Lutein Tabletting Compression Loss via Particle Size Control

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Solution Overview

Problem

Current lutein tablets suffer from high compression loss during the tableting process, leading to reduced shelf life due to lutein being extracted from the hydrocolloid matrix, which loses its protective effect and is prone to oxidation.

Innovation Solution

A solid formulation comprising milled carotenoids (lutein and zeaxanthin) with a specific particle size distribution, combined with modified food starches and glucose syrup, which minimizes the compression loss by embedding lutein within a stable matrix, thereby reducing the amount of lutein on the tablet surface and protecting it from oxidation.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Stability of the object's composition

If lutein is embedded in a hydrocolloid matrix for protection, then stability is improved, but compression loss increases during tableting

Engineering Contradiction:
Improvelutein stabilityVSAvoidcompression loss
Core Design Contradiction:
Stability of the object's compositionVSLoss of substance

Solution Approach 1:

The patent changes the particle size parameter of lutein from conventional sizes to a specific range (D[3,2] of 0.6-1.5 μm and D[v,0.5] of 1.1-3.5 μm). This parameter modification allows lutein to be more effectively embedded in the hydrocolloid matrix, reducing compression loss during tableting while maintaining stability protection.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent creates a composite formulation combining milled lutein particles with specific hydrocolloids (modified food starches), glucose syrup, and antioxidants. This composite structure ensures lutein is properly embedded and protected within the matrix, resolving the contradiction between stability and compression loss.

Inventive Principle:
Principle #40Composite materials

2Quantity of substance

If lutein is present on tablet surface for availability, then bioavailability is improved, but oxidation resistance decreases

Engineering Contradiction:
Improvelutein availabilityVSAvoidoxidation susceptibility
Core Design Contradiction:
Quantity of substanceVSObject-affected harmful factors

Solution Approach 1:

The hydrocolloid matrix acts as a protective shell or film surrounding the lutein particles. This matrix embedding protects lutein from oxidation while the formulation ensures controlled availability, resolving the contradiction between surface availability and oxidation resistance.

Inventive Principle:
Principle #30Flexible shells and thin films

Solution Approach 2:

The patent incorporates water-soluble antioxidants (such as sodium ascorbate) within the hydrocolloid matrix, creating a chemically protective environment that prevents oxidation. This inert-like protective atmosphere allows lutein to maintain stability while remaining available.

Inventive Principle:
Principle #39Inert atmosphere (Inert environment)

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 formulation achieves a compression loss of ≤12%, enhancing the stability and shelf life of lutein tablets by maintaining lutein within the matrix, ensuring it remains protected and effective.

Implementation Method 1

embedding lutein within a stable matrix, thereby reducing the amount of lutein on the tablet surface

Methodology Applied
Scientific EffectPhysical embedding/encapsulation:

Implementation Method 2

the hydrocolloid which protects lutein from degradation and oxidation

Methodology Applied
Scientific EffectProtective barrier effect:

Implementation Method 3

at least one water-soluble antioxidant (preferably sodium ascorbate)... protecting it from oxidation

Methodology Applied
Scientific EffectAntioxidant protection: Oxidation

Implementation Method 4

a milled carotenoid has the following particle size distribution: D [3,2] in the range of from 0.6 to 1.5 μm and D [v, 0.5] in the range of from 1.1 to 3.5 μm

Methodology Applied
Scientific EffectMechanical milling/size reduction: Abrasion

Data Source

PatentUS20240023589A1Tablettable formulation of lutein and/or zeaxanthin
Publication Date: 2024.01.25 DSM IP ASSETS BV
  • US20240023589A1 patent drawing

AI summary

Solid formulations include a milled carotenoid, at least one hydrocolloid, a glucose syrup, sucrose and at least one water-soluble antioxidant (preferably sodium ascorbate), wherein the carotenoid is selected from the group consisting of lutein and zeaxanthin and any mixture thereof, wherein the hydrocolloid is selected from the group consisting of modified food starches and any mixtures thereof, and wherein the milled carotenoid has the following particle size distribution:D [3,2] in the range of from 0.6 to 1.5 μm and D [v, 0.5] in the range of from 1.1 to 3.5 μm, all D values as measured by laser diffraction (Malvern Instruments Ltd, Malvern, UK, Mastersizer 3000) according to the Fraunhofer scattering model. The solid formulation is in form of granules which are used for dietary supplements and pharmaceuticals, such as e.g. multi-vitamin and/or multi-mineral tablets and surprisingly show a low compression loss.