METHOD OF DECOMPOSING CONSTITUENTS OF A TEST SAMPLE AND ESTIMATING FLUORESCENCE LIFETIME
The present invention relates to a method of decomposition of a test sample into constituents thereof. The method proceeds by optically imaging the test sample to obtain a corresponding unknown time-domain resolved signal and decomposes the unknown time-domain resolved signal by comparing the unknown time-domain resolved signal with time-domain resolved reference signals. Furthermore, the method allows the determination of the presence or absence of constituents. Relative quantities may also be determined if sample material properties are known or taken into account. Lifetime decay of the constituents may also be estimated by handling effect of light diffusion in the test sample as time decay.
1 . A method for decomposing a test sample into one or a plurality of constituents, the method comprising:
optically imaging the test sample to obtain a corresponding unknown time-domain resolved signal; and
decomposing the unknown time-domain resolved signal by comparing the unknown time-domain resolved signal with time-domain resolved reference signals.
2 . A method according to claim 1 , wherein the time-domain resolved reference signals are individually recorded for each of the constituents in a reference sample using the time-domain optical imaging apparatus;
3 . A method according to claim 1 , further comprising analyzing decomposed unknown time-domain resolved signal for determining constituents present in the test sample.
4 . A method according to claim 1 , further comprising performing a quantitative analysis for determining relative fractional contributions of the constituents in the test sample.
5 . A method according to claim 1 wherein decomposing the unknown time-resolved signal comprises a least squares fitting of the unknown time-resolved signal to the time-resolved reference signals.
6 . A method according to claim 1 wherein one of the constituents is a known fluorophore.
7 . A method according to claim 6 wherein another constituent is an autofluorescent medium.
8 . A method according to claim 6 wherein another consistuent is a second known fluorophore.
9 . A method according to claim 4 further comprising determining a relative quantity of at least one of the constituents.
10 . A method according to claim 9 , wherein determining the relative quantity of at least one of the constituents comprises locating the at least one constituent at substantially the same position in the test sample and in the corresponding reference sample.
11 . A method according to claim 9 , wherein determining the relative quantity of at least one of the constituent comprises individually determining the position of each of the at least one constituent in the corresponding reference sample and in the test sample, and the optical properties of the reference sample and test sample.
12 . A method according to claim 9 wherein the reference samples and the test sample are in vitro.
13 . A method according to claim 9 further comprising measuring a relative steady-state fluorescence intensity ratio of two of the constituents, and determining a fluorophore quantity fraction Ci for each of the constituents from an estimated fluorescence signal intensity fraction f i for each of the constituents on the reference sample.
14 . A method for estimating multiple fluorescence lifetime of one or a plurality of constituents of an in vivo test sample, the method comprising:
estimating lifetime of the one or the plural constituents using lifetime fitting procedures by handling effect of light diffusion in the test sample as a time delay; and
estimating contribution fractions of multiple decays through data fitting with known individual decay of constituents.