PLGA Nanoparticle Nanogel Delivery for Sustained AMD Treatment

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Solution Overview

Problem

Current treatments for age-related macular degeneration (AMD) suffer from a narrow therapeutic index, rapid drug clearance, frequent dose instillation, adverse effects, and poor therapeutic outcomes, necessitating a method for local delivery of anti-angiogenic agents like sunitinib to minimize dose frequency and enhance effectiveness.

Innovation Solution

Development of poly(lactic-co-glycolic acid) (PLGA)-based nanoparticles loaded with sunitinib, combined with a thermal reversible nanogel, for sustained drug delivery to the eye, providing a sustained release profile and reducing dosing frequency.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Quantity of substance

If systemic administration of anti-VEGF agents is used, then therapeutic coverage is broad, but therapeutic effectiveness is poor and clearance is rapid

Engineering Contradiction:
Improvetherapeutic coverageVSAvoidtherapeutic effectiveness
Core Design Contradiction:
Quantity of substanceVSReliability

Solution Approach 1:

The patent uses intravitreal injection as an intermediary delivery route to bypass systemic circulation and deliver anti-VEGF agents directly to the ocular site. This mediator approach overcomes the rapid clearance and poor effectiveness of systemic administration by placing the drug in close proximity to the target tissue, allowing sustained local action without relying on systemic distribution.

Inventive Principle:
Principle #24Intermediary (Mediator)

2Reliability

If frequent dose instillation is performed, then therapeutic effectiveness is maintained, but patient compliance decreases and adverse effects increase

Engineering Contradiction:
Improvetherapeutic effectivenessVSAvoidpatient compliance
Core Design Contradiction:
ReliabilityVSEase of operation

Solution Approach 1:

The patent employs sustained-release formulations and ocular implant devices that pre-load therapeutic agents for prolonged delivery. This preliminary action stores the drug in a reservoir or matrix that releases it gradually over weeks or months, eliminating the need for frequent patient-administered doses while maintaining therapeutic effectiveness and improving compliance.

Inventive Principle:
Principle #10Preliminary action

3Loss of time

If local delivery of sunitinib is implemented, then dosing frequency is reduced, but delivery precision must be increased

Engineering Contradiction:
Improvedosing frequencyVSAvoiddelivery precision
Core Design Contradiction:
Loss of timeVSManufacturing precision

Solution Approach 1:

The patent applies local quality by designing ocular-specific delivery systems including intravitreal implants, ocular inserts, and targeted nanocarriers that concentrate sunitinib precisely at the retinal and choroidal sites. These systems ensure the drug is delivered exactly where needed in the eye with controlled release kinetics, reducing dosing frequency while maintaining high delivery precision through localized formulation design.

Inventive Principle:
Principle #3Local quality

Data Source

PatentUS20250367118A1Nanoparticles and nanogel drug compositions for treatment of age-related macular degeneration
Publication Date: 2025.12.04 UNIV OF SOUTH FLORIDA
  • US20250367118A1 patent drawing
  • US20250367118A1 patent drawing
  • US20250367118A1 patent drawing

AI summary

Disclosed are nanoparticles and nanogel drug compositions and the use thereof for treating age-related macular degeneration.