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Floating microorganism adhesive porous hydrogel and preparation method thereof

A technology of porous hydrogel and floating organisms, applied in the direction of drug combination, pharmaceutical formula, medical preparations containing active ingredients, etc., can solve the problems of low mechanical properties of hydrogel, time-consuming, low crystallinity, etc., to achieve improved Effects of bioavailability, prolonged residence time, and mild reaction conditions

Inactive Publication Date: 2013-05-29
SHENYANG PHARMA UNIVERSITY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] The existing commonly used porous hydrogel preparation methods include: (1) Freeze-drying method: This method uses the principle of sublimation of a deep-cooled solvent to produce a pore structure to prepare a porous hydrogel. The operation is simple and does not require additional chemistry. Drugs, without high temperature or heating, but the polymers prepared by this method are usually amorphous and have low crystallinity, which may reduce the stability of some drugs; (2) Porogenic method: in the presence of porogens Prepare the gel under certain conditions, and then soak, rinse or dissolve the porogen with water or acid solution, leaving holes in their original positions to obtain a porous structure
The disadvantages are that the process of dissolving, washing, soaking and removing the porogen takes time, which prolongs the material preparation cycle; a small amount of uneluted porogen is easy to remain in the product; the porosity of the pore structure is poor; (3) Emulsion template method: This method prepares an intermediate phase emulsion droplet template. During the polymerization process, the template droplets are evenly dispersed in the polymer continuous phase; hole
The solution polymerization phase separation method may lead to low mechanical properties of the hydrogel, which limits the application of the product; while the modified thermal phase separation method is only suitable for the preparation of temperature-sensitive porous hydrogels, and the pore size and porosity control is more difficult

Method used

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  • Floating microorganism adhesive porous hydrogel and preparation method thereof
  • Floating microorganism adhesive porous hydrogel and preparation method thereof
  • Floating microorganism adhesive porous hydrogel and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0027] Implementation example one Nimodipine pectin calcium porous hydrogel

[0028] Add 0.5 g nimodipine to 20 mL 5 g / L surfactant aqueous solution to form a suspension, stir, add 1 g pectin to dissolve to form a uniform and viscous mixture, add the above mixture to 100 mL 50 g / L of calcium chloride solution, add all the solution and continue to stir for 15 minutes, filter, wash with 100 mL of water, and dry to obtain nimodipine calcium pectin porous hydrogel.

Embodiment 2

[0029] Implementation example two nimodipine pectin calcium-chitosan porous hydrogel

[0030] Add 0.6 g of nimodipine to 20 mL of 5 g / L surfactant aqueous solution to form a suspension, stir, add 1 g of pectin to dissolve to form a uniform and viscous mixture, and add the above mixture to 100 mL of 20 g / L calcium chloride solution (containing chitosan with a concentration of 2 g / L), add all of it and continue to stir for 20 minutes, filter, wash with 100 mL of water, and dry to obtain nimodipine pectin calcium-chitosan Sugar porous hydrogel.

[0031] Refer to the two appendices of the Pharmacopoeia of the People's Republic of China (2005 Edition) C The second method of dissolution test device, the paddle method is used for the release test, the dissolution medium is 900 mL of 0.1 mol / L hydrochloric acid solution, the temperature is (37±0.5) ℃, the rotation speed is 50 r / min, and 100 mg of porous Add the hydrogel into the dissolution vessel, sample 5 mL at regular intervals,...

Embodiment 3

[0033] Implementation example three Ketoprofen sodium alginate-chitosan porous hydrogel

[0034] Add 0.8 g ketoprofen to 40 mL of 5 g / L surfactant aqueous solution to form a suspension, stir, add 0.8 g sodium alginate to dissolve and form a uniform viscous mixture, add the above mixture to 100 mL of 30 g / L calcium chloride solution (containing chitosan with a concentration of 2 g / L), add all of it and continue to stir for 30 minutes, filter, wash with 100 mL of water, and dry to obtain ketoprofen calcium alginate- Chitosan porous hydrogel.

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Abstract

The invention discloses a preparation method of a floating bioadhesive porous hydrogel. The porous hydrogel is a non-effervescent granule and is prepared by adopting an orifice-coagulating bath method, wherein the method is simple, and reaction conditions are mild. A micropill is prepared from drugs and a carrier, wherein the carrier is a natural high molecular polysaccharide substance, has biocompatibility and bioadhesion, is sensitive to the pH value and does not have toxic side effect. The preparation method of the micropill comprises the following steps of: firstly, adding water-insolubledrugs into a solution containing surfactants, and stirring or ultrasonically dispersing uniformly; stirring at a higher speed; adding polysaccharides for dissolving to form uniform viscous mixture; then adding the mixture into a chitosan coagulating bath containing calcium chloride in a form of droplets for cross-linking curing; washing with water; and drying to obtain the micropill. The preparedmicropill has good floatability, bioadhesion and sustained release property in the stomach, and has bioadhesion and pulsed sustained release property in the intestinal tract.

Description

technical field [0001] The invention belongs to the field of pharmaceutical preparations, and in particular relates to a floating bioadhesive porous hydrogel and a preparation method thereof. Background technique [0002] The gastric floating drug delivery system refers to a preparation that can maintain its own density less than that of the gastric content after oral administration, and is in a floating state in the gastric juice. Gastric floating sustained-release preparations have great advantages in improving drug efficacy and reducing drug toxicity, and have become one of the hotspots in pharmaceutical research. According to different floating mechanisms, gastric floating preparations can be divided into effervescent floating preparations and non-effervescent floating preparations. Non-effervescent floating preparations float in the gastric juice because their own density is smaller than that of the contents. Effervescent flotation preparations usually contain an effe...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A61K9/06A61K47/36A61K45/00A61P29/00A61P9/12A61P1/04
Inventor 朱澄云李美琴王中彦韩国华冀艳艳孙国祥徐峰王艳娇王岩阚启明
Owner SHENYANG PHARMA UNIVERSITY
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