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Ophthalmic medicine-carried amnion and preparation method thereof

An amniotic membrane and drug-loaded technology, which is applied in the field of medical application or transplanted biomaterials, can solve the problem of long-term sustained release of drugs, unstable exogenous growth factor content, and inability to withstand surgical sutures. Pulling and other problems, to achieve the effect of wound healing, good tissue compatibility, no toxic side effects

Inactive Publication Date: 2011-08-31
CHONGQING MEDICAL UNIVERSITY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, there are many studies on: 1. Preparation of drugs into nano-medicines to improve the penetration of drugs on the ocular surface and the residence time of drugs on the ocular surface, but there is still the problem of frequent drops of drugs in nano-ophthalmics; The drug storage system is to put the drug on a certain carrier, and achieve the purpose of treatment through the release of the drug, but the general carrier cannot bear the pulling of the surgical suture because it is not a bioactive film, and is not easy to fix on the ocular surface
In the prior art, there is a Chinese invention patent application titled "drug amniotic membrane and its preparation method" published on September 26, 2007 (CN101040616A). The drug amniotic membrane contains exogenous cell growth factors, and its preparation method It is prepared by immersing the amniotic membrane in a preservation solution containing exogenous cell growth factors, and then cryopreserved or freeze-dried at a low temperature; it can make the amniotic membrane biologically active after long-term storage, and can also be used to extract the amniotic membrane from the preservation solution. The exogenous cell growth factor absorbed in the medium is slowly released to the wound surface, which is beneficial to wound healing. It is said that it can be used for the repair of ophthalmic wounds; The content of growth factors is unstable, and the amount is not easy to control, and the repeatability is poor. Therefore, it is difficult for the prepared drug amniotic membrane to have a long-term sustained-release effect of the drug

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0016] Example 1 Preparation of Gatifloxacin-loaded Chitosan Nanoparticles Adhesively Linked Amniotic Membrane

[0017] 1. Preparation of chitosan nanoparticle suspension loaded with gatifloxacin

[0018] Weigh 0.2g chitosan, dissolve it in 200ml concentration of 1.5mg / ml glacial acetic acid solution and stir evenly, add 0.2g sodium polyphosphate to the chitosan acetic acid solution to make the concentration 1.0mg / ml, stir Evenly, the stirring speed is 700-800r / min, and the reaction time is half an hour, then add 300mg of gatifloxacin raw material drug, and stir evenly, that is, the chitosan nanometer loaded with gatifloxacin with a particle size of 100-300nm particle suspension;

[0019] 2. Preparation of dry powder of chitosan nanoparticles loaded with gatifloxacin

[0020] The gatifloxacin chitosan nanoparticle suspension prepared in step 1 was centrifuged (5000r / min, 30min, 4°C,) to remove the supernatant, and the remaining part was frozen overnight in a -20°C refrigerat...

experiment example 1

[0024] [Experimental example 1] In vitro bacteriostatic experiment of amniotic membrane gelled with chitosan nanoparticles loaded with gatifloxacin

[0025] Method: A modified agar diffusion method was used. According to the method of Example 1, the gelled amniotic membrane (diameter 3 mm, height 0.5 mm) loaded with chitosan nanoparticles at a concentration of 3 mg / ml gatifloxacin was prepared under sterile conditions. In addition, the amniotic membrane (diameter 3 mm, height 0.5 mm) prepared with a concentration of 3 mg / ml gatifloxacin-fibrin glue was used as a control group. The tested strains were Streptococcus pneumoniae (clinical strains), Staphylococcus aureus and standard strains of Pseudomonas aeruginosa. The test strains were inoculated on the agar plate, and the inoculation amount was 10 5 cfu / ml; Place the prepared amniotic membrane loaded with chitosan nanoparticles gelled with gatifloxacin and the amniotic membrane loaded with ordinary gatifloxacin-fibrin glue...

experiment example 2

[0027] [Experimental Example 2] Determination of drug concentration in rabbit aqueous humor after transplantation of gatifloxacin-loaded chitosan nanoparticles gel-linked amniotic membrane

[0028]Method: According to the method of Example 1, the gelled amniotic membrane loaded with chitosan nanoparticles at a concentration of 3 mg / ml gatifloxacin was prepared under aseptic conditions. Thirty New Zealand white rabbits were randomly divided into 6 groups with 5 rabbits in each group. The left eye was the control eye, and the right eye was the experimental eye. The experimental eye was sutured and fixed on the corneoscleral limbus with chitosan nanoparticles gel-linked amniotic membrane loaded with gatifloxacin in diameter. The control eye was instilled with gatiza at a concentration of 3 mg / ml. Star eye drops, a total of 4 times an hour. 6h after the operation of the experimental eye and 2h, 1d, 2d, 3d, 4d, and 5d after the last eye drop of the control eye, 0.2ml of aqueous hu...

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Abstract

The invention provides an ophthalmic medicine-carried amnion which comprises fibrin glue, fresh amnion or preserved amnion. The ophthalmic medicine-carried amnion is further characterized by comprising gatifloxacin-carried chitosan nanoparticles. A preparation method of the ophthalmic medicine-carried amnion comprises the steps of: preparing gatifloxacin-carried chitosan nanoparticles suspension liquid, preparing gatifloxacin-carried chitosan nanoparticles dry powder and preparing medicine-carried amnion. The gatifloxacin, the chitosan nanoparticles, the fibrin glue and the amnion can mutually play a role in synergetic beneficiation and multiple slow release, and can prolong the release of the contained medicine, so that the medicine is more durable in local effective concentration after the use of the amnion, and the medicine can not be frequently used; and the invention has the advantages of being low in allergic reaction rate, good in histocompatibility, free of side effects, capable of being absorbed gradually, healing the wound and filling in gaps, good for healing the wound, and capable of withdrawing a medicine slow release carrier without operation and the like.

Description

technical field [0001] The invention belongs to medical application or transplantation biomaterials, in particular to a drug-loaded amniotic membrane used in ophthalmology and a preparation method thereof. Background technique [0002] Ocular surface diseases, including pterygium, keratitis, corneal perforation, ocular surface chemical burns, and ocular surface trauma, are common diseases in ophthalmology, often leading to vision loss in patients. It is of great significance to take active and effective treatment measures for it in the work of preventing and curing blindness. The conventional treatment method is eye drops or eye drops combined with surgical application or transplantation of new membranous materials to repair the ocular surface; currently, the biomaterials used for the ocular surface are mainly amniotic membranes, and simple amniotic membrane application or transplantation can be difficult during the operation. There is a characteristic of being easy to curl...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61L27/54A61L27/36A61L15/44A61L15/40A61K31/496A61K47/36A61P27/02
Inventor 赵敏王岚周文君赵媛吴静牟彦
Owner CHONGQING MEDICAL UNIVERSITY
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