Publications by authors named "Xing Tang"

The therapeutic efficacy of intervertebral disc (IVD) infections treated with intravenous vancomycin (VCM) is often limited by inadequate blood supply to the IVD. In this study, we developed a localized and sustained-release drug delivery system for the intradiscal administration of VCM. First, VCM-loaded multivesicular liposomes (VCM-MVLs) were prepared using a two-step emulsification process, and we investigated the effects of the preparation process and formulation composition on the quality of the MVLs.

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Touch screens have been extensively utilized in vehicle information systems; however, few studies have centered on the reduction of the touchscreen interaction task load and the increase of body discomfort when driving on unpaved roads. This study aimed to explore the relationship between the system interface elements' design features and interaction task load in vehicle simulated vibration environments. Using a touch screen computer and E-prime software, we investigated the interaction task load and body parts discomfort of 18 participants in varied vibration frequency environments and interface design elements.

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Disulfiram (Allensworth et al.), an "old drug" for the treatment of chronic alcohol dependence, has received extensive attention due to its potential antitumor activity for new medical applications. However, the application of DSF in cancer therapy was limited by its extremely terrible solubility in water.

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Optoelectronic logic gates (OELGs) have become one of the excellent candidates for logic devices in the post Moore era, with great potential for complex optical computing, secure optical communication, and image processing. As an important component of OELGs, bipolar photodetectors (BPDs) face problems such as limited logic functionality, narrow response range, slow response speed, and high-power consumption. Here, we propose a self-powered BPD with a back-to-back structure based on HgTe quantum dot (QD) and organic material PBDB-T:Y6 stacking.

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Oral delivery of peptide and protein drugs (PDs) is hindered by the impermeable intestinal mucosa, which consists of both the mucus layer and the epithelium. Therefore, double-layer (mucus layer and epithelium) overcoming nanocarriers need to be designed to enhance the transporting efficiency of PDs. However, the requirements for surface properties to penetrate these two barriers are quite distinct.

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To address challenges such as limited loading capacity, restricted targeting precision, and low yield of natural exosomes as drug carriers, the fusion of liposomes and exosomes to create hybrid vesicles has emerged as a viable solution approach. While current research mainly focuses on designing functionalized liposomes, less attention is given to how liposome membrane materials affect the elasticity of these hybrids and their delivery efficiency. This study utilized milk exosomes (mExos) as model exosomes, and generated hybrid vesicles with varying elasticity through the fusion of phospholipids with differing chain lengths, examining the disparities among various hybrid vesicles in their ability to overcoming the gastrointestinal barriers.

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Purpose: Tylvalosin Tartrate (TAT), a new-generation macrolide antibiotic, undergoes significant degradation in the stomach and in vivo rapid elimination upon oral administration, resulting in poor bioavailability. This study developed TAT enteric amorphous pellets by liquid layering (TAT/EAP-LL) with pH-sensitive and burst release characteristics, to enhance drug stability in the stomach and concentration enrichment in the duodenum.

Methods: The drug loading layer, isolation layer and enteric layer were formed on the surface of the blank core pellets.

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Norcantharidin (NCTD), an antitumor agent with an increased leukocyte function, has been used for the treatment of hepatocellular carcinoma (HCC) in clinical. However, the clinical application of NCTD is limited due to its inadequate hydrophilicity and lipophilicity, short half-life (t), as well as adverse effects such as vascular irritation, cardiotoxicity, and nephrotoxicity. Herein, a lactoferrin (Lf) and DSPE-mPEG functionalized liposomes loaded with norcantharidic acid (NCA), an active metabolite of NCTD, was constructed for the targeted therapy of HCC.

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Objectives: Subclinical myocardial involvement is common in systemic lupus erythematosus (SLE), but differences between new onset and longstanding SLE are not fully elucidated. This study compared myocardial involvement in new onset versus longstanding SLE using cardiovascular magnetic resonance (CMR).

Materials And Methods: We prospectively enrolled 24 drug-naïve new onset SLE patients, 27 longstanding SLE patients, and 20 healthy controls.

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Background: Neurodermatitis is a chronic skin condition characterized by intense itching and skin thickening due to neurological dysfunction. Its persistent nature poses a challenge to effective treatment, significantly impacting patients' quality of life. Wet cupping therapy is increasingly being used in clinics to manage neurodermatitis, so it is imperative to assess the evidence regarding its effectiveness and safety.

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Article Synopsis
  • Clinical outcomes for peritoneal carcinomatosis (PC) remain poor, but microsphere-based intraperitoneal chemotherapy shows promise based on preclinical studies.
  • This review discusses current treatment strategies for PC, the advantages of using microspheres, the complications of peritoneal adhesions they cause, and possible solutions to these issues.
  • Future research should focus on improving microsphere formulations with biocompatible materials and optimal sizes to enhance drug distribution and tumor targeting, potentially improving treatment efficacy for PC.
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  • Antibiotic resistance is a growing issue, and researchers are exploring antimicrobial peptides like LC-AMP-I1 from venom as potential solutions.
  • LC-AMP-I1 shows strong antibacterial effects against multidrug-resistant bacteria, prevents biofilm formation, and has low toxicity to human cells.
  • In experiments, LC-AMP-I1 worked well with traditional antibiotics and effectively reduced bacterial growth in an infection model, suggesting it could be a promising alternative to standard treatments.
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Article Synopsis
  • * Key cellular components like cyclins, CDKs, and their inhibitors play a critical role in regulating the smooth progression of the cell cycle.
  • * Targeting the cell cycle with specific drugs can provide effective cancer treatment options due to their high specificity and lower toxicity, which could lead to advances in chemotherapy.
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Peritoneal carcinomatosis (PC) is caused by metastasis of primary tumor cells from intra-abdominal organs to the peritoneal surface. Intraperitoneal (IP) chemotherapy allows close contact of high concentrations of therapeutic agents with cancer cells in the peritoneal cavity to prolong patient survival. However, conventional IP chemotherapy is prone to rapid elimination from the peritoneal cavity and lacks specificity towards cancer cells.

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  • The text discusses the importance of polymer gels in advanced technologies like biomedical engineering and energy harvesting, emphasizing their mechanical properties.
  • It points out the lack of systematic reviews linking molecular interactions to the mechanical characteristics of polymer gels, highlighting the need for a comprehensive understanding.
  • The review focuses on both molecular and structural engineering approaches to enhance polymer gel mechanics and summarizes key applications and future perspectives in this area.
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Background: Lung adenocarcinoma (LUAD) is one of the respiratory diseases with high mortality and incidence. As an important angiogenic factor, (Endothelial cell-specific molecule 1) ESM1 plays an important role in the occurrence and development of LUAD. However, the role and molecular mechanism of ESM1 on LUAD metabolic reprogramming and angiogenesis remain unclear.

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The aim of this study was to prepare sodium glycocholate liposomes (SGC-Lip) encapsulating semaglutide (Sml) to improve oral bioavailability and better exert hypoglycemic effect. In this paper, SGC-Lip was prepared by reverse-phase evaporation method with particle size around 140 nm, potential around -27 mV, rounded morphology and better stability. The hypoglycemic and intestinal uptake effects of SGC-Lip and cholesterol-containing liposomes (CH-Lip) were comparatively investigated in rats, and the oral safety of SGC-Lip was examined by cytotoxicity assay.

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Acute lung injury (ALI) arises from an excessive inflammatory response, usually progressing to acute respiratory distress syndrome (ARDS) if not promptly addressed. There is currently a limited array of effective treatments available for ALI. In this study, we developed disulfide bond-bridged prodrug self-assembled nanoparticles (referred to as DSSS NPs).

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Milk exosomes (mExos) have demonstrated significant promise as vehicles for the oral administration of protein and peptide drugs owing to their superior capacity to traverse epithelial barriers. Nevertheless, certain challenges persist due to their intrinsic characteristics, including suboptimal drug loading efficiency, inadequate mucus penetration capability, and susceptibility to membrane protein loss. Herein, a hybrid vesicle with self-adaptive surface properties (mExos@DSPE-Hyd-PMPC) was designed by fusing functionalized liposomes with natural mExos, aiming to overcome the limitations associated with mExos and unlock their full potential in oral peptide delivery.

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The robust operation of quantum entanglement states is crucial for applications in quantum information, computing, and communications. However, it has always been a great challenge to complete such a task because of decoherence and disorder. Here, we propose theoretically and demonstrate experimentally an effective scheme to realize robust operation of quantum entanglement states by designing quadruple degeneracy exceptional points.

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Attributing to their broad pharmacological effects encompassing anti-inflammation, antitoxin, and immunosuppression, glucocorticoids (GCs) are extensively utilized in the clinic for the treatment of diverse diseases such as lupus erythematosus, nephritis, arthritis, ulcerative colitis, asthma, keratitis, macular edema, and leukemia. However, long-term use often causes undesirable side effects, including metabolic disorders-induced Cushing's syndrome (buffalo back, full moon face, hyperglycemia, etc.), osteoporosis, aggravated infection, psychosis, glaucoma, and cataract.

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Article Synopsis
  • Bulleyaconitine A (BLA) is being explored as a treatment for rheumatoid arthritis (RA) due to its anti-inflammatory, pain-relieving, and bone repair properties.
  • Long-acting microspheres (BLA-MS) were created to deliver BLA effectively within joint cavities, showing a drug loading of 23.93% and an encapsulation efficiency of 95.73%.
  • In studies with collagen-induced arthritis rats, BLA-MS significantly reduced paw swelling and inflammatory markers, indicating potential for future clinical use in treating RA.
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Vincristine (VCR), as a cytotoxic drug, is used clinically to treat acute lymphatic leukemia and breast cancer, and commonly used clinically as vincristine sulfate (VCRS). However, its clinical use is limited by unpredictable pharmacologic characteristics, a narrow therapeutic index, and neurotoxicity. The pH gradient method was used for active drug loading of VCRS, and the process route mainly includes the preparation of blank liposomes and drug-loaded liposomes.

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Purpose: Traditional progesterone (PRG) injections require long-term administration, leading to poor patient compliance. The emergence of long-acting injectable microspheres extends the release period to several days or even months. However, these microspheres often face challenges such as burst release and incomplete drug release.

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Tumor vaccines have demonstrated a modest response rate, primarily attributed to their inefficient delivery to dendritic cells (DCs), low cross-presentation, DC-intrinsic immunosuppressive signals, and an immunosuppressive tumor microenvironment (TME). Here, draining lymph node (DLN)-targeted and tumor-targeted nanovaccines were proposed to address these limitations, and heterocyclic lipidoid (A18) and polyester (BR647) were synthesized to achieve dual-targeted cancer immunotherapy. Meanwhile, oligo hyaluronic acid (HA) and DMG-PEG-Mannose were incorporated to prepare dual-targeted nanovaccines encapsulated with STAT3 siRNA and model antigens.

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