Institute of Pharmaceutical Technology, Sri Padmavathi Mahila Visvavidyalayam, (Women’s University), Tirupati, India
Email: [email protected]
Received: 28 Feb 2019, Revised and Accepted: 04 Jul 2019
Objective: Quercetin is therapeutically hampered because of its poor solubility. The present investigation was aimed to prepare quercetin loaded nanosponges topical gel to enhance the solubility and efficacy of the drug.
Methods: Quercetin nanosponges were prepared by emulsion solvent diffusion method. Developed nanosponges optimized by particle size, SEM, entrapment efficiency, FT-IR, DSC, P-XRD, In vitro studies. The optimized formulation of nanosponges was loaded into a topical gel and it was characterized by ex-vivo, in vivo Pharmacodynamic and kinetic studies.
Results: The particle size and zeta potential of optimized nanosponges were found to be 188.3 nm and-0.1mV. Surface morphology was studied using SEM Analysis which showed tiny sponge-like structure and entrapment efficiency was found to be 96.5 %. In vitro drug release of optimized nanosponges was found to be 98.6% for 7hours. Optimized nanosponges entrapped gel was prepared by using carbopol 934 and hydroxypropyl methylcellulose as gelling agents. The prepared nanogels were homogenous and ex-vivo skin permeation studies of the optimized nanosponges gel was found to be 98.1% for 5 h, quercetin loaded nanosponges has shown higher skin permeation efficiency (18.4µg/cm2±2.1) compared to pure quercetin gel. The pharmacokinetic and pharmacodynamic studies showed that the quercetin loaded nanosponges has shown more effective when compared to marketed formulation.
Conclusion: Quercetin loaded nanosponges gel has shown a significant increase in activity (p<0.05) compared to the marketed formulation (Voveran Emulgel).
Keywords: Nanosponges, Nanosponges gel, Quercetin, In vitro, Ex-vivo studies, In vivo studies
© 2019 The Authors. Published by Innovare Academic Sciences Pvt Ltd. This is an open-access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/)
The plant and plant parts are used for therapeutic properties like Dacus carota, Ocimum sanctum, Curcuma domestica valet on, Glycyrrhiza glabra, Foeniculum vulgar, Cuscuta reflexa and Withinia sommifera were known as the best examples for anti-inflammatory, antidiabetic, and anti-hypercholesterolemia [Soon am park et al.; 2013, Wang Q et al.;2018]. Flavonoids are a group of plant metabolites found in a variety of fruits and vegetables, which are 15 carbon atom phenolic molecules. Quercetin is one of the vital bioflavonoid present in more than twenty plant materials which is known for its therapeutic activities like anti-inflammatory, antihypertensive, antidiabetic, antioxidant and anti-obesity [Qi Tan, Weidong Liu, et al.;2011]. Quercetin name was derived from the Latin word quercetum means oak forest belonging to the class flavanols. Quercetin is chemically 2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxychromen-4-one, having one OH group attached at positions 3, 5, 7, 31, and 41 positions [Soheirn. abdel rehaman et al. 2014]. Quercetin is yellow in color which is sparingly soluble in water and completely soluble in alcohol, which belongs to BCS class II drugs [Chen-Yu G et al.; 2012]. It is also available as an abundant dietary supplement present in the red grapes, onions, buckwheat, bark, olive oil, green tea, red wine, cranberries [Gulian quan et al.:2015]. Quercetin has a most remarkable property of anti-inflammatory conditions as it stops the formation of prostaglandins, cyclooxygenase (COX) as well as histamine release. Quercetin is mostly consumed orally, but the drawback is that it has low oral bioavailability . The absorption of quercetin was low in the gastrointestinal tract due to its poor solubility. Quercetin was enzymatically hydrolyzed and it was glucuronidated or converted into the sulfated form of quercetin when taken orally . The bioavailability of this quercetin was nearly 44 % when taken orally because most of the drug metabolized by the liver and is eliminated from the intestinal cells through an efflux mechanism . So the topical drug delivery system has the advantage to overcome these problems . The structure and composition of the drug were the major barriers for this type, but the formulation of the polymer type drug delivery can overcome this problem [10, 11]. Nanosponge has a 3-dimensional structure with tiny channels and mesh-like structure on the surface, when the solution is mixed with the polymers it forms a mesh-like structure, with naturally biodegradable polymer as the backbone which results in the formation of pockets like structure in which drug can be loaded . Physically these nanosponges are in the form of dry powder which can be formulated as orally, topically and parentally. A wide variety of drugs can be loaded into the nanosponges but the drug molecular weight should be less than 400 daltons . Nanosponges due to its nano size can be successfully incorporated into the topical gel, effectively releases the drug with increased stability, bypasses the first pass metabolism and reduces the gastric irritation. Due to its small size, they can freely circulate into the blood until they get attached to the specific target site. Hence the objective of the present study is to increase the solubility of poorly aqueous soluble quercetin by formulating quercetin into nanosponges. Quercetin containing nanosponges loaded into the gel was characterized by in vitro drug release, in vivo pharmacokinetic and pharmacodynamic studies.
Quercetin, Ethylcellulose, Polyvinyl alcohol was purchased from SD. Fine-chemicals Ltd, Dichloromethane was purchased from Merck limited, Mumbai, Hydroxypropyl methylcellulose (HPMC), Carbopol 934, HPLC methanol was purchased from HiMedia. Triethanolamine, Glycerine and Methylparaben and Propylparaben have purchased from Merck limited, Mumbai. Microorganisms (Staphylococcus aureus, E. coli, Proteus vulgaris, Bacillus subtilis) obtained from HiMedia.
Preparation of quercetin-loaded nanosponges
Quercetin loaded nanosponges were formulated by using the emulsion solvent diffusion method using ethyl cellulose as polymer and quercetin as a drug. Required quantities of the drug and polymer were added into the solvent dichloromethane and mixed well. The above solution was added into the external aqueous phase containing required quantities of polyvinyl alcohol and 150 ml of water [14, 15] in a continuous stirring process at 1200 rpm for 30 min on a magnetic stirrer. The formed nanosponges were filtered and dried in the oven. The formulation composition of quercetin-loaded nanosponges was given in table 1.
Table 1: Formulation composition of quercetin-loaded nanosponges
|S. No.||Formulation code||Drug: Ethyl cellulose (mg)||PVA(mg)||Water(ml)|
Quercetin loaded nanosponges gel
A nanosponge showing a high percentage of drug release F4 was converted into a topical gel using polymers carbopol 934 and hydroxypropyl methylcellulose (HPMC). Carbopol934 and hydroxypropyl methylcellulose  were weighed and soaked for 24h in the required quantity of water and stirred using a mechanical stirrer at 1000 rpm [16, 17]. In the above-formed gel required quantities of glycerin, methylparaben, propylparaben, and triethanolamine were added with continuous and slow stirring for 30 min. Composition of quercetin-loaded nanosponges gel was given in table 2.
Table 2: The composition of topical gels using different concentrations of polymers (Carbopol 934 and HPMC)
|S. No.||Formulation code||Composition||Ratios of polymers|
Evaluation of quercetin-loaded nanosponges
Scanning electron microscopy
Scanning electron microscopy (JOEL-JSM-IT500) was used for surface morphology and structural elucidation of the formed nanosponges. The formed images were captured, particles size and surface morphology were studied [18, 19].
Particle size and zeta potential
The particle size and zeta potential of the formed quercetin loaded nanosponges were determined by using the Horiba zeta sizer . The dispersion was mixed, thoroughly diluted with water and then analyzed. Each sample was analyzed in triplicates and the average of the three values was noted.
Differential scanning calorimeter
Differential scanning calorimeter (Metler Toledo, Switzerland) studies were done to find out the chemical compatibility between the polymers and drug. For this, the melting point of the pure drug was compared to the melting point of the drug in the formulation [21, 22]. The instrument was calibrated with tin as standard material. 5 mg of the sample was taken in an aluminum crucible and heated at a rate of 10 °C in the temperature range of 100-300 °C.
X-ray diffraction studies
The crystalline nature of the drug in the pure quercetin and quercetin loaded nanosponges was evaluated by using these P-XRD studies [23, 24]. Powder X-ray diffractometer (Regaku-mini plus 500) was done by using k-beta (x2) filtered, Cu–k, alpha radiation, and at a voltage of 30kv, and 15 mA.
Drug compatibility with excipients
Drug compatibility study of pure quercetin, ethylcellulose, and nanosponges formulated using quercetin was carried out by potassium bromide pellets by applying pressure of 100 kg to form a pellet [25, 26]. They formed pellet was scanned in the region of 4000-600 cm-1 using (FTS300 Spectrophotometer (Glab), Canton, MA).
The amount of quercetin present in the quercetin loaded nanosponges was determined by taking 10 mg of quercetin-loaded nanosponges in 10 ml of phosphate buffer pH 7.4 and kept aside for 24h and then after 24h the solution was stirred using a magnetic stirrer (Remi equipment, Mumbai) at 1000 rpm for 30 min and filtered. The filtered solution absorbance was measured by using a UV visible spectrophotometer (Shimadzu, Japan) at 372 nm.
In vitro drug release studies
The release rates of quercetin-loaded nanosponges were investigated using the dialysis membrane, which is having a pore size of 2.4 nm and a molecular weight of 12,000-14,000 daltons was used. This dialysis membrane was soaked 12 h before using in distilled water. 100 ml of phosphate buffer of pH 7.4 was taken in a beaker [26, 27]. The beaker was placed on a magnetic stirrer (Remi equipment, Mumbai) at 100 rpm and at a temperature of 37 °C. An aliquot of 5 ml of the sample was taken at regular intervals; an equal amount of fresh buffer was replaced in the beaker to maintain sink conditions . The samples were measured using UV-visible spectrophotometer (Shimadzu, Japan) at a wavelength of 372 nm.
Characterization of quercetin-loaded nanosponges gel
Physical examination of gel
The formed quercetin loaded nanosponges gel was physically tested for the presence of any aggregates and uniformity by visually after it was stored in a container.
The pH of the gel
The pH of the quercetin loaded nanosponges gel was determined by using a digital pH meter (Remi equipment, Mumbai).
The viscosity of the gel was determined by Brookfield LV Viscometer . The prepared quercetin loaded nanosponges gel of 5g was taken in a beaker and by selecting spindle number 64 the viscosity of the gel was noted.
Percentage of drug content
10 mg of the gel was placed in 10 ml of phosphate buffer of pH 7.4 and the solution was kept aside for 24h and the solution was stirred on a magnetic stirrer (Remi equipment, Mumbai) for 30 min and filtered . The absorbance of a filtered solution was measured by using a UV spectrophotometer (Shimadzu, Japan) at 372 nm.
Antimicrobial activity by a zone of inhibition method
The 20 ml of sterilized broth was taken individually into four Petri dishes and inoculated with four different types of bacteria (Staphylococcus aureus, E. coli, Proteus vulgaris, Bacillus subtilis). The subcultured bacteria were spread on the solidified nutrient broth and four wells were kept on the solidified agar medium of 6 mm to place quercetin loaded nanosponges gel . The Petri dishes were incubated at 35-37 °C for 24h. Then the zone of inhibition of microbial growth was measured using the scale in centimeters.
Ex-vivo skin permeation studies and flux value determination
The ex-vivo skin permeation studies were performed using goatskin in the modified Franz diffusion cell. Goatskin, which was brought from a local slaughterhouse, the hair on the goatskin was removed by using the razor and the skin was wiped with isopropyl alcohol. Goatskin was mounted in between donor and receptor compartment. The donor compartment of the diffusion cell was placed with 500 mg of quercetin-loaded nanosponges gel and the receptor compartment was filled with phosphate buffer of pH 7.4 [31, 32]. The entire setting was placed on the magnetic stirrer (Remi equipment, Mumbai) with an rpm of 100 and temperature 37 °C was maintained. Then aliquot of 5 ml of the sample was taken at regular intervals of time 0,0.25,0.5,1,2,3,4,6,8,12,24 h and a freshly prepared buffer of 5 ml was placed back into the receptor compartment to maintain the sink conditions. The samples were measured using the UV spectrophotometer (Shimadzu, Japan) at 372 nm. The obtained results were subjected for the skin permeation parameters like flux, permeation coefficient, lag time and diffusion coefficient by plotting a graph between percentage cumulative drug release on the y-axis and time on the x-axis. The data obtained were also subjected to mathematical models like zero order, first order, Higuchi, Korsmeyer-peppas model .
According to the International Council for Harmonization of technical requirements for pharmaceutical for human use (ICH) guidelines, the stability studies of the prepared quercetin loaded nanosponges gel and quercetin pure gel were conducted. The prepared gels were studied under two variations 25±2 °C (refrigerator temperature) and 40±2 °C (accelerated stability condition) for a period of three months [34, 35]. Parameters like pH, drug content, homogeneity, in vitro drug release studies were conducted.
In vivo anti-inflammatory activity
Anti-inflammatory activity studies were carried in male Wistar rats. Animals were procured from Sri Venkateswara Enterprises, Bangalore. The animals were housed under the standard environmental conditions like humidity (55±5%) ambient temperature (25±1 °C) and 12/12h dark and light cycles. All the protocols and experimental procedures which were used for the anti-inflammatory study were as per the guidelines of a committee for the purpose of control and supervision of experiments on animals (CPCSEA) and which was approved by institutional animal ethics committee bearing Reg. No.1677/PO/Re/ S/2012/CPCSEA/IAEC/25 dt.3.05.2018. The in vivo pharmaco-dynamic activity was performed to find out the efficacy of the quercetin loaded nanosponges gel in animals. For this study male Wistar albino rats were used. They were grouped into five and all the animals were kept at an optimum weight of 150-200g and age of 10-12 w [35, 36]. Group I was treated as the control without any treatment, Group II was normal with only carrageenan (1%w/v) inducer, Group III was treated with marketed Voveran gel, Group IV with pure quercetin gel and Group V with quercetin loaded nanosponges gel. Carrageenan solution (1%w/v in normal solution) was used as an inducer to produce inflammation. The animals were kept in observation for 10 min for any behavioral changes. The thickness of the paw was measured (mm) at regular time intervals as 0,30 min,1hr,2hr,3hr,4hr after inducing carrageenan to plantar region of the left hind paw, quercetin loaded nanosponges gel and pure quercetin gel was applied to the sole of the paw where the inflammation was induced. The paw volume was noted using plethysmometer . The percentage of inhibition of paw volume of rats was calculated by using the formula.
% inhibition of edema = V control- V test/V control
In vivo pharmacokinetic study
Pharmacokinetic parameters were done to estimate the concentration of the drug in the blood. Three groups of rats were taken each group containing randomly six rats, which were housed under normal conditions; the rats were fastened overnight before the experiment with free access to water. The study was conducted with three groups Group I control, Group II for the pure quercetin gel and Group III for quercetin loaded nanosponges gel. Drug concentration was estimated by RP-HPLC method using methanol: orthophosphoric acid (65:35) as a mobile phase, with glibenclamide an internal standard and C18 as a column having dimensions (4.6x250 mm, 5 µm) (Shimadzu, Japan) with a flow rate of 0.8 ml/min [38,39]. Blood samples were collected at different time intervals from male Wistar albino rats from retro-orbital into Eppendorf tubes containing sodium citrate as an anticoagulant.
Treatment of plasma samples
The working solution containing the plasma samples spiked with various concentrations of the quercetin with a fixed amount of internal standard was transferred into a clean centrifugation tube. To this 400 µl of methanol was added which acts as a protein precipitant and the solution was vortex mixed and centrifuged at 5000 rpm (Remi equipment, Mumbai) for five minutes. The supernatant solution was separated and injected into an HPLC column using a Hamilton syringe and analyzed at the wavelength of 372 nm .
Scanning electron microscopy
The photographs of quercetin-loaded nanosponges using scanning electron microscope are shown in fig. 1(a) to fig. 1(c). The formed nanosponges were spherical in shape with tiny mesh-like structure. The size and shape were unaffected even after encapsulating the quercetin drug in the nanosponges.
Particle size and zeta potential
All measurements were performed in triplicates for measuring the size and zeta potential of the particles at a temperature of 25±2 °C . The dispersions were diluted by using double distilled water to ensure that scattering of light was within the range of sensitivity. The average particle size of the optimized nanosponges was found to be 188.3 nm with a polydispersity index of 0.13, which indicates that it has a homogenous particle distribution. Homogeneity of the particles was measured by the polydispersity index, which varies from 0 to 1 the value closer to zero indicates more homology between the particles. Zeta potential of the optimized nanosponges was found to be-0.1mV. This indicates that the formed quercetin loaded nanosponges were stable through electrostatic repulsion and thereby avoiding the repulsion between the particles. The concentration of the polymer plays an important role in the size of the nanosponges from F1 to F5 (1.1 nm, 17.9 nm, 18.2 nm, 188.3 nm, 289.9 nm) as the concentration of the polymer increases with respect to the drug the size of the nanosponges increases. Thus polymer and drug ratio plays an important role in particle size analysis. The zeta size fig. 2(a) and potential for F1 to F5 (-22.0mV,-11.9mV,-18.3mV,-0.1mV,-3.6mV) was shown in fig. 2(b).
Fig. (1a, 1b, 1c): Scanning electron microscopy images
Fig. (2a, 2b) Zeta size and zeta potential
Differential scanning calorimetry (DSC)
The Differential scanning calorimetry (DSC) thermograms showed that compatibility between polymer and drug. The thermograms showed the melting point range of 303.6 °C for pure quercetin drug and 297.85 °C for the quercetin loaded nanosponges. Both the peaks in thermogram are same, which showed that quercetin loaded nanosponges have the same crystalline state of quercetin in pure form . The DSC thermograms of pure quercetin fig. 3 (a) and quercetin loaded nanosponges were shown in the fig. 3(b).
X-Ray diffraction studies
P-X-ray diffractograms of the pure quercetin and the quercetin loaded nanosponges were taken and analyzed . The diffractograms of the pure quercetin showed 2Ө values as follows (12.46,14.14,15.73,16.43,18.14,19.9,20.8,25.05,27.8,28.4,30.8). This implies that the drug has high crystalline nature and the quercetin loaded nanosponges also show similar 2Ɵ values in quercetin loaded nanosponges, they both exhibit the same intense sharp peaks. Which indicates the crystalline nature of the quercetin was not lost in the quercetin loaded nanosponges when compared to the pure form. The slight difference is only due to the reduction in size, which implicates the enhancement in the dissolution and solubility of the nanosponges. X-ray diffractogram of pure quercetin fig. 4(a) and quercetin nanosponges were shown in fig. 4(b).
Drug-excipient compatibility study
Fourier infrared spectroscopy (FT-IR) was one of the most quickened and efficient identifiers of the encapsulated chemical molecules . The characteristic peak intensities of pure quercetin molecules are as follows it shows O-H stretching at 3400 cm-1,=C-H stretch at 2930 cm-1, C=O stretching at 1680 cm-1, aromatic C=C stretch at 1510 cm-1 and 1610 cm-1 and aromatic C-O stretch at1220 cm-1. The pure quercetin drug and the quercetin loaded nanosponges have shown the same characteristic peaks which implicate there is no chemical interaction between the polymer and drug. An (FT-IR) Fourier infrared spectroscopy spectrum of pure quercetin fig. 5(a), ethylcellulose fig. 5(b) and optimized quercetin nanosponges were shown in fig. 5(c).
Quercetin pure drug (3a)
Quercetin loaded nanosponges (3b)
Fig. (3a, 3b): DSC differential scanning calorimetry thermograms
Diffractogram of pure quercetin (4a)
Diffractogram of quercetin loaded nanosponges (4b)
Fig. 4: X-ray diffractogram of pure quercetin (4a), quercetin loaded nanosponges (4b)
Entrapment efficiency was measured for all the formulations from F1-F9 the amount of drug entrapped in the nanosponges was found to be in the range of 90-97% from F1-F5 as the drug entrapped was reduced from F6-F9 this is because as the volume of water and the quantity of polyvinyl alcohol was increased the nanosponges formed were irregular in size and shape and lead to the formation of aggregates and entrapment efficiency is also decreased. Formulations from F6-F9 were discarded for further studies as their entrapment efficiency is very low. The entrapment efficiency of various formulations from F1-F9 was tabulated in table 3.
Table 3: Entrapment efficiency of quercetin loaded nanosponges
|S. No.||Formulation||Entrapment efficiency (%)||Zeta size(nm)||Zeta potential (mV)|
The values are given as mean±SD, n=3
Pure quercetin (5a)
Ethyl cellulose (5b)
Quercetin loaded nanosponges (5c)
Fig. (5a, 5b, 5c): Fourier transform infrared spectroscopy
In vitro release studies
In vitro release studies were done by using a phosphate buffer of pH 7.4. All the formulations of nanosponges were subjected to in vitro drug release studies by using a dialysis membrane. The formulation F4 has shown the maximum cumulative percentage of drug release 98.6% for 7h; the F4 has shown the highest release in 7 h when compared to all other formulations. The cumulative drug release profile was obtained by taking time on x-axis and % cumulative percent of drug release on the y-axis . The release studies were performed for all the formulations F0 (Pure drug), F1, F2, F3, F4, F5. The amount of drug release was found to be 98% for formulation F4 in 7h, for F3 it is 90.5%in 6h, F2 70%, F1 63.5%, F5 79.4% and pure drug 39% at the end of 7h. When compared from F0-F5, the F4 has shown the highest drug release when compared to all other formulations this may be accredited because of the high solubility of the drug. The optimized F4 formulation followed the zero-order drug release profile. Percentage cumulative drug release profile from F0-F5 was given fig. 6. The concentration of polymer played an important role in the release characteristics.
Fig. 6: Comparative in vitro dissolution profile of different quercetin loaded nanosponges formulations, mean±SD, n=3
Characterization of quercetin-loaded nanosponges of gels
The prepared gels were homogenous and they exhibit no aggregates, they were transparent in nature and smooth in appearance. The physicochemical properties like pH, viscosity and drug content of the formulated gels were calculated and tabulated in table 4 . All the prepared gels from X1-X6 has shown a pH range of 6.8-7.0. This is considered as acceptable ranges to reduce the skin irritation. The viscosity of the gels plays an important role in the extrudability and the release of the drug. Gels with high viscosity may not extrude that easily from the tube and low viscous gels may flow easily from the tube that is the reason there should be an optimum viscosity for the gels. The viscosity of the formed gels ranges from 8,300-48,700cps, the viscosity variation was due to change in the concentrations of the polymers (carbapol934 and hydroxypropyl methylcellulose) as the concentration of the polymer hydroxyl propyl methyl cellulose increased there was an increase in the viscosity of the gel. The drug content of the gels from X1-X6 was found to be in the range 95-98% and given in table 4.
Table 4: Evaluation of physicochemical properties of quercetin loaded nanosponges gel
|S. No.||Carbopol 934:HPMC||Viscosity (cps)||Appearance||Drug content (%)||pH|
The values are given as mean±SD, n=3
Staphylo coccus aureus Bacillus subtilis Proteous vulgaris Escherechia coli
Fig. 7: Antimicrobial effect of quercetin-loaded nanosponges gel against bacteria Staphylococcus aureus, Bacillus subtilis, Proteus vulgaris, Escherichia coli studies by a zone of inhibition method
Antimicrobial activity by a zone of inhibition method
This study was determined by using the bacterial strains Staphylococcus aureus, Escherichia coli, Proteus vulgaris, Bacillus subtilis obtained from HiMedia. The antimicrobial activity was carried out for optimized formulation X1 quercetin loaded nanosponges gel . The gel showed that they were microbiologically inert towards the bacterial strains. The zone of inhibition was reported for Staphylococcus aureus was 2.9 cm2, Escherichia coli was 3.2 cm2, Proteus vulgaris was 3.0 cm2 and Bacillus subtilis was 3.4 cm2 were represented in fig. 7.
Ex-vivo skin permeation studies and flux value determination
The quercetin loaded nanosponges gel and pure quercetin gel were subjected to ex-vivo skin permeation studies using goatskin. The amount of drug permeated through the goat skin into the receptor compartment was measured by taking the samples at regular intervals of time . Among all the formulations, the cumulative percent of drug permeated through the skin for the optimized X1 gel loaded with F4 formulation was found to be 95% for four hours and the cumulative percentage of drug release for pure quercetin gel X6 it showed 50% for 24h. The cumulative percent of drug diffused was given in (fig. 8). Highest ex-vivo skin permeation from X1 may be attributed due to the increased solubility of the drug within the gel matrix into the test media. The permeation parameters were calculated from a graph by plotting the cumulative percent drug release on the y-axis versus time on the x-axis. The flux was calculated from the slope of the graph and was found as18.4µg/cm2/h for quercetin nanosponges and 10.3µg/cm2/h for pure quercetin and the flux value was more for quercetin nanosponges than pure quercetin gel. The lag time, permeation coefficient, diffusion coefficient was calculated for quercetin nanosponges gel and pure celecoxib gel and the values are as follows (0.03, 0.98h) (3.12, 2.1 kg) (0.0234, 0.16 mol/m3). The data obtained from the ex-vivo skin permeation studies were subjected to the kinetic data modeling to find out the release mechanism studies from the quercetin loaded nanosponges gel. From the fig. 8 and it was found that the nanosponges loaded quercetin gel release follows zero-order mechanism which governs the release of the drug. From the equation R2=0.99, the drug release follows the Higuchi model which indicates it follows the diffusion mechanism (fickian n<0.5). The quercetin loaded nanosponges gel showed the best release when compared to pure quercetin gel.
The studies were performed as per ICH guidelines for the optimized F4 formulation which was converted into a polymer-based topical gel. The physical appearance of this gel was observed it does not show any variations and they appear smooth, uniform distribution without any aggregate formation for a period of three months. This implies that the formed quercetin loaded nanosponges gel and pure quercetin gel were stable. The percentage of drug content, in vitro drug release studies, shows no significant change in the drug content and percent of drug release. It was concluded that optimized formulation (X1) and pure quercetin gel were stable during the period of 3 mo of stability studies. The results were tabulated in table 5.
Fig. 8: Ex-vivo skin permeation studies of pure quercetin gel and quercetin loaded nanosponges gel
Table 5: Stability studies for the optimized quercetin loaded nanosponges gel
|Temperatures||25±2 °C||40±2 °C|
|Time in days||pH||Drug content||Homogeneity||In vitro drug release||pH||Drug content||Homogeneity||In vitro drug release|
|Freshly prepared||7.0±0.1||98.5||Smooth and transparent||98.6 %||7.0±0.2||97.5||Smooth and transparent||98.6%|
|30 d||7.0±0.2||98.5||Smooth and transparent||97.2 %||7.0±02||97.5||Smooth and transparent||97.2%|
|60 d||6.9±0.1||97.8||Smooth and transparent||97.2 %||6.8±02||96.9||Smooth and transparent||97.2%|
|90 d||6.8±0.2||97.6||Smooth and transparent||97.0 %||6.7±0.3||96.9||Smooth and transparent||97.0%|
The values are given as mean±SD, n=3.
Anti-inflammatory activity was carried out using carrageenan-induced paw edema method. For quercetin loaded nanosponges gel and pure quercetin gel. For this study male, Wistar albino rats were selected which were grouped into five, each group containing six animals, weighing 150-200g. The anti-inflammatory test results are as follows the percentage inhibition of paw volume for Group III was 76.2%, Group IV 40.4% and Group V 96.4% which is indicated in the fig. 9. From the results, it is evident that there is a significant difference (*p<0.005) between the pure quercetin gel and quercetin loaded nanosponges gel. The data were subjected to ANOVA (Graph Pad Prism, software), it was found that the F ratio was 3.0 (fc<ft). So there is a significant difference between the pure quercetin and quercetin loaded nanosponges gel. Quercetin loaded nanosponges gel shows effective inhibition when compared to the marketed gel and pure quercetin gel (quercetin loaded nanosponges gel>marketed gel>pure quercetin gel).
Fig. 9: Percent edema inhibition of quercetin loaded nanosponges gel, marketed gel and pure quercetin gel, P<0.05 compared with disease control values were expressed as mean±SEM observation, ANOVA (FC>ft) there is a significant difference
The current analytical method as mentioned above was applied for the study of pharmacokinetic parameters of pure quercetin and quercetin loaded nanosponges gel. The chromatogram of quercetin showing retention time of 7.6 having internal standard (glibenclamide) peak at 3.1 was shown in fig. 10. The mean plasma concentration versus time profile of pure quercetin gel and quercetin loaded nanosponges gel after topical administration of both the gels were summarized as follows C max (15.5, 27.05µg/ml), T max (4,2h), t1/2(10, 9.7h), AUC (90,126 µg/ml) as follows. The mean plasma concentration (AUC), C max, T max, t1/2 was statistically significant (*p<0.05) when compared to the pure quercetin gel and quercetin loaded nanosponges gel. Pure quercetin gel and quercetin loaded nanosponges gel which is given fig. 11. Quercetin loaded nanosponges gel has shown fast absorption with C max (27.05µg/ml) and more AUC (126 µg/ml) as it contains the tiny size of nanosponges (188.3 nm) which makes the drug more permeable when compared to pure quercetin gel through the skin.
Fig. 10: HPLC chromatogram of quercetin
Fig. 11: Plasma concentration time profile of pure quercetin gel and quercetin nanosponges gel in rats n=6, Data presented as mean±SD
From above all the results it can be concluded that the nanosponges prepared with ethyl cellulose and drug quercetin by emulsion solvent diffusion method were effectively incorporated into the topical gel. The quercetin loaded nanosponges gel showed more for anti-inflammatory activity when compared to pure quercetin gel and marketed Voveran Emulgel.
All the authors have contributed equally
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