Cryo-silicified Biological Libraries for RNA Preservation

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Solution Overview

Problem

Current methods for preserving biological samples, such as formalin fixation and paraffin embedding, often result in degraded or chemically modified RNA, making it difficult to extract high-quality genetic and proteomic information from cells and tissues.

Innovation Solution

The use of cryo-silicification, a process that involves exposing samples to silicon-containing compounds at room temperature followed by incubation at 0° C to 80° C, which allows for dry, long-term storage and subsequent rehydration of cells, enabling the preservation of intact biological information like RNA, DNA, and proteins.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Duration of action of stationary object

If formalin fixation and paraffin embedding are used to preserve biological samples, then long-term storage is enabled, but RNA degradation and chemical modification occur

Engineering Contradiction:
Improvestorage durationVSAvoidRNA integrity
Core Design Contradiction:
Duration of action of stationary objectVSReliability

Solution Approach 1:

The patent changes the physical-chemical parameters of preservation by using cryo-silicification instead of formalin fixation. This involves transforming the sample from a hydrated state to a dehydrated siliceous matrix at low temperatures, fundamentally altering the preservation mechanism to prevent RNA degradation while maintaining long-term storage capability

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent employs phase transitions in the cryo-silicification process, where biological samples are frozen and then transformed into a stable dehydrated state through silicification. This phase change from hydrated to dehydrated state allows long-term preservation without the chemical degradation caused by formalin fixation

Inventive Principle:
Principle #36Phase transitions

2Reliability

If cryo-silicification is used to preserve biological samples, then RNA integrity is maintained, but storage conditions require specialized equipment

Engineering Contradiction:
ImproveRNA integrityVSAvoidstorage equipment requirements
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The patent applies preliminary action by performing cryo-silicification and dehydration processing before storage. This pre-treatment transforms the biological samples into a stable dehydrated state that can be stored without specialized cryogenic equipment, eliminating the need for continuous freezing while preserving RNA integrity

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The patent replaces expensive, complex cryogenic storage infrastructure with simple, ambient temperature storage conditions. The dehydrated cryo-silicified samples can be stored in standard laboratory freezers or even at room temperature, significantly reducing equipment requirements and operational costs

Inventive Principle:
Principle #27Cheap short-living objects (Disposable)

3Duration of action of stationary object

If dehydrated cryo-silicified cells are stored, then long-term stability is achieved, but rehydration and analysis complexity increases

Engineering Contradiction:
Improvestorage stabilityVSAvoidanalysis process complexity
Core Design Contradiction:
Duration of action of stationary objectVSDevice complexity

Solution Approach 1:

The patent applies self-service by designing the cryo-silicification process to naturally preserve all biological molecules (RNA, DNA, proteins) in their native states within the siliceous matrix. Upon rehydration, the samples automatically restore their functional properties without requiring complex recovery protocols or specialized processing steps

Inventive Principle:
Principle #25Self-service

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

Cryo-silicification and subsequent dehydration enable the retention of RNA integrity for extended periods, allowing for effective analysis and reconstitution of biological samples, including genetic and proteomic information, without the need for aldehyde fixation or paraffin embedding.

Implementation Method 1

The method includes obtaining a sample that includes a cell and cryo-silicifying the sample to create a cryo-silicified sample

Methodology Applied
Scientific EffectCryo-silicification: Precipitation

Implementation Method 2

the method further includes dehydrating the cryo-silicified sample to create a dehydrated cryo-silicified sample

Methodology Applied
Scientific EffectDehydration: Desiccation

Implementation Method 3

cryo-silicified cells, dehydrated cryo-silicified cells

Methodology Applied
Scientific EffectCryo-preservation: Freezing

Data Source

PatentUS20220389413A1Biological libraries and methods of preparing and using same
Publication Date: 2022.12.08 UNM RAINFOREST INNOVATIONS
  • US20220389413A1 patent drawing
  • US20220389413A1 patent drawing
  • US20220389413A1 patent drawing

AI summary

A biological library that includes a plurality of cryo-silicified cells, a plurality of dehydrated cryo-silicified cells, or both, where the cryo-silicified cells and/or the dehydrated cryo-silicified cells contain accessible biological information. In some embodiments, the biological information includes genetic information, proteomic information, or transcriptomic information. Members of the library may be analyzed to identify changes in the biological information associated with a medical condition or response to treatment. When the library includes B lymphocytes, cellular material from the B lymphocytes may be used to produce an antibody.