Patent Grant
11166916
This application claims priority of Taiwanese Patent Application No. 108145453, filed on Dec. 12, 2019.
The present disclosure relates to a carbon quantum dot and a method of preparing the same. The present disclosure also relates to use of this carbon quantum dot to treat a bacterial infection and to inhibit bacterial growth and biofilm formation.
Bacterial pathogens, or disease-producing microorganisms, can infect a host by one of several mechanisms and cause significant morbidity and mortality. They may enter through a break in the skin, they may be introduced by vector transmission, or they may interact with a mucosal surface. Disease ensues following infection of the host, when the potential of the pathogen to disrupt normal bodily functions is fully expressed. Common bacterial pathogens include Staphylococcus aureus (such as methicillin-resistant Staphylococcus aureus (MRSA)), Escherichia coli, Pseudomonas aeruginosa, and Salmonella enteritidis.
Biofilms are medically and industrially important because they can accumulate on a wide variety of substrates and are resistant to antimicrobial agents and detergents. Microbial biofilms develop when microorganisms adhere to a surface and produce extracellular polymers that facilitate adhesion and provide a structural matrix. Therefore, inhibiting adhesion to surfaces is important. These surfaces may be inert, non-living materials or living tissues. Recently, medical devices or materials (such as urinary catheters, vascular grafts, and contact lenses) have been widely used. However, improper cleaning and storage of such devices or materials may cause biofilm formation, which can lead to bacterial infections (such as endocarditis, osteomyelitis, sinusitis, urethral infections, chronic prostatitis, and keratitis).
Carbon quantum dots (CQDs), which serve as a new type of carbon material, not only has good stability and biocompatibility, but also has abundant surface functional groups and a special structure of graphene carbon group. CQDs have been widely used in light chemicals, biological imaging, biomedical engineering, and other fields because of the superior photoluminescence properties.
It has been reported that CQDs prepared from biogenic polyamines (PAs) (such as putrescine, spermidine, and spermine) have been used as an antibacterial agent for topical treatment of bacterial infection. For instance, Jian H. J. et al. disclose a one-step method to synthesize carbon quantum dots from biogenic polyamines. Briefly, CQDs from polyamines (CQDPAs) were prepared by directly pyrolyzing putrescine, spermidine, or spermine at 210° C., 240° C., 270° C., or 300° C. for 3 hours in the solid state. The thus obtained CQDPAs were then dispersed in deionized (DI) water and sonicated for 30 minutes. Larger particles were removed by centrifugation with a relative centrifugal force (RCF) of 20000 g for 60 minutes. The CQDPAs in the supernatant were collected and purified through dialysis. The experimental results reveal that the yields of the CQDPAs product obtained from spermine (CQDSpms) or putrescine (CQDPuts) are relatively low compared to those of CQDs from spermidine (CQDSpds) synthesized at 210-270° C. Furthermore, relative to free spermidine, CQDSpds exhibit much higher antibacterial activity not only against non-multidrug-resistant bacteria but also against multidrug-resistant bacteria (MRSA) due to their strong disintegration effect on the bacterial membrane. Topical ocular administration of CQDSpds can induce the opening of the tight junction of corneal epithelial cells, thereby leading to great antibacterial treatment of Staphylococcus aureus-induced bacterial keratitis in rabbits. The experimental results indicate that CQDSpds are a promising antibacterial candidate for clinical applications in treating eye-related bacterial infections and even persistent bacteria induced infections. (Jian H. J. et al. (2017), ACS Nano, 11:6703-6716).
In spite of the aforesaid, there is still a need to develop a new carbon quantum dot that can more satisfactorily inhibit bacterial growth and biofilm formation.
Accordingly, in a first aspect, the present disclosure provides a carbon quantum dot produced by the step of:
subjecting dopamine and spermine to a pyrolysis treatment at 250° C.
In a second aspect, the present disclosure provides a composition including a carbon quantum dot as described above.
In a third aspect, the present disclosure provides a method for treating a bacterial infection, which includes administering to a subject in need thereof a carbon quantum dot as described above.
In a fourth aspect, the present disclosure provides a method for inhibiting bacterial growth and biofilm formation, which includes applying a carbon quantum dot as described above onto an object.
In a fifth aspect, the present disclosure provides a process for producing a carbon quantum dot, which includes the step of:
subjecting dopamine and spermine to a pyrolysis treatment at 250° C.
The above and other objects, features and advantages of the present disclosure will become apparent with reference to the following detailed description and the exemplary embodiments taken in conjunction with the accompanying drawings, in which:
It is to be understood that, if any prior art publication is referred to herein, such reference does not constitute an admission that the publication forms a part of the common general knowledge in the art, in Taiwan or any other country.
For the purpose of this specification, it will be clearly understood that the word “comprising” means “including but not limited to”, and that the word “comprises” has a corresponding meaning.
Unless defined otherwise, all technical and scientific terms used herein have the meaning commonly understood by a person skilled in the art to which the present disclosure belongs. One skilled in the art will recognize many methods and materials similar or equivalent to those described herein, which could be used in the practice of the present disclosure. Indeed, the present disclosure is in no way limited to the methods and materials described.
The present disclosure provides a carbon quantum dot produced by the step of:
subjecting dopamine and spermine to a pyrolysis treatment at 250° C.
According to the present disclosure, a ratio of dopamine to spermine ranges from 1:0.25 (w/w) to 1:4 (w/w). In an exemplary embodiment, the ratio of dopamine to spermine is 1:0.42 (w/w). In another exemplary embodiment, the ratio of dopamine to spermine is 1:2.33 (w/w). In yet another exemplary embodiment, the ratio of dopamine to spermine is 1:1 (w/w).
According to the present disclosure, the carbon quantum dot may have a particle size ranging from 3 to 10 nm. In an exemplary embodiment, the carbon quantum dot has a particle size of 4 nm.
According to the present disclosure, the carbon quantum dot may have a zeta potential ranging from +5 to +50 mV. In an exemplary embodiment, the carbon quantum dot has a zeta potential of +33 mV.
According to the present disclosure, the carbon quantum dot may have a covalent bond selected from the group consisting of C—C, C—O, C—N, C═C, C═O, C═N, and combinations thereof.
It should be appreciated that the operating conditions of the pyrolysis treatment may vary, depending on the peripheral instruments and equipment used, the proportion of the amounts of dopamine and spermine used, etc. The actual operating conditions necessary for the pyrolysis treatment are well known in the art, and can be determined without undue experimentation.
According to the present disclosure, the pyrolysis treatment may be conducted at 250° C. for 2 to 4 hours. In an exemplary embodiment, the pyrolysis treatment is conducted at 250° C. for 2 hours.
The present disclosure also provides a method for treating a bacterial infection, which includes administering to a subject in need thereof a carbon quantum dot as described above.
As used herein, the term “treat” or “treatment” means lessening, inducing stasis of, or postponing or reducing the progression, development, onset, or severity of the disease or condition or severity of one or more symptoms associated with a disease or disorder or condition described herein, or ameliorating existing uncontrolled or unwanted symptoms, preventing additional symptoms, or relieving or alleviating the intensity and/or duration of a manifestation of a disorder experienced by a subject. The term “treat” also includes prophylactically preventing, curing, healing, altering, remedying, ameliorating, improving, or affecting a condition (e.g., a disease), the symptoms of the condition, or the predisposition toward the condition.
As used herein, the term “bacterial infection” refers to the undesired proliferation or presence of invasion of pathogenic microbes in a host organism. This includes the excessive growth of microbes that are normally present in or on the body of a mammal or other organism. More generally, a bacterial infection can be any situation in which the presence of a bacterial population(s) is damaging to a host mammal. Thus, a bacterial infection exists when excessive numbers of a bacterial population are present in or on a mammal's body, or when the effects of the presence of a bacterial population(s) are damaging the cells or other tissue of a mammal.
According to the present disclosure, the bacterial infection may be selected from the group consisting of keratitis, conjunctivitis, endocarditis, osteomyelitis, sinusitis, urinary tract infection, chronic prostatitis, meningitis, and combinations thereof. In an exemplary embodiment, the bacterial infection is keratitis.
According to the present disclosure, the carbon quantum dot may be prepared in the form of a pharmaceutical composition. The pharmaceutical composition may be formulated into a suitable dosage form for parenteral or topical administration using technology well known to those skilled in the art.
The pharmaceutical composition according to the present disclosure may be administered via one of the following parenteral routes: intraperitoneal injection, intrapleural injection, intramuscular injection, intravenous injection, intraarterial injection, intraarticular injection, intrasynovial injection, intrathecal injection, intracranial injection, intraepidermal injection, subcutaneous injection, intradermal injection, intralesional injection, and sublingual administration. In certain embodiments, the pharmaceutical composition is formulated into a suitable dosage form for intravenous injection. In other embodiments, the pharmaceutical composition is formulated into a suitable dosage form for subcutaneous injection.
The pharmaceutical composition according to the present disclosure may be formulated into an external preparation suitable for topical application to the skin using technology well known to those skilled in the art. The external preparation includes, but is not limited to, emulsions, gels, ointments, creams, patches, liniments, powder, aerosols, sprays, lotions, serums, pastes, foams, drops, suspensions, salves, and bandages.
The dosage and frequency of administration of the pharmaceutical composition according to the present disclosure may vary depending on the following factors: the severity of the disease to be alleviated, the route of administration, and the age, physical condition and response of the subject to be treated.
The present disclosure also provides a method for inhibiting bacterial growth and biofilm formation, which includes applying a carbon quantum dot as described above onto an object.
As used herein, the term “biofilm formation” refers to the attachment of microorganisms to surfaces and the subsequent development of multiple layers of cells.
As used herein, the term “inhibition” or “inhibiting” refers to a decrease of biofilm associated microorganism formation and/or growth. The microorganisms may include gram-positive or gram-negative bacteria, yeasts, and fungi.
According to the present disclosure, the object may be a medical device, a medical instrument, a dressing, a bandage, a food preparation surface, a food packaging surface, a manufacturing surface, a consumer good, a water treatment system, a water delivery system, or a ventilation system.
In certain embodiments, the object may be selected from the group consisting of a denture, a mouth guard, a dairy line, a water line, an adhesive bandage, a component of an HVAC system, a component of a water treatment facility, a component of a vacuum or a vacuum cleaner, a vacuum cleaner bag, a vacuum cleaner filter, an air filter, a component of a cooling tower, a toy, a window, a door, a window frame, a doorframe, a medical instrument, a dental instrument, a bathroom tile, a kitchen tile, food industry processing instruments, hospital tables and beds, an animal water dish, a washing machine, a dishwasher, a towel, a dish, a bowl, a utensil, a cup, a glass, a cutting board, a dish drying tray, a whirlpool bathtub, a sink, a toilet, a toilet seat, a swimming pool, a birdbath, a planter, a garden hose, a fish pond, an oil pipe, a gas pipe, a dairy line filter, a line used in food and beverage manufacturing, a cosmetic container, an outdoor pond liner, a tap and water spout, a humidifier, a humidifier filter, a bathroom tile, a bathroom fixture, a toilet lid, a swimming pool liner, a swimming pool skimmer, a swimming pool filter, a hot tub line, a hot tub filter, a washing machine liner, a dishwasher liner, an animal water dish, a food storage container, a beverage storage container, a plate, a cup, a fork, a knife, a spoon, a garbage bag, and a counter top.
According to the present disclosure, biofilm formation may be caused by a microbe selected from the group consisting of Staphylococcus aureus (such as mexillin-resistant Staphylococcus aureus (MRSA)), Escherichia coli, Pseudomonas aeruginosa, Salmonella enteritidis, and combinations thereof.
The disclosure will be further described by way of the following examples. However, it should be understood that the following examples are solely intended for the purpose of illustration and should not be construed as limiting the disclosure in practice.
General Experimental Materials:
Escherichia coli
Staphylococcus aureus
Pseudomonas aeruginosa
Salmonella enteritidis
Staphylococcus aureus
The experimental data are expressed as mean±standard error of the mean (SEM), and were analyzed via Student's t-test so as to assess the difference between all the groups. Statistical significance is indicated by p<0.05.
A. Pyrolysis of dopamine at different temperatures 0.04 g of dopamine was evenly mixed with 0.5 mL of deionized water, and the resultant mixture was heated at a designated temperature (230° C., 250° C., or 270° C.) for 2 hours. The solid residue thus obtained was allowed to cool to room temperature, followed by adding 5 mL of deionized water. Subsequently, centrifugation at 20,000 g was performed for 60 minutes, and the resultant supernatant was collected, followed by conducting dialysis using a dialysis membrane with a molecular weight cut-off value of 1 kDa and deionized water for 10 hours, so as to obtain a dialysate. The dialysate was diluted 10-fold by deionized water, followed by obtaining a UV-visible absorption spectrum and a fluorescence spectrum using a monochromatic microplate spectrophotometer (Synergy 4 Multi-Mode, Biotek Instruments, Winooski, Vt., USA).
Moreover, only the dialysate obtained at a pyrolysis temperature of 250° C. had a fluorescent light emission intensity measured at a wavelength of 460 nm (see
B. Pyrolysis of Dopamine with Various Polyamines at 250° C.
Samples 1-6 were prepared using the recipe shown in Table 2 and according to the method described in section A of this example, except that only the pyrolysis temperature of 250° C. was applied.
Subsequently, the resultant dialysate of each sample was collected and then subjected to UV-visible absorption spectroscopy and fluorescence spectroscopy as described in section A of this example.
Referring to
This result indicated that pyrolysis of spermidine or dopamine alone or pyrolysis of dopamine with various polyamines (e.g., spermine, spermidine, and putrescine) at 250° C. can successfully generate carbon quantum dots. The carbon quantum dots of samples 1 and 3-6 are represented by CQDDA, CQDSPD/CQDDA-SPM, CQDDA-SPD, and CQDDA-PUT, respectively.
C. Morphological Analysis
Morphological analysis of CQDDA-SPM obtained in section B of this example was performed using a Tecnai G2 S-Twin transmission electron microscope (Philips/FEI, Hillsboro, Oreg., USA). The experimental results show that CQDDA-SPM had a particle size of about 4 nm and a lattice fringe of about 0.23 nm.
D. Fourier Transform Infrared Spectroscopy (FTIR)
A suitable amount of a respective one of CQDDA, CQDSPD, and CQDDA-SPM obtained in section B of this example and spermidine was freeze-dried, and the respective resultant freeze-dried powder was mixed with potassium bromide in a ratio of 1:99 (wt/wt), followed by compressing into a tablet. Each tablet was subjected to FTIR analysis using an Agilent Cary 640 FT-IR spectrometer (Santa Clara, Calif., USA).
Referring to
E. X-Ray Photoelectron Spectroscopy (XPS)
The atomic ratio (N/C) of nitrogen and carbon at an outermost surface of CQDSPD and CQDDA-SPM obtained in section B of this example was measured using an ESCALAB 250 spectrometer (VG Scientific, East Grinstead, UK). The operating conditions applied are described as follows. The X-ray excitation source was Al Kα X-ray, and peaks of Cis and N1s were measured.
Referring to
Referring to
These results indicate that the chemical bonding and bonding structure on the surface of CQDDA-SPM are different from those of CQDSPD.
F. Zeta Potential Analysis
A suitable amount of a respective one of CQDDA, CQDDA-SPM, CQDDA-SPD, and CQDDA-PUT obtained in section B of this example was dissolved in a 5 mM phosphate buffer (pH 7.4). The respective resultant mixture was subjected to zeta potential analysis using a Zetasizer Nano instrument (Nano ZS, Malvern Instruments, Worcestershire, UK).
Referring to
A. Preparation of Tested Bacterial Strains
A respective one of Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, Salmonella enteritidis, and MRSA was inoculated into a LB broth, followed by incubation in a thermostatic shaking incubator (37° C.) until an OD600 value of 1.0 was reached. The respective resultant culture was centrifuged at 3,000 g for 10 minutes, and the cell pellet thus obtained was washed with a 5 mM phosphate buffer (pH 7.4), followed by suspending with a LB broth. The resultant bacterial broths of Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, Salmonella enteritidis, and MRSA (each of such five bacterial suspensions contained a bacterial concentration of 1×104 CFU/mL) were used for the following experiment.
B. Preparation of CQDDA-SPM-1 and CQDDA-SPM-2
CQDDA-SPM-1 and CQDDA-SPM-2 were prepared generally according to the procedures described in the abovementioned section B of Example 1, except that: for CQDDA-SPM-1, the ratio of dopamine to spermine is 1:2.33 (w/w), and for CQDDA-SPM-2, the ratio of dopamine to spermine is 1:0.42 (w/w).
C. Preparation of DA Solutions and SPM Solutions
A suitable amount of a respective one of dopamine and spermine was dissolved in deionized water, so as to obtain DA solutions having different concentrations (0.05-5000 μg/mL), and SPM solutions having different concentrations (0.05-5000 μg/mL).
D. Preparation of CQD Solutions
A suitable amount of a respective one of CQDDA, CQDSPD, CQDDA-SPM, CQDDA-SPD, CQDDA-PUT, CQDDA-SPM-1, and CQDDA-SPM-2 was freeze-dried, and the respective resultant freeze-dried powder was dissolved in deionized water, followed by dilution with a 5 mM phosphate buffer (pH 7.4), so as to obtain seven CQD solutions having different concentrations (0.05-50 μg/mL).
E. Evaluation of Antimicrobial Effect of CQDDA-SPM
A respective one of the five CQD solutions (i.e., CQDDA, CQDSPD, CQDDA-SPM, CQDDA-SPD, and CQDDA-PUT solutions), the DA solutions, and the SPM solutions and a respective one of the bacterial broths of Staphylococcus aureus and Escherichia coli were mixed in a 5 mM phosphate buffer (pH 7.4), and the respective resultant mixture was incubated in a thermostatic shaking incubator (37° C.) for 1 hour, followed by addition of a suitable amount of LB broth. After incubation with shaking for 18 hours, the respective resultant culture was subjected to serial dilution with a LB broth, so as to obtain seven dilutions (101 to 107).
Thereafter, 1 μL of the respective dilution was subjected to spread plate procedure. The number of surviving bacteria was counted, and the minimum inhibitory concentration to inhibit the growth of 90% of a bacterial isolate (MIC90) was determined according to the technique well known to and routinely used by one skilled in the art.
As shown in Table 3 below, for Staphylococcus aureus and Escherichia coli, the MIC90 values of CQDDA-SPM were significantly lower than those of the other four CQDs, DA, and SPM, indicating that the CQDDA-SPM of the present disclosure is effective in inhibiting the growth of bacteria.
Staphylococcus
aureus
Escherichia coli
F. Evaluation of Antimicrobial Effect of CQDDA-SPM, CQDDA-SPM-1, and CQDDA-SPM-2
A respective one of the four CQD solutions (i.e., CQDDA, CQDDA-SPM, CQDDA-SPM-1, and CQDDA-SPM-2 solutions) and the SPM solutions and a respective one of bacterial broths of Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, Salmonella enteritidis, and MRSA were mixed in a 5 mM phosphate buffer (pH 7.4), and the respective resultant mixture was subjected to antimicrobial activity analysis according to the method described in section E of this example.
As shown in Table 4 below, for the five bacterial pathogens, the MIC90 values of CQDDA-SPM, CQDDA-SPM-1, and CQDDA-SPM-2 were significantly lower than those of CQDDA and SPM, indicating that the CQDDA-SPM, CQDDA-SPM-1, and CQDDA-SPM-2 of the present disclosure are effective in inhibiting the growth of bacteria.
Staphylococcus
Escherichia
Pseudomonas
Salmonella
aureus
coli
aeruginosa
enteritidis
Materials:
A. Preparation of CQDDA-SPM Solutions
A suitable amount of CQDDA-SPM was dissolved in deionized water, so as to obtain two CQDDA-SPM solutions respectively having 100 and 200 μg/mL of CQDDA-SPM.
Methods:
Contact lenses (Alcon, DAILIES DAILIES® AquaComfort Plus®) were divided into 3 groups, including two experimental groups (i.e., experimental groups 1 and 2) and one control group (n==2 for each group). The contact lenses of the experimental group 1 and the experimental group 2 were respectively immersed in 100 μg/mL CQDDA-SPM solution and 200 μg/mL CQDDA-SPM solution, and the contact lenses of the control group were not treated with CQDDA-SPM. The contact lenses of each group were respectively added to the bacterial broth of Staphylococcus aureus prepared in section A of Example 2 (the concentration of the bacterial broth was adjusted to 1×108 CFU/mL). All the groups were cultivated in an incubator (37° C.) for 48 hours.
Thereafter, the contact lenses of each group were taken out, and biofilm formation was visually observed. Subsequently, 2 mL of phosphate-buffered saline (PBS) was added to a respective one of the contact lenses of each group, followed by shaking for 9 minutes. Subsequently, the resultant liquid portion was collected and was diluted 10-fold by PBS. 100 μL of the respective resultant dilution was obtained, and was coated onto a LB agar plate using spread plate technique, followed by cultivation in an incubator (37° C.) for 18 hours. The number of colonies on the LB agar plates of each group was counted, and the total bacterial count of each group was further calculated based on the dilution ratio. The bacterial viability percentage (%) was calculated using the following Equation (I):
A=(B/C)×100 (I)
Referring to
This result indicates that the CQDDA-SPM of the present disclosure is effective in inhibiting growth of biofilm associated bacteria and killing biofilm associated bacteria, and hence can be used as an anti-biofilm agent for inhibiting bacterial growth and biofilm formation on an object (such as a medical device, a bandage, a food preparation surface, a consumer good, a water delivery system, etc.).
A. Test Animals
New Zealand white rabbits (16-20 weeks old, a body weight of 3-3.5 Kg) were purchased from National Laboratory Animal Breeding and Research Center (Taipei, Taiwan, ROC). The rabbits were kept in an animal room with an independent air conditioning system under the following laboratory conditions: a 12 hour light/12 hour dark cycle, a temperature of 20-24° C., and a relative humidity of 55-65%. Furthermore, water and feed were provided ad libitum for all the experimental animals. All animal testing procedures were approved by the National Institutes of Health and were carried out in accordance with the ARVO Statement for the Use of Animals in Ophthalmic and Vision Research.
B. Preparation of CQDDA-SPM-Treated Contact Lenses
Contact lenses (Alcon, DAILIES DAILIES® AquaComfort Plus®) were immersed in 200 μg/mL CQDDA-SPM solution prepared in section A of Example 3 for 1 hour, and the thus obtained CQDDA-SPM-treated contact lenses were used for the following experiment.
C. Induction of Bacterial Keratitis
The New Zealand white rabbits were divided into a control group and an experimental group (n==6 for each group). The cornea of each rabbit in the experimental group and the control group was cut to form a wound having an area of about 3 mm×3 mm using sterile surgical scissors and a blade. Thereafter, 50 μL of the bacterial broth of Staphylococcus aureus prepared in section A of Example 2 (the concentration of the bacterial broth was adjusted to 1×108 CFU/mL) was topically instilled into the ocular surface of the respective rabbit, so as to induce bacterial keratitis.
D. Application of CQDDA-SPM-Treated Contact Lenses
The upper and lower eyelids of each rabbit were passively kept closed for 2 minutes, and thereafter, for the experimental group, the CQDDA-SPM-treated contact lens obtained in the above section B was placed on the eye of each rabbit. For the control group, an untreated contact lens was placed on the eye of each rabbit. After a 4-hour rest, the contact lens was removed from the eye of each rabbit. On Day 0.5, Day 1, and Day 3 after the treatment, the eye of each rabbit was subjected to analyses set forth in sections E and F below. Furthermore, Day 14 after the treatment, all the rabbits were sacrificed by virtue of 95% CO2, and the corneal tissue of the respective rabbit was obtained using a sterile surgical blade, and was subjected to analyses set forth in sections E and F below.
E. Morphological Observation
The change in anterior segment morphometry of each rabbit was analyzed using a method slightly modified from that described by Jian H. J. et al. (2017), ACS Nano, 11:6703-6716. Briefly, the anterior segment morphology (i.e., corneal and lens clarity, the degree of anterior chamber activity, and status of iris) of the rabbit eye was observed by slit-lamp biomicroscopy (Topcon Optical, Tokyo, Japan), and seven parameters, including conjuncitivitis, chemosis, iritis, fibrin accumulation, hypopyon, stromal infiltration, and stromal edema, were assessed visually by scoring on a scale from 0 to 4 (the higher the scale, the more serious the ocular symptom was).
Referring to
F. Determination of Central Corneal Thickness
The central corneal thickness of each rabbit was determined using an ultrasonic pachymeter equipped with a hand-held solid probe (DGH Technology, Exton, Pa., USA).
Referring to
G. Histopathologic Analysis
0.02 g of the corneal tissue of each group was fixed with a 4% paraformaldehyde solution (in PBS) at room temperature for 2 hours, and the fixed tissue sample was then embedded with paraffin, followed by slicing to obtain a tissue section having a thickness of 5 μm. The tissue section was stained using a hematoxylin and eosin (H&E) staining protocol well-known to those skilled in the art, and was observed under an optical microscope (Carl Zeiss, Oberkochen, Germany) at 200× magnification.
Referring to
H. Determination of Viable Bacteria Count
0.2 g of the corneal tissue of the respective group was added to 2 mL of PBS, and the thus obtained mixture was homogenized using a homogenizer, and was then diluted 20-fold by PBS. 0.1 mL of the respective dilution was coated onto a mannitol salt agar (MSA) plate (containing 10 g/L mannitol, 75 g/L NaCl, 10 g/L peptone, 1 g/L beef extract, and 15 g/L agar) using spread plate technique, followed by cultivation in an incubator (37° C.) for 24 hours. The number of colonies on the MSA plate of each group was counted, and the total bacterial count of each group was further calculated based on the dilution ratio.
Referring to
Summarizing the above test results, it is clear that the CQDDA-SPM of the present disclosure is effective in treating a bacterial infection and inhibiting bacterial growth and biofilm formation.
All patents and references cited in this specification are incorporated herein in their entirety as reference. Where there is conflict, the descriptions in this case, including the definitions, shall prevail.
While the disclosure has been described in connection with what are considered the exemplary embodiments, it is understood that this disclosure is not limited to the disclosed embodiments but is intended to cover various arrangements included within the spirit and scope of the broadest interpretation so as to encompass all such modifications and equivalent arrangements.
| Number | Date | Country | Kind |
|---|---|---|---|
| 108145453 | Dec 2019 | TW | national |
| Entry |
|---|
| Harroun et al. ACS Infectious Disease 2017 3:777-779 (Year: 2017). |
| Jian et al. ACS Nano 2017 11:6703-6716 (Year: 2017). |
| Xiao et al. Nanomaterials 2018 8:854, 1-13 (Year: 2018). |
| Lan et al. Journal of Materials Chemistry B 2017 5:5265-5271 (Year: 2017). |
| Number | Date | Country | |
|---|---|---|---|
| 20210177763 A1 | Jun 2021 | US |
