| 1 |
Hollow porphyrinic MOF |
Zr4+ and TCPP |
Doxorubicin (DOX), indocyanine green (ICG) |
pH, thermo |
Carcinoma (4T1) cell |
Release: 65% pH5 |
22
|
| IC50: 0.11 μg mL−1
|
| % Cell viability: 8% |
| 2 |
PEG/PA@ZJU-64-NSN |
Zn2+ and H2BTDBA |
Procainamide hydrochloride (PA) |
pH |
Heart, stomach (oral route) |
Release: 100% (physiological environment), 40% (stomach environment) |
176
|
| 3 |
Mg-MOF-74 |
Mg2+ and H4dhtp |
α-Cyano-4-hydroxycinnamate |
— |
HeLa |
The saturated loading capacity: 625 mg g−1
|
139
|
| % Cell viability: 5% |
| 4 |
Curcumin@N3-bio-MOF-100 |
Zn2+ and N3-BPDC |
Curcumin |
pH |
4T1 |
Release: 88.42% pH5 |
137
|
| 5 |
γ-Cyclodextrin-MOF@ Eudragit®RS |
K+ and γ-cyclodextrin |
Indomethacin |
— |
Anti-inflammatory (oral route) |
Release: 82.36% |
160
|
| 6 |
MXene/MOF-5 |
Zn2+ and H2BDC |
Doxorubicin/pCRISPR |
pH |
HEK-293, PC12, HepG2, and HeLa |
Release: 50% |
198
|
| Loading efficiency (%): 46 |
| % Cell viability: 9.9% |
| 7 |
Fe3O4–NH2@PDA@Au@MIL101-NH2
|
Fe3+ and NH2-BDC |
Doxorubicin |
Thermal |
HeLa |
The saturated loading capacity: 34.31 mg g−1
|
124
|
| % Cell viability: 10% |
| 8 |
Zn-MOF-74@CS |
Zn2+, Mn2+, TEA, and H4dhtp |
Doxorubicin |
— |
HeLa |
The saturated loading capacity: 113 mg g−
|
125
|
| % Cell viability: 5% |
| 9 |
HKUST-1 |
Cu2+ and trimesic acid |
Paracetamol |
— |
Antipyretics and analgesics (oral route) |
Loading efficiency (%): 63.41% |
163
|
| 10 |
γ-Cyclodextrin-MOF |
K+ and γ-cyclodextrin |
Florfenicol and enrofloxacin |
— |
Antibacterial (oral route) |
MIC: +E. coli: 0.1 μg mL−1
|
168
|
| +S. aureus: 1.6 μg mL−1
|
| 11 |
Ru-90@bio-MOF-1 |
Zn2+ and BPDC |
Ru-90 |
pH |
Human melanoma A375, the non-tumor mouse L929 |
Release: 43.11% (pH 5), 25.36% (pH 7.4) |
141
|
| IC50 (μM): 43.8 (A375), 31.5 (L929) |
| 12 |
CS-g-PAA/PU/magnetic MIL-53 |
Fe3+ and terephthalic acid |
Temozolomide and paclitaxel |
pH, thermo |
U-87 MG glioblastoma cells |
Release: 90% at pH5, 43 °C |
133
|
| % Cell viability: ∼25% |
| Loading efficiency (%): 80 |
| 13 |
MgAl-LDH/Fe-MOF/D-Man |
Al3+, Mg2+, and NH2-BDC |
Methotrexate, doxorubicin |
pH |
MDA-MB 231 |
Release: 45.2% (pH 5), 18.82% (pH 7.4) |
122
|
| 14 |
Bio-MOF(Zn)@CMS/GQDs |
Zn2+ and CMS/GQD |
Curcumin, doxorubicin |
pH |
HepG2 |
Loading efficiency (%): CUR (54.2) and DOX (43.2) |
199
|
| 15 |
FU@Eu-MOF |
Eu3+ and H3BTC |
Fucoidan |
pH |
A549 |
Release: 85.3% pH 5 |
142
|
| 16 |
CuO-MOF |
Fe3+ and Cu3(BTC)2
|
Doxorubicin |
pH |
— |
Release: 98.9% pH 5 |
123
|
| 17 |
Bio-MOF/polydopamine |
Zn2+ and curcumin |
Doxorubicin |
pH/NIR |
HeLa |
Release: 60.83% pH 5 |
200
|
| IC50: 0.032 mg mL−1
|
| 18 |
Zr MOF UiO-66 |
Zr4+ and BDC |
Dichloroacetate, 5-fu |
pH |
MCF-7, HEK293 |
Loading efficiency (%): 27.5 |
128
|
| IC50: 0.2 mg mL−1
|
| 19 |
DOX/AS1411@PEGMA@GQDs@γ-CD-MOF |
K+ and γ-cyclodextrin |
Doxorubicin |
pH |
MCF-7 |
Loading efficiency (%): 89.1% |
201
|
| 20 |
CS/Zn-MOF@GO |
Zn2+ and H2BDC |
5-Fu |
pH |
MCF-7 |
Loading efficiency (%): 45% |
129
|
| Release: 41.47% pH 5 |
| 21 |
GQDs@Bio-MOF |
Cd+ and TEA |
5-Fu |
pH |
HT 29 |
Loading efficiency (%): 42.4% |
202
|
| Release: 63.2% pH 5 |
| 22 |
Al-MOF/GO |
Al3+ and GO |
5-Fu |
pH |
MCF 7 and MCF 10A |
Loading efficiency (%): 78.4% |
130
|
| Release: 63.1% |
| 23 |
DHA-UIO-66-NH2
|
Zr4+ and BDC-NH2
|
5-Fu |
pH |
MCF 7 |
IC50: 10.82 μM |
203
|
| 24 |
UiO-66-NH2
|
Zr4+, BDC-NH2
|
Temozolomide |
Ultrasound intervention |
U251, SHG44 |
Release: 100% |
134
|
| % Cell viability: ∼20% |
| 25 |
ZnMOF-CS-FA |
Zn2+ and TPA |
Methotrexate |
pH |
HCT116 |
Loading efficiency (%): 78% |
146
|
| Release: ∼95% pH 5, ∼25% pH 7.4 |
| 26 |
CMC/Cu-MOF |
Cu2+ and terephthalic acid |
Ibuprofen |
pH |
Anti-inflammatory (oral route) |
Release: pH 1.2 (20%), pH 6.8 (40%), pH 7.4 (70%) |
204
|
| 27 |
UiO-66-PDC |
Zr4+ and H2BDC |
Ibuprofen |
pH |
Anti-inflammatory (oral route) |
Release: pH 2 (10%), pH 7.4 (100%) |
162
|
| 28 |
MIL-100/sodium dodecyl sulfate |
Fe3+ and BTC |
Insulin |
pH |
Diabetes treatment (oral route) |
Release: 70% (pH 7.4) |
172
|
| 29 |
ZIF-8 |
Zn2+ and 2-MIM |
Indomethacin |
pH |
Anti-inflammatory (oral route) |
Release: 90% |
161
|
| The saturated loading capacity: 1210 mg g−1
|
| 30 |
CMC-Zn-MEL@TC |
Zn2+ and carboxymethyl cellulose |
Tetracycline |
pH |
Antibacterial (oral route) |
Release: 100% |
170
|
| The antibacterial efficiency: +E. coli: 99% |
| +S. aureus: 99% |
| 31 |
Fe3O4@PAA@MIL-100(Cr) |
— |
Ciprofloxacin |
pH |
Antibacterial (oral route) |
Loading efficiency: 50% |
205
|
| Release: 80% at pH 7.4 |
| 32 |
ZIF-8/GO/MgFe2O4
|
Mg2+, Zn2+, and 2-methyl imidazole |
Tetracycline |
pH |
Antibacterial (oral route) |
Release: 92% at pH 7.4 |
169
|
| Inhibition zone: +E. coli: 22 mm |
| +S. aureus: 25 mm |
| 33 |
U-CD-MOF |
K+ and γ-cyclodextrin |
Caffeic acid |
pH |
Antibacterial (oral route) |
Release: 100% |
171
|
| 34 |
UiO-67 |
Zr4+ and BDPC |
Brimonidine |
— |
Eye drops |
Adsorption capacity for the drug: 600 mg g−1
|
177
|
| Release: 50% |
| 35 |
SiRNA@MOF |
Zn2+ and 2-methyl imidazole |
TNFα siRNA |
pH |
Treatment of ulcerative colitis (oral route) |
Release: +100% to 54.71% (pH 1.5), to 30.2% (pH 6.8) to 11.3% (pH 7.4) |
206
|
| 36 |
NH2-MIL101 |
— |
Exendin-4 |
pH |
Diabetes treatment (oral route) |
Release: 100% pH 7.4 |
175
|
| 37 |
CD-MOF |
K+ and γ-cyclodextrin |
Honokiol |
pH |
Anticancer, control gastric acidity (oral) |
Release: pH 1.2 (19%), pH 6.8 (46%), pH 7.4 (∼94%) |
173
|
| 38 |
MIL-100(Fe) |
Fe3+ and H3BTC |
Genistein |
pH |
Antioxidant and antiangiogenic (oral route) |
The saturated loading capacity: 271 mg g−1
|
207
|
| 39 |
Bio-MOF-100 |
Zn2+ and 4,4′-biphenyldicarboxylic acid |
Rifampicin, isoniazid, pyrazinamide |
pH |
Anti-tuberculosis (oral route) |
Loading efficiency: 66% |
208
|
| % Cell viability: 0% |
| 40 |
MIL-100(Fe) |
Fe2+ and BTC |
Diclofenac |
pH |
Anti-osteoarthritis (oral route) |
Release: 92% at pH 7.4 |
209
|