XYLOGLUCAN CONJUGATED FUNCTIONALIZED GRAPHENE OXIDE AS A NANO CARRIER SYSTEM FOR pH RESPONSIVE TARGETED DRUG DELIVERY OF FUCOIDAN

Objective: Marine polysaccharides are materializing in the field of biomedicine owing to its promising properties, including high biocompatibility, excellent biodegradability, nontoxic nature, abundance and low cost. Fucoidan (FU), a sulphated marine polysaccharide extracted from brown seaweed, shows a promising application prospect as an anticancer model drug. In order to enhance the stability, biocompatibility and drug loading capacity, xyloglucan was chosen as a targeting ligand, conjugated onto the surface of chitosan functionalized graphene oxide for targeted delivery of fucoidan. Methods: Firstly, Graphene oxide (GO) was prepared by modified Hummer’s method and functionalized with chitosan (CS) via amidation process, further conjugated with xyloglucan (XG). The resulting conjugate, GO-CS-XG, was used to deliver fucoidan through a nanocarrier drug delivery method. The developed GO-CS-XG-FU nanosystem was analyzed for its physiochemical characterization, morphology, hemolytic activity, anti- inflammatory and anticancer activity. Results: The FU loading efficiency and capacity were 75.7% and 83.4%, respectively. XG ligands on the nanoparticle may lead the nanoparticles to actively target cancer cells. Hemolytic activity of the FU-loaded GO-CS-XG nanosystem shows negligible activity, thus making it a potential candidate for biomedical applications. In vitro drug release analysis of FU from GO-CS-XG was lesser at physiological pH but under acidic conditions, it was significantly increased. Results of in vitro cell viability studies indicate that the efficiency of fucoidan was improved upon conjugation with the nanosystem (GO-CS-XG) against human histiocytic lymphoma (U 937) cell line. Conclusion: As a result, we propose a new multifunctional graphene-based targeted platform by using xyloglucan polysaccharide as targeting nanomaterial for pH-responsive anticancer drug delivery with high efficacy. The purpose of the study was to functionalize the GO surface with CS via an amide bond. A novel multifunctional platform was designed by conjugating XG onto the surface of GO-CS. GO-CS-XG conjugate system was structurally and morphologically analyzed by UV-Visible, FT-IR, TEM, SEM and zeta potential. FU was used as an anti-tumor model drug to evaluate drug loading and release properties, as well as the effect of pH. In addition, the anticancer activity of pH-responsive FU loaded drug delivery systems was evaluated by MTT assay.


INTRODUCTION
Drug conjugation to macromolecular carriers has emerged as a viable technique in the field of drug delivery systems in recent years. Because of their biocompatibility, biodegradability, non-toxicity, and simplicity of availability from natural resources, polysaccharides have attracted increased interest in drug delivery methods. Polysaccharides-based drug delivery systems are fascinating due to their numerous advantages such as prolonged half-life, solubility of drugs, improved pharmacokinetics, increased drug accumulation in tumor tissues via enhanced permeability and retention effect [1][2][3].
The most salient derivative of graphene is graphene oxide (GO) which consists of a wide range of oxygen-containing functional groups such as carboxyl, hydroxyl and epoxy groups on its surface. Due to its enormous surface area, π-stacking, and hydrophobic interactions, GO has attracted interest as a suitable drug carrier [4]. However, GO's dispersion in biological solution is limited, resulting in the development of aggregates, limiting its use in biomedical applications. Therefore, functionalization of GO is necessary in order to build an efficient nanocarrier system to improve its stability, biocompatibility and more prominently, interaction with the target molecules to release the drugs in a controlled way at the specific target site [5].
For example, chitosan (CS) is widely used in the study of GO-based targeted drug delivery systems due to its prominent properties such as high biocompatibility, biodegradability, bacteriostatic action, nontoxic and abundance in nature. Moreover, the positive nature of CS with free amino groups and hydroxyl groups on the polymeric chains made more beneficial for surface adhesion and enables crosslinking with the carboxyl groups of GO on its surface [6]. Thus chitosan-functionalized graphene oxide (GO-CS) nanocarrier enables good biocompatibility and bioadhesive property, which enables the prolonged retention onto the targeted substrate.
Xyloglucan (XG) is also a natural polysaccharide obtained from tamarind seeds. It is composed of a (1 → 4)-linked β-D-glucan backbone chain at O-6 position of D-glucopyranosyl residues with α-D-xylopyranose or with 2-O-β-D-galactopyranosyl-α-D-xylopyranose [7]. XG has gained considerable attention to carry out the work because of its striking properties, which include high viscosity, broad pH tolerance, non-carcinogenicity, biocompatibility, mucoadhesivity in situ gelation and high drug loading capacity [8]. Due to these versatile properties, XG is considered to be an attractive and functional polymer which is particularly suitable as a nanocarrier for drug delivery systems [9]. However, until now, no targeted drug delivery systems based on xyloglucan as targeting ligand have been synthesized. Therefore, we made XG a polysaccharide of choice as a targeting ligand in the chitosan functionalized GO drug delivery systems. Sulphated polysaccharides extracted from marine algae are excellent drug candidates for pharmaceutical applications. Over the past years, many researchers have investigated on sulphated polysaccharides-based nanomaterials for biomedical application such as antimicrobial activity, drug delivery, gene delivery, tissue engineering, wound dressing and cancer therapy [10,11]. Fucoidan (FU), a naturally occuring sulphated polysaccharides mainly comprised of fucose residues and sulphate groups extracted from marine brown seaweed Sargassum wightii. It has various biological properties such as antiviral, anticoagulant, anti-tumor, anti-inflammatory, antioxidant, immunomodulating and anticoagulant [12,13]. A vast number of studies have been conducted on the use of fucoidan as a reducing and stabilizing agent in the biosynthesis of metal nanoparticles. However, the use of FU as a model anticancer drug for GO nano carrier-based targeted drug delivery system still remain undetected.
The purpose of the study was to functionalize the GO surface with CS via an amide bond. A novel multifunctional platform was designed by conjugating XG onto the surface of GO-CS. GO-CS-XG conjugate system was structurally and morphologically analyzed by UV-Visible, FT-IR, TEM, SEM and zeta potential. FU was used as an anti-tumor model drug to evaluate drug loading and release properties, as well as the effect of pH. In addition, the anticancer activity of pH-responsive FU loaded drug delivery systems was evaluated by MTT assay.

Collection of seaweed material
The brown seaweed sargassum wightii was collected from marine water seashore was identified and authenticated by Dr. M. Ganesan, Scientist of Marine Algal Research Station, CSMCRI (Central Salt and Marine chemicals Research Institute) Mandapam Camp, Tamil Nadu, India. The seaweed was washed thoroughly with tap water and distilled water to remove extraneous materials and shade-dried for 5 d and oven-dried at 60 °C until a constant weight was obtained, then was grind into a fine powder using the electric mixer and stored at 4 °C for future use.

Extraction of fucoidan
Extraction of fucoidan from brown seaweed Sargassum wightii was done by the accompanying methods [14,15] with some modification. Algal powder was mixed with 100 ml of 85% ethanol and stirred at room temperature for 12h. In order to remove pigments, proteins and lipids, then centrifuged at 970g for 10 min. The resultant residue was then washed with acetone and left overnight to dry at room temperature. 10 gm of the algal sediment was then collected and mixed with distilled water and placed at 70 °C on a hot plate with constant stirring for 1h. The solutions were then centrifuged at 3800g for 10 min to this 1% CaCl2 was added in order to precipitate alginates. The solutions were then centrifuged at 3273 g for 10 min to remove unwanted impurities. The supernatant was collected and 95% ethanol was added until a final concentration of 70% was reached and stored at 4 °C overnight in order to obtain ethanol-precipitated fucoidan, was then recovered by centrifugation at 3800g for 30 min, and the precipitated fucoidan was lyophilized and stored for further analysis.

Synthesis of graphene oxide (GO)
Graphene oxide (GO) was synthesized from graphite powder according to a modified Hummer's method [16,17]. Briefly, graphite powder was poured into the cold solution of concentrated H2So4 and NaNO3. Then, KMno4 was gradually added to this solution upon continuous stirring under ice bath medium maintaining a temperature of 10-15 °C. The reaction mixture was then stirred at 40 °C for 24h. The reaction was terminated at room temperature by the addition of distilled water and H2O2 (30%). The resultant solution was washed several times with 10% dilute HCl and distilled water in order to remove metal ions and centrifuged at 800 rpm for 20 min. The obtained graphite oxide powder was sonicated for 1h to yield nanographene oxide. The resulting GO was freeze-dried to obtain as loose powder and stored for further use.

CS functionalized GO
Chitosan was attached on to the surface of GO via an amidation process [18] to form GO-CS. In brief, GO (1 mg/ml, 50 ml) was first sonicated in distilled water (50 ml) for 30 min, EDC (100 mg) and NHS (75 mg) both are dissolved in water (30 ml) were added to this GO dispersion under constant stirring in order to activate the carboxyl residues of GO and kept under constant stirring. To this mixture chitosan in acetic acid (75 ml) was added dropwise and stirred at room temperature for 24h. The reacted product was centrifuged and washed several times with distilled water to remove the unreacted CS. The CS functionalized GO conjugate was freeze-dried and stored for further use.

Synthesis of GO-CS-XG conjugate
GO-CS-XG was synthesized by conjugating XG onto the surface of the intermediate product GO-CS. Initially, GO-CS (100 mg) was dispersed in 100 ml of distilled water and subjected to sonication followed by the addition of XG solution (50 ml). The mixture was kept under magnetic stirring for 24 h at room temperature, then centrifuged and freeze-dried, resulting in the formation of GO-CS-XG.

Loading of FU onto GO-CS-XG conjugate
FU was loaded on to the GO-CS-XG system by simply mixing FU to GO-CS-XG solution followed by overnight stirring. The solution was centrifuged twice at 8000 rpm for 20 min to remove the unbound FU retained in the supernatant. The final product GO-CS-XG-FU was lyophilized and stored for further use.

FU loading capacity (%)
Mass of loaded FU Mass of nanocarrier ×100

Characterization techniques
UV-Visible absorption spectra for the samples were performed using Perkin Elmer UV-Vis spectrophotometer (Model: Lambda 35). The samples were placed in a quartz cell. UV-Visible absorption spectra for these samples scanned in the wavelength ranging from 200 to 800 nm. The FTIR analysis was done with a Perkin Elmer (spectrum two model) Fourier Transform Infrared spectrophotometer over the range of 400-4000 cm− 1 ; powdered samples were mixed with potassium bromide and pelletized, which were used to confirm the presence of functional groups on the surface of GO, GO-CS, GO-CS-XG and GO-CS-XG-FU. Zeta potentials were measured using Horiba SZ 100 Nanopartica. All the Experiments were carried in triplicates. Morphological analysis of the samples were done by Scanning electron microscopy (Carl Zeiss Evo 18 model) and Transmission electron microscopy by (FEI Tecnai, G2 20Twin). TEM images were obtained by placing a drop of sample on a copper grid and evaporated at room temperature. Surface morphology and roughness of the samples were visualized by Atomic force microscopy (Nanosurf Easy Scan 2).

In vitro hemolysis assay
The hemolytic activity of GO-CS-XG, free fucoidan and fucoidanloaded nanocarrier was analyzed on Human red blood cells [19]. Fresh human RBCs were removed from 5 ml of the citrated blood by centrifugation at 500g for 10 min. The cells were washed with phosphate-buffered saline (PBS) in order to remove the plasma and the process has been repeated 2 to 3 times to obtain serum-free blood cells and then it is resuspended in 20 ml of PBS. A stock of 5 % haematocrit suspension was used in this analysis. 100μl of diluted RBC suspension was treated with equal volumes of each sample at different concentrations (20, 40, 60, 80 and 100 μg/ml) and incubated for 30 min at 25 °C. After incubation, the mixture was centrifuged at 500g for 10 min and the absorbance of the supernatant was determined at 540 nm using a microplate reader (Epoch Microplate; BioTek). RBCs suspended in 2% Triton-X and PBS was used as the positive and negative controls respectively, the percentage of hemolysis of RBCs was calculated using the formula

Anti-inflammatory assay
An anti-inflammatory activity was performed by the membrane stabilization method [20,21]. In brief, 5 ml of whole blood was collected and mixed with equal volume of Alsever's solution and centrifugation at 500g for 5 min. The RBC pellets were further washed with isosaline and the same process was repeated for 3 times and then resuspended in water. Different concentrations (20,40,60,80and100μg/ml) of GO-CS-XG, FU, GO-CS-XG-FU were prepared to which 0.3 ml of HRBC was added along with 0.3 ml of PBS and 0.5 ml of hypo saline, which was subjected to incubation at 37 °C for 30 min. The suspension was then centrifuged at 3000 rpm for 5 min and measured at 540 nm using a microplate reader (Epoch microplate spectrophotometer; BioTek).
pH stimuli-responsive release study FU release profile was investigated under two different pH environments (PBS at pH 5.3 and pH7.4) at 37 °C for a period of 50h. FU containing GO-CS-XG Nps (3 ml) was placed in a dialysis bag in 7 ml PBS and stirred continuously. At time intervals, 3 ml of the release solution was taken out and fresh PBS was added into the medium to keep the volume constant. The release of Fu from GO-CS-XG Nps was measured by UV-Vis spectroscopy at the wavelength of 262.6 nm using a calibration curve.

Mechanism of FU release
To investigate the drug release mechanism of loaded FU from GO-CS-XG-FU, various models, including Zero order, First order, Higuchi, Korsmeyer-Peppas model, Hixson Crowell, were employed to fit the accumulative release data and to understand the drug release kinetics [22,23].

Zero-order model
To observe the release kinetics, data obtained from in vitro FU release studies were plotted as cumulative percent of FU released (% Qt) vs time (t).

Qt = Q0=K0t
Where Q0 is the initial amount of FU in solution, Qt is the amount of FU dissolved in time t and K0 is the zero-order release constant expressed in units of concentration/time.

First-order model
Release kinetics which followed the first order can be expressed by the equation: Where C0 is the initial concentration of FU, K is the first-order rate constant and t is the time. Hence the drug release kinetics data obtained from in vitro study are plotted as cumulative log percent of FU remaining vs time (t).

Higuchi model
Higuchi equation can be represented in the simplified form Where KH is the Higuchi dissolution constant. The data obtained were plotted against Cumulative percent drug released vs square root of time (√t).

Korsmeyer-peppas model
60 percent of drug release data were fitted in the Korsmeyer-Peppas model and described by the following equation to observe the mechanism of drug release.

Mt/M∞ = Kkpt n
Where Kkp is the Korsmeyer release rate constant, n is the release exponent, and Mt/M∞ is the proportion of FU released at time t. The n value is used to differentiate between different releases. If n is 0.45 ≤ n, the diffusion mechanism is Fickian, 0.45<n<0.89 is non-Fickian, n = 0.89 is Case II transport, and n>0.89 is super case II transport in this model [23]. A graph is displayed between cumulative log percent of FU released (log Mt/M∞) vs log time (log t) to evaluate release kinetics.
To study release kinetics, a graph is plotted between cumulative log percent of FU released (log) vs log time

Hixson-crowell model
Hixson-Crowell showed a relationship between drug release and time which can be expressed by the equation as follows Where W0 is the initial amount of FU in the pharmaceutical dosage form and Wt is the remaining amount of FU in the pharmaceutical dosage form at time t; KHC is the Hixson-Crowell constant relating to the surface volume. To investigate the release kinetics, data from in vitro drug release were plotted against time as the cube root of drug % remaining in matrix.

Cytotoxicity study
The in vitro cytotoxicity of prepared samples was studied on human histiocytic lymphoma cells, U 937 by MTT assay.

MTT cytotoxicity assay
A cell count of 10 5 U 937 cells was seeded in 96-plates for 24h. After 24 h of cell adhesion, the cells were treated with different concentrations (20-100 μg/ml) of GO-CS-XG, free FU, GO-CS-XG-FU to evaluate the cytotoxicity of the prepared nanocarrier and FU loaded nanocarrier and further incubated for 24, 48 and 72h respectively. After incubation, the medium was replaced with 100 μl of MTT in PBS and subjected to further incubation of 4h at 37 °C. Finally, the medium was removed and the formazan crystals formed in the cells were dissolved in 100 μl of DMSO. In a microplate reader, light absorbance was measured at 570 nm. Cell viability was calculated as a percentage relative to untreated control.

Statistical analysis
Statistical analysis was performed using Graph pad prism 9 software. All the measurements were repeated thrice and data were expressed as mean±SD. Data were analyzed using a one-way analysis of variance (ANOVA). A "p" value of less than 0.05 (p<0.05) was considered to be statistically significant.

UV-Visible analysis
The UV-Vis spectra of GO, GO-CS, GO-CS-XG and GO-CS-XG-FU are shown in fig. 1a-d respectively. The UV visible spectrum thus obtained gives a characteristic peak at 230 nm for GO nanoparticles ascribed to a π-π* transitions of-C=C-bonds [24], with a slight rise in peak at 265 nm which corresponds to the n-π* transitions of-C=O-bond ( fig. 1a), and these peaks slightly shifted to a single peak at 260 nm ( fig. 1b) when the surface of the GO was functionalized with chitosan. Binding of xyloglucan on to the surface of GO-CS ( fig. 1c) was observed by a peak at 281 nm. It was observed that the loading of FU exhibited a strong peak at 275 nm, indicating that the FU drug was successfully conjugated on the nanocarrier system GO-CS-XG nanoparticles ( fig. 1d).

FTIR spectroscopy
The functional groups and interactions of GO, GO-CS, GO-CS-XG and GO-CS-XG-FU were confirmed by FT-IR analysis ( fig. 2 and 3). FT-IR spectrum of GO ( fig. 2) showed the absorption peak at 1740 cm -1 , 1636 cm -1 and 1400 cm -1 are attributed to the C=O stretching vibration, C=C stretching vibration of the sp 2 carbon skeletal or epoxy groups and O-H deformation vibrations of ketone groups, respectively. The peak at 3431 cm -1 and 2918 cm -1 clearly states O-H stretching vibration and the saturated C-H bond vibration. The weak band at 1200 cm -1 and two sharp peaks at 1103 cm -1 and 1029 cm -1 were due to the C-OH stretching and the vibrations of epoxy (C-O-C) groups present at the edges of the GO planes. These results of GO showed that ample of hydroxyl, carboxyl and epoxy groups were presented on the surface of GO [25].
In the FT-IR spectrum of GO-CS ( fig. 2), the shifts in the characteristic absorption peaks revealed that these alterations could be related to the reaction of GO carboxyl groups with the amino groups of chitosan [26] in order to form an amide I at 1623 cm -1 , in addition to this, a band at 1567 cm -1 (amide II) is a characteristic of the N-H bonds of Nacetyl groups. Presence of carboxylate groups at 1400 cm -1 . The prominent peak at 1740 cm -1, indicating the presence of-COOH group at 1740 cm -1 in GO is almost shifted to 1720 cm -1 . These observations clearly indicate the functionalization of GO with CS.

Fig. 2: FT-IR spectra of (a) GO, (b) GO-CS
The FT-IR spectra of GO-CS-XG and GO-CS-XG-FU are shown in fig. 3. Conjugation of xyloglucan to GO-CS ( fig. 3) results in the ring opening, which leads to the formation of amide linkage between the aldehyde group of xyloglucan units and free amino groups present on the surface of GO-CS and the peak at 1720 cm -1 for-CO groups disappeared. A broad absorption band at 3431 cm -1 attributed to the hydroxyl (O-H) stretching. A band at 2921 cm -1 to 2843 cm -1 is due to the asymmetric vibration of the carbohydrate ring-C-H bonds. The region from 1239 to 1030 cm -1 is typical of xylose [26,27], corresponding to the C-OH vibrations of the glycosidic C-O-C bonds. It is clearly evident that the xyloglucan was effectively conjugated to the GO-CS system via intermolecular or ionic interactions.
Furthermore, the loading of FU on to the GO-CS-XG nanocarrier system ( fig. 3) shows the presence of peaks at 1243 cm -1 and 850 cm -1 indicates the stretching vibrations of-SO3 groups and the bending vibration of C-O-S, thus depicting the successful loading of drug with the GO-CS-XG nanocarrier system by means of non-covalent binding to form GO-CS-XG-FU.   . 5a-d).
GO nanoparticles (fig. 5a) showed a crumpled flake with its intrinsic folding. GO-CS showed some morphologies different from the GO, a layered sheath-like structure indicating a proper adhesion between GO and chitosan matrix ( fig. 5b). TEM image of GO-CS-XG and GO-CS-XG-FU ( fig. 5c and 5d) were found to be wrinkled with particles embedded within the surface. From the TEM analysis it is clear that this nanocarrier system GO-CS-XG brings an intrinsic change in its structure upon functionalization, conjugation and loading of drug.

Atomic force microscopy (AFM)
AFM images of the nanocarrier system GO, GO-CS and GO-CS-XG-FU are shown in fig. 6a-c. It gives an idea about the surface morphology of the prepared samples. It is observed that the average thickness of the GO is 0 to 5μm. Fig. 6a depicts the three-dimensional image of GO and the surface is layer by layer like morphological (wave-like morphology) of GO. The corresponding two-dimensional structure were clearly indicates the layer by layer morphological structure. The stacking of GO layers together during sample preparation for AFM investigation causes the variance in GO thickness. Fig. 6b

Drug loading and encapsulation efficiency
FU was loaded onto the GO-CS-XG nanocarrier via a simple mixing and sonication method. The unbound drug was removed by centrifugation and the loading capacity and entrapment efficiency of FU on GO-CS-XG nanocarrier were calculated by measuring the concentration of unbound drug-using UV-Vis at 262.6 nm included in table 1. Based on the results the entrapment efficiency and loading capacity of GO-CS-XG-FU are higher than the others and are as high as 75.79% and 83.45%, respectively, which may be due to the ionic interactions between FU and the GO-CS-XG. As a result, GO-CS-XG appears to be a promising drug carrier candidate.

Zeta potential
Further evidence for the successful functionalization and loading of FU to the nanocarrier GO-CS-XG was analyzed in the zeta potential of the sample; fig. 7a-d shows the zeta potential values obtained for the GO-CS-XG-FU nanosystem at varies stages of synthesis. The Zeta potential of GO-CS (average value 26.8±0.82mv) became positive after conjugation with GO (average value-24.4±0.7mv). The cationic polysaccharide CS shielded the negative charge of the graphene oxide nanoparticles and offsets its charge. After functionalization of GO-CSNps with the neutral charge polysaccharide XG, surface zeta potential changed to an average value of-20.4±0.37mv indicating the conjugation of XG with the GO-CSNps. Changes in the zeta potential of GO-CS-XG-FU with an average value of-15.9±0.9mv due to the conjugation of sulphated polysaccharide fucoidan, thus indicating successful loading of the FU drug onto the surface of GO-CS-XG nanoparticles.

In vitro hemolysis assay
In this study, the hemocompatibilty was evaluated using human blood in terms of hemolysis. The in vitro hemolytic assay was evaluated for each sample (FU, GO-CS-XG, GO-CS-XG-FU) at five different concentrations; 20,40,60,80 and 100 μg/ml. Triton X-100 and PBS were used as positive and negative controls, respectively.

Anti-inflammatory assay
The predominant basis for a nanoparticle to be biocompatible is it shouldn't cause any inflammation. Anti-inflammatory activity was evaluated by human red blood cells membrane stabilization method. GO-CS-XG, FU and GO-CS-XG-FU showed 82.56%, 86.23% and 90.62% stabilization at a concentration of 100μg/ml, respectively in accordance with diclofenac sodium salt as standard ( fig. 10). Thus percentage of stabilization increases with increase in concentration. In order to enhance the release of anti-cancer drug within the tumor cells and to avoid the undesired release in blood circulation, it is prominent to have a pH-responsive drug release from the nanocarrier system. Therefore it is important to investigate controlled drug release from the fucoidan-loaded GO-CS-XG based nanocarriers at 37 °C in different pH environments (PBS at pH 5.3 and pH 7.4) for a period of 60h ( fig. 11).
In the current study, we have chosen fucoidan (FU) as a model drug extracted from the marine brown algae Sargassum wightii to exhibit the release from a xyloglucan mediated GO-CS nanocarrier. As seen in fig. 11 at physiological pH, there was a slower release rate at controlled manner in FU from GO-CS-XG nanocarrier was only 30% of the total bound FU after 60 h, which can due to the ionic interactions between the drug FU and the GO-CS-XG nanocarrier system. In case of acidic condition (pH 5.3), the release rate of FU was dramatically enhanced to 70%, leading to a higher preferred release of FU, it means that the drug-loaded wasn't released fully even after 60 hr still 30% of the drug is retained in the system for circulation. Thus GO-CS-XG nanocarrier system has a significant improvement in prolonged releasing which can sustain up to 60 h. To investigate the kinetics and release mechanism of FU from GO-CS-XG-FU formulation, various kinetic models were applied-Zero order, First order, Higuchi, Hixson Crowell and Korsmeyer-Peppas model at pH 7.4 and pH 5.3 respectively and interpreted in the form of graphical presentation and evaluated by correlation coefficient (R 2 ) represented in fig. 12a- In addition, the n value of Korsmeyer-Peppas model can be used to characterize the release mechanism of FU. In this model, the release mechanism of FU at pH 7.4 (R2 = 0.98463) implies that the drug release from the system follows anomalous (non-fickian) diffusion (n =0.643) and at pH 5.3 (R2 = 0.87905) follows the fickian diffusion mechanism (n = 0.41).

In vitro cytotoxicity
The cytotoxicity of FU-loaded GO-CS-XG based pH-responsive nanocarrier system, free FU and GO-CS-XG were evaluated by MTT assay against human histiocytic lymphoma (U 937) cells for periods of 24h, 48h and 72h.
As depicted in fig. 13 a-c, the cell viability decreased as the incubation time increased, thus exhibiting time-dependent cytotoxicity. Upon 24h of exposure, the GO-CS-XG-FU showed 33% of cell death when compared to free FU, which shows a 20% cell death at a concentration of 100μg/ml, almost 13% of the efficacy of FU is increase when FU loaded on to GO-CS-XG nanocarrier system. After 72h of incubation, the cell viability of GO-CS-XG-FU was around 18.3%, almost 82% of cells died at a concentration of 100μg/ml. From the cytotoxicity results, it can be understood that drug-loaded GO-CS-XG-FU showed significant cytotoxicity against U 937 cells compared to FU and GO-CS-XG. Hence the development of the GO-CS-XG nanocarrier system has the potential for targeted delivery of cancer drugs, thus proving the efficacy of FU as a suitable candidate through this nanocarrier system. Morphological changes in U 937 cells are shown in fig. 14a-b. In conclusion, we have developed a promising platform for anticancer drug delivery system with high dug loading and efficiency. To specifically target the cancer cells, chitosan functionalized graphene oxide was conjugated with the targeting ligand xyloglucan The targeted and pH-responsive GO-CS-XG drug delivery was loaded with fucoidan, an anticancer model drug extracted from marine brown algae Sargassum wightii. The in vitro release of FU was at a faster and higher rate in the case of acidic medium compared to physiological conditions. This pH-sensitive drug release with high entrapment efficiency makes this nanocarrier system a prominent candidate for targeted drug delivery system. Hemolysis studies provide excellent biocompatibility by showing no toxic effect on RBCs. Better stabilization was achieved via an antiinflammatory assay. FU-loaded GO-CS-XG drug delivery systems were tested for cytotoxicity activity against human lymphoma (U937) cells exhibited higher cytotoxicity of 82% at higher concentration upon exposure to a period of 72h, which is well defined from the MTT assay. Therefore this present study is brief screening of polysaccharides as a new drug carrier system along with GO for targeted drug delivery.