LONG-LASTING HYDROGEL FOR USE AGAINST DRUG-RESISTANT BACTERIA AND PREPARATION METHOD AND USE THEREOF

Abstract

A long-lasting hydrogel for use against drug-resistant bacteria, and a preparation method and use thereof are provided. In the present disclosure, polyvinyl alcohol (PVA) is mainly adopted as a matrix, and phytic acid and honey including glucose and fructose are added to modify the PVA to obtain the hydrogel. During preparation of the antimicrobial hydrogel, no toxic chemical crosslinking agent or initiator is added, and the antimicrobial hydrogel is mainly obtained by crosslinking PVA, phytic acid, and monosaccharides through ester bonds, hydrogen bonds, and electrostatic adsorption. In addition, the hydrogel obtained by adding phytic acid and honey to the PVA matrix exhibits a significant long-lasting antimicrobial effect for Staphylococcus aureus (S aureus), drug-resistant S. aureus, and Pseudomonas aeruginosa (P. aeruginosa), and the antimicrobial effect can last for about 3 months.

Claims

1. A preparation method of a long-lasting hydrogel for use against drug-resistant bacteria, comprising the following steps: 1) Preparation of a hydrogen bond-containing synthetic or semi-synthetic polymer material solution by dissolving a hydrogen bond-containing synthetic or semi-synthetic polymer material in deionized water, and heating and stirring a first mixture solution to obtain the hydrogen bond-containing synthetic or semi-synthetic polymer material solution; 2) Preparation of a mixed solution by mixing the hydrogen bond-containing synthetic or semi-synthetic polymer material solution, a phytic acid solution, and honey in a mass ratio of 5:5:2, stirring a second mixture solution until the second mixture solution is homogeneous and free of impurities and allowing the second mixture solution to stand for bubble removal to obtain a transparent mixed solution; 3) Pre-curing treatment of the transparent mixed solution by pre-curing the transparent mixed solution under heating in an 80° C. water bath until a resulting pre-cured solution is brown and viscous and has a film on a surface of the resulting pre-cured solution, and removing the film to obtain a pre-cured hydrogel solution; and 4) Preparation of an antimicrobial hydrogel by pouring the pre-cured hydrogel solution into a prepared mold, and conducting repetitive operation of freeze-thaw cycles to obtain a cured hydrogel.

2. The preparation method of the long-lasting hydrogel for use against drug-resistant bacteria according to claim 1, further comprising the following step: 5) Demolding the cured hydrogel by taking a fully-cured hydrogel out from the mold after the cured hydrogel is fully cured, and storing the fully-cured hydrogel in a refrigerator.

3. The preparation method of the long-lasting hydrogel for use against drug-resistant bacteria according to claim 1, wherein in step 1), the hydrogen bond-containing synthetic or semi-synthetic polymer material solution has a solid content of 10% to 20%; a dissolution temperature is 60° C.; and the stirring is conducted for 24 h at a rotational speed of 800 rpm/min.

4. The preparation method of the long-lasting hydrogel for use against drug-resistant bacteria according to claim 1, wherein in step 2), the phytic acid solution has a mass percentage concentration of 1% to 5%.

5. The preparation method of the long-lasting hydrogel for use against drug-resistant bacteria according to claim 1, wherein in step 2), the honey has a high monosaccharide content, and specifically, each glucose and fructose content in the honey is greater than 20%.

6. The preparation method of the long-lasting hydrogel for use against drug-resistant bacteria according to claim 1, wherein in step 4), in the freeze-thaw cycles, freezing is conducted at −48° C. for 2 h and thawing is conducted at room temperature for 30 minutes; and three freeze-thaw cycles are adopted.

7. The preparation method of the long-lasting hydrogel for use against drug-resistant bacteria according to claim 1, wherein in step 1), the hydrogen bond-containing synthetic or semi-synthetic polymer material is one or more selected from the group consisting of polyvinyl alcohol (PVA), polyethylene glycol (PEG), and a cellulose derivative.

8. A long-lasting hydrogel for use against drug-resistant bacteria prepared by the preparation method according to claim 1.

9. A method of using the long-lasting hydrogel for use against drug-resistant bacteria according to claim 8, comprising the step of providing the long-lasting hydrogel in a skin wound dressing.

10. The long-lasting hydrogel for use against drug-resistant bacteria according to claim 8, wherein the preparation method of the long-lasting hydrogel for use against drug-resistant bacteria further comprising the following step: 5) Demolding the cured hydrogel by taking a fully-cured hydrogel out from the mold after the cured hydrogel is fully cured and storing the fully-cured hydrogel in a refrigerator.

11. The long-lasting hydrogel for use against drug-resistant bacteria according to claim 8, wherein in step 1), the hydrogen bond-containing synthetic or semi-synthetic polymer material solution has a solid content of 10% to 20%; a dissolution temperature is 60° C.; and the stirring is conducted for 24 h at a rotational speed of 800 rpm/min.

12. The long-lasting hydrogel for use against drug-resistant bacteria according to claim 8, wherein in step 2), the phytic acid solution has a mass percentage concentration of 1% to 5%.

13. The long-lasting hydrogel for use against drug-resistant bacteria according to claim 8, wherein in step 2), the honey has a high monosaccharide content, and specifically, each glucose and fructose content in the honey is greater than 20%.

14. The long-lasting hydrogel for use against drug-resistant bacteria according to claim 8, wherein in step 4), in the freeze-thaw cycles, freezing is conducted at −48° C. for 2 h and thawing is conducted at room temperature for 30 minutes; and three freeze-thaw cycles are adopted.

15. The long-lasting hydrogel for use against drug-resistant bacteria according to claim 8, wherein in step 1), the hydrogen bond-containing synthetic or semi-synthetic polymer material is one or more selected from the group consisting of PVA, PEG, and a cellulose derivative.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0030] FIG. 1 is a schematic diagram illustrating a structure of the antimicrobial hydrogel based on PVA, phytic acid, and honey:

[0031] FIG. 2 shows in vitro antimicrobial effects of the antimicrobial hydrogel for S. aureus, drug-resistant S. aureus, and P. aeruginosa after the antimicrobial hydrogel is placed at a constant temperature of 37° C. for 24 h; and

[0032] FIG. 3 shows in vitro antimicrobial effects of the antimicrobial hydrogel for S. aureus, drug-resistant S. aureus, and P. aeruginosa after the antimicrobial hydrogel is placed at a constant temperature of 37° C. for three months.

DETAILED DESCRIPTION OF THE EMBODIMENTS

[0033] The present disclosure is described in further detail below with reference to the accompanying drawings and specific examples.

Example 1

[0034] 1) Preparation of a PVA solution with a solid content of 10%: 1 g of PVA was added to 9 g of deionized water, a resulting mixture was stirred at 60° C. and 800 rpm/min for 24 h to allow dissolution to obtain a transparent and viscous PVA solution, and the PVA solution was stored for later use. [0035] 2) Preparation of a mixed solution: 5 g of a phytic acid solution with a mass percentage concentration of 1% and 2 g of honey were added to 5 g of the PVA solution with a solid content of 10%, and a resulting solution was thoroughly stirred at 70° C. and 700 rpm/min until there were no impurities, and then allowed to stand for 0.5 h to remove bubbles to obtain a transparent mixed solution. The vacuum bubble removal method was not adopted here because the viscous solution would cause a large number of bubbles to accumulate on a surface; resulting in difficult bubble removal. [0036] 3) Pre-curing treatment of the mixed solution: the mixed solution was pre-cured under heating in an 80° C. water bath for 2 h to obtain a light-brown and viscous pre-cured solution with a film on a surface thereof, and then the film was removed with tweezers to obtain pre-cured hydrogel solution. The film was formed due to the rapid water loss of a surface solution during heating. [0037] 4) Preparation of an antimicrobial hydrogel: the pre-cured hydrogel solution was poured into a prepared mold, and three freeze-thaw cycles were conducted to obtain a cured hydrogel, which was elastic. [0038] 5) Demolding of the cured hydrogel: after the cured hydrogel was fully cured, the fully-cured hydrogel was taken out from the mold and stored in a refrigerator.

Example 2

[0039] 1) Preparation of a PVA solution with a solid content of 15%: 1.5 g of PVA was added to 8.5 g of deionized water, a resulting mixture was stirred at 60° C. for 24 h to allow dissolution to obtain a transparent and viscous PVA solution, and the PVA solution was stored for later use. [0040] 2) Preparation of a mixed solution: 5 g of a phytic acid solution with a mass percentage concentration of 1% and 2 g of a honey solution were added to 5 g of the PVA solution with a solid content of 15%, and a resulting solution was thoroughly stirred at 70° C. and 700 rpm/min, and then allowed to stand for 0.5 h to remove bubbles to obtain a transparent mixed solution. [0041] 3) Pre-curing treatment of the mixed solution: the mixed solution was pre-cured under heating in an 80° C. water bath for 2 h to obtain a light-brown and viscous pre-cured solution with a film on a surface thereof, and then the film was removed with tweezers to obtain pre-cured hydrogel solution. [0042] 4) Preparation of an antimicrobial hydrogel: the pre-cured hydrogel solution was poured into a prepared mold and three freeze-thaw cycles were conducted to obtain a cured hydrogel, which was elastic. [0043] 5) Demolding of the cured hydrogel: after the cured hydrogel was fully cured, the fully-cured hydrogel was taken out from the mold and stored in a refrigerator.

Example 3

[0044] 1) Preparation of a PVA solution with a solid content of 20%: 2 g of PVA was added to 8 g of deionized water and a resulting mixture was stirred at 60° C. for 24 h and then stored for later use. [0045] 2) Preparation of a mixed solution: 5 g of a phytic acid solution with a mass percentage concentration of 1% and 2 g of a honey solution were added to 5 g of the PVA solution with a solid content of 20% and a resulting solution was thoroughly stirred at 70° C. and then allowed to stand for bubble removal to obtain a transparent mixed solution. [0046] 3) Pre-curing treatment of the mixed solution: the mixed solution obtained after the bubble removal was pre-cured under heating in an 80° C. water bath to obtain a light-brown and viscous pre-cured solution with a film on a surface thereof, and then the film was removed with tweezers to obtain a pre-cured hydrogel solution. [0047] 4) Preparation of an antimicrobial hydrogel: the pre-cured hydrogel viscous solution was poured into a prepared mold and then freeze-thaw cycles were conducted for curing to obtain an elastic antimicrobial hydrogel. [0048] 5) Demolding of the cured hydrogel: after the cured hydrogel was fully cured, the fully-cured hydrogel was taken out from the mold and stored in a refrigerator.

[0049] In Examples 1, 2, and 3, a mass concentration of PVA in the antimicrobial hydrogel is changed; because PVA is mainly to serve as a skeleton in the hydrogel, the mass concentration of PVA can be changed to adjust the mechanical properties of the hydrogel. Which can be described specifically as follows: when the concentration of PVA increases from 10% to 20%, the mechanical strength Young's modulus of the antimicrobial hydrogel will increase accordingly. Since an antimicrobial hydrogel is used for human skin, and the excellent elasticity and low mechanical strength of a hydrogel can improve the use comfort, but do not affect the antibacterial activity of the hydrogel, the mass percentage concentration of PVA is preferably 10%.

[0050] Structures of the antimicrobial hydrogels in Examples 1, 2, and 3 are shown in FIG. 1, and a crosslinked structure of the hydrogel includes covalent ester bonds, non-covalent hydrogen bonds, and electrostatic interactions. In vitro antimicrobial effects of the antimicrobial hydrogel for S. aureus, drug-resistant S. aureus, and P. aeruginosa are shown in FIG. 2, and it can be seen that an inhibitory zone diameter (IZD) of the antimicrobial hydrogel is much larger than an IZD of an antibiotic. The blank in FIG. 2 indicates a blank group and the Anti in FIG. 2 indicates an antibiotic group. FIG. 3 shows antimicrobial effects of the hydrogel in FIG. 2 after being placed for 3 months. It can be seen that, after three months, the bacteria have developed resistance to the antibiotic, but the antimicrobial hydrogel still exhibits a prominent antimicrobial effect. Indicating the durability of antimicrobial activity of the antimicrobial hydrogel of the present disclosure.

[0051] IZD data of in vitro antimicrobial activity for an experimental group (mass percentage concentration of phytic acid: 1%), a blank control group, and an antibody group in Example 1 are shown in Table 1, and white filter papers of the control group and the antibody group each have a size of 6 mm.

TABLE-US-00001 TABLE 1 IZD data of in vitro antimicrobial activity for an experimental group (mass percentage concentration of phytic acid: 1%), a blank control group, and an antibody group Experimental Bacterium type group (1%) Control group Antibody group S. aureus 10.74 mm <6 mm 8.4 Drug-resistant 9.5 mm <6 mm <6 mm S. aureus P. aeruginosa 10.6 mm <6 mm 10.3 mm

Example 4

[0052] 1) Preparation of a PVA solution with a solid content of 10%: 1 g of PVA was added to 9 g of deionized water and a resulting mixture was stirred at 60° C. for 24 h and then stored for later use. [0053] 2) Preparation of a mixed solution: 5 g of a phytic acid solution with a mass percentage concentration of 2.5% and 2 g of a honey solution were added to 5 g of the PVA solution with a solid content of 10% and a resulting solution was thoroughly stirred at 70° C. and then allowed to stand for bubble removal to obtain transparent mixed solution. [0054] 3) Pre-curing treatment of the mixed solution: the mixed solution obtained after the bubble removal was pre-cured under heating in an 80° C. water bath to obtain a light-brown and viscous pre-cured solution with a film on a surface thereof, and then the film was removed with tweezers to obtain a pre-cured hydrogel solution. [0055] 4) Preparation of an antimicrobial hydrogel: the pre-cured hydrogel viscous solution was poured into a prepared mold and then freeze-thaw cycles were conducted for curing to obtain an elastic antimicrobial hydrogel. [0056] 5) Demolding of the cured hydrogel: after the cured hydrogel was fully cured, the fully-cured hydrogel was taken out from the mold and stored in a refrigerator.

[0057] IZD data of in vitro antimicrobial activity for an experimental group (mass percentage concentration of phytic acid: 2.5%), a blank control group, and an antibody group in Example 4 are shown in Table 2, and white filter papers of the control group and the antibody group each have a size of 6 mm.

TABLE-US-00002 TABLE 2 IZD data of in vitro antimicrobial activity for an experimental group (mass percentage concentration of phytic acid: 2.5%), a blank control group, and an antibody group Experimental Bacterium type group (2.5%) Control group Antibody group S. aureus 12.9 mm <6 mm 8.4 Drug-resistant 10.7 mm <6 mm <6 mm S. aureus P. aeruginosa 11.5 mm <6 mm 10.3 mm

Example 5

[0058] 1) Preparation of a PVA solution with a solid content of 10%: 1 g of PVA was added to 9 g of deionized water, and a resulting mixture was stirred at 60° C. for 24 h and then stored for later use. [0059] 2) Preparation of a mixed solution: 5 g of a phytic acid solution with a mass percentage concentration of 5% and 2 g of a honey solution were added to 5 g of the PVA solution with a solid content of 10% and a resulting solution was thoroughly stirred at 70° C. and then allowed to stand for bubble removal to obtain a transparent mixed solution. [0060] 3) Pre-curing treatment of the mixed solution: the mixed solution obtained after the bubble removal was pre-cured under heating in an 80° C. water bath to obtain a light-brown and viscous pre-cured solution with a film on a surface thereof, and then the film was removed with tweezers to obtain pre-cured hydrogel solution. [0061] 4) Preparation of an antimicrobial hydrogel: the pre-cured hydrogel viscous solution was poured into a prepared mold and then freeze-thaw cycles were conducted for curing to obtain an elastic antimicrobial hydrogel. [0062] 5) Demolding of the cured hydrogel: after the cured hydrogel was fully cured, the fully-cured hydrogel was taken out from the mold and stored in a refrigerator.

[0063] IZD data of in vitro antimicrobial activity for an experimental group (mass percentage concentration of phytic acid: 5%), a blank control group, and an antibody group in Example 5 are shown in Table 3, and white filter papers of the control group and the antibody group each have a size of 6 mm.

TABLE-US-00003 TABLE 3 IZD data of in vitro antimicrobial activity for an experimental group (mass percentage concentration of phytic acid: 5%), a blank control group, and an antibody group Experimental Bacterium type group (5%) Control group Antibody group S. aureus   15 mm <6 mm 8.4 Drug-resistant 11.5 mm <6 mm <6 mm S. aureus P. aeruginosa 14.5 mm <6 mm 10.3 mm

[0064] In Examples 1, 4, and 5, the phytic acid content in the hydrogel is changed, that is, the mass percentage concentration of phytic acid is increased from 1% to 5%. It can be seen from the in vitro antibacterial data in Tables 1 to 3 that the increase of the phytic acid content can increase the IZD of the antimicrobial hydrogel, and this is because the increased mass concentration of phytic acid increases a content of ester bonds and improves a crosslinking density of the hydrogel, thereby destroying the cell walls of bacteria and effectively inhibiting the activity of bacteria.