Hydroxyalkyl Starch Selective Macrophage Targeting for Hematological Neoplasms

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Current treatments for hematological neoplasms, such as leukemia and lymphoma, often result in severe side effects due to the non-selective nature of chemotherapy drugs, which can lead to tumor recurrence during recovery periods.

Innovation Solution

The use of hydroxyalkylated starch (HAS) as a therapeutic agent to reduce tumor growth rate and cancer cell proliferation while minimizing toxic side effects, potentially combined with standard chemotherapy drugs to reduce their dosage and frequency.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If chemotherapy drugs are used to treat hematological neoplasms, then tumor growth rate and cancer cell proliferation are reduced, but severe toxic side effects occur

Engineering Contradiction:
Improvetumor growth reductionVSAvoidtoxic side effects
Core Design Contradiction:
ProductivityVSObject-affected harmful factors

Solution Approach 1:

The patent uses hydroxyalkyl starch as an intermediary substance that selectively binds to hematological neoplasm cells through macrophage-mediated recognition. This intermediary approach allows the treatment to target cancer cells indirectly while sparing healthy cells, thereby reducing toxic side effects while maintaining tumor growth reduction efficacy

Inventive Principle:
Principle #24Intermediary (Mediator)

Solution Approach 2:

The patent changes the parameter of selectivity by using hydroxyalkyl starch with specific molecular weight and substitution degree parameters. These parameter optimizations enable the starch to be recognized by macrophages associated with neoplasm cells, achieving selective targeting without the non-specific toxicity of conventional chemotherapy

Inventive Principle:
Principle #35Parameter changes

2Reliability

If chemotherapy drugs are administered repeatedly to prevent tumor recurrence, then treatment efficacy is maintained, but toxic side effects accumulate and health deteriorates

Engineering Contradiction:
Improvetreatment efficacyVSAvoidaccumulated toxicity
Core Design Contradiction:
ReliabilityVSObject-affected harmful factors

Solution Approach 1:

By using hydroxyalkyl starch as a repeatable intermediary treatment that accumulates in neoplasm-associated macrophages, the patent enables continuous or repeated administration without cumulative toxicity. The intermediary selectively targets diseased cells, allowing reliable long-term treatment efficacy while avoiding the accumulated harm that plagues conventional chemotherapy

Inventive Principle:
Principle #24Intermediary (Mediator)

3Productivity

If standard chemotherapy dosage is used to ensure treatment effectiveness, then tumor control is achieved, but recovery periods are required due to toxicity

Engineering Contradiction:
Improvetumor controlVSAvoidrecovery period
Core Design Contradiction:
ProductivityVSDuration of action of moving object

Solution Approach 1:

The hydroxyalkyl starch intermediary enables continuous treatment without recovery periods because it selectively accumulates only in neoplasm-associated macrophages. This selective intermediary approach maintains effective tumor control while eliminating the toxic recovery intervals required by conventional chemotherapy, allowing uninterrupted treatment duration

Inventive Principle:
Principle #24Intermediary (Mediator)

Data Source

PatentUS10272102B2Hydroxyalkyl starch for the treatment of hematological neoplasms
Publication Date: 2019.04.30 FRESENIUS KABI DEUTSCHLAND GMBH
  • US10272102B2 patent drawing
  • US10272102B2 patent drawing
  • US10272102B2 patent drawing

AI summary

The present invention relates to hydroxyalkyl starch or a pharmaceutical preparation thereof for the treatment of a hematological neoplasm, especially by effectively reducing proliferation rate of cancer cells and inhibiting cancer cell growth and wherein the hydroxyalkyl starch has a mean molecular weight (MW) above 20 and below 1300 kDa and a molar substitution (MS) in the range of from 0.1 to 1.5, wherein the alkylation may be an ethylation, propylation or butylation or mixes thereof; and wherein the alkyl may be further substituted.