Table 1.
Therapeutic Compound | Nanocarrier | Drug Location | Loading-retention Strategy | Release Mechanism |
In vitro Evaluation (Bacteria) |
In vitro Evaluation (Eukaryotic cells) |
In vivo | Ref. |
Antibiotic(s) | ||||||||
Vancomycin | MSNs | Surface | Covalent bonding | None |
S. aureus E. coli |
Raw 264.7 LO2 |
Mouse | 29 |
Gentamicin Neomycin Kanamycin |
MSNs | Surface | Covalent bonding | None |
B. cereus S. aureus E. coli S. typhimurium |
None | None | 30 |
Barbituric acid-N-halamine | Silica NP | Surface | Coating with pMMA copolymer | Chlorine release |
P. aeruginosa S. aureus |
None | None | 31 |
Tetramethylpiperidine- N-halamine | Silica NP | Surface | Coating with pMMA copolymer | Chlorine release |
S. aureus E. coli |
None | None | 32 |
Tetracycline | Silica NP | Silica matrix | Loading on silica polymerization | Dissolution of SiO2 NPs | E. coli | HEK 293T | None | 33 |
Vancomycin | H-MSNs vs RH-MSNs vs R-SiO2NPs |
Internal void Surface/void Surface |
Diffusion into silica/roughness | Morphology-dependent diffusion | E. coli | None | None | 34 |
Chlorhexidine | Round vs rod MSNs |
Mesopores | Direct loading | Diffusion |
S. sobrinus S. mutans C. albicans |
None | None | 35 |
Ampicillin | SBA-15 SBA-15-NH2 MCM-41 |
Mesopores | Direct loading | Diffusion | None | None | None | 36 |
Doxycycline | Several MCM-41 compositions | Mesopores | Direct loading | Diffusion | K. pneumoniae | None | None | 37 |
Lomefloxacin | Metal-doped MCM-41 | Mesopores | Direct loading | Diffusion | E. coli | None | None | 38 |
Polymyxin B | MSNs: RAW, NH2 or COOH | Mesopores | Direct loading | Diffusion |
E. coli A. baumannii P. aeruginosa |
HepG2 HFF-1 HEK-293 |
None | 39 |
Chlorhexidine | MONs | Mesopores | Direct loading | Redox-driven MON dissolution |
E. coli S. aureus |
HUVEC L929 |
None | 40 |
Rifampicin | HMM MSNs | Mesopores | Direct loading | Diffusion | S. aureus | RAW264.7 Caco-2 |
None | 41,42 |
Gentamicin Rifamycin |
SiO2 NPs | Silica matrix | Loading on silica polymerization | Proteolysis of a collagen coating |
P. aeruginosa S. aureus |
L929 | None | 44 |
Gentamicin | MSNs | Mesopores | Embedment in dental cement | Diffusion | S. aureus | MC3T3 | None | 45 |
Chlorhexidine | MSNs | Mesopores | Embedment in dental cement | Diffusion | S. mutans | None | None | 46 |
Gentamicin | MSNs | Mesopores | Embedment in dental cement | Diffusion | S. aureus | None | None | 47 |
Vancomycin | MSNs | Mesopores | Embedment in collagen scaffold | Diffusion | S. aureus | Rat BMSCs | Rabbit | 49 |
Gentamycin | Dendritic MSNs | Mesopores | Electrospinning on polycaprolactone fibers |
Diffusion | E. coli | None | None | 50 |
Chlorhexidine | Ca–Si mesoporous nanoparticles (MCSNs) | Mesopores | Direct loading | Diffusion | E. faecalis | MC3T3-E1 | None | 48 |
Ciprofloxacin | MSNs | Mesopores | Lipid layer | pH-driven coating detachment | S. typhimurium | RAW 264.7 HeLa |
Mouse | 52 |
Gentamicin | MSNs | Mesopores | Lipid layer | Bacteria-mediated coating degradation | S. aureus | RAW 264.7 MC3T3-E1 |
Mouse | 53 |
Ampicillin | MSNs | Mesopores | Ca phosphate-folic acid coating | pH-driven coating dissolution |
E. coli S. aureus |
HEK-293 | Mouse | 54 |
Proteins | ||||||||
Lysozyme | MSNs | Surface | Electrostatic interaction | Not specified (pH driven detachment) |
E. coli | HEK-293 LO2 |
Mice | 55 |
MSNs | Pores | Direct loading | Adsorption | E. coli | None | None | 56 | |
HMSNs | Surface | Direct loading | Adsorption | E. coli | None | Mice | 57 | |
HMSNs | Particle cavity | Direct loading | Cavity loading | E. coli | None | None | 58 | |
Concanavalin A | MSNs | Surface | Covalent bond | Grafting | E. coli | None | None | 109 |
Bactofencin A | MSE vs MSN | Mesopores | Direct loading | Diffusion | S. aureus | HEK-293 | None | 59 |
Peptide | ||||||||
LL37 | SiO2 NPs vs MSNs | None/LL37 | Electrostatic interaction | Surface adsorption vs pore release | E. coli | Hemolysis | None | 60 |
NZX | MSNs | NZX | Direct loading | Pore release | M. bovis | THP-1 | Mice | 61 |
Extract | ||||||||
Eucalyptus, orange and cinnamon essential oils | MSNs | Mesopores | None | Diffusion |
S. aureus E. coli C. albicans |
L929 | None | 62 |
Red propolis extract | MSNs | Mesopores | None | Diffusion | S. aureus | None | None | 63 |
Tea tree oil | MSNs | Mesopores | Coating with PEI layer | pH-driven coating detachment | E. coli | None | None | 64,65 |
Abbreviations: HMM, Hiroshima mesoporous material; HMSNs, hollow mesoporous silica nanoparticles; MCM-41, Mobil composition of matter; MONs, mesoporous organosilica nanoparticles; MSNs, mesoporous silica nanoparticles; PEI, poly(ethyleneimine); PMMA, poly(methyl methacrylate); RH-MSNs, rough hollow mesoporous silica nanoparticles; R-SiO2NP, rough silica nanoparticles; SBA-15, Santa Barbara amorphous. Prokaryotic cell lines: A. baumannii, Acinetobacter baumannii; B. Cereus, Bacillus cereus; C. albicans, Candida albicans; E. coli, Escherichia coli; E. faecalis, Enterococcus faecalis; K. pneumoniae, Klebsiella pneumoniae; M. Bovis, Mycobacterium bovis; M. tuberculosis,Mycobacterium tuberculosis; P. aeruginosa,Pseudomonas aeruginosa; S. aureus, Staphylococcus aureus; S. mutans, Staphylococcus mutans; S. typhimurium, Salmonella typhimurium; S. sobrinus, Staphylococcus sobrinus. Eukaryotic cell lines: BMSC, bone mesenchymal stem cells; Caco-2, human colorectal adenocarcinoma; HEK-293, human embryonic kidney cells; HeLa, human cervix adenocarcinoma; HepG2, human hepatoma; HFF-1, human foreskin fibroblasts; L929, mouse fibroblasts; LO2, human hepatocytes; MC3T3-E1, mouse preosteoblasts; RAW 264.7, mouse macrophages; THP-1, human monocytes.