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A review of drug delivery systems based on nanotechnology and green chemistry: green nanomedicine

Jahangirian, Hossein, Ghasemian lemraski, Ensieh, Webster, Thomas J, Rafiee-Moghaddam, Roshanak, Abdollahi, Yadollah·2017·International Journal of Nanomedicine
DOI 10.2147/ijn.s127683PMC PMC5396976
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Figure 1 A schematic representation of some of the unique advantages of magnetic nanomaterials for hyperthermia-based therapy and controlled drug delivery. Abbreviation: BBB, blood–brain barrier.
Figure 1 A schematic representation of some of the unique advantages of magnetic nanomaterials for hyperthermia-based therapy and controlled drug delivery. Abbreviation: BBB, blood–brain barrier.CC BY-NC · PubMed Central
Figure 2 Schematic illustration of the synthesis of soybean phospholipid-encapsulated MoS2. Abbreviations: MoS2, molybdenum disulfide; NIR, near infrared absorbing dyes.
Figure 2 Schematic illustration of the synthesis of soybean phospholipid-encapsulated MoS2. Abbreviations: MoS2, molybdenum disulfide; NIR, near infrared absorbing dyes.CC BY-NC · PubMed Central
Figure 3 Schematic image of different drug-delivering vehicles and releasing techniques between NCM and FA-CCM. Abbreviations: FA, folic acid; GSH, glutathione; PEG, poly(ethylene glycol); Cur, curmine; NCM, noncross-linked micelle; PDS, pyridyldisulfide; DTT, dithiothreitol.
Figure 3 Schematic image of different drug-delivering vehicles and releasing techniques between NCM and FA-CCM. Abbreviations: FA, folic acid; GSH, glutathione; PEG, poly(ethylene glycol); Cur, curmine; NCM, noncross-linked micelle; PDS, pyridyldisulfide; DTT, dithiothreitol.CC BY-NC · PubMed Central
Figure 4 A schematic illustration for the synthesis of hydrophilic CuInS2 QDs for in vitro bioimaging. Abbreviations: GSH, glutathione; QDs, quantum dots.
Figure 4 A schematic illustration for the synthesis of hydrophilic CuInS2 QDs for in vitro bioimaging. Abbreviations: GSH, glutathione; QDs, quantum dots.CC BY-NC · PubMed Central
Figure 5 Schematic diagram for the synthesis of pullulan-stabilized AuNPs. Abbreviations: AuNPs, gold nanoparticles; EDC, 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride.
Figure 5 Schematic diagram for the synthesis of pullulan-stabilized AuNPs. Abbreviations: AuNPs, gold nanoparticles; EDC, 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride.CC BY-NC · PubMed Central
Figure 6 Schematic image of the modification of SWCNTs with the antitumor drug DOX for targeting and accelerated destroying of breast cancer. Abbreviations: DOX, doxorubicin; FA, folic acid; PEG, poly(ethylene glycol); SWCNTs, single-walled carbon nanotubes; NIR, near-infrared.
Figure 6 Schematic image of the modification of SWCNTs with the antitumor drug DOX for targeting and accelerated destroying of breast cancer. Abbreviations: DOX, doxorubicin; FA, folic acid; PEG, poly(ethylene glycol); SWCNTs, single-walled carbon nanotubes; NIR, near-infrared.CC BY-NC · PubMed Central
Figure 7 One example of using CNTs as a multifunctional insulin carrier. Abbreviations: CNTs, carbon nanotubes; EDC, 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride; NHS, N-hydroxysulfosuccinimide.
Figure 7 One example of using CNTs as a multifunctional insulin carrier. Abbreviations: CNTs, carbon nanotubes; EDC, 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride; NHS, N-hydroxysulfosuccinimide.CC BY-NC · PubMed Central
Figure 8 Schematic illustration of the preparing and in vitro osteogenic effect of PlGF-2-/BMP-2-loaded heparin–HTCC nanocomplexes. Abbreviations: BMP-2, bone morphogenic protein-2; PlGF, placental growth factor; GF, Dual-growth factor-loaded; HTCC, heparin–N-(2-hydroxyl) propyl-3-trimethyl ammonium chitosan chloride.
Figure 8 Schematic illustration of the preparing and in vitro osteogenic effect of PlGF-2-/BMP-2-loaded heparin–HTCC nanocomplexes. Abbreviations: BMP-2, bone morphogenic protein-2; PlGF, placental growth factor; GF, Dual-growth factor-loaded; HTCC, heparin–N-(2-hydroxyl) propyl-3-trimethyl ammonium chitosan chloride.CC BY-NC · PubMed Central
Figure 9 Schematic image of transformable core–shell-based nanocarriers.
Figure 9 Schematic image of transformable core–shell-based nanocarriers.CC BY-NC · PubMed Central

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Authors
Jahangirian, H., Ghasemian lemraski, E., Webster, T. J., Rafiee-Moghaddam, R., & Abdollahi, Y.
Venue
International Journal of Nanomedicine
Publisher
Informa UK Limited
Published
2017-04
Volume
Volume 12
Pages
2957-2978
ISSN
1178-2013
DOI
10.2147/ijn.s127683
PMC
PMC5396976
Cited by
496
References
0
Language
en
Licence
creativecommons.org/licenses/by-nc/3.0/ (unspecified)

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Jahangirian, H., Ghasemian lemraski, E., Webster, T. J., Rafiee-Moghaddam, R., & Abdollahi, Y. (2017). A review of drug delivery systems based on nanotechnology and green chemistry: green nanomedicine. International Journal of Nanomedicine. https://doi.org/10.2147/ijn.s127683