AIM To recognize the characteristic findings of micrQliver cancer (MLC) and to evaluate the effect of CT arterial portography (CTAP) and CT hepatic arteriography (CTHA) in diagnosis of MLC. METHODS Between April 1996 ...AIM To recognize the characteristic findings of micrQliver cancer (MLC) and to evaluate the effect of CT arterial portography (CTAP) and CT hepatic arteriography (CTHA) in diagnosis of MLC. METHODS Between April 1996 to December 1998, CTAP and CTHA were performed in 12patients with MLC, which were not detect ed byconventional CT examinations. After CTHA, 3 mL-- 5 mL mixture of lipiodol, doxorubic in andmitomycin C were injected into hepatic arterythrough the catheter, and then followed up by CTthree or four weeks later (Lipiodol CT LP-CT).RESULTS A total of 22 micro--tumors (0 .2 cm 0.6 cm in diameter ) were detected in 12patients, which manifested as small perfusiondefects in CTAP and small round enhancement inCTHA. The rate of detectability of CTAP andCTHA was 68.2% (15/ 22) and 77.3% (17/ 22)respectively, and the rate of the simultaneoususe of both procedures reached 86. 4% (19/ 22 ).All micro--tumors were demonstrated as punctatelipiodol deposit fool in LP--CT. After LP--CT, theelevated serum level of Q-fetoprotein (AFP)dropped to the normal level in all patients.CONCLUSION The CTAP and CTHA are the mostsensitive imaging methods for detecting microIiver cancer. Confirmed by the change of theelevated serum AFP level and lipiodol depositfool in LP-CT, small perfusion defects in CTAPand punctate enhancement in CTHA may suggestmicro--liver cancer.展开更多
Epithelial ovarian cancer(EOC) is the leading cause of death among all gynecological malignancies. Despite the technological and medical advances over the past four decades, such as the development of several biologic...Epithelial ovarian cancer(EOC) is the leading cause of death among all gynecological malignancies. Despite the technological and medical advances over the past four decades, such as the development of several biological markers(mRNA and proteins biomarkers), the mortality rate of ovarian cancer remains a challenge because of its late diagnosis, which is specifically attributed to low specificities and sensitivities. Under this compulsive scenario, recent advances in expression biology have shifted in identifying and developing specific and sensitive biomarkers, such as micro RNAs(miRNAs) for cancer diagnosis and prognosis. MiRNAs are a novel class of small non-coding RNAs that deregulate gene expression at the posttranscriptional level, either by translational repression or by mRNA degradation. These mechanisms may be involved in a complex cascade of cellular events associated with the pathophysiology of many types of cancer. MiRNAs are easily detectable in tissue and blood samples of cancer patients. Therefore, miRNAs hold good promise as potential biomarkers in ovarian cancer. In this review, we attempted to provide a comprehensive profile of key miRNAs involved in ovarian carcinoma to establish mi RNAs as more reliable non-invasive clinical biomarkers for early detection of ovarian cancer compared with protein and DNA biomarkers.展开更多
This study proposes a novel transformer oil micro-water detection method based on the ultrasonic pulse-echo technique,optimised by a sparrow search algorithm(SSA)to enhance the prediction performance of a random fores...This study proposes a novel transformer oil micro-water detection method based on the ultrasonic pulse-echo technique,optimised by a sparrow search algorithm(SSA)to enhance the prediction performance of a random forest(RF)model.Initially,finite element simulations were conducted to select optimal ultrasonic frequencies of 2 and 2.5 MHz.An accelerated thermal ageing experiment was performed using#25 Karamay oil samples,and ultrasonic pulse-echo signals were collected via a custom-built detection platform.Variational mode decomposition was employed to extract effective echoes from the raw pulse-echo signals.Temporal and frequency domain analyses yielded 162 dimensional features,which were subsequently filtered to 88 key parameters using the maximum information coefficient method.A transformer oil micro-water detection model was then developed by integrating the SSA with RF and trained using K-fold cross-validation.The model achieved an impressive average prediction accuracy of 97.34%over 10 cross-validation runs.The testing set demonstrated a prediction accuracy of 96.40%,a remarkable improvement of 16.53%compared to the unoptimised RF model.The findings provide a solid foundation for the rapid detection of micro-water content in transformer oil using the ultrasonic pulse-echo method.展开更多
Pringe array is proposed as the cooperated target in the precise torsion angle detection. The target fringe array image is generated according to the structure of the optical system, and the torsion angle detection al...Pringe array is proposed as the cooperated target in the precise torsion angle detection. The target fringe array image is generated according to the structure of the optical system, and the torsion angle detection algorithm is analyzed in response to the gray distribution of the image. The factors affecting the detection precision of the fringe torsion angle are analyzed theoretically and numerically. It indicates that the detection precision of the torsion angle is 1 angular second or even less, carefully selecting the detector array. Significantly, experiments are performed to demonstrate the precision and the results match well with the simulations.展开更多
In this work,we have developed a sensitive,simple,and enzyme-free assay for detection of micro RNAs(mi RNAs)by means of a DNA molecular motor consisting of two stem-loop DNAs with identical stems and complementary loo...In this work,we have developed a sensitive,simple,and enzyme-free assay for detection of micro RNAs(mi RNAs)by means of a DNA molecular motor consisting of two stem-loop DNAs with identical stems and complementary loop domains.In the presence of mi RNA target,it can hybridize with one of the stem-loop DNA to open the stem and to produce a mi RNA/DNA hybrid and a single strand(ss)DNA,the ss DNA will in turn hybridize with another stem-loop DNA and finally form a double strand(ds)DNA to release the mi RNA.One of the stem-loop DNA is double-labeled by a fluorophore/quencher pair with efficiently quenched fluorescence.The formation of ds DNA can produced specific fluorescence signal for mi RNA detection.The released mi RNA will continuously initiate the next hybridization of the two stem-loop DNAs to form a cycle-running DNA molecular motor,which results in great fluorescence amplification.With the efficient signal amplification,as low as 1 pmol/L mi RNA target can be detected and a wide dynamic range from 1 pmol/L to 2 nmol/L is also obtained.Moreover,by designing different stem-loop DNAs specific to different mi RNA targets and labeling them with different fluorophores,multiplexed mi RNAs can be simultaneously detected in one-tube reaction with the synchronous fluorescence spectrum(SFS)technique.展开更多
Facing the body＇s EEG（electroencephalograph, 0.5–100 Hz, 5–100 μV） and ECG＇s（electrocardiogram,〈 100 Hz, 0.01–5 mV） micro signal detection requirement, this paper develops a pervasive application micro sign...Facing the body＇s EEG（electroencephalograph, 0.5–100 Hz, 5–100 μV） and ECG＇s（electrocardiogram,〈 100 Hz, 0.01–5 mV） micro signal detection requirement, this paper develops a pervasive application micro signal detection ASIC chip with the chopping modulation/demodulation method. The chopper-stabilization circuit with the RRL（ripple reduction loop） circuit is to suppress the ripple voltage, which locates at the single-stage amplifier＇s outputting terminal. The single-stage chopping core＇s noise has been suppressed too, and it is beneficial for suppressing noises of post-circuit. The chopping core circuit uses the PFB（positive feedback loop） to increase the inputting resistance, and the NFB（negative feedback loop） to stabilize the 40 dB intermediate frequency gain. The cascaded switch-capacitor sample/hold circuit has been used for deleting spike noises caused by non-ideal MOS switches, and the VGA/BPF（voltage gain amplifier/band pass filter） circuit is used to tune the chopper system＇s gain/bandwidth digitally. Assisted with the designed novel dry-electrode, the real test result of the chopping amplifying circuit gives some critical parameters： 8.1 μW/channel, 0.8 μVrms（@band-widthD100 Hz）, 4216–11220 times digitally tuning gain range, etc. The data capture system uses the NI CO＇s data capturing DAQmx interface,and the captured micro EEG/ECG＇s waves are real-time displayed with the PC-Labview. The proposed chopper system is a unified EEG/ECG signal＇s detection instrument and has a critical real application value.展开更多
Array based detection techniques with fluorescence signal reading is a powerful tool for multiple targets analysis. However,when applied fluorescence array for micro RNA detection, time-consuming multi-steps surface s...Array based detection techniques with fluorescence signal reading is a powerful tool for multiple targets analysis. However,when applied fluorescence array for micro RNA detection, time-consuming multi-steps surface signal amplification is usually required due to the low abundance of micro RNA in total RNA expressions, which impairs detection efficiency and limits its application in point of care test(POCT) manner. Herein, DNA cascade reactors(DCRs) functionalized photonic crystal(PC)array was fabricated for express and sensitive detections of mi RNA-21 and mi RNA-155. DCRs were assembled by interval conjugation of self-quenched hairpin DNA probes to single strand DNA nanowire synthesized by rolling circle amplification,which generated cascade DNA hybridization reactions in response to target mi RNAwith instant fluorescence recovery signal. PC array patterns with multi-structure colors further amplified fluorescence with their respective photonic bandgaps(PBGs)matching with the emission peaks of fluorescence molecules labelled on DCRs. The as-prepared DCRs functionalized PC array demonstrated express and sensitive simultaneous detections of mi RNA-21 and mi RNA-155 with hundreds f M detection limits only in 15 min, and was successfully applied in fast quantifications of low abundance mi RNAs from cell lysates and spiked mi RNAs from human serum, which would hold great potential for disease diagnosis and therapeutic effect monitoring with a POCT manner.展开更多
基金Supported by“9.5”National Major Project of National Cammittee of Sciences and Technology,No.96-907-03-02.
文摘AIM To recognize the characteristic findings of micrQliver cancer (MLC) and to evaluate the effect of CT arterial portography (CTAP) and CT hepatic arteriography (CTHA) in diagnosis of MLC. METHODS Between April 1996 to December 1998, CTAP and CTHA were performed in 12patients with MLC, which were not detect ed byconventional CT examinations. After CTHA, 3 mL-- 5 mL mixture of lipiodol, doxorubic in andmitomycin C were injected into hepatic arterythrough the catheter, and then followed up by CTthree or four weeks later (Lipiodol CT LP-CT).RESULTS A total of 22 micro--tumors (0 .2 cm 0.6 cm in diameter ) were detected in 12patients, which manifested as small perfusiondefects in CTAP and small round enhancement inCTHA. The rate of detectability of CTAP andCTHA was 68.2% (15/ 22) and 77.3% (17/ 22)respectively, and the rate of the simultaneoususe of both procedures reached 86. 4% (19/ 22 ).All micro--tumors were demonstrated as punctatelipiodol deposit fool in LP--CT. After LP--CT, theelevated serum level of Q-fetoprotein (AFP)dropped to the normal level in all patients.CONCLUSION The CTAP and CTHA are the mostsensitive imaging methods for detecting microIiver cancer. Confirmed by the change of theelevated serum AFP level and lipiodol depositfool in LP-CT, small perfusion defects in CTAPand punctate enhancement in CTHA may suggestmicro--liver cancer.
基金the ICMR New Delhi for financial support (Grant No. 3/2/2/136/2012/NCD-Ⅲ)
文摘Epithelial ovarian cancer(EOC) is the leading cause of death among all gynecological malignancies. Despite the technological and medical advances over the past four decades, such as the development of several biological markers(mRNA and proteins biomarkers), the mortality rate of ovarian cancer remains a challenge because of its late diagnosis, which is specifically attributed to low specificities and sensitivities. Under this compulsive scenario, recent advances in expression biology have shifted in identifying and developing specific and sensitive biomarkers, such as micro RNAs(miRNAs) for cancer diagnosis and prognosis. MiRNAs are a novel class of small non-coding RNAs that deregulate gene expression at the posttranscriptional level, either by translational repression or by mRNA degradation. These mechanisms may be involved in a complex cascade of cellular events associated with the pathophysiology of many types of cancer. MiRNAs are easily detectable in tissue and blood samples of cancer patients. Therefore, miRNAs hold good promise as potential biomarkers in ovarian cancer. In this review, we attempted to provide a comprehensive profile of key miRNAs involved in ovarian carcinoma to establish mi RNAs as more reliable non-invasive clinical biomarkers for early detection of ovarian cancer compared with protein and DNA biomarkers.
基金National Natural Science Foundation of China,Grant/Award Number:52077177。
文摘This study proposes a novel transformer oil micro-water detection method based on the ultrasonic pulse-echo technique,optimised by a sparrow search algorithm(SSA)to enhance the prediction performance of a random forest(RF)model.Initially,finite element simulations were conducted to select optimal ultrasonic frequencies of 2 and 2.5 MHz.An accelerated thermal ageing experiment was performed using#25 Karamay oil samples,and ultrasonic pulse-echo signals were collected via a custom-built detection platform.Variational mode decomposition was employed to extract effective echoes from the raw pulse-echo signals.Temporal and frequency domain analyses yielded 162 dimensional features,which were subsequently filtered to 88 key parameters using the maximum information coefficient method.A transformer oil micro-water detection model was then developed by integrating the SSA with RF and trained using K-fold cross-validation.The model achieved an impressive average prediction accuracy of 97.34%over 10 cross-validation runs.The testing set demonstrated a prediction accuracy of 96.40%,a remarkable improvement of 16.53%compared to the unoptimised RF model.The findings provide a solid foundation for the rapid detection of micro-water content in transformer oil using the ultrasonic pulse-echo method.
基金the National Natural Science Foundation of China under Grant No.61275002.
文摘Pringe array is proposed as the cooperated target in the precise torsion angle detection. The target fringe array image is generated according to the structure of the optical system, and the torsion angle detection algorithm is analyzed in response to the gray distribution of the image. The factors affecting the detection precision of the fringe torsion angle are analyzed theoretically and numerically. It indicates that the detection precision of the torsion angle is 1 angular second or even less, carefully selecting the detector array. Significantly, experiments are performed to demonstrate the precision and the results match well with the simulations.
基金the National Natural Science Foundation of China(21335005,21472120)the Fundamental Research Funds for the Central Universities(GK201501003,GK201303003)the Excellent Doctor Innovation Project of Shaanxi Normal University
文摘In this work,we have developed a sensitive,simple,and enzyme-free assay for detection of micro RNAs(mi RNAs)by means of a DNA molecular motor consisting of two stem-loop DNAs with identical stems and complementary loop domains.In the presence of mi RNA target,it can hybridize with one of the stem-loop DNA to open the stem and to produce a mi RNA/DNA hybrid and a single strand(ss)DNA,the ss DNA will in turn hybridize with another stem-loop DNA and finally form a double strand(ds)DNA to release the mi RNA.One of the stem-loop DNA is double-labeled by a fluorophore/quencher pair with efficiently quenched fluorescence.The formation of ds DNA can produced specific fluorescence signal for mi RNA detection.The released mi RNA will continuously initiate the next hybridization of the two stem-loop DNAs to form a cycle-running DNA molecular motor,which results in great fluorescence amplification.With the efficient signal amplification,as low as 1 pmol/L mi RNA target can be detected and a wide dynamic range from 1 pmol/L to 2 nmol/L is also obtained.Moreover,by designing different stem-loop DNAs specific to different mi RNA targets and labeling them with different fluorophores,multiplexed mi RNAs can be simultaneously detected in one-tube reaction with the synchronous fluorescence spectrum(SFS)technique.
基金Project supported by the National Natural Science Foundation of China(Nos.61527815,31500800,61501426,61471342)the National Key Basic Research Plan(No.2014CB744600)+1 种基金the Beijing Science and Technology Plan(No.Z141100000214002)the Chinese Academy of Sciences’Key Project(No.KJZD-EW-L11-2)
文摘Facing the body＇s EEG（electroencephalograph, 0.5–100 Hz, 5–100 μV） and ECG＇s（electrocardiogram,〈 100 Hz, 0.01–5 mV） micro signal detection requirement, this paper develops a pervasive application micro signal detection ASIC chip with the chopping modulation/demodulation method. The chopper-stabilization circuit with the RRL（ripple reduction loop） circuit is to suppress the ripple voltage, which locates at the single-stage amplifier＇s outputting terminal. The single-stage chopping core＇s noise has been suppressed too, and it is beneficial for suppressing noises of post-circuit. The chopping core circuit uses the PFB（positive feedback loop） to increase the inputting resistance, and the NFB（negative feedback loop） to stabilize the 40 dB intermediate frequency gain. The cascaded switch-capacitor sample/hold circuit has been used for deleting spike noises caused by non-ideal MOS switches, and the VGA/BPF（voltage gain amplifier/band pass filter） circuit is used to tune the chopper system＇s gain/bandwidth digitally. Assisted with the designed novel dry-electrode, the real test result of the chopping amplifying circuit gives some critical parameters： 8.1 μW/channel, 0.8 μVrms（@band-widthD100 Hz）, 4216–11220 times digitally tuning gain range, etc. The data capture system uses the NI CO＇s data capturing DAQmx interface,and the captured micro EEG/ECG＇s waves are real-time displayed with the PC-Labview. The proposed chopper system is a unified EEG/ECG signal＇s detection instrument and has a critical real application value.
基金supported by the National Natural Science Foundation of China(21635005,21605083,21974064)the National Research Foundation for Thousand Youth Talents Plan of China,Specially-appointed Professor Foundation of Jiangsu Province,Program for innovative Talents and Entrepreneurs of Jiangsu Province。
文摘Array based detection techniques with fluorescence signal reading is a powerful tool for multiple targets analysis. However,when applied fluorescence array for micro RNA detection, time-consuming multi-steps surface signal amplification is usually required due to the low abundance of micro RNA in total RNA expressions, which impairs detection efficiency and limits its application in point of care test(POCT) manner. Herein, DNA cascade reactors(DCRs) functionalized photonic crystal(PC)array was fabricated for express and sensitive detections of mi RNA-21 and mi RNA-155. DCRs were assembled by interval conjugation of self-quenched hairpin DNA probes to single strand DNA nanowire synthesized by rolling circle amplification,which generated cascade DNA hybridization reactions in response to target mi RNAwith instant fluorescence recovery signal. PC array patterns with multi-structure colors further amplified fluorescence with their respective photonic bandgaps(PBGs)matching with the emission peaks of fluorescence molecules labelled on DCRs. The as-prepared DCRs functionalized PC array demonstrated express and sensitive simultaneous detections of mi RNA-21 and mi RNA-155 with hundreds f M detection limits only in 15 min, and was successfully applied in fast quantifications of low abundance mi RNAs from cell lysates and spiked mi RNAs from human serum, which would hold great potential for disease diagnosis and therapeutic effect monitoring with a POCT manner.
