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. 2022 Jun 18;10(2):33. doi: 10.3390/medsci10020033

Human Trial for the Effect of Plasma-Activated Water Spray on Vaginal Cleaning in Patients with Bacterial Vaginosis

Yongwoo Jang 1,2,*, Junsoo Bok 2, Dong Keun Ahn 3, Chang-Koo Kim 4, Ju-Seop Kang 1,*
Editors: José Schneider, Antoni Torres
PMCID: PMC9227462  PMID: 35736353

Abstract

Underwater plasma discharge temporally produces several reactive radicals and/or free chlorine molecules in water, which is responsible for antimicrobial activity. Hence, it can simply sanitize tap water without disinfectant treatment. Additionally, the spraying technique using cleaning water exploits deep application in the narrow and curved vaginal tract of patients. Herein, we attempted a clinical trial to evaluate the vaginal cleaning effect of spraying plasma-activated water (PAW) to patients with vaginitis (46 patients). The efficacy was compared with treatment with betadine antiseptics used to treat bacterial vaginosis (40 patients). To evaluate the cleaning effect, Gram staining of the vaginal secretions was conducted before and after spraying PAW or betadine treatment (BT). Consequently, PAW-sprayed (PAWS) patients (22.3%) showed a better vaginal cleaning effect against Gram-positive and -negative bacteria than BT patients (14.4%). Moreover, 18 patients in the BT group showed worsened vaginal contamination, whereas five patients in the PAWS group showed worsened vaginal contamination. Taken together, the noncontact method of spraying cleaning water to the vagina exhibited a reliable vaginal cleaning effect without further bacterial infection compared with BT. Therefore, we suggest a clinical application of the spraying method using PAW for vaginal cleaning to patients with vaginitis without disinfectants and antibiotics.

Keywords: plasma-activated water, underwater plasma discharge, bacterial vaginosis, vaginal cleaning

1. Introduction

Bacterial vaginosis is the most common disease of vaginitis and is caused by unbalanced changes in the vaginal microbiome [1]. Its abnormal vaginal microbiota is likely associated with a reduced overall number of Lactobacilli species and the predominance of anaerobic microorganisms such as Gardnerella vaginalis and Atopobium vaginae species [2,3]. Generally, the clinical symptoms present vaginal discharges with a fish-like odor and urinary pain.

Currently, it is believed that the overgrowth of anaerobic species, predominantly Gardnerella vaginalis, creates a structured and polymicrobial biofilm barrier that is strongly attached to the vaginal epithelium [4,5]. In fact, several studies have supported that Gardnerella vaginalis is most of the bacterial composition in vitro biofilm formation models [3,6,7,8]. The microbiota is embedded in a polymeric matrix of extracellular nucleic acids, polysaccharides, and proteins [9,10]. Thus, it is likely that vaginal bacteria within biofilms are difficult to clearly eliminate using antibiotics, which is a common treatment for bacterial vaginosis [11]. This situation is considered to be correlated with high recurrence rates of bacterial vaginosis.

As an alternative therapeutic approach, spraying plasma-activated water (PAW) would be a promising way to destroy biofilms and then remove infected bacteria firmly attached to biofilms. It is known that, because the cold atmospheric-pressure plasma is discharged in water, PAW is disinfected by plasma exposure [12,13]. Therefore, PAW has potential antimicrobial activity within biofilms without causing bacterial resistance [14,15,16,17].

Generally, plasma irradiation at atmospheric pressure induces various ionized gases and free radicals that originate primarily from oxygen and nitrogen gases in the air and water [18,19,20]. In particular, oxygen-derived free radicals such as superoxide anions and hydroxyl ions are responsible for the antibacterial activity [21,22,23]. Additionally, many previous studies also support that underwater plasma exposure to chlorinated tap water can increase free residual chlorine molecules such as hypochlorous acid and hypochlorite ions, eliminating harmful microorganisms [24,25]. Because tap water can potentially be contaminated, depending on the surrounding environment, it must be sanitized for use as cleaning water. In this regard, plasma discharge in water would be a promising technology for easily and safely disinfecting tap water. In a previous preliminary study, we found a potential of PAW to patients with bacterial vaginosis (5 patients) [26]. However, there are still few studies related to the bacterial vaginosis of PAW when compared to the numerous studies showing the antibacterial effect of PAW. Considering this point, the vaginal cleaning effect of spraying sterilized water using PAW and the antibacterial effect of PAW to bacterial pathogens related to bacterial vaginosis can be considered.

In this study, we first attempted to clarify the cleaning effect of the spraying PAW compared with betadine treatment as control in vaginitis patients (control group; 40 patients, experimental group; 46 patients).

2. Materials and Methods

2.1. Ethical Consideration

This study was a single-institution, randomized, and comparative study performed at a Roen medical center. The study was approved by the Institutional Review Board of the Korea National Institute for Bioethics Policy (P01-202109-11-003).

2.2. Patient Characteristics and Trial Design

Among the patients who visited the hospital for suspected vaginitis, the gynecologists observed the color, smell, and viscosity of vaginal discharge to first select suspected patients with bacterial vaginosis. Finally, clinical trial participants were selected for the following conditions: (1) women who tested positive for 9 STD (sexually transmitted disease) polymerase chain reaction (PCR) tests; (2) those who had not undergone a hysterectomy; and (3) those who were willing to voluntarily participate in the clinical trial and comply with the clinical trial plan. Ninety-four vaginitis-suspected patients participated in this clinical study. They were randomly divided into the control group (47 patients) and the experimental group (47 patients). The patients in the control group were treated with a topical betadine, and the patients in the experimental group were treated by spraying plasma-activated water for 1 min (approximately 150~200 mL). Finally, the number of STD-positive patients was 40 in the control group and 46 in the experimental group.

2.3. Preparation of Plasma-Activated Water

PAW was prepared using an underwater plasma-generating device as previously reported [26]. Briefly, the atmospheric plasma was discharged for 10 min in a cleaning solution container with 3 L of tap water. Subsequently, the plasma-activated water in the cleaning solution container was sprayed on the patients of the experimental group using a spraying nozzle for 1 min.

2.4. Methods

To identify bacterial vaginosis, PCR analysis was conducted for the following STD-related bacteria: Gardnerella vaginalis, Mycoplasma hominis, Mycoplasma genitalium, Neisseria gonorrhoeae, Trichomonas vaginalis, Ureaplasma urealyticum, Ureaplasma parvum, Chlamydia trachomatis, and Treponema pallidum. These target transcripts were measured by using the commercial kit according to the manufacturer’s instruction (INFINATM STI 12, BIOWITHUS, Seoul, Korea). The Gram-positive test was performed using the vaginal secretion of all patients in the control and experimental groups before and after the application of betadine treatment or plasma-activated water spraying. Gram and PCR tests were conducted according to the institutional protocol of a Roen medical center (Seoul, Korea). The classification of bacteria was determined by the Gram stain (positive or negative) and morphologies (round shape, rod shape, or oval shape). According to these criteria, the vaginal bacteria were classified into the following five types according to the results of Gram staining as follows: Gram-positive cocci, Gram-positive bacilli, Gram-positive coccobacilli, Gram-negative bacilli, and Gram-negative coccobacilli. In addition, the grades were counted as the average number of each bacterium that was visible in the field when the microscopic field moved at random 10 times. In this regard, the samples were divided into four stages according to the number of bacteria visible as follows: rare (0~1), few (2~4), moderate (5~30), and heavy (over 30) stages.

2.5. Statistical Analyses

The data in Figure 1 are expressed as means ± standard deviation (SD). Statistical significance was analyzed using Student’s t test. All statistical analyses were performed using GraphPad Prism 7 software (GraphPad Software Inc., San Diego, CA, USA). In Figure 1, all comparisons showed a non-significant difference between two groups (p >0.05).

Figure 1.

Figure 1

Beeswarm boxplot of the percentage of reduced bacteria, including Gram-positive cocci (A), Gram₋positive bacilli (B), Gram₋positive coccobacilli (C), Gram₋negative bacilli (D), and Gram₋negative coccobacilli (E), in betadine treatment (BT, blue) and plasma₋activated water sprayed (PAWS, red) patients. (F) Beeswarm boxplot of the number of overgrowth cases after the application of BT or PAWS. All the results are expressed as means ± standard deviation (SD).

3. Results

For this clinical study, we examined and analyzed the control (40 patients) and experimental (46 patients) groups, except for STD PCR-negative patients, from each group (Supplementary Tables S1 and S2). The control group was treated with the topical betadine, and the experimental group was treated by spraying plasma-activated water for 1 min. To determine a quantitative change in vaginal bacteria, we performed the Gram stain test from the vaginal secretion of all patients in the control and experimental groups before and after the application of betadine treatment or plasma-activated water spraying. The vaginal bacteria were classified into the following five types according to the results of Gram staining as follows: Gram-positive cocci, Gram-positive bacilli, Gram-positive coccobacilli, Gram-negative bacilli, and Gram-negative coccobacilli. When observing the results of Gram staining with a microscope, the samples were divided into four stages according to the number of bacteria visible as follows: rare (0~1), few (2~4), moderate (5~30), and heavy (over 30) stages. Based on this result, we evaluated the reduced number of bacteria before and after betadine treatment or plasma-activated water spraying according to the following standard. The 25% reduction in bacteria indicates a decrease in one stage, such as from heavy to moderate or from moderate to few. Thus, we deemed 50% for the decrease in two stages, 75% for the decrease in three stages, and 100% for the decrease in four stages.

Table 1 shows a reduced mean percentage of all bacteria, including Gram-positive and -negative bacteria. The PAWS (22.29%) patients had a slightly increased effect on vaginal cleaning compared with those with betadine treatment (BT, 14.37%). Specifically, the PAWS group showed a reduction of 20.56 ± 4.32 and 27.38 ± 6.88 in Gram-positive and -negative bacteria compared with the BT group (12.11 ± 5.04 and 20.65 ± 4.32), respectively.

Table 1.

A summary of the results of a percentage of reduced bacteria in the betadine-treated and plasma-activated water (PAW)-sprayed patients.

BT PAWS
All bacteria Number of samples 87 83
Average 14.37 22.29
Standard deviation 44.07 33.36
Standard error of mean 4.73 3.66
Gram-positive bacteria Number of samples 64 62
Average 12.11 20.56
Standard deviation 40.33 34.03
Standard error of mean 5.04 4.32
Gram-negative bacteria Number of samples 23 21
Average 20.65 27.38
Standard deviation 53.65 31.53
Standard error of mean 11.19 6.88

Figure 1 is a beeswarm boxplot representing each value for a mean percentage of reduced bacteria between the BT and PAWS groups. The comparisons between BT and PAWS patients in the Gram-positive bacteria including cocci, bacilli, and coccobacilli are shown in Figure 1A–C, and their comparisons in the Gram-negative bacteria such as bacilli and coccobacilli are shown in Figure 1D,E. Overall, betadine swabs from patients with vaginitis show a broad treatment deviation in vaginal cleaning before and after treatment. In this regard, the PAWS group presented a better vaginal cleaning effect and narrow treatment deviation on vaginal cleaning compared with the BT group. Remarkably, the mean and standard deviation values for the reduced percentage of Gram-positive coccobacilli between the BT and PAWS groups were 7.14 ± 55.42 and 31.25 ± 35.94, respectively (Figure 1C). Regarding Gram-negative coccobacilli, the values were 21.15 ± 66.81 in the BT group and 20.83 ± 36.67 in the PAWS group (Figure 1E). Interestingly, 18 patients in the BT group showed worsened bacterial vaginosis, whereas 5 patients in the PAWS group showed worsened bacterial vaginosis (Figure 1F). Detailed information on the bacterial types and overgrowth is shown in Table 2. Additionally, Table 3 and Table 4 are raw results of patients in BT and PAWS groups for vaginal cleaning effect.

Table 2.

A summary of the results of bacterial overgrowth case in the patients after treatment of betadine and PAW.

Gram Stain Before After Patient No.
Betadine-treated patients Gram-positive cocci - few B8
- rare B17
rare few B18
Gram-positive bacilli few moderate B2
few moderate B7
moderate heavy B14
moderate heavy B27
Gram-positive cocobacilli few moderate B8
rare few B17
- moderate B25
- few B33
- heavy B38
- moderate B39
Gram-negative bacilli - rare B2
rare few B8
Gram-negative cocobacilli - moderate B5
- few B14
- heavy B17
PAW-
sprayed patients
Gram-positive cocci - few P5
Gram-positive bacilli - heavy P1
- few P21
Gram-negative cocobacilli moderate heavy P14
- rare P19

Table 3.

A summary of the results of Gram stain in the betadine-treated patients. The minus (−) and plus (+) signs indicate the reduction and increase of bacteria, respectively.

Patient No. Gram-Positive Cocci Gram-Positive Bacilli Gram-Positive Coccobacilli Gram-Negative Bacilli Gram-Negative Coccobacilli
Before After % Before After % Before After % Before After % Before After %
B1 few rare 25 heavy rare 75
B2 few moderate −25 - rare −25
B3 heavy heavy 0
B4 few rare 25
B5 few few 0 few few 0 heavy moderate 25 moderate few 50 - moderate −75
B6 few - 50 few rare 25 heavy heavy 0 heavy - 100
B7 few moderate −25 heavy few 50
B8 - few −50 moderate moderate 0 few moderate −25 rare few −25
B9 heavy heavy 0
B10 heavy moderate 25
B11 few rare 25
B12 heavy few 50 heavy - 100 heavy - 100
B13 moderate rare 50 moderate - 75 heavy - 100
B14 moderate heavy −25 - moderate −75
B15 moderate moderate 0 few - 50
B16 heavy rare 75 few - 50 rare rare 0
B17 - rare −25 heavy rare 75 rare few −25 rare - 25 - few −50
B18 rare few −25 rare - 25 heavy heavy 0 heavy heavy 0
B19 heavy few 50
B20 heavy heavy 0 rare - 25 rare - 25
B21 rare rare 0 rare rare 0 heavy heavy 0 rare - 25 few few 0
B22 heavy heavy 0
B23 few few 0 few few 0 heavy heavy 0 moderate - 75
B24 heavy moderate 25 heavy heavy 0
B25 heavy rare 75 - moderate −75
B26 rare rare 0
B27 moderate heavy −25
B28 heavy heavy 0
B29 few few 0 heavy moderate 25 few few 0 few few 0 few few 0
B30 heavy rare 75
B31 heavy moderate 25
B32 moderate moderate 0
B33 heavy heavy 0 - few −50
B34 heavy heavy 0
B35 moderate few 25 heavy - 100 heavy - 100
B36 heavy rare 75 moderate - 75
B37 few - 50 heavy heavy 0 moderate moderate 0
B38 heavy few 50 - heavy −100 - heavy −100
B39 heavy heavy 0 - moderate −75
B40 heavy heavy 0

Table 4.

A summary of the results of Gram stain in the plasma-activated water sprayed patients. The minus (−) and plus (+) signs indicate the reduction and increase of bacteria, respectively.

Patient No. Gram-Positive Cocci Gram-Positive Bacilli Gram-Positive Coccobacilli Gram-Negative Bacilli Gram-Negative Coccobacilli
Before After % Before After % Before After % Before After % Before After %
P1 heavy moderate 25 - heavy −100 heavy - 100 heavy moderate 25 heavy - 100
P2 heavy rare 75
P3 heavy moderate 25
P4 heavy moderate 25
P5 - few −50 moderate moderate 0 moderate moderate 0
P6 heavy heavy 0 few - 50
P7 few rare 25 heavy - 100
P8 heavy heavy 0
P9 heavy heavy 0
P10 heavy moderate 25
P11 few few 0
P12 moderate few 25 moderate few 25 few - 50
P13 heavy rare 75 rare rare 0
P14 moderate moderate 0 heavy heavy 0 moderate heavy −25
P15 few few 0
P16 heavy moderate 25 heavy heavy 0 heavy heavy 0
P17 heavy heavy 0
P18 moderate few 25
P19 heavy few 50 moderate moderate 0 - rare −25
P20 rare rare 0 rare rare 0 heavy heavy 0 rare rare 0 few few 0
P21 - few −50 heavy few 50 heavy few 50
P22 heavy heavy 0 Few rare 25
P23 heavy rare 75
P24 heavy heavy 0
P25 heavy rare 75 heavy few 50 few - 50
P26 heavy heavy 0
P27 heavy heavy 0
P28 heavy heavy 0
P29 heavy heavy 0
P30 few rare 25
P31 heavy heavy 0 few few 0 rare - 25 rare - 25
P32 heavy heavy 0
P33 heavy moderate 25
P34 few - 50 heavy rare 75 moderate moderate 0
P35 heavy moderate 25
P36 heavy few 50
P37 heavy heavy 0
P38 heavy rare 75
P39 few rare 25 heavy heavy 0 few - 50 heavy moderate 25
P40 heavy moderate 25
P41 heavy moderate 25 few - 50 few - 50
P42 heavy rare 75
P43 heavy few 50
P44 heavy moderate 25 rare - 25
P45 heavy few 50
P46 rare rare 0

4. Discussion

In the present clinical study, we performed a randomized comparison of vaginal cleaning effects between BT and PAWS groups. As a result, we present a similar vaginal cleaning effect between BT (14.37 ± 44.07) and PAWS patients (22.29 ± 33.36) in the current study. For vaginal cleaning, current clinical results support that application with spraying PAW to patients is an effective method similar to BT. This human trials were designed as noninferiority trials, which determine whether a new experimental treatment is no less efficacious than an active control treatment already in use. If it is similar to the effect of betaine, and plasma-activated water spraying can replace the chemical betadine, it is believed that it has great advantages in treating patients with vaginitis. This finding is consistent with vaginal cleaning effect of PAW to patients (five patients) with bacterial vaginosis in a previous preliminary study [26]. In addition to the vaginal cleaning effect, the antibacterial effect of PAW on overgrown bacteria related to bacterial vaginosis could be expected, because numerous studies have shown the antibacterial effect of PAW [14,15,16,17].

Generally, swabs of betadine at the vaginal site of a suspected infection and the administration of antibiotics are common treatments for bacterial vaginosis. In the case of chemical antiseptic treatment, safety concerns are associated with topical use, particularly in the long term. Additionally, unexpected contamination is possible during the treatment process. Eighteen cases of bacterial vaginosis occurred in patients who received betadine treatment (Figure 1F). In some cases, bacterial infection is further exaggerated in the deep area of the vaginal tract that was not treated enough with betadine. The secondary contamination of treatment tools such as swabs can also occur.

Therefore, the PAW method, which is a topical non-contact method, is a safe, effective, and simple treatment method compared to the betadine swab method, which is a contact treatment method in the patient with bacterial vaginosis.

5. Conclusions

In this study, PAWS patients showed a slightly better outcome concerning vaginal cleaning with lower variability than those receiving BT. Considering these points, spraying cleaning water disinfected by plasma discharge to vaginitis patients is a promising cleaning method.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/medsci10020033/s1, Table S1: A summary on the results of STD PCR test in the betadine-treated patients; Table S2: A summary on the results of STD PCR test in the plasma-activated water sprayed patients.

Author Contributions

Conceptualization, Y.J., D.K.A. and C.-K.K.; methodology, J.-S.K.; analysis, Y.J., J.B. and J.-S.K.; writing—original draft preparation, Y.J.; writing—review and editing, C.-K.K. and J.-S.K.; visualization, J.B.; supervision, Y.J. and J.-S.K. All authors have read and agreed to the published version of the manuscript.

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki and was approved by the Institutional Review Board of Korea National Institute for Bioethics Policy (P01-202109-11-003).

Informed Consent Statement

Informed consent was obtained from all the subjects involved in the study.

Data Availability Statement

The data generated are included within the manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

Funding Statement

This research was funded by the National Research Foundation of Korea grant (No. 2021R1A2C1094837) and the GRRC program of Gyeonggi province (GRRC AJOU 2016B03, Photonics-Medical Convergence Technology Research Center).

Footnotes

Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Data Availability Statement

The data generated are included within the manuscript.


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