Hydrophilic drug and hydrophobic drug co-loaded target composite nano-drug preparation and preparation method thereof
A nano-drug, hydrophobic drug technology, applied in the direction of drug combination, pharmaceutical formula, non-active ingredient medical preparations, etc., to achieve good therapeutic effect, delay drug resistance, reduce toxicity effect
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Embodiment 1
[0030] 1) Add 150 ml concentrated sulfuric acid and concentrated nitric acid to 50 mgMWCNTs (H2 SO 4 :HNO 3 =3:1) in the mixture was oxidized at 100 °C for 4 h to obtain truncated CNTs, which were centrifuged at 6000 rpm, precipitated in an ultrasonic tank and washed with acetone for 5 times to remove impurities, and then vacuum-dried at 40 °C for 16 h, The obtained black powdery substance is truncated multi-walled carbon nanotubes (CNTs). The as-prepared CNTs have a highly hydrophilic surface and are soluble in aqueous solution because strong acid oxidation not only truncates CNTs but also changes the chemical properties of their surface, i.e., their surface is highly carboxylated. Dissolve 50 mg of CNTs in 50 ml of deionized water, add 3 equivalents of 1-ethyl-(3-dimethylaminopropyl) carbodiimide hydrochloride (EDC) to activate at room temperature for 2 h, and then Add 3 equivalents of N-hydroxysuccinimide (NHS) and a certain amount of polyethylene glycol (H 2 N-PEG-NH 2...
Embodiment 2
[0036] Example 2 In vitro experiments on breast cancer cells,
[0037] Using HER-2-positive breast cancer cells SKBR-3, SKBR-3 cells were combined with doxorubicin (ADM)) HER-2-specific monoclonal antibody Fab fragment targeting carbon nanotube drug PEG-CNTs- AntiHER2 Fab-ADM , paclitaxel (Taxol) HER-2 specific monoclonal antibody Fab fragment targeting carbon nanotube drug PEG-CNTs- AntiHER2 Fab -Taxol and HER-2 targeting carbon nanotube loaded hydrophilic drug doxorubicin and hydrophobic The drug preparation of two anticancer drugs paclitaxel (PEG-CNTs-AntiHER2 Fab-ADM-Taxol) was co-cultured for 48h, and the cell viability was detected by MTT. ADM and Taxol single drug group ( p <0.05, n=6).
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