Compositions and methods for targeted delivery to cells
US-2024390271-A1 · Nov 28, 2024 · US
US12569450B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12569450-B2 |
| Application number | US-202017776481-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 9, 2020 |
| Priority date | Nov 13, 2019 |
| Publication date | Mar 10, 2026 |
| Grant date | Mar 10, 2026 |
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.
The present disclosure provides nanoparticles comprising methyl palmitate and at least one serumglobular protein and uses thereof.
Opening claim text (preview).
The invention claimed is: 1 . A composition comprising nanoparticles comprising methyl palmitate and albumin, wherein the nanoparticles comprise methyl palmitate and albumin in a weight ratio (w/w) between 5:1 and 2:1. 2 . The composition according to claim 1 , wherein the average diameter size of the nanoparticles is comprised between 180 nm and 240 nm. 3 . A method for producing the nanoparticles according to claim 1 , comprising the following steps: preparing a first solution comprising methyl palmitate, preparing a second solution comprising albumin, adding the second solution to the first solution to obtain a third solution comprising methyl palmitate and albumin in a weight ratio (w/w) comprised between 2:2.5 and 2:20, mixing the third solution thereby allowing the production of nanoparticles in the solution, and separating the nanoparticles. 4 . The method according to claim 3 , wherein the separating step is carried out by centrifugation of the solution containing the nanoparticles. 5 . The method according to claim 3 , wherein the separating step is carried out at a temperature comprised between 4° C. and 9° C. 6 . A kit comprising the composition according to claim 1 and at least one active principle or at least one imaging agent, said at least one active principle or said at least one imaging agent being contained in at least one Secondary Administered Nanoparticle, for separate and sequential use in inhibiting the phagocytic activity of the macrophages and in increasing the bioavailability of said active principle and/or said imaging agent in a mammal.
Manufacture or treatment of nanostructures · CPC title
Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery · CPC title
Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca · CPC title
Processes · CPC title
Organic compounds, e.g. fats, sugars · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.