Design and synthesis of nano-biomaterials based on graphene and local delivery of cerebrolysin into the injured spinal cord of mice, promising neural restoration

Spinal cord injury (SCI) is an incurable and catastrophic health issue with no clinical solution. As part of cascade reactions, the inflammatory process and fibrous glial scar production aggravate the amount of lesion through a secondary damage mechanism, encouraging scientists from other disciplines to investigate new paths for solving this problem. Graphene oxide (GO) and its derivatives are among the most promising biomedical and nerve tissue regeneration materials due to their remarkable chemical, mechanical, and electrical properties. This paper designs and introduces a new GO-based nanomaterial to minimize inflammation and stimulate neurite regrowth. To improve biocompatibility, biodegradability, and cell proliferation, GO plates were modified with polyethylene glycol (PEG) and Au nanoparticles as neuroprotective and antibacterial agents, respectively. Preliminary biological investigations on bone marrow derived mesenchymal stem cells (BM-MSCs) with various concentrations of a graphenic nanocarrier indicated a lack of cell toxicity and an enhancement in BM-MSC proliferation of about 10% after 48 hours. Therapeutic nanostructures were used in the T10 segment of a mouse SCI model. The pathological and immunohistochemical data revealed that refilling tissue cavities, decreasing degeneration, and establishing neuroregeneration resulted in a considerable improvement of hind limb motor function. Furthermore, compared to the nanocomposite mixture alone, the intraspinal delivery of cerebrolysin (CRL) had a more satisfying impact on nerve regrowth, cystic cavity, hemorrhage avoidance, and motor function enhancement. This study demonstrates the potential of graphenic nanomaterials for SCI treatment and neuroregeneration applications.


Introduction
SCI, a serious medical problem, is correlated with intrusive damage to sensory, motor, and voluntary actions at the injury site.Recovery and complete care of damaged nerves have been more challenging than for other tissues due to nervous system structure and function complexities.Progress has been made in understanding the degeneration mechanism and treatment methods.Still, almost three million people worldwide suffer from SCI, with tragic personal and social consequences and high nancial costs (more than four billion dollars annually). [1][2][3] Cascade interactions such as cystic cavitation, generation of glial scar, and the aggregation of inhibitors associated with myelin appear in the SCI lesion site microenvironment during the acute process. 4By completing the process of glial scar formation, functional nerve recovery leads to failure in nervous tissue regeneration and movement restoration. 5,6One challenge to efficient neurogenesis is how to rebuild the microenvironment for nerve tissue improvement.Functional studies and clinical trials are utilized to resolve these obstacles, including cell 7 and biomaterial placement, 8 growth factor release, 9 inhibitory matrix disruption, 10,11 endogenous neurite outgrowth, and axonal cytoskeleton stimulation. 6,12Using cells, biomolecules, biomaterials, or combinations thereof as effective methods can provide the least invasive form of SCI treatment.][15] Regenerative medicine, a brilliant eld of medicine in recent decades, is an exciting method in which injured organs, tissues, or cells are renewed through special continuous strategies.Recently, regenerative medicine has been used to repair and regenerate bone, muscle, heart, nerve tissue, etc.In addition to stem cell therapy, biomaterials or a combination thereof have been used for neuroregeneration. 16raphene-based nanomaterials (GBNs) are one of the most promising structures for nanotechnology applications due to their superior physicochemical properties.GBNs are used extensively in biomedical areas such as biomedicine, 17 drug/ gene delivery, 18 neuroscience, 19 bioimaging, 20 phototherapy, 21 biosensor fabrication, 22 and tissue engineering. 23In addition to the signicant characteristics of graphene (G), GO, and partially reduced GO (rGO), as well as other graphene derivatives with greater versatility and hydrophilicity for bio-applications, 24,25 can enhance neural differentiation and axonal coordination through recording and stimulating neural electrical signals. 9,26he biocompatibility and toxicity of GBNs are currently a source of concern.Various parameters, including diameter, concentration, chemical compositions of the surface, lateral dimension, and aggregation conditions, decisively impact cytotoxicity. 27,28Proper functionalization of the GO surface is therefore essential for designing a nanocarrier system with high in vivo biocompatibility and biodegradability, good solubility in the body's physiological environment, and the development of antibacterial properties.
PEG is a synthetic polymer that is remarkably hydrophilic, biocompatible, and Food and Drug Administration (FDA) approved for graing on GO sheets covalently and non-covalently.PEG modication could delay the circulation time and improve the in vivo pharmacokinetics for effective drug delivery.Furthermore, it has shown activities such as neuroprotection, anti-inammatory properties, suppression of conversions in the SCI environment, and the ability to cross the blood-spinal cord barrier. 29,30esides PEGylation, additional chemical functionalization should be examined to develop the antibacterial activities of GO materials.Subsequently, chitosan or metal antibacterial agents (silver nanoparticles (AgNPs), gold nanoparticles (AuNPs), zinc oxide (ZnO), and others) can be used.2][33] In order to enhance conductivity and anti-inammatory activity, the combination of AuNPs with GO can be an attractive approach to develop cell proliferation and nerve improvement.
On the other hand, local drugs, trophic factors, and cell delivery provide an exceptional opportunity to localize carriers at the injury site.][36] CRL, a low-molecular-weight peptide, is a porcine braindriven preparation that contains a balanced composition of several neurotrophic factors to develop neuroprotection, neuroplasticity, and neuroregeneration in various brain diseases. 37t was used as a model medication to examine the manufactured smart nanocarrier's loading and release behavior and improve neural regeneration in SCI challenges.
This study aimed to assess the creation and usage of GObased nano-biomaterials as a neuro-stimulator and drug carrier for SCI treatment.GO was chosen due to its excellent physicochemical qualities and ease of reaction.The GO surface was rst modied with PEG and AuNPs to enhance biocompatibility, physiological solubility, antibacterial properties, and conductivity of GO to improve treatment quality and reduce regeneration time.Meanwhile, the encapsulation and release abilities of the CRL were evaluated using GO plates.The injectable nanostructures were employed in a mouse's damaged thoracic spinal cord aer analyzing in vitro cell toxicity.The functional improvement was measured two weeks aer surgery.Histological examinations were also performed to conrm the tissue response, neurite presence, and glial scar density in the lesion microenvironment (Fig. 1).

Characterization apparatus
2.2.1 Fourier transform infrared spectrometry (FTIR).FTIR was used to investigate the structure of the synthesized nanobiocomposites (Bruker Vector-22 FT-IR spectrometer).The wavenumber (cm −1 ) vs. transmittance percent of each sample was measured in the 400 to 4000 cm −1 range, using a KBr pellet technique.
2.2.3 Thermogravimetric analysis (TGA).The Q500 (TGA Q500) analyzer was used to perform TGA.Nanomaterials were weighed and evaluated in a nitrogen environment.The temperature range was measured from 47 to 675 °C at a scanning rate of 10 °C min −1 .
2.2.4 Ultraviolet-visible spectrophotometry (UV-Vis).UV-Vis spectra were performed with a Philips PU 8620 Ultraviolet spectrophotometer at the absorption maximum (l max ) using a 1 cm quartz cell.
2.2.5 Field emission scanning electron microscopy (FESEM).To determine the surface morphology and elemental composition of GBM, the samples were sputter-coated with a thin gold lm.This coating makes them conductive for examination at 30 kV using a MIRA3 FESEM microscope equipped with energy-dispersive X-ray spectroscopy (EDX).
2.2.6 Dynamic light scattering (DLS).The charge of the surface, average dimension, and the polydispersity index (PDI) of the prepared nano-biomaterials were evaluated using a DLS (Microtrac, Nanotrac Wave) with a laser light wavelength of 780 nm at room temperature in deionized water (DW).

Preparation of GO-PG
As described previously, GO was prepared through the modied Hummers' procedure. 38,39Then, 100 mg of GO was dispersed in 100 mL of DW in a sonication bath for two hours.Then 10 mg of PEG was added to the GO suspension and stirred vigorously at 500 rpm and 60 °C for 24 h.The color changed from brown to black.The obtained solid was washed with DW ve times for purication, centrifuged at 12 000 rpm for 5 minutes, and dried at 40 °C.

Preparation of GO
In brief, 100 mg of GO in 100 mL of ethanol : DW (20 : 80) was dispersed by ultrasonication for one hour to obtain one mg mL −1 solution.Then 0.5 mL of TEOS and 0.5 mL of APTES were inserted and redispersed for 30 minutes.The homogeneous solution was moved to the hotplate.Aer adding 100 mL ammonia, the mixture was soly stirred at 125 rpm and 40 °C for 12 hours and turned black.Then the amino-functionalized GO precipitate was washed with ethanol and distilled water to remove the unreacted chemicals.The obtained GO-SiO 2 -NH 2 planes were redispersed in DW and mixed with HAuCl 4 $3H 2 O aqueous solution (2.5 mL, 0.01 M).Subsequently, the suspension was mixed with magnetic stirring at 96 °C for 30 minutes.Au nanoparticles were placed on the amine groups and the GO nanosheets.Finally, the prepared hybrids were ltered, washed with DW three times, and dried at 40 °C in a vacuum atmosphere.

Loading of CRL
70 mg of CRL solution in DW was added to 40 mL of GO aqueous dispersion (1 mg mL −1 ) and stirred at room temperature (20 °C) for 24 h.Aer centrifugation at 10 000 rpm, the solution was ltered.The GO-CRL was washed with DW to remove a small quantity of solubilized unbound drug and dried under vacuum at room temperature.The loading ratio of CRL (wt%) was derived from UV absorbance at 268 nm and calculated using the equations below.

Entrapment efficiency (%) = the initial amount of drug
− the amount of drug in the supernatant/the initial amount of drug × 100 Loading efficiency (%) = the initial amount of drug − the amount of drug in the supernatant/amount of nanocarrier × 100

CRL release studies
GO-CRL (10 mg) in 5 mL of phosphate-buffered solution (PBS; pH 7.4) was placed in a dialysis bag (14 kDa MWCO) and transferred to a 10 mL buffer solution for 14 days at 37 °C.At predened intervals (1, 2, 3, ., 14 days), the supernatant was collected and replaced with an equal amount of fresh buffer.The amount of CRL released was measured using a UV-Vis spectrophotometer and calculated using the equation below.
Drug release (%) = P (amount of drug in release solution at time t)/amount of drug loaded in the nanocarrier × 100

Isolation of BM-MSCs and culturing
As explained previously, BM-MSCs were extracted from the tibia and femur bones of mice.The animal's whole body was dissected aer immersing in 70% (v/v) ethanol.Applying micro dissecting scissors and a surgical scalpel, muscles, ligaments, and tendons were carefully separated from the bones.Aer transferring into ice-cold sterile PBS, the ends of the marrow cavity were cleaned with medium until the bones turned white before centrifugation at 2500 rpm for 5 minutes.The supernatant was removed, and a 5 mL total medium (containing DMEM, 10% FBS, and 100 U per mL penicillin-streptomycin) was added before transferring the suspension to a cell culture ask.This ask was then placed within a humidied environment maintained at 37 °C, with a 5% CO 2 concentration, in order to attain a cellular conuence ranging from 70% to 90%.Following the 3 rd passage and elimination of macrophages, lipids, and blood cells, the BM-MSCs were characterized employing CD44, CD34, and CD90 surface markers using the ow cytometry technique in the previous study. 39ach specimen underwent a thorough cleansing process employing 70% ethanol, followed by desiccation within a sterile hood.Subsequently, a 30 minute UV irradiation sterilization procedure was administered prior to their utilization in both in vitro and in vivo investigations.Notably, these assessments were conducted on a minimum of three separate occasions.

MTT assay
The BM-MSCs at 70% conuency were detached by trypsin and then centrifuged at 1000 rpm for 5 minutes at room temperature.The cells were seeded in 96-well plates with 200 mL complete DMEM medium and incubated overnight to adhere to the dishes.Aer removing the old media, the cells were treated with various quantities of GO, GO-PG, GO-Au, GO-CRL, and NC + CRL (0.1, 1, 10, 20, 40, 100, and 150 mg mL −1 ) and placed in an incubator set at 37 °C for durations of 24, 48, and 72 hours.The 96 wells were rinsed with PBS and incubated for 4 hours in darkness with 100 mL MTT in the culture medium (0.4 mg mL −1 medium) at 37 °C.The NC + CRL group is symbolized as a complex of GO-PG, GO-Au, and GO-CRL 1 : 1 : 1, used in the animal model.Aer discarding the MTT-containing medium, 200 mL of DMSO was added to dissolve the insoluble violet formazan produced by live cells.Ultimately, the spectrophotometric microplate ELISA reader (Multiskan MK3, Thermo Electron Corporation) was employed to measure the absorbance of the formazan solution at a wavelength of 570 nm, and the results were represented as optical density (OD) aer blank subtraction.
Cell viability (%) = OD (test)/OD (control) × 100 Nanoscale Advances Paper 2.9 Reactive oxygen species (ROS) studies Intracellular reactive oxygen species or radicals (ROS) were measured using 2 ′ ,7 ′ -dichlorodihydrouorescein diacetate (DCFH-DA, Sigma-Aldrich).First, 5 × 10 4 cells were placed per well onto chamber slides and cultivated for 24 hours.The cell medium was then removed, and the cells were treated for 48 hours with GO, GO-PG, GO-Au, GO-CRL, and NC + CRL (the control cells received no therapeutic nanomaterials).Aer rinsing the cells twice with PBS, 10 mM per L DCFH-DA was applied to the cells, and they were located in a dark incubator at 37 °C for 30 minutes.In order to remove uncombined probes, cells were washed twice with PBS and treated with DAPI for 30 minutes in a dark environment before rinsing with PBS and then examined under a uorescence microscope (Nikon E1000M, Japan).

SCI modeling in mice
The  40 were randomly divided into three triplicate groups (n = 12 per group), including the injury (I) group (SCI with no injection), the (I + NC) group (SCI with a complex of GO-PG and GO-Au 1 : 1 in 100 mg per mL injection), and the (I + NC + CRL) group (SCI with a complex of GO-PG, GO-Au, and GO-CRL 1 : 1 : 1 in 100 mg per mL injection).The NC and CRL symbols were used instead of (GO-PG and GO-Au) and GO-CRL, respectively, to simplify the characters.All mice were anesthetized with ketamine and xylazine (80 : 20 mg kg −1 ) intraperitoneally before the surgery.A longitudinal incision was made along the lower thoracic vertebrae to expose the spinal column, and a laminectomy was performed at the T10 segment.The compression approach resulted in the injury (0.3 mm, 15 s), and 50 mL of the therapeutic nanomaterials corresponding to each group were injected into the lesion space.Aer the procedure, the incision was sutured in layers and the creatures were situated in a separate enclosure under a warm lamp for 0.5-1 hour before being transferred to their home cages.Furthermore, mouse bladders were manually emptied twice a day until the reex of the urine system returned.They received a constant dose of ciprooxacin (2 mg kg −1 ) and sterile normal saline for 5 days.

Locomotor function test
The Basso, Beattie, and Bresnahan (BBB) test was applied to measure the locomotion activity of the hind limbs following SCI.The BBB test involves a 21-point locomotor assessment scale administered for 4 minutes every day for two weeks by two unrelated observers.

Histological and immunouorescence studies
At two weeks post-injury, the mice were put into deep anesthesia with intraperitoneal injections of xylazine-ketamine (20 : 80 mg kg −1 ).Then they were sacriced utilizing the usual perfusion-xation method, which included sterile normal saline and paraformaldehyde 4% circulation.A 1 cm spinal cord slice was taken via a dorsal laminectomy and submerged in 4% paraformaldehyde at 4 °C.Fixed tissues were placed horizontally in paraffin and cut into 5 mm sections with a microtome.Aer transferring the segments to the slides, they were stained with hematoxylin and eosin (H&E) stains and studied using an optical microscope (Nikon Eclipse E100).

Statistical analysis
Data were expressed as the mean ± SD of at least three different experiments (n $ 3).GraphPad Prism (8.0.2) and ImageJ Fiji were utilized for quantitative analysis.The means of the data sources were calculated using the Student's t-test and one-way ANOVA.All statistical analyses determined the signicance value as P < 0.05.The absorption bands at 3360 cm −1 and 3400 cm −1 represent the primary aliphatic amine (N-H) groups, while the peak at 3400 cm −1 overlaps with the hydroxyl groups of GO.The peaks associated with C-H and C]C stretching vibrations of GO appeared at 2925, 2962, and 1635 cm −1 respectively.Additionally, the peak at 1068 cm −1 that corresponds to Si-O-Si bonds overlaps with that of C-O-C at 1065 cm −1 , which indicates the successful functionalization of GO with TEOS and APTES. 41,42The GO-Au spectrum should be comparable to the GO-SiO 2 -NH 2 peaks owing to the emergence of Au peaks in the far-infrared, but a new peak at 462 cm −1 might be possible and be attributable to the presence of Au nanoparticles. 43Further analytical procedures, such as XRD, were utilized to conrm the presence of AuNPs on GO sheets.In the spectrum of GO-PG (Fig. S1E †), the peaks of C]O and C-O became sharper and shied to 1736 cm −1 and 1080 cm −1 respectively, because of the interactions between the GO's carboxylic acid and hydroxyl groups with O-H groups of PEG.The existence of peaks at 2877 cm −1 and 1456 cm −1 attributed to the -CH 2 (sp 3 ) and CH plane bending groups of PG and also the peak at 1635 cm −1 (C]C) of GO indicated graing of PEG onto GO-PG. 44

XRD
The crystalline structures of GO, GO-PG, GO-SiO 2 -NH 2 , and GO-Au have been investigated by XRD diffraction patterns.As shown in

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Nanoscale Advances the diffractograms (Fig. S2 †), the GO-PG diffractogram exhibits a broad peak at 2q = 21.3°(120),slightly different from the GO-PEG pattern in the previous study, 39 indicating a reduction in the crystallinity and development of an amorphous system with an interlayer spacing of d = 9.1 Å which may be due to weak interactions or a low degree of PEGylation.The broader and shorter diffraction pattern of GO-SiO 2 -NH 2 at 2q = 22.4°with an interplanar distance d = 3.96 Å compared to the GO pattern displays the silane functionalization of GO.The GO-Au pattern, besides the extensive GO-SiO 2 -NH 2 peak, contains ve sharp peaks at diffraction angles of 38.28°, 44.48°, 64.6°, 77.44°, and 81.58°, corresponding to the characteristic gold crystalline sheets (111), ( 200), ( 220), (311), and ( 222) respectively (ICDD code 00-002-1095). 45t should be noted that in diffraction patterns, the characteristic GO peak has vanished because of complete exfoliation and the existence of oxygen-containing groups.Moreover, the addition of PEG, TEOS, and APTES prevents aggregation and restacking of GO sheets.The presence of a broad peak observed in the diffractograms of GO-PG and GO-SiO 2 -NH 2 near the natural graphite angle can be attributed to a partial reduction of graphene oxide (GO) induced by graing reactions.

TGA/DTG
As shown in the TGA/DTG diagrams (Fig. S3a and b †), the weight loss near 100 °C is due to the evaporation of water molecules between layers.Almost 20% of the GO-PG mass decreases at 150-250 °C and 25% declines close to 250-350 °C, respectively, owing to the loss of groups of oxygen and PEG.The weight loss between 300 and 600 °C is attributed to the pyrolysis of carbon skeletal structures and the release of carbon dioxide into the atmosphere. 46The GO-SiO 2 -NH 2 and GO-Au patterns display tremendous thermal stability against GO, forming a silica layer and gold nanoparticles on the GO surface. 40Two negligible weight reductions in areas less than 100 °C and 170-250 °C suggest the presence of moisture and oxygen groups, respectively.Due to silyl group decomposition, almost 25% of weight loss occurred between 250 and 350 °C.The other declination level near 420-450 °C illustrates the degradation of inert Au nanoparticles.As can be seen, the composites' thermal stability was signicantly increased due to the successful surface modication of GO. 45,47 3.4 FESEM and EDX FESEM images in Fig. 2 illustrate GO, GO-PG, and GO-Au nanocomposite morphological structure.GO sheets exhibit a planar structure with wrinkled surfaces.GO-PG depicts an extensive at system, owing to H-bonding interactions between PEG and GO surfaces.In the gure of GO-Au, the white stains on the surface of GO related to the existence of silyl groups and Au nanoparticles are distributed uniformly on the GO surface.
Meanwhile, to record the conrmation of the elemental combination of the GO-PG and GO-Au nanocomposites, EDX was employed (Table 1).The elemental analysis data demonstrated that the modication reactions on the GO sheets were executed successfully.

DLS
In order to measure the size of nano-biocomposites, we have used dynamic light scattering (DLS) in water at room temperature.The suspended sizes of GO, GO-Au, and GO-PG were 170 nm, 226 nm, and 427 nm, respectively.Zeta potential and

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polydispersity analyses (Table 2) of the prepared nanomaterials showed that the PG and Au could increase the zeta potential of GO sheets by contributing negative charges to their surface, making them more stable and less prone to agglomeration in DW at room temperature.The spectrum of GO-PG was identical to that of GO, except for a greater absorbance, which may be attributed to non-covalent PEGylation.

In vitro drug loading and release evaluation
In this research, non-covalent drug loading was carried out at room temperature overnight.The presence of carboxylic acid groups on GO electrostatically interacts with CRL's amine groups, causing increased loading.Fig. 3b shows that CRL molecules were successfully loaded onto GO sheets, as evidenced by the characteristic absorption peak of CRL (268 nm) and GO-CRL.The loading concentration of CRL (92%) and the entrapment efficiency (96.5%) were determined using UV-Vis spectrophotometry.The in vitro release tests were carried out for 14 days, employing PBS at a temperature of 37 °C.According to the ndings (Fig. 3c), the low quantity of CRL released from the nanocarrier (39.68% in the rst week) increases to 80.27% aer 14 days.This phenomenon could be attributed to the removal of   the adsorbed drug from the nanocarrier as well as the solid electrostatic interaction between the CRL's amine groups and the nanocarrier's carboxylic acid groups.The calibration standard curve of CRL is shown in Fig. S4.†

MTT study
For biomedical applications, ideal nanomaterials must be biocompatible.A standard MTT assay was used to examine the in vitro cytotoxicity of the produced nano-biomaterials on BM-MSCs.Fig. 4 demonstrates the cytotoxicity results with a series of doses (0.1, 1, 10, 20, 40, 100, and 150 mg mL −1 of GO-PG, GO-Au, GO-CRL, and NC + CRL in a complete medium for 24, 48, and 72 hours.According to the ndings, the cell viability of entire nanomaterials was greater than 80% except in high doses of GO-Au (100 and 150 mg mL −1 ).It can be deduced that no noticeable cytotoxicity was observed in the prepared nanocomposites aer 24 hours.Cell proliferation for GO increased to more than 92% aer 48 and 72 hours of exposure due to covalent and noncovalent interplays between hydrophilic GO and medium proteins.Here, through the activation of the GO surface, a noticeable enhancement in cell proliferation was achieved, reaching approximately 106% and 115% improvement when GO plates were graed with both Au and PEG.In addition, due to the low PEGylation degree of GO, GO-PG increased cell growth and proliferation by around 5% compared to our earlier study.
Regarding the GO-CRL and NC + CRL groups, cell viability increased to almost 120% and 133% in 72 hours, showing more effective interactions even with the small amount of CRL.Using GraphPad Prism, the effective concentration (EC 50 ) values of GO, GO-PG, and GO-Au were 48, 53, and 10 mg mL −1 , respectively.Numerous previous investigations have shown that dimension, concentration, chemistry of the surface, and shape may impact the cytotoxicity of products based on graphene. 28,49-51

ROS study
Intracellular ROS levels might be increased by exposing cells to nanomaterials, which is the primary feature of intracellular oxidative stress. 52ROS can cause intracellular lipid peroxidation, protein inactivation (via nitration and oxidation), mitochondrial malfunction, and apoptosis or necrosis.DCFH-DA is one of the most widely utilized methods for directly assessing a cell's redox status compared to alternative ROS detection techniques. 53In this system, H 2 DCFDA, a non-uorescent lipid-permeable compound, is transformed into 2 ′ ,7 ′ -dichlorouorescein (DCF) (green uorescence) by an intracellular esterase reaction.4][55] As shown in Fig. 5a and b, the levels of ROS aer 48 hours for GO, GO-Au, GO-PG, GO-CRL, and NC + CRL, respectively, were 0.093 ± 0.011, 0.28 ± 0.027, 0.37 ± 0.010, 0.086 ± 0.011, and 0.088 ± 0.005, which is considered a good score compared to prior studies.In this regard, Chen et al. have indicated that modication of the GO surface with Au increases the level of ROS by around 4.7. 56These ndings may be attributed to the nanomaterials' acceptable average lateral size and fewer edges.Furthermore, the combination of the nanomaterials in the NC + CRL group caused a desirable reduction in ROS levels due to both the pharmacological effect of CRL and covalent and non-covalent interactions among its functional groups with the oxygenated groups of GO-PG and GO-Au.Meanwhile, the nuclei in the core of cells stained with DAPI (blue) showed a round morphology with no fragmentation.These results correlate with the MTT assay, indicating that the prepared nanomaterials are not only less toxic but also more biocompatible aer 48 and 72 hours.In future studies, more detailed cellular investigations will be examined (Fig. 5a).Nanoscale Advances Paper

BBB tests
Recovery of locomotor function was assessed with BBB score for injured animals at the T10 level for 4 minutes during the initial 2 weeks past injury (subacute phase).The locomotion behavior of animals in all groups was exactly equivalent immediately aer injury, indicating a lack of motor function (Fig. 5c).Then, in comparison with the (I) group (1.8 points), the motor function in the (I + NC) and (I + NC + CRL) groups was restored astonishingly, with higher BBB ratings (6.12 and 12.32 points, respectively).Besides that, with continuously increased drug release into spinal cord lesion sites, the BBB score of the (I + NC + CRL) group was considerably higher than that of the other groups 7 days following surgery, demonstrating that (I + NC + CRL) had a superior therapeutic inuence on functional improvement.

Histology and immunohistochemistry studies
Encouraged by the exceptional capabilities of graphenic nanobiomaterials and their potential to repair neurites, we investigated the tissue response of the damaged mouse spinal cord to a complex of GO-PG, GO-Au, and local delivery of CRL into the wounded location in the subacute phase.
According to the mouse spinal cord diameter, we selected 50 mL of mixed nanomaterials to place into the damaged site and release CRL locally.Further studies will be performed in the chronic phase (over a longer period of time) in the mouse model.The H&E stains of sagittal sections indicated the standard histopathology of the control (without injury), (I), (I + NC), and (I + NC + CRL) groups two weeks aer surgery in Fig. 6a.Numerous neuronal cells were observed in the control group, and myelinated axons were shown with thin arrowheads.Multiple cystic cavities (asterisks), hemorrhage (arrowheads), and round-shaped nucleus cells, most probably activated astrocytes (thick arrows), were seen surrounding the lesion site in the (I) group.The cavity area and hemorrhage percent were calculated using Fiji ImageJ.The cavity area in the (I) group was 5 ± 1.263 mm 2 , which was reduced to 2.5 ± 0.2 mm 2 and 1.7 ± 0.131 mm 2 in the (I + NC) and (I + NC + CRL) groups, respectively, indicating less visible and smaller-sized cavitation (Fig. 6b).The bleeding rate was also decreased from 14.5% ± 0.592 (I) to 3.25% ± 0.424 (I + NC) and 3.27% ± 0.430 (I + NC + CRL) (Fig. 6c).Moreover, a band of tightly compacted cells with oval nuclei could be identied at the rostral, medial, and caudal hemispheres, which most likely represented lymphocytes.
To evaluate the effect of synthetic nano-biomaterials on neurite regeneration, we used immunouorescence staining for GFAP (red), NF (green), and DAPI (blue) by double labeling.For nucleus staining, DAPI was utilized (Fig. 7a).GFAP, a marker of reactive astrocyte detection and glial scar formation, hindered neuroregeneration in injured areas.Fig. 7b demonstrates that GFAP was expressed substantially in the (I) group, near the lesion location, at around 48% ± 1.431.Treatments with the (I + NC) and (I + NC + CRL) signicantly lowered GFAP accumulation to 33% ± 1.756 and 23% ± 1.652, respectively, indicating that CRL affects astrogliosis in comparison with (I + NC) and (I) groups.The NF immunouorescence labeling was then utilized to trace and detect nerve ber renewal and axonal regeneration.NF-positive nerve bers were evident in the rostral, central, and caudal portions of the (I + NC) and (I + NC + CRL) groups as compared to the (I) group.The percentages of NF expression

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Nanoscale Advances were calculated as 25% ± 2.847, 37% ± 0.545, and 52% ± 1.907 for the (I), (I + NC), and (I + NC + CRL) groups, respectively.For the group (I + NC + CRL), particularly extensive lengths of nerve bers were seen in the center of the lesion.Fig. 7c depicts a signicant difference in the quantitative analysis of NF expression.These data show that compared to group (I), treatment groups (I + NC) and (I + NC + CRL) signicantly reduced glial scar formation, cavity areas, bleeding, and increased neurite counts.In addition, local delivery of CRL at the lesion site accelerated the improvement process two weeks aer the injury.
8][59][60] Topography and surface chemistry of tissue engineering biomaterials have essential roles in inuencing cell behaviors (differentiation, proliferation, directed growth of nerve cells, brosis, and inammation) and regulating intracellular signaling pathways to affect gene expression.Zhang and coworkers found that surface modication of PLLA-aligned nanobers with GO nanosheets enhances surface roughness, resulting in optimal contact for cell growth. 61Encapsulating several neurotrophic factors into biomaterials increases cell growth, proliferation, differentiation, migration, and neurite regeneration.However, nerve development is greatly inuenced by the amount, duration, and location of neurotrophic substances released in vivo.

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In this study, we found that injecting graphene-based nanobiomaterials into the lesion cavity lled the damaged hole and reduced astrocyte hyperactivities for glial scar formation, hemorrhage, edema, and necrosis.On the other hand, the electrical ability of reduced GO sheets increases connectivity and stimulates neurite sprouting and outgrowth.Furthermore, smart delivery of CRL (I + NC + CRL group) into the damaged microenvironment 7 days aer injury (concurrent with nerve stimulation) enhances locomotor hindlimb activity and accelerates neuroregeneration more effectively than the (I + NC) group.

Conclusions
This paper reports the creation of new biocompatible GO-based nanomaterials for nerve tissue engineering and neuroregeneration.Nanocomposites were functionalized with PEG and Au nanoparticles to improve conductivity, antibacterial, and neuroprotective characteristics, resulting in an optimal microenvironment for neurite regeneration.The abundance of oxygen-containing groups on the nanocomposites' surface establishes a constructive interplay with the proteins of the medium.This interaction not only fosters the proliferation of BM-MSCs but also maintains an optimal level of reactive oxygen species (ROS), which is highly favorable.Two weeks aer injection of a mixture of prepared nano-biomaterials into the mouse spinal cord lesion site, a cascade of improvements became evident.Notably, there was an increase in functional locomotor scoring of the BBB.This positive trend was coupled with a reduction in cavity dimensions, instances of bleeding, astrocyte activation, and scar formation.Moreover, a marked enhancement in both reconnection and the regeneration of neurites was prominently observed.Local distribution of CRL signicantly enhanced these results and SCI improvement.We highly suggest electrical stimulation of these materials, combined with cells and growth factors, to increase neural tissue repair and hindlimb functional recovery, providing a potentially curative approach for CNS disorders.

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Nanoscale Advances

3. 1
Fig.S1† shows the FT-IR spectra of GO, GO-SiO 2 -NH 2 , GO-Au, PEG, and GO-PG.According to Fig.S1B, † the peaks at 1133 cm −1 and 1624 cm −1 are due to Si-O-C and C-N bonds.The absorption bands at 3360 cm −1 and 3400 cm −1 represent the primary aliphatic amine (N-H) groups, while the peak at 3400 cm −1 overlaps with the hydroxyl groups of GO.The peaks associated with C-H and C]C stretching vibrations of GO appeared at 2925, 2962, and 1635 cm −1 respectively.Additionally, the peak at 1068 cm −1 that corresponds to Si-O-Si bonds overlaps with that of C-O-C at 1065 cm −1 , which indicates the successful functionalization of GO with TEOS and APTES.41,42The GO-Au spectrum should be comparable to the GO-SiO 2 -NH 2 peaks owing to the emergence of Au peaks in the far-infrared, but a new peak at 462 cm −1 might be possible and be attributable to the presence of Au nanoparticles.43Further analytical procedures, such as XRD, were utilized to conrm the presence of AuNPs on GO sheets.In the spectrum of GO-PG (Fig.S1E †), the peaks of C]O and C-O became sharper and shied to 1736 cm −1 and 1080 cm −1 respectively, because of the interactions between the GO's carboxylic acid and hydroxyl groups with O-H groups of PEG.The existence of peaks at 2877 cm −1 and 1456 cm −1 attributed to the -CH 2 (sp 3 ) and CH plane bending groups of PG and also the peak at 1635 cm −1 (C]C) of GO indicated graing of PEG onto GO-PG.44

Fig. 1
Fig. 1 Schematic representation of the procedure.

3. 6
UV-Vis spectra UV-Vis absorption spectra, an effective method for characterizing graed AuNPs on GO sheets, are demonstrated in Fig. 3a.At 230 and 300 nm, the absorption peaks correspond to p / p* (C]C) and n / p* (C]O) excitation in the GO curve.The n / p* peak shows a bit of red shi aer Au and PEG modication, owing to GO partial reduction.Meanwhile, a new peak at 525 nm has emerged in the GO-Au curve, indicating the presence of Au nanoparticles in GO sheets.

Fig. 2
Fig. 2 FESEM images of GO, GO-PG, and GO-Au with a scale bar of 2 mm and 200 nm.

Fig. 4
Fig.4MTT assay was used to determine the cytotoxicity and biocompatibility of different GO-PG, GO-Au, GO-CRL, and NC + CRL doses on BM-MSCs after 24, 48, and 72 hours.The p-value for a significant difference between NC + CRL and control groups was 0.0001 (n = 3, mean + SD).

Fig. 5
Fig. 5 ROS generation in BM-MSCs after incubation with GO, GO-Au, GO-PG, GO-CRL, and NC + CRL for 48 hours.DCFH-DA and DAPI were used to detect ROS and cell nuclei, respectively.(a) Fluorescence microscope images with a scale bar of 50 mm, (b) quantitative ROS levels of nanocomposites (**p < 0.001, ***p < 0.0001).(c) Results of motor function evaluation of mice hind limbs using the BBB scale 1-14 days after injury.Data are expressed as mean ± SD (****p < 0.0001, determined by one-way ANOVA).

Fig. 6
Fig. 6 H&E staining was used to examine the histology of nerve tissue regeneration two weeks after surgery.Images from an optical microscope are exhibited at scales of 1 mm and 50 mm.(a) In the groups, the magnified pictures revealed cystic cavities (asterisks), bleeding (arrowheads), astrocytes (thick arrows), lymphocytes (thin arrows), and myelinated axons (thin arrowheads).Quantitative data for cavity areas and bleeding percent at longitudinal section lesion sites in the spinal cord (b and c).Mean ± SD, **p = 0.0031, ***p = 0.00045, and *p = 0.015 for cavity area and p # 0.000001 for hemorrhage percent, n = 12 per group.

Table 2
DLS analysis of GO, GO-Au, and GO-PG