ANTIBACTERIAL ACTIVITY OF CHLOROGENIC ACID PHYTOVESICLES AGAINST RESISTANT BACTERIA: DEVELOPMENT, OPTIMIZATION AND EVALUATION

Objective: To investigate the in vitro antibacterial activity of a naturally occurring polyphenol chlorogenic acid (CGA) and compares it with formulated chlorogenic acid phytovesicles against 4 different bacterial strains; two gram positive [ Staphylococcous aureus and Bacillus subtilis] and two gram negative strains [ Klebsiella pneumonia and Escherichia coli ]. Methods: CGA phytovesicles were developed and optimized using central composite design to improvise CGA’s physicochemical properties. Bactericidal activity was evaluated using agar diffusion, minimum inhibitory concentration (MIC) and time kill assay. The effect of pH and temperature on the antimicrobial activity was determined. Results: The optimized CGA phytovesicles showed entrapment of 96.89% with 30 times better lipophilic solubility than the plain drug. The inhibition zone sizes for CGA phytovesicle ranged from 17-25 mm as compared to 15-20 mm of plain CGA while the MIC values ranged 200-250 µg/ml as compared to 500-550 µg/ml of plain CGA. CGA phytovesicles exhibited a strong bactericidal effect at MIC with a log reduction in the range of 0.90-2.04 in Colony forming units (CFUs) at 24h for different strains as compared to 1.38-2.17 of plain CGA. Furthermore, the antibacterial effect was found to augment with increasing temperature but decreased with alkaline pH. Conclusion: Results strongly supports the hypothesis of potential use of CGA phytovesicles as a mode of drug delivery for its antibacterial use against different resistant bacteria. Staphylococcous aureus, Bacillus subtilis, Klebsiella pneumonia, Escherichia coli antimicrobial activity against these test bacteria indicate that there is a possibility of CGA phytovesicle as an alternative source of potential antibacterial agent.


INTRODUCTION
Phytochemicals are the bioactive plant compounds present in functional foods like fruits, vegetables, grains etc. These bioactive compounds not just promote good health but play a major role in prevention of chronic diseases [1]. These bioactive plant compounds which are also known as secondary plant metabolites, possess various benefits including antibacterial properties against pathogenic and spoilage microbes [2]. The increasing antibiotic resistance, limited spectrum and multiple side effects with synthetic agents at an alarming rate, prevails the natural antimicrobials. Unlike the synthetic antibiotics, natural antimicrobials don't target a particular reaction rather act on various groups of biomolecules in a pathogen thus there is no occurrence of resistance which makes them more alluring candidate [3]. However these bioactive compounds or secondary metabolites are limited in their efficacy because of poor absorption with limited solubility in lipophilic phases and instability at different physiological pH values [4].
The antibacterial efficacy of these secondary metabolites in plants depends on the chemical structure of active components and their concentration. Various phytochemicals present in plants with antibacterial effect includes saponin, flavonoids, thiosulfinates, glucosinolates, phenolics, and organic acids. Among them, Chlorogenic acid (CGA), a polyphenolic derivative of caffeic acid and quinic acid holds as a promising physiologically active substance present in foods such as coffee beans, tea and different fruits like apples, grapes, plums etc [5]. CGA has been reported to have antimicrobial activity against gram negative as well as gram positive bacteria [6]. The antimicrobial activity of polyphenolic derivatives has been imputed by their structure, their pH and sodium chloride concentration which results in physiological changes in pathogens and consequent cell death [7]. It also possesses other activities such as chemopreventive, antimutagenic, antioxidative, hypoglycemic, antiviral and anti-inflammatory. Its properties are attributed to the phenolic hydroxyl groups and it is characterized by relatively low toxicity and side effects. Till date there have been several literatures on antimicrobial efficiency of CGA against various strains having mechanism of disrupting the cell membranes of microbes [6] and inhibiting the bacterial fatty acid synthesis [8]. It has also been studied against various resistant strains as a synergistic agent along with standard antibiotics [9,4]. Despite its safety and effectiveness the use of CGA is limited by its low bioavailability [10]. Low bioavailability is attributed to extensive metabolism, thus despite of having a good hydrophilicity (40 mg/ml), it has low bioavailability (17-24%) and permeability (Biopharmaceutical classification system class III), which in turn affects its biological activities [11]. Moreover, CGA undergoes oxidation during storage or processing [12]. Complexation with phospholipid has not only shown to increase bioavailability by limiting the metabolism and increase in lipophilic solubility, but will also form stable phytovesicular form of CGA because of complexation [13]. Also CGA possesses polar hydroxyl groups in its structure which favours binding with phospholipid to form a phytovesicular complex [14].
Present work is thus aimed to develop and optimize phytovesicular complexes of CGA to improve its bioavailability, permeability and stability which should in turn enhance its antibacterial efficiency against these gram positive and gram negative bacteria. This enhanced activity can act as a source of an antibiotic alternative for drug development against array of infections. Four different bacterial strains Staphylococcous aureus, Bacillus subtilis, Klebsiella pneumonia and Escherichia coli were selected which causes various infections like soft tissue infections, joint infections, Urinary tract infections, nosocomial infections etc. Antibacterial efficiency against them was evaluated using agar diffusion assay, measuring minimum inhibitory concentration (MIC), time kill assay. Further the role of pH and temperature on antibacterial was also evaluated and compared against plain CGA.

Materials
CGA was purchased from Chemsworth, Surat-394230, India. Dimethyl sulfoxide (DMSO), Dichloromethane, N-hexane were obtained from Merck Pvt. Ltd. India. Various bacterial growth mediums like Mueller-Hinton agar (MHA), Mueller-Hinton Broth(MHB) were purchased from Himedia Lab. Pvt. Ltd. Phospholipon 90H was obtained as a gratis sample from Lipoid, Germany. All the other chemicals were of analytical grade.

Culture conditions
Organisms obtained were sub cultured in nutrient broth and nutrient agar. A loopful of organisms were transferred from the cultures obtained, in a freshly prepared nutrient broth suspension in an aseptic environment. Similarly a loopful of culture was streaked on an agar slant and incubated at 37 °C for 24h. The sub culturing was done every two months.

Standard antibiotic
Gentamycin (GEN) was used as a standard antibiotic to compare the antibacterial activity of CGA. Gentamycin (Gentalab) of Laborate pharmaceuticals India Ltd. was obtained from a local pharmacy shop.

Formulation of CGA phytovesicles by central composite design
Central composite design was used to study the influence of different process and formulation variables such as drugphospholipid ratio (X1), reaction time (X2) and reaction temperature(X3) on the quality attributes of phytovesicular complex i.e. partition coefficient and entrapment efficiency (table 1). The effect of these three independent variables at three different levels was evaluated by carrying out trials for 20 different combinations. The data obtained was statically analyzed and validated by Design expert® software (Version 11.0, Stat-Ease Inc., Minneapolis, MN). The design constructed gave the following polynomial Eq. 1.0. Y = b0 + b1X1 + b2X2 + b3X3 + b11X12 + b22X22 + b33X32 + b12X1X2 + b23X2X3 + b13X1X3 ……..Eq. 1.0 Where Y is the response for all the 20 combinations, b0 is the intercept while b1 to b33 are coefficients to the variables X1 X2 X3(main factors). The interaction terms (X1X2, X2X3, and X1X3) showed concurrent changes in response as the factors change. While the linearity was measured by polynomial terms (X12, X22, X32). Briefly, CGA and Phospholipon 90H were refluxed with 20 ml of dichloromethane at different molar ratios, reaction times and temperatures. The volume was then reduced to 3-5 ml by continuously stirring and to it 10 ml of n-hexane was added to precipitate the complex. n-hexane was allowed to evaporate at room temperature for 24-48 h. Percentage yield was calculated and the dried complex was further stored in a glass bottle at room temperature [15].

Analytical method of analyzing CGA
Estimation of CGA content in the complex was carried out by UV spectrophotometer (Jasco (V-630), Japan.) Also Calibration of CGA was performed in methanol, ultrapure water and phosphate buffer saline pH 6.8 (PBS). A standard stock solution of 1000 ppm was prepared, and from this, a 10 ppm solution was prepared to determine the λmax and calibration curves. Various validation parameters like linearity, intraday precision study, interday accuracy study, robustness, ruggedness were determined in accordance with the ICH guidelines [16].

Entrapment efficiency and partition coefficient
Phytovesicles equivalent to 10 mg of drug were accurately weighed in 100 ml beaker to which 50 ml of 6.8 pH phosphate buffer was added. The beaker was then subjected to stirring on a magnetic stirrer for 4 h and then allowed to stand for 1h. Clear supernatant was decanted while the sludge was subjected to centrifugation at 5000 rpm for 15 min. The supernatant obtained after centrifugation was filtered with Whatman filter paper (0.45 µm) and was measured for UV absorbance at 328.8 nm. Entrapment efficiency was calculated by following formula Eq. 2.0 [17] Entrapment ef�iciency = Solubility of CGA and CGA phytovesicles in both oil and water phase was determined by calculating partition coefficient using shake flask method with water and n-octanol. 10 mg equivalent of phytovesicles were taken in a conical flask to which 10 ml of water and n-octanol was added and then placed upon rotary shaker for 24 h. The mixture was then transferred to a separating funnel and was allowed to stand for 30 min. The amount of drug in both phases was determined by UV spectrophotometer in triplicate. Same procedure was carried out for the plain drug. Concentration in both the phases was calculated using calibration curve equation and partition coefficient was calculated by using equation 3.0. [13] Partition coef�icient = Co/Cw …… Eq. 3.0 Where Co-concentration in oil phase, Cw-concentration in water phase.

Fourier transform infra-red (FT-IR) spectroscopy
The IR spectra of the samples (CGA, Phospholipon 90H, phytovesicles and their physical mixture) were recorded with Fourier transform infrared spectrophotometer (Shimadzu-IRAFFINITY-1, Japan) in the region of 4000 cm -1 to 400 cm -1 . Pellets were prepared by triturating sample with potassium bromide using glass pestle and mortar in the ratio 1:100. The mixture was then introduced into the sample holder and scanned. The interaction between CGA and Phospholipon 90H was studied with the spectrums obtained [18].

Differential scanning calorimetery (DSC)
Thermograms of CGA, Phospholipon 90H, Phytovesicles and their physical mixture were recorded using a differential scanning calorimeter (DSC 60 PLUS, Shimadzu, Japan). The thermal behaviour was studied by heating each individual sample in aluminium seal sample pan under nitrogen gas flow at the heating rate of 5 °C/min from 0 to 300 °C [19].

Particle size analysis and zeta potential
The particle size, polydispersity index and zeta potential of phytovesicles were determined by a Zetasizer Nano ZS90 (Malvern Instruments Ltd., Massachusetts, USA). For measurement phytovesicles (10 mg) were dispersed in 10 ml deionized water and measured [18].

Scanning electron microscopy (SEM)
SEM imaging of CGA phytovesicles, Phospholipon 90H and CGA was performed by a scanning electron microscope (JEOL, JSM-6390LV, Tokyo, Japan). The sample was mounted on specimen stubs using carbon tape and was coated over with gold using ion sputtering device (JFC 1600). The measurements were performed at 20kV using different magnifications [19].

Agar diffusion assay
Antibacterial activity of CGA and CGA phytovesicles against Staphylococcous aureus, Bacillus subtilis, Klebsiella pneumonia and Escherichia coli was determined by agar diffusion assay. All the bacterial isolates were grown in nutrient broth and standardized in saline solution to a turbidity of 0.5 McFarland standards. Using sterile cotton swabs the bacterial inoculum (50 µl) were then spread onto MHA plates by lawn culture. Wells were created onto the MHA plates using sterilized cork borer (6 mm). Test solutions (100 µl) prepared by dissolving the CGA and CGA phytovesicles in DMSO at a concentration of 2, 4, 8, 16, 32 mg/ml were then carefully loaded into the wells. Gentamycin (GEN) was used as a standard while DMSO was used as negative control. After loading of the sample the plates were kept in refrigerator for 30 min so that the drug will diffuse before the organisms starts growing. Plates were then further incubated at 37 °C for 24 h and observed for growth and inhibition zones around the wells which were then further compared with antibiotic. All measurements were performed in triplicates [20].

Minimum inhibitory concentration (MIC)
Minimum inhibitory concentration of CGA and CGA phytovesicles for Staphylococcous aureus, Bacillus subtilis, Klebsiella pneumonia and Escherichia coli was determined by broth dilution method. Stock solutions of CGA and CGA phytovesicles were prepared at 1000 µg/ml. 11 sterile test tubes were labelled and arranged. Tubes 2-11 were loaded with 500 µl of MHB. While to tubes 1 and 2, 1000 µl of CGA stock solution was added. Two fold serial dilution was then performed by pipetting out 500 µl of the mixture from test tube 2 to 3 and consecutive transferring mixture till tube 9. 500 µl of mixture from tube 9 was discarded. Tube 10 and tube 11 served as growth control (with no antibiotic) and broth control respectively. All test tubes were inoculated except the 11th test tube with 500 µl of bacterial inoculums (0.5 McFarland standard). The tubes were then further incubated at 37 °C for 24 h. MIC was determined by the lowest concentration showing no visible growth. All measurements were performed in triplicates. The whole procedure was carried out in a laminar air flow in a sterile condition. Also, pippete tips were changed with each transfer so as to avoid the carryover of antibiotic [4].  [4].

Effect of pH on antibacterial activity
A change in the antibacterial activity with changes in pH was determined.  [20].

Effect of temperature on antibacterial activity
The role of temperature was determined by using the method described by Kabir et al. [20]. The test solutions of CGA and CGA phytovesicles were exposed to concentration equivalent to MIC, at two different temperatures. After which the test sample was added to 1000 µl of MHB and 500 µl of bacterial inoculum (for all the 4 strains Staphylococcous aureus, Bacillus subtilis, Klebsiella pneumonia and Escherichia coli) and incubated in a rotary shaker.
To determine the CFUs the samples were diluted 10 folds before plating them on MHA plates. The whole experiment was performed in triplicate.  Statistically significant coefficients with p value of 0.0480 for Y1 and 0.0120 for Y2 were obtained for both the responses. Regression analysis showed that drug-phospholipid ratio (X1) had a direct relationship and reaction time (X2) with reaction temperature (X3) had an inverse relationship on partition coefficient (Y1). Indicating that partition coefficient values increased with increasing drug phospholipid ratio and decreased with increasing reaction time and temperature. This is because increase in drug phospholipid ratio causes higher quantity of phospholipid to remain in an uncomplexed form forming additional layers encircling CGA phytovesicles rendering good lipophilic character to it [21]. While with increasing reaction time and temperature the phytovesicles formed were sticky and less free flowing owing to the phase transitioning of phospholipid at higher temperature resulting into less solubility.

Optimization of CGA phytovesicles by central composite design
On the other hand for entrapment efficiency (Y2), drug-phospholipid ratio (X1) and reaction temperature(X3) had direct relationship while reaction time(X2) having an inverse relationship. It was found that highest reaction time of 3.6 h gave entrapment of 83.44% while at 1h it gave entrapment of 96.86%. This may be due dissociation in hydrogen bonding between CGA phenolic group and choline group of Phospholipon 90H with longer reaction times. Thus it shows the appropriate time required for CGA to complex with that of phospholipid while the increase in entrapment efficiency with increasing drug-phospholipid ratio and reaction temperature can be attributed to increased phospholipid content at required transition temperature which favors better entrapment of CGA complex [22].

Fig. 2: 3D surface plots of CGA phytovesicles (a) Partition coefficient (b) Entrapment efficiency
Similar relationship was seen in contour plots and 3D response curves ( fig. 1 and 2 respectively). Depending on these observations optimal values of the variables were drawn i.e. 1:3, 1h, 60 °C respectively. Batch F7 was thus selected as the optimized batch showing highest entrapment with highest partition coefficient where the drug CGA and phospholipid were in the molar ratio of 1:3 thus having better prospects to complex sufficiently with optimum reaction time of 1h with 60 °C of reaction temperature.
The models obtained for both the dependent variables were further validated by preparing an additional batch as per the optimal values of independent variables-1:3, 1h, 60 °C. The predicted values for partition coefficient and entrapment efficiency of CGA phytovesicles from quadratic and 2FI model (respectively) and the actual values from the prepared batch were compared. The partition coefficient and entrapment efficiency of the prepared batch as per optimized conditions were found to be 0.9554 and 93.65±0.25% respectively as compared to 0.9265 and 90.85±0.02 % of the predicted values given by model showing its practicability. Bias was calculated using the Eq. 6.0 was found (-3.1%) for partition coefficient and (-3.08%) for entrapment efficiency demonstrating the robustness of the generated models [23]. Relative standard deviations of intra and inter day measurements in all the solvents was less than 2%. The limit of quantification and limit of detection values obtained were 0.06 µg/ml and 0.02 µg/ml for methanol and ultrapure water; 0.10 µg/ml and 0.03 µg/ml for pH 6.8 PBS. The results obtained were in agreement with the literature reported by Navarra et al. [24] and Shikov et al. [25].

Entrapment efficiency and partition coefficient
Entrapment efficiency of optimized CGA phytovesicles was 96.89±1.24 % [14] while the partition coefficient of CGA phytovesicle was found to be 0.977±0.36 as compared to 0.036±0.43 of CGA [26]. This increase in partition coefficient is attributed to the complexation between CGA and phospholipid. The CGA phytovesicle showed better solubility (30 times more) in oil phase (4.830 mg/ml) with solubility in water phase of 4.939 mg/ml as compared to plain CGA which showed 0.16 mg/ml of solubility in oil phase and 4.414 mg/ml solubility in water phase. Thus the phytovesicle formed was more ampiphilic in nature. Leptihn et al. [27] reported that pka, LogP and hydrophobicity play a major role for a molecule to exert antimicrobial activity. CGA in phytovesicular form showed higher logP values with optimum hydrophobicity thus having propensity for improved antimicrobial activity [27].  (fig. 3). The spectra of Phospholipon 90H gave characteristic C-H stretching band of long chain fatty acid at 2916.37 cm -1 and 2848.86 cm -1 [28]. Also, a C=O band at 1467.83 cm -1 ; a − a (so3)3 band at 923.90 cm -1 and a P-O-C stretch at 968.27 cm -1 [29]. The spectra of the physical mixture showed all the characteristic bands as those present in CGA and Phospholipon 90H. While in the spectrum of CGA phytovesicle was different from CGA and Phospholipon 90H with absence of 908.47 cm -1 , 817.82 cm -1 , 923.90 cm -1 , 968.27 cm -1 peaks. The peak at 3672.47 cm -1 shifted left to 3687.90 cm -1 . Furthermore, the absence of aromatic stretch peaks has been previously attributed to successful formation of phytovesicular complex [30] indicating the hydrogen bonding between phenolic group of CGA with choline group of Phospholipon 90H [14].  Fig. 4 shows the thermograms of CGA, Phospholipon 90H, physical mixture and CGA Phytovesicles. CGA showed two sharp endothermic peaks at with onset at 195.01 °C and 202.56 °C which is in consistent with the literature reports [31]. Thermogram of Phospholipon 90H showed a sharp endothermic peak at onset of 101.43 °C and additional endothermic peaks at onset of 57.20 °C, and 177.69 °C. The physical mixture of CGA and Phospholipon 90H retained characteristics peaks of both CGA and Phospholipon 90H, however a new characteristic peak was seen at onset of 70.45 °C which can be attributed to the probable depression in melting endotherm of Phospholipon 90H, complex or eutectic formation. CGA phytovesicle exhibited an endotherm with an onset at 61.52 °C and also an endotherm close to characteristic physical mixture peak at 70.45 °C which clearly indicates the Phytovesicular complex formation. Additionally, disappearance of other characteristic endotherms of CGA and Phospholipon 90H, corroborates the formation of phytovesicular complex. Particle size, zeta potential and SEM: The mean particle diameter of optimized phytovesicular complex was found to be 808.6±1.8 nm and the polydispersity index obtained as 0.78±0.06 indicating a narrow range of particle size distribution [32]. The Zeta potential was found to be (-) 18   Agar diffusion assay is a standard susceptibility testing for antimicrobials where the antimicrobial agent diffuses into the agar plates and inhibits the growth of the test organism forming growth inhibition zones. Balouiri et al. [33] referred to it as a technique to screen or quantify the antimicrobial effect. CGA in phytovesicular form will give a larger zone of inhibition than plain CGA because of its higher penetrability across cell membrane with higher partition coefficient value [33]. The results obtained from agar diffusion assay are illustrated in table 3. CGA was found to be highly active against all the 4 strains. The zone of inhibition for CGA phytovesicle ranged between 17-25 mm as compared to CGA showing zone of 15-20 mm at 32 mg/ml¯. With increasing concentrations of both the samples, evenly increasing zones of inhibition were found with maximum activity at 32 mg/ml¯ and a zone of 25 mm ( fig. 7). While the zones obtained with standard antibiotic Gentamycin at equivalent concentration were in the range 30-33 mm [34].

Minimum inhibitory concentration
MIC values for CGA and CGA phytovesicles are given in  [35]. A relatively higher lipophilic solubility of CGA phytovesicle is responsible for higher microbial membrane permeability ultimately leading to its disruption and cell death. This shows the efficiency of CGA in phytovesicular form with higher antibacterial activity.

Time kill assay
The effect of time on bactericidal activity of CGA and CGA phytovesicles in all the 4 strains was determined and shown in fig. 8. There was sharp decrease in the number of viable cells obtained with Escherichia coli and Bacillus subtilis after 6h of incubation and a linear decrease in the number of viable cells was found with Staphylococcous aureus and Klebsiella pneumonia after 12h. This higher resistance with the latter two strains can be explained with the basis of different cell wall composition [36]. A relatively higher lethal effect was observed with CGA phytovesicle after 6h of incubation as compared to moderate lethal effect after 12h with CGA. This strong bactericidal effect at MIC with a log reduction (1.5 times) in the range of 0.90-2.04 in CFUs at 24h for different strains as compared to 1.38-2.17 of plain CGA can be attributed to the efficiency of phytovesicular form of CGA in crossing the lipid bilayer of the cell and exerting its antimicrobial properties. Moreno et al. [37] reported that the antimicrobial effect of phenolic derivatives is related to inactivation of enzymes in the cell, which are further dependent on rate at which alterations in the cellular membrane and cellular penetration takes place. CGA in phytovesicular form crosses the lipid bilayer of the cell membrane more easily as compared to plain CGA. This loss in integrity of cell membrane causes cell death [37]. Thus a more lethal effect was obtained in phytovesicular form than plain CGA which increased the cell membrane permeability [38].

Effect of pH on antibacterial activity
Almajano et al. [39] outlined that antimicrobial effect of phenolic derivatives is governed by pH. Thus the effect of pH on antimicrobial activity on CGA and CGA phytovesicles was assessed and shown in fig. 9. It was found that at pH 10, no bactericidal effect was exerted, while at pH 7 a very weak bactericidal effect was exerted. On the other hand very lethal bactericidal effect was seen at pH 4. The reason for this was described by Narita et al. [40] that phenolic derivatives are more stable under acidic pH conditions. At higher pH (≥7) CGA undergoes irreversible structural changes [41]. It has been reported by Wen et al. [42] that antimicrobial activity of weak acids such as CGA depends on the ionization state and proportion of undissociated molecules of caffeic acid and quinic acid. Hence pH appeared to be a crucial factor in the bactericidal activity of CGA and parallel effect was seen on the antibacterial activity of CGA phytovesicles with less CFUs at lower pH as compared to plain CGA.

Effect of temperature on antibacterial activity
An effect of temperature on the bactericidal effect of CGA and CGA phytovesicles was studied which showed that a moderate bactericidal effect was observed at 37 °C and a marked bactericidal effect was obtained at 50 °C for all the 4 strains especially on Escherichia coli ( fig. 10). While CGA phytovesicles showed further reduction in the CFUs with increased temperature. This was explained by Kabir et al. [20] and Lou et al. [43] who reported that the role of temperature in antimicrobial action was due to increased permeability of CGA through the bacterial cell walls. They also highlighted that the mechanism for temperature mediated membrane permeability may be because of cell wall disruption at specific temperature leading to cell death [20]. Hence the role of temperature in bactericidal effect of CGA and CGA phytovesicles was determined.

CONCLUSION
In present study, phytovesicular delivery of CGA provided a greater antibacterial activity over plain CGA. Increased antibacterial activity of CGA in phyovesicular form can be attributed to its improved lipophilic solubility (partition coefficient), which in turn should facilitate an increase in its permeability across bacterial cell wall bilayer. Thereby, reducing the MIC and kill time nearly to half of its plain drug form. The antibacterial activity was largely dependent on both pH and temperature. Phytovesicles exerted a marked antimicrobial action on both Gram negative [Klebsiella pneumonia and Escherichia coli] and Gram positive [Staphylococcous aureus and Bacillus subtilis] microbes. In order of sensitivity to CGA phytovesicles, the microorganisms are Escherichia coli>Bacillus subtilis>Staphylococcous aureus>Klebsiella pneumonia. All these strains are associated with various types of infections including Urinary tract infections, wound infections, meningitis, nosocomial infections etc. Demonstration of enhanced antimicrobial activity against these test bacteria indicate that there is a possibility of CGA phytovesicle as an alternative source of potential antibacterial agent.