30 times of the amount of cefprozil.

[0094] (B) Weigh the prescri...

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PUM

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Abstract

The invention relates to cefprozil lipidosome, a preparation method thereof and granules comprising the same. The cefprozil lipidosome comprises the following components in proportion by weight: 1 cefprozi, 1.25-5 hydrogenated soybean lecithin, 1.25-5 egg yolk lecithin, 2.5-10 cholesterin and 0.1-3 vitamin E. The cefprozil granules not only conform to the requirements of Chinese pharmacopoeia, but also has the advantages of more stable storage at normal temperature, faster drug effect-taking, and obviously improved bioavailability compared with the common cefprozil pharmaceutical composition.

Description

technical field [0001] The invention relates to a cefprozil liposome, a preparation method thereof and granules containing it. The cefprozil granules are more stable than common cefprozil pharmaceutical compositions, exhibit faster drug effects and have significant bioavailability The improved advantages belong to the technical field of medicine. Background technique [0002] Acute cholecystitis is a common disease. In my country, according to literature reports, it ranks second among acute abdominal surgical diseases, second only to acute appendicitis, and is more common than acute intestinal obstruction and ulcer perforation. The disease is more common in middle-aged people aged 35 to 40, and women are more likely to suffer from it than men, especially women who are obese and have multiple pregnancies. The onset of acute cholecystitis is due to obstruction of the cystic duct by stones, resulting in the retention of bile in the gallbladder, followed by bacterial infection...

Claims

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Application Information

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IPC IPC(8): A61K9/127A61K9/16A61K31/545A61P1/16A61P31/04
Inventor 王丽燕
Owner 王丽燕
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