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1.
Biomater Adv ; 154: 213641, 2023 Nov.
Article in English | MEDLINE | ID: mdl-37804685

ABSTRACT

In this study, a wound dressing of electrospun polycaprolactone (PCL) fibers incorporating the antimicrobial peptide (AMP) nisin was fabricated. Nisin was physically adsorbed to the PCL fibers and tested for antibacterial activity against both Staphylococcus aureus (S. aureus) and Pseudomonas aeruginosa (P. aeruginosa). The PCL fibers had an average diameter of 1.16 µm ± 0.42 µm and no significant change in diameter occurred after nisin adsorption. X-ray photoelectron spectroscopy (XPS) analysis of the fibers detected nitrogen indicative of adsorbed nisin and the signal was used to quantify the levels of coverage on the fiber surfaces. In vitro nisin release studies showed a burst release profile with 80 % of the nisin being released from the fibers within 30 min. Air plasma pre-treatment of the PCL fibers to render them hydrophilic improved nisin loading and release. Antibacterial testing was performed using minimum inhibitory concentration (MIC) and surface attachment assays. The released nisin remained active against both Gram positive S. aureus and Gram negative P. aeruginosa, which has previously been difficult to achieve with single polymer fiber systems. Mammalian cell culture of the nisin coated fibers with L-929 mouse fibroblasts and human epidermal keratinocytes (HEKa) showed that the nisin did not have a significant effect on the biocompatibility of the PCL fibers. The results presented here demonstrate that the physical adsorption, which is a post-treatment, overcomes the potential limitations of harsh chemicals and fabrication conditions of electrospinning from organic solvents and provides a drug loading system having effective antibacterial properties in wound dressings.


Subject(s)
Nisin , Staphylococcal Infections , Mice , Animals , Humans , Nisin/pharmacology , Nisin/chemistry , Staphylococcus aureus , Pseudomonas aeruginosa , Anti-Bacterial Agents/pharmacology , Anti-Bacterial Agents/chemistry , Mammals
2.
Macromol Biosci ; 23(1): e2200347, 2023 01.
Article in English | MEDLINE | ID: mdl-36353916

ABSTRACT

Nanofibrous microspheres (NFM) are emerging as prominent next-generation biomimetic injectable scaffold system for stem cell delivery and different tissue regeneration where nanofibrous topography facilitates ECM-like stem cells niches. Addition of osteogenic bioactive nanosilicate platelets within NFM can provide osteoconductive cues to facilitate matrix mediated osteogenic differentiation of stem cells and enhance the efficiency of bone tissue regeneration. In this study, gelatin nanofibrous microspheres are prepared containing fluoride-doped laponite XL21 (LP) using the emulsion mediated thermal induce phase separation (TIPS) technique. Systematic studies are performed to understand the effect of physicochemical properties of biomimicking NFM alone and with different concentrations of LP on human dental follicle stem cells (hDFSCs), their cellular attachment, proliferation, and osteogenic differentiation. The study highlights the effect of LP nanosilicate with biomimicking nanofibrous injectable scaffold system aiding in enhancing stem cell differentiation under normal physiological conditions compared to NFM without LP. The laponite-NFM shows suitability as excellent injectable biomaterials system for stem cell attachment, proliferation and osteogenic differentiation for stem cell transplantation and bone tissue regeneration.


Subject(s)
Nanofibers , Osteogenesis , Humans , Gelatin/pharmacology , Gelatin/chemistry , Microspheres , Nanofibers/chemistry , Dental Sac , Cell Differentiation , Stem Cell Transplantation , Tissue Scaffolds/chemistry , Tissue Engineering/methods
3.
Biomater Adv ; 139: 212981, 2022 Aug.
Article in English | MEDLINE | ID: mdl-35882137

ABSTRACT

Stem cells based novel treatment modality for degenerative and immune dysfunction diseases created a huge demand of suitable carriers to support ex-vivo production of quality stem cells, and effective in-vivo transplantation of stem cells and their fate. In spite of promising candidature of nanofibrous microspheres (NFM) to recreate native stem cell niches to be used for possible scaling-up for ex-vivo stem cells expansion, it remains fairly unexplored. A systematic study on the stem cell-NFM interaction comparative with commercial microspheres (CM) has been performed for the first time. Gelatin NFM with variable physicochemical properties such as size, surface properties, surface chemistry, and variable degradability were prepared using microemulsion coupled with thermally induced phase separation (TIPS) method. Effect of physicochemical properties of NFM and their cellular interaction such as binding, morphology, metabolic activity and proliferation studies were performed using human bone marrow-derived mesenchymal stem cells (hBMSCs), human dental follicle stem cells (hDFSCs) and human gingival fibroblast (HGF) cells and compared with the commercial and solid microspheres. Gelatin NFM supports excellent cell binding, proliferation, metabolic activities and chemical cues specific differentiation. All out-turns indicate that NFM stand to be an outstanding candidate for ex-vivo cells' expansion and injectable carriers for stem cell transplantation.


Subject(s)
Gelatin , Nanofibers , Gelatin/chemistry , Humans , Microspheres , Nanofibers/chemistry , Stem Cell Niche , Stem Cell Transplantation
4.
ACS Appl Bio Mater ; 2(12): 5340-5348, 2019 Dec 16.
Article in English | MEDLINE | ID: mdl-35021534

ABSTRACT

Gelatin nanofibers have gained significant attention for different biomedical applications, as they provide a suitable environment for cell attachment, growth, and proliferation compared to the other biopolymers and synthetic polymers. Airbrushing/solution-blow-spinning could overcome the limitation of the conventional electrospinning method of nanofiber preparation. The present study reports the fabrication of nano/microfibers from commercially available low-molecular-weight gelatin of animal origin as a first-time study. The effect of various airbrushing parameters, namely, the concentration of gelatin solution, air pressure, and polymer solution flow rate on the fiber quality, morphology, and diameters, was studied. Finally, the biological evaluation of the airbrushed gelatin nanofibers was performed using human bone marrow-derived mesenchymal stem cells (hBMSCs). Gelatin nanofibers exhibit excellent biocompatibility and support the growth of hBMSCs similar to electrospun gelatin nanofibers. Our airbrushing technique is an easy, low-cost, and scalable method to fabricate the gelatin nanofibers for different biomedical applications such as tissue engineering, wound healing, and substrate for delivery of bioactive molecules.

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