A UiO-66 3D photonic crystal optical sensor for highly efficient chlorobenzene vapor detection

Chlorobenzene (C₆H₅Cl) is a flammable liquid with high vapor activity, which is a severe threat to the environment and human health. Therefore, it is essential to develop a highly efficient sensor to detect C₆H₅Cl vapor. Herein, we developed a UiO-66 three-dimensional photonic crystal (3D PC) optical sensor and investigated its sensing properties toward the C₆H₅Cl vapor. The UiO-66 3D PCs optical sensor shows a high sensitivity of C₆H₅Cl vapor, in the concentrations range of 0–500 ppm, the reflectance intensity response to be 0.06% ppm with a good linear relationship, detection limit can reach 1.64 ppm and the quality factor is 10.8. Additionally, the UiO-66 3D PC optical sensor demonstrated great selectivity with the values of selectivity (S) varying from 2.24 to 10.65 for the C₆H₅Cl vapor as compared with carbon tetrachloride (CCl₄), dichloromethane (CH₂Cl₂), 1,1,2-trichloroethane (C₂H₃Cl₃), benzene (C₆H₆), deionized water (H₂O), ethanol (C₂H₅OH) and methyl alcohol (CH₃OH) vapors. Moreover, the UiO-66 3D PC optical sensor shows an ultrafast optical response time and recovery times of 0.5 s and 0.45 s with exceptional stability and repeatability to 500 ppm C₆H₅Cl vapor. These excellent sensing properties are attributed to the efficacy of signal transduction, increased porosity and gas adsorption sites, which are intrinsically endowed by the design of the 3D optical structure. The design and fabrication of this UiO-66 3D PC optical sensor might open up potential applications for the detection of the C₆H₅Cl vapor.

Chlorobenzene (C₆H₅Cl) is a flammable liquid with high vapor activity, which is a severe threat to the environment and human health.     

Corrosion kinetics and mechanisms of ZrC1−x ceramics in high temperature water vapor

The corrosion kinetics and mechanisms of ZrC_1−x ceramics in water vapor between 800 and 1200 °C were investigated. The results showed that there was only cubic ZrO₂ phase in the corrosion layer when corroded at 800 °C, while a scale layer consisted of a mixture of cubic and monoclinic ZrO₂ phases when corroded at 1000 °C and 1200 °C. A series of crystallographic relationships at the ZrC/c-ZrO₂ interface were detected. The c-ZrO₂ formed near the interface retained some crystallographic orientations of the initial ZrC before corrosion, presenting an “inheritance in microstructure” between c-ZrO₂ and ZrC. The corrosion behavior mainly followed a parabolic relationship. The incremental rate of weight gain increased with increased corrosion temperature and decreased C/Zr ratio and the carbon vacancy was passive to the decrease of corrosion rate. The main corrosion controlling mechanism changed from phase boundary reactions to surface diffusion and then to grain boundary diffusion with increased temperature.

Studies on the corrosion kinetics and mechanisms of ZrC_1−x ceramics in water vapor are reported for the first time.     

Dynamic activation of cystic fibrosis transmembrane conductance regulator by type 3 and type 4D phosphodiesterase inhibitors

The diseases of cystic fibrosis, chronic obstructive pulmonary disease (COPD), and chronic bronchitis are characterized by mucus-congested and inflamed airways. Anti-inflammatory agents that can simultaneously restore or enhance mucociliary clearance through cystic fibrosis transmembrane conductance regulator (CFTR) activation may represent new therapeutics in their treatment. Herein, we report the activation of CFTR-mediated chloride secretion by phosphodiesterase (PDE) 4 inhibitors in T84 monolayer using (125)I anion as tracer. In the absence of forskolin, the iodide secretion was insensitive to PDE4 inhibitor L-826,141 [4-[2-(3,4-bis-difluoromethoxyphenyl)-2-[4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)phenyl]-ethyl]-3-methylpyridine-1-oxide], roflumilast, or to PDE3 inhibitor trequinsin. However, these inhibitors potently augmented iodide secretion after forskolin stimulation, with efficacy coupled to the activation states of adenylyl cyclase. The iodide secretion from PDE3 or PDE4 inhibition was characterized at first by a prolonged efflux duration, followed by progressively elevated peak efflux rates at higher inhibitor concentrations. Paralleled with an increased phosphor-cAMP response element-binding protein formation, the CFTR activation dissociated from a global cAMP elevation and was blocked by H89 [N-[2-((p-bromocinnamyl)amino)ethyl]-5-isoquinolinesulfonamide]. 2-(4-Fluorophenoxy)-N-[(1S)-1-(4-methoxyphenyl)ethyl]nicotinamide, a stereoselective PDE4D inhibitor, augmented iodide efflux more efficiently than its less potent (R)-isomer. The peak efflux from maximal PDE4 and PDE3 inhibition matched that from full adenylyl cyclase activation. These data suggest that PDE3 and PDE4 (mainly PDE4D) form the major cAMP diffusion barrier in T84 cells to ensure a compartmentalized CFTR signaling. Together with their potent anti-inflammatory properties, the potentially enhanced airway mucociliary clearance from CFTR activation may have contributed to the efficacy of PDE4 inhibitors in COPD and asthmatic patients. PDE4 inhibitors may represent new opportunities to combat cystic fibrosis and other respiratory diseases in future.     

A flexible biomimetic superhydrophobic and superoleophilic 3D macroporous polymer-based robust network for the efficient separation of oil-contaminated water

The development of stable 3D surfaces for oil/water separation has been of great interest to researchers. Inspired by the lotus leaf, in this study, a superhydrophobic stable and robust surface was generated by the combination of n-octadecyltrichlorosilane, silica, polypyrrole and polyurethane (ODTCS–SiO₂–PP–PU). The constructed 3D network displayed superhydrophobic and superoleophilic behavior with a high water contact angle of 154.7° ± 0.8°. The superhydrophobic behavior of the porous material was found to be stable for months. Apart from the hydrophobicity analysis of the material, the various forms of the materials were investigated via scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR), and energy-dispersive X-ray spectroscopy (EDX). Under the force of gravity, hexane displayed an exceptionally high flux of 102 068 Lm⁻² h⁻¹ through ODTCS–SiO₂–PP–PU. The macroporous network of ODTCS–SiO₂–PP–PU displayed fewer chances of fouling, which is a common issue with membranes. Moreover, its porous network displayed good absorption capacity for various non-polar organic solvents. The maximum absorption capacity observed for toluene was 34 times its own weight. The separation efficiency of various non-polar organic solvents from water was observed in the range of 99.5 to 99.8%. ODTCS–SiO₂–PP–PU, due to its superhydrophobicity, 3D porous network, extraordinarily high flux, good absorption capacity, and excellent separation capability, has been established as a good candidate for the separation of organic and oil contaminants from water.

Superhydrophobic polyurethane for oil and water separation.     

Arrangement of water molecules and high proton conductivity of tunnel structure phosphates,KMg1−xH2x(PO3)3·yH2O

A fast proton conductor was investigated in a mixed-valence system of phosphates with a combination of large cations (K⁺) and small cations (Mg²⁺), which resulted in a new phase with a tunnel structure suitable for proton conduction. KMg_1−xH_2x(PO₃)₃·yH₂O was synthesized by a coprecipitation method. A solid solution formed in the range of x = 0–0.18 in KMg_1−xH_2x(PO₃)₃·yH₂O. The structure of the new proton conductor was determined using neutron and X-ray diffraction measurements. KMg_1−xH_2x(PO₃)₃·yH₂O has a tunnel framework composed of face-shared (KO₆) and (MgO₆) chains, and PO₄ tetrahedral chains along the c-direction by corner-sharing. Two oxygen sites of water molecules were detected in the one-dimensional tunnel, one of which exists as a coordination water of K⁺ sites. Multi-step dehydration was observed at 30 °C and 150 °C from thermogravimetric/differential thermal analysis measurements, which reflects the different coordination environments of the water of crystallization. Water molecules are connected to PO₄ tetrahedra by hydrogen bonds and form a chain along the c-axis in the tunnel, which would provide an environment for fast proton conduction associated with water molecules. The KMg_1−xH_2x(PO₃)₃·yH₂O sample with x = 0.18 exhibited high proton conductivity of 4.5 × 10⁻³ S cm⁻¹ at 150 °C and 7.0 × 10⁻³ S cm⁻¹ at 200 °C in a dry Ar gas flow and maintained the total conductivity above 10⁻³ S cm⁻¹ for 60 h at 150 °C under N₂ gas atmosphere.

A fast proton conductor exhibiting high proton conductivity of 7.0 × 10⁻³ S cm⁻¹ at 200 °C in a dry Ar gas flow was developed by designing water chains in a rigid tunnel framework.     

A comprehensive review of recent developments in 3D printing technique for ceramic membrane fabrication for water purification

Additive manufacturing (AM), which is also commonly known as 3D printing, provides flexibility in the manufacturing of complex geometric parts at competitive prices and within a low production time. However, AM has not been used to a large extent in filtration and water treatment processes. AM results in the creation of millions of nanofibers that are sublayered on top of each other and compressed into a thin membrane. AM is a novel technique for fabricating filtration membranes with different shapes, sizes and controlled porosity, which cannot be achieved using conventional process such as electrospinning and knife casting. In this paper, we review the advantages and limitations of AM processes for fabricating ceramic membranes. Moreover, a brief background of AM processes is provided, and their future prospects are examined. Due to their potential benefits for fabrication and flexibility with different materials, AM methods are promising in the field of membrane engineering.

Additive manufacturing (AM), which is also commonly known as 3D printing, provides flexibility in the manufacturing of complex geometric parts at competitive prices and within a low production time.     

A new 3D concentration gradient maker and its application in building hydrogels with a 3D stiffness gradient

For a deeper knowledge of phenomena at cell and tissue level, for understanding the role on bimolecular signalling and for the development of new drugs it is important to recreate in vitro environments that mimic the physiological one. Spatial gradients of soluble species guide the cells’ morphogenesis, and they range in a three‐dimensional (3D) environment. Gradients of mechanical properties, which have a 3D pattern, could lead cell migration and differentiation. In this work, a new 3D Concentration Gradient Maker able to generate 3D concentration gradients of soluble species was developed, which could be used for differential perfusion of scaffolds. The same device can be applied to build hydrogel matrixes with a 3D gradient of mechanical properties. Computational dynamic fluid analysis was used to develop the gradient generator; the validation of the 3D gradient of stiffness was carried out using finite elements analysis and experimental studies. The device and its application could bring improvements in studying phenomena related to cell chemotaxis and mechanotaxis, but also to differentiation in the simultaneous presence of gradients in both soluble chemical species and substrate stiffness. Copyright © 2014 John Wiley & Sons, Ltd.     

A sensitive and simplified radioimmunoassay for 1,25-dihydroxyvitamin D3

A sensitive radioimmunoassay system for 1 alpha,25-dihydroxyvitamin D3 [1,25(OH)2D3] with an improved extraction procedure has been developed. Following one-step extraction and prepurification of 1,25(OH)2D3 by 'Extrelut-1' minicolumns final purification was achieved by high-performance liquid chromatography (HPLC) using a radial compression separation system equipped with a mu Porasil cartridge. The HPLC method applied allows the purification of 4 extracts/h. Recovery of 1,25(OH)2[3H]D3 after HPLC was 77 +/- 2.6% (mean +/- SD, n = 51). Since the recovery of 1,25(OH)2[3H]D3 was very reproducible, addition of labelled steroid to each single serum sample for monitoring recovery was omitted. The sensitivity of the assay was 0.8 pg/tube resulting in a detection limit of 3 ng/l, when 1 ml of serum was extracted. Intra-assay and inter-assay coefficients of variation were 12% and 16.8%, respectively. Serum 1,25(OH)2D3 concentration in 30 normal subjects (mean age: 25 yr) was 55 +/- 12 ng/l (mean +/- SD). In 55 elderly patients (mean age: 77 yr) the 1,25(OH)2D3 serum level was 32 +/- 12 ng/l (mean +/- SD) and in three patients with chronic renal failure on 1,25(OH)2D3 therapy 146 +/- 67 ng/l (mean +/- SD). Patients with chronic renal failure had reduced 1,25(OH)2D3 serum levels (mean 5.4 ng/l, range less than 3-11 ng/l, n = 10). In one patient with renal failure, following kidney transplantation the serum 1,25(OH)2D3 and creatinine levels were monitored from the 4th to the 12th post-surgical day: a highly significant negative correlation (r = 0.85) was found.     

Design and fabrication of polypyrrole/expanded graphite 3D interlayer nanohybrids towards high capacitive performance

Polypyrrole/expanded graphite (PPy/EG) nanohybrids, with a hierarchical structure of a three dimensional EG framework with a thick PPy coating layer, have been synthesized via a vacuum-assisted intercalation in situ oxidation polymerization method. In the synthesis, pyrrole monomers were intercalated into the irregular pores of EG with the assistance of a vacuum pump. Subsequently, the intercalated pyrrole monomers assembled on both sides of the EG nanosheets and formed PPy by an in situ polymerization method. As electrode materials, the typical PPy/EG10 sample with an EG content of 10% had a high specific capacitance of 454.3 F g⁻¹ and 442.7 F g⁻¹ (1.0 A g⁻¹), and specific capacitance retention rate of 75.9% and 73.3% (15.0 A g⁻¹) in 1 M H₂SO₄ and 1 M KCl electrolytes, respectively. The two-electrode symmetric supercapacitor showed a high energy density of 47.5 W h kg⁻¹ at a power density of 1 kW kg⁻¹, and could retain superb stability after 2000 cycles. The unique self-supporting structure feature and homogeneous PPy nanosphere coating combined the contributions of electrochemical double layer capacitance and pseudo-capacitance, which made the nanohybrids an excellent electrode material for high performance energy storage devices.

Polypyrrole/expanded graphite nanohybrids with a hierarchical structure were synthesized as electrode materials, and showed outstanding energy storage performance.     

A comparison between acoustic output indices in 2D and 3D/4D ultrasound in obstetrics.

OBJECTIVE: Three-dimensional (3D) ultrasound is gaining popularity in prenatal diagnosis. While there are no studies regarding the safety of 3D ultrasound, it is now widely performed in non-medical facilities, for non-diagnostic purposes. The present study was aimed at comparing the acoustic output, as expressed by thermal index (TI) and mechanical index (MI), of conventional two-dimensional (2D) and 3D/4D ultrasound during pregnancy. METHODS: A prospective, observational study was conducted, using three different commercially available machines (iU22, Philips Medical Systems; Prosound Alfa-10, Aloka; and Voluson 730 Expert, General Electric). Patients undergoing additional 3D/4D ultrasound examinations were recruited from those scheduled for fetal anatomy and follow-up exams. Fetuses with anomalies were excluded from the analysis. Data were collected regarding duration of the exam, and each MI and TI during 2D and 3D/4D ultrasound exams. RESULTS: A total of 40 ultrasound examinations were evaluated. Mean gestational age was 31.1 +/- 5.8 weeks, and mean duration of the exam was 20.1 +/- 9.9 min. Mean TIs during the 3D (0.27 +/- 0.1) and 4D examinations (0.24 +/- 0.1) were comparable with the TI during B-mode scanning (0.28 +/- 0.1, P = 0.343). The MIs during the 3D volume acquisitions were significantly lower than those in the 2D B-mode ultrasound studies (0.89 +/- 0.2 vs. 1.12 +/- 0.1, P = 0.018). The 3D volume acquisitions added 2.0 +/- 1.8 min of actual ultrasound scanning time (i.e. not including data processing and manipulation, or 3D displays, which are all post-processing steps). The 4D added 2.2 +/- 1.2 min. CONCLUSIONS: Acoustic exposure levels during 3D/4D ultrasound examination, as expressed by TI, are comparable with those of 2D B-mode ultrasound. However, it is very difficult to evaluate the additional scanning time needed to choose an adequate scanning plane and to acquire a diagnostic 3D volume.     

Anti-H antibody of unusually high titer showing variable reactivities against group A red cells and broad thermal amplitude in a patient with lymphoma

We report a case of a patient with high titer anti-H antibody showing broad thermal amplitude and variable reactivities against group A red cells. A 62-year-old Korean female was diagnosed with diffuse large B cell lymphoma involving multiple organs. Her ABO/RhD type was A+ and her genotype was ABO*A.01.01/ABO*O.01.02. Antibody screening test (AST) and antibody identification test (IDT) were strongly positive for all reagent cells. Anti-human globulin (AHG) test revealed an antibody titer of 1:256 for 37?°C phase and trace positivity for poly- and mono-specific C3d. Reactivity was stronger for O+ red cells than that for A+ red cells across all temperatures tested (4?°C, room temperature (RT) and 37?°C). This was also found for AHG phase. Anti-IH was ruled out based on agglutination of O+ cord cells (CCs). Antibody was determined as IgM anti-H after DTT treatment. Three batches of 10 A+ red cells from random donors were tested with three consecutive serums for crossmatching using tube method. Interestingly, out of thirty A+ red cells tested, 20 cells at RT, 11 cells at 37?°C and 11 cells in the AHG phase showed reactivity of greater than 2+. The patient was transfused with 6 units of packed RBCs subsequently. Chemotherapy (R-CHOP regimen) and Helicobacter pylori eradication were then started. Her antibody titer gradually decreased following such treatment. In conclusion, we identified a case of patient with high titer anti-H with broad thermal amplitude, suggesting that anti-H antibodies might need to be considered for cases with pan-agglutination in AST and IDT.     

Determination of 25-hydroxyvitamin D3 in serum by high performance liquid chromatography and isotope dilution-mass spectrometry

Four different HPLC methods for analysis of 25-hydroxyvitamin D3 in serum were evaluated with a method based on isotope dilution-mass spectrometry (ID-MS). Method I utilized Sephadex LH-20 chromatography as the only prepurification step. No correlation with the ID-MS method was obtained. Method II utilized Sephadex LH-20 chromatography and a subsequent reversed phase HPLC step as prepurification. The correlation coefficient was 0.99 (regression coefficient 1.2 and intercept - 3.9 micrograms/l). Method III included open silicic acid chromatography and straight phase HPLC as prepurification. The correlation when compared with the ID-MS method was 0.94 (regression coefficient 1.2 and intercept - 0.4 micrograms/l). In method IV Sep-pak C18 chromatography and open silicic acid chromatography were used as prepurification. The correlation coefficient when compared with the ID-MS method was 0.97 (regression coefficient 0.8 and intercept 0.1 microgram/l). It is concluded that a single Sephadex LH-20 step is not sufficient as prepurification and that method IV had an accuracy sufficient for its intended use to analyse 25-hydroxyvitamin D3 in serum from cattle.     

Persistent and automatic intraoperative 3D digitization of surfaces under dynamic magnifications of an operating microscope

One of the major challenges impeding advancement in image-guided surgical (IGS) systems is the soft-tissue deformation during surgical procedures. These deformations reduce the utility of the patient’s preoperative images and may produce inaccuracies in the application of preoperative surgical plans. Solutions to compensate for the tissue deformations include the acquisition of intraoperative tomographic images of the whole organ for direct displacement measurement and techniques that combines intraoperative organ surface measurements with computational biomechanical models to predict subsurface displacements. The later solution has the advantage of being less expensive and amenable to surgical workflow. Several modalities such as textured laser scanners, conoscopic holography, and stereo-pair cameras have been proposed for the intraoperative 3D estimation of organ surfaces to drive patient-specific biomechanical models for the intraoperative update of preoperative images. Though each modality has its respective advantages and disadvantages, stereo-pair camera approaches used within a standard operating microscope is the focus of this article. A new method that permits the automatic and near real-time estimation of 3D surfaces (at 1 Hz) under varying magnifications of the operating microscope is proposed. This method has been evaluated on a CAD phantom object and on full-length neurosurgery video sequences (∼1 h) acquired intraoperatively by the proposed stereovision system. To the best of our knowledge, this type of validation study on full-length brain tumor surgery videos has not been done before. The method for estimating the unknown magnification factor of the operating microscope achieves accuracy within 0.02 of the theoretical value on a CAD phantom and within 0.06 on 4 clinical videos of the entire brain tumor surgery. When compared to a laser range scanner, the proposed method for reconstructing 3D surfaces intraoperatively achieves root mean square errors (surface-to-surface distance) in the 0.28–0.81 mm range on the phantom object and in the 0.54–1.35 mm range on 4 clinical cases. The digitization accuracy of the presented stereovision methods indicate that the operating microscope can be used to deliver the persistent intraoperative input required by computational biomechanical models to update the patient’s preoperative images and facilitate active surgical guidance.     

A simplified high-performance liquid chromatographic method for determination of vitamin D3, 25-hydroxyvitamin D2 and 25-hydroxyvitamin D3 in human serum.

Measurement of the serum level of 25-hydroxyvitamin D is the most useful parameter in evaluating vitamin D status. The serum level of vitamin D is a useful parameter in studying short time effects after exposure to ultraviolet light and absorption of the vitamin after oral administration. A method for simultaneous determinations of vitamin D3 25-hydroxyvitamin D2 and 25-hydroxyvitamin D3 is described. Serum or plasma was extracted by methanol-isopropanol (90:10, v/v) and hexane. The hexane layer was injected in to a reversed-phase (C18) high-performance liquid chromatographic (HPLC) system. 25-hydroxyvitamin D2 and 25-hydroxyvitamin D3 were eluted by methanol-water (85:15, v/v), and vitamin D3 by a linear gradient of methanol-water (85:15) and methanol-isopropanol-water (87.5:10:2.5), and detected by u.v. absorption. This method gave separate determinations of the D2 and D3 forms of 25-hydroxyvitamin D, but owing to an interfering peak the method does not measure vitamin D2. The assay was very sensitive with a detection limit of 5 nmol l-1 for 25-hydroxyvitamin D2 and D3 and vitamin D3 by using 0.5 ml serum or plasma for analysis, so that for low vitamin D3 levels more than 1 ml of serum is desirable.     

A comparative study of Cu-anchored 0D and 1D ZnO nanostructures for the reduction of organic pollutants in water

In this work, Cu NPs were loaded at a fixed percentage (5 wt%) on 1D, (1D + 0D) and 0D ZnO nanostructures to investigate the effect of the support morphology on the reduction of organic pollutants in water. The synthesized materials were characterized by high-resolution transmission electron microscopy (HR-TEM), ultraviolet-visible spectroscopy (UV-Vis), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), N₂ adsorption–desorption and X-ray photoelectron spectroscopy (XPS). The results reveal that the loading of Cu NPs decreases the optical band gap, and a slight change in the crystallite sizes increases the specific surface area value of the nanocomposites. The TEM images reveal that 1D ZnO has an average width of 44.7 nm and an average length of 211 nm, while 0D ZnO has an average diameter of 54.5 nm. The HR-TEM and XPS data confirm the loading of metallic Cu NPs on the surface of the ZnO nanostructures. The pure ZnO and nanocomposites were tested for 4-nitrophenol (4-NP) reduction in the presence of NaBH₄ at room temperature. The obtained results show that pure ZnO nanostructures have no catalytic performance, while the nanocomposites showed good catalytic activities. The catalytic reduction efficiency of 4-NP was found to follow the order of Cu/0DZnO > Cu/(1D + 0D)ZnO > Cu/1DZnO. The complete reduction of 4-NP has been observed to be achievable within 60 s using the Cu/0DZnO nanocomposite, with a k_app value of 8.42 min⁻¹ and good recyclability of up to five cycles. This nanocomposite was then applied in the reduction of organic dyes in water; it was found that the reduction rate constants for the methylene blue, Congo red, and acriflavine hydrochloride dyes were 1.4 min⁻¹, 1.2 min⁻¹, and 3.81 min⁻¹, respectively. The high catalytic performance of this nanocomposite may be due to the small particle size, high specific surface area, and the high dispersion of Cu NPs on the surface of ZnO.

Catalytic reduction of 4-NP over Cu/ZnO nanocomposites.     

A 2D/3D correspondence building method for reconstruction of a patient-specific 3D bone surface model using point distribution models and calibrated X-ray images

Constructing a 3D bone surface model from a limited number of calibrated 2D X-ray images (e.g. 2) and a 3D point distribution model is a challenging task, especially, when we would like to construct a patient-specific surface model of a bone with pathology. One of the key steps for such a 2D/3D reconstruction is to establish correspondences between the 2D images and the 3D model. This paper presents a 2D/3D correspondence building method based on a non-rigid 2D point matching process, which iteratively uses a symmetric injective nearest-neighbor mapping operator and 2D thin-plate splines based deformations to find a fraction of best matched 2D point pairs between features extracted from the X-ray images and those extracted from the 3D model. The estimated point pairs are then used to set up a set of 3D point pairs such that we turn a 2D/3D reconstruction problem to a 3D/3D one, whose solutions are well studied. Incorporating this 2D/3D correspondence building method, a 2D/3D reconstruction scheme combining a statistical instantiation with a regularized shape deformation has been developed. Comprehensive experiments on clinical datasets and on images of cadaveric femurs with both non-pathologic and pathologic cases are designed and conducted to evaluate the performance of the 2D/3D correspondence building method as well as that of the 2D/3D reconstruction scheme. Quantitative and qualitative evaluation results are given, which demonstrate the validity of the present method and scheme.