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. 2018 Dec 16;10(4):282. doi: 10.3390/pharmaceutics10040282

Table 1.

Summary of characterization features of GBNs, type of graphene nanomaterial, and inclusion criteria based on reported therapeutic and/or diagnostic role of graphene in the overall system developed. The figures mentioned in this table can be found in each referenced study and represent examples from the revised studies where therapeutic and/or diagnostic relevance of graphene is clearly illustrated.

Graphene-Based Nanomaterial Graphene Type Coating Theranostic
System Size
(D or D × T)
Zeta-Potential/
Colloidal Stability in Serum
Proven Graphene Therapeutic Relevance Proven Graphene Diagnostic Relevance Ref.
Au@PLA-(PAH/GO)n GO 1.5 µm n.r. USI (Figure 2)
s.e. Au@PLA
[61]
UCNPs-NGO/ZnPc GO PEG ≈ 300 × 1.5 nm (GO) + 40 nm (UCNPs) n.r. PTT (Figure 3 and Figure S4) [85]
GO-HA-Ce6 GO ≈ 440 nm n.r.
1 d stability
PTT (Figure 3)
s.e. Ce6
[52]
ICG-GO-FA GO PEG-FA ≈ 200 nm n.r.
3 h stability
PTT (Figure S3, Figure 2 and Figure 3)
s.e. ICG
[86]
GO-AuNS GO ≈ 0.8 μm −19 mV
10 days
PTT (Figure 6)
s.e. AuNS
[70]
GQD-Cur GO ≈ 150 nm (GQD-Cur)
3–6 nm (GQD)
n.r. PL (Figure 6) [78]
GO-Abs/Cy7 GO 100–600 × 1.2 nm n.r. PAT (Figure 3
and Figure 9)
s.e. Cy7
PAI (Figure 3 and Figure 6)
s.e. Cy7
[72]
GDH GO HA ≈ 120 nm (GDH)
≈ 30 nm (GO)
n.r.
7 days
PTT (Figure 5a) [62]
PheoA+GO:FA-BSA-c-PheoA GO PEG-FA ≈ 180 nm ≈ −30 mV
n.r.
PTT + PDT
(Figure 7 and Figure 9)
s.e. Pheo
[47]
GO-PEG-ZnS:Mn-DOX GO PEG-ZnS:Mn n.r. n.r. PL (Figure 4)
s.e. ZnS:Mn
[53]
CPGA GO PEG ≈ 230 × 15 nm ≈ −25 mV
7 d stability
PTT (Figure 3)
s.e. Au and Cy5.5
PAI (Figure 2)
FI (Figure 2)
s.e. Au
[56]
GO@Gd-PEG-FA/DOX GO PEG-FA n.r ≈ −6 mV PTT (Figure 6) [75]
GO/AuNS-PEG/Ce6 GO PEG ≈ 400 × 18 nm ≈ −38 mV
1 d stability
PTT (Figure 2b)
s.e. AuNS
[87]
GO/Bi2Se3/PVP GO ≈ 150 nm ≈ −18 mV (GO)
n.r.
PTT (Figure 5d)
s.e. Bi2Se3
[92]
GO/UCNPs ZnFe2O4 GO PEG ≈ 400 nm ≈ −17 mV
n.r.
PTT (Figure 2d)
PDT+PTT (Figure 3)
s.e. UCNPs
[48]
GO/MnWO4/PEG GO PEG ≈ 130 nm ≈ −26 mV
n.r.
PTT (Figure 3) [5]
LOGr-Pc-LHRH LOGr PEG ≈ 80 nm n.r.
n.r.
PTT (Figure 3a
and Figure 6b)
PDT (Figure 6c)
s.e. Pc
[81]
GO-DOX NGO PEG ≈ 30 × 6 nm n.r. PAI (Figure 5) s.e. Cy 5.5 [71]
ICG-FeCl3@GO NGO _ ≈ 40 nm n.r. PTT (Figure 3d)
s.e. ICG
[83]
GO@Ag-DOX-NGR NGO DSPE-PEG-NGR ≈ 40 nm −29 mV PTT (Figure 6)
s.e. Ag
[76]
GO-PEG-DVDMS NGO PEG ≈ 20.5 × 1.5 nm n.r. PTT (Figure 2a, Figure 3a and Figure 3d)
s.e. DVDMS
[88]
IO/GO-COOH NGO OA ≈ 50 × 20 nm n.r. PTT (Figure 5)
s.e. IO
MRI (Figure 3)
s.e. IO
[60]
GO-PEG-CysCOOH NGO PEG-CysCOOH < 50 × 2 nm n.r.
1 d stability
PTT (Figure 2 and
Figure 4)
s.e. CysCOOH
PAI (Figure 3)
s.e. CysCOOH
[73]
Au@NGO NGO ≈ 98 nm ≈ −28 mV
n.r.
SERS (Figure 3)
s.e. Au
[68]
NGO-PEG-FA NGO PEG-FA ≈ 100 nm n.r PTT (Figure 4, Figure 5, Figure 6 and Figure 7 FI (Figure 3) [7]
NGO-IR-808 NGO PEG ≈ 20–40 × 3 nm n.r. PTT (Figure 2, Figure 3 and Figure 7)
s.e. IR-808
FI (Figure 4 and Figure 6)
IR-TI (Figure 7)
s.e. IR-808
[67]
NGO-PEG-ICG/PTX NGO PEG-ICG < 100 × 1 nm ≈ −30 mV
14 d stability
PTT (Figure 4, Figure S5 and Figure 6)
s.e. ICG
FI (Figure 5)
s.e. ICG
[91]
NGO-UCNPs-Ce6 NGO OA ≈ 100 nm (GO)+
48 nm (UCNPs)
n.r. PTT (Figure S4,
Figure 7 and Figure 8)
PDT+PTT (Figure 3,
Figure 7 and Figure 8)
s.e. UCNPs
[57]
UCNP@NGO NGO OA ≈ 100 nm (GO)+
55 nm (UCNPs)
n.r. PTT (Figure 2, Figure 4 and Figure 5)
s.e. UCNPs
[64]
BSA/nano-rGO rGO BSA ≈ 70 nm ≈ −30 mV
30 d stability
PTT (Figure 3) PAI (Figure 4 and Figure 5) [74]
rGONM-PEG-Cy7-RGD rGO PEG ≈ 61 nm n.r. PTT (Figure 2) [46]
rGO-Fe2O3@AuNPs rGO NH2-PEG ≈ 610 nm −21.1 mV
> 5 h
PTT (Figure 3a)
s.e. Fe2O3@Au NPs
[50]
rGO nanosheets rGO HA ≈ 115 nm ≈ −60 mV
n.r.
PTT (Figure 4a
and Figure 5a)
s.e. ICG
[69]
131I-RGO-PEG rGO PEG ≈ 50 × 3.5 nm n.r.
7 days
PTT (Figure 2)
s.e. 131I
γ-image (Figure 3)
s.e. 131I
[51]
rGO-AuNRVe rGO PEG ≈ 74 nm n.r. PTT (Figure 2)
s.e. AuNR
PAI (Figure 5)
s.e. AuNR
[79]
anti-EGFR-PEG-rGO@
CPSS-Au-R6G
rGO PEG-Anti-EGFR < 200 nm n.r. PTT (Figure S5
and Figure 7b)
s.e. AuNPs
[6]
ICG-PDA-rGO rGO PDA 1–5 μm × 1 nm n.r. PTT (Figure 3
and Figure 8)
s.e. ICG
PAI (Figure 4
and Figure 6)
IR-TI (Figure 7)
s.e. ICG
[59]
rGO-GSPs rGO PEG ≈ 100 nm n.r.
3 d stability
PTT (Figure 2a
and Figure 2b)
s.e. AuNPs
PAI (Figure 2d
and Figure 2e)
s.e. AuNPs
[66]
rGO-mfHSA rGO mfHSA ≈ 200 nm −25 mV
2 d stability
PTT (Figure 3c) [93]
FA-PEG-Lip@rGO/Res rGO PEG-FA ≈ 220 nm ≈ −24 mV
7 d stability
PTT (Figure 7b) IR-TI (Figure 7a) [58]
ArGO rGO APGA ≈ 115 nm ≈ −38 mV
28 d stability
PTT (Figure 5b
and Figure 6a)
IR-TI (Figure 5a) [77]
AAP10-pDA/rGO rGO pDA 300 nm × 3.5 nm n.r. PTT (Figure 2)
s.e. pDA
[90]
cGdots GQDs ≈ 5 nm n.r.
n.r.
All therapeutic outcomes came from GQDs All diagnostic outcomes came from GQDs [45]
GQDs GQDs 2–6 nm n.r. All therapeutic outcomes came from GQDs All diagnostic outcomes came from GQDs [44]
PLA-PEG-grafted GQDs
(f-GQDs)
GQDs PLA-PEG ≈ 22 × 1.7 nm ≈ −4 mV
n.r.
PL (Figure 4) [55]
AS1411@GQD GQDs ≈ −13 mV
n.r.
PTT (Figure 6a
and Figure 6b)
s.e. AS1411
[84]
HA-GQD
-SiO2 NPs
GQDs ≈ 40 nm n.r. PDT (Figure 6)
s.e. HA and SiO2
[94]
GQDs@Cys-BHC GQDs ≈ 5 nm n.r. FI (Figure 8) [82]
Fe3O4@SiO2@GQDs-FA/DOX GQDs ≈ 25 nm ≈ −18 mV
n.r.
PL (Figure 3)
FI (Figure 5)
[80]
GQD-MSN--DOX GQDs 50-80 nm n.r. PTT (Figure 6
and Figure 9)
[89]
GQD-PEG-P GQDs PEG 8 × 1 nm ≈ + 14 mV
n.r.
PTT (Figure 3) FI (Figure 5) [49]
DOX@GQD-P-Cy GQDs ≈ 15 nm ≈ −4 mV (w/o) DOX
n.r.
FI (Figure 4d–e)
s.e. DOX by FRET
[54]
DL-GQD-comp GQDs ≈ 220 nm n.r. PL (Figure 5) [63]
IR780/GQDs-FA GQDs 8.5 × 1.5 nm n.r. PTT (Figure 5a and Figure 5b) s.e. IR780 FI (Figure 6)
IR-TI (Figure 7a)
s.e. IR780
[65]
SCNA
(DOX/GQD)
GQDs HTPGS < 5 nm n.r.
4 h stability
PTT (Figure 5e) CLSMI (Figure 4) [8]

Table 1 abbreviations: GO—Graphene oxide; NGO—Nanographene oxide; rGO—Reduced Graphene oxide; GQDs—Graphene Quantum Dots; D—Diameter; D × T—Diameter × Thickness; d–day(s); n.r.—not reported; s.e.—synergic effect with; CLSMI—confocal laser scanning microscopy imaging; FI—fluorescence imaging; FRET—fluorescence resonance energy transfer; IR-TI—infrared thermal imaging; MRI—magnetic resonance imaging; PAI—photoacoustic imaging; PAT—photoacoustic therapy; PDT—photodynamic therapy; PL—Photoluminescence; PTT—photothermal therapy; SERS—Super Enhanced Raman Spectroscopy; USI—ultra sound imaging. AAP10—Antiarrhythmic peptide 10 (promotes bystander effect); Abs—integrin αvβ3 mAb (targeting ligand); Ag—silver; anti-EGFR—anti-epidermal growth factor receptor (targeting ligand); APGA—amphiphilic poly-γ-glutamic acid; ArGO—rGO coated with amphiphilic poly-γ-glutamic acid; AS1411—aptamer of 26-base guanine-rich short oligonucleotide (targeting ligand); Au—gold; AuNPs—gold nanoparticles; AuNRVe—gold nanorod vesicles; AuNR—Gold nanorods; AuNS—Gold nanostars; Bi2Se3—Bismuth Selenide; BHC—Berberine hydrochloride; BSA—bovine serum albumin; Ce6—Chlorin e6 (photosensitizer); cGdots—carboxylated graphene dots; Cy5.5—Cyanine 5.5 (NIR dye and photosensitizer); Cy7—Cyanine 7 (NIR dye and photosensitizer); Cys—Cysteamine hydrochloride (NIR dye); Cys-COOH—Cysteine- rich Carboxy-terminal domain CPGA—theranostic probe formed by Cy5.5 (NIR dye) labelled-matrix metalloproteinase-14 (MMP-14) substrate (CP) conjugated onto the GO/Au complex (GA); CPSS—carbon porous silica nanosheets; Cur—curcumin; DL-GQD-comp—doxorubicin hydrochloride loaded GQD complex; DOX—doxorubicin hydrochloride; DSPE—1,2-distearoyl-sn-glycero-3-phosphoethanolamine; DVDMS—bis[1-[6,7-bis[2-(sodium carbonate ethyl]-1,3,5,8,-tetramethyl-2-vinyl-porphin-4-yl]ethyl]ether (photosensitizer); FA—Folic acid (target ligand); FeCl3—Iron chloride; Fe2O3 and Fe3O4—Iron oxide nanoparticles; Gd—Gadolinium; GDH—Graphene–DOX conjugate in HA nanogel; GSPs—gold superparticles; HA—hyaluronic acid (target ligand); HA-GQD—complex of Hypocrellin A (photosensitizer), HA and GQD; HTPGS—N-acetyl histidine-functionalized D-α-tocopherol polyethylene glycol 1000 succinate; 131I—Iodine-131 (radioisotope); ICG—NIR fluorescence dye; IO—iron oxide; IR780—IR780 iodide (NIR dye); IR-808—Heptamethine indocyanine dye (photosensitizer); LHRH—luteinizing hormone-releasing hormone peptide; Lip—Phospholipids; LOGr—low-oxygen graphene; mfHSA—multifunctional human serum albumin—HSA functionalized with indocyanine green (ICG) and lactobionic acid (LA); MnWO4—manganese tungstate; MSN—mesoporous silica nanoparticles; NGR—Asn-Gly-Arg peptide (target ligand); OA—Oleic acid; P—porphyrin; PAH—poly (allylamine hydrochloride); Pc—phthalocyanine; P-Cy—Cyanine 5.5 dye conjugated to GQD though a cathepsin D-responsive peptide (P); PDA or pDA—Polydopamine (reduces GO improves water solubility and biocompatibility and increases NIR absorption); PEG—Polyethylene glycol; PheoA—Pheophorbide A (photosensitizer); PLA—polylactic acid; PTX—Paclitaxel; PVP—polyvinylpyrrolidone; R6G—Rhodamine 6G; Res—Resveratrol; rGONM—reduced graphene oxide nanomesh; RGD—arginine–glycine–aspartic acid-based peptide (target ligand); SCNA—size-changeable graphene quantum dot nanoaircraft; SiO2 NPs—silicon dioxide nanoparticles; UCNPs—upconversion luminescence nanoparticles; ZnFe2O4—Zinc ferrite nanoparticles; ZnPc—Zinc phthalocyanine (photosensitizer); ZnS:Mn—manganese-doped zinc sulfide nanoparticles.