Tetrazole derivatives
US-2024382468-A2 · Nov 21, 2024 · US
US8968784B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-8968784-B2 |
| Application number | US-31378408-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 24, 2008 |
| Priority date | May 22, 2006 |
| Publication date | Mar 3, 2015 |
| Grant date | Mar 3, 2015 |
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.
A method for preparing hydro/organo gelators from disaccharide sugars by biocatalysis and their use in enzyme-triggered drug delivery. Controlled delivery of an anti-inflammatory, chemopreventive drug is achieved by an enzyme-triggered drug release mechanism via degradation of encapsulated hydrogels. The hydro- and organo-gelators are synthesized in high yields from renewable resources by using a regioselective enzyme catalysis and a known chemopreventive and anti-inflammatory drug, curcumin, is encapsulated in the gel matrix and released by enzyme triggered delivery. The release of the drug occurs at the physiological temperature and control of the drug release rate is achieved by manipulating the enzyme concentration and temperature. The by-products formed after the gel degradation clearly demonstrated the site specificity of degradation of the gelator by enzyme catalysis. The present invention has applications in developing cost effective, controlled drug delivery vehicles from renewable resources, with a potential impact on pharmaceutical research and molecular design and delivery strategies.
Opening claim text (preview).
The invention claimed is: 1. A drug-delivery composition, comprising: a) a hydro/organo gel prepared by assembly of gelators to form nano-aggregates, wherein the gelator is prepared from an esterification reaction between amygdalin and a fatty acid; and b) a hydrophobic drug encapsulated in said gel; wherein said drug is capable of release upon enzyme mediated degradation of said gel. 2. The composition of claim 1 , wherein the hydro/organo gel is prepared…
Related publications grouped by family.
Free tools are coming soon. Tell us what you want to track and we'll notify you.
Answers are generated from the same data shown on this page.