Manganese ion coated nanoparticles for delivery of compositions into the central nervous system by nasal insufflation

US9375400B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9375400-B2
Application numberUS-201214343534-A
CountryUS
Kind codeB2
Filing dateSep 14, 2012
Priority dateSep 14, 2011
Publication dateJun 28, 2016
Grant dateJun 28, 2016

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  1. Title

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  2. Abstract

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  4. Key dates

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  5. First independent claim

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Abstract

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The compositions and methods of the disclosure particularly target the divalent metal transporter expressed on olfactory nerve terminals to transport divalent cation-coated or cation-containing nanoparticles to all regions of brain. It has been found that such divalent cation-containing nanoparticles, including those nanoparticles comprising manganese have affinity for the metal transport receptor proteins. Although this receptor has particular affinity for manganese, it is contemplated that other divalent ions, including magnesium, calcium, and the like may also be bound to such receptors leading to transport of the nanoparticles into the intracellular cytoplasm. Nanoparticles have been developed, therefore, as vehicles for parenteral delivery of genes, proteins and drugs. The present disclosure encompasses embodiments of nanoparticle-based compositions and methods for the use thereof for the delivery of genes, oligonucleotides, including but not limited to small interfering RNA, and other small molecule drugs, into the brain by nasal insufflation.

First claim

Opening claim text (preview).

We claim: 1. A nanoparticle delivery vehicle, comprising: a core comprising a plurality of cross-linked chitosan molecules or cross-linked thiolated chitosan molecules; and a plurality of manganese ions bonded to said cross-linked chitosan molecules or thiolated chitosan molecules. 2. The nanoparticle vehicle of claim 1 , wherein the core further comprises a therapeutic agent is attached to, or embedded in, the core. 3. The nanoparticle vehicle of claim 2 , wherein said therapeutic agent is a plurality of nucleic acid molecules bonded to the plurality of cross-linked chitosan molecules or cross-linked thiolated chitosan molecules of the nanoparticle core. 4. The nanoparticle vehicle of claim 3 , wherein the nucleic acid is an siRNA. 5. The nanoparticle vehicle of claim 1 , wherein the cross-linked chitosan molecules or the cross-linked thiolated chitosan molecules are cross-linked by a chelator selected from the group consisting of: L-(+)-Tartaric acid, ethylenediamine-N,N,N;-triacetic acid, protoporphyrin IX, nitrilotriacetic acid, mercaptosuccinic acid, and ethylenediaminetetraacetic acid, and wherein the manganese ions are chelated by the chelator. 6. A pharmaceutical composition comprising a nanoparticle delivery vehicle according to claim 1 and a pharmaceutically acceptable carrier. 7. The nanoparticle vehicle of claim 1 , wherein the cross-linked chitosan molecules or cross-linked thiolated chitosan molecules are cross-linked by a metal ion chelator and the manganese is chelated to said chelator. 8. A nanoparticle delivery vehicle comprising: a core comprising a plurality of cross-linked chitosan molecules or cross-linked thiolated chitosan molecules, wherein the cross-linked chitosan molecules or the cross-linked thiolated chitosan molecules are cross-linked by a chelator selected from the group consisting of: L-(+)-tartaric acid, ethylenediamine-N,N,N-triacetic acid, protoporphyrin IX, nitrilotriacetic acid, mercaptosuccinic acid, and ethylenediaminetetraacetic acid, a plurality of manganese ions, wherein the manganese ions are bonded to the cross-linking chelator, and a therapeutic agent, wherein said therapeutic agent is a plurality of nucleic acid molecules bonded to the cross-linked chitosan molecules or cross-linked thiolated chitosan molecules of the core. 9. A pharmaceutical composition comprising a nanoparticle delivery vehicle according to claim 8 , and a pharmaceutically acceptable carrier.

Assignees

Inventors

Classifications

  • interfering nucleic acids [NA] · CPC title

  • Microemulsions or submicron emulsions; Preconcentrates or solids thereof; Micelles, e.g. made of phospholipids or block copolymers (A61K9/0026 takes precedence) · CPC title

  • Chelates, e.g. Gd-DOTA or Zinc-amino acid chelates; Chelate-forming compounds, e.g. DOTA or ethylenediamine being covalently linked or complexed to the pharmacologically- or therapeutically-active agent · CPC title

  • using biolistic methods · CPC title

  • Inorganic compounds · CPC title

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What does patent US9375400B2 cover?
The compositions and methods of the disclosure particularly target the divalent metal transporter expressed on olfactory nerve terminals to transport divalent cation-coated or cation-containing nanoparticles to all regions of brain. It has been found that such divalent cation-containing nanoparticles, including those nanoparticles comprising manganese have affinity for the metal transport recep…
Who is the assignee on this patent?
Sanchez-Ramos Juan, Sava Vasyl, Song Shijie, and 3 more
What technology area does this patent fall under?
Primary CPC classification A61K9/1652. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Jun 28 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). 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).