[Effect of the change in serum concentration on serum fluorescence spectrum].

The spectral analysis technology applied to some blood diseases diagnosis is convenient and speedy. The experimental result shows that the line type and peak value of the fluorescence spectra of serum excited by ultraviolet radiation with different wavelength remain the same, but the fluorescence peak value changes with the wavelength of the blazed light. The present paper studied how the serum fluorescence spectrum changes with the serum concentration, adopting Shimadzu Corporation (Japan) fluorescence photometer RF5301, and provided the experiment basis for disease diagnosis by hemanalysis. The experimental result shows that the fluorescence spectrum of serum is different under the excitation of different monochromatic light, the relative fluorescence intensity of serum increases with the serum concentration when excitated with 220, 230 and 310-420 nm monochromatic light, but the serum fluorescence intensity decreases while the serum concentration increases when the excitation monochromatic light is between 240 nm and 420 nm. The experimental research found that the serum concentration quenching and absorption effect is not obvious when the experimental sample is excitated by 220, 230 and 310 to 420 nm monochromatic light, and the fluorescence stimulation plays the main role. The serum concentration quenching and absorbing effect is obvious, so the fluorescence intensity becomes weaker and weaker with serum concentration increasing when the sample is excitated by 240 nm to 300 nm monochromatic light. This work provides the experimental basis for the choice of serum concentration in the study of serum fluorescence spectrum.

[Measurement and analysis of absorption spectrum of human blood].

The present paper puts forward a method of disease diagnosis by using the technology of spectrum analysis of human blood serum. The generation mechanism of absorption spectrum is explained and the absorption spectra of the normal blood serum and the sick blood serum are listed from the experiments of absorption spectrometry. Though the value of absorbency of the sick blood serum is almost equal to that of the normal blood serum in the most absorption spectra, there are some differences around 278 nm in the absorption spectrum. The absorbency of the blood serum with hyperglycemia is greater than that of the normal blood serum at 285 nm in the spectrum, and besides, there comes a peak shift of absorption with hyperglycemia. In the absorption spectrum of the blood serum with hypercholesterolemia, there is a clear absorption peak at 414 nm. However there is not any peak at that wavelength in the absorption spectrum of the normal blood serum. Through comparing the characters of the spectrum, we can judge if the blood sample is or not, and this blood analysis is a new method for the diagnosis of disease. Compared with other methods of blood measurements, the method of absorption spectrum analysis of blood serum presented in this paper, is more convenient for measurement, simpler for analysis, and easier to popularize.

[Experimental investigation of fluorescence spectra of serum excitated with different wavelength light].

In the present paper the fluorescence spectra of the blood serum excited with different wavelength were measured with the fluorescence photometer RF5301 (SHIMADZU) made in Japan. The relationship between the fluorescence spectra of the serum and the wavelength of the excitation light was studied during the experiment. The experimental results show that the linetype and peak wavelength of the fluorescence spectra of serum excited by ultraviolet radiation with different wavelength are almost the same, and they do not depend on the excitation wavelength. But the fluorescence peak value changes with the excitation wavelength. There are two high intensity emission intervals in the fluorescence spectra. One of these is from about 300 nm to 410 nm, and the other is below 310 nmr The fluorescence spectra are mostly centralized in the first interval, and the wavelengths of fluorescence peaks were found around two locations: one is near 330 nm and the other is near 370 nm. At this time the strife phenomena occur. When the excitation wavelength is about 250 nm or higher, the fluorescence peak only occurs at 330 nm, and the optimal excitation wavelength is 300 nm. While the wavelength is greater than 320 nm, the fluorescence intensity of the first interval begins to fall, while that of the other augments. And at this time the peak of wavelength of fluorescence is 452 nm. This study provides the experimental foundations for advanced study and applications of the characteristics of fluorescence spectrum of blood serum, and also offers the references to the wavelength selection of excitation light in the application of the photo-induced fluorescence spectra diagnostic technology.

[Effect of glucose concentration in human serum on fluorescence intensity].

Blood plays an important role in the clinical diagnosis and treatment; many diseases may lead to changes in the blood composition or characteristic properties. Therefore, the analysis of blood sugar will be of great importance. The present paper studies the difference of fluorescence intensity stimulated by light wave between normal blood serum and hyperglycemia blood serum. The result shows that the average grey level of fluorescence image at 365 nm increases obviously with the changes in the concentration of glucose; however, the average grey changes little at 353, 369 and 405 nm. This shows that the main effect of serum glucose on the fluorescence intensity peak appears at 365 nm. Because the fluorescence intensity has something to do with the concentration of the fluorescence material, the blood glucose concentration influences directly the fluorescence intensity at 365 nm. Therefore, it is possible to judge blood sugar content, and to make sure whether the content exceeds the normal value or not by comparing the fluorescence intensity of the blood serum measured at 365 nm. This technique of optical measurement provides an experimental basis for the diagnosis of blood diseases.

[Analysis and application of excitation fluorescence intensity of blood].

The analysis technique of fluorescence is adopted to study the intensity of excitation fluorescence of blood in the present paper. The theoretical analysis and differences of normal and abnormal blood (hyperglycemia, hyperlipemia) are presented. The theoretical analysis was proved by experiment results. It was discovered that blood sugar consistency has an effect on blood fluorescence. In other words, with the same excitation wavelength and with blood sugar consistency increasing, the fluorescence intensity increases gradually. It is obvious that blood sugar is also a kind of fluorescein, and its consistency has an effect on fluorescence intensity, which is identical with the theoretical analysis, indicating that the experiment is successful, and it is possible to distinguish blood sugar consistency by comparing the fluorescence intensity in blood. It was also discovered that the higher the cholesterin content, the more intense the fluorescence. When excitation wavelength is especially 435 nm, the phenomenon is very obvious. The study paves a new way for the blood quick check and diagnosis of diseases.