Hydroxypropyl Cellulose Research Articles

Multifunctional composite flexible films of hydroxypropyl cellulose and silver nanowires

Flexible wearable devices have aroused attentions since the booming flexible electronic technologies, as well as the requirements for improved comfortableness and real-time monitoring for complex motion state of human body. Developing a flexible integrated wearable device with multi functions provides a promising route for next-generation wearable devices. Meanwhile, transparency and biocompatibility are also considered a lot. Herein, hydroxypropyl cellulose/silver nanowires (HPC/AgNWs) flexible composite films were fabricated with a facile two-step method. The fabricated composite films exhibited sufficient transparency and mechanical strength. More importantly, the HPC/AgNWs composite films afforded good motion sensing performances with current sensitivity as high as 350 %. It can accurately identify different bending angles and frequencies, and remained stable for more than 1000 bending cycles. Apart from being employed as motion sensors, the fabricated HPC/AgNWs could be also used for electrical heating and electromagnetic shielding. The films could be heated to more than 60°C at 3.0 V in 57 seconds, and the electromagnetic shielding efficiency reached more than 99.9 %. This study contributed a feasible strategy for the preparation of multifunctional flexible films which are expected to be further applicated in the field of wearable devices.

The potential of new eco-friendly formulations in enhancing the protection of ceramic artifacts

This study focuses on transforming the consolidation formulations based on Hydroxypropyl cellulose (HPC), which is an eco-friendly bio-based cellulosic polymer with inherent hydrophilic characteristics to a hydrophobic one. This will be done via integrating the polymer with nano-silica and hydrophobic nano-silica, to enhance its consolidating properties to be in line with the global trend of replacing conventional materials with eco-friendly alternatives. Three different formulations were prepared, including HPC polymer solely, HPC integrated with nano-silica (NS), and HPC integrated with hydrophobic nano-silica (HNS). Primarily, nano-silica and hydrophobic nano-silica were synthesized and characterized using TEM and XRD. Subsequently, the prepared formulations were applied to artificial ceramic artifacts to evaluate their physical and mechanical properties, encompassing parameters such as water absorption, color change, contact angle, SEM/EDX, and digital microscopy. The results revealed that the incorporation of hydrophobic nano-silica significantly enhanced the mechanical and the physical properties of the cellulosic polymer, besides the extreme change that happened to its hydrophilic properties which was developed to a very good hydrophobic one. The success of these consolidation formulations can pave the way for the utilization of bio-based polymers with their inherent eco-friendly nature in the consolidation and restoration processes of cultural heritage artifacts, which can help in the contribution to the expanding body of knowledge in sustainable materials for conservation purposes.

Effect of hydroxy propyl cellulose grade and foam quality on foam granulation of a high drug load formulation

Foam granulation is a relatively newer wet granulation process whereby foamed binder solutions are added to the powders in the mixer to reduce localized over-wetting encountered during the wet granulation. This study is the first to investigate the effect of binder grade and foam quality on foam granulation process and granule properties of a high drug load formulation. Two different HPC grades, HPC LF (two times more viscous) and HPC EXF at an equivalent 7.4%w/w solution concentration, and foam quality of 50%, 90% and binder solution dripped were added to a high drug load (81%w/w) formulation for wet granulation. The granules were evaluated for compactibility and resultant compact strengths. The 50% foam quality of either HPC LF and HPC EXF resulted in lowest impeller power reading and water activity compared to 90% foam quality or dripped HPC solution. Granules prepared with 50% foam quality also exhibited smaller granule size, wider size distribution and higher specific surface area, resulting in higher compactibility. Whilst the granules prepared with different foamed HPC grades were not significantly different in compression behavior, they were higher in compact strengths, suggesting that foam mixing was more efficient in binder distribution compared to binder liquid penetration and distribution.

Triple-Responsive, Multimodal, Visual Electronic Skin toward All-in-One Health Management for Gestational Diabetes Mellitus.

Gestational diabetes mellitus (GDM) is one of the most common metabolic disorders during pregnancy, leading to serious complications for pregnant women and a threat to life safety of infants. Therefore, it is particularly important to establish a multipurpose monitoring pathway to important physiological indicators of pregnant women. In this work, three kinds of double network hydrogels are prepared with poly(vinyl alcohol) (PVA), borax, and cellulose ethers with varying substituents of methyl (methyl cellulose, MC), hydroxypropyl (hydroxypropyl cellulose, HPC), or both (hydroxypropyl methyl cellulose, HPMC), respectively. The corresponding toughness (143.9, 102.3, and 135.9 kJ cm-3) and conductivity (0.69, 0.45, and 0.51 S m-1) of the hydrogels demonstrate that PB-MC was endowed with the prominent performance. Molecular dynamics simulations further revealed the essence that hydrogen bond interactions between PVA and cellulose ethers play a critical role in regulating the structure and properties of hydrogels. Thermochromic capsule powders (TCPs) were subsequently doped in to achieve a composite hydrogel (TCPs@PB-MC) to indicate the change in human body temperature. Furthermore, the process of the TCPs@PB-MC response to glucose, pH, and temperature was tracked in-depth through the electrochemical window. This work provides a novel strategy for all-in-one health management of GDM.

Preparation of Gel Forming Polymer-Based Sprays for First Aid Care of Skin Injuries

Currently, there are several types of materials for the treatment of wounds, burns, and other topical injuries available on the market. The most used are gauzes and compresses due to their fluid absorption capacity; however, these materials adhere to the surface of the lesions, which can lead to further bleeding and tissue damage upon removal. In the present study, the development of a polymer-based gel that can be applied as a spray provides a new vision in injury protection, respecting the requirements of safety, ease, and quickness of both applicability and removal. The following polymeric sprays were developed to further obtain gels based on different polymers: hydroxypropyl cellulose (HPC), polyvinyl pyrrolidone (PVP) and hydroxypropyl methylcellulose (HPMC) using polyethylene glycol (PEG) as a plasticizer. The developed sprays revealed suitable properties for use in topical injuries. A protective film was obtained when sprayed on a surface through a casting mechanism. The obtained films adhered to the surface of biological tissue (pig muscle), turning into a gel when the exudate was absorbed, and proved to be washable with saline solution and contribute to the clotting process. Moreover, biocompatibility results showed that all materials were biocompatible, as cell viability was over 90% for all the materials.

Controlled micro-scale ink droplet spreading on cotton fabrics via cellulose-based coatings for greener textile inkjet printing

Inkjet printing of cotton fabric is considered a cleaner, efficient and revolutionary technology in textile coloration industry. However, due to the good hydrophilicity of cotton fibers, ink droplet spreading was difficult to be prevented, causing the problems of poor image resolution, low dye utilization efficiency and reduced product quality. Hence, in this study, cellulose-based coatings were fabricated on the cotton surface to adjust the surface hydrophilicity and prevent ink droplet spreading. Results showed that, cellulose derivatives like hydroxypropyl cellulose (CMHPC) and hydroxyethyl methyl cellulose (HEMC) could form continuous and uniform cellulose film coatings on fiber surface. Because there are fewer hydrophilic side groups in HEMC structure, the hydrophilicity of cotton fabric and the ink spreading was effectively controlled. From microscope observation, the spreading lengths of a single droplet were significantly decreased by HEMC from 276.27 to 66.95 μm. The K/S values representing color depth were improved from 9.44 to 19.41. Furthermore, industrial application was conducted to verify the laboratory results, showing that higher image quality was obtained in practical application using HEMC. This work provides a more potential and greener application of cellulose-based coatings to promote the development of textile inkjet printing.

Sustainable, super-stable thermochromic material by coupling hydroxypropyl cellulose and sodium carboxymethyl cellulose

Hydroxypropyl cellulose (HPC) is a green thermochromic material in energy-saving buildings, anti-counterfeiting, and data security fields. However, the high lower critical solution temperature (LCST) of HPC, around 42 °C (higher than the human thermal comfort temperature), limits its thermochromic sensitivity, poor stability, and short lifespan. Herein, we developed a durable, high-performance cellulose-based thermochromic composite with a lower LCST and easy preparation capability by combining HPC with sodium carboxymethyl cellulose (CMC). In such thermochromic cellulose, CMC constructs a hydrophilic skeleton to enable uniform dispersion of HPC, and functions as a stronger competitor to attract the water molecules compared to HPC, both of which trigger high thermochromic sensitivity and low LCST (just 32.5 °C) of our CMC/HPC. In addition, CMC/HPC shows superior stability, such as 100-day working capability and 60-time recyclability. This advancement marks a significant step forward in creating sustainable, efficient thermochromic materials, offering new opportunities for energy conservation in the building.

Consolidation materials used with illuminated and non-illuminated paper manuscripts and historical leather bindings: a review

Purpose This study aims to focus on the main materials used in consolidation processes of illuminated paper manuscripts and leather binding. Design/methodology/approach For each material, chemical structure, chemical composition, molecular formula, solubility, advantages, disadvantages and its role in treatment process are presented. Findings This study concluded that carboxy methyl cellulose, hydroxy propyl cellulose, methyl cellulose, cellulose acetate, nanocrystalline cellulose, funori, sturgeon glue, poly vinyl alcohol, chitosan, chitosan nanoparticles (NPs), gelatin, aquazol, paraloid B72 and hydroxyapatite NPs were the most common and important materials used for the consolidation of illuminated paper manuscripts. For the leather bindings, hydroxy propyl cellulose, polyethylene glycol, oligomeric melamine-formaldehyde resin, acrylic wax SC6000, pliantex, paraloid B67 and B72, silicone oil and collagen NPs are the most consolidants used. Originality/value Illuminated paper manuscripts with leather binding are considered one of the most important objects in libraries, museums and storehouses. The uncontrolled conditions and other deterioration factors inside the libraries and storehouses lead to degradation of these artifacts. The brittleness, fragility and weakness are considered the most common deterioration aspects of illuminated paper manuscripts and leather binding. Therefore, the consolidation process became vital and important to solve this problem. This study presents the main materials used for consolidation process of illuminated paper manuscripts and leather bindings.

Topical Meloxicam Hydroxypropyl Guar Hydrogels Based on Low-Substituted Hydroxypropyl Cellulose Solid Dispersions.

Meloxicam (MX) is a poorly water-soluble drug with severe gastrointestinal side effects. Topical hydrogel of hydroxypropyl guar (HPG) was formulated using a solid dispersion (SD) of MX with hydroxypropyl cellulose (LHPC) as an alternative to oral administration. The development of a solid dispersion with an adequate MX:LHPC ratio could increase the topical delivery of meloxicam. Solid dispersions showed high MX solubility values and were related to an increase in hydrophilicity. The drug/polymer and polymer/polymer interactions of solid dispersions within the HPG hydrogels were evaluated by SEM, DSC, FTIR, and viscosity studies. A porous structure was observed in the solid dispersion hydrogel MX:LHPC (1:2.5) and its higher viscosity was related to a high increase in hydrogen bonds among the -OH groups from LHPC and HPG with water molecules. In vitro drug release studies showed increases of 3.20 and 3.97-fold for hydrogels with MX:LHPC ratios of (1:1) and (1:2.5), respectively, at 2 h compared to hydrogel with pure MX. Finally, a fitting transition from zero to first-order model was observed for these hydrogels containing solid dispersions, while the n value of Korsmeyer-Peppas model indicated that release mechanism is governed by diffusion through an important relaxation of the polymer.

CONSERVATION OF A PAINTED WOODEN COFFIN AT DAHSHUR ARCHAEOLOGICAL AREA

This paper aims to document the conservation processes of a polychrome wooden coffin in the Dahshur archaeological area dating back to the late period. The exterior part of the coffin is decorated with a painted layer. Visual observation, 2D Program, and Optical Microscopy (OM) were used. wood identification. The coffin was in a bad condition. It was covered with a thick layer of dust, losing parts of the painted and gesso layers, as well as other parts of these layers, were lost. Some parts were missing from the head area of the lid coffin. The conservation processes of the wooden coffin included mechanical and chemical cleaning, reattachment of the separated parts of the ground layer and painted layers, filling the edge of the painted layer, and consolidating the painted layer. The conservation process included mechanical cleaning using soft brushes, chemical cleaning using ethyl alcohol and distilled water for painting, stabilization of the separated gesso layer using Paraloid B72, filling cracks of the gesso layers using glass microballoon with Paraloid B72 and consolidating the painted layer with calcium oxide nanoparticles with Klucel G (hydroxypropyl cellulose) 0. 5%

Efficient carbon dioxide capture from flue gas and natural gas by a robust metal–organic framework with record selectivity and excellent granulation performance

The design of porous materials for CO2 capture from flue gas and natural gas is highly demanded. However, it is challenging to target materials that combine high CO2 capacity and CO2 selectivity. In this work, we report a robust metal–organic framework (MOF) Zn-ox-mtz with one dimensional channels and narrow windows for excellent CO2 capture from CO2/N2 (simulated flue gas) and CO2/CH4 (simulated natural gas) with high selectivity. Zn-ox-mtz exhibits a high CO2 capacity (58.0 STP cm3 g−1 at 15 kPa), excellent CO2/N2 (15/85, S > 106) and CO2/CH4 (50/50, S > 105) selectivity and good chemical stability. In addition, the practical separation performance is demonstrated by breakthrough experiments under various process conditions. A efficient separation is achieved with the impressive CO2 capacity of 2.60 ± 0.12 mmol g−1 at 298 K. Importantly, the outstanding performance is sustained under high humidity. The molecular sieving mechanism investigated by theoretical calculations indicated that CO2 with small molecular size is tightly trapped by multiple C = O···H-C hydrogen bonding and O = C···O forces in the cavity while CH4 and N2 with larger molecular size display overlarge energy barrier to cross the contract pore windows. Moreover, the granulation of Zn-ox-mtz by hydroxypropyl cellulose is realized with high MOF loading (93.8 %) and the granulated Zn-ox-mtz beads retained the excellent CO2/N2 and CO2/CH4 separation performance.

3D Printing of Luminescent Perovskite Quantum Dot–Polymer Architectures

AbstractOrganic–inorganic perovskite quantum dot (PQD)–polymer composites are emerging optoelectronic materials with exceptional properties that are promising widespread application in next‐generation electronics. Advances in the utilization of these materials depend on the development of suitable fabrication techniques to create 3D architectures composed of PQD–polymer for sophisticated optoelectronics. This study introduces a straightforward and effective method for producing 3D architectures of PQD‐encapsulated high‐performance composites (PQD‐HPCs) through direct‐ink writing (DIW). This method employs an ink composed of prefabricated PQDs and hydroxypropyl cellulose (HPC) in dichloromethane (DCM). HPC, an appropriate organic‐soluble polymer, exhibits optical transparency in the highly volatile DCM and enables the formulation of a stable, room‐temperature extrudable ink. The architectures, which are printed by adjusting the halide ratios (Cl, Br, and I) for the compositions of CH3NH3PbBr1.5I1.5, CH3NH3PbBr3, and CH3NH3PbBr1.5Cl1.5, exhibit single peak photoluminescence emissions of red (639 nm), green (515 nm), and blue (467 nm). Optimizing the printing parameters of DIW enables the precise fabrication of programmed and complex PQD‐HPC 3D architectures for advanced anti‐counterfeiting and information encryption. This method has the potential to enhance the functionality of modern printed electronic devices significantly.

Successful vitrification of equine embryos >300 microns without puncture or aspiration.

Equine embryos >300 μm require puncture before vitrification. Protocols that do not require pre-puncture would make vitrification easier and allow for its widespread use. To design a successful vitrification protocol for embryos >300 μm without puncture as a pre-treatment. Experimental in vivo study. Thirty-eight embryos were divided into 3 groups (G1: ≤300 μm, n = 11; G2: >300-500 μm, n = 20; G3: >500 μm, n = 7). Embryos were vitrified using a human vitrification kit. Following a 15 min exposure to equilibration solution (ES; 7.5% DMSO +7.5% ethylene glycol [EG] in a base medium [BM] of M199 HEPES-buffered medium [H199] + hydroxypropyl cellulose + gentamycin), embryos were exposed for ≤90 s to a vitrification solution (15% DMSO +15% EG + 0.5 M trelahose in BM), loaded onto a Cryolock and plunged into LN2. Warming was undertaken by plunging the Cryolock tip into 1 mL of H199 + 20% FBS + pen/strep +1 M sucrose at 42°C for 1 min. The embryos were then moved to a 0.5 M sucrose solution for 4 min, then placed in Vigro Hold for 4 min prior to transfer to a recipient. Pregnancy rates were 81.8% (9/11) for G1, 80% (16/20) for G2, and 0% (0/7) for G3. The largest embryo to survive was 480 μm. Limited numbers and only one pregnancy was followed to term. Equine embryos ≤480 μm can be successfully vitrified using a protocol with a longer exposure time to the ES. This does not appear to have a negative effect on early embryonic development.

DESIGN, DEVELOPMENT, AND CHARACTERIZATION OF LORATADINE SUSTAINED RELEASED BUCCAL FILM: IN VITRO AND IN VIVO STUDY IN BEAGLE DOGS

Objective: The aim of this work was to develop and evaluate bucco-adhesive films of Loratadine (LTD) for sustained release use. Methods: Design of twelve different sustained released buccal film formulas using Carbopol, pectin, sodium alginate, glycerol, carboxymethyl cellulose (CMC), hydroxypropyl cellulose (HPC), Gelatin, Hydroxyethyl cellulose (HEC), and Hydroxypropyl methylcellulose (HPMC) as mucoadhesive polymers. Films were evaluated for physicochemical properties, thickness, swelling, moisture content, drug content, in vitro dissolution. The pharmacokinetic parameters of optimal formula were evaluated in beagle dogs. Results: The selected film formula (F6) showed accepted content and muco-adhesion properties. The in vitro release study showed prolonged release of drug from films over 10 h in optimal formulation. The bioavailability studies performed using beagle dogs model showed that there was 113.45% increase in the AUC0-24 of selected film compared with oral market tablets. Conclusion: Bucco-adhesive films is a promising dosage form for improving the bioavailability of loratadine.

Fabrication of CuO nanoparticles embedded novel chitosan/hydroxypropyl cellulose bio-nanocomposites for active packaging of jamun fruit

The study herein was intended to develop CuO nanoparticles (CuO NPs) embedded in chitosan (CS) and hydroxypropyl cellulose (HPC) based bio-nanocomposites with improved functional properties to prolong the shelf life of fruits using eco-friendly solvent casting technique. ATR-FTIR spectroscopy revealed hydrogen bonding interactions between the CS, HPC and CuO NPs. The homogeneity of the CuO NPs distributed bio-nanocomposites was verified by SEM images with minimum aggregations. Bio-nanocomposites showed improved mechanical properties (tensile strength of 33 MPa) with excellent UV-light blocking ability (4% of %transmittance at 360 nm and 20% transparency at 600 nm), also, a significant decrease in moisture adsorption (5.27%), water vapour permeability (2.47%), oxygen permeability (1.39%), and biodegradability (12.58%) compared to control CS/HPC blend film. Furthermore, CuO NPs induced CS/HPC bio-nanocomposites exhibited strong antimicrobial properties against B. subtilis, S. aureus, P. aeruginosa, E. coli, and C. albicans as well as antioxidant properties. Moreover, 0.8% of CuO NPs embedded in CS/HPC bio-nanocomposite film extended the shelf life of packed jamun fruits confirming the potential of prepared bio-nanocomposites to serve as an active food packaging material.

Assessment of the structural change of DNA by binding with a small molecule based on capillary sieving electrophoresis.

In this study, capillary sieving electrophoresis (CSE) using polymer solutions was used to evaluate the structural changes in nucleic acids upon complexation with small molecules. As the model target and nucleic acids, L-tyrosinamide (Tyr-Am) and its aptamer, which is a type of DNA specifically binding to Tyr-Am, were selected. CSE was conducted using a capillary filled with background solution (BGS) containing hydroxypropyl cellulose (HPC) as a sieving matrix. When Tyr-Am or tyrosine was added to the BGS in CSE, the ratio of mobility differences of the Tyr-Am-aptamer complex increased compared to that of the free aptamer without the addition of Tyr-Am. In contrast, when other amino acids or their analogs were added, results showed no apparent change or decreases in electrophoretic mobility. These results indicate that the proposed method can be applied to assess structural changes in nucleic acids that target small molecules.

Optimizing Nonsink Dissolution Testing for Amorphous Solid Dispersions: Exploring Sample Handling Variables.

This study aims to investigate key variables affecting the dissolution of amorphous pharmaceuticals. We examined sample treatment methods (centrifugation vs syringe filtration), time delays between sample collection and processing (immediate, 2, or 24 h), and different sample preparations (bare powder, capsules, or tablets). These factors were evaluated through both sink and nonsink dissolution experiments, using controlled supersaturation conditions (sink index ≈ 0.1) with amorphous solid dispersions (ASDs) containing low-substituted hydroxypropyl cellulose (L-HPC) and either indomethacin or posaconazole as model drugs. Our results highlighted the significant impact of syringe filtration on nonsink dissolutions, particularly the notable reduction in dissolved drug concentration, possibly due to filtration-induced precipitation. Moreover, introducing a delay of 2 or 24 h between sample collection and quantitation under nonsink conditions led to substantial concentration changes. This effect was not as pronounced when samples underwent centrifugation, and only the analysis was delayed for 2 h. The findings also emphasize the importance of accounting for delays introduced by pharmaceutical formulations, particularly in assessing the kinetic-solubility profiles of ASDs. This research offers valuable insights into the field of ASDs, enhancing our understanding of how these variables can influence dissolution results.

Water and Oxygen Barrier Properties of All-Cellulose Nanocomposites.

Hydroxypropyl cellulose (HPC) is potentially interesting as a biobased, rigid food packaging material, but its stiffness and strength are somewhat low, and its water and oxygen transport rates are too high. To improve these characteristics, we investigated nanocomposites of HPC and cellulose nanocrystals (CNCs). These high-aspect-ratio nanoparticles display high stiffness and strength, and their high crystallinity renders them virtually impermeable. Exchanging the counterions of sulfate-ester decorated CNCs with cetyltrimethylammonium ions affords particles that are dispersible in ethanol (CTA.CNC) and allows solvent casting of HPC/CTA.CNC nanocomposite films, which, even at a CTA.CNC content of 90 wt %, are highly transparent. The introduction of CTA.CNC considerably increases the Young's modulus (Ey) and upper tensile strength (σUTS). For example, in the nanocomposite with 90% CTA.CNC, Ey = 7.6 GPa is increased 20-fold and σUTS = 42.7 MPa is more than doubled in comparison to HPC, whereas the extensibility (1.1%) remains appreciable. Composites with a CTA.CNC content of 70 wt % or less show a lower water vapor permeability (6.4-9.2 × 10-5 g μm m-2 s-1 Pa-1) than the neat HPC (1.5 × 10-4 g μm m-2 s-1 Pa-1), whereas the oxygen permeability (5.6 × 10-7-1.3 × 10-6 cm3 μm m-2 s-1 Pa-1) is reduced by 1 order of magnitude compared to HPC (3.2 × 10-6 cm3 μm m-2 s-1 Pa-1). The biobased nanocomposites retain their mechanical integrity at a relative humidity of 75% but readily disintegrate in water.

Trace polymer coated clarithromycin spherulites: Formation mechanism, improvement in pharmaceutical properties and development of high-drug-loading direct compression tablets

Clarithromycin (CLA) is a high dose antibiotic drug exhibiting poor flowability and tabletability, making the tablet development challenging. This study aims to develop spherulitic CLA by introducing trace amount of polymer in crystallization solution. Its formation mechanism, physicochemical properties and potential for the direct compression (DC) tablets development were also investigated. Morphological analyses and the in situ observation on crystallization process revealed that the CLA spherulites are formed by fractal branching growth from both sides of the threadlike precursor fibers. 1H NMR analysis and nucleation time monitoring indicated that the existence of hydroxypropyl cellulose in solution slowed down the crystal nucleation and growth rate by forming hydrogen bonding interactions with CLA molecules, making the system maintain high supersaturation, providing high driving forces for CLA spherulitic growth. In comparison to commercial CLA, the CLA spherulites exhibit profoundly improved flowability, tabletability and dissolution behaviors. XPS, contact angle and Raman mapping analysis confirmed the presence of a thin HPC layer on the surfaces and interior of CLA spherulitic particles, resulting in increasing powder plasticity, interparticulate bonding strength and powder wettability, thus better tabletability and dissolution performances. The improved flowability and tabletability of CLA spherulites also enabled the successful development of DC tablet formulation with a high CLA loading (82.8 wt%) and similar dissolution profiles to reference listed drug. This study provides a novel solid form of CLA with superior manufacturability for further development.

Injectable and Thermosensitive Hydrogel with Platelet-Rich Plasma for Enhanced Biotherapy of Skin Wound Healing.

The rapid and effective healing of skin wounds resulted from severe injuries and full-layer skin defects remains a pressing clinical challenge in contemporary medical practice. The reduction of wound infection and rapid healing is helpful to rebuild and repair skin tissue. Here, a thermosensitive chitosan-based wound dressing hydrogel incorporating β-glycerophosphate (GP), hydroxy propyl cellulose (HPC), graphene oxide (GO), and platelet-rich plasma (PRP) is developed, which exhibits the dual functions of antibacterial properties and repair promotion. GP and HPC enhance the mechanical properties through forming hydrogen bonding connection, while GO produces local heat under near-infrared light, leading to improved blood circulation and skin recovery. Notably, antibacterial properties against Pseudomonas aeruginosa, and control-release of growth factors from PRP are also achieved based on the system. In vitro experiments reveal its biocompatibility, and ability to promote cell proliferation and migration. Animal experiments demonstrate that the epithelial repair and collagen deposition can be promoted during skin wound healing in Sprague Dawley rats. Moreover, a reduction in wound inflammation levels and the improvement of wound microenvironment are observed, collectively fostering effective wound healing. Therefore, the composite hydrogel system incorporated with GO and PRP can be a promising dressing for the treatment of skin wounds.