Flow Cell Spectrophotometer Integrated in Liquid Handler

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Solution Overview

Problem

Current liquid handling and spectrophotometry systems face challenges in integrating sample preparation and analysis, particularly with small sample volumes, leading to inefficiencies and sample wastage, as they require separate apparatus and are not compatible with automated liquid handlers.

Innovation Solution

A combined liquid handling and photometric system that includes a flow cell spectrophotometer integrated within an automated liquid handler, enabling high-throughput UV readings with minimal sample consumption (down to 3-5 µL) and maintaining accuracy, allowing for consistent protein and polypeptide concentration measurements and sample reuse.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If separate apparatus are used for liquid handling and spectrophotometry, then each apparatus can be optimized for its specific function, but the system becomes more complex and less compatible with automated liquid handlers

Engineering Contradiction:
Improvefunctional optimizationVSAvoidsystem integration
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The patent combines the spectrophotometer and liquid handler into a single integrated apparatus. The flow cell spectrophotometer is positioned within the liquid handler body, allowing optical measurements to be performed during liquid handling operations. This merging eliminates the need for separate apparatus and improves compatibility with automated systems while maintaining functional optimization through dedicated components for each function.

Inventive Principle:
Principle #5Merging (Combining)

2Measurement precision

If traditional spectrophotometers are used with small sample volumes, then measurement accuracy can be maintained, but sample consumption increases and reuse becomes difficult

Engineering Contradiction:
Improvereading accuracyVSAvoidsample consumption
Core Design Contradiction:
Measurement precisionVSLoss of substance

Solution Approach 1:

The patent employs a flow cell spectrophotometer that allows dynamic sampling and measurement. The system can aspirate small volumes of sample (3-5 µL) into the flow cell for measurement, then dispense the same sample back into the original container for reuse. This dynamic approach enables multiple measurements from the same small sample volume, reducing sample consumption while maintaining accuracy through controlled flow through the optical path.

Inventive Principle:
Principle #15Dynamics

3Productivity

If plate readers are integrated into automated liquid handlers, then high-throughput analysis can be achieved, but the integration is challenging and expensive

Engineering Contradiction:
Improvethroughput capabilityVSAvoidintegration difficulty
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

The patent creates a universal integrated apparatus where the flow cell spectrophotometer can be incorporated into automated liquid handlers. The system performs multiple functions: liquid handling, optical measurement, and sample reuse capability. This multi-functional design achieves high-throughput analysis capability while simplifying integration compared to plate reader systems, as the flow cell can be directly positioned within the liquid handler body without requiring complex plate mounting and positioning mechanisms.

Inventive Principle:
Principle #6Universality (Multi-functionality)

4Reliability

If minimum sample volumes are required for accurate readings, then measurement reliability is improved, but available sample quantity is reduced for other purposes

Engineering Contradiction:
Improvereading accuracyVSAvoidsample availability
Core Design Contradiction:
ReliabilityVSQuantity of substance

Solution Approach 1:

The patent implements sample recovery through the flow cell spectrophotometer system. After optical measurement, the sample in the flow cell is dispensed back into the original container rather than being discarded. This recovery mechanism allows the minimum required sample volume for accurate readings (3-5 µL) to be reused for subsequent measurements or other experimental purposes, thereby maintaining both reading accuracy and sample availability.

Inventive Principle:
Principle #34Discarding and recovering

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

This solution provides accurate and efficient analysis of small sample volumes with minimal sample consumption, enabling standardized methods for mass spectrometric analysis and improving the integration of sample preparation and spectrophotometric measurements within automated systems.

Implementation Method 1

Optical spectrophotometric techniques, including UV-visible (ultraviolet-visible) optical absorption spectroscopy and colorimetry, are used extensively in organic chemical and biochemical assays

Methodology Applied
Scientific EffectUV absorption spectroscopy: Absorption Spectroscopy

Data Source

PatentEP3671220B1Apparatus for handling and spectrophotometry of small liquid samples
Publication Date: 2023.02.22 THERMO FINNIGAN LLC
  • EP3671220B1 patent drawingFigure 1A
  • EP3671220B1 patent drawingFigure 1B
  • EP3671220B1 patent drawingFigure 1C

AI summary

A system (1) comprises: (a) a robotic arm (4); (b) a needle capillary (8) coupled to the robotic arm (4); (c) a cell (11) coupled to the robotic arm (4) comprising: a housing (7); first and second windows (34a, 34b) disposed within the housing (7) and defining a width of an internal chamber (27) therebetween; a collimating lens (36a) optically coupled to the first window (34a); a focusing lens (36b) optically coupled to the second window (34b); an inlet port fluidically coupled to a first end of the internal chamber (27); and an outlet port fluidically coupled to a second end of the internal chamber (27); (d) a pump (30); (e) first and second tubings (12, 16) fluidically coupled, respectively, between the needle capillary (8) and the inlet port and between the pump (30) and the outlet port; (f) a light source (24); (g) a photodetector (26); and (h) first and second optical fibers (18, 20) optically coupled, respectively, between the light source (24) and the collimating lens (36a) and between the photodetector (26) and the focusing lens (36b).