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Nano-gold micelles loaded Dox and Elacridar for reversing drug resistance of breast cancer 纳米金胶束装载阿霉素和艾拉西达逆转乳腺癌耐药
IF 2.3 4区 工程技术 Q1 BIOCHEMICAL RESEARCH METHODS Pub Date : 2022-11-07 DOI: 10.1049/nbt2.12102
Liu-Jing Wen, Yue-Sheng Wang, Jie Zhang

The aim of this study was to provide a new effective carrier for rescuing the sensitivity of drug-resistant in breast cancer cells. Nano-gold micelles loaded with Dox and Elacridar (FP-ssD@A-E) were chemically synthesised. With the increase in the amount of Dox and Elacridar, the encapsulation rate of FP-ssD@A-E gradually increased, and the drug loading rate gradually decreased. FP-ss@A-E had a sustained-release effect. Dox, Elacridar, FP-ss@AuNPs, and FP-ssD@A-E significantly improved cell apoptosis, in which, FP-ssD@A-E was the most significant. FP-ssD@A-E significantly decreased the cell viability and improved the Dox uptake. The levels of VEGFR-1, P-gp, IL-6, and i-NOS were significantly decreased after Dox, Dox + Elacridar, FP-ss@AuNPs, and FP-ssD@A-E treatment. It was worth noting that FP-ssD@A-E had the most significant effects. The prepared FP-ssD@A-E micelles, which were spherical in shape, uniform in particle size distribution, and had good drug loading performance and encapsulation efficiency.

本研究旨在为挽救乳腺癌耐药细胞的敏感性提供一种新的有效载体。用化学方法合成了负载Dox和Elacridar (FP-ssD@A-E)的纳米金胶束。随着Dox和Elacridar用量的增加,FP-ssD@A-E的包封率逐渐增加,载药率逐渐降低。FP-ss@A-E有持续释放的效果。Dox、Elacridar、FP-ss@AuNPs和FP-ssD@A-E均能显著改善细胞凋亡,其中FP-ssD@A-E效果最为显著。FP-ssD@A-E显著降低细胞活力,提高Dox摄取。Dox、Dox +埃拉克达、FP-ss@AuNPs和FP-ssD@A-E治疗后,VEGFR-1、P-gp、IL-6和i-NOS水平均显著降低。值得注意的是,FP-ssD@A-E的效果最为显著。制备的FP-ssD@A-E胶束呈球形,粒径分布均匀,具有良好的载药性能和包封效率。
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引用次数: 0
Effect of different physical factors on the synthesis of spherical gold nanoparticles towards cost-effective biomedical applications 不同物理因素对球形金纳米颗粒合成的影响及其在生物医学上的应用
IF 2.3 4区 工程技术 Q1 BIOCHEMICAL RESEARCH METHODS Pub Date : 2022-11-03 DOI: 10.1049/nbt2.12100
Zahra Bahmanyar, Fatemeh Mohammadi, Ahmad Gholami, Mehdi Khoshneviszadeh

Gold nanoparticles (AuNPs) have great potential to contribute to numerous application fields of biomedicine, which are highly dependent on their physicochemical properties, such as size and shape. Due to the final characteristics, nanoparticles (NPs) are primarily affected by different factors of reaction conditions; the present study aimed to evaluate the effects of manipulating the main physical parameters of the Turkevich method to optimise the fabrication of citrated capped AuNPs in a spherical shape, desirable final size, and efficiency. For this purpose, various experiments of citrate-capped spherical AuNPs synthesis were designed to study the roles of a wide range of initial pH values and temperature of reaction, Na3Cit/HAuCl4 molar ratio, and two order reagent additions, method I and method II, in the final characterisations and reaction efficacy. Prepared NPs synthesised with different experiments were characterised by dynamic light scattering, UV-Visible, and fourier transform infrared spectroscopy. Furthermore, NPs obtained from optimised synthesis conditions were more detailed using UV-Visible, transmission electron microscopy, and XRD. The findings indicated that the final size and synthesis efficacy of citrated capped spherical AuNPs were significantly affected by all studied synthesis parameters and the order addition of reagents. The higher initial reaction temperature and Na3Cit/HAuCl4 Molar ratio provided a smaller particle size with desirable synthesis efficacy. Besides, final optimised NPs were provided in cubic crystal structures, and each NP's single crystal was obtained. In sum, our findings indicated that optimising synthesis conditions could improve size distribution, morphology, crystallite size, and structures of final NPS, as well as efficiency, which is a principal factor associated with future cost-effective productions on large scales. Further studies are needed in this regard.

金纳米粒子(AuNPs)在生物医学的众多应用领域具有巨大的潜力,这些领域高度依赖于其物理化学性质,如尺寸和形状。由于最终的特性,纳米颗粒主要受到反应条件的不同因素的影响;本研究旨在评估操纵Turkevich方法的主要物理参数以优化球形柠檬酸封端AuNPs的制备、理想的最终尺寸和效率的效果。为此,设计了柠檬酸盐封端的球形AuNPs合成的各种实验,以研究宽范围的初始pH值和反应温度、Na3Cit/HAuCl4摩尔比以及两级试剂添加(方法I和方法II)在最终表征和反应效果中的作用。通过动态光散射、紫外可见光谱和傅立叶变换红外光谱对通过不同实验合成的纳米颗粒进行了表征。此外,使用UV-Visible、透射电子显微镜和XRD对从优化的合成条件获得的NP进行了更详细的分析。研究结果表明,柠檬酸封端的球形AuNPs的最终尺寸和合成效率受到所有研究的合成参数和试剂添加顺序的显著影响。较高的初始反应温度和Na3Cit/HAuCl4摩尔比提供了较小的颗粒尺寸和期望的合成效率。此外,最终优化的NP以立方晶体结构提供,并获得每个NP的单晶。总之,我们的研究结果表明,优化合成条件可以改善最终NPS的尺寸分布、形态、晶粒尺寸和结构,以及效率,这是未来大规模生产具有成本效益的主要因素。在这方面需要进一步研究。
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引用次数: 3
Dutasteride nanoemulsion preparation to inhibit 5-alpha-hair follicle reductase enzymes in the hair follicle; an ex vivo study 抑制毛囊内5- α -毛囊还原酶的杜他雄胺纳米乳制备离体研究
IF 2.3 4区 工程技术 Q1 BIOCHEMICAL RESEARCH METHODS Pub Date : 2022-10-31 DOI: 10.1049/nbt2.12101
Mehri Memar Bashi Aval, Elham Hoveizi, Reza Mombeiny, Mostafa Kazemi, Saeedeh Saeedi, Shima Tavakol

Alopecia is a treatable disorder that usually occurs due to high levels of 5-alpha dihydrotestosterone in hair follicles. To enhance the storage capacity of hair follicles and alleviate the inherent characteristics of dutasteride, 5-alpha reductase inhibitor, a prolonged-release nanocarrier was synthesised, and its influence on rat abdomen's skin was investigated. Results showed the lower ratio of S/Co (higher ethanol concentration) increased the hydrodynamic nanocarriers' particle size due to thermodynamic disturbance and Ostwald ripening. In contrast, an increase in surfactant through a decrease in interfacial tension resulted in smaller nanocarriers of 32.4 nm. Moreover, an increase in viscosity had an inverse correlation with the nanoemulsions' particle size. Nanocarriers containing ethanol showed less entrapment efficacy, perhaps due to the rapid dissolution of dutasteride into ethanol during nanoemulsification, while, based on Stokes' equation, the addition of ethanol resulted in smaller particle size and stability of the system. Skin permeation analysis using Franz diffusion cells showed nanocarriers could pass through the skin and release dutasteride for 6 days. In conclusion, the optimum concentration of ingredients is decisive in guaranteeing the ideal particle size, stability, and skin permeation of nanocarriers. The Present dutasteride nanocarrier would promise a prolonged and sustained-release drug delivery system for Alopecia therapy.

脱发是一种可治疗的疾病,通常是由于毛囊中5- α -二氢睾酮水平高而引起的。为了提高毛囊的储存能力,缓解5- α还原酶抑制剂杜他雄胺的固有特性,合成了一种缓释纳米载体,并研究了其对大鼠腹部皮肤的影响。结果表明,较低的S/Co比(较高的乙醇浓度)由于热力学干扰和奥斯特瓦尔德成熟导致水动力纳米载体粒径增大。相比之下,通过降低界面张力来增加表面活性剂可以得到更小的32.4 nm纳米载体。此外,粘度的增加与纳米乳液的粒径呈负相关。含乙醇的纳米载体的包封效果较差,这可能是由于在纳米乳化过程中度他雄胺迅速溶解到乙醇中,而根据Stokes方程,乙醇的加入使体系的粒径更小,稳定性更强。Franz扩散池皮肤渗透分析表明,纳米载体可以通过皮肤并释放杜他雄胺6天。综上所述,最佳成分浓度是保证纳米载体理想粒径、稳定性和透皮性的决定性因素。本发明的杜他雄胺纳米载体有望成为治疗脱发的长效缓释药物输送系统。
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引用次数: 2
Human embryonic stem cells cultured on hydrogels grafted with extracellular matrix protein-derived peptides with polyethylene glycol joint nanosegments 人胚胎干细胞的水凝胶培养与细胞外基质蛋白衍生肽与聚乙二醇联合纳米段
IF 2.3 4区 工程技术 Q1 BIOCHEMICAL RESEARCH METHODS Pub Date : 2022-10-06 DOI: 10.1049/nbt2.12091
Abdullah A. Alarfaj, Abdurahman H. Hirad, Murugan A. Munusamy, S. Suresh Kumar, Akon Higuchi

Human pluripotent stem cells (hPSCs) can be proliferated on completely synthetic materials under xeno-free cultivation conditions using biomaterials grafted with extracellular matrix protein (ECM)-derived peptides. However, cell culture biomaterials grafted with ECM-derived peptides must be prepared using a high concentration of peptide reaction solution (e.g. 1000 μg/ml), whereas the ECM concentration of the ECM-coated surface for hPSC culture is typically 5 μg/ml. We designed a polyethylene glycol (PEG) joint nanosegment (linker) to be used between base cell culture biomaterials and bioactive ECM-derived peptides to enhance the probability of contact between ECM-derived peptides and cell binding receptors of hPSCs. Vitronectin-derived peptides with glycine joint nanosegments (GCGG) were conjugated onto poly (vinyl alcohol-co-itaconic acid) hydrogels via PEG joint nanosegments, and human embryonic stem cells (hESCs) were cultivated on these hydrogels. hESCs could successfully be cultivated on hydrogels while maintaining their pluripotency and differentiation potential to differentiate into cells that are induced from three germ layers in vitro and in vivo, where only a 50 μg/ml ECM-derived peptide concentration was used when the PEG joint nanosegments were introduced into peptides that were grafted onto hydrogel surfaces. The joint nanosegments between bioactive peptides and base cell culture biomaterials were found to contribute to efficient hESC attachment and proliferation.

利用细胞外基质蛋白(ECM)衍生多肽的生物材料,可以在无异种培养条件下在完全合成的材料上增殖人类多能干细胞(hPSCs)。然而,用ECM衍生肽嫁接的细胞培养生物材料必须使用高浓度的肽反应溶液(例如1000 μg/ml)制备,而用于hPSC培养的ECM包被表面的ECM浓度通常为5 μg/ml。我们设计了一种聚乙二醇(PEG)连接纳米段(连接器),用于基础细胞培养生物材料和生物活性ecm衍生肽之间,以提高ecm衍生肽与hPSCs细胞结合受体之间的接触概率。将带甘氨酸关节纳米段(GCGG)的玻璃质连接蛋白衍生肽通过PEG连接纳米段偶联到聚乙烯醇-共衣康酸水凝胶上,在此水凝胶上培养人胚胎干细胞(hESCs)。hESCs在水凝胶上成功培养,同时保持其多能性和分化潜能,在体外和体内分化为三种胚层诱导的细胞,当将PEG连接纳米片段引入到水凝胶表面的肽中时,仅使用50 μg/ml的ecm衍生肽浓度。生物活性肽与基础细胞培养材料之间的关节纳米段有助于hESC的有效附着和增殖。
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引用次数: 0
The effect of Klotho protein complexed with nanomaterials on bone mesenchymal stem cell performance in the treatment of diabetic ischaemic ulcer Klotho蛋白复合纳米材料对骨间充质干细胞在糖尿病缺血性溃疡治疗中的作用
IF 2.3 4区 工程技术 Q1 BIOCHEMICAL RESEARCH METHODS Pub Date : 2022-09-26 DOI: 10.1049/nbt2.12099
Rui Tang, Gang Zhao, Yuqiao Wang, Ruixue Zhang

A lack of angiogenesis is the key problem in the healing of diabetic foot ulcers. Stem cells have already been proven to have a high potential for angiogenesis. The most important aspects of stem cell therapy are improving the microenvironment, cell homing and continuous factor stimulation. We investigated the effect of Klotho protein to heal wounds by promoting the proliferation and migration of bone mesenchymal stem cells and endothelial cells in vitro. Based on the above study, we produced a compound material by using poly(lactic-co-glycolic acid) (PLGA), chitosan microspheres and gelatin through electro spining technology. The structure of the compound material, just like a sandwich, is that two pieces of PLGA nanofiber films clamped gelatin film which contained chitosan microspheres. In the in vitro release experiment, we could detect the release of Klotho after seven days in the compound material, but the release time was approximately 40 hours for the chitosan microspheres. After seeded bone mesenchymal stem cells (BMSCs) on the surface of the compound material, we observed morphologies of the chitosan microsphere, the PLGA nanofiber and BMSCs by scanning electron microscopy. The nanofiber mesh biological tissue materials could supply an appropriate microenvironment and cell factors for the survival of BMSCs. Compared with the control group, the biological tissue material seeded with BMSCs significantly promoted angiogenesis in the lower limb of diabetic C57BL/6J mice and accelerated diabetic foot wound healing. The compound biomaterial which could continuously stimulate BMSCs through releasing Klotho protein could accelerate wound healing in the diabetic foot and other ischemic ulcers.

血管生成的缺乏是糖尿病足溃疡愈合的关键问题。干细胞已经被证明在血管生成方面具有很高的潜力。干细胞治疗最重要的方面是改善微环境、细胞归巢和持续因子刺激。我们在体外研究了Klotho蛋白通过促进骨间充质干细胞和内皮细胞的增殖和迁移来促进伤口愈合的作用。在此基础上,采用电纺丝技术,以聚乳酸-羟基乙酸(PLGA)、壳聚糖微球和明胶为原料制备了复合材料。这种复合材料的结构就像三明治一样,两片聚乳酸纳米纤维薄膜夹住了含有壳聚糖微球的明胶薄膜。体外释放实验表明,壳聚糖微球的释放时间约为40小时,而Klotho的释放时间约为7 d。将骨间充质干细胞(BMSCs)植入复合材料表面后,通过扫描电镜观察壳聚糖微球、PLGA纳米纤维和BMSCs的形态。纳米纤维网状生物组织材料可为骨髓间充质干细胞的存活提供适宜的微环境和细胞因子。与对照组相比,植入BMSCs的生物组织材料显著促进糖尿病C57BL/6J小鼠下肢血管生成,加速糖尿病足创面愈合。该复合生物材料通过释放Klotho蛋白持续刺激骨髓间充质干细胞,可促进糖尿病足及其他缺血性溃疡的创面愈合。
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引用次数: 1
Biosynthesis of silver nanoparticles using Lawsonia inermis and their biomedical application 银纳米粒子的生物合成及其生物医学应用
IF 2.3 4区 工程技术 Q1 BIOCHEMICAL RESEARCH METHODS Pub Date : 2022-08-30 DOI: 10.1049/nbt2.12096
Eman Alhomaidi, Saade Abdalkareem Jasim, Hawraz Ibrahim M. Amin, Marcos Augusto Lima Nobre, Mehrdad Khatami, Abduladheem Turki Jalil, Saja Hussain Dilfy

Developing biosynthesis of silver nanoparticles (Ag-NPs) using plant extract is an environmentally friendly method to reduce the use of harmful chemical substances. The green synthesis of Ag-NPs by Lawsonia inermis extract and its cellular toxicity and the antimicrobial effect was studied. The physical and chemical properties of synthesised Ag-NPs were investigated using UV-visible spectroscopy, infrared spectroscopy, X-ray diffraction (XRD), scanning, and transmission electron microscopy. The average size of Ag-NPs was 40 nm. The XRD result shows peaks at 2θ = 38.07°, 44.26°, 64.43°, and 77.35° are related to the FCC structure of Ag-NPs. Cytotoxicity of synthesised nanoparticles was evaluated by MTT toxicity test on breast cancer MCF7 cell line. Observations showed that the effect of cytotoxicity of nanoparticles on the studied cell line depended on concentration and time. The obtained IC50 was considered for cells at a dose of 250 μg/ml. Growth and survival rates decreased exponentially with the dose. Antimicrobial properties of Ag-NPs synthesised with extract were investigated against Escherichia coli, Salmonella typhimurium, Bacillus cereus, and Staphylococcus aureus to calculate the minimum inhibitory concentration and the minimum bactericidal concentration of (MBC). The results showed that the synthesised Ag-NPs and the plant extract have antimicrobial properties. The lowest concentration of Ag-NPs that can inhibit the growth of bacterial strains was 25 μg/ml.

利用植物提取物生物合成纳米银是一种减少有害化学物质使用的环保方法。本文研究了白刺槐提取物绿色合成Ag-NPs及其细胞毒性和抗菌作用。采用紫外可见光谱、红外光谱、x射线衍射(XRD)、扫描电镜和透射电镜对合成的Ag-NPs的理化性质进行了研究。Ag-NPs的平均尺寸为40 nm。XRD结果表明,2θ = 38.07°、44.26°、64.43°和77.35°的峰与Ag-NPs的FCC结构有关。对乳腺癌MCF7细胞株进行MTT毒性试验,评价合成纳米颗粒的细胞毒性。结果表明,纳米颗粒对细胞毒性的影响与浓度和时间有关。在250 μg/ml的剂量下考虑细胞的IC50。生长和存活率随剂量呈指数下降。以提取液合成的Ag-NPs对大肠杆菌、鼠伤寒沙门菌、蜡样芽孢杆菌和金黄色葡萄球菌的抑菌性能进行研究,计算最小抑菌浓度和最小杀菌浓度。结果表明,所合成的Ag-NPs和植物提取物均具有抗菌性能。抑制菌株生长的Ag-NPs最低浓度为25 μg/ml。
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引用次数: 7
Lipid-coated bismuth nanoflower as the thermos-radio sensiti for therapy of lung metastatic breast cancer: Preparation, optimisation, and characterisation 脂质包被铋纳米花作为热放射敏感性治疗肺转移性乳腺癌:制备,优化和表征
IF 2.3 4区 工程技术 Q1 BIOCHEMICAL RESEARCH METHODS Pub Date : 2022-08-29 DOI: 10.1049/nbt2.12097
Shushu Xue, Junrong Jiao, Si Miao, Lijun Wang, Yang Liu, Qingjie Zhang, Qiyue Wang, Yu Xi, Yuanyuan Zhang

Lung metastatic breast cancer (LMBC) leads to a large number of deaths in women with breast cancer, and radiotherapy has been considered the common assay for tumour therapy except for surgery. However, radiotherapy still faces problems of low efficiency due to resistance and easily induced side effects. Here, the authors designed lipid-decorated bismuth-based nanoflowers (DP-BNFs) as both a radiosensitiser and a photothermal therapy agent for LMBC treatment. The BNFs were prepared by oxidation of bismuth nitrate and subsequent reduction using sodium borohydride. The preparation parameters and formulation of DP-BNFs were optimised via a single-factor experiment, with the factors including reaction temperature, a molar ratio of reducing agents, and the types and amount of decorated lipid materials. The result indicated that the BNFs prepared at 170°C with the Bi/NaBH4 ratio of 1:0.7 exhibited the best yield and particle size around 160 nm. After being spray dried with lactose to prepare dry powder inhalation (DP-BNF@Lat-MPs), their effects on improving therapeutic efficiency of the radiotherapy and photothermal therapy combination were measured using the western blot assay to determine the tumour apoptosis. In a word, DP-BNF@Lat-MPs could be a novel inhalable integrated microsphere that provides a new possibility for thermoradiotherapy of LMBC.

肺转移性乳腺癌(LMBC)导致大量乳腺癌妇女死亡,放射治疗一直被认为是除手术外肿瘤治疗的常用方法。然而,放射治疗仍然面临着由于耐药和易诱发副作用而效率低的问题。在这里,作者设计了脂质修饰的铋基纳米花(DP-BNFs)作为LMBC治疗的放射增敏剂和光热治疗剂。采用硝酸铋氧化和硼氢化钠还原法制备了bnf。通过单因素实验,以反应温度、还原剂的摩尔比、修饰脂质材料的种类和用量为影响因素,对dp - bnf的制备参数和配方进行优化。结果表明,当Bi/NaBH4比为1:7 . 0时,在170℃条件下制备的bnf产率最高,粒径在160 nm左右。经乳糖喷雾干燥制备干粉吸入(DP-BNF@Lat-MPs)后,采用western blot法检测其对放疗和光热联合治疗的疗效。总之,DP-BNF@Lat-MPs可能是一种新型的可吸入集成微球,为LMBC的热放疗提供了新的可能性。
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引用次数: 0
The role of size in PEGylated liposomal doxorubicin biodistribution and anti-tumour activity 大小在聚乙二醇化脂质体阿霉素生物分布和抗肿瘤活性中的作用。
IF 2.3 4区 工程技术 Q1 BIOCHEMICAL RESEARCH METHODS Pub Date : 2022-08-18 DOI: 10.1049/nbt2.12094
Saba Dadpour, Amin Mehrabian, Mahdieh Arabsalmani, Elaheh Mirhadi, Anis Askarizadeh, Mohammad Mashreghi, Mahmoud Reza Jaafari

The size of nanoliposome-encapsulated drugs significantly affects their therapeutic efficacy, biodistribution, targeting ability, and toxicity profile for the cancer treatment. In the present study, the biodistribution and anti-tumoral activity of PEGylated liposomal Doxorubicin (PLD) formulations with different sizes were investigated. First, 100, 200, and 400 nm PLDs were prepared by remote loading procedure and characterised for their size, zeta potential, encapsulation efficacy, and release properties. Then, in vitro cellular uptake and cytotoxicity were studied by flow cytometry and MTT assay, and compared with commercially available PLD Caelyx®. In vivo studies were applied on BALB/c mice bearing C26 colon carcinoma. The cytotoxicity and cellular uptake tests did not demonstrate any statistically significant differences between PLDs. The biodistribution results showed that Caelyx® and 100 nm liposomal formulations had the most doxorubicin (Dox) accumulation in the tumour tissue and, as a result, considerably suppressed tumour growth compared with 200 and 400 nm PLDs. In contrast, larger nanoparticles (200 and 400 nm formulations) had more accumulation in the liver and spleen. This study revealed that 90 nm Caelyx® biodistribution profile led to the stronger anti-tumour activity of the drug and hence significant survival extension, and showed the importance of vesicle size in the targeting of nanoparticles to the tumour microenvironment for the treatment of cancer.

纳米脂质体包封药物的大小显著影响其治疗癌症的疗效、生物分布、靶向能力和毒性特征。在本研究中,研究了不同大小的聚乙二醇化脂质体阿霉素(PLD)的生物分布和抗肿瘤活性。首先,通过远程加载工艺制备了100nm、200nm和400nm的pld,并对其尺寸、zeta电位、封装效率和释放性能进行了表征。然后,通过流式细胞术和MTT法研究其体外细胞摄取和细胞毒性,并与市售PLD Caelyx®进行比较。体内研究应用于携带C26结肠癌的BALB/c小鼠。细胞毒性和细胞摄取试验未显示pld之间有统计学上的显著差异。生物分布结果显示,Caelyx®和100 nm脂质体制剂在肿瘤组织中具有最多的阿霉素(Dox)积累,因此与200和400 nm脂质体相比,可显著抑制肿瘤生长。相比之下,更大的纳米颗粒(200和400纳米配方)在肝脏和脾脏中积累更多。本研究表明,90 nm的Caelyx®生物分布曲线使药物具有更强的抗肿瘤活性,从而显着延长生存期,并显示了囊泡大小在将纳米颗粒靶向肿瘤微环境以治疗癌症方面的重要性。
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引用次数: 7
Functional characteristics of the rigid elytra in a bamboo weevil beetle Cyrtotrachelus buqueti 竹象鼻虫硬翅的功能特征
IF 2.3 4区 工程技术 Q1 BIOCHEMICAL RESEARCH METHODS Pub Date : 2022-08-12 DOI: 10.1049/nbt2.12095
Xin Li, Yu Zheng

The bamboo weevil beetle, Cyrtotrachelus buqueti, has evolved a particular flight pattern. When crawling, the beetle folds the flexible hind wings and stuffs under the rigid elytra. During flight, the hind wings are deployed through a series of deployment joints that are passively driven by flapping forces. When the hind wings are fully expanded, the unfolding joint realises self-locking. At this time, the hind wings act as a folded wing membrane and flap simultaneously with the elytra to generate aerodynamics. The functional characteristics of the elytra of the bamboo weevil beetle were investigated, including microscopic morphology, kinematic properties and aerodynamic forces of the elytra. In particular, the flapping kinematics of the elytra were measured using high-speed cameras and reconstructed using a modified direct linear transformation algorithm. Although the elytra are passively flapped by the flapping of the hind wings, the analysis shows that its flapping wing trajectory is a double figure-eight pattern with flapping amplitude and angle of attack. The results show that the passive flapping of elytra produces aerodynamic forces that cannot be ignored. The kinematics of the elytra suggest that this beetle may use well-known flapping mechanisms such as a delayed stall and clap and fling.

竹象鼻虫(Cyrtotrachelus buqueti)进化出了一种特殊的飞行模式。爬行时,甲虫折叠灵活的后翅,塞进坚硬的鞘翅下。在飞行过程中,后翼通过一系列由扑翼力被动驱动的展开关节展开。当后翼完全展开时,展开接头实现自锁。此时,后翼充当折叠的翼膜,并与鞘翅同时拍打以产生空气动力。研究了竹象鼻虫鞘翅的微观形态、运动特性和气动力等功能特征。特别地,利用高速摄像机测量了鞘翅的扑动运动学,并使用改进的直接线性变换算法进行了重建。虽然鞘翅是被动受后翼扑动的,但分析表明其扑动翼轨迹为双8字形,具有扑动幅度和迎角。结果表明,鞘翅被动扑动会产生不可忽视的气动力。鞘翅的运动学表明,这种甲虫可能使用众所周知的拍打机制,如延迟失速和拍击和投掷。
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引用次数: 2
Enhancement of antibacterial activity through phyto-fabrication of silver nanoparticles with Ficus thonningii aqueous extracts 无花果水提物制备纳米银增强抗菌活性的研究
IF 2.3 4区 工程技术 Q1 BIOCHEMICAL RESEARCH METHODS Pub Date : 2022-08-09 DOI: 10.1049/nbt2.12093
Dickens A. Ondigo, Were L. L. Munyendo, Dickson Andala, Apollo O. Maima, Josephat M. Mosweta, Kevin W. Odhiambo

The World Health Organisation reports higher levels of bacterial resistance to cephalosporins and carbapenems of above 54%. The sufficient redox capabilities of Ficus thonningii phytochemicals for Ag+ reduction to Ag0 and ultimately aggregation to nucleation are exploited for the first time in attempting to enhance the antibacterial activity. Solution colour change to brown due to surface plasmon resonance phenomenon confirmed nanoparticle fabrication with a UV/Vis absorption peak at 426 nm. Fourier Transform Infrared spectra revealed functional groups (C=C at 1620–1680 cm−1; C=H at 1400–1600 cm−1 aromatics) for encapsulation, stabilisation, and reduction of the silver ion. The Dynamic Light Scattering technique verified F. thonningii encapsulated silver nanoparticles particle size of 57.84 nm with a negative zeta potential (−19.8 mV) as proof of stability. The surface, shape and topographical features were shown by Scanning Electron Microscopy as spherical orientations. An enhanced antimicrobial efficacy was displayed by the nanoparticles (inhibition zones of 26.1, 24.1 and 15.2 mm from 11.5, 10.6 and 6.5 mm) for Staphylococcus aureus, Streptococcus pyrogenes and Escherichia coli, respectively, compared to Flucloxacillin standard that was in the ranges of 21.5, 23.5 and 25.7 mm. The enhanced potency provides a basis for diversified approaches of generating novel drugs for treating bacterial infections.

世界卫生组织报告说,细菌对头孢菌素和碳青霉烯类的耐药性高于54%。本文首次利用榕树植物化学物质充分的氧化还原能力,将Ag+还原为Ag0并最终聚集成核,试图提高榕树植物的抗菌活性。由于表面等离子体共振现象,溶液颜色变为棕色,证实了纳米颗粒的制备,其紫外/可见吸收峰位于426 nm。傅里叶变换红外光谱显示官能团(C=C,在1620-1680 cm−1;C=H (1400-1600 cm−1芳烃)用于包封、稳定和还原银离子。动态光散射技术验证了F. thonningii封装的银纳米粒子粒径为57.84 nm, zeta电位为负(- 19.8 mV),证明了其稳定性。扫描电镜显示其表面、形状和地形特征为球形取向。与氟氯西林对金黄色葡萄球菌、热原链球菌和大肠杆菌的抑制范围分别为21.5、23.5和25.7 mm相比,纳米颗粒对金黄色葡萄球菌、热原链球菌和大肠杆菌的抑制范围分别为26.1、24.1和15.2 mm。效力的增强为开发治疗细菌感染的新药提供了多种途径。
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引用次数: 1
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IET nanobiotechnology
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