Background Vulnerable plaques play an important role in the onset of sudden cardiac events and strokes. How to stabilize vulnerable plaques is still a challenge to medical science. Alprostadil is a biologically active...Background Vulnerable plaques play an important role in the onset of sudden cardiac events and strokes. How to stabilize vulnerable plaques is still a challenge to medical science. Alprostadil is a biologically active substance with strong activity on vessel. Our study assessed the stabilizing effects of an alprostadil liposome microsphere preparation (ALMP) on vulnerable plaques in the brachiocephalic artery of apolipoprotein E (Apo E) knockout mice. Methods Seventy-two male Apo E-knockout mice were fed a high-fat diet beginning at eight weeks of age. At week 17, they were divided randomly into groups for treatment with a high dose (3.6 μg, kg-1. d-1) or low dose (1.8 μg. kg-1 . d-1) of an ALMP, or 0.2 ml/d normal saline (control group), The drug was administered using a micro-capsule pump. Twenty weeks after drug administration, pathological changes in the vulnerable plaques within the brachiocephalic artery were assessed, and levels of anti-mouse monocyte/macrophage monoclonal antibody (MOMA-2) and superoxide anions in the plaques were detected using immunofluorescence. The soluble intercellular adhesion molecule-1 (ICAM-1) expression was measured by ELISA, and the expression of matrix metalloproteinase-9 (MMP-9) and CD40 mRNA was measured using RT-PCR. Thrombospindin-1 (TSP-1) expression was detected using Western blotting. Results Compared with the control group, ALMP treatment significantly reduced the plaque area in the brachiocephalic artery (P 〈0.01), significantly lowered the contents of the lipid core (P 〈0.01 ), significantly reduced the number of ruptured fibrous caps (P 〈0.05), and increased the thickness of the fibrous cap and significantly reduced the incidence of intra-plaque hemorrhage (P 〈0.05). ALMP treatment significantly reduced the expression of MOMA-2, superoxide anion, MMP-9, ICAM-1 and CD40 in the plaques (P 〈0.01), decreased plasma ICAM-1 expression (P 〈0.01 ), and increased the expression of TSP-1. Conclusions Treatment with ALMP can stabilize vulnerable plaques by inhibiting inflammation.展开更多
Introduction The use of supercritical fluids such as supercritical CO<sub>2</sub>(scCO<sub>2</sub>) has provided a ’clean’ and effective alternative to traditional methods of protein delive...Introduction The use of supercritical fluids such as supercritical CO<sub>2</sub>(scCO<sub>2</sub>) has provided a ’clean’ and effective alternative to traditional methods of protein delivery systems.Here。展开更多
The thermally expandable microspheres(TEMs) were prepared via suspension polymerization with acrylonitrile(AN), methyl methacrylate(MMA) and methyl acrylate(MA) as monomers and n-hexane as the blowing agent. M...The thermally expandable microspheres(TEMs) were prepared via suspension polymerization with acrylonitrile(AN), methyl methacrylate(MMA) and methyl acrylate(MA) as monomers and n-hexane as the blowing agent. Meanwhile, a novel type of functional and conductive thermal expandable microsphere was obtained through strongly covering the surface of microsphere by conductive polymers with the mass loading of 1.5%. The optimal conditions to prepare high foaming ratio and equally distributed microcapsules were investigated with AN-MMA-MA in the proportion of 70%/20%/10%(m/m/m), and 25 wt% of n-hexane in oil phase. The further investigation results showed that the unexpanded TEMs were about 30 μm in diameter and the maximum expansion ratio was nearly 125 times of original volume. The polypyrrole(PPy) was smoothly coated on the surface of the TEMs and the expansion property of PPy-coated TEMs was almost the same as the uncoated TEMs. Moreover, the structure and expanding performance of TEMs and PPy-coated TEMs were characterized by scanning electron microscopy(SEM), laser particle size analyzer and dilatometer(DIL).展开更多
文摘Background Vulnerable plaques play an important role in the onset of sudden cardiac events and strokes. How to stabilize vulnerable plaques is still a challenge to medical science. Alprostadil is a biologically active substance with strong activity on vessel. Our study assessed the stabilizing effects of an alprostadil liposome microsphere preparation (ALMP) on vulnerable plaques in the brachiocephalic artery of apolipoprotein E (Apo E) knockout mice. Methods Seventy-two male Apo E-knockout mice were fed a high-fat diet beginning at eight weeks of age. At week 17, they were divided randomly into groups for treatment with a high dose (3.6 μg, kg-1. d-1) or low dose (1.8 μg. kg-1 . d-1) of an ALMP, or 0.2 ml/d normal saline (control group), The drug was administered using a micro-capsule pump. Twenty weeks after drug administration, pathological changes in the vulnerable plaques within the brachiocephalic artery were assessed, and levels of anti-mouse monocyte/macrophage monoclonal antibody (MOMA-2) and superoxide anions in the plaques were detected using immunofluorescence. The soluble intercellular adhesion molecule-1 (ICAM-1) expression was measured by ELISA, and the expression of matrix metalloproteinase-9 (MMP-9) and CD40 mRNA was measured using RT-PCR. Thrombospindin-1 (TSP-1) expression was detected using Western blotting. Results Compared with the control group, ALMP treatment significantly reduced the plaque area in the brachiocephalic artery (P 〈0.01), significantly lowered the contents of the lipid core (P 〈0.01 ), significantly reduced the number of ruptured fibrous caps (P 〈0.05), and increased the thickness of the fibrous cap and significantly reduced the incidence of intra-plaque hemorrhage (P 〈0.05). ALMP treatment significantly reduced the expression of MOMA-2, superoxide anion, MMP-9, ICAM-1 and CD40 in the plaques (P 〈0.01), decreased plasma ICAM-1 expression (P 〈0.01 ), and increased the expression of TSP-1. Conclusions Treatment with ALMP can stabilize vulnerable plaques by inhibiting inflammation.
文摘Introduction The use of supercritical fluids such as supercritical CO<sub>2</sub>(scCO<sub>2</sub>) has provided a ’clean’ and effective alternative to traditional methods of protein delivery systems.Here。
基金the National Natural ScienceFoundation of China(Nos.21206171,21376010)the Project of Natural Science Foundation of Beijing(No.2152012)+1 种基金the Young Elite Teacher Project(No.27170115004/027)the Project of 2011 Collaborative Innovation for Green Printing and Publishing Technology and the Project of Beijing Municipal Commission of Educatio (No.km201410005007)for the financial supports
文摘The thermally expandable microspheres(TEMs) were prepared via suspension polymerization with acrylonitrile(AN), methyl methacrylate(MMA) and methyl acrylate(MA) as monomers and n-hexane as the blowing agent. Meanwhile, a novel type of functional and conductive thermal expandable microsphere was obtained through strongly covering the surface of microsphere by conductive polymers with the mass loading of 1.5%. The optimal conditions to prepare high foaming ratio and equally distributed microcapsules were investigated with AN-MMA-MA in the proportion of 70%/20%/10%(m/m/m), and 25 wt% of n-hexane in oil phase. The further investigation results showed that the unexpanded TEMs were about 30 μm in diameter and the maximum expansion ratio was nearly 125 times of original volume. The polypyrrole(PPy) was smoothly coated on the surface of the TEMs and the expansion property of PPy-coated TEMs was almost the same as the uncoated TEMs. Moreover, the structure and expanding performance of TEMs and PPy-coated TEMs were characterized by scanning electron microscopy(SEM), laser particle size analyzer and dilatometer(DIL).