Curcumin-based magnetic nanostructured system for dual response of imaging and therapeutics
US-2020038525-A1 · Feb 6, 2020 · US
US11723920B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11723920-B2 |
| Application number | US-202117530002-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 18, 2021 |
| Priority date | Apr 25, 2019 |
| Publication date | Aug 15, 2023 |
| Grant date | Aug 15, 2023 |
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A nanotherapeutic having platinum complexes encapsulated by a nanoformulation containing at least one spinel ferrite of formula CuFe2O4, NiFe2O4, CoFe2O4, and MnFe2O4 deposited on mesoporous silica. A method of preparing the nanotherapeutic that involves mixing a metal(II) salt and a Fe(III) salt with the mesoporous silica nanoparticles to form a powdery mixture, calcining the powdery mixture to form the nanoformulation, and mixing the nanoformulation with the platinum complex. A method for treating cancer with the nanotherapeutic.
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The invention claimed is: 1. A method for treating a proliferative disorder, the method comprising administering a nanotherapeutic to a subject in need of therapy, wherein the nanotherapeutic comprises: a nanoformulation comprising: mesoporous silica nanoparticles in the form of monodispersed spherical silica having a particle size distribution of about 80 nm; and spinel ferrite nanoclusters of formula (I) MFe 2 O 4 (I) wherein M is at least one transition metal element selected from the group consisting of Cu and Ni; wherein: the spinel ferrite nanoclusters are impregnated on the mesoporous silica nanoparticles; and the spinel ferrite nanoclusters are present in an amount of 25-35 wt % relative to a total weight of the nanoformulation, and cisplatin encapsulated within pores of the nanoformulation, wherein the nanoformulation has a cisplatin release at a pH 5 at 37° C. for 72 h of 60-80 wt. %; wherein the pores of the nanoformulation have a pore diameter in a range of 10-25 nm, and the nanoformulation has a pore volume in a range of 0.05 0.3 cm 3 /g, a BET surface area in a range of 15-70 m 2 /g, and a saturation magnetization value in a range of 7-15 emu/g; and wherein the proliferative disorder is a cancer selected from the group consisting of breast cancer, ovarian cancer, cervical cancer, testicular cancer, colon cancer, bladder cancer, and lung cancer. 2. The method of claim 1 , wherein the nanotherapeutic further comprises one or more pharmaceutically acceptable carriers and/or excipients selected from the group consisting of a buffer, an inorganic salt, a fatty acid, a vegetable oil, a synthetic fatty ester, a surfactant, and a polymer. 3. The method of claim 1 , wherein the cisplatin is present at a concentration of 0.01-10 mmol/g relative to a total weight of the nanoformulation. 4. The method of claim 1 , wherein 0.5-800 mg/kg of the nanotherapeutic is administered per body weight of the subject. 5. The method of claim 1 , wherein the cancer proliferative disorder is breast cancer. 6. The method of claim 1 , wherein the subject is a mammal.
Platinum; Compounds thereof · CPC title
Inorganic compounds · CPC title
Antineoplastic agents · CPC title
Esters of carboxylic acids, e.g. fatty acid monoglycerides, medium-chain triglycerides, parabens or PEG fatty acid esters · CPC title
Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery · CPC title
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