Porous SBA-15/cellulose membrane with prolonged anti-microbial drug release characteristics for potential wound dressing application

Cellulose ◽  
2020 ◽  
Vol 27 (5) ◽  
pp. 2737-2756
Author(s):  
Zhi Shen ◽  
Ning Cai ◽  
Yanan Xue ◽  
Bo Yu ◽  
Jianzhi Wang ◽  
...  
Polymer ◽  
2021 ◽  
pp. 123786
Author(s):  
Weiwei Fan ◽  
Zetian Zhang ◽  
Yang Liu ◽  
Junchao Wang ◽  
Zhengjun Li ◽  
...  

2021 ◽  
Vol 36 (5) ◽  
pp. 431-443
Author(s):  
Swetha Andra ◽  
Satheesh kumar Balu ◽  
Rajalakshmi Ramamoorthy ◽  
Murugesan Muthalagu ◽  
Devisri Sampath ◽  
...  

Wound healing properties of some herbs have been known for decades. Recently, electrospun mats have been used as a wound dressing material due to the high surface area of fiber and ease of incorporation of drug into the fiber matrix. In this aspect, the incorporation of herbal extracts in electrospun matrix could provide synergistic effect for wound healing. In the present work, extracts from Cissus quadrangularis (CQ) and Galinsoga parviflora Cav (GP) were loaded into the PVA solution in different proportions. These solutions were used to produce nanofibrous mat in electrospinning and the characteristics of the mat were analyzed. The morphology of the fiber was analyzed using scanning electron microscope (SEM), the presence of functional groups was identified using Fourier transform infrared spectroscopy (FTIR). The result of drug release shows that the GP extract loaded PVA nanofibrous mat has sustained drug release of 28% after 8 h of incubation compared to CQ loaded PVA nanofibrous mat. This trend follows as the concentration of GP increases in the mixture. The antimicrobial efficiency of the prepared mat was evaluated against both Gram-negative bacteria E. coli and Gram-positive bacteria S. aureus. The prepared nanofibrous mat has shown excellent antibacterial activity, cell viability, hemocompatibility, and sufficient tensile properties which indicates that it could be a promising biomaterial for wound dressing application.


2020 ◽  
Vol 3 (10) ◽  
pp. 7219-7227
Author(s):  
Ho Ying Huang ◽  
Artiom Skripka ◽  
Liana Zaroubi ◽  
Brandon L. Findlay ◽  
Fiorenzo Vetrone ◽  
...  

2014 ◽  
Vol 122 ◽  
pp. 175-183 ◽  
Author(s):  
Bhavesh D. Kevadiya ◽  
Shalini Rajkumar ◽  
Hari C. Bajaj ◽  
Shiva Shankaran Chettiar ◽  
Kalpeshgiri Gosai ◽  
...  

Materials ◽  
2021 ◽  
Vol 14 (23) ◽  
pp. 7266
Author(s):  
Kamil P. Grela ◽  
Dominik M. Marciniak ◽  
Bożena Karolewicz

This article covers the design and evaluation of a novel drug vehicle: a thermosensitive, injectable, high-oil-content (50% w/w) emulgel providing a controlled release of lipophilic pharmaceuticals. Different vegetable (castor, canola, olive, peanut, grapeseed, linseed), mineral (paraffin) and semisynthetic (isopropyl myristate, oleic acid) oils were screened for ibuprofen (IBU) solubility and for their capacity for high-shear emulsification in a 17% (w/w) aqueous solution of poloxamer 407. Chosen emulgels were subject to a rheological evaluation, a syringeability test (TA.XT texture analyser; 2 mL syringe; 18 G, 20 G and 22 G needles) and a drug release study (48 h; cellulose membrane; 0.05 mol/L phosphate buffer at pH 7.4). Castor oil turned out to be an optimal component for IBU incorporation. Blank and drug-loaded castor oil emulgels were susceptible to administration via a syringe and needle, with the absolute injection force not exceeding 3 kg (29.4 N). The drug release test revealed dose-dependent, quasi-linear kinetics, with up to 44 h of controlled, steady, linear release. The results indicate the significant potential of high-oil-content, oil-in-water thermosensitive emulgel formulations as vehicles for the controlled release of lipophilic APIs.


Polymers ◽  
2019 ◽  
Vol 11 (5) ◽  
pp. 808 ◽  
Author(s):  
Zhi Shen ◽  
Ning Cai ◽  
Yanan Xue ◽  
Vincent Chan ◽  
Bo Yu ◽  
...  

The sustained release of antimicrobial therapeutics for wound dressing has become an attractive design strategy for prolonging the timespan of wound dressings and for reducing the risk of chronic wound infection. Recently, cellulose-based membrane has become a preferred option of wound dressings for the treatment of burn wounds and skin ulcers. In this work, novel cellulose membrane incorporated with mesoporous silica particles (SBA-15) was developed as an antimicrobial wound dressing with desirable sustained release functionality for targeting persistent bacterial pathogens. Attributed to a coated layer of calcium carbonate (CaCO3), SBA-15 particles were free from corrosion in alkaline condition during the preparation of cellulose-based composite membranes. SEM, TEM and BET results showed that the morphology, specific surface area, pore size and pore volume of pristine SBA-15 were preserved after the incorporation of CaCO3-coated SBA-15 into the cellulose matrix, while the mesoporous structure of SBA-15 was significantly disrupted without the use of CaCO3 coating. The resultant composite membranes containing 30 wt% SBA-15 (denoted as CM-Ca2-SBA(30%)) achieved 3.6 wt% of antimicrobial drug loading. Interestingly, CM-Ca2-SBA(30%) demonstrated the sustained release property of chloramphenicol for 270 h, driven by a two-stage drug release processes of SBA-15/cellulose. The water vapor permeability (WVTR) and swelling properties of composite membranes were shown to have complied with the primary requirements of wound dressing. Antibacterial assays revealed that strong antibacterial activities (144 h) of the composite membranes against Staphylococcus aureus and Eschericia coli were achieved. All results displayed that the strategy of coating silica with CaCO3 helps to obtain cellulose–silica composite membranes with desirable sustained release profiles and strong antibacterial activities. The antibacterial SBA-15/cellulose composite membranes show potential for the application of wound dressing.


2020 ◽  
Vol 2020 ◽  
pp. 1-15
Author(s):  
Woan Sean Tan ◽  
Palanisamy Arulselvan ◽  
Shiow-Fern Ng ◽  
Che Norma Mat Taib ◽  
Murni Nazira Sarian ◽  
...  

Chronic wounds represent serious globally health care and economic issues especially for patients with hyperglycemic condition. Wound dressings have a predominant function in wound treatment; however, the dressings for the long-lasting and non-healing wounds are still a significant challenge in the wound care management market. Astonishingly, advanced wound dressing which is embedded with a synthetic drug compound in a natural polymer compound that acts as drug release carrier has brought about promising treatment effect toward injured wound. In the current study, results have shown that Vicenin-2 (VCN-2) compound in low concentration significantly enhanced cell proliferation and migration of HDF. It also regulated the production of pro-inflammatory cytokines such as IL-6, IL-1β, and TNF-α from HDF in wound repair. Treatment of VCN-2 also has facilitated the expression of TGF-1β and VEGF wound healing maker in a dose-dependent manner. A hydrocolloid film based on sodium alginate (SA) incorporated with VCN-2 synthetic compound which targets to promote wound healing particularly in diabetic condition was successfully developed and optimized for its physico-chemical properties. It was discovered that all the fabricated film formulations prepared were smooth, translucent, and good with flexibility. The thickness and weight of the formulations were also found to be uniform. The hydrophilic polymer comprised of VCN-2 were shown to possess desirable wound dressing properties and superior mechanical characteristics. The drug release profiles have revealed hydrocolloid film, which is able to control and sustain the VCN-2 released to wound area. In short, hydrocolloid films consisting of VCN-2 formulations are suitably used as a potential wound dressing to promote restoration of wound injury.


2018 ◽  
Vol 89 (5) ◽  
pp. 801-813 ◽  
Author(s):  
Bing Li ◽  
Dapeng Li ◽  
Yanni Yang ◽  
Lu Zhang ◽  
Ke Xu ◽  
...  

In this study, direct deposition, 1,2,3,4-butanetetracarboxylic acid (BTCA) crosslinking, chelating and ultraviolet (UV) photo-grafting methods were employed to bond alginate-Ca2+/poly( N-isopropylacrylamide) (PNIPAAm) interpenetrating network hydrogel onto cotton fabric surface for wound dressing applications. Infrared spectroscopy confirmed the presence of alginate-Ca2+/PNIPAAm hydrogels on the cotton fabrics. Scanning electron microscopy was used to investigate surface and cross-section morphologies. Differential scanning calorimetry and three-dimensional video microscopy indicated that fabric-supported hydrogels maintained the thermal-sensitive property with a lower critical solution temperature (LCST) of around 34–35℃. The results of water vapor permeation revealed that the water vapor transmission rate at 37℃ was significantly higher than that at 25℃ for the shrink and collapse of the hydrogels above the LCST. Moreover, the breaking stress of the fabric-supported hydrogels was similar to that of the original cotton fabrics, but much larger than the hydrogels by themselves. The UV photo-grafting provided the strongest peel strength, followed by the BTCA crosslinking, the chelating and the direct deposition method. The cotton fabric-supported alginate-Ca2+/PNIPAAm hydrogels were stiffer than the original cotton fabric due to the high glass transition temperature of PNIPAAm (about 140℃). The in vitro drug release experiment confirmed that the cumulative release amount was much higher at around 37℃ (above the LCST) than at 25℃ (below the LCST). This showed that the fabric-supported thermal-sensitive hydrogels had functions of keeping the wound area breathable and comfortable, and provided controlled drug release with good mechanical properties, indicating a great potential and significance for wound dressing applications.


Sign in / Sign up

Export Citation Format

Share Document