*Corresponding Author:
H. M. Ashvini
Department of Pharmaceutics, Acharya & B M Reddy college of Pharmacy, Bengaluru-560 107, India
[email protected]
Date of Submission 21 February 2018
Date of Revision 18 September 2018
Date of Acceptance 11 February 2019
Indian J Pharm Sci 2019;81(2):302-308  

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Clarithromycin-loaded chitosan nanoparticles were prepared and evaluated for antibacterial activity against Streptococcus pneumonia. Infrared and differential scanning calorimetry studies ruled out any possibility of interaction between clarithromycin and excipients used. Formulations were prepared using ionic gelation method. From the results, it was found that percent entrapment efficiency of formulations ranged between 12.1±0.67 to 59.45±4.05 %, particle size between 155.31±23.36 to 360.05±26.06 nm with narrow size distributions except F1, F2, F3 and zeta potential between +11.96±0.5 to +26.83±0.4 mV. The in vitro drug release was found to be good with 75.1±1.01, 72.4±2.14, 68.1±1.96 and 65±1.52 % release for F4, F5, F6 and F7, respectively. From the results of kinetic studies, formulations were found to be more linear towards Higuchi model with R2 value ranging from 0.843 to 0.964 indicating that drug release mechanism by diffusion and n value of Korsemeyer-Peppas plot was found to be less 0.5 indicating Fickian diffusion. In vitro antibacterial activity was performed against Streptococcus pneumonia. Their minimum inhibition concentration values of F4 and F5 was 1/4th and 1/2th of minimum inhibition concentration of clarithromycin. Results of in vitro antibacterial studies showed that, the clarithromycin nanoparticles have more antibacterial property than intact drug.


Clarithromycin, chitosan nanoparticles, antibacterial activity

Chitosan (CS) is a linear copolymer of β-(1-4)- linked 2-acetamido-2-deoxy-beta-D-glucopyranose and 2-amino-2-deoxy-3-D-glucopyranose, obtained by deacetylation of its parent polymer chitin, the second most abundant in nature after cellulose [1]. The bactericidal action of CS is well known and is due to an electrostatic interaction between NH3+ groups of CS and phosphoryl groups of phospholipid components and lipopolysaccharides of bacterial cell membranes. This leads to an increase in the permeability formation of pores and finally disrupts the bacterial cell wall [2-4].

Bacterial infectious diseases ranging from cutaneous infection to deep-seated life-threatening infections such as pneumonia, endocarditis, septicaemia, osteomyelitis, and other metastatic complications [5-7]. Antibiotic are the usual treatment for bacterial infection [8]. Bacterial infectious disease is still responsible for considerable global mortality despite antibiotic treatment [9-11]. The major challenges faced by localized treatment of respiratory tract infections are the rapid absorption and clearance of antibiotics from the lungs. A critical obstacle and challenge for bacterial infectious therapy concerns the limited availability of effective biocompatible delivery system for most hydrophobic therapeutic and antimicrobial resistance. Intracellular infections and acquired resistance of infectious microbes are also key challenges [12].

The clinical treatment failure of bacterial infectious disease is associated with low bioavailability of antibiotics, side effects of antibiotics, tissue and cellular barriers, biofilm-related infection and the emergence of resistant bacteria. Polymeric nanoparticles (NPs) and microparticles have been shown to have the potential to provide controlled drug delivery to the lungs, with sustained release of drugs so as to prolong drug action, reduce side effects, and to improve the patient compliance [13].

Nanotechnology in medicine is already largely considered and explored in many medical areas, especially in drug delivery. NPs encapsulating antibiotics have shown great probability in substituting the administration of antibiotics in their free form. Polymeric NPs deliver antibiotics into very dense tissue and inaccessible cells. In case of NPs, the major fraction of the API can be released due to the smaller particle size and with this, shorter the diffusional distance between inner matrix and the environment [14]. Designing a NP formulation for antibacterial drug may prolong therapeutic by decrease the frequency of dosing and also improve the efficacy of drug and patient compliance. Literature indicated that NP formulations of antibiotics have better antibacterial effect than conventional formulation.

Clarithromycin (CLM) is a broad spectrum antibiotic [15], which has been widely used to treat respiratory tract infections caused by Pseudomonas aeruginosa, Chlamydophila pneumoniae, Klebsiella pneumonia, Mycoplasma pneumonia, Streptococcus pneumonia and Haemophilus influenza [16]. CLM is practically insoluble in water and its poor solubility is pH-dependent [17]. Acid stability of CLM makes it suitable for oral administration. Despite CLM being absorbed from GI tract, systemic bioavailability of CLM is relatively poor (55 %) [18]. CLM exerts its antibacterial action by binding to the 50s ribosomal subunit of susceptible organisms and by inhibiting protein synthesis through translocation of aminoacyl transfer-RNA [19].

Polymers used for NP construction are either natural or synthetic. Natural polymers include albumin, collagen, gelatin, CS, haemoglobin and alginate. Among water-soluble polymers available, CS is one of the most extensively studied [20]. The 5 key advantages that polymeric drug delivery products can offer are; localized and sustained delivery of drug, stabilization of the drug, release rate, which is less dependent on the drug properties and steady release rate with time.

In the present research work, formation of antibiotic NPs seems to be a good choice for treatment of respiratory tract infections. Using these NPs, the dose and dosing frequency of CLM and side effects could be minimized, patient’s compliance improved by direct delivering of drug into lungs.

Materials and Methods

CLM was obtained from Calyx Pharmaceuticals. CS was purchased from Sigma Aldrich (85 % deacetylation). Sodium tripolyphosphate was purchased from Yarrow Chem Pvt., Ltd., Mumbai. High performance liquid chromatography (HPLC) grade water, acetonitrile and methanol were purchase from S. D. Fine-Chem, Mumbai, India. Potassium dihydrogen phosphate was purchased from Finar Reagents and o-phosphoric acid was obtained from Merck Chemicals. All other chemicals used were of analytical grade or HPLC grade.

Preparation of CLM-loaded CS NPs:

CLM-loaded CS NPs were prepared by ionic gelation method [21-23]. CS was dissolved in an aqueous solution of acetic acid at concentrations, 0.1, 0.25 and 0.5 %) under magnetic stirring at room temperature. CLM was dissolved in CS solution, to get concentration of 1 mg/ml. Triphenyl phosphate (TPP) aqueous solution (0.25 %) was added drop-wise using a syringe and needle (Table 1). pH of the CS solution was maintained at 4-4.5. Stirring was continued for about 30 min. The resultant NPs suspension was centrifuged at 15 000 rpm for 15 min (Remi cold centrifuge). Supernatant was collected and used for determining the encapsulation efficiency.

Formulation CS conc. CS:STPP ratio
F1 0.1 % 1:1
F2 1:1.5
F3 1:2
F4 0.2 % 1:1
F5 1:1.5
F6 1:2
F7 0.5 % 1:1
F8 1:1.5
F9 1:2

Table 1: Composition of Chitosan Nanoparticles

Encapsulation efficiency:

CLM content in NPs were determined by a fully validated HPLC method [24-32] after appropriate dilution with HPLC grade acetonitrile. About 20 μl was injected into a HPLC system (Shimadzu LC-20AT) equipped with a UV detector (at 205 nm) and Phenomenex Kinetex 5 μ C18 (250×4.6 mm i.d., 5 μm particle size) column. Optimised mobile phase, acetonitrile (0.1 M):potassium dihydrogen phosphate (50:50) was used, at flow rate of 1 ml/min and at a wave length of 205 nm. Three samples from each formulation were injected into HPLC column with appropriate dilution. Entrapment efficiency (EE %) in the CS-NPs were calculated according to the Eqn. [33,34], % EE = total amount of CLM loading–free CLM in the supernatant/ total amount of CLM loading×100.

Size of NPs, surface morphology and zeta potential:

Mean particle size and zeta potential of prepared NPs were measured using a Malvern Nano ZS 90 (Malvern Instruments, UK) after appropriate dilution with double-distilled water. The mean particle size and distribution were measured based on photon correlation spectroscopy (dynamic light scattering) technique. The particle surface charge was quantified as zeta potential using Malvern Nano ZS 90 (Laser Doppler Electrophoresis).

Scanning electron microscopy (SEM):

The morphology of NPs was investigated using SEM (EM-LEO435VP, Carl Zeiss SMT Inc., NY).

Differential scanning calorimetry (DSC):

Thermograms of CLM, NPs, physical mixture of CLM with polymer and NPs were carried out using DSC Shimadzu 60 with TDA trend line software to evaluate any possible interaction. The analysis was performed at a rate of 10.0° /min from 10° to 300°.

Fourier-transform infrared spectroscopy (FTIR):

FTIR of intact CLM, NPs and physical mixture were obtained from FTIR spectrophotometer, model Tensor 27, Bruker. Spectra were obtained by ATR technique. The scanning range was 4000-400 cm-1.

In vitro drug release:

In vitro release patterns were studied using conventional dialysis technique [35]. In this method CLM-loaded CS NP suspension (equivalent to 10 mg) was placed in a dialysis bag, which was immersed in a beaker containing 100 ml phosphate buffer (pH 7.4), continuous to acceptor fluid and dialyzed. Acceptor compartment was agitated continuously using a magnetic stirrer, sink the condition and the temperature was maintained at 37±1°. The drug which diffuses out of NPs into the continuous phase was periodically sampled and assayed using HPLC according to the method described for encapsulation efficiency. The mean calculated values were obtained from 3 replicates. In order to understand the kinetic and mechanism of drug release, the result of in vitro drug release study of NPs were fitted with various kinetic models [36,37].

Stability studies:

The stability of different formulations was evaluated after the formulations were stored at room temperature and at 4° in a freeze for a period of 6 mo. Samples were collected at every 1 mo interval and were viewed for sedimentation. Any changes in the particle size and zeta potential were assessed [38,39].

Antibacterial activity of the NP suspension:

Minimum inhibitory concentration (MIC) of CLM NPs was determined by micro-dilution technique using S. pneumoniae. In vitro antibacterial assays were carried out adopting the Kirby Baurer method according to the National Committee for Clinical Laboratory Standards procedures for aerobic testing. Mueller-Hinton agar was used as growth media. To the sterile nutrient agar plates 100 μl of the test organism was aseptically transferred and spread using a sterile L-shaped glass rod. The organism was allowed to settle on the medium for 5 min (seeding). Using a sterile cork borer, three bores of 6 mm were made and 100 μl of the test sample (CLM, 1 mg/ml) as a positive control and blank as negative control was transferred aseptically into the bore. The plates were incubated for 24 h at 37º. The tests were done in triplicates and the zones of inhibition were measured using standard HiMedia scale [40-42].

Results and Discussion

CLM-loaded CS NPs were prepared by ionic gelation method. Ionic gelation method was selected because of following interesting features: 1) NPs are formed spontaneously as a result of molecular linkage between negatively charged TPP phosphate ions and positively charged CS amino group. 2) NPs are obtained spontaneously under mild conditions without involving high temperature, organic solvent, and sonication. 3) Provides a continuous release of entrapped drug for prolonged time. CS mucoadhesive character increases residual time at the site of absorption. Initial trials were addressed in the selection of the optimal ratios for the formation of NPs of TPP and CS.

Encapsulation efficiency was in range of 12.1±0.67 to 57.56±1.31 %. High encapsulation (57.56±1.31 %) of CLM in NPs indicated efficient loading of the drug, due to its low aqueous solubility. From these results, it was observed as the CS concentration increased from 0.1 to 0.2 %, encapsulation also increased at constant TPP concentration. But further increase in CS concentration led to a decrease in the encapsulation, which might be due to insufficient TPP to cross link. At a constant CS concentration, as the ratio of TPP increased, encapsulation increased due to more cross linking.

The results of particle size are reported in Table 2. Mean particle size ranged from 155.31±23.26 to 399.95±16.50 nm. The mean particle size increased with increase in CS concentration. Lower the CS concentration, lower the viscosity, which resulted in better solubility and interaction between CS and TPP, and thus smaller particle size (F1, F2, F3) [43]. Further increase in CS concentration resulted in increased particle size due to precipitation, this might be due to increase in the viscosity of the CS solution. Available TPP could not crosslink CS strongly, which led to increase in the particle size. In case of 0.2 and 0.5 % CS concentration, as concentration of CS increased to 0.5 %, viscosity of solution increased, thus available TPP was not able to completely cross link, leading to increase in the particle size with decrease in encapsulation. At s constant CS concentration, increase in the TPP ratio resulted in increase in the particle size, but the yield decreased.

Formulation code Encapsulation efficiency (%) Mean particle size (nm) PDI Zeta potential (mV)
F1 22.10±0.67 155.31±23.26 0.70±0.04 +14.12±0.10
F2 38.71±3.44 182.18±15.10 0.76±0.20 +13.81±0.03
F3 45.82±1.13 208.14±16.50 1.00±0.00 +11.96±0.50
F4 67.41±2.61 285.93±23.26 0.19±0.03 +26.83±0.40
F5 79.56±1.31 297.87±15.10 0.21±0.02 +25.10±0.30
F6 45.15±4.05 302.12±14.03 0.19±0.02 +23.97±0.23
F7 55.38±1.01 332.90±13.95 0.24±0.03 +25.13±0.91
F8 41.99±1.40 399.95±16.50 0.35±0.02 +22.20±0.91
F9 38.15±2.04 360.05±26.06 0.41±0.01 +19.33±0.21

Table 2: Characteristics of Clarithromycin-Loaded Chitosan Nanoparticles

The value of polydispersity index (PDI) can range from 0.00 (mono-dispersed systems) to 1.00 (highlydispersed systems), where PDI value greater than 0.50 indicate a relatively broader size distribution [44]. However narrow size distribution was observed for all NPs and all NPs exhibited a relative mono-dispersed distribution except F1, F2 and F3.

From the results it was observed that as CS concentration increased, zeta potential also increased (F1, F4, F7). More the concentration of CS, more the unneutralised amine group on the surface of NPs, stronger the electrostatic repulsion between particles. Whereas increase in the TPP volume ratio decreased the zeta potential, due to more interaction was observed. This confirmed that the formation of NPs greatly depend on the concentration of free amine groups to cross link with TPP. Based on the above results, 0.2 % CS formulations were selected for further studies.

DSC thermogram of pure CLM showed a sharp endothermic peak at 221.81° (figure 1). The thermograms of formulation showed the same endothermic peak at similar temperature, this further confirmed that there was no drug to polymer interaction. The DSC thermogram of CLM, physical mixture and NPs are shown in figure 1. Sharp endothermic peak at 223.01° (figure 1a) corresponding to its melting temperature of CLM. However, no sharp endotherm was seen at 223.01° in figure 1b and c, which indicated that crystallinity of CLM has been reduced significantly in NPs. Hence, it could be concluded that the drug was present in the formulation in the amorphous phase and might have been homogeneously dispersed in the polymer matrix.


Figure 1: DSC thermograms
(a) Clarithromycin, (b) physical mixture and (c) clarithromycinloaded NPs

The FTIR spectra of CLM-loaded NPs, CLM and physical mixture of CLM and polymer are shown in figure 2. CLM showed characteristic peaks of OCH3 stretching at 2880 cm-1, CH2 stretching at 2827 cm-1, C-CH3 stretching at 2943 cm-1, C=O stretching at 1727 cm-1, C-O bending at 1366 cm-1, C-N bending at 1171 cm-1. The spectra of both physical mixture and NPs did not show any prominent changes in the peak position in comparison to CLM spectra. These results revealed that there was no chemical interaction between CLM and CS.


Figure 2: FTIR spectra
(a) Clarithromycin, (b) physical mixture and (c) clarithromycinloaded NPs

The dissolution profile of intact CLM and selected CLM-loaded NPs are shown in figure 3. In vitro drug release studies was carried out in phosphate buffer (pH 6.8) for 48 h. Release profile of CLM from NPs could be divided into two phases: initial burst release of around 10 % at 1 h followed by slow release for 48 h. As the TPP ratio increased, release decreased due to tight bonding. As the CS concentration increased, release decreased at constant TPP concentration. These result showed that initial release during first 2 h was 14, 12, 11 and 8 % for F4, F5, F6 and F7, respectively. The burst release of drug could be due to dissolution of the surface drug that is poorly entrapped in polymer matrix, slow release is due to diffusion of drug present in the core of CS NPs.


Figure 3: In vitro dissolution profiles
In vitro dissolution profiles of clarithromycin-loaded chitosan NPs (-▲-) F4, (-■-) F5, (-♦-) F6 and (-●-) F7

From the results it was evident that all the formulations were more linear towards Higuchi model with R2 value ranging from 0.843 to 0.964 indicating that drug release mechanism was by diffusion. In Korsemeyer-Peppas plot, the slope value for all formulations was found to be less 0.5 indicating Fickian diffusion. Kinetic data is mentioned in Table 3.

Formulation code Zero Order First order Higuchi Korsemeyer-Peppas
R2 R2 R2 n value
F4 0.9095 0.8789 0.984 0.3050
F5 0.8434 0.8539 0.9691 0.4574
F6 0.9664 0.8854 0.9936 0.3512
F7 0.9299 0.8667 0.9832 0.2142

Table 3: Kinetic Data of Selected Formualtions

The SEM image of F4 (figure 4) was found to be uniform and roughly spherical and sub spherical in shape, separated from each other, suggesting possible stabilisation of the NPs due to positive surface charges.


Figure 4: SEM image of F4 formulation

Results of 6 mo stability studies showed that there was no change in the appearance, particle size, zeta potential and PDI, stored at refrigerator condition (F4, F5, F6, F7, F8). While at room temperature, there was agglomeration of particles. Thus, refrigerator condition is suitable for storage of CS NPs.

The mean MICs of NPs are shown in figure 5. The MIC of the CLM NPs was determined against a Gram-positive pathogens S. pneumoniae. The MIC values for the standard CLM solution was 32 μg/ml and for the CS formulations, F4, F5, F6 and F7, these were 8, 16, 32 and 32 μg/ml, respectively. Based on these results, it was observed that particle size and release of drug from formulation had influenced the MIC. F4 formulation showed lower particle size and greater release of CLM when compared to other formulations, hence, the MIC of F4 is lower than that of other formulations. Due to stability issues remaining formulations were not further evaluated.


Figure 5: MIC and zone of inhibition of clarithromycin and clarithromycin-loaded NPs
Bar diagrams represent minimum inhibitory concentration image and zone of inhibition in mm image of clarithromycin (CLM) and clarithromycin-loaded NPs F4, F5, F6 and F7

In vitro antibacterial activity of CLM NPs was determined by agar disc diffusion assay. Large and clear zones of inhibitions were observed around discs impregnated with CLM NPs, which clearly demonstrated the antibacterial effect of CLM NPs. The mean diameter of the inhibitory zones for F4 and F5 formulations was 27 and 29 mm, respectively which were greater than those of the remaining formulation and CLM, as shown in figure 5.

This paper described the preparation of NPs using a hydrophilic polymer, which is non-toxic and biocompatible. The present study demonstrated that CS NPs prepared by ionic gelation method can be used to load CLM. NPs with efficient CLM loading were obtained, the concentration of CS strongly influenced the particle size. The results showed that these NPs could be suitable for treatment of respiratory tract infections caused by S. pneumoniae.


The authors thank Calyx Chemicals and Pharmaceuticals Ltd., for providing CLM as gift sample for this work. Authors also thank to Dr. Divakar Goli, Principal, Acharya & B M Reddy College of Pharmacy, Bangalore for providing required facilities to carry out this research work.

Conflict of interest

The authors state that they have no conflicts of interest.