Protein-polysaccharide based nanogel/hydrogel composite with controlled continuous delivery of drug for enhanced wound healing.

Carbohydr Polym

Key Laboratory of Synthetic and Biological Colloids, Ministry of Education, School of Chemical and Material Engineering, Jiangnan University, Wuxi 214122, China. Electronic address:

Published: May 2025


Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

In the development of drug delivery vehicles for full-thickness skin wounds, achieving a specific drug concentration at the active site remains a key challenge. In this work, we reported a novel protein-polysaccharide bio-based composite hydrogel (SG@CRG) with controlled continuous drug delivery for enhanced wound healing. This composite hydrogel was prepared by incorporating drug embedded spirulina protein isolate nanogels (SG) into carboxymethyl chitosan based hydrogel (CRG) network, which exhibited rapid gelation and excellent mechanical properties. Notably, the release rate of the embedded drug could be tuned by adjusting the proportion of SG within the composite hydrogels. In vitro experiments demonstrated that the composite hydrogel exhibited excellent antibacterial activity against both gram-positive and gram-negative bacteria (inhibition rates at 12 h for S. aureus and E. coli were 99.77 % and 98.64 %, respectively), and good biocompatibility. Additionally, the hydrogel could effectively alleviate excessive inflammation and oxidative stress damage. Lastly, a full-thickness mouse skin model was established to assess its wound healing performance in vivo, which found that the composite hydrogel markedly accelerated wound healing (the healing ratios achieved by day 7 and day 12 were 78.37 % and 99.13 %, respectively, compared to 56.99 % and 84.50 % in the control group) by diminishing inflammation, promoting granulation tissue regeneration, increasing collagen deposition, and accelerating angiogenesis. Altogether, this innovative protein-polysaccharide bio-based composite hydrogel provides new insights and technical support for the development of more efficient wound treatment method, showing its potential application as a wound healing drug delivery vehicle.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.carbpol.2025.123407DOI Listing

Publication Analysis

Top Keywords

wound healing
20
composite hydrogel
20
drug delivery
12
controlled continuous
8
enhanced wound
8
protein-polysaccharide bio-based
8
bio-based composite
8
composite
7
drug
7
hydrogel
7

Similar Publications

Purpose: To clinically validate the nursing diagnosis "Inadequate Nutritional Intake" based on elements identified within a specific situation theory framework in the context of children with cancer.

Methods: This is a diagnostic accuracy study following the Standards for Reporting Diagnostic Accuracy Studies (STARD) protocol. Specifically, it refers to the clinical validation phase of the nursing diagnosis Inadequate nutritional intake, using a cross-sectional design.

View Article and Find Full Text PDF

Dermal Filler Use in Patients Undergoing Chemotherapy and Radiation Therapy.

JMIR Dermatol

September 2025

College of Osteopathic Medicine, Rocky Vista University, 8401 S Chambers Road, Parker, CO, 80112, United States, 1 9253236431.

Dermal fillers have gained increasing popularity for their ability to enhance facial symmetry, restore volume, and improve skin texture. However, their use in patients with cancer undergoing active chemotherapy and radiation therapy poses unique challenges, as these treatments can alter both the safety profile and efficacy of filler procedures. Chemotherapy can interfere with normal wound healing and immune responses, warranting a more cautious and individualized approach when considering dermal fillers in this population.

View Article and Find Full Text PDF

Bilayered chitosan scaffolds: a novel approach to mimicking native skin architecture.

Biomed Mater

September 2025

Department of Nanobiotechnology, Faculty of Biological Sciences, , Tarbiat Modares University, Tehran, P.O. Box 14115-154, Iran, Tehran, Tehran Province, 14115-154, Iran (the Islamic Republic of).

It is essential to develop new strategies for wound treatment and skin reconstruction, particularly by scaffolds that replicate the structure and function of native skin. A bilayer scaffold was developed using three-dimensional (3D) bioprinting, based on a uniform chitosan-based formulation for both layers, maintaining material uniformity while offering structural support and promoting cell adhesion. The upper chitosan layer, embedded with NHEK-Neo, is stiffer and mimics the epidermis, while the softer lower layer contains embedded HFFs and HFSCs, mimicking the dermis.

View Article and Find Full Text PDF

In recent years, the incidence of orthopedic diseases has increased significantly, while traditional treatments often face limitations such as limited efficacy and pronounced side effects. The development of nanomedicine technology provides novel strategies for orthopedic disease treatment. As an emerging two-dimensional (2D) nanomaterial, black phosphorus nanosheets (BPNS) demonstrate remarkable potential in treating orthopedic diseases due to their unique physicochemical properties, superior biocompatibility, and the fact that their degradation product-elemental phosphorus-constitutes an essential component of bone tissue.

View Article and Find Full Text PDF

The ferroptosis-associated gene TIMP1 facilitates skin scar formation through the interaction with CST3 in fibroblasts.

Int Immunopharmacol

September 2025

Medical Center of Burn Plastic and Wound Repair, the First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang 330006, Jiangxi, China. Electronic address:

Skin scar formation is a critical pathological process in wound healing, but its underlying regulatory mechanisms remain incompletely elucidated. By integrating analyses of Bulk-RNA seq and single-cell RNA sequencing (scRNA-seq) data, we identified that ferroptosis-related biological processes potentially play a key role in skin scar formation. Further mechanistic studies demonstrated that in human dermal fibroblast cells, the ferroptosis regulator TIMP metallopeptidase inhibitor 1 (TIMP1) significantly promotes fibroblast differentiation toward a mature phenotype through interactions with cystatin C (CST3), characterized by upregulated expression of myofibroblast differentiation markers such as α-smooth muscle actin (α-SMA) and connective tissue growth factor (CTGF), along with enhanced cell proliferation and migration abilities.

View Article and Find Full Text PDF