Page 370 - IJB-9-1
P. 370

International Journal of Bioprinting                          Micro/nano-3D hemostats for rapid wound healing



            Table 3. Biomaterials for fabricating micro/nanostructures as hemostatic agents
             Hemostatic material  Hemostatic mechanism  Role in wound healing  Limiting factors      References
             Synthetic polymers
               Polyethylene   Tissue adhesion  Carrier for therapeutic agents  Expensive; risk of residue  [64,210,211]
               glycol (PEG)
               Polyurethane  Platelet aggregation;   Antibacterial agent  Slow biodegradation; poor biocompati-  [212-214]
                            coagulation initiator                        bility; long polymerization time
             Natural polymers
               Collagen and   Platelet activation  Promotes cell growth and proliferation  Poor resistance to degradation; risk of   [7,124,183,184,200]
               gelatin                                                   immune response
               Fibrinogen,   Blood clot formation;   Revascularization; promotes epidermal   Expensive; risk of immune response  [185-187]
               fibrin       platelet aggregation  thickness; promotes fibroblast and
                                              fibrocyte proliferation
               Hyaluronic acid  Tissue adhesion  Wound moisture; promotes fibroblast   Expensive; difficult to remove  [186,188-190]
                                              migration and collagen deposition
               Cellulose    Platelet aggregation;   Antibacterial agent  Slow biodegradation         [191-193]
                            coagulation factor
                            activation
               Chitosan     Platelet and blood cell   Antibacterial agent; promotes gran-  Poor biocompatibility; slow degradation  [194-198]
                            adhesion and aggrega-  ulation tissue formation; promotes
                            tion              fibroblast proliferation
               Alginate     Tissue adhesion   Wound moisture; promotes tissue gran-  Low mechanical strength and chemical   [53,55,199]
                                              ulation and fibroblast proliferation  stability
               Curcumin     Immuno-regulator  Antibacterial agent; anti-inflammatory;   Poor bioavailability and absorption;   [215-218]
                                              antioxidant; anti-carcinogenic  chemical instability
             Metal-containing materials
               Silver (Ag)  Platelet activation  Antibacterial agent     No biodegradation; difficult to remove;   [68,219-222]
               Zinc (Zn)    Blood cell aggregation  Antibacterial agent; epithelization;   toxic at high concentrations  [68,174,190,216]
                                              revascularization; promotes cell prolif-
                                              eration
               Iron (Fe)    Blood cell aggregation;   Revascularization                              [40,68,171,215,219]
                            thrombin stabilizer
               Cerium (Ce)  Blood cell aggregation  Anti-inflammatory                                [223-225]
               Gold (Au)    Phagocytosis      Enzymatic activity modulation,                         [226-228]
                                                anti-carcinogen

            electrical, light, and ultrasound stimulations, play a role   subsequent wound healing in hydrogels infused with
            in  determining  stem  cell behavior [44,74] . Topographical   micro/nanostructures.  Figure 3C shows the comparative
            modifications can modulate monocyte attachment     effects in hemostasis and subsequent wound healing
            and macrophage differentiation.  Figure 3A shows the   between a hemostatic agent made of quaternized chitosan, a
            polarization of naïve (M0) macrophages to pro- (M1) or   hydrogel, and a hydrogel infused with near-infrared (NIR)-
            anti-inflammatory (M2) phenotypes.  Electrification at   responsive micro/nanostructures . These examples show
                                                                                         [79]
            different power densities for a sustained amount of time is   the significance of utilizing materials that allow for a more
            also an effective means of killing bacteria . For example,   fine-tuned response to stimuli in micro/nanostructures
                                             [70]
            Figure 3B shows the bacterial killing rate in a topical wound   when designing scaffolds seeded with growth factors and
            dressing as a function of the time of white light irradiation   cells that require controlled activation .
                                                                                             [45]
            (400–800 nm) at different power densities .
                                             [71]
                                                               4. Micro/nanostructures in hemostatic
               Micro/nanostructures also have an inherent ability to
            respond to stimuli, such as temperature, and translate these     application
            cues to create a more dynamic 3D microenvironment. Thus,   Appropriate material selection and fabrication techniques
            photothermal and photodynamic therapy has been utilized   are necessary for designing and fabricating scaffolds
            to initiate the onset of more rapid hemostasis and support   and micro/nanostructures for rapid hemostasis. When

            V                                              362                      https://doi.org/10.18063/ijb.v9i1.648
            Volume 9 Issue 1 (2023)olume 9 Issue 1 (2023)
   365   366   367   368   369   370   371   372   373   374   375