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1.
Int Immunopharmacol ; 131: 111922, 2024 Apr 20.
Article in English | MEDLINE | ID: mdl-38522137

ABSTRACT

Streptococcus equi subsp. zooepidemicus (SEZ) is a zoonotic bacterial pathogen that causes life-threatening infections and various diseases such as meningitis, endocarditis and pneumonia. With the use of antibiotics being severely restricted in the international community, an alternative to antibiotics is urgently needed against bacterial. In the present study, the herbal extract magnolol protected mice against SEZ infection, reflected by increased survival rate and reduced bacterial burden. A pro-inflammatory form of cell death occurred in SEZ-infected macrophage. Magnolol downregulated the expression of pyroptosis-related proteins and reduced the formation of cell membrane pores in infected macrophages to suppress the development of subsequent inflammation. We further demonstrated that magnolol directly suppressed SEZ-induced macrophage pyroptosis, which partially protected macrophages from SEZ infection. Our study revealed that magnolol suppressed inflammation and protected mice against SEZ infection, providing a possible treatment for SEZ infection.


Subject(s)
Biphenyl Compounds , Lignans , Streptococcal Infections , Streptococcus equi , Animals , Mice , Streptococcus equi/physiology , Pyroptosis , Macrophages/microbiology , Inflammation , Anti-Bacterial Agents , Streptococcal Infections/drug therapy , Streptococcal Infections/microbiology
2.
Clin Drug Investig ; 44(3): 149-162, 2024 Mar.
Article in English | MEDLINE | ID: mdl-38300386

ABSTRACT

BACKGROUND AND OBJECTIVES: Camrelizumab plus rivoceranib showed significant clinical benefits in progression-free survival and overall survival compared to sorafenib in patients with unresectable hepatocellular carcinoma (HCC). This study aimed to assess its cost effectiveness from the perspective of Chinese health care system. METHODS: A Markov state-transition model was developed based on the Phase 3 randomized CARES-310 clinical trial data. Health state utility values were obtained from the CARES-310 clinical trial, and direct medical costs were derived from the relevant literature and local charges. The measured outcomes included quality-adjusted life-years (QALYs) and the incremental cost-effectiveness ratio (ICER). Probabilistic and one-way sensitivity analyses were performed to assess the uncertainty of the model. RESULTS: In the base-case analysis, the incremental effectiveness and cost of camrelizumab plus rivoceranib versus sorafenib were 0.41 QALYs and $13,684.84, respectively, resulting in an ICER of $33,619.98/QALY, lower than the willingness-to-pay threshold of China ($35,864.61/QALY). Subgroup analyses revealed that the ICERs of camrelizumab plus rivoceranib versus sorafenib were $35,920.01 and $29,717.98 in patients with ALBI grade 1 and grade 2, respectively. One-way sensitivity analyses indicated that the cost of camrelizumab, the proportion of patients receiving subsequent treatment in the camrelizumab plus rivoceranib group, and the cost of rivoceranib were the most significant factors in the base-case analysis. Probabilistic sensitivity analysis suggested that the probabilities of cost effectiveness of camrelizumab plus rivoceranib were 61.27%, 51.46%, and 82.78% for any grade, and ALBI grade 1 and grade 2, respectively. CONCLUSIONS: Camrelizumab plus rivoceranib was more cost effective than sorafenib as first-line therapy for unresectable HCC in the Chinese setting.


Subject(s)
Antibodies, Monoclonal, Humanized , Carcinoma, Hepatocellular , Liver Neoplasms , Pyridines , Humans , Sorafenib/therapeutic use , Carcinoma, Hepatocellular/drug therapy , Cost-Effectiveness Analysis , Liver Neoplasms/drug therapy , Cost-Benefit Analysis , Delivery of Health Care
3.
Biosensors (Basel) ; 13(2)2023 Feb 03.
Article in English | MEDLINE | ID: mdl-36831991

ABSTRACT

A typical colorimetric sandwich-type sensor relies on dual antibodies/aptamers to specifically visualize the targets. The requirement of dual antibodies/aptamers and low signal intensity inevitably increases the design difficulty and compromises the sensing sensitivity. In this work, a novel sandwich-type aptasensor was developed using single aptamer-functionalized magnetic nanoparticles as a specific recognition unit to target cancer cells and a bimetallic metal-organic frameworks (MOFs)-based nanozymes as a colorimetric signal amplification unit. The well-defined crystalline structure of UIO-66 MOFs enabled the introduction of Fe/Zr bimetal nodes, which possessed integrated properties of the peroxidase-like nanozyme activity and direct coordinately binding to the cell surface. Such a novel construction strategy of sandwich-type aptasensors achieved simple, sensitive, and specific detection of the target cancer cells, which will inspire the development of biosensors.


Subject(s)
Aptamers, Nucleotide , Biosensing Techniques , Metal Nanoparticles , Metal-Organic Frameworks , Nanoparticles , Neoplasms , Metal-Organic Frameworks/chemistry , Colorimetry , Aptamers, Nucleotide/chemistry , Metal Nanoparticles/chemistry , Limit of Detection , Neoplasms/diagnosis
4.
Anal Chem ; 95(8): 4227-4234, 2023 02 28.
Article in English | MEDLINE | ID: mdl-36795965

ABSTRACT

Fluorescence-assisted digital counting analysis allowed sensitive quantification of targets by measuring individual fluorescent labels. However, traditional fluorescent labels suffered from low brightness, small size, and sophisticated preparation procedures. Herein, engineering fluorescent dye-stained cancer cells with magnetic nanoparticles were proposed to construct single-cell probes for fluorescence-assisted digital counting analysis by quantifying the target-dependent binding or cleaving events. Various engineering strategies of cancer cells including biological recognition and chemical modification were developed for rationally designing single-cell probes. Introduction of suitable recognition elements into single-cell probes allowed digital quantification of each target-dependent event via counting the colored single-cell probes in the representative image taken using a confocal microscope. The reliability of the proposed digital counting strategy was corroborated by traditional optical microscopy- and flow cytometry-dependent counting technologies. The advantages of single-cell probes, including high brightness, big size, ease of preparation, and magnetic separation, contributed to the sensitive and selective analysis of targets of interest. As proof-to-concept assays, indirect analysis of exonuclease III (Exo III) activity, as well as direct quantitation of cancer cells, were investigated, and the potential in biological sample analysis was also assessed. This sensing strategy will open a new avenue for the development of biosensors.


Subject(s)
Biosensing Techniques , Nanoparticles , Neoplasms , Reproducibility of Results , Spectrometry, Fluorescence , Biosensing Techniques/methods , Fluorescent Dyes/metabolism , DNA Probes
5.
Polymers (Basel) ; 14(18)2022 Sep 06.
Article in English | MEDLINE | ID: mdl-36145866

ABSTRACT

Hydrogels based on nanocomposites (NC) structure have acquired a great deal of interest, but they are still limited by relatively low mechanical strength, inevitably losing elasticity when applied below subzero temperatures, due to the formation of ice crystallization. In this study, an anti-freezing and mechanically strong Laponite NC organohydrogel was prepared by a direct solvent replacement strategy of immersing Laponite NC pre-hydrogel into ethylene glycol (EG)/water mixture solution. In the organohydrogel, a part of water molecules was replaced by EG, which inhibited the formation of ice crystallization even at extremely low temperatures. In addition, the formation of hydrogen bonds between Laponite and the monomers of N-isopropylacrylamide (NIPAM) and hydroxyethyl acrylate (HEA) endowed the organohydrogels with high mechanical strength and toughness. The NC organohydrogel can maintain its mechanical flexibility even at -25 °C. The compressive stress, tensile stress, and elongation at the break of N5H5L reached 3871.71 kPa, 137.05 kPa, and 173.39%, respectively, which may be potentially applied as ocean probes in low temperature environment.

6.
Anticancer Agents Med Chem ; 21(15): 1996-2003, 2021.
Article in English | MEDLINE | ID: mdl-33292141

ABSTRACT

BACKGROUND: Interleukin-11 (IL-11) could promote invasion and metastasis of cancer cells, however, its mechanism is unclear. OBJECTIVE: This study aimed to investigate the effects of recombinant human IL-11 (rhIL-11) on lung cancer cell metastasis and growth. METHODS: Human lung cancer cell, A549, was cultured and subcutaneously injected into mice to establish Xenograft tumor models. Tumor models were divided into control, rhIL-11 transplantation (250 µg/kg/day), and rhIL-11 transplantation (500 µg/kg/day) group. Tumor volumes were recorded and measured 6 times. Hypoxia- Inducible Factor 1α (HIF1α), snail, slug, Signal Transducers/Activators of Transcription-3 (STAT3), E-cadherin, twist, and vimentin levels were evaluated using western blot and Real-Time PCR (RT-PCR). RESULTS: Sizes of subcutaneous tumors increased following measurement time. rhIL-11 treatment significantly enhanced HIF1α and STAT3 expression in rhIL-11 treatment groups compared to the control group (p<0.05). However, no remarkable differences were discovered between rhIL-11 (250 µg/kg/day) and rhIL-11 (500 µg/kg/day) group (p>0.05). rhIL-11 treatments significantly increased twist, and slug expressions compared to control group (p<0.05), especially for rhIL-11 (500 µg/kg/day) treatment, which triggered significantly higher effects on twist and slug expressions compared to those in the control group (p<0.05). Vimentin and snail mRNA levels were significantly up-regulated and E-cadherin level was significantly down-regulated in rhIL-11 treatment groups compared to the control group (p<0.05). Meanwhile, rhIL-11 at a dosage of 500 µg/kg/day triggered remarkably higher effects on vimentin, snail, and E-cadherin expressions compared to those in rhIL-11 (250 µg/kg/day) group (p<0.05). CONCLUSION: rhIL-11 transplantation promoted growth and Epithelial-Mesenchymal Transition (EMT) of A549 cells, which might be associated with STAT3/HIF-1α/EMT signaling pathway activation.


Subject(s)
Adenocarcinoma of Lung/therapy , Antineoplastic Agents/metabolism , Hypoxia-Inducible Factor 1, alpha Subunit/metabolism , Interleukin-11/metabolism , Lung Neoplasms/therapy , STAT3 Transcription Factor/metabolism , Adenocarcinoma of Lung/metabolism , Adenocarcinoma of Lung/pathology , Animals , Cell Proliferation , Drug Screening Assays, Antitumor , Epithelial-Mesenchymal Transition , Female , Humans , Lung Neoplasms/metabolism , Lung Neoplasms/pathology , Mice , Recombinant Proteins/metabolism , Signal Transduction , Tumor Cells, Cultured
7.
Bioorg Med Chem Lett ; 27(2): 282-287, 2017 01 15.
Article in English | MEDLINE | ID: mdl-27913181

ABSTRACT

Squaric acid and its derivatives are versatile synthons and have demonstrated applications in medicinal chemistry, notably as non-classical bioisosteric replacements for functional groups such as carboxylic acids, alpha-amino acids, urea, guanidine, peptide bonds and phosphate/pyrophosphate linkages. Surprisingly, no reports have appeared concerning its possible application as a nucleobase substitute in nucleosides. A preliminary investigation of such an application is reported herein. 3-Amino-4-((1R,4S)-4-(hydroxymethyl)cyclopent-2-en-1-yl)amino-cyclobut-3-ene-1,2-dione, 3-((1R,4S)-4-(hydroxymethyl)cyclopent-2-en-1-yl)amino-4-methoxycyclobut-3-ene-1,2-dione, and 3-hydroxy-4-((1R,4S)-4-(hydroxymethyl)cyclopent-2-en-1-yl)amino-cyclobut-3-ene-1,2-dione sodium salt were synthesized. Computational analyses of their structures and preliminary antitumor and antiviral screening results are reported.


Subject(s)
Antineoplastic Agents/pharmacology , Antiviral Agents/chemical synthesis , Cyclobutanes/pharmacology , Nucleosides/pharmacology , Antineoplastic Agents/chemical synthesis , Antineoplastic Agents/chemistry , Antiviral Agents/chemistry , Cell Line, Tumor , Cell Proliferation/drug effects , Cyclobutanes/chemical synthesis , Cyclobutanes/chemistry , Dose-Response Relationship, Drug , Drug Screening Assays, Antitumor , Humans , Models, Molecular , Molecular Structure , Nucleosides/chemical synthesis , Nucleosides/chemistry , Structure-Activity Relationship
8.
J Am Chem Soc ; 134(38): 15644-7, 2012 Sep 26.
Article in English | MEDLINE | ID: mdl-22963012

ABSTRACT

A new solution-based method to fabricate Cu(2)ZnSn(S,Se)(4) (CZTSSe) thin films is presented. Binary and ternary chalcogenide nanoparticles were synthesized and used as precursors to form CZTSSe thin films. The composition of the CZTSSe films can be easily controlled by adjusting the ratio of the nanoparticles used. The effect of compositional adjustment on device performance is illustrated. Laboratory-scale photovoltaic cells with 8.5% total-area efficiency (or 9.6% active-area efficiency) were demonstrated without anti-reflective coatings. Material characterization data revealed the formation of a bilayer microstructure during thermal processing and suggested a path forward on device improvement.

9.
Zhong Xi Yi Jie He Xue Bao ; 9(12): 1277-85, 2011 Dec.
Article in Chinese | MEDLINE | ID: mdl-22152764

ABSTRACT

This paper introduces the development and application of health-related quality of life (HRQOL) scales in research on coronary heart disease (CHD). Currently, the scales for CHD patients have been more systematically developed and widely used in foreign countries, while domestically in China, they are developed successfully but problematically; research in this field has started later and the scales introduced are limited and not suitable for the entire range of domestic CHD patients. Thus, this paper introduces 26 HRQOL scales in research on CHD, including five generic scales, ten disease-specific scales from abroad and eleven scales originating from China. With the deficiency of HRQOL scales, especially that in traditional Chinese medicine and specific scales, this paper analyzes and summarizes the problems existing in development of scales. The authors also provide solutions in order to help the development and application of scales in further studies.


Subject(s)
Coronary Disease , Health Status , Medicine, Chinese Traditional/methods , Quality of Life , Surveys and Questionnaires/standards , Coronary Disease/physiopathology , Coronary Disease/psychology , Humans
10.
J Food Prot ; 73(4): 715-9, 2010 Apr.
Article in English | MEDLINE | ID: mdl-20377961

ABSTRACT

The purpose of this research was to investigate the influence of sucrose at 2.0, 4.0, and 8.0% as a protectant during freeze-drying on the viability and membrane properties of Lactobacillus casei Zhang. Membrane properties were determined using zeta potential, hydrophobicity, fluidity, and integrity before and after freeze-drying. Exposing L. casei Zhang to sucrose protected it from drastic changes in cell surface electrophoretic mobility and hydrophobicity in contrast with the untreated condition, and the effect was dose related. Sucrose caused an increase in membrane fluidity compared with the control sample. Moreover, 2.0% sucrose decreased the general polarization values less than 4.0 or 8.0% sucrose, while 4.0% sucrose and 8.0% sucrose had no significant difference in decreasing general polarization values (P < 0.05). L. casei Zhang freeze-dried in the presence of 2.0% sucrose retained up to 23.7% membrane integrity, whereas cells freeze-dried with 4.0 and 8.0% sucrose had 32.4 and 37.6% membrane integrity compared with that of L. casei Zhang before freeze-drying. Correspondingly, the number of survivors of L. casei Zhang, determined by the plate count method, decreased from 8.02 to 0.63 log CFU/ml after freeze-drying in the absence of sucrose. However, in the presence of 2.0, 4.0, and 8.0% sucrose, the numbers of survivors were 2.01, 2.87, and 3.20 log CFU/ml after freeze-drying, respectively. The present work suggested that sucrose was an effective membrane protectant at 2.0, 4.0, or 8.0% on the surface zeta potential, hydrophobicity, fluidity, and integrity of L. casei Zhang.


Subject(s)
Cell Membrane/drug effects , Cryoprotective Agents/pharmacology , Freeze Drying , Lacticaseibacillus casei/drug effects , Sucrose/pharmacology , Colony Count, Microbial , Dose-Response Relationship, Drug , Food Microbiology , Hydrophobic and Hydrophilic Interactions , Lacticaseibacillus casei/cytology , Lacticaseibacillus casei/physiology , Membrane Fluidity , Membrane Lipids , Membrane Potentials , Microbial Viability , Probiotics
11.
Biochemistry (Mosc) ; 73(6): 669-75, 2008 Jun.
Article in English | MEDLINE | ID: mdl-18620532

ABSTRACT

Pholiota nameko polysaccharide (PNPS-1) has been isolated and purified by enzymatic hydrolysis, hot water extraction, ethanol precipitation, and ion-exchange and gel-filtration chromatography. The anti-inflammatory activity of PNPS-1 was evaluated in rodents using xylene-induced ear edema, egg albumin-, carrageenin-, and formaldehyde-induced paw edema, cotton pellet granuloma test, adhesion of peritoneal leukocytes in vitro, and ulcerogenic activity. The results showed that PNPS-1 (5 mg/ear) inhibited topical edema in the mouse ear and at 100, 200, and 400 mg/kg (intraperitoneally) it significantly suppressed the development of egg albumin-, carrageenin-, and formaldehyde-induced paw edema in the animals. PNPS-1 (100, 200, and 400 mg/kg, per oral) significantly inhibited the growth of granuloma tissues induced by subcutaneously implanted cotton pellets in rats by 10.96, 18.07, and 43.75%, respectively. PNPS-1 also inhibited spontaneous and phorbol-12-myristate-13-acetate-activated adhesion of peritoneal leukocytes in vitro. Further, both acute as well as chronic administration of PNPS-1 (100, 200, and 400 mg/kg, per oral) did not produce any gastric lesion in rats. In conclusion, these data indicated that PNPS-1 possesses significant anti-inflammatory activity suggesting its potential as an anti-inflammatory agent for use in the treatment of various inflammatory-related diseases.


Subject(s)
Agaricales/chemistry , Anti-Inflammatory Agents/therapeutic use , Inflammation/drug therapy , Polysaccharides/therapeutic use , Animals , Anti-Inflammatory Agents/isolation & purification , Anti-Inflammatory Agents/pharmacology , Cells, Cultured , Drug Evaluation, Preclinical , Edema/pathology , Female , Granuloma/pathology , Granuloma/prevention & control , Macrophages, Peritoneal/drug effects , Macrophages, Peritoneal/pathology , Male , Mice , Phytotherapy , Plant Extracts/isolation & purification , Plant Extracts/pharmacology , Plant Extracts/therapeutic use , Polysaccharides/isolation & purification , Polysaccharides/pharmacology , Rats , Rats, Sprague-Dawley
12.
Int J Biol Macromol ; 43(3): 232-7, 2008 Oct 01.
Article in English | MEDLINE | ID: mdl-18582932

ABSTRACT

Lipopolysaccharide from cow placenta (LPS-CP-2) has been isolated and purified by hot phenol-water extraction, enzyme hydrolysis, chloroform-petroleum ether method, ion-exchange and gel-filtration chromatography. Also, LPS-PS-2 was evaluated for antitumor activity against Ehrlich ascites carcinoma (EAC)-bearing Swiss albino mice. LPS-PS-2 caused significant (P<0.05) decrease in tumor volume, and viable cell count; and it prolonged the life span of EAC-tumor-bearing mice. Hematological profile indicates that LPS-CP-2 possessed protective action on the haemopoietic system. Further, administration of LPS-CP-2 reduced the tumor volume of both DLA and EAC cell lines in a dose-dependent way. The LPS-PS was found to be devoid of pyrogenic response in the rabbits. These results indicate that LPS-PS exhibited significant antitumor activity without pyrogenic response, suggesting its potential as antitumor agent.


Subject(s)
Antineoplastic Agents/isolation & purification , Antineoplastic Agents/pharmacology , Carcinoma, Ehrlich Tumor/drug therapy , Lipopolysaccharides/isolation & purification , Lipopolysaccharides/pharmacology , Placenta/chemistry , Animals , Antineoplastic Agents/therapeutic use , Carcinoma, Ehrlich Tumor/blood , Carcinoma, Ehrlich Tumor/pathology , Cattle , Cell Line, Tumor , Cell Survival/drug effects , Female , Lipopolysaccharides/therapeutic use , Mice , Pregnancy , Pyrogens/metabolism , Rabbits
13.
Zhonghua Jie He He Hu Xi Za Zhi ; 27(8): 546-8, 2004 Aug.
Article in Chinese | MEDLINE | ID: mdl-15388005

ABSTRACT

OBJECTIVE: To investigate the activity and clinical efficacy of toremifene plus mitomycin, vindesin and cisplatin regimen (MVP) in non-small cell lung cancer (NSCLC). METHODS: A549 cells were seeded into 96 wells at the concentration of 10 x 10(4)cells/well and exposed to different agents. Seventy-two hours later, the cytotoxicity of the agents were evaluated with the method of MTT. The clinical trial included 63 patients with chemtherapy-naive NSCLC and 30 patients who had received chemotherapy (Pre-treatment arm). The chemotherapy-naive patients were randomly divided into the toremifene-treatment arm and the control arm. Each patient was given MVP chemotherapy. Five days before the chemotherapy, those in the toremifene-treatment group and pre-treatment arm started toremifene 420 mg daily orally for 7 days. The response was evaluated after two cycles of chemotherapy and toxic side effects and the survival of the patients were followed up. RESULTS: Toremifene decreased the IC(50) of chemotherapeutic agents and increased their cytotoxicity. In the clinical trial, the response rate and median survival were 47% and 11 months in the toremifene-treatment arm and 32% and 9 months in the control arm, respectively. The difference between the two arms was not significant. The response rate and median survival were 17% and 7 months in the pre-treatment arm, respectively. The toxicity among the three groups was not significantly different. CONCLUSIONS: Toremifene can improve the cytotoxicity of cisplatin, mitomycin and vindesin. Toremifene plus MVP regimen is safe and effective in the treatment of NSCLC.


Subject(s)
Antineoplastic Agents, Hormonal/administration & dosage , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Carcinoma, Non-Small-Cell Lung/drug therapy , Lung Neoplasms/drug therapy , Toremifene/administration & dosage , Aged , Antineoplastic Combined Chemotherapy Protocols/pharmacology , Carcinoma, Non-Small-Cell Lung/mortality , Carcinoma, Non-Small-Cell Lung/pathology , Cell Division/drug effects , Cisplatin/administration & dosage , Female , Follow-Up Studies , Humans , Inhibitory Concentration 50 , Lung Neoplasms/mortality , Lung Neoplasms/pathology , Male , Middle Aged , Mitomycins/administration & dosage , Survival Rate , Tumor Cells, Cultured , Vindesine/administration & dosage
14.
J Acoust Soc Am ; 114(4 Pt 1): 1898-904, 2003 Oct.
Article in English | MEDLINE | ID: mdl-14587590

ABSTRACT

In this paper we study the bubble dynamics driven by an aspherical acoustic field, based on the theory of hydrodynamics. Evolution equations for an aspherical bubble are derived under the aspherical acoustic driving. The numerical calculations show that the aspherical bubble can oscillate stably and periodically under suitable conditions, which is out of the explanation of spherical perturbation theory. Furthermore, under some controlling parameters, the aspherical distortion can either grow rapidly, leading to the bubble's breakdown, or decay gradually making the bubble spherical, which is similar to the result of the perturbation theory driven by a spherical ultrasound.

15.
J Acoust Soc Am ; 111(6): 2632-7, 2002 Jun.
Article in English | MEDLINE | ID: mdl-12083195

ABSTRACT

The dependence of the single bubble sonoluminescence (SBSL) on the waveforms of the driving ultrasound has been investigated by both experiment and numerical calculation. Three types of non-simple-harmonic waves, the rectangular, triangular and as well as the sinusoidal wave with a pulse, are used to drive the SBSL in our research. The triangular wave is the most effective, while the rectangular wave is the worst and the sinusoidal wave in the middle. However, the rectangular wave drives the brightest SBSL among those waves if the sound pressure amplitude keeps constant. When we use a simple-harmonic wave with a pulse as the driving sound, stable and periodic SBSL flashes have been observed. An increase in the flash intensity can be observed as the pulse is put at a suitable phase related to the sinusoidal wave. All of the observations are investigated numerically. Well qualitative agreements between the numerical simulations and the experimental measurements have been achieved.

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