Lipid Nanoparticle Delivery of MicroRNAs for Treatment-Resistant Cancer

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Solution Overview

Problem

Current treatments for glioblastoma (GBM) and triple-negative breast cancer (TNBC) are limited by resistance to standard therapies, such as ionizing radiation and temozolomide, and lack effective targeting mechanisms, leading to poor prognosis and limited treatment options for these aggressive cancers.

Innovation Solution

Nanoparticles, specifically liposomes and lipid nanoparticles, encapsulating microRNAs like miR-603 or anti-miR-21, functionalized with a targeting moiety, are administered to specifically target and deliver therapeutic agents to cancer cells, enhancing radiation sensitivity and reducing cancer cell proliferation.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If standard therapies (ionizing radiation and temozolomide) are used to treat glioblastoma, then initial treatment response is achieved, but tumor progression and recurrence occur due to development of resistance

Engineering Contradiction:
Improvetreatment effectivenessVSAvoidtreatment durability
Core Design Contradiction:
ReliabilityVSDuration of action of stationary object

Solution Approach 1:

The patent applies preliminary action by using nanoparticles to deliver microRNAs that preemptively sensitize cancer cells to radiation therapy before the actual treatment occurs. The microRNAs are delivered in advance to modulate gene expression and make the tumor cells more vulnerable to subsequent radiation, preventing resistance development rather than responding to it after it occurs.

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The patent uses nanoparticles as an intermediary delivery system to transport microRNAs across the blood-brain barrier and into tumor cells. These nanoparticles act as mediators that facilitate the delivery of therapeutic agents specifically to the tumor site, enabling precise modulation of tumor cell sensitivity to radiation therapy.

Inventive Principle:
Principle #24Intermediary (Mediator)

2Adaptability or versatility

If conventional treatments are applied to triple-negative breast cancer, then general cancer therapy is provided, but effective targeting mechanisms are lacking leading to poor prognosis

Engineering Contradiction:
Improvetreatment applicabilityVSAvoidtreatment efficacy
Core Design Contradiction:
Adaptability or versatilityVSReliability

Solution Approach 1:

The patent applies local quality by functionalizing nanoparticles with specific targeting moieties that recognize and bind to receptors uniquely or preferentially expressed on triple-negative breast cancer cells. This enables the therapeutic agent to be delivered specifically to the tumor tissue rather than systemically, achieving localized treatment effect with enhanced efficacy for this specific cancer subtype.

Inventive Principle:
Principle #3Local quality

Solution Approach 2:

The patent employs parameter changes by modifying the physical and chemical properties of the nanoparticle delivery system, including size, surface charge, and surface functionalization, to optimize tumor penetration, cellular uptake, and targeted delivery to triple-negative breast cancer cells, thereby adapting the treatment to the specific characteristics of this aggressive cancer type.

Inventive Principle:
Principle #35Parameter changes

Data Source

PatentUS20240209361A1Treating cancer
Publication Date: 2024.06.27 REGENTS OF THE UNIVERSITY OF MINNESOTA
  • US20240209361A1 patent drawing
  • US20240209361A1 patent drawing
  • US20240209361A1 patent drawing

AI summary

This document relates to methods and materials for treating cancer. For example, this document provides nanoparticles (e.g., liposomes and LNPs) encapsulating one or more microRNAs and/or one or more anti-microRNAs. In some cases, nanoparticles (e.g., liposomes and LNPs) encapsulating one or more microRNAs and/or one or more anti-microRNAs can be administered to a mammal (e.g., a human) having cancer to treat the mammal.