IP Library Patent Application 14841325
Patent Application
App. No. 14/841,325

COMPOSITIONS OF PARTICULATE COFORMULATION

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Quick Facts
Patent No.
US None
App. No.
14/841,325
Abstract

Embodiments of the invention provide a composition of a particulate coformulation which includes particles containing an active substance and an additive, wherein each particle contains a relative additive concentration increasing radially outwards from a particle center to a particle surface along a finite gradient. In one example, the particle surface is an additive-rich surface without a distinct physical boundary between the particle center and the particle surface. The relative additive concentration may have a continuous rate of change across the finite gradient. In some examples, an active substance:additive ratio of the particle surface is sufficiently low to form a protective surface layer around the active substance. Generally, the particle surface is free of the active substance.

Claims (24)

1 . A composition of a particulate coformulation, comprising:

an active substance and an additive, which is a solid dispersion of one component in the other, but which has a finite gradient in the relative additive concentration, which concentration increases radially outwards from the core to the surface of the particles, so that the particles have an additive-rich surface region but do not possess separate core and coating layers with a distinct physical boundary between them, wherein the coformulation is or comprises a pharmaceutical or nutraceutical agent or a foodstuff.

2 . The composition of claim 1 , wherein the active substance:additive ratio, at the particle surfaces, is sufficiently low for the additive to form a protective surface layer around the active substance.

3 . The composition of claim 1 , wherein the additive is a taste masking agent or an odor masking agent.

4 . The composition of claim 2 , wherein the additive is a taste masking agent or an odor masking agent.

5 . The composition of claim 1 , wherein the active substance is present in a crystalline form and the additive is present in an amorphous form, and wherein differential scanning calorimetry analysis or X-ray diffraction analysis of the coformulation indicates reduced active substance crystallinity compared to that of the active substance alone.

6 . The composition of claim 1 , wherein the relative additive concentration is up to about 60% by weight.

7 . The composition of claim 2 , wherein the relative additive concentration is up to about 60% by weight.

8 . The composition of claim 4 , wherein the relative additive concentration is up to about 60% by weight.

9 . A composition of a particulate coformulation, comprising:

particles comprising:

an active substance, the active substance comprising a pharmaceutical agent, a nutritional agent, an herbicidal agent, a pesticidal agent, or combinations thereof; and

an additive, wherein each particle comprises a relative additive concentration increasing radially outwards from a particle center to a particle surface along a finite gradient, and wherein both the active substance and the additive comprise different pharmaceutically active substances for co-administration.

10 . The composition of claim 9 , wherein the particle surface is an additive-rich surface without a distinct physical boundary between the particle center and the particle surface.

11 . The composition of claim 10 , wherein the relative additive concentration has a continuous rate of change across the finite gradient.

12 . The composition of claim 10 , wherein an active substance:additive ratio of the particle surface is sufficiently low to form a protective surface layer around the active substance.

13 . The composition of claim 10 , wherein the particle surface is free of the active substance.

14 . The composition of claim 9 , wherein the particle surface comprises a concentration of about 5% or less by weight of the active substance.

15 . The composition of claim 14 , wherein the concentration of the active substance is about 2% or less by weight.

16 . The composition of claim 15 , wherein the concentration of the active substance is about 1% or less by weight.

17 . The composition of claim 16 , wherein the concentration of the active substance is about 0.5% or less by weight.

18 . The composition of claim 17 , wherein the concentration of the active substance is about 0% by weight.

19 . The composition of claim 9 , wherein a central region of each particle comprises a concentration of about 90% or greater by weight of the active substance.

20 . The composition of claim 19 , wherein the concentration of the active substance is about 95% or greater by weight.

Assignments (2)
RELEASE OF SECURITY INTEREST Recorded Apr 17, 2020
From: TC LENDING, LLC, AS COLLATERAL AGENT
To: NEKTAR THERAPEUTICS
Reel/Frame 053180/0009 →
GRANT OF SECURITY INTEREST IN UNITED STATES PATENTS Recorded Oct 6, 2015
From: NEKTAR THERAPEUTICS
To: TC LENDING, LLC, AS COLLATERAL AGENT
Reel/Frame 036796/0562 →