Extranodal lymphomas presenting as soft tissue sarcomas to a sarcoma service over a two-year period.

Non-Hodgkin's lymphoma usually presents with lymphadenopathy at multiple sites but can also involve any part of the musculoskeletal system. Occasionally the presentation is with a soft tissue mass. The presentation of large, superficial lymphomatous masses is similar both clinically and radiologically to that of soft tissue sarcomas. The six cases of lymphoma presenting to the Exeter Sarcoma Service as suspected soft tissue sarcomas, over a two-year period (2002-2004), are presented. We describe the clinical and imaging characteristics of these tumours and their subsequent management. Our cases showed variability in presentation. Only one of the six cases presented with pain and one with tenderness. Four of the cases had no lymphadenopathy and the other two had lymphadenopathy restricted to one nodal basin. Overlying soft tissue swelling occurred in four cases and in distal limb swelling beyond the mass in one case. Radiologically, lymphomas are known to be likely to exhibit confluent lymphadenopathy that is rare in patients with soft tissue sarcoma. Confluent lymphadenopathy was demonstrated in only one case of this series of patients. It is thought that lymphomas infiltrate across anatomical fascial planes more readily than sarcomas and in four of our six cases this feature was present. Clinical history, examination and MRI are insufficient to differentiate between soft tissue sarcoma and lymphoma and the importance of obtaining a pathological diagnosis prior to surgery is clear. It is crucial to differentiate lymphoma from sarcoma in order to avoid unnecessary excisional procedures in lymphoma patients.     

Acrolein-Induced Toxicity—Defective Mitochondrial Function as a Possible Mechanism

Administration of acrolein (2.5 mg/kg body weight/day) to rats for 45 days depleted the glutathione level in liver, which triggered an imbalance in the antioxidant defense, resulting in lipid peroxidation. Enhanced lipid peroxidation damaged the membranous structure of mitochondria, which was indicated by the loss of lamellae, and increased the oxidation of exogenously added NADH. Loss in membrane integrity altered the activities of the tricarboxylic acid cycle enzymes and levels of cytochromes. Decreased rate of ADP—stimulated oxygen uptake, respiratory coupling ratio, and ATP synthesis—were also observed. We report that the acrolein-induced toxicity is mediated through the depletion of GSH leading to impairment of rat liver mitochondrial function. Received: 24 November 1998     

Oligomeric proanthocyanidins protect myocardium by mitigating left ventricular remodeling in isoproterenol‐induced postmyocardial infarction

Extracellular matrix (ECM) remodeling is a major pathophysiological process during post‐myocardial infarction (MI). The activation, differentiation, and proliferation of cardiac fibroblasts to myofibroblasts regulate the expression of ECM proteins. The signaling by bone morphogenetic protein (BMP‐4), an extracellular ligand of the TGF‐β family, has recently been identified as an essential pathway in regulating cardiovascular dysfunctions including myocardial fibrosis. Oligomeric proanthocyanidins (OPC) are well known for their cardioprotective activity. The primary aim of the study was to investigate BMP‐4‐mediated ECM turnover in cardiac fibrosis during isoproterenol‐induced post‐MI and its downregulation by OPC. Myocardial injury was evaluated by assaying serum markers LDH and CK. Oxidative stress and the enzymatic and nonenzymatic antioxidant levels were assessed to support the cardioprotective nature of OPC. The total collagen level was analyzed by measuring hydroxyproline levels. The ISO‐induced group showed a significant decrease in the levels of antioxidants due to severe oxidative stress and increased expression of BMP‐4 which reflects the increased expression of MMP 2 and 9 with a concomitant increase and deposition of fibrillary collagens type I and III responsible for the fibrotic scar formation as evidenced in the histological analysis.BMP‐4 activation, thus, is strongly associated with cardiac fibrosis which was downregulated upon OPC supplementation. This study provides an evidence supporting the antifibrotic effect of OPC via regulation of BMP‐4‐mediated ECM turnover and also substantiates the remarkable antioxidant efficacy of OPC against isoproterenol induced severe oxidative stress and subsequent post‐MI cardiac fibrosis.     

One-step solution synthesis of a two-dimensional semiconducting covalent organometallic nanosheet via the condensation of boronic acid

In this work, a 2D covalent organometallic nanosheet (COMS) was designed and successfully synthesized through the one-step conjunction of a terpyridine–metal–terpyridine (TMT) sandwich coordinate motif with borate ester covalent heterocyclic (B₃O₃) linkage via the condensation of boronic acid. The obtained 2D COMS with a cobalt coordination center (2D COMS-Co) showed promising p-type semiconducting properties.

A 2D covalent organometallic nanosheet (COMS-Co) was synthesized through the one-step conjunction of sandwich coordinate motif with covalent heterocyclic linkage via the condensation of boronic acid, and it showed promising semiconducting properties.

Two-dimensional (2D) metal–organic frameworks (MOFs) obtained by using the strong bonding effects between metal ions and organic molecule species have aroused great interest;^1–8 these include coordination nanosheets, which are a class of 2D materials featuring metal complex motifs.^9–12 Covalent bonds are considered to be an effective way to fabricate covalent organic frameworks (COFs) such as COF-1, which is mainly constructed by a phenyl ring and borate ester to form covalent heterocyclic (B₃O₃) linkage.^13–15 Based on the synergistic effects of metal coordination and covalent interactions, Jiang and co-workers demonstrated the important role of central metals in controlling π-electronic functions through Mpc-COF.¹⁶ Nevertheless, the coordination bond forms spontaneously within the ring of the porphyrin heterocycle and not as the linkage between organic components. In addition, the connections made between metal ions and ligand motifs cannot facilitate the proper tuning of the physicochemical properties of the structure.¹⁷ Combining the covalent and coordinate features may provide an opportunity to design new 2D materials and thus, the synergetic enhancement in many unique properties can be achieved. As far as we know, the fabrication of 2D semiconducting materials that combine the covalent heterocyclic linkage and coordinate linkage has not been reported. Therefore, it is a pressing need to construct a functional 2D organic framework through a one-step synthesis strategy, which would be a more attractive approach.Herein, we first proposed an efficient one-step strategy to synthesize a 2D material by the synergy of covalent and organometallic interactions; it was named as a covalent organometallic nanosheet (2D COMS-M, M = cobalt (Co)). The as-proposed 2D COMS-Co was constructed by linking the borate ester covalent heterocyclic (B₃O₃) structure and terpyridine (tpy) metal coordination motif (TMT) (Fig. 1).Open in a separate windowFig. 1(a) Synthesis route of the semiconducting 2D COMS. (b) Design principles of COMS via the condensation of boronic acid. (c) The calculated cross-sectional view of 2D COMS-Co.In order to explore the extended construction of 2D COMS, the self-condensation ligand 4-phenylborate-2,2′; 6′,2′′-terpyridine (L¹) integrated with CoCl₂ as the Co²⁺ carrier was employed through an anhydrous and oxygen-free hydrothermal reaction at 120 °C under argon, and the typical synthesis process is depicted in Fig. 1a (for details, please see ESI^†). Starting from the condensation reaction of boronic acid (Fig. 1b), H₂O could be generated and played a key role in dissolving CoCl₂ and further releasing Co²⁺ ions (CoCl₂ is practically insoluble in mesitylene and dioxane). This was followed by coordination between the terpyridine motifs and the released Co²⁺ ions to obtain 2D COMS. This novel strategy could achieve crystalline 2D materials by self-controlling the release of Co²⁺ through the one-step condensation reaction of boronic acid. The calculated cross-sectional view of 2D COMS-Co indicates that the thickness of the monolayer 2D COMS-Co is 0.69 nm (Fig. 1c). The dual synergistic connecting effects of covalence and coordination in 2D COMS-Co provided nanosheet-like morphology with significant improvement in the semiconducting performance. The hole mobility of the 2D COMS-Co-based FET device could reach to 5.7 × 10⁻⁵ cm² V⁻¹ s⁻¹ with an ON–OFF ratio of 221, which demonstrated the potential application of 2D COMS-Co in semiconducting devices.The scanning electron microscopy (SEM) image (Fig. 2a) reveals that 2D COMS-Co has a uniform micron-sized nanosheet-like structure. Furthermore, the transmission electron microscopy (TEM) image indicates that the as-synthesized 2D COMS-Co consists of few multi-layers. Fig. 2c shows an enlarged image of the selected area visualized with high-resolution TEM (HRTEM), where the section enclosed by white lines depicts lattice fringes. Moreover, the selected area electron diffraction (SAED, inset of Fig. 2c) image shows a circular ring pattern that reveals the well-defined crystalline structure of 2D COMS-Co; these results are in agreement with our X-ray diffraction data (Fig. S2, ESI^†). Most interestingly, the atomic force microscopy (AFM) image (Fig. 2d) clearly demonstrates that the selected thickness of 2D COMS-Co is 2.07 nm, and the resultant thickness is three times less than the calculated value of 0.69 nm (Fig. 1c), indicating its uniform three-layer stacked structure. The above results collectively provide strong evidence of typical 2D features for COMS-Co. Moreover, the high-angle annular dark-field (HAADF) image and the scanning transmission electron microscopy (STEM) elemental mapping further revealed that the C (red), B (cyan), N (green), O (blue) and Co (pink) elements are homogeneously distributed on the selected area of 2D COMS-Co (Fig. 2e–k). The electronic structure of 2D COMS-Co was further characterized by four-probe scanning tunnel microscopy (STM) (please see details in ESI^†). The high-resolution STM imaging revealed that the 2D COMS-Co flake has a layered flake structure with uniformly distributed hexagonal hole morphology and the resultant holes have a diameter of 4.72 nm (Fig. 2l); this observation is in accordance with the proposed structure of 2D COMS-Co (Fig. S8, ESI^†).Open in a separate windowFig. 2Morphological characterization of 2D COMS-Co. (a) SEM image of powder. (b) TEM image. (c) HRTEM image (d) AFM image. (e) HAADF image. (f–k) STEM elemental mapping. (l) STM image.Due to the covalence and coordination effects, the absorption peak of 2D COMS-Co obtained from the UV-vis measurements (Fig. 3a) is red-shifted in comparison to that for ligand L¹, and the optical band gap is calculated to be 1.85 eV. Furthermore, density functional theory (DFT) calculations revealed that the highest occupied molecular orbital (HOMO) of 2D COMS-Co was dominated by the π orbital of the B₃O₃ linkage and the phenyl ring, whereas the π* orbital of TMT was responsible for the lowest unoccupied molecular orbital (LUMO). Additionally, the calculated electronic band gap of 2D COMS-Co was 1.89 eV, which was in accordance with the optical band gap, confirming the successful synthesis of 2D COMS-Co. Fig. 3b displays the X-ray photoelectron spectroscopy (XPS) spectrum of 2D COMS-Co, in which the appearance of the binding energy peak at 192.2 eV is significantly different from that for L¹ (191.1 eV), which can be ascribed to the –C–B–O₂ structure.^18,19 Compared to the observation for L¹, the N 1s peak for 2D COMS-Co shifted to a higher binding energy value (399.2 eV for COMS-Co and 397.5 eV for L¹). The skewing of the peaks toward higher binding energy was induced by the contribution of N atoms in terpyridine to the metal center. Therefore, the XPS results clearly provide evidence of the existence of both covalent and coordination effects in the as-prepared 2D COMS-Co. The Fourier transform infrared (FT-IR) spectra in Fig. 3c show that the –B(OH)₂ bands (around 3500 cm⁻¹) of the ligand L¹ are significantly attenuated compared to that observed for 2D COMS-Co. In addition, the B–O stretching vibrations at 1351 cm⁻¹ can be observed for 2D COMS-Co but not for L¹.^13,20–22 Thus, the above results show that the expected B₃O₃ rings for 2D COMS-Co have indeed been formed. Notably, the nitrogen adsorption–desorption isotherms reveal that the Brunauer–Emmett–Teller (BET) specific surface area of 2D COMS-Co is as high as 598 m² g⁻¹ (Fig. 3d); it surpasses those of other layered materials, including the reported graphene oxide paper (10 m² g⁻¹), clays (10 to 100 m² g⁻¹), and pillared clays (50 to 300 m² g⁻¹), and is in the range of the values of the most porous zeolites and many porous carbons.^13,23 This drastic enhancement can be assigned to the uniform porous structure of the as-synthesized 2D COMS-Co.Open in a separate windowFig. 3(a) UV-vis spectra of L¹ and 2D COMS-Co (left), electron distribution on HOMO/LUMO and the orbital energy gap (right). (b) XPS B 1s and N 1s spectra of L¹ and 2D COMS-Co. (c) FT-IR spectra of L¹ and 2D COMS-Co. (d) N₂ adsorption and desorption isotherms of 2D COMS-Co (inset: stacking porous view).The above results show that the 2D COMS-Co units arranged in periodic strips can provide conducting pathways for charge carrier transport through TMT and central cobalt ions. 2D COMS-Co was employed to function as the active semiconducting channel in a field-effect transistor (FET) device. As shown in Fig. 4a, the individual 2D COMS-Co sample is deposited on an Si wafer as the semiconducting layer to construct the FET device. The 2D COMS-Co-based FET device delivered hole mobility of 5.7 × 10⁻⁵ cm² V⁻¹ S⁻¹ and an ON/OFF ratio of 221, which were comparable with those of previously reported 2D MOFs (Table S1^†). Therefore, these results collectively demonstrate the potential application of 2D COMS-Co in semiconducting devices.Open in a separate windowFig. 4(a) Schematic of the FET device employing 2D COMS-Co as the semiconducting layer. (b) Transfer curve of the 2D COMS-Co-based FET device with the inset showing an optical and model diagram of the device; V_G is the gate-source voltage and I_D is the drain current.In summary, a novel two-dimensional covalent organometallic nanosheet (COMS) was designed and successfully synthesized through the strategy of one-step conjunction of a TMT sandwich coordinate motif with B₃O₃ linkage. This facile strategy could achieve crystalline 2D COMS-Co by self-controlling the release of Co²⁺ through a one-step condensation reaction of boronic acid. The systematic characterization demonstrated the successful preparation of porous and crystalline 2D COMS-Co. Particularly, the as-prepared 2D COMS-Co-based FET device presented hole mobility of 5.7 × 10⁻⁵ cm² V⁻¹ S⁻¹ and an ON/OFF ratio of 221, which demonstrated the potential application of 2D COMS-Co in semiconducting devices. Therefore, we envision that this work will open a new avenue for the synthesis of two-dimensional semiconducting covalent organometallic materials by using covalence and coordination dual synergistic connection effects via a one-step facile strategy.