Compressed 3-NOP Tablets for Sustained Rumen Release

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Solution Overview

Problem

Current formulations of 3-nitrooxypropanol for reducing methane production in ruminants exhibit rapid disintegration and instantaneous release, which is not suitable for long-term methane reduction, as methane production in ruminants increases slowly after feeding.

Innovation Solution

Compressed tablets comprising 3-nitrooxypropanol and gluten, which remain intact and slowly release the active ingredient into aqueous media over an extended period, providing a slow and sustained release of the active compound.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Speed

If 3-nitrooxypropanol is supplemented as 10% on silicon dioxide, then the active ingredient is instantly released into the aqueous rumen fluid, but this instant release is not suitable for long term methane reduction as methanogenic archaea increase slowly after feeding

Engineering Contradiction:
Improverelease speed of active ingredientVSAvoidduration of methane reduction
Core Design Contradiction:
SpeedVSDuration of action of moving object

Solution Approach 1:

The patent changes the physical and chemical parameters of the tablet formulation by using compressed tablets with specific density (0.6-1.2 g/cm³), hardness (5-20 kp), and water stability (less than 10% weight loss after 24 hours). These parameter changes enable the tablet to maintain structural integrity and control the release rate of 3-nitrooxypropanol, transforming it from instant release to sustained release over 4-24 hours, matching the slow increase of methanogenic archaea after feeding.

Inventive Principle:
Principle #35Parameter changes

2Duration of action of moving object

If a compressed tablet formulation is used to achieve slow release, then the release duration is extended to 2-24 hours, but the tablet must maintain integrity and resist disintegration in aqueous media

Engineering Contradiction:
Improverelease duration of active ingredientVSAvoidtablet integrity in aqueous media
Core Design Contradiction:
Duration of action of moving objectVSStability of the object's composition

Solution Approach 1:

The patent employs composite tablet formulations combining 3-nitrooxypropanol (0.01-10 wt%) with excipients including starch (10-50 wt%), microcrystalline cellulose (10-50 wt%), and binders (5-20 wt%). This composite structure creates a matrix that controls drug release while maintaining tablet integrity in aqueous environments, achieving both extended release duration and structural stability through the synergistic properties of different materials.

Inventive Principle:
Principle #40Composite materials

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

The compressed tablets effectively inhibit methanogenic archaea growth, leading to sustained methane reduction in ruminants by maintaining the active ingredient's integrity and controlled release over 2-24 hours, addressing the limitations of rapid disintegration and instantaneous release in existing products.

Implementation Method 1

only slowly release the active into aqueous media over an extended period of time, such as 2-24 hours

Methodology Applied
Scientific EffectDiffusion: Diffusion

Implementation Method 2

show no disintegration over a long period of time and only slowly release the active into aqueous media

Methodology Applied
Scientific EffectDissolution:

Implementation Method 3

3-Nitrooxypropanol and structural analogues thereof have been reported to inhibit the growth of methanogenic archaea and thus significantly reducing the methane production in ruminants

Methodology Applied
Scientific EffectInhibition of microbial growth:

Data Source

PatentUS20240342095A1Compressed tablets
Publication Date: 2024.10.17 DSM IP ASSETS BV
  • US20240342095A1 patent drawing
  • US20240342095A1 patent drawing

AI summary

Compositions are formed of a compressed mixture which includes a powderous formulation of a carrier and 3-nitrooxypropanol or derivatives thereof as an active ingredient, and a gluten. The composition remains intact in water after 24 hours.