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Antibacterial effects of chitosan-based hydrogels containing Trachyspermum ammi essential oil on pathogens isolated from dogs with otitis externa

BMC Veterinary Research volume 20, Article number: 130 (2024) Cite this article

Abstract

Background

Growing antibiotic resistance has made treating otitis externa (OE) increasingly challenging. On the other hand, local antimicrobial treatments, especially those that combine essential oils (EOs) with nanoparticles, tend to be preferred over systemic ones. It was investigated whether Ajwain (Trachyspermum ammi) EO, combined with chitosan nanoparticles modified by cholesterol, could inhibit the growth of bacterial pathogens isolated from OE cases in dogs. In total, 57 dogs with clinical signs of OE were examined and bacteriologically tested. Hydrogels of Chitosan were synthesized by self-assembly and investigated. EO was extracted (Clevenger machine), and its ingredients were checked (GC-MS analysis) and encapsulated in chitosan-cholesterol nanoparticles. Disc-diffusion and broth Micro-dilution (MIC and MBC) examined its antimicrobial and therapeutic properties.

Results

Staphylococcus pseudintermedius (49.3%) was the most common bacteria isolated from OE cases, followed by Pseudomonas aeruginosa (14.7%), Escherichia coli (13.3%), Streptococcus canis (9.3%), Corynebacterium auriscanis (6.7%), Klebsiella pneumoniae (2.7%), Proteus mirabilis (2.7%), and Bacillus cereus (1.3%). The investigation into the antimicrobial properties of Ajwain EO encapsulated in chitosan nanoparticles revealed that it exhibited a more pronounced antimicrobial effect against the pathogens responsible for OE.

Conclusions

Using chitosan nanoparticles encapsulated with EO presents an effective treatment approach for dogs with OE that conventional antimicrobial treatments have not cured. This approach not only enhances antibacterial effects but also reduces the required dosage of antimicrobials, potentially preventing the emergence of antimicrobial resistance.

Peer Review reports

Background

Ajwain, scientifically known as Trachyspermum ammi (T. ammi), belongs to the Apiaceae family and the Apiales order. The well-known T. ammi fruit or dried seeds are regarded as a highly nutrient-dense or therapeutically enhanced component of the plant [1,2,3]. In medieval Persian medicine and pharmaceutical manuscripts, Ajwain is called Zenyan or Nankhah. It has been utilized in Persian medicine for thousands of years. The plant contains several bioactive compounds of pharmacological significance, including saponins, phenolic compounds, carbohydrates, fats, fiber, volatile oil, glycosides, and minerals. In modern medicine, Ajwain has been used for various purposes such as bronchodilation, cardiac stimulation, carminative effects, digestive stimulation, diuretic properties, Galactagogue, hypoglycemic effects, anti-inflammatory properties, analgesic effects, antibiotic activity, and as an ant filarial agent [1]. The essential oil (EO) extracted from the dried seeds of T. ammi contains approximately 50% Thymol, a potent germicide, anti-spasmodic, and fungicide. Thymol is considered a fourth-generation herbal antibiotic as it can effectively kill bacteria resistant to common third-generation antibiotics and multi-drug-resistant microbial pathogens. Ajwain essential oil also contains phenol, benzene methyl, and γ-terpinene, which exhibit antibacterial activity similar to Thymol [4].

Numerous studies have extensively investigated the antimicrobial properties of EOs and their constituents. However, EOs are volatile and delicate compounds prone to enzymatic reactions and susceptible to degradation when exposed to oxygen, light, moisture, and heat. These factors can compromise their biological properties, leading to decreased activity and increased toxicity, which limits their traditional use [5, 6]. To overcome the limitations and challenges associated with EOs, researchers have explored the encapsulation of EOs within drug delivery systems. This approach allows for the controlled release of the active compounds, enhancing the bioavailability and efficacy of the EOs and achieving an optimal pharmacokinetic profile [5, 7].

Chitosan (CS) and its derivatives have found remarkable applications in the biomedical field, particularly in the controlled release of active substances. CS is commonly modified to form a hydrogel (HG) for this purpose [8, 9]. Nano-gels, on the other hand, are HGs that possess nanoscale dimensions. A HG is a cross-linked polymer chain network forming a macromolecular structure [10]. These cross-linked polymeric networks, known as HG, can mimic soft tissues and create a moist environment. CS, a linear polysaccharide, demonstrates pH-responsive self-assembling properties. It is preferred for constructing HGs due to its inherent intermolecular and intramolecular hydrogen bonding capabilities and its versatile reactive amino groups [11].

Canine Otitis Externa (OE) is a common skin disease affecting dogs, accounting for approximately 20% of small-animal counseling cases [12,13,14]. This condition is multifactorial, and it manifests with various clinical signs, including head shaking, ear scratching, ceruminous or purulent discharge, self-inflicted skin lesions, malodor, swelling, and pain [15]. Staphylococcus spp. is the most frequently isolated bacterial species from the ear canals of dogs with OE. However, other bacteria, such as Streptococcus spp., Pseudomonas spp., Corynebacterium spp., Escherichia coli, and other Enterobacteriaceae, can also be involved [16, 17]. Diagnosis of OE typically involves palpation of the ear canal, visual inspection, and Otoscope examination. Cytology and bacterial culture are commonly used diagnostic tools. In cases of colonization by opportunistic bacteria, veterinarians may face therapeutic challenges [16, 18].

Topical antimicrobial therapy is the preferred treatment approach for OE, as systemic medications are less effective. However, conventional drugs often encounter bacterial resistance. Hence, EOs are being explored as alternative therapies, and further studies are needed to determine their efficacy against the bacteria that cause OE [15, 17]. In this study, Nano-gels were produced by creating amid linkages between the amino groups in CS and the carboxyl group of Cholesterol (CHOL). The study aimed to investigate the potential effects of T. ammi EO encapsulated in CS-CHOL Nano-gels as a green carrier against bacterial pathogens isolated from cases of OE. The current study seeks to provide a solution to the pressing demand for therapeutic alternatives in treating infections caused by antibiotic-resistant bacteria.

Results

Direct cytology results

Based on the results of cytological analysis of swabs obtained from dogs suffering from OE, the frequency of gram-positive cocci, gram-negative rods, gram-positive rods, and gram-positive cocci/rods were 58.66%, 33.33%, 1.33%, and 6.66%, respectively.

Bacterial culture results

A total of 75 bacterial species were isolated from dogs with OE, indicating their involvement in causing the condition. Among these, Staphylococcus pseudintermedius was the most frequently observed bacterium, with a frequency of 37 (49.3%). Following S. pseudintermedius, the next most commonly identified bacteria were Pseudomonas aeruginosa (11 (14.7%)), Escherichia coli (10 (13.3%)), Streptococcus canis (7 (9.3%)), Corynebacterium auriscanis (5 (6.7%)), Klebsiella pneumoniae (2 (2.7%)), Proteus Mirabilis (2 (2.7%)), and Bacillus cereus (1 (1.3%)). The isolated bacterial species were identified based on several criteria, including Gram morphology, culture morphology, and specific biochemical tests associated with each species. The identification process followed the guidelines and references provided by Markey et al. and Quinn, widely recognized references in bacterial identification [19, 20].

Antibiotic susceptibility results

No antibiotic can provide 100% effectiveness against all isolated bacteria. However, the isolated bacteria in this study demonstrated satisfactory susceptibility to certain antibiotics. Specifically, they showed sensitivity to Amikacin, Gentamicin, Cephalothin, and Ceftriaxone. S. pseudintermedius exhibited high sensitivity to Amikacin, Cephalothin, and Gentamicin while showing notable resistance to Penicillin G, Ampicillin, and Oxytetracycline. In general, Penicillin G, Erythromycin, and Ampicillin demonstrated the highest levels of antibiotic resistance among the bacteria examined (Table 1). The quality control strains used in the study yielded results following the guidelines set by the CLSI, indicating that the test conditions were appropriate and reliable [21].

Table 1 Antimicrobial resistance percentage of isolated bacteria from dogs with OE
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GC/MS analysis results

Using gas chromatography/mass spectrometry (GC/MS) analysis, the study identified 11 compounds present in T. ammi EO, which was extracted in the present study (Table 2). Among these compounds, Thymol was present in a notably high percentage, accounting for 48% of the EO composition.

Table 2 Chemical analysis of EO of T. ammi by GC/MS
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SEM & successful encapsulating of EO in CS-CHOL nano-gel

SEM analysis revealed that the produced Nano-gels exhibited a diameter of less than 100 nm, indicating their nanoscale size. Furthermore, the Nano-gels displayed a uniform and spherical morphology (Fig. 1). The encapsulation efficiency of the EO was determined to be 67.23%, indicating a substantial accumulation of the EO within the Nano-gels.

Fig. 1
figure 1

Scanning electron microscopy (SEM) image of CS-CHOL Nano-gel

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Antibacterial Effect of free and encapsulated EO based on disk diffusion method

The findings indicate that the antibacterial effects of T. ammi EO encapsulated in CS-CHOL Nano-gel are more pronounced than those of the free form of T. ammi EO (Fig. 2). Negative control discs containing CS-CHOL Nano-gel alone did not affect the six bacterial strains tested. The most significant inhibitory effect of T. ammi EO was observed against S. pseudintermedius. On the other hand, the lowest inhibitory effect of T. ammi EO encapsulated in CS-CHOL Nano-gel was observed against P. aeruginosa (Fig. 2). The results were considered significant when the p-value was less than 0.05 for the T. ammi EO and T. ammi EO encapsulated in CS-CHOL Nano-gel groups.

Fig. 2
figure 2

The diagram of the inhibition zone diameter of the selected microbial strains against the disc containing T. ammi EO encapsulated in CS-CHOL Nano-gel (a) and a disc containing T. ammi EO (b). P, P-value; Staph, S. pseudintermedius; Strep, S. canis, Cor, C. auriscanis; Pseudo, P. aeruginosa; Pro, P. Mirabilis

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MIC and MBC findings

The results of MIC tests showed a more significant inhibitory effect of T. ammi EO encapsulated in CS-CHOL Nano-gel compared to CS-CHOL Nano-gel without T. ammi EO (P < 0.05) (Fig. 3-a) and T. ammi EO (P < 0.05) (Table 3). In both repetitions of the experiment, the results were the same. By comparing the MIC of T. ammi EO and CS-CHOL Nano-gel with T. ammi EO, with S. pseudintermedius, S. canis, C. auriscanis, E. coli, and P. Mirabilis, the P-value was less than 0.05, and significant results were reported. Comparison MBC of T. ammi EO and T. ammi EO encapsulated in CS-CHOL Nano-gel for S. pseudintermedius, S. canis, and E. coli bacteria reported significant results (Table 3).

Fig. 3
figure 3

The MIC of T. ammi EO encapsulated in CS-CHOL Nano-gel (Name of bacteria-Nano CCL) and CS-CHOL Nano-gel without T. ammi EO (Name of bacteria-CCL) on the selected bacteria (a). The MBC of T. ammi EO encapsulated in CS-CHOL Nano-gel (Name of bacteria-Nano CCL) and CS-CHOL Nano-gel without T. ammi EO (Name of bacteria-CCL) on the selected bacteria (b)

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T. ammi EO encapsulated in CS-CHOL Nano-gel had an excellent inhibitory effect on S. pseudintermedius, S. canis, P. aeruginosa, and P. Mirabilis, so the mean MIC for these bacteria was 112.5 ppm. The mean MIC for C. auriscanis and E. coli was 137.5 ppm, which indicates that higher amounts of T. ammi EO encapsulated in CS-CHOL Nano-gel are needed. Among the tested bacterial samples, S. pseudintermedius and S. canis were the most sensitive to T. ammi EO encapsulated in CS-CHOL Nano-gel (Table 3), and their mean MIC was 68.75 ppm. CS-CHOL Nano-gel with T. ammi EO shows a satisfactory bactericidal effect (MBC) for S. pseudintermedius and S. canis (Fig. 3-b). In general, there is little difference between MIC and MBC values.

Table 3 Statistical analysis and comparison of MIC and MBC of T. ammi EO and T. ammi EO encapsulated in CS-CHOL Nano-gel with each selected bacteria separately by T-test
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Discussion

Various studies have employed different cross-linking methods to synthesize Nano-gels to microencapsulate EOs. These methods include self-assembly, ionic cross-linking, cross-linking polymerization, crystallization, radiation cross-linking, and functional group cross-linking. Each method offers unique advantages and can be tailored to meet specific requirements regarding the desired properties and applications of the Nano-gels [22]. The present study utilized self-assembly to create Nano-gels composed of CS polymer modified with cholesterol. These Nano-gels possess unique characteristics such as high biocompatibility, low toxicity, and biodegradability, making them suitable for producing nanometer-sized carriers for microencapsulating EOs [8]. CS is a polymer derived from acetyl glucosamine and is obtained by partially deacetylating chitin through alkaline treatment [23]. CS has limited surface activity due to the absence of hydrophobic segments. However, the surface activity of CS can be enhanced through chemical modifications [24].

The hydrophilic nature of chitosan (CS) is a crucial characteristic that allows for creation of self-assembled nanoparticles by incorporating hydrophobic components into CS. This property makes CS well-suited for applications in drug delivery. The hydrophobic cavities within CS can serve as storage compartments for various bioactive materials. The drug’s therapeutic efficiency can be improved by binding targeted components to the drug-loaded nanoparticles’ surface [8, 25]. In synthesis, non-polar cholesterol is bound to the CS polymer using EDC (Cross-linker). When this complex is placed in a polar environment, the non-polar heads of cholesterol accumulate inside the complex. In contrast, the polar heads are oriented towards the outside, forming a spherical complex structure. This connection has been confirmed through electron microscopy [26].

The present study confirmed the shape and size of the Nano-gels through SEM imaging, which revealed well-separated spherical nanoparticles without any aggregation. This lack of aggregation can be attributed to the positive charges on the CS, which prevent the Nano-gels from sticking together. Previous research by Kosaraju et al. (2006) has reported that interactions between polyphenols and matrix polymers can result in smooth surface particles. Therefore, intermolecular or intramolecular interactions may contribute to the relatively smooth surface of the nanoparticles [27].

The antimicrobial properties of T. ammi EO have been demonstrated in various studies [28]. The present study analysis of the EO revealed that the main components were Thymol (48%) and p-Cymene (23%). These compounds contribute significantly to the antimicrobial activity of T. ammi EO, which is consistent with findings from other research studies. In 2023, Mishra et al. identified Thymol as the primary component of T. ammi EO through GC-MS analysis [29]. Researchers have also investigated the antibacterial mechanism of Thymol. It has been found that Thymol increases the permeability of the bacterial cell membrane. It can disrupt the outer membrane of bacteria, leading to the release of lipopolysaccharide (LPS) and increased cytoplasmic permeability to ATP [30, 31].

In the current study, the loading capacity of T. ammi EO in the Nano-gel was determined to be 67.23%, indicating successful storage of the EO in the Nano-gel. The structure of the Nano-gel was also found to protect the EO and control its release effectively. The durability of EO-containing nanoparticles can be attributed to the slow and stable release of active components within the nanoparticles [32]. Previous research by Yang et al. in 2009 demonstrated that nanoparticles containing garlic EO remained stable for up to five months [33]. Recent studies have highlighted the substantial potential of nanoparticles functionalized with EOs for antimicrobial activity against multidrug-resistant pathogens. This antimicrobial activity is attributed to the improved stability and solubility of EOs and the reduced evaporation and degradation of active EO components [6]. In 2022, Zarenejad et al. combined T. ammi EO with CS nanoparticles and compared it with free EO, showing better efficiency of the EOs combined with nanoparticles [34].

The free and encapsulated T. ammi EO demonstrated excellent inhibitory activity against S. pseudintermedius and S. canis. The growth-inhibiting activity of the encapsulated T. ammi EO was more pronounced than that of the free EO against P. Mirabilis and C. auriscanis. Statistical analysis of the MIC and MBC results in the present study indicated that the encapsulated T. ammi EO exhibited a strong antibacterial effect against Gram-positive bacteria, such as S. pseudintermedius and S. canis, as well as Gram-negative E. coli. Furthermore, no significant difference was observed in the MIC and MBC results between the CS-CHOL Nano-gel without T. ammi EO, and T. ammi EO encapsulated in CS-CHOL Nano-gel in P. Mirabilis species. Similar findings were reported by Zarenejad et al. in 2022, where no substantial difference in effectiveness was observed in Pseudomonas spp. when evaluating the efficacy of EOs. The reduced antibacterial effect of T. ammi EO against Gram-negative bacteria can be attributed to the unique cell walls of these bacteria, which provide them with greater resistance to the antimicrobial activity of the EO [34].

Several studies conducted on OE have reported findings similar to the current research regarding the isolation of infectious agents and their antibiotic resistance patterns. In 2023, Abani et al. isolated Staphylococcus spp., Streptococcus spp., Pseudomonas spp., and Enterobacteriaceae spp. from cases of OE in dogs, and these isolates showed evident antibiotic resistance, similar to the findings of the present study [17]. Similarly, in 2016, De Martino et al. updated the microbiological causes of Otitis in dogs in the Campania region of Italy. They identified Staphylococcus spp., Pseudomonas spp., E. coli, and Proteus spp. as important pathogens causing ear infections in dogs. In this study, the isolated bacterial strains demonstrated a significant level of resistance to at least four classes of antimicrobial drugs that were utilized [35]. Bugden conducted a study in 2012 on bacteria isolated from the ears of 3,541 dogs with Otitis in Australia. The most commonly isolated bacteria were Pseudomonas spp. (35.5%), Staphylococcus spp. (24.3%), Proteus spp. (6.8%), streptococci spp. (6.2%), and E. coli (4.2%). Most isolates showed sensitivity to Gentamicin but were highly resistant to Polymyxin B treatment. Streptococci spp. also exhibited increased resistance to all antibiotics used in the study [36]. In the present study, among the total of 75 isolated bacteria, S. pseudintermedius accounted for 49.3%, P. aeruginosa for 14.7%, E. coli for 13.3%, S. canis for 9.3%, and C. auriscanis for 7% of the total isolates. These findings are consistent with the prevalence of these bacterial species in cases of OE [17, 35, 36].

In order to mitigate the adverse effects and potentially reverse antimicrobial resistance, one effective treatment strategy is to reduce the usage of antimicrobials. Additionally, the development of drug combinations has emerged as a novel approach to controlling resistant pathogens. Combining antimicrobials with EOs against resistant bacteria can broaden the antimicrobial spectrum, thereby reducing the emergence of resistant variants and minimizing the reliance on a single antimicrobial agent [37, 38]. For instance, in a study conducted by Rosato et al. in 2007, the use of Pelargonium graveolens EO was found to reduce the minimum effective dose of Norfloxacin against B. cereus, B. subtilis, E. coli, and Staphylococcus spp., demonstrating an apparent synergistic effect [39]. Other studies have reported that EOs such as Eremanthus erythropappus and Origanum vulgare can enhance the action of beta-lactam antibiotics against both Gram-positive and Gram-negative bacteria that produce beta-lactamase enzymes [37].

Conclusion

There is an undeniable and urgent need for alternative treatment options for infections caused by antibiotic-resistant bacteria. Addressing this issue requires proactive initiatives and efforts from the scientific and medical communities. Developing novel therapies, exploring alternative antimicrobial agents, promoting antimicrobial stewardship programs, and implementing infection prevention and control measures are some of the key strategies that can help combat the challenge of antibiotic resistance. It is crucial to prioritize research and funding in this area to ensure the availability of effective treatment options for patients affected by antibiotic-resistant infections. The present study’s findings support the effectiveness of T. ammi EO in HGs against the pathogens responsible for OE. The superior antibacterial effects observed with EO encapsulated in HGs, compared to free EOs and CS-CHOL Nano-gel, indicate the potential of such HGs in combination with other commonly used antimicrobials for treating OE. This approach offers a way to reintroduce EOs and antimicrobials that may have been abandoned due to widespread resistance. Combining these agents in HGs can enhance the antibacterial effects, and the required dosage of antimicrobials may be reduced, potentially preventing the emergence of antimicrobial resistance.

Methods

Materials

Polysaccharide Chitosan (Sigma, USA) with low molecular weight and about 8% degree of deacetylation was purchased; Brain heart infusion (BHI), mannitol salt agar (MSA) and Mc-Conkey (Merck, Germany); Mueller-Hinton agar (MHA) (Oxoid, UK); API-Coryne system (BioMerieux, France); 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC), Cholesterol, Acetic acid, Dimethyl sulfoxide (DMSO), blank paper discs were obtained from Padtan-Teb Company, Iran; Commercial antibiotic disks (Oxoid Ltd, UK); and fruit of T. ammi plant was purchased from Pakan Seed Company (Isfahan, Iran) with herbarium stock number, 293-0303-1.

Animals

Investigations were conducted into fifty-seven dogs with OE referred to the Veterinary Hospital of Small Animals. The most important signs in the history of affected animals included itching of the ear, abnormal secretions, and malodorous ears. In clinical examination, symptoms such as redness of the auricle and external ear canal, pain in palpation of the ear, abnormal secretion, and malodorous ear were observed. OE was confirmed in all cases by otoscope and cytological examination. Animals with any history of other diseases or antibiotic therapy within the last two months were excluded from this study. If several cases from the same housing were referred with OE, sampling was conducted from only one.

Sampling & bacteriological process

Samples were collected from dogs that exhibited signs of OE, including ear itching, abnormal secretions, and odor. The sampling procedure involved using sterile swabs to collect samples from the end of the vertical part of the external ear. Three sterile swabs were taken to prevent contamination before conducting an otoscope examination. Each swab was used for different analyses, including cytological and bacterial cultures. A third swab was replaced if any swabs became contaminated or damaged during the procedure. Care was taken to ensure that the swab made minimal contact with the outer portion of the ear canal and the surrounding hairs when entering and exiting during the sampling process. The swab was rotated 360° inside the ear canal for approximately five seconds. Following sample collection, the swabs were rolled onto cytological slides and fixed with heat. Gram staining was performed on the slides and was subsequently evaluated microscopically. The swabs were sent to a laboratory within two hours for further analysis.

The process related to bacteriology, including aerobic cultivation in blood agar (Columbia agar with 5% sheep blood), BHI, MSA, and MacConkey. The cultures were incubated at 37 °C for 24 to 48 h. Bacterial species were identified by Gram morphological and biochemical characteristics (TSI, Urease test, IMViC, Motility test, Lecithinase Test, oxidase, Catalase, Nitrate reduction, and Coagulase.), as described by Murray et al. and Markey et al. [20, 40]. . Corynebacterium spp. was identified by the API-Coryne system according to the manufacturer’s instructions.

Preparation of T. ammi EO

The fruit of the T. ammi plant was purchased, and after confirming the purity of the seed, the EO was extracted from the milled powder of the fruit by steam distillation using a Clevenger machine. EO was dehydrated with sodium sulfate. It was kept in a dark glass container with a closed lid, away from light, and at a cool temperature [41].

GC/MS analysis of EO

The EO compounds were identified using GC/MS. The system consisted of an Agilent 6890 gas chromatograph with an Agilent 5973 mass-selective detector (Agilent, USA). Since the compounds in EOs are known as volatile substances in terms of molecular weight and polarity, the process of separating and identifying the components of EO was carried out by gas chromatography combined with mass spectrometry.

Synthesis of chitosan nano-gel

The Nano-gel was prepared using a self-assembly method involving CS and cholesterol (CHOL) with the assistance of an EDC cross-linker [42, 43]. To prepare a 0.5% CS solution, 1 gr of CS was added to 200 µl of a 1% acetic acid solution (v/v). The mixture was then placed on a magnetic stirrer and stirred at a speed of 500 rpm for 20 min. The resulting solution, which had a semi-transparent appearance and a fragile yellow color, was subjected to homogenization using an ultrasonic sonicator (Elmasonic, E30H, Germany) for 20 min. The sonicator was operated at a power of 70 watts. After the homogenization process, a stock solution with a concentration of 5000 ppm was obtained.

To incorporate CHOL into the CS solution, 215 mg of CHOL was initially dissolved in 10 µl of ethanol. Subsequently, 178 µl of EDC was added to the CHOL solution, and the mixture was kept in darkness for a short period. To the formation of amid linkages between the carboxyl groups of CHOL (C26H45COOH) and the amino groups of CS (a [1,2,3,4]-2-amino-2-deoxy B-D-glucan), the CHOL-EDC mixture was added dropwise, slowly, to a solution containing 75 µl of CS while stirring on a magnetic stirrer. To ensure a complete formation of amid linkages between CS and CHOL, The resulting mixture was left to stir on a magnetic stirrer for 24 h to allow for adequate linkage formation. Next, the pH of the mixture was adjusted to a range of 8.5-9 by adding sodium hydroxide while continuing to mix on a magnetic stirrer. As the pH gradually increased, gel formation was observed. To separate the formed Nano-gel particles, the mixture was centrifuged for 5 min at a speed of 9000 rpm. This centrifugation step aimed to separate the Nano-gel particles from the rest of the solution. Following the centrifugation step, the supernatant solution was carefully separated from the white Nano-gel deposits that had formed on the wall of the centrifuge tube. The centrifugation process was repeated twice using ethanol to eliminate impurities that did not participate in the reaction, including EDC, CS, and CHOL. After each centrifugation, the supernatant solution was discarded.

The resulting Nano-gel particles were dispersed in a 1% acetic acid solution. The dispersion was filtered using a filter with a pore size of 0.2 mm to obtain a uniform particle size. This filtration step helped to remove any larger particles or aggregates from the Nano-gel suspension. Subsequently, the filtered Nano-gel particles were dried thoroughly using a vacuum dryer. The dried Nano-gel was then stored in a dark glass container at a cool temperature.

SEM was employed to investigate the morphology and size of the CS-CHOL Nano-gel. The SEM analysis was conducted at an accelerating voltage of 70 kV to obtain detailed information about the structure and size distribution of the Nano-gel particles.

Encapsulation of T. ammi EO in CS-CHOL nano-gel

A total of 0.5 µl of T. ammi EO was dissolved in 1 µl of DMSO, then 0.5 µl of the solution was diluted with deionized water to reach a final volume of 10 µl. This solution was named Solution Number 1. CS-CHOL Nano-gel (1 mg) was added to 1 µl of Solution Number 1 and kept for 24 h at room temperature. It was centrifuged for 15 min at 12,000 rpm and 20 °C to separate the particles. In the end, two separate phases were created; the supernatant was discarded, and the sediment containing CS-CHOL Nano-gel encapsulated with T. ammi EO was used for microbial tests. The optical absorbance of the supernatant was taken by UV-Vis spectrophotometry using а Varioskan Flash Multimode Reader (Thermo Scientific, Waltham, MA) at a wavelength of 280 nm to calculate the Loading efficiency of the EO according to the formula [1].

$$Loading\;Efficiency \% =\left[\frac{OD r-OD s }{OD r}\right]\times 100$$
(1)

Chosen isolates of bacteria

Six bacterial strains that exhibited higher abundance in dogs affected by OE were selected for the next steps: S. pseudintermedius, S. canis, P. aeruginosa, E. coli, C. auriscanis, and P. Mirabilis. These strains were preserved in glycerol broth and stored at -80 °C. The selected strains were utilized to examine the impact of free EO and encapsulated EO.

Antimicrobial susceptibility tests

In order to assess the antibacterial activity, 30 µl of T. ammi EO and T. ammi EO in CS-CHOL Nano-gel (100 µg ml− 1) were separately inoculated onto blank paper discs. These discs serve as a means to release antibacterial substances into the culture medium containing the targeted bacteria. Subsequently, MHA plates were prepared under standard conditions and inoculated with microbial strains isolated from cases of OE using surface culture plating. The paper discs were then placed onto the agar plates and incubated at 37 °C for 18–24 h. After incubation, the antibacterial susceptibility was evaluated by measuring the diameter of the inhibition zones around the discs. The negative control was a blank disc coated with unencapsulated CS-CHOL Nano-gel (Fig. 4).

Fig. 4
figure 4

Determination of the antimicrobial sensitivity of the EO by the disc diffusion method on Pseudomonas. K: CS-CHOL Nano-gel as a negative control disk; Z: free T. ammi EO; Z + N: T. ammi EO in CS-CHOL Nano-gel

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The antimicrobial susceptibility patterns of the isolated bacterial strains were determined using the disk diffusion test on MHA. The test was performed following the recommendations of the Clinical Laboratory Standards Institute (CLSI) as described in the 33rd Edition of the M100 guidelines (2023) [21]. Commercial antibiotic disks (Oxoid Ltd, UK) containing the following drugs and concentrations were used: Amikacin (Ak30; 30 µg), Ampicillin (Amp2; 2 µg), Ceftriaxone (Cro30; 30 µg), Cephalothin (Kf30; 30 µg), Gentamicin (Cn10; 30 µg), Enrofloxacin (Enr5; 5 µg), Erythromycin (E15; 15 µg), Oxytetracycline (Ot30; 30 µg), Rifampicin (Rd5; 5 µg), and Penicillin G (P5; 5 units). The selection of drugs was based on the strains and their clinical use.

After incubation for 24 h at 37 °C, the diameters of the inhibitory zones around the antibiotic disks were measured and evaluated according to CLSI guidelines. The strains were classified as sensitive or resistant to the drug, with intermediate susceptibility considered resistant. Only the percentage of resistance is reported in the results. Strains obtained from the American Type Culture Collection (ATCC), such as E. coli 25,922, S. aureus 25,923, S. pneumoniae 49,619, and P. aeruginosa 27,853, were used for quality control.

Determination of MIC and MBC values

The MIC of encapsulated T. ammi EO in CS-CHOL Nano-gel against the bacteria isolated from cases of OE in dogs was determined using the in vitro broth microdilution method. The experimental protocol used in the present study was based on the methods described by Sharifi and Nayeri Fasaei [41] and Firmino et al. [44]. The MIC was determined in 96-well polystyrene plates. For this test, 100 µg of T. ammi EO in CS-CHOL Nano-gel solution under aseptic conditions was serially diluted in a BHI to attain final concentrations of 25 to 0.19 µg ml− 1. Next, 100 µl of bacterial culture previously set at a concentration of ∼ 5 × 105 CFU ml− 1 was added.

Each bacterial isolate was subjected to individual testing in a separate experiment, and each experiment was repeated twice. Two wells were utilized in each microplate for the positive and negative controls. The positive control consisted of 100 µl of BHI broth and 100 µl of microbial suspension. Conversely, the negative control contained 100 µl of BHI broth and 100 µl T. ammi EO in CS-CHOL Nano-gel. The microplates were then incubated aerobically at 37 °C for 24 h. After incubation, the wells were visually examined, and the optical absorbance was measured using an ELISA reader. The MIC was determined to be the lowest concentration of T. ammi EO in CS-CHOL Nano-gel, at which no visible growth was detected in the wells. To assess the effects of the CS-CHOL Nano-gel without T. ammi EO, the MIC was determined individually for each bacterium.

The MIC of the EO alone was also determined to compare the effects of T. ammi EO alone with the effects of the EO encapsulated in CS-CHOL Nano-gel. To enhance the solubility of T. ammi EO, it was diluted 1:10 with a 1.5% DMSO solution. DMSO is widely recognized as non-toxic when used at concentrations below 10% (v/v) [45]. To determine the MBC, 50 µl of each well that exhibited no visible growth in the MIC test were cultured on a blood agar medium and incubated at 37 °C for 24 h. The MBC was defined as the lowest concentration at which the original bacterial growth was reduced by a minimum of 99.9% [44, 46].

Statistical analysis

The collected data was analyzed using SPSS 25.0 software (SPSS Inc., Chicago, IL). A comparison between T. ammi EO, CS-CHOL Nano-gel encapsulated with T. ammi EO, and CS-CHOL Nano-gel without T. ammi EO was conducted using an independent t-test with four repetitions.

Data availability

All relevant data is contained within the manuscript. The data generated and analyzed during the current study are available from the corresponding author on request.

Abbreviations

T. ammi :

Trachyspermum ammi

EO :

Essential Oil

HG:

Hydrogel

CS:

Chitosan

OE:

Otitis Externa [inflammation of the external ear canal

DMSO:

Dimethyl sulfoxide

CHOL:

Cholesterol

EDC:

Ethylcarbodiimide hydrochloride

SEM:

Scanning Electron Microscopy

GC/MS:

Gas Chromatography-Mass Spectrometry

References

  1. Goyal S, Chaturvedi V, Dhingra G, Tanwar S, Sharma K, Singh S. Trachyspermum ammi: a review on traditional and modern pharmacological aspects. Biol Sci. 2022;2(4):324–37.

    Google Scholar 

  2. Kedia A, Dubey NK. Essential oil of Trachyspermum ammi (L.) Sprague ex Turrill-Phytochemistry and therapeutics. Bioactives and Pharmacology of Medicinal plants. Apple Academic; 2023. pp. 83–95.

  3. Gupta BD, Kar A, Narayan S, Thakur CP, Mukherjee PK, Haldar PK. Ultra-performance liquid chromatography‐quadrupole time‐of‐flight tandem mass spectrometry‐based metabolite profiling, quality evaluation, and marker analysis of Trachyspermum ammi (L.) Sprague by high‐performance thin‐layer chromatography. J Sep Sci. 2023;46(10):2200872.

    Article  CAS  Google Scholar 

  4. Nouri Gharajalar S. Antibacterial activity of Ajwain essential oil against some zoonotic bacteria. J Zoonotic Dis. 2021;5(2):26–33.

    Google Scholar 

  5. Cimino C, Maurel OM, Musumeci T, Bonaccorso A, Drago F, Souto EMB, et al. Essential oils: Pharmaceutical applications and encapsulation strategies into lipid-based delivery systems. Pharmaceutics. 2021;13(3):327.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Chouhan S, Sharma K, Guleria S. Antimicrobial activity of some essential oils—present status and future perspectives. Medicines. 2017;4(3):58.

    Article  PubMed  PubMed Central  Google Scholar 

  7. Zare MR, Khorram M, Barzegar S, Asadian F, Zareshahrabadi Z, Saharkhiz MJ, et al. Antimicrobial core–shell electrospun nanofibers containing Ajwain essential oil for accelerating infected wound healing. Int J Pharm. 2021;603:120698.

    Article  CAS  PubMed  Google Scholar 

  8. Muñana-González S, Veloso-Fernández A, Ruiz-Rubio L, Pérez-Álvarez L, Vilas-Vilela JL. Covalent cross-linking as a strategy to prepare Water-Dispersible Chitosan Nanogels. Polymers. 2023;15(2):434.

    Article  PubMed  PubMed Central  Google Scholar 

  9. Gonçalves MM, Maluf DF, Pontarolo R, Saul CK, Almouazen E, Chevalier Y. Negatively charged chitosan nanoparticles prepared by ionotropic gelation for encapsulation of positively charged proteins. Int J Pharm. 2023:123164.

  10. Gallo E, Diaferia C, Rosa E, Smaldone G, Morelli G, Accardo A. Peptide-based hydrogels and nanogels for delivery of doxorubicin. Int J Nanomed. 2021:1617–30.

  11. Wang Z, Yang L, Fang W. Chitosan-based hydrogels. Chitin Chitosan: Prop Appl. 2019:97–144.

  12. Kwon J, Yang M-H, Ko H-J, Kim S-G, Park C, Park S-C. Antimicrobial resistance and virulence factors of Proteus mirabilis isolated from dog with chronic otitis externa. Pathogens. 2022;11(10):1215.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Korbelik J, Singh A, Rousseau J, Weese JS. Characterization of the otic bacterial microbiota in dogs with otitis externa compared to healthy individuals. Vet Dermatol. 2019;30(3):228–e70.

    Article  PubMed  Google Scholar 

  14. Tambella AM, Attili AR, Beribè F, Galosi M, Marchegiani A, Cerquetella M, et al. Management of otitis externa with an led-illuminated gel: a randomized controlled clinical trial in dogs. BMC Vet Res. 2020;16(1):1–14.

    Article  Google Scholar 

  15. Vercelli C, Pasquetti M, Giovannetti G, Visioni S, Re G, Giorgi M, et al. In vitro and in vivo evaluation of a new phytotherapic blend to treat acute externa otitis in dogs. J Vet Pharmacol Ther. 2021;44(6):910–8.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Leonard C, Thiry D, Taminiau B, Daube G, Fontaine J. External ear canal evaluation in Dogs with Chronic Suppurative Otitis Externa: comparison of Direct Cytology, Bacterial Culture and 16S Amplicon Profiling. Veterinary Sci. 2022;9(7):366.

    Article  Google Scholar 

  17. Ebani VV, Pieracci Y, Cagnoli G, Bertelloni F, Munafò C, Nardoni S, et al. In Vitro Antimicrobial activity of Thymus vulgaris, Origanum vulgare, Satureja montana and their mixture against clinical isolates responsible for Canine Otitis Externa. Veterinary Sci. 2023;10(1):30.

    Article  Google Scholar 

  18. Bajwa J. Canine otitis externa—treatment and complications. Can Veterinary J. 2019;60(1):97.

    Google Scholar 

  19. Quinn PJ. Clinical Veterinary Microbiology: United Kingdom: Wolfe; 1994.

  20. Markey B, Leonard F, Archambault M, Cullinane A, Maguire D. Clinical Veterinary Microbiology E-Book: Elsevier Health Sciences; 2013.

  21. Wayne P. CLSI. M100. Performance standards for antimicrobial susceptibility testing. 33rd Edition. Clinical and Laboratory Standards Institute2023.

  22. Beyki M, Zhaveh S, Khalili ST, Rahmani-Cherati T, Abollahi A, Bayat M, et al. Encapsulation of Mentha Piperita essential oils in chitosan–cinnamic acid nanogel with enhanced antimicrobial activity against aspergillus flavus. Ind Crops Prod. 2014;54:310–9.

    Article  CAS  Google Scholar 

  23. Şenel S, McClure SJ. Potential applications of chitosan in veterinary medicine. Adv Drug Deliv Rev. 2004;56(10):1467–80.

    Article  PubMed  Google Scholar 

  24. Elsabee MZ, Morsi RE, Al-Sabagh A. Surface active properties of chitosan and its derivatives. Colloids Surf B. 2009;74(1):1–16.

    Article  CAS  Google Scholar 

  25. Jaber N, Aiedeh K. Sorption behavior and release kinetics of iron (II) ions by oleoyl chitosan polymeric nanoparticles. J Drug Deliv Sci Technol. 2019;54:101354.

    Article  CAS  Google Scholar 

  26. Tavasoli B, Khanmohammadi S, Yahyaei M, Barshan-tashnizi M, Mehrnejad F. Insight into molecular mechanism of human insulin encapsulation into the polyacrylic acid/deoxycholic acid-modified chitosan nanogel: an experimental and molecular dynamics investigation. J Mol Liq. 2023;369:120850.

    Article  CAS  Google Scholar 

  27. Kosaraju SL, D’ath L, Lawrence A. Preparation and characterisation of chitosan microspheres for antioxidant delivery. Carbohydr Polym. 2006;64(2):163–7.

    Article  CAS  Google Scholar 

  28. Bairwa R, Sodha R, Rajawat B. Trachyspermum ammi. Pharmacogn Rev. 2012;6(11):56.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  29. Mishra PK, Kakatkar AS, Gautam RK, Kumar V, Debbarma A, Chatterjee S. Effect of Ajwain (Trachyspermum ammi) extract and gamma irradiation on the shelf-life extension of rohu (Labeo rohita) and seer (Scomberomorus guttatus) fish steaks during chilled storage. Food Res Int. 2023;163:112149.

    Article  CAS  PubMed  Google Scholar 

  30. Tian L, Wang X, Liu R, Zhang D, Wang X, Sun R, et al. Antibacterial mechanism of Thymol against Enterobacter sakazakii. Food Control. 2021;123:107716.

    Article  CAS  Google Scholar 

  31. Yuru W, Tianyu L, Chao L, Yuanyuan T, Yuan L, Xingyu P, et al. Antibacterial effect of Thymol against fish-derived drug-resistant Aeromonas veronii in vitro and its mechanism. Acta Agriculturae Zhejiangensis. 2022;34(7):1412.

    Google Scholar 

  32. Ziaee M, Moharramipour S, Mohsenifar A. Toxicity of C arum copticum essential oil-loaded nanogel against S itophilus granarius and T ribolium confusum. J Appl Entomol. 2014;138(10):763–71.

    Article  CAS  Google Scholar 

  33. Yang F-L, Li X-G, Zhu F, Lei C-L. Structural characterization of nanoparticles loaded with garlic essential oil and their insecticidal activity against Tribolium castaneum (Herbst) (Coleoptera: Tenebrionidae). J Agric Food Chem. 2009;57(21):10156–62.

    Article  CAS  PubMed  Google Scholar 

  34. Zarenezhad E, Ranjbar N, Firooziyan S, Ghoorkhanian M, Osanloo M. Promising larvicidal effects of chitosan nanoparticles containing laurus nobilis and trachyspermum ammi essential oils against Anopheles Stephensi. Int J Trop Insect Sci. 2022;42(1):895–904.

    Article  Google Scholar 

  35. De Martino L, Nocera FP, Mallardo K, Nizza S, Masturzo E, Fiorito F, et al. An update on microbiological causes of canine otitis externa in Campania Region, Italy. Asian Pac J Trop Biomed. 2016;6(5):384–9.

    Article  Google Scholar 

  36. Bugden D. Identification and antibiotic susceptibility of bacterial isolates from dogs with otitis externa in a ustralia. Aust Vet J. 2013;91(1–2):43–6.

    Article  CAS  PubMed  Google Scholar 

  37. Yap PSX, Lim SHE, Hu CP, Yiap BC. Combination of essential oils and antibiotics reduce antibiotic resistance in plasmid-conferred multidrug resistant bacteria. Phytomedicine. 2013;20(8–9):710–3.

    Article  CAS  PubMed  Google Scholar 

  38. Valcourt C, Saulnier P, Umerska A, Zanelli M, Montagu A, Rossines E, Joly-Guillou M-L. Synergistic interactions between doxycycline and terpenic components of essential oils encapsulated within lipid nanocapsules against gram negative bacteria. Int J Pharm. 2016;498(1–2):23–31.

    Article  CAS  PubMed  Google Scholar 

  39. Rosato A, Vitali C, De Laurentis N, Armenise D, Milillo MA. Antibacterial effect of some essential oils administered alone or in combination with Norfloxacin. Phytomedicine. 2007;14(11):727–32.

    Article  CAS  PubMed  Google Scholar 

  40. Murray PR, Baron EJ, Jorgensen JH, Landry ML, Pfaller MA. Manual of clinical microbiology: volume. Volume 2. ASM; 2006.

  41. Sharifi A, Nayeri Fasaei B. Selected plant essential oils inhibit biofilm formation and luxs-and pfs‐mediated quorum sensing by Escherichia coli O157: H7. Lett Appl Microbiol. 2022;74(6):916–23.

    Article  CAS  PubMed  Google Scholar 

  42. Wang Y-S, Liu L-R, Jiang Q, Zhang Q-Q. Self-aggregated nanoparticles of cholesterol-modified chitosan conjugate as a novel carrier of epirubicin. Eur Polymer J. 2007;43(1):43–51.

    Article  Google Scholar 

  43. Quiñones JP, Peniche H, Peniche C. Chitosan based self-assembled nanoparticles in drug delivery. Polymers. 2018;10(3):235.

    Article  PubMed  PubMed Central  Google Scholar 

  44. Firmino DF, Cavalcante TT, Gomes GA, Firmino N, Rosa LD, de Carvalho MG, Catunda FE Jr. Antibacterial and antibiofilm activities of Cinnamomum sp. essential oil and cinnamaldehyde: antimicrobial activities. The Scientific World Journal. 2018;2018.

  45. Summer K, Browne J, Hollanders M, Benkendorff K. Out of control: the need for standardised solvent approaches and data reporting in antibiofilm assays incorporating dimethyl-sulfoxide (DMSO). Biofilm. 2022;4:100081.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  46. Schwalbe R, Steele-Moore L, Goodwin AC. Antimicrobial susceptibility testing protocols: Crc; 2007.

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Acknowledgements

The authors are sincerely grateful to the Laboratory of Microbiology and Immunology, Faculty of Veterinary Medicine, University of Tehran, and University of Tehran’s Veterinary Hospital of Small Animals.

Funding

This research received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors.

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Authors and Affiliations

  1. Department of Microbiology and Immunology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran

    Niloofar Jelokhani Niaraki, Bahar Nayeri Fasaei & Seyed Mehdi Joghataei

  2. Department of Internal Medicine, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran

    Shahram Jamshidi

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  1. Niloofar Jelokhani Niaraki
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Contributions

Conceptualization, SJ, and BNF; methodology, BNF; software, NJN and SMJ; validation, SJ, and BNF; formal analysis, NJN; investigation, NJN; resources, NJN; data curation, NJN and SMJ; writing—original draft preparation, SMJ; writing—review and editing, SMJ and BNF; supervision, SJ and BNF; project administration, BNF; funding acquisition, SJ All authors have read and agreed to the published version of the manuscript.

Corresponding author

Correspondence to Bahar Nayeri Fasaei.

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Due to obtaining the consent of the animal owners and their presence, as well as respecting the patient’s rights and humane principles during sampling, the need for ethics approval by the ethics committee of the Faculty of Veterinary Medicine of the University of Tehran, Iran, was waived. Verbal informed consent was obtained from all owners to collect samples from the dogs. The ethics committee approved verbal informed consent. The researchers dated and signed the consent form indicating that “I have read and explained this consent form to the participant before receiving the participant’s consent, and the participant had knowledge of its contents and understood it.

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Niaraki, N.J., Jamshidi, S., Fasaei, B.N. et al. Antibacterial effects of chitosan-based hydrogels containing Trachyspermum ammi essential oil on pathogens isolated from dogs with otitis externa. BMC Vet Res 20, 130 (2024). https://doi.org/10.1186/s12917-024-03971-7

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BMC Veterinary Research

ISSN: 1746-6148

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