Optical sensor for in situ measurement of analytes

Abstract

An implantable sensor for use in the detection of quantitative measurement of an analyte in subcutaneous fluid, the sensor being biodegradable or hydrolysable in vivo. The sensor incorporates an assay for the analyte, the readout of which is a detectable or measurable optical signal which can, when the sensor is in operation in a subcutaneous location, be interrogated transcutaneously by external optical means.

What is claimed is:  
     
       1. A sensor for the detection or quantitative measurement of an analyte in subcutaneous fluid, said sensor being characterised in that it can function in a subcutaneous location with no physical connection to the external environment, said sensor incorporating an assay for said analyte the readout of which is a detectable or measurable optical signal, which optical signal can, when the sensor is in operation in a subcutaneous location, be interrogated transcutaneously by external optical means and said sensor being biodegradable or hydrolysable in vivo. 
     
     
       2. A sensor as claimed in  claim 1  wherein said assay is a binding assay, the readout of which is a detectable or measurable optical signal. 
     
     
       3. A sensor as claimed in  claim 2  wherein said binding assay is a competitive binding assay the components of which include an analyte binding agent and an analyte analog. 
     
     
       4. A sensor as claimed in  claim 3  wherein said analyte analog is labelled with a first chromophore and said analyte binding agent is labelled with a second chromophore, the emission spectrum of said first chromophore overlapping with the absorption spectrum of said second chromophore. 
     
     
       5. A sensor as claimed in  claim 3  wherein the binding agent is an antibody, an Fab fragment, a lectin, a hormone receptor, a drug receptor, an aptamer or a molecularly-imprinted polymer. 
     
     
       6. A sensor as claimed in  claim 2 , wherein said detectable or measurable optical signal is generated by fluorescence energy transfer, fluorescence polarisation, fluorescence quenching, phosphorescence, luminescence enhancement, luminescence quenching, diffraction or plasmon resonance. 
     
     
       7. A sensor as claimed in  claim 1 , which comprises an injectable or implantable matrix material, the components of said assay being suspended in said matrix material. 
     
     
       8. A sensor as claimed in  claim 1 , which comprises a plurality of microparticles. 
     
     
       9. A sensor as claimed in  claim 8  wherein said microparticles are solid microparticles and the components of said assay are uniformly dispersed in said solid microparticles. 
     
     
       10. A sensor as claimed in  claim 8  wherein said microparticles are hollow microparticles and the components of said assay are encapsulated inside said hollow microparticles. 
     
     
       11. A sensor as claimed in  claim 1 , which comprises a plurality of liposomes, the components of said assay being encapsulated inside said liposomes. 
     
     
       12. A sensor as claimed in  claim 1 , which comprises a hollow chamber having a wall portion enclosing a central space containing the components of said assay means. 
     
     
       13. A sensor as claimed in  claim 1 , which comprises a plurality of empty erythrocytes which have been loaded with the components of said assay. 
     
     
       14. An analytical system for the detection or quantitative measurement of an analyte in subcutaneous fluid, which analytical system comprises a sensor as claimed in  claim 1 , together with optical means suitable for the trans-cutaneous interrogation of said sensor. 
     
     
       15. A method of detecting or quantitatively measuring an analyte in the subcutaneous fluid of a mammal, which method comprises the steps of: 
       (a) injecting or implanting a sensor for the detection or quantitative measurement of an analyte in subcutaneous fluid as claimed in  claim 1  into a subcutaneous location on said mammal;  
       (b) allowing the assay of said sensor to reach thermodynamic equilibrium;  
       (c) interrogating the readout of said assay using optical means; and  
       (d) relating the measurement obtained in (c) to the concentration of analyte.