System and method for the analysis of bodily fluids

Abstract

A system for the rapid characterization of multi-analyte fluids, in one embodiment, includes a light source, a sensor array, and a detector. The sensor array is formed from a supporting member into which a plurality of cavities may be formed. A series of chemically sensitive particles are, in one embodiment positioned within the cavities. The particles may be configured to produce a signal when a receptor coupled to the particle interacts with the analyte. Using pattern recognition techniques, the analytes within a multi-analyte fluid may be characterized.

Description

PRIORITY CLAIM [0001] This application claims priority to U.S. Provisional Application No. 60 / 179,369 entitled “METHOD AND SYSTEM FOR COLLECTING AND TRANSMITTING CHEMICAL INFORMATION,” filed Jan. 31, 2000, U.S. Provisional Application No. 60 / 179,424 entitled “SYSTEM AND METHOD FOR THE ANALYSIS OF BODILY FLUIDS” filed Jan. 31, 2000, U.S. Provisional Application No. 60 / 179,294 entitled “SYSTEM AND METHOD FOR IDENTIFYING NUCLEIC ACIDS IN A FLUID SAMPLE,” filed Jan. 31, 2000, U.S. Provisional Application No. 60 / 179,380 entitled “METHOD OF PREPARING A SENSOR ARRAY,” filed Jan. 31, 2000, U.S. Provisional Application No. 60 / 179,292 entitled “SYSTEM FOR TRANSFERRING FLUID SAMPLES THROUGH A SENSOR ARRAY,” filed Jan. 31, 2000 and U.S. Provisional Application No.60 / 179,293 entitled “PORTABLE SENSOR ARRAY SYSTEM,” filed Jan. 31, 2000.STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT [0002] Research leading to this invention was federally supported, in part, by grant No. 1R01GM5730...

AI Technical Summary

Benefits of technology

[0017] Herein we describe a system and method for the analysis of a fluid containing one or more analytes. The system may be used for either liquid or gaseous fluids. The system, in some embodiments, may generate patterns that are diagnostic for both the individual analytes and mixtures of the analytes. The system in some embodiments, is made of a plurality of chemically sensitive particles, formed in an ordered array, capable of simultaneously detecting many different kinds of analytes rapidly. An aspect of the system is that the array may be formed using a microfabrication process, thus allowing the system to be manufactured in an inexpensive manner.

[0021] In an embodiment, the optical detector may be integrated within the bottom of the supporting member, rather than using a separate detecting device. The optical detectors may be coupled to a microprocessor to allow evaluation of fluids without the use of separate detecting components. Additionally, a fluid delivery system may also be incorporated into the supporting member. Integration of detectors and a fluid delivery system into the supporting member may allow the formation of a compact and portable analyte sensing system.

Problems solved by technology

Arrays based on SAW crystals yield extremely sensitive responses to vapor, however, engineering challenges have prevented the creation of large SAW arrays having multiple sensor sites.

Additionally, limited chemical diversity and the lack of understanding of the molecular features of such systems makes their expansion into more complex analysis difficult.

When these sensors are exposed to volatile reagents, some of the volatile reagents adsorb into the polymer layers, leading to small changes in the electrical resistance of these layers.

Although the above described electronic nose provides an impressive capability for monitoring volatile reagents, the system possesses a number of undesirable characteristics that warrant the development of alternative sensor array systems.

Moreover, the electronic nose systems are expensive (e.g., the Aromascan system costs about $50,000 / unit) and bulky (≧1 ft3).

Furthermore, the functional elements for the currently available electronic nose are composed of conductive polymer systems which possess little chemical selectivity for many of the analytes which are of interest to the military and civilian communities.

However, the LATs lack the ability to be utilized for multiple, real time analyte detection schemes as the nature of the response intrinsically depends on a cooperative effect of the entire collection of microspheres.

Although quite promising for the detection of DNA fragments, these arrays are generally not designed for non-DNA molecules, and accordingly show very little sensitivity to smaller organic molecules.

Moreover, while a number of prototype DNA chips containing up to a few thousand different nucleic acid probes have been described, the existing technologies tend to be difficult to expand to a practical size.

As a result, DNA chips may be prohibitively expensive for practical uses.

Methods for manufacturing large numbers of reproducible sensors, however, has yet to be developed.

Moreover, no methods for acquisitions of data streams in a simultaneous manner are commercially available with this system.

Optical alignment issues may also be problematic for these systems.

Since the identification and isolation of the appropriate antibodies is time consuming, these techniques are limited to a single agent per testing module and there is no opportunity to evaluate the amount of agent present.

Most antibody methods are relatively insensitive and require the presence of 10 to 10 organisms.

The fastest methods are generally agglutination reactions, but these methods are less sensitive due to difficulties in visual interpretation of the reactions.

These detection schemes do not, however, appear to allow the simultaneous detection of multiple analytes on a single detector platform.

As with antibody-antigen reactions this approach has not been developed for the simultaneous detection of multiple analytes.

However, the current limitations of these testing methods are related to delays caused by specimen preparation, amplification, and detection.

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