Hydrogel Toxin-Absorbing or Binding Nanoparticles

US2017079909A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2017079909-A1
Application numberUS-201515126342-A
CountryUS
Kind codeA1
Filing dateMar 20, 2015
Priority dateMar 20, 2014
Publication dateMar 23, 2017
Grant date

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The present invention provides for compositions comprising a polymeric hydrogel impregnated with a toxin-absorbing or binding nanoparticle. The present invention also provides for the use of the above compositions for decreasing or neutralizing the effect of a toxin, or for treating or preventing an infection by a microbe that produces a toxin, in a subject. The exemplary toxin is a biological toxin such as a viral, bacterial, fungal, plant or animal toxin.

First claim

Opening claim text (preview).

1 . A composition comprising a polymeric hydrogel impregnated with a toxin-absorbing or binding nanoparticle, wherein said nanoparticle comprises a) an inner core comprising a non-cellular material, and b) an outer surface comprising a cellular membrane configured for absorbing or binding said toxin. 2 . The composition of claim 1 , wherein the polymeric hydrogel comprises a material selected from the group consisting of poly(ethylene glycol) dimethacrylate (PEGDMA), silicone, gelatin, chitosan, alginate, polyester, poly(vinyl alcohol) and polyacrylamide, polyethylene oxide, polyvinyl alcohol, Carbopol®, polyacrylamidomethylpropanesulfonate, polyacrylic acid, a salt of acrylic acid (including sodium and sulfopropyl acrylate, 2-hydroxyethyl methacrylate), agarose, methylcellulose, hyaluronan, and copolymers thereof. 3 . (canceled) 4 . The composition of claim 1 , wherein, during use, the polymeric hydrogel comprises at least about 1% water (w/w). 5 . The composition of claim 1 , wherein the polymeric hydrogel possess a degree of flexibility suitable to be applied to a tissue or an organ. 6 . (canceled) 7 . The composition of claim 1 , wherein the inner core of the nanoparticle comprises a polymeric particle core, a silica particle core, or a metal, e.g., gold, particle core. 8 - 10 . (canceled) 11 . The composition of claim 1 , wherein the inner core of the nanoparticle comprises a biocompatible or a synthetic material selected from the group consisting of poly(lactic-c-glycolic acid) (PLGA), polylactic acid (PLA), polyglycolic acid (PGA), polycaprolactone (PCL), polylysine, and polyglutamic acid. 12 . The composition of claim 1 , wherein the inner core of the nanoparticle supports the outer surface of the nanoparticle. 13 . (canceled) 14 . The composition of claim 1 , wherein the cellular membrane of the nanoparticle comprises a plasma membrane or an intracellular membrane. 15 . (canceled) 16 . The composition of claim 1 , wherein the nanoparticle has a diameter from about 10 nm to about 10 um. 17 . The composition of claim 1 , wherein the nanoparticle substantially lacks constituents of the cell from which the cellular membrane is derived. 18 . (canceled) 19 . The composition of claim 1 , wherein the nanoparticle substantially maintains natural structural integrity or activity of the cellular membrane or the constituents of the cellular membrane. 20 . The composition of claim 1 , wherein the nanoparticle is biocompatible or biodegradable. 21 . The composition of claim 1 , wherein the inner core of the nanoparticle comprises PLGA and the outer surface of the nanoparticle comprises a plasma membrane derived from a red blood cell. 22 - 23 . (canceled) 24 . The composition of claim 1 , wherein the cellular membrane of the outer surface of the nanoparticle is configured to absorb or bind to a biological toxin. 25 - 32 . (canceled) 33 . The composition of claim 1 , wherein the polymeric hydrogel comprises hydrated polymeric networks that are either physically or covalently crosslinked with each other and/or with the nanoparticle(s). 34 . The composition of claim 1 , which further comprises a therapeutic agent, a prophylactic agent, a diagnostic or marker agent, a prognostic agent, an isolation agent, a monitoring agent, or a combination thereof. 35 - 48 . (canceled) 49 . The composition of claim 1 , which is configured to be a part of scaffolds in tissue engineering. 50 . (canceled) 51 . The composition of any of claim 1 , which is a toxin-neutralizing antimicrobial hydrogel. 52 - 54 . (canceled) 55 . A method for decreasing or neutralizing the effect of a toxin, or for treating or preventing an infection by a microbe that produces a toxin, in a subject, which method comprises administering, to a subject in need, or to cells of said subject, an effective amount of a composition of claim 1 . 56 - 74 . (canceled) 75 . A method of preserving therapeutic functionality of a toxin-absorbing or binding nanoparticle, which method comprises impregnating a toxin-absorbing or binding nanoparticle in a polymeric hydrogel to form a composition comprising said polymeric hydrogel impregnated with said toxin-absorbing or binding nanoparticle, wherein said nanoparticle comprises a) an inner core comprising a non-cellular material, and b) an outer surface comprising a cellular membrane configured for absorbing or binding said toxin. 76 - 80 . (canceled)

Assignees

Inventors

Classifications

  • Polyesters, e.g. poly(lactide-co-glycolide) · CPC title

  • Biocides, antimicrobial agents, antiseptic agents · CPC title

  • Hydrogels or hydrocolloids · CPC title

  • Biologically active materials, e.g. therapeutic substances {(A61L27/227 takes precedence)} · CPC title

  • Reptiles (antigens from snakes A61K39/38) · CPC title

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What does patent US2017079909A1 cover?
The present invention provides for compositions comprising a polymeric hydrogel impregnated with a toxin-absorbing or binding nanoparticle. The present invention also provides for the use of the above compositions for decreasing or neutralizing the effect of a toxin, or for treating or preventing an infection by a microbe that produces a toxin, in a subject. The exemplary toxin is a biological …
Who is the assignee on this patent?
Univ California
What technology area does this patent fall under?
Primary CPC classification A61K9/06. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Thu Mar 23 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).