A Study on Processing Defects and Parameter Optimization in Abrasive Suspension Jet Cutting of Carbon-Fiber-Reinforced Plastics

Abrasive suspension jet (ASJ), an accurate cold-cutting technology, can address traditional processing issues relating to carbon-fiber-reinforced plastics (CFRPs) like tool wear, interlayer delamination, large heat-affected zone, and low surface roughness. This study employed the use of an ASJ to cut CFRPs and an ultra-depth optical microscope to scan the cut surface to analyze interlayer delamination, surface roughness, kerf taper, and shoulder damage. Regression analysis was conducted to establish a prediction model for cutting quality based on surface roughness, kerf taper, and shoulder damage. Various types of CFRP cutting quality were analyzed using jet parameters. It was found that the use of ASJ to process CFRP results in the following defects: The range of surface roughness variation is from 0.112 μm to 0.144 μm. Surface roughness is most influenced by stand-off distance, followed by traverse speed and jet pressure. The range of kerf taper variation is from 4.737° to 10.1°. Kerf taper is most influenced by stand-off distance, followed by jet pressure and traverse speed. The range of shoulder damage variation is from 3.384 μm2 to 10 μm2. Shoulder damage is most influenced by jet pressure, followed by traverse speed and stand-off distance. A prediction model for cutting quality was developed based on surface roughness, kerf taper, and shoulder damage, providing data support for ASJ cutting of CFRPs. The optimal parameter combination is a stand-off distance of 1 mm, a jet pressure of 30 MPa, and a traverse speed of 30 mm/min

Hybrid Mesoporous–Microporous Nanocarriers for Overcoming Multidrug Resistance by Sequential Drug Delivery

Combination chemotherapy with a modulator and a chemotherapeutic drug has become one of the most promising strategies for the treatment of multidrug resistance (MDR) in cancer therapy. However, the development of nanocarriers with a high payload and sequential release of therapeutic agents poses a significant challenge. In this work, we report a type of hybrid nanocarriers prepared by polydopamine (PDA) mediated integration of the mesoporous MSN core and the microporous zeolite imidazolate frameworks-8 (ZIF-8) shell. The nanocarriers exploit storage capacities for drugs based on the high porosity and molecular sieving capabilities of ZIF-8 for sequential drug release. Particularly, large amounts of an anticancer drug (DOX, 607 μg mg^–1) and a MDR inhibitor curcumin (CUR, 778 μg mg^–1) were sequentially loaded in the mesoporous core via π–π stacking interactions mediated by PDA and in the microporous shell via the encapsulation during ZIF-8 growth. The sustained release of DOX was observed to follow earlier and faster release of CUR by acid-sensitive dissolution of the ZIF-8 shell. Furthermore, the nanoparticles showed good biocompatibility and effective cellular uptake in in vitro evaluations using drug-resistant MCF-7/ADR cancer cells. More importantly, the preferentially released CUR inhibited the drug efflux function of the membrane P-glycoprotein (P-gp), which subsequently facilitated the nuclear transportation of DOX released from the PDA-MSN core, and, in turn, the synergistic effects on killing MDR cancer cells. The hybrid mesoporous–microporous nanocarrier holds great promise for combination chemotherapy applications on the basis of sequential drug release

Dissecting the effect of ileal faecal diversion on the intestine using single‐cell sequencing

Abstract Background Although ileal faecal diversion is commonly used in clinical settings, complications accompany it. Elucidating the intestinal changes caused by ileal faecal diversion will help resolve postoperative complications and elucidate the pathogenic mechanisms of associated intestinal disorders, such as Crohn's disease (CD). Therefore, our study aimed to provide new insights into the effects of ileal faecal diversion on the intestine and the potential mechanisms. Methods Single‐cell RNA sequencing was performed on proximal functional and paired distal defunctioned intestinal mucosae from three patients with ileal faecal diversion. We also performed in vitro cellular and animal experiments, tissue staining and analysed public datasets to validate our findings. Results We found that the epithelium in the defunctioned intestine tended to be immature, with defective mechanical and mucous barriers. However, the innate immune barrier in the defunctioned intestine was enhanced. Focusing on the changes in goblet cells, we demonstrated that mechanical stimulation promotes the differentiation and maturation of goblet cells through the TRPA1‐ERK pathway, indicating that the absence of mechanical stimulation may be the main cause of defects in the goblet cells of the defunctioned intestine. Furthermore, we found obvious fibrosis with a pro‐fibrotic microenvironment in the defunctioned intestine and identified that monocytes may be important targets for faecal diversion to alleviate CD. Conclusions This study revealed the different transcription landscapes of various cell subsets and the potential underlying mechanisms within the defunctioned intestine, when compared to the functional intestine, based on the background of ileal faecal diversion. These findings provide novel insights for understanding the physiological and pathological roles of the faecal stream in the intestine