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Novel Tubeimoside I liposomal drug delivery system in combination with gemcitabine for the treatment of pancreatic cancer. 新型 Tubeimoside I 脂质体给药系统与吉西他滨联合治疗胰腺癌。
Pub Date : 2024-01-01 Epub Date: 2024-09-03 DOI: 10.1080/17435889.2024.2382076
Shuhui Li, Yuansheng Liu, Xiaojun Sui, Yuzhen Zhuo, He Siqi, Zhang Sijia, Zhang Hui, Li Dihua, Zhang Dapeng, Yang Lei

Aim: To evaluate the anti-pancreatic cancer effect of novel Tubeimoside I multifunctional liposomes combined with gemcitabine.Methods: Liposomes were prepared through the thin film hydration method, with evaluations conducted on parameters including encapsulation efficiency (EE%), particle size, polydispersity index (PDI), zeta potential (ZP), storage stability, and release over a 7-day period. The cellular uptake rate, therapeutic efficacy in vitro and in vivo and the role of immune microenvironment modulation were evaluated.Results: The novel Tubeimoside I multifunctional liposomal exhibited good stability, significant anti-cancer activity, and immune microenvironment remodeling effects. Furthermore, it showed a safety profile.Conclusion: This study underscores the potential of Novel Tubeimoside I multifunctional liposomal as a promising treatment option for pancreatic cancer.

目的:评估新型 Tubeimoside I 多功能脂质体联合吉西他滨的抗胰腺癌效果:方法:采用薄膜水合法制备脂质体,并对其封装效率(EE%)、粒度、多分散指数(PDI)、ZP、储存稳定性和 7 天释放等参数进行评估。对细胞摄取率、体外和体内疗效以及免疫微环境调节作用进行了评估:结果:新型 Tubeimoside I 多功能脂质体具有良好的稳定性、显著的抗癌活性和免疫微环境重塑作用。此外,它还显示出良好的安全性:本研究强调了新型 Tubeimoside I 多功能脂质体作为胰腺癌治疗选择的潜力。
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引用次数: 0
Sol-gel synthesis of magnesium oxide nanoparticles and their evaluation as a therapeutic agent for the treatment of osteoarthritis. 氧化镁纳米粒子的溶胶凝胶合成及其作为骨关节炎治疗剂的评估。
Pub Date : 2024-01-01 Epub Date: 2024-08-07 DOI: 10.1080/17435889.2024.2382421
Sen Mei, Fangchao Jiang, Na Liu, Zhizi Feng, Yu Zheng, Wei Yang, Weizhong Zhang, Yingna Cui, Weiming Wang, Jin Xie, Nan Zhang

Aim: We synthesized MgO NPs via sol-gel reaction and investigated them as carriers to deliver Mg2+ to the affected joint for osteoarthritis (OA).Materials & methods: The physicochemical properties of samples were characterized by transmission electron microscope (TEM), dynamic light scattering (DLS) and x-ray diffraction (XRD). The release of Mg2+ was monitored by ICP-MS. The potential cytotoxicity was evaluated using MTT assay. The efficacy and biosafety were evaluated in a rabbit OA model.Results: MgO NPs can prolong the Mg2+ release time from 0.5 h to 12 h. No significant cytotoxicity was observed when concentrations below 250 μg/ml. Intra-articular samples could effectively alleviate the degeneration and destruction of the cartilage.Conclusion: this study demonstrates the potential of MgO NPs as a safe and effective treatment of OA. Simultaneously, the size of the particles may play a significant role in influencing the therapeutic outcome.

目的:我们通过溶胶-凝胶反应合成了氧化镁 NPs,并研究了将其作为载体将 Mg2+ 输送到受影响关节以治疗骨关节炎(OA)。材料与方法:透射电子显微镜(TEM)、动态光散射(DLS)和 X 射线衍射(XRD)对样品的理化性质进行了表征。ICP-MS 监测了 Mg2+ 的释放。使用 MTT 试验评估了潜在的细胞毒性。在兔 OA 模型中评估了药效和生物安全性。研究结果当浓度低于 250 μg/ml 时,未观察到明显的细胞毒性。关节内样本可有效缓解软骨的退化和破坏。结论:本研究表明氧化镁氧化物具有安全有效治疗 OA 的潜力。同时,颗粒的大小可能会对治疗效果产生重要影响。
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引用次数: 0
Enhancing radiotherapy for melanoma: the promise of high-Z metal nanoparticles in radiosensitization. 加强黑色素瘤的放射治疗:高 Z 值金属纳米粒子在放射增敏方面的前景。
Pub Date : 2024-01-01 Epub Date: 2024-10-09 DOI: 10.1080/17435889.2024.2403325
Abolfazl Bemidinezhad, Shaghayegh Radmehr, Negin Moosaei, Zohreh Efati, Prashant Kesharwani, Amirhossein Sahebkar

Melanoma is a type of skin cancer that can be challenging to treat, especially in advanced stages. Radiotherapy is one of the main treatment modalities for melanoma, but its efficacy can be limited due to the radioresistance of melanoma cells. Recently, there has been growing interest in using high-Z metal nanoparticles (NPs) to enhance the effectiveness of radiotherapy for melanoma. This review provides an overview of the current state of radiotherapy for melanoma and discusses the physical and biological mechanisms of radiosensitization through high-Z metal NPs. Additionally, it summarizes the latest research on using high-Z metal NPs to sensitize melanoma cells to radiation, both in vitro and in vivo. By examining the available evidence, this review aims to shed light on the potential of high-Z metal NPs in improving radiotherapy outcomes for patients with melanoma.

黑色素瘤是一种治疗难度很大的皮肤癌,尤其是晚期患者。放疗是黑色素瘤的主要治疗方法之一,但由于黑色素瘤细胞的放射抗性,其疗效可能有限。最近,人们对使用高Z金属纳米粒子(NPs)来提高黑色素瘤放疗的效果越来越感兴趣。本综述概述了黑色素瘤放疗的现状,并讨论了通过高Z金属纳米粒子实现放射增敏的物理和生物机制。此外,它还总结了利用高Z金属氮氧化物在体外和体内使黑色素瘤细胞对辐射敏感的最新研究。通过研究现有证据,本综述旨在阐明高Z值金属氮氧化物在改善黑色素瘤患者放疗效果方面的潜力。
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引用次数: 0
Mineralo-organic particles inhibit influenza A virus infection by targeting viral hemagglutinin activity. 矿物有机微粒通过靶向病毒血凝素活性抑制甲型流感病毒感染。
Pub Date : 2024-01-01 Epub Date: 2024-09-25 DOI: 10.1080/17435889.2024.2403326
Huan-Jung Chiang, Hsin-Hsin Peng, Kuo-Feng Weng, Kuei-Ching Hsiung, Chieh-Yu Liang, Shun-Li Kuo, David M Ojcius, John Ding-E Young, Shin-Ru Shih

Aim: Mineralo-organic particles, naturally present in human body fluids, participate in ectopic calcification and inflammatory diseases. These particles coexist with influenza A virus (IAV) in the same microenvironment during viral infection. Our objective was to investigate the functional consequences of the potential interactions between these particles and the virions.Materials & methods: We used in vitro models, including electron microscopy, fluorescence microscopy, hemagglutination assay and viral infection assays to examine the interactions.Results: Mineralo-organic particles bind to IAV virions through interactions involving particle-bound fetuin-A and mineral content, effectively engaging viral hemagglutinin. These interactions result in hindered viral infection.Conclusion: These findings uncover the novel interactions between mineralo-organic particles and IAV, highlighting the impact of virus microenvironment complexity.

目的:天然存在于人体体液中的矿物有机微粒参与了异位钙化和炎症性疾病。在病毒感染期间,这些颗粒与甲型流感病毒(IAV)共存于同一微环境中。我们的目的是研究这些颗粒与病毒之间潜在相互作用的功能性后果:我们使用了体外模型,包括电子显微镜、荧光显微镜、血凝试验和病毒感染试验来研究这些相互作用:结果:矿物-有机颗粒通过与颗粒结合的胎盘素-A和矿物成分的相互作用与 IAV 病毒结合,有效地与病毒血凝素结合。这些相互作用导致病毒感染受阻:这些发现揭示了矿物有机微粒与 IAV 之间的新型相互作用,凸显了病毒微环境复杂性的影响。
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引用次数: 0
Nanoparticles for the treatment of inflammatory conditions. 用于治疗炎症的纳米颗粒。
Pub Date : 2024-01-01 Epub Date: 2024-01-17 DOI: 10.2217/nnm-2023-0324
Christina Janko, Mehtap Civelek, Iwona Cicha, Helmut Spielvogel, Harald Unterweger, Christoph Alexiou
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引用次数: 0
Nanomedicine-mediated drug delivery for potential treatment of inflammatory bowel disease: a narrative review. 纳米药物介导的药物输送用于炎症性肠病的潜在治疗:综述。
Pub Date : 2024-01-01 Epub Date: 2024-01-29 DOI: 10.2217/nnm-2023-0267
Zhina Majdzadeh Ardekani, Ana L Lorenzo-Leal, Horacio Bach

Background & aims: Inflammatory bowel disease (IBD) is a condition characterized by chronic inflammation of the gastrointestinal tract, manifesting as either Crohn's disease (CrD) or ulcerative colitis (UC). Current treatment options for CrD and UC primarily focus on symptom management. In recent years, advancements in nanotechnology have increased the clinical applicability of nanoparticles (NPs) in treating IBD. This review explores the current research on NP-mediated drug-delivery systems for IBD treatment and assesses its advantages and limitations. Results: The authors examine diverse nanomedicine applications for IBD and address the current challenges and prospects in the field to advance nanomediated therapies in the future. Conclusion: Innovative NP-based treatment strategies promise a reliable and effective approach to IBD management.

背景与目的:炎症性肠病(IBD)是一种以胃肠道慢性炎症为特征的疾病,表现为克罗恩病(CRD)或溃疡性结肠炎(UC)。目前治疗克罗恩病和溃疡性结肠炎的方法主要集中在症状控制上。近年来,纳米技术的进步提高了纳米粒子(NPs)在治疗 IBD 方面的临床应用。本综述探讨了目前以 NP 为介导的 IBD 治疗药物递送系统的研究情况,并评估了其优势和局限性。结果:作者研究了纳米医学在 IBD 中的各种应用,并探讨了该领域当前面临的挑战和未来推进纳米介导疗法的前景。结论:基于 NP 的创新治疗策略有望成为治疗 IBD 的可靠而有效的方法。
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引用次数: 0
Oxidative stress-induced neurotoxicity of quantum dots and influencing factors. 量子点氧化应激诱导的神经毒性及其影响因素
Pub Date : 2024-01-01 Epub Date: 2024-04-12 DOI: 10.2217/nnm-2023-0326
Qing Fang, Meng Tang

Quantum dots (QDs) have significant potential for treating and diagnosing CNS diseases. Meanwhile, the neurotoxicity of QDs has garnered attention. In this review, we focus on elucidating the mechanisms and consequences of CNS oxidative stress induced by QDs. First, we discussed the pathway of QDs transit into the brain. We then elucidate the relationship between QDs and oxidative stress from in vivo and in vitro studies. Furthermore, the main reasons and adverse outcomes of QDs leading to oxidative stress are discussed. In addition, the primary factors that may affect the neurotoxicity of QDs are analyzed. Finally, we propose potential strategies for mitigating QDs neurotoxicity and outline future perspectives for their development.

量子点(QDs)在治疗和诊断中枢神经系统疾病方面具有巨大潜力。与此同时,量子点的神经毒性也引起了人们的关注。在这篇综述中,我们重点阐述了量子点诱导中枢神经系统氧化应激的机制和后果。首先,我们讨论了 QDs 进入大脑的途径。然后,我们从体内和体外研究中阐明了 QDs 与氧化应激之间的关系。此外,我们还讨论了 QDs 导致氧化应激的主要原因和不良后果。此外,还分析了可能影响 QDs 神经毒性的主要因素。最后,我们提出了减轻 QDs 神经毒性的潜在策略,并概述了这些策略的未来发展前景。
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引用次数: 0
Development and evaluation of berberine-loaded bigel for the treatment of hyperpigmentation on B16F10 melanoma cell line. 开发和评估用于治疗 B16F10 黑色素瘤细胞系色素沉着的小檗碱负载 bigel。
Pub Date : 2024-01-01 Epub Date: 2024-07-26 DOI: 10.1080/17435889.2024.2370759
Bharti Mangla, Pankaj Kumar, Zuber Ahamad, Shamama Javed, Waquar Ahsan, Geeta Aggarwal

Aim: The aim of this study was to optimize, develop, characterize and evaluate a topical nanobigel (BG) formulation containing Berberine (BRB) that exhibits anti-melanogenic properties.Materials & methods: The Berberine-loaded bigel (BRB@BG) formulation was prepared by homogenously mixing the optimized hydrogel and oleogel. BRB@BG was characterized in vitro and cytotoxicity study was conducted to evaluate its effects on murine skin melanoma B16F10 cell lines.Results: The optimized BRB@BG exhibited uniform texture with nanometric size, desirable spreadability and extrudability, suitable for topical applications. Cytotoxicity studies revealed that BRB@BG had a lower IC50 value (4.84 μg/ml) on B16F10 cell lines compared with drug alone.Conclusion: In conclusion, the developed BRB@BG formulation showed good potential as safe and effective topical treatment for hyperpigmentation.

目的:本研究旨在优化、开发、表征和评估一种含有小檗碱(BRB)、具有抗黑色素生成特性的局部纳米凝胶(BG)配方。材料与方法:将优化的水凝胶和油凝胶均匀混合,制备出小檗碱负载 bigel(BRB@BG)配方。对 BRB@BG 进行了体外表征和细胞毒性研究,以评估其对小鼠皮肤黑色素瘤 B16F10 细胞系的影响。结果显示优化后的 BRB@BG 具有纳米级的均匀质地、理想的铺展性和挤出性,适合局部应用。细胞毒性研究表明,与单独使用药物相比,BRB@BG 对 B16F10 细胞株的 IC50 值(4.84 μg/ml)更低。结论总之,所开发的 BRB@BG 制剂显示出作为安全有效的色素沉着局部治疗药物的良好潜力。
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引用次数: 0
Recent advances in nanostructured delivery systems for vancomycin. 万古霉素纳米结构给药系统的最新进展。
Pub Date : 2024-01-01 Epub Date: 2024-08-15 DOI: 10.1080/17435889.2024.2377063
Mohabbat Ansari, Mohsen Shahlaei, Simzar Hosseinzadeh, Sajad Moradi

Despite the development of new generations of antibiotics, vancomycin remained as a high-efficacy antibiotic for treating the infections caused by MRSA. Researchers have explored various nanoformulations, aiming to enhance the therapeutic efficacy of vancomycin. Such novel formulations improve the effectiveness of drug cargoes in treating bacterial infections and minimizing the risk of adverse effects. The vast of researches have focuses on enhancing the permeation ability of vancomycin through different biological barriers especially those of gastrointestinal tract. Increasing the drug loading and tuning the drug release from nanocarrier are other important goal for many conducted studies. This study reviews the newest nano-based formulations for vancomycin as a key antibiotic in treating hospitalized bacterial infections.

尽管新一代抗生素不断问世,但万古霉素仍是治疗 MRSA 感染的高效抗生素。研究人员探索了各种纳米制剂,旨在提高万古霉素的疗效。这些新型制剂提高了药物在治疗细菌感染方面的有效性,并将不良反应的风险降至最低。大量研究的重点是提高万古霉素通过不同生物屏障(尤其是胃肠道屏障)的渗透能力。提高纳米载体的载药量和药物释放量也是许多研究的重要目标。本研究综述了万古霉素作为治疗住院细菌感染的主要抗生素的最新纳米制剂。
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引用次数: 0
Antitumoral melatonin-loaded nanostructured lipid carriers. 抗肿瘤褪黑激素纳米脂质载体。
Pub Date : 2024-01-01 Epub Date: 2024-08-02 DOI: 10.1080/17435889.2024.2379757
Lorena Bonilla-Vidal, Marta Świtalska, Marta Espina, Joanna Wietrzyk, Maria Luisa García, Eliana B Souto, Anna Gliszczyńska, Elena Sánchez-López

Aim: Cancer constitutes the second leading cause of death worldwide, with conventional therapies limited by significant side effects. Melatonin (MEL), a natural compound with antitumoral properties, suffers from instability and low solubility. To overcome these issues, MEL was encapsulated into nanostructured lipid carriers (MEL-NLC) containing rosehip oil to enhance stability and boost its antitumoral activity.Methods: MEL-NLC were optimized by a design of experiments approach and characterized for their physicochemical properties. Stability and biopharmaceutical behavior were assessed, along with interaction studies and in vitro antitumoral efficacy against various cancer cell lines.Results: Optimized MEL-NLC exhibited desirable physicochemical characteristics, including small particle size and sustained MEL release, along with long-term stability. In vitro studies demonstrated that MEL-NLC selectively induced cytotoxicity in several cancer cell lines while sparing healthy cells.Conclusion: MEL-NLC represent a promising alternative for cancer, combining enhanced stability and targeted antitumoral activity, potentially overcoming the limitations of conventional treatments.

目的:癌症是全球第二大死因,传统疗法因副作用大而受到限制。褪黑素(MEL)是一种具有抗肿瘤特性的天然化合物,但存在不稳定和溶解度低的问题。为了克服这些问题,我们将褪黑素封装到含有玫瑰果油的纳米结构脂质载体(MEL-NLC)中,以提高其稳定性并增强其抗肿瘤活性。研究方法通过实验设计方法对 MEL-NLC 进行了优化,并对其理化性质进行了表征。对其稳定性和生物制药行为进行了评估,同时还进行了相互作用研究和体外抗肿瘤效果研究。结果:优化后的 MEL-NLC 具有理想的理化特性,包括小粒径、持续释放 MEL 以及长期稳定性。体外研究表明,MEL-NLC 可选择性地诱导多种癌细胞株产生细胞毒性,同时保护健康细胞。结论:MEL-NLCMEL-NLC 是一种很有前景的癌症替代疗法,它结合了更强的稳定性和靶向抗肿瘤活性,有可能克服传统疗法的局限性。
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引用次数: 0
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Nanomedicine (London, England)
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