ABSTRACT
PURPOSE: To investigate the CT features of drug-resistant pulmonary tuberculosis (DR-PTB) and the diagnostic value of CT in DR-PTB diagnosis to provide imaging evidence for the timely detection of drug-resistant Mycobacterium tuberculosis. MATERIALS AND METHODS: A total of 1546 cases of pulmonary tuberculosis (PTB) with complete clinical data, chest CT images and defined drug sensitivity testing results were consecutively enrolled; 516 cases of DR-PTB were included in the drug-resistant group, and 1030 cases of drug-sensitive pulmonary tuberculosis (DS-PTB) were included in the drug-sensitivity group. Comparative analyses of clinical symptoms and imaging findings were conducted. Univariate and logistic regression analyses were performed, a regression equation model was developed, and the receiver operating characteristic (ROC) curve was constructed. RESULTS: In the univariate analysis, some features, including whole-lung involvement, multiple cavities, thick-walled cavities, collapsed lung, disseminated lesions along the bronchi, bronchiectasis, emphysema, atelectasis, calcification, proliferative lesions, encapsulated effusion, etc., were observed more frequently in the DR-PTB group than in the DS-PTB group, and the differences were statistically significant (p<0.05). Exudative lesions and pneumoconiosis were observed more frequently in the drug-sensitivity group than in the drug-resistant group (p<0.05). Logistic regression analysis indicated that whole-lung involvement, multiple cavities, thick-walled cavities, disseminated lesions along the bronchi, bronchiectasis, and emphysema were independent risk factors for DR-PTB, and exudative diseases were protective factors. The total prediction accuracy of the regression model was 80.6%, and the area under the ROC curve (AUC) was 82.6%. CONCLUSION: Chest CT manifestations of DR-PTB had certain characteristics that significantly indicated the possibility of drug resistance in tuberculosis patients, specifically when multifarious imaging findings, including multiple cavities, thick-walled cavities, disseminated lesions along the bronchi, whole-lung involvement, etc., coexisted simultaneously. These results may provide imaging evidence for timely drug resistance detection in suspected drug-resistant cases and contribute to the early diagnosis of DR-PTB.
ABSTRACT
BACKGROUND: To explore the correlation of flash dual source computed tomography perfusion imaging (CTPI) and regional lymph node metastasis of non-small cell lung cancer (NSCLC), and to evaluate the value of CT perfusion parameters in predicting regional lymph node metastasis of NSCLC. METHODS: 120 consecutive patients with NSCLC confirmed by postoperative histopathology were underwent flash dual source CT perfusion imaging in pre-operation. The CT perfusion parameters of NSCLC, such as blood flow (BF), blood volume (BV), mean transit time (MTT) and permeability (PMB) were obtained by the image post-processing. Then microvessel density (MVD), luminal vascular number (LVN), luminal vascular area (LVA) and luminal vascular perimeter (LVP) of NSCLC were counted by immunohistochemistry. These cases were divided into group A (patients with lymph node metastasis, 58 cases) and group B (patients without lymph node metastasis, 62 cases) according to their pathological results. The CT perfusion parameters and the microvessel parameters were contrastively analysed between the two groups. Receiver operating characteristic (ROC) curve was used to assess the diagnostic efficiency of CT perfusion parameters in predicting regional lymph node metastasis of NSCLC in pre-operation. RESULTS: Group A presented significantly lower LVA, BF and higher MTT, PMB than Group B (P < 0.05), while BV, LVN, LVP and MVD were no significant difference (P > 0.05). Correlation analysis showed that BF was correlated with LVA and LVP (P < 0.05), while BV, MTT and PMB were not correlated with LVN, LVA and LVP (P > 0.05). All the perfusion parameters were not correlated with MVD. According to the ROC curve analysis, when BF < 85.16 ml/100 ml/min as a cutoff point to predict regional lymph node metastasis of NSCLC, the sensitivity, specificity, accuracy, positive predictive value and negative predictive value were 60.8, 81.7, 71.5, 75.6 and 69.5% respectively. CONCLUSION: Flash dual source CT perfusion imaging can non-invasively indicate the luminal vascular structure of tumor and BF can be used as one of the important indexes in predicting regional lymph node metastasis of NSCLC in pre-operation.
Subject(s)
Carcinoma, Non-Small-Cell Lung/pathology , Lung Neoplasms/pathology , Lymphatic Metastasis/diagnosis , Neovascularization, Pathologic/diagnostic imaging , Perfusion Imaging , Tomography, X-Ray Computed , Adult , Aged , Carcinoma, Non-Small-Cell Lung/blood supply , Carcinoma, Non-Small-Cell Lung/diagnosis , Carcinoma, Non-Small-Cell Lung/surgery , Correlation of Data , Feasibility Studies , Female , Humans , Lung/blood supply , Lung/diagnostic imaging , Lung/pathology , Lung Neoplasms/blood supply , Lung Neoplasms/diagnosis , Lung Neoplasms/surgery , Lymph Nodes/pathology , Lymph Nodes/surgery , Lymphatic Metastasis/pathology , Male , Microvessels/diagnostic imaging , Middle Aged , Neoplasm Staging , Neovascularization, Pathologic/pathology , Neovascularization, Pathologic/surgery , Predictive Value of Tests , Preoperative PeriodABSTRACT
OBJECTIVE: To explore the correlation between dual source computed tomography perfusion imaging (CTPI) and microvascular parameters, and evaluate the value of CTPI in the differential diagnosis of solitary pulmonary nodule (SPN). METHODS: 65 consecutive patients with SPN who successfully underwent pre-operative CT perfusion imaging with dual source CT and received a final diagnosis by postoperative pathology. The cases were divided into malignant, benign and inflammatory groups according to the pathological results. CT perfusion parameters, such as blood flow (BF), blood volume (BV), mean transit time (MTT) and permeability surface (PMB) were obtained by performing CTPI of SPNs. The postoperative specimens of SPNs were immunohistochemically stained for CD34 and SMA to detect microvessel density (MVD) and luminal vascular parameters, such as luminal vascular number (LVN), luminal vascular area (LVA) and luminal vascular perimeter (LVP). The receiver operating characteristic (ROC) curve was used to assess the diagnostic efficiency of CT perfusion parameter in diagnosing malignant SPNs. RESULTS: In these 65 cases, malignant, benign and inflammatory SPNs were respectively 39, 14 and 12 cases. Significant difference was observed in LVN/MVD, LVA and LVP among the three groups (P < 0.05). The correlation between CT perfusion parameters (BF, BV and PMB) and the luminal vascular parameters was stronger than that with MVD (P < 0.05). PMB has the strongest correlation with LVN/MVD. Using BF≥60ml/100ml/min, BV≥6.34ml/100ml and PMB≥13.35ml/100 ml/min for the diagnosis, the area under the curve (AUC) of the ROC curve was 0.760, the sensitivity was 82% and the specificity was 61%. CONCLUSIONS: The main indicators reflecting blood perfusion of SPN are the degree of lumen or maturity of microvessels (LVN, LVA and LVP), not just the number of microvessels (e.g. MVD). CT perfusion imaging can be used as an important method to non-invasively evaluate tumour angiogenesis and help to distinguish malignant SPNs from benign and inflammatory SPNs.
Subject(s)
Lung Neoplasms/diagnosis , Lung/blood supply , Microvessels/pathology , Perfusion Imaging/methods , Solitary Pulmonary Nodule/diagnosis , Adult , Aged , Antigens, CD34/immunology , Antigens, CD34/metabolism , Blood Volume , Diagnosis, Differential , Female , Humans , Immunohistochemistry , Lung/pathology , Lung Neoplasms/blood supply , Lung Neoplasms/pathology , Male , Middle Aged , Neovascularization, Pathologic , Predictive Value of Tests , Prognosis , Regional Blood Flow , Solitary Pulmonary Nodule/blood supply , Solitary Pulmonary Nodule/pathology , Tomography, X-Ray Computed , Young AdultABSTRACT
Scaffold-based techniques are a vital assistance tool to support main structure and enhance the resolution of target structure. In this study, a custom-made micro-extrusion bioprinting system was built and utilized to fabricate different scaffold structures such as log-pile scaffold and two-ring scaffold. This approach showed tremendous potential because of its ability to produce microscale channels with almost any shape. We were able to fabricate these scaffolds by using a custom-made 3D bioprinter to print hydrogel solution, mostly composed of Pluronic F-127, then wash away hydrogen by phosphate buffer saline (PBS) after crosslinking of main structure. We were able to achieve the desired scaffold structure by feeding G-codes data into user interface (Pronterface) and then translating that model into a program that utilizes a customized programming language, which instructs the microfabrication printer nozzles to dispense the hydrogel at specific locations. This fundamental study will be used to print increasingly viable and complex tissue shapes with living cells.
ABSTRACT
An ionic liquid dispersive liquid-liquid microextraction high-performance liquid chromatography (IL-DLLME-HPLC) method for effective enrichment and determination of nitrite ion in water and biological samples was developed. The method was based on the reaction of nitrite ion with p-nitroaniline in the presence of diphenylamine in acid media and IL-DLLME of azo product. The optimization of reaction and extraction conditions, such as kind and concentration of acid, reaction time, volume of reaction solvent, temperature, kind of extraction and dispersive solvent, volume of extraction and dispersive solvent, addition of salt, extraction and centrifugal time were studied. Under the optimal conditions, 1-octyl-3-methylimidazolium bis[(trifluoromethyl)sulfonyl]imide IL-DLLME procedure provided high enrichment factor of 430 and good extraction recovery of 91.7% for nitrite ion. The linearity was observed in the range of 0.4-500.0 µg L⻹ with good correlation coefficient (r²=0.9996). The relative standard deviations (RSDs) for five replicate measurements varied between 1.5% and 4.8%. The limit of detection of the method (S/N=3) was 0.05 µg L⻹. The interference effect of some anions and cations was also tested. The developed method allowed achieving an excellent enrichment factor, yielding a lower LOD in comparison with other methods. Moreover, the proposed method was able to analyze nitrite ion in water and biological samples with satisfactory recovery ranged from 96.5% to 107.3%.
Subject(s)
Chemical Fractionation/methods , Chromatography, High Pressure Liquid/methods , Nitrites/analysis , Saliva/chemistry , Water/chemistry , Adult , Female , Humans , Ionic Liquids/chemistry , Methanol , Nitrites/isolation & purification , Reproducibility of Results , Rivers/chemistry , Sensitivity and Specificity , Water Pollutants, Chemical/analysis , Water SupplyABSTRACT
The paper described a new ionic liquid, 1,3-dibutylimidazolium hexafluorophosphate, as extraction solvent for extraction and preconcentration of organophosphorus pesticides (fenitrothion, parathion, fenthion and phoxim) from water and fruit samples by dispersive liquid-liquid microextraction combined with high-performance liquid chromatography. The effects of experimental parameters, such as extraction solvent volume, disperser solvent and its volume, extraction and centrifugal time, sample pH, extraction temperature and salt addition, on the extraction efficiency were investigated. An extraction recovery of over 75% and enrichment factor of over 300-fold were obtained under the optimum conditions. The linearity relationship was also observed in the range of 5-1000 microgL(-1) with the correlation coefficients (r(2)) ranging from 0.9988 to 0.9999. Limits of detection were 0.01-0.05 microgL(-1) for four analytes. The relative standard deviations at spiking three different concentration levels of 20, 100 and 500 microgL(-1) varied from 1.3-2.7, 1.4-1.9 and 1.1-1.7% (n=7), respectively. Three real samples including tap water, Yellow River water and pear spiked at three concentration levels were analyzed and yielded recoveries ranging from 92.7-109.1, 95.0-108.2 and 91.2-108.1%, respectively.
Subject(s)
Chemical Fractionation/methods , Chromatography, High Pressure Liquid/methods , Fruit/chemistry , Organophosphorus Compounds/analysis , Pesticides/analysis , Water Pollutants, Chemical/analysis , Chemical Fractionation/instrumentation , Imidazoles/chemistry , Ionic Liquids/chemistry , Limit of DetectionABSTRACT
Using 1-octyl-3-methylimidazolium hexafluorophosphate ([C(8)MIM][PF(6)]) ionic liquid as extraction solvent, organophosphorus pesticides (OPPs) (parathion, phoxim, phorate and chlorpyifos) in water were determined by dispersive liquid-liquid microextraction (DLLME) combined with high-performance liquid chromatography (HPLC). The extraction procedure was induced by the formation of cloudy solution, which was composed of fine drops of [C(8)MIM][PF(6)] dispersed entirely into sample solution with the help of disperser solvent (methanol). Parameters including extraction solvent and its volume, disperser solvent and its volume, extraction time, centrifugal time, salt addition, extraction temperature and sample pH were investigated and optimized. Under the optimized conditions, up to 200-fold enrichment factor of analytes and acceptable extraction recovery (>70%) were obtained. The calibration curves were linear in the concentration range of 10.5-1045.0 microg L(-1) for parathion, 10.2-1020.0 microg L(-1) for phoxim, 54.5-1089.0 microg L(-1) for phorate and 27.2-1089.0 microg L(-1) for chlorpyifos, respectively. The limits of detection calculated at a signal-to-noise ratio of 3 were in the range of 0.1-5.0 microg L(-1). The relative standard deviations for seven replicate experiments at 200 microg L(-1) concentration level were less than 4.7%. The proposed method was applied to the analysis of four different sources water samples (tap, well, rain and Yellow River water) and the relative recoveries of spiked water samples are 99.9-115.4%, 101.8-113.7% and 87.3-117.6% at three different concentration levels of 75, 200 and 1000 microg L(-1), respectively.