| Literature DB >> 36015200 |
Nithya Rani Raju1, Ekaterina Silina2, Victor Stupin3, Natalia Manturova4, Saravana Babu Chidambaram5,6, Raghu Ram Achar1.
Abstract
The healing of wounds is a dynamic function that necessitates coordination among multiple cell types and an optimal extracellular milieu. Much of the research focused on finding new techniques to improve and manage dermal injuries, chronic injuries, burn injuries, and sepsis, which are frequent medical concerns. A new research strategy involves developing multifunctional dressings to aid innate healing and combat numerous issues that trouble incompletely healed injuries, such as extreme inflammation, ischemic damage, scarring, and wound infection. Natural origin-based compounds offer distinct characteristics, such as excellent biocompatibility, cost-effectiveness, and low toxicity. Researchers have developed biopolymer-based wound dressings with drugs, biomacromolecules, and cells that are cytocompatible, hemostatic, initiate skin rejuvenation and rapid healing, and possess anti-inflammatory and antimicrobial activity. The main goal would be to mimic characteristics of fetal tissue regeneration in the adult healing phase, including complete hair and glandular restoration without delay or scarring. Emerging treatments based on biomaterials, nanoparticles, and biomimetic proteases have the keys to improving wound care and will be a vital addition to the therapeutic toolkit for slow-healing wounds. This study focuses on recent discoveries of several dressings that have undergone extensive pre-clinical development or are now undergoing fundamental research.Entities:
Keywords: biomaterials; multifunctional dressings; nanoparticles; smart wound dressings; tissue regeneration
Year: 2022 PMID: 36015200 PMCID: PMC9414988 DOI: 10.3390/pharmaceutics14081574
Source DB: PubMed Journal: Pharmaceutics ISSN: 1999-4923 Impact factor: 6.525
Figure 1Factors affecting wound healing.
Figure 2Characteristic features of multifunctional smart wound dressings.
Figure 3Flow chart of article selection and review process.
Figure 4Types of dressings, applications, pros and cons.
Summary of recent advances in hydrogel dressings.
| Dressing Composition | Dressing Material Evaluated/ | Key Findings | Reference |
|---|---|---|---|
| Gelatin methacrylate (GM), methacrylate of silk fibroin (MSF), stem cells (SC) and platelet concentrate plasma (PCP) | Gauze, GM/MSF, GM/MSF/PCP, GM/MSF/PCP/SC | Wound healing, reepithelialisation, and collagen deposition are all accelerated. | [ |
| N-carboxyethyl chitosan, hyaluronic acid–aldehyde, insulin and adipic acid dihydrazide | Control, hydrogel, hydrogel + insulin | Expedited re-epithelialization and neovascularization; shortened inflammatory phase; increased granulation tissue formation; facilitated collagen deposition | [ |
| Polymerized ionic liquid (PL), konjac glucomannan (K) and electrical stimulation (ES) | Control, PL-K-0, PL-K-5, PL-K-10, PL-K-20, ES, PL-K-ES-20 | It has great mechanical qualities and biocompatibility, and it disinfect quickly and effectively | [ |
| Poly [2-(methacryloyloxy) ethyl] dimethyl-(3-sulfopropyl) ammonium hydroxide (SBMA), quaternized chitosan methacrylate (QCS) and Gelatin methacrylate (GelMA) | Control, SQG hydrogel | Improves granulation tissue development and collagen deposition by demonstrating good cell activity, hemocompatibility, and histocompatibility | [ |
| Cannabidiol (CD), Zinc (Zn2+) ions and the alginate polymer (Alg) | Control group, Tegaderm™ group (3M), Alg@Zn group, CD/Alg@Zn group | Controlling of inflammatory infiltration, collagen deposition and granulation tissue production, and blood vessel formation | [ |
| Gelatin meth acryloyl (GMa), Cerium oxide nanoparticles (CeNs) and an antimicrobial peptide (AMP) | GMa-Dopa, GMa-Dopa-AMP, GMa-Dopa-CeNs, GMa-Dopa-AMP-CeNs | Spray ability, adhesiveness, antibacterial activity, as well as the ability to scavenge ROS and regenerating skin are all promising | [ |
| Gelatin (G), methacrylic anhydride (M), sodium tetraborate and oxidized dextran (BD) | GelMA/OD/Borax hydrogel | Efficiently stopped the bleeding, decreasing bioburden and hastened the healing of the wound | [ |
| blank group, positive group (PBS) and G-M-BD | |||
| G-M-BD-L prepolymer solution, G-M-BD prepolymer solution | |||
| Rose Bengal (RB), graphene oxide (GO), polyvinyl Alcohol (PVA) hybrid hydrogel and chitosan microspheres | PVA, GO/PVA, β-GO/PVA, and β-GO/RB/PVA HDs | Biocompatibility and water-absorbing capability are desirable, as is an antimicrobial impact | [ |
| N-(9-fluorenylmethoxy carbonyl)-L-phenylalanine (Fmoc-F) and berberine chloride (BBR) | Control, Fmoc-F/BBR, Fmoc-F/BBR + Light | Antibacterial and anti-biofilm action has been improved | [ |
| Chitosan hydrogel membrane (CS), Cerium oxide nanoparticles (CeO2) from | CS, CS-1% CeO2, CS-5% CeO2 | Showed excellent microbicidal, antioxidant activity and proven to accelerate healing time and closure | [ |
Summary of recent advances in film dressings.
| Dressing Composition | Dressing Material Evaluated/ | Key Findings | Reference |
|---|---|---|---|
| Sodium alginate and pectin loaded with simvastatin (SIM) | Control, Saline, Hydrogel film, Kaltostat® commercial dressing, SIM-hydrogel film | Better angiogenic effect contributed accelerated healing, quicker re-epithelialization and improved collagen deposition | [ |
| Saline, Cytol centella cream, PVA film (100%), (70:30) PSP/PVA film | Hastened wound closure and reepithelialisation | [ | |
| Xyloglucan dressing (XG) and Concanavalin A © | Saline, XG, XGC | Non-toxic, homogenous, angiogenesis, remodelling, early epithelialization | [ |
| Chitosan film (CF) loaded with Vancomycin (V) | Saline, Burn, Burn vancomycin, Burn + CF, Burn + VCF2 | Controlled drug release, remarkable antimicrobial effect and enhanced wound recovery | [ |
| Polycaprolactone (PCL), Gelatin, poly (perfluoro decyl methacrylate) + poly (dimethyl siloxane) + poly (perfluoro decyl methacrylate (PMFA) | PCL-Gelatin, PCL-PMFA, PCL G + F | Non-adherent ability and constant drainage performance | [ |
| Ofloxacin (O), tea tree (T) and lavender oil (L) in gellan gum hydrogel film | Blank, O, L, T, OL, OT | Antibacterial and wound-healing properties are notable | [ |
Summary of recent advances in sponge dressings.
| Dressing Composition | Dressing Material Evaluated/ | Key Findings | Reference |
|---|---|---|---|
| Chitosan, alginate, hyaluronic acid, genipin | Medical gauze, CAHS1, CAHS2 and CAHS3 | Facilitates wound closure and haemostatic | [ |
| Kang Fuxin (K), Alginate (AG) and carboxymethyl chitosan (CMC) | Control, AC, AG, ACK-5, ACK-10, ACK-15 | Good moisture transmission, plasticity, antimicrobial features, low cytotoxicity, and haemostatic | [ |
| Chain based sponge dressing (CSD) | CSD and gauze | Achieved haemostasis quickly | [ |
| Janus polyurethane, Superhydrophobic silica nanoparticles, super hydrophilic polyurethane (PU) | Saline, PU Sponge, Janus PU sponge | Reduced the risk of infection, excessive wetting and accelerated the efficiency of healing | [ |
| Platelet rich plasma (PRP), collagen sponge scaffold (CSS) with modified polydopamine (PDA) | PDA-CSS-PRP, CSS-PRP, CSS and Normal Saline | Fast angiogenesis, rapid collagen arrangement leading to less scar development | [ |
| Corn stalk (CS), silver nanoparticles (AgNPs) and chitin sponge (CH) | Control, polyvinyl formal sponge, CH-CS-AgNPs, CH-CS, CH | Biocompatibility and nontoxicity, fast wound closure rate | [ |
| Chitosan and H. syriacus petroleum ether extract (SPC) | Control, Standard Mebo®, SPC-plain, SPC-low, SPC-medium, SPC-high | Perfect re-epithelization and epidermal remodelling | [ |
| recombinant collagen (rCOL) | Implantation test with rCOL, COL | Perfect biocompatibility with no sensitivity, no toxicity, no stimulation reactions observed and excellent haemostatic effect | [ |
| Saline, rCOL sponge extraction | |||
| Saline, Saline extraction, Solvent saline, Seasame oil Solvent extraction, non-polar solvent extraction | |||
| Control, Gelatin sponge, ADDS-CS3, ADDS-CS2 | Excellent haemostatic properties | [ |
Summary of recent advances in nanofiber dressings.
| Dressing Composition | Dressing Material Evaluated/ | Key Findings | Reference |
|---|---|---|---|
| Antimicrobial peptide KRWWKWWRRC (K), Collagen nanosheet (CN) | Blank, CN, KCN, | Good reepithelialisation, rapid wound closure and low inflammation | [ |
| Poly (caprolactone) (PCL), Poly (vinyl alcohol) (PVA), collagen nanofibers (Col), | Control, PCL/PVA/Col, PCL/PVA/Col/Ex 1%, PCL/PVA/Col/Ex 5%, PCL/PVA/Col/Ex 10% | Hemocompatible, cytocompatibility, and prevent bacterial penetration | [ |
| Nanofiber mat of cellulose acetate (CA) loaded with parathyroid hormone related protein (Pthrp-2) | CA, CAP-1%, CAP-5% | Promoted epithelialization, collagen deposition and blood vessel formation | [ |
| Distilled water, betadine ointment, MOS-PS-AgNPs-25, MOS-PS-AgNPs-50, MOS-PS-AgNPs-100 | Supports wound tightening and tissue generation as well | [ | |
| mupirocin® ointment, magnetite ointment, zinc oxide/magnetite ointment, control | Granulation tissue, collagen density and epithelization improvements observed | [ | |
| Bilayer scaffold consists curcumin dextran nanoparticles (CDN), cerium oxide nanoparticles (CON) loaded Gelatin cryogel layer and polyvinyl alcohol-poly (vinylpyrrolidone)-iodine-potassium iodide layer (GCL) | Control, GCL, GCL-CDN-CON, Tegaderm pad commercial | Strong antioxidant, antibacterial and faster wound closure | [ |
Summary of recent advances in foam dressings.
| Dressing Composition | Dressing Material Evaluated/ | Key Findings | Reference |
|---|---|---|---|
| Mesostructured cellular silica foams (MCF) decorated with silver ions (Ag) | Control, MCF and MCF-Ag | MCF-Ag antibacterial haemostatic agent with splendid water absorption and antibacterial capacity | [ |
| Polyurethane biomacromolecule combined foam (PUC), asiaticoside (AS), Silver nanoparticle (AgNPs) | PUC-AS-AgNPs, commercial gauze | shorter wound closure time, higher reepithelialisation and less pain score | [ |
| Hyaluronic acid, a cell wall fragment of | LimpiAD foam | Prevented skin lesions or any sign of skin damage | [ |
Summary of recent advances in gauze dressings.
| Dressing Composition | Dressing Material Evaluated/ | Key Findings | Reference |
|---|---|---|---|
| Gauze (G), Quat 188, silver nanoparticles (AgNPs), oxytetracyline hydrochloride (Ox) and salicyl-imine-chitosan biopolymer (SIC) | Gauze fabric, Dermazin Ointment, G/Ag NPs/Ox, G/Ag NPs/Ox/CS, fabrics/Ag NPs/Ox/SIC-0.2, G/Ag NPs/Ox/SIC-0.4, G/Ag NPs/Ox/SIC-0.6 | Promoting fibrosis and collagen reorganization | [ |
| Cotton guaze (CG), chitosan (C), Gelatin (G) and alginate (A) | Control, CG and AGCCg-5 | High fluid absorption, excellent biocompatibility, hemocompatibility, haemostatic performance, low cost, reliability, safety, and a simple manufacturing process | [ |
| Amino-modified cotton gauze (CG), poly (carboxybetaine-co-dopamine methacrylamide) (PCM) copolymer, silver nanoparticles (AgNPs) | Blank, Pristine CG, PCM@AgNPs-CG | Showed excellent hemocompatibility, cytocompatibility, reduced the inflammatory response and wound infection | [ |
| Gauze, polydopamine, perfluorocarbon and silver nanoparticle (Lotus@Gauze) | Vaseline® petrolatum gauze, Atrauman®Ag gauze, Lotus@Gauze, Irradiated Vaseline® petrolatum gauze, Irradiated atrauman®Ag gauze, Irradiated Lotus@Gauze | Antiadhesive and antibacterial gauzes | [ |
Summary of recent studies in plant extracts and proteases.
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| Control, Povidine ointment, | Wound healing is faster and wound contraction is better. | [ | |
| Silver sulphadiazine cream, aqueous cream, 10% BME aqueous cream, 2.5% BME aqueous cream, 0.625% BME aqueous cream | Angiogenesis, collagenation, and re-epithelization all improved, as did antibacterial and antioxidant activities | [ | |
| Serine protease (Tricuspidin) from | Tricuspidin & Trypsin | Excellent proteolytic ability, anti-inflammatory effect | [ |
| Tricuspidin & PBS | |||
| Gel, Gel (Mebo), PM, UA, and OA gels | Non-toxic & improve wound healing | [ | |
| Control, mupirocin® ointment, P, PG, PGC | Decreasing the length of healing time and stimulates MRSA-infected wound regeneration | [ | |
| Cysteine protease (Drupin) from | Saline, Neosporin, papain, Fd-protein rich fraction, drupin, drupin-IAA | Controlled expression of MMP’s, increased collagen production, cellular migration and proliferation | [ |
| Bromelain based Escghar ex (ESX) | ESX group, Gel arm group | Good debridement activity of the formulation | [ |
| Serine protease (SP), Antiquorin (Aq) | Saline, Aq, SP + Aq | Improved platelet aggregation and quick haemostatis | [ |
Figure 5Phytochemicals from various plant sources that have been found to be effective in wound treatments.