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1.
Opt Express ; 32(2): 1635-1649, 2024 Jan 15.
Article En | MEDLINE | ID: mdl-38297711

High throughput has become an important research direction in the field of super-resolution (SR) microscopy, especially in improving the capability of dynamic observations. In this study, we present a hexagonal lattice structured illumination microscopy (hexSIM) system characterized by a large field of view (FOV), rapid imaging speed, and high power efficiency. Our approach employs spatial light interference to generate a two-dimensional hexagonal SIM pattern, and utilizes electro-optical modulators for high-speed phase shifting. This design enables the achievement of a 210-µm diameter SIM illumination FOV when using a 100×/1.49 objective lens, capturing 2048 × 2048 pixel images at an impressive 98 frames per second (fps) single frame rate. Notably, this method attains a near 100% full field-of-view and power efficiency, with the speed limited only by the camera's capabilities. Our hexSIM demonstrates a substantial 1.73-fold improvement in spatial resolution and necessitates only seven phase-shift images, thus enhancing the imaging speed compared to conventional 2D-SIM.

2.
Opt Express ; 30(5): 7938-7953, 2022 Feb 28.
Article En | MEDLINE | ID: mdl-35299546

Three-dimensional structured illumination microscopy (3D-SIM) plays an essential role in biological volumetric imaging with the capabilities of improving lateral and axial resolution. However, the traditional linear 3D algorithm is sensitive to noise and generates artifacts, while the low temporal resolution hinders live-cell imaging. In this paper, we propose a novel 3D-SIM algorithm based on total variation (TV) and fast iterative shrinkage threshold algorithm (FISTA), termed TV-FISTA-SIM. Compared to conventional algorithms, TV-FISTA-SIM achieves higher reconstruction fidelity with the least artifacts, even when the signal-to-noise ratio (SNR) is as low as 5 dB, and a faster reconstruction rate. Through simulation, we have verified that TV-FISTA-SIM can effectively reduce the amount of required data with less deterioration. Moreover, we demonstrate TV-FISTA-SIM for high-quality multi-color 3D super-resolution imaging, which can be potentially applied to live-cell imaging applications.


Lighting , Microscopy , Algorithms , Artifacts , Imaging, Three-Dimensional/methods , Lighting/methods , Microscopy/methods
3.
Pediatr Emerg Care ; 29(9): 988-91, 2013 Sep.
Article En | MEDLINE | ID: mdl-23974718

OBJECTIVES: Early reports on pneumomediastinum studied the adult population, and recent analyses of pneumomediastinum in pediatric patients contain small numbers of patients. We aimed to summarize the experience of a larger number of pediatric patients with spontaneous pneumomediastinum (SPM) in a tertiary children's facility in northern Taiwan. METHODS: We performed a retrospective chart review of clinical manifestations and outcome of SPM on pediatric patients who were admitted to our hospital during a 10-year period. RESULTS: Forty-three patients (49.4%) had primary SPM, with a male predominance in adolescents. None of the 16 patients younger than 6 years had primary SPM; 43 of 71 patients older than 6 years had secondary SPM (0% vs 60.6%, P < 0.05). The common causes of secondary SPM were asthmatic exacerbation, pneumonia or lower respiratory tract infections, or choking. Ten patients had normal frontal chest radiograph finding (sensitivity, 89.1%); the lateral neck radiographs clearly demonstrated subcutaneous emphysema in 9 of these 10 patients. CONCLUSIONS: All patients younger than 6 years with SPM were secondary; therefore, they should be vigilantly examined for predisposing causes. For adolescent patients with SPM with no catastrophic events, asthma with exacerbation should be considered first, and extensive or invasive diagnostic examinations are not needed. Primary SPM usually requires conservative treatment only with no sequel or recurrence. Lateral neck radiograph has a higher sensitivity for the demonstration of subcutaneous emphysema in doubtful cases.


Mediastinal Emphysema/epidemiology , Adolescent , Age Factors , Airway Obstruction/complications , Asthma/complications , Child , Child, Preschool , Comorbidity , Cough/complications , Diagnostic Imaging/methods , Female , Foreign Bodies/complications , Foreign Bodies/diagnostic imaging , Humans , Infant , Length of Stay/statistics & numerical data , Male , Mediastinal Emphysema/diagnostic imaging , Radiography , Respiratory Tract Infections/complications , Retrospective Studies , Rupture, Spontaneous , Subcutaneous Emphysema/diagnostic imaging , Subcutaneous Emphysema/epidemiology , Symptom Assessment , Taiwan/epidemiology
4.
J Infect Chemother ; 19(4): 782-6, 2013 Aug.
Article En | MEDLINE | ID: mdl-23196653

The aim of this study was to estimate the prevalence of macrolide-resistant Mycoplasma pneumoniae in Taiwan and to compare the clinical courses of pediatric patients with macrolide-resistant (MR) M. pneumoniae and macrolide-susceptible (MS) M. pneumoniae infection. Patients were among the children admitted to Chang Gung Children's Hospital with mycoplasmal pneumonia between February and December 2011. Detection for macrolide resistance was performed after informed consent was obtained. We retrospectively reviewed medical records and compared the clinical courses of two groups of patients of 73 children enrolled into our study. The rate of macrolide resistance in M. pneumoniae was 12.3 %. Longer hospital stay was observed in the MR patients than MS patients [median, 7 days vs. 5 days (P = 0.019)]. Clinical features or radiographic or laboratory findings are not helpful to differentiate MR from MS mycoplasmal pneumonia. Early diagnosis of MR mycoplasmal pneumonia is crucial for the best management of these patients and obviates the need for extensive etiological searches of these nonresponding cases.


Anti-Bacterial Agents/pharmacology , Macrolides/pharmacology , Mycoplasma pneumoniae/drug effects , Pneumonia, Mycoplasma/microbiology , Adolescent , Anti-Bacterial Agents/therapeutic use , Child , Child, Preschool , DNA, Bacterial/analysis , Drug Resistance, Bacterial , Female , Genes, Bacterial/genetics , Hospitalization , Humans , Infant , Macrolides/therapeutic use , Male , Microbial Sensitivity Tests , Mutation , Mycoplasma pneumoniae/genetics , Mycoplasma pneumoniae/isolation & purification , Pharynx/microbiology , Pneumonia, Mycoplasma/drug therapy , Prevalence , RNA, Ribosomal, 23S/genetics , Retrospective Studies , Taiwan/epidemiology , Treatment Outcome
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