Separation of nanoparticles
US-2015375180-A1 · Dec 31, 2015 · US
US10358456B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10358456-B2 |
| Application number | US-201815933076-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 22, 2018 |
| Priority date | Mar 22, 2017 |
| Publication date | Jul 23, 2019 |
| Grant date | Jul 23, 2019 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Platinum(II) complexes with various selones (L) having the general formula PtL2Cl2 are disclosed. The platinum(II) complexes of the invention inhibit growth of cancer cells in vitro and are useful for treatment of proliferative disorders such as cancers and/or tumors.
Opening claim text (preview).
The invention claimed is: 1. A platinum (II) complex of formula PtL 2 Cl 2 , wherein L is of formula Ia, Ib, Ic, or Id: wherein R 4 and R 4′ are independently hydrogen, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, t-butyl, pentyl, isopentyl, phenyl, or benzyl. 2. A method of making the platinum (II) complex of claim 1 , said method comprising: (a) adding a solution of tetrahaloplatinate (II) in a polar aprotic solvent to a solution of a compound of formula Ia, Ib, Ic, or Id in a solvent under inert gas to form a reaction mixture, and (b) stirring the reaction mixture to form the platinum (II) complex as a precipitate. 3. The method of claim 2 , further comprising filtering the platinum (II) complex. 4. A pharmaceutical composition comprising the platinum (II) complex of claim 1 ; and a pharmaceutically acceptable carrier and/or excipient. 5. The pharmaceutical composition of claim 4 , which comprises 0.1-400 μM of the platinum (II) complex relative to the total volume of the composition. 6. The pharmaceutical composition of claim 5 , wherein the pharmaceutically acceptable carrier and/or excipient is at least one 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. 7. The pharmaceutical composition of claim 5 , further comprising a chemotherapeutic agent. 8. A method for treating cervical cancer, breast cancer, or both in a subject in need of therapy, the method comprising administering to the subject a sufficient amount of the pharmaceutical composition of claim 4 . 9. The method of claim 8 , wherein 1-300 mg/kg of the platinum (II) complex is administered per body weight of the subject. 10. The method of claim 8 , wherein the subject is a mammal.
containing heavy metals, e.g. hemin, hematin, melarsoprol · CPC title
Platinum compounds · CPC title
Antineoplastic agents · CPC title
Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca · CPC title
without a metal-carbon linkage · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.