Table 2.
Antimicrobial additive (Inorganic nanoparticles) | Other additive(s) | Synthesis method | Content | Antimicrobial capability | Application | Refs |
---|---|---|---|---|---|---|
AgNPs | ----- | Reduction of Ag ions by SF solution using a microfluidic device | 125 μg/mL AgNO3 | Live/dead assay: Maximum bacterial death at 3 h RE (2 h): E. coli (>75%) in an infected mouse model |
Surgical site infections | [65] |
AgNPs | Polylactic acid (PLA) Nano hydroxyapatite (nHA) Polydopamine (PDA) |
Reduction of Ag ions by SF and fabrication of SF/Ag/nHA/PLA composites | 50 mM AgNO3 solution | Turbidity test against E. coli and S. aureus (24 h): Lower absorbance of the medium containing the scaffolds |
Bone TE | [67] |
Ag NPs | ----- | SF as the reducing and stabilizing agent for preparation of SF-AgNPs solutions under light | 0–153.6 mg/L | MRSA: MIC (19.2 mg/L) MBC (76.8 mg/L) CLSM and SEM (10 h): No biofilm formation at concentrations higher than MIC |
General biomedical applications | [66] |
AgNPs | ----- | Dip-coating Tasar SF nanofibrous mats in AgNPs solution | 1 mM AgNO3 solution | ZOI (12 h): S. aureus (10 mm) E. coli (14mm) P. aeruginosa (8 mm) S. epidermidis (10 mm) |
Skin TE | [78] |
AgNPs | ----- | Dip-coating and microwave irradiation of SF fibers in AgNO3 solution | 0.5, 1 and 1.5 mmol L−1 of AgNO3 solutions | Diffusion assay (24 h): S. aureus, M. tuberculosis, and E. coli (dose-dependent antibacterial activity) |
Wound healing | [90] |
Ag doped hydroxy appetite (HA) NPs | Chitosan (CS) Strontium (Sr) | Freeze-dried AgSrHA/CS/SF cryogels | ----- | Turbidity test (24 h): Growth inhibition of E. coli and S. epidermidis |
Bone TE | [91] |
AgNPs | Strontium nanotubes (SNT) Titanium (Ti) Polydopamine (PDA) |
SF/Ag coating on PDA modified SNTs (created by anodizing Ti) | Turbidity test and ZOI (24 h): Antibacterial activity against S. aureus and E. coli RE (1–5 d): S. aureus and E. coli (100–70%) |
Bone TE | [92] | |
AgNPs | ------ | The SF solution containing AgNO3 was exposed to light to form SF/AgNPs films | 0.1–2 % AgNO3 | ZOI (2 d): Antibacterial activity at 0.5–1% against S. aureus and kanamycin resistant E. coli (quantitative data N/A) |
Bone TE | [93] |
AgNPs | ----- | In situ reduction of Ag ions and fabrication of AgNPs loaded SF gels | 26.5±1.24 ppm | MIC (6±1.32 ppm) and ZOI (11±2.12mm) against S. aureus after 2 d |
Wound healing | [94] |
AgNPs | Carboxymethyl chitosan (CMC) | In situ synthesis of AgNPs in SF solution, and fabrication of freeze-dried AgNPs-SF-CMC sponges | AgNO3 solution (0.05 wt%) | Turbidity test and ZOI (24 h): Significantly lower OD values and larger inhibition zones against S. aureus and P. aeruginosa compared to control without Ag NPs and compared to AQUACEL® Ag | Wound healing | [95] |
AgNPs | ----- | In situ reduction reaction between SF and silver nitrate under light | 153.6 and 384 mg/L of SF-AgNPs solution | SEM (7 d): Significant reduction of S aureus biofilm at 384 mg/L of SF-NS solution compared with saline. |
Sinusitis treatment | [96] |
AgNPs | ----- | Impregnation of silk fibers with AgNPs using in situ (AgNO3 solution) and ex situ (colloidal AgNPs solution) approaches | AgNO3 solution (4 mM) | Higher antibacterial activity of in situ prepared fibers after 24 h P. aeruginosa: ZOI (3.3±0.5 mm), RE (99.9%) S. aureus: ZOI (2.4±0.4 mm), RE (95%) |
Wound healing | [77] |
AgNPs | ----- | Electrospinning SF/AgNO3 solution and irradiation with UV to obtain SF/AgNPs nanofibers | 0.1%, 0.5%, and 1% wt/v | No antibacterial activity at 0.1% and 0.5% against S. aureus and S. epidermidis ZOI (24 h) at 1%: S. aureus (6.5 mm) S. epidermidis (5.6 mm) P. aeruginosa (9.3 mm) |
Wound healing | [97] |
AgNPs | ----- | Dip-coating and in situ photoreduction of Ag ions on SF sutures | 0.5 wt/v % AgNO3 solution | Inhibition zone against S. aureus and E. coli after 24 h (Diameter N/A) RE (24 h-bacteria in solution): E. coli (78%), S. aureus (81%) RE (24 h-adhered bacteria): E. coli (34%), S. aureus (35%) |
Suture | [98] |
Ag@AgCl NPs | Cellulose acetate (CA) | Photocatalytic reduction and in situ formation of Ag@AgCl NPs on SF/CA composite membranes | 0.1 M AgNO3 aqueous solution | ZOI (24 h): E. coli (13.99 mm) S. aureus (12.59 mm) |
Antibacterial applications | [99] |
AuNPs | ----- | Reduction of AuNPs by SF solution | 0.5 mM SF-AuNPs colloidal solution | RE (24 h): E. fecalis (85.19 ± 3.24 %) S. aureus (32.34 ± 1.70 %) E. coli (77.95 ± 9.59 %) P. aeruginosa (63.38 ± 4.26 %) |
Nanoparticles with antibacterial and anticancer properties | [69] |
AuNPs AgNPs |
Nano-hydroxyapatite (nHA) | In situ reduction of AgNPs and AuNPs by SF/nHA solution and fabrication of hydrogels | 0, 0.1, 0.5 and 1% HAuCl4·3H2O and AgNO3 | Turbidity test and resazurin assay (24 h): SF/AgNPs (0.1–1 %): Antibacterial activity against MSSA, MRSA, S. epidermidis, E. coli, and P. aeruginosa SF/AuNPs (≥0.5%): Antibacterial activity against MSSA, MRSA, S. epidermidis, E. coli, and P. aeruginosa No antibacterial activity against S. epidermidis |
Bone regeneration | [68] |
Diamino-2-pyrimidinethiol-functionalized Au NPs (DAPT-Au NPs) | ----- | Aqueous SF/Au-DAPT membranes | 27 μg/cm2 | MIC and ZOI (20 h): E. coli and MDR E. coli (4 μg/mL, ~14 mm) Inhibition of growth after 20 h. |
Wound healing | [100] |
Ca2+ | Polyethylene glycol diglycidyl ether (PEG-DE) | Freeze-dired Ca2+ loaded SF-PEG-DE porous material | 1.8, 3.6, 5.4, and 7.2%, (w/w) | CFU and turbidity test (6 h): Inhibitory effect on the bacterial growth and propagation of E. coli and S. aureus |
Hemostatic material | [86] |
Calcium peroxide (CPO) | Gelatin (GL) Human keratin (HK) | Physical blending to make composite film scaffolds | 20% CPO | ZOI (24 h): E. coli (3.55 ± 0.24 mm) S. aureus (2.89 ± 0.20 mm) |
Urethral TE | [87] |
CuBTC MOF particles | ----- | Formation of CuBTC MOF on silk yarns by immersing in Cu(OAc)2.2H2O, and H3BTC solution | 2–8 dipping cycles | ZOI (24 h- IV-cycle 4): E. coli (7.7 mm) S. aureus (6.5 mm) ZOI (24 h- IV-cycle 10): E. coli (8.0 mm) S. aureus (7.5 mm) |
Wound healing and medical applications | [70] |
Graphene oxide (GO) | ----- | Electrospinning | 5 wt% GO | Survival rate after 18 h: E. coli (35.7 ± 3.6 %) S. aureus (41.6 ± 0.3%) SEM: Shrunken morphology of E. coli on the SF/GO nanofibers |
Wound dressing | [80] |
Graphene oxide (GO) Reduced GO (RGO) Graphene (Gr) |
----- | Electrospinning | 1 wt% | RE (24 h): Antibacterial activity of SF/GO, SF/RGO, and SF/Gr against S. aureus (92.8%, 98.6%,80.6%) and E. coli (70.3%, 84.9%, 69.5%) |
TE | [101] |
Reduced Graphene oxide (GO) TiO2 |
----- | Electrospinning | 0.01 wt% | RE against S. aureus: SF/RGO: 94.8% SF/TiO2: 83.6% SF/GO/TiO2: 84.9% |
TE | [102] |
MgOH2 nanorods | Polyvinyl alcohol Sodium Alginate | Freeze-dried Hydrogels | 0.3 wt% | Crystal violet assay (24 h): Inhibition of P. aeruginosa biofilm formation |
TE and general biomedical applications | [103] |
MoSe2 nanosheets | ----- | Exfoliation of MoSe2 nanosheets by carboxyl-modified SF (CMSF) solution | MoSe2–CMSF nanosheets (50 μg mL−1) | Live/dead assay, SEM, turbidity test, and CFU (6 h): Antibacterial activity against E. coli and B. subtilis |
Wound dressing | [76] |
TiO2 | ----- | TiO2 /SF blend membranes | TiO2/SF weight ratios: 1/1000, 3/1000, 5/1000, and 10/1000 | 1/1000 samples showed the highest antibacterial activity ZOI (24 h): S. aureus (19.0±0.2) E. coli (17.0±0.1) P. aeruginosa (13.0±0.2) |
Skin TE and wound dressing | [85] |
TiO2 | Chitin (Ch) Glycerol (Gly) | Freeze-dried SF/Ch/TiO2 wound dressings | 0.5, 1.5, 3.0 % (w/w) TiO2 | ZOI (24 h): S. aureus (19 mm) E. coli (20–22 mm) CFU (3% TiO2): 5-fold decrease in number of colonies |
Wound dressing | [84] |
ZnO NPs | Sodium alginate (SA) | Dip-coating SF fibers functionalized with SA in ZnO NPs solution | 0.5% suspension of ZnO NPs | ZOI (2–6 d): S. aureus (1.9–0.5 mm) |
Suture | [83] |
ZnO NPs | Hyaluronic acid (HA) | Co-axial electrospinning | 1, 3, and 5% w/v ZnO NPs | ZOI (24 h) (5% ZnO fibers): E. coli (2.93±0.12 mm) S. aureus (3.37±0.12 mm) CFU (24 h): E. coli (28±2 colonies) S. aureus (6±1 colonies) |
Burn wound healing | [82] |
Porous ZnO NPs (PZ) | ----- | Dip-coating silk thread in PZ solution | 50 mM Zn(NO3)2·6H2 O initial solution | RE (6–8 h): S. aureus and E. coli (~80%) Suppressing bacterial infection in a mouse model (2 w) |
Suture | [81] |
MDR, multi drug resistanat; MSSA, methicillin-susceptible Staphylococcus aureus; S. epidermidis, Staphylococcus epidermidis; MBC, minimum bactericidal concentration; SEM, scanning electron microscopy; CLSM, confocal laser scanning microscopy