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5 protocols using 1 3 5 benzene tricarboxylic acid btc

1

Synthesis of Metal-Organic Frameworks

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VOSO4·xH2O, 1,3,5-benzene tricarboxylic acid (BTC), adenine, DMF, ethanol (≥99.5%) and, methanol (99.8%) were purchased from Sigma-Aldrich and used as supplied. All aqueous solutions were prepared with deionized water.
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2

Synthesis of Metal-Organic Frameworks

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EXAMPLE 1

Chemicals and Materials

All reagents were used as purchased without further purification. 1,3,5-benzene tricarboxylic acid (BTC), Cu(NO3)2.3H2O, Co(NO3)2.6H2O, Ni(NO3)2.6H2O, Zn(NO3)2.6H2O, FeCl2.6H2O, N,N-dimethylformamide (DMF) and ethanol were obtained from Sigma-Aldrich. Acetonitrile was obtained from Sigma-Aldrich. Toluene, cyclohexane and methylcyclohexane were used as purchased from Sigma-Aldrich. New 10 mL and 20 mL kimble scintillation vials were used for the synthesis of various metal organic frameworks (MOFs).

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3

Synthesis and Functionalization of Metal-Organic Frameworks

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Iron (III) chloride hexahydrate (98%, Alfa Aesar, Schiltigheim, France), 1,3,5-benzenetricarboxylic acid (BTC, 95%, Sigma-Aldrich, Saint-Quentin-Fallavier, France) and absolute ethanol (99%, Carlo Erba, Val-de-Reuil, France) were used for MOF synthesis. PBS (11.9 mM, pH 7.4 ± 0.1) was purchased from Life Technology Co., Ltd. (Saint Aubin, France). It contains 11.9 mM phosphates, 137 mM NaCl and 2.7 mM KCl. Gem-MP (CH12F2N3OP) was purchased from Toronto Research Chemicals, Canada. Phosphated β-cyclodextrin sodium salt (CD-P, Cyclolab, CY-2017.1, molecular formula: C42H70O47P4Na4) was used for coating. Milli-Q water was obtained from a Millipore apparatus equipped with a 0.22 μm filter. Reagents and solvents were used without further purification.
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4

Doxorubicin-Loaded Nanoscale Metal-Organic Frameworks

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Doxorubicin (DOX, 98%), citric acid (≥99.5%), sodium phosphate monobasic dihydrate (≥99%, NaH2PO4·2H2O), hydrochloric acid (HCl, 34–37%), sodium hydroxide (NaOH, ≥97%) potassium chloride (powder, ≥99%) and deferoxamine mesylate salt (≥92.5%) were purchased from Sigma-Aldrich (Saint-Quentin-Fallavier, France). γ-CD was purchased from Cyclolab (Budapest, Hungary). Dimethylsulfoxide (DMSO, ACS) was from Panreac Applichem (Barcelona, Spain). Deuterated DMSO (DMSO-d6, 99.8% D) and water (D2O, 99.9% D) were obtained from Eurisotop (Gif sur Yvette, France). 1,5-13C2 citric acid was obtained from CortecNet (Les Ulis, France). 1,3,5-benzenetricarboxylic acid (BTC, 95%, Sigma-Aldrich, Saint-Quentin-Fallavier, France), aluminum nitrate nonahydrate (98%, Sigma-Aldrich, Saint-Quentin-Fallavier, France) and trimethyl trimesate (98%, Sigma-Aldrich, Saint-Quentin-Fallavier, France) and absolute ethanol (99%, Carlo Erba, Val-de-Reuil, France) were used for the synthesis of nanoMOFs. Water was purified by a Millipore MilliQ system.
Phosphate buffer saline (PBS, pH 7.4, containing 9.5 mM phosphates) was purchased from Life Technologies (Saint-Aubin, France) and was used for DOX release study.
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5

Synthesis of Metal-Organic Frameworks

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EXAMPLE 1

Chemicals and Materials

All reagents were used as purchased without further purification. 1,3,5-benzene tricarboxylic acid (BTC), Cu(NO3)2.3H2O, Co(NO3)2.6H2O, Ni(NO3)2.6H2O, Zn(NO3)2.6H2O, FeCl2.6H2O, N,N-dimethylformamide (DMF) and ethanol were obtained from Sigma-Aldrich. Acetonitrile was obtained from Sigma-Aldrich. Toluene, cyclohexane and methylcyclohexane were used as purchased from Sigma-Aldrich. New 10 mL and 20 mL kimble scintillation vials were used for the synthesis of various metal organic frameworks (MOFs).

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