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Innovations in targeted drug delivery: From nanotechnology to clinical applications 靶向给药的创新:从纳米技术到临床应用
Pub Date : 2025-12-09 DOI: 10.1016/j.nxnano.2025.100336
Akash Srivastava, Asad Ahmad, Shaiber Siddiqui, Anas Islam
Targeted drug delivery systems (TDDS) have emerged as transformative platforms for enhancing therapeutic precision while minimizing systemic toxicity. By exploiting mechanisms such as the enhanced permeability and retention (EPR) effect, ligand-based active targeting, and stimulus-responsive release, these systems offer improved pharmacokinetics and site-specific action. Clinical success stories underscore their translational impact—liposomal formulations like Doxil® reduce doxorubicin-related cardiotoxicity by nearly 50 %, while lipid nanoparticle-based Onpattro® became the first FDA-approved RNA interference therapy, paving the way for mRNA vaccine technologies. Despite such milestones, challenges persist, including tumor heterogeneity, immunogenicity, and regulatory complexities, which hinder broader clinical adoption. Emerging strategies—hybrid nanocarriers, AI-driven drug release, and integration with digital health—are reshaping the future of personalized medicine. This review provides a comprehensive analysis of current nanocarrier platforms, clinical progress, regulatory trends, and innovations driving the next generation of targeted drug delivery.
靶向给药系统(TDDS)已经成为提高治疗精度同时最小化全身毒性的变革性平台。通过利用增强渗透性和滞留性(EPR)效应、基于配体的主动靶向和刺激响应释放等机制,这些系统提供了更好的药代动力学和位点特异性作用。临床成功案例强调了它们的转化影响-脂质体制剂如Doxil®可将阿霉素相关的心脏毒性降低近50% %,而基于脂质纳米颗粒的Onpattro®成为fda批准的第一个RNA干扰疗法,为mRNA疫苗技术铺平了道路。尽管取得了这些里程碑,但挑战依然存在,包括肿瘤异质性、免疫原性和监管复杂性,阻碍了更广泛的临床应用。新兴战略——混合纳米载体、人工智能驱动的药物释放以及与数字健康的整合——正在重塑个性化医疗的未来。这篇综述全面分析了当前的纳米载体平台、临床进展、监管趋势以及推动下一代靶向药物递送的创新。
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引用次数: 0
The influence of ion beam-synthesized InSb nanocrystals on current-voltage characteristics of SiO2 layers in MOS structures 离子束合成InSb纳米晶对MOS结构中SiO2层电流-电压特性的影响
Pub Date : 2025-12-09 DOI: 10.1016/j.nxnano.2025.100340
Alexander K. Fedotov , Valeria Yu. Leonenko , Julia A. Fedotova , Ida E. Tyschenko
Current density (J) as a function of electric field (E) at different temperatures (T) is studied in Al/SiO2<InSb> /Si/Al metal-oxide-semiconductor (MOS) structures fabricated using silicon-on-insulator and ion-beam synthesis technologies. The MOS structures containing SiO2 layers implanted with Sb+ and In+ ions are investigated both before and after annealing at 800 and 1100 ℃. Annealing leads to the formation of InSb nanocrystals (5 – 25 nm in diameter) to result in a unique charge distribution within SiO2. Three distinct types of J(E, T) behavior are observed in the temperature range 2 < T < 300 K and at electric fields up to ±6.7 × 105 V/cm. At E < 4 × 104 V/cm, all samples exhibit ohmic conduction, whereas at higher fields (E > 2 ×105 V/cm) the J(E, T) dependences follow the space charge-limited current (SCLC) models: Below 40 K, the Mott-Gurney law applies, indicating monoenergetic traps near the SiO2 midgap. Above 40 K, the J(E, T) behavior is consistent with the Mark-Helfrich SCLC model, revealing an exponential energy distribution of traps in the “tails” of localized states in SiO2. These localized states are associated with an implantation-induced structural disorder. An energy band diagram of the annealed MOS structures has been developed to directly correlate the Fermi-level shifts and the evolution of trap states with the formation of InSb nanocrystals. This correlation provides a benchmark insight into the redistribution of free and localized charges in modified SiO2<InSb> layers and explains their influence on the observed J(E, T) characteristics. The contribution of this work lies in establishing a direct link between the nanocrystal-induced disorder and the charge redistribution in modified oxide layers subjected to annealing.
采用绝缘体上硅和离子束合成技术制备了Al/SiO2<;InSb>; /Si/Al金属氧化物半导体(MOS)结构,研究了不同温度(T)下电流密度(J)随电场(E)的变化规律。研究了在800℃和1100℃退火前后注入Sb+和In+离子的SiO2层MOS结构。退火可形成InSb纳米晶体(直径5 - 25 nm),从而使SiO2内部具有独特的电荷分布。在温度范围2 <; T <; 300 K和电场高达±6.7 × 105 V/cm时,观察到三种不同类型的J(E, T)行为。在E <; 4 × 104 V/cm时,所有样品都表现出欧姆传导,而在更高的场(E >; 2 ×105 V/cm)下,J(E, T)依赖关系遵循空间电荷限制电流(SCLC)模型:低于40 K时,适用莫特-格尼定律,表明SiO2中隙附近存在单能阱。在40 K以上,J(E, T)行为符合Mark-Helfrich SCLC模型,揭示了SiO2中局域态“尾部”陷阱的指数能量分布。这些局部状态与植入引起的结构紊乱有关。本文建立了退火MOS结构的能带图,直接将费米能级位移和阱态的演化与InSb纳米晶体的形成联系起来。这种相关性为研究修饰SiO2<;InSb>; 层中自由电荷和定域电荷的再分布提供了基准,并解释了它们对观察到的J(E, T)特性的影响。这项工作的贡献在于建立了纳米晶体诱导的无序和经过退火的修饰氧化物层中的电荷重新分配之间的直接联系。
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引用次数: 0
Naringenin and quercetin nanoparticles as a dual strategy for topical management of diabetic retinopathy 柚皮素和槲皮素纳米颗粒作为局部治疗糖尿病视网膜病变的双重策略
Pub Date : 2025-12-08 DOI: 10.1016/j.nxnano.2025.100332
Janhavi S. Ganore , Umesh D. Laddha , Prashant S. Adhav , Chanchal S. Pagar , Sanjay J. Kshirsagar , Neelam L. Dashputre , Pavan B. Udavant
Diabetic retinopathy (DR) is a complication associated with diabetes that impacts the retinal microvasculature and leads to vision problems. The currently available treatments for diabetic retinopathy are invasive and associated with pain and side effects, which lead to patient noncompliance. This research aims to formulate nanoparticles of two PPAR-γ agonists, viz. quercetin and naringenin, by using two different polymers, as HPMC-Poloxamer and PLGA, respectively. For optimization, a 32 Factorial design was used. The HPH pressure and PLGA concentration were independent variables for naringenin nanoparticles; Poloxamer concentration and HPH pressure were independent variables for quercetin nanoparticles. The particle size, PDI, and entrapment efficiency were the responses. The optimized batch of naringenin showed a particle size of 187.1 nm, PDI 0.117, and percent entrapment of 91 %, whereas the optimized quercetin batch showed a particle size of 185 nm, PDI 0.289, and 82.5 % entrapment. The optimized batch was further subjected to spray drying and characterized by various in-vitro, ex-vivo, and in-vivo methods. Nanoparticles showed spherical shape with smooth morphology in the SEM study, and XRD confirmed the entrapment of both drugs in the selected polymers. In vitro drug release study showed the comparatively rapid drug release of quercetin (90.55 ± 0.972 %) and more sustained drug release of naringenin (48.90 ± 0.894 %) at the end of 10 h. Differences in the release of drugs are characteristic of particular polymers used during preparation. This will prevent competition between two drugs to bind to receptors. Results from the isotonicity study, ex-vivo examination indicate the non-irritant nature and safety of the formulation. The in-vivo study on Wistar rats suggests formulation containing a combination of nanoparticles showed a synergistic effect in reducing VEGF, an important factor in diabetic retinopathy, than the individual treatment with nanoparticles of the particular drug. The study finding suggests that treatment with a combination of nanoparticles of quercetin and naringenin prepared by two different polymers having different drug release patterns can be considered as an alternate non-invasive therapy approach for the treatment of diabetic retinopathy.
糖尿病视网膜病变(DR)是一种与糖尿病相关的并发症,它会影响视网膜微血管并导致视力问题。目前可用的治疗糖尿病视网膜病变是侵入性的,并伴有疼痛和副作用,这导致患者不遵守。本研究旨在制备两种PPAR-γ激动剂,即槲皮素和柚皮素的纳米颗粒,分别使用两种不同的聚合物,分别为HPMC-Poloxamer和PLGA。为了优化,采用32因子设计。HPH压力和PLGA浓度是柚皮素纳米颗粒的自变量;波洛沙姆浓度和HPH压力是槲皮素纳米颗粒的独立变量。粒径、PDI和捕集效率是响应。柚皮素的粒径为187.1 nm, PDI为0.117,包封率为91% %;槲皮素的粒径为185 nm, PDI为0.289,包封率为82.5 %。优化后的批料进一步进行喷雾干燥,并通过各种体外、离体和体内方法进行表征。在SEM研究中,纳米颗粒呈球形,形貌光滑,XRD证实了所选聚合物中两种药物的包埋。体外释药研究表明,槲皮素的释药速度较快(90.55 ± 0.972 %),柚皮素的释药速度较慢(48.90 ± 0.894 %),释药时间为10 h。药物释放的差异是制备过程中使用的特定聚合物的特征。这将防止两种药物在与受体结合时相互竞争。等渗性研究和离体试验结果表明该制剂无刺激性和安全性。Wistar大鼠体内研究表明,与单独使用特定药物的纳米颗粒治疗相比,含有纳米颗粒组合的配方在降低VEGF(糖尿病视网膜病变的重要因素)方面具有协同作用。该研究结果表明,槲皮素和柚皮素纳米颗粒的联合治疗可以被认为是治疗糖尿病视网膜病变的一种替代的非侵入性治疗方法。
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引用次数: 0
Sennoside-functionalized ZrO₂ nanoparticles via Cassia angustifolia: Gram-selective antibacterial and anticancer nanoplatform with green synthesis 以决明子为原料的senno苷功能化的ZrO 2纳米粒子:绿色合成的革兰氏选择性抗菌抗癌纳米平台
Pub Date : 2025-12-06 DOI: 10.1016/j.nxnano.2025.100330
Aarti Jathar , Samreen Fatema , Mazahar Farooqui , Abhay Dashrath , Dattatraya Jirekar , Pramila Ghumare
Sennoside-functionalized zirconium dioxide nanoparticles (Sen–ZrO₂ NPs) were engineered via a single-step green synthesis route using Cassia angustifolia leaf extract as both a bio reductant and stabilizer. Structural characterization confirmed phase-pure tetragonal ZrO₂ formation through X-ray diffraction (XRD), while Fourier-transform infrared spectroscopy (FTIR) verified sennoside anchoring via characteristic CO and O–H vibrations at 1680 cm⁻¹ and 3605 cm⁻¹. Scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM/EDS) revealed spherical morphologies with uniform elemental distribution. The Sen–ZrO₂ NPs exhibited pronounced Gram-selective antibacterial activity, demonstrating a fourfold potency enhancement against Staphylococcus aureus (MIC = 64 µg mL⁻¹) compared to unmodified ZrO₂. Time-kill assays further demonstrated a rapid 4-log reduction in bacterial viability within 6 h. Against MCF-7 breast cancer cells, the nanoparticles displayed dose-dependent cytotoxicity (IC₅₀ = 61.44 µg mL⁻¹), representing a 2.3-fold improvement over bare ZrO₂. This dual bioactivity is attributed to sennoside-mediated redox modulation and surface functionalization, which act synergistically to enhance membrane disruption and reactive oxygen species (ROS) generation. This work establishes a sustainable plant-engineered ZrO₂ nanoplatform with integrated antibacterial–anticancer functionality, presenting a viable green approach to advanced nanotherapeutics for combating antimicrobial resistance and cancer.
以决明子叶提取物为生物还原剂和稳定剂,通过一步绿色合成工艺制备了senno苷功能化二氧化锆纳米粒子(Sen-ZrO₂NPs)。结构表征通过x射线衍射(XRD)证实了相纯四方ZrO₂形成,而傅里叶变换红外光谱(FTIR)证实了sennoside通过1680 cm⁻¹ 和3605 cm⁻¹的特征CO和O-H振动锚定。扫描电子显微镜和能量色散x射线能谱分析(SEM/EDS)显示其呈球形,元素分布均匀。Sen-ZrO₂NPs表现出明显的革兰选择性抗菌活性,与未修饰的ZrO₂相比,对金黄色葡萄球菌(MIC = 64 µg mL⁻¹)的效力增强了四倍。时间杀伤试验进一步表明,细菌活力在6 h内迅速降低4对数。对MCF-7乳腺癌细胞,纳米颗粒显示出剂量依赖性的细胞毒性(IC₅₀= 61.44 µg mL⁻¹),比裸ZrO₂提高2.3倍。这种双重生物活性归因于sennoside介导的氧化还原调节和表面功能化,它们协同作用以增强膜破坏和活性氧(ROS)的产生。这项工作建立了一个具有综合抗菌抗癌功能的可持续植物工程ZrO 2纳米平台,为对抗抗生素耐药性和癌症的先进纳米治疗提供了可行的绿色途径。
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引用次数: 0
Characterization of cadmium-doped nZVI residuals: Structure, morphology, and photoelectrochemical properties 掺杂镉的nZVI残留物的表征:结构、形态和光电化学性质
Pub Date : 2025-12-05 DOI: 10.1016/j.nxnano.2025.100327
Camila Morales-Navas , Annelis O. Sánchez-Álvarez , Joesene J. Soto-Pérez , Eduardo Larios , Arnulfo Rojas , Carlos R. Cabrera
This study explores a novel approach to reuse the residual material generated after environmental remediation processes using nanoscale zero-valent iron (nZVI) nanoparticles. While nZVI has been evaluated for the removal of heavy metal ions in contaminated areas, it has yet to provide a definitive solution. We propose utilizing the residual nZVI material for photo-harvesting in photoelectrochemical cells. Here, we report on the material's transformation into a Fe0/FexOy Cd1−xFexOy catalyst and investigate its potential through X-ray photoelectron spectroscopy (XPS), inductively coupled plasma (ICP), transmission electron microscopy (TEM), and X-ray diffraction (XRD). On the other hand, traditional characterization methods were also employed to validate the versatility of the Cathodic Particle Coulometry (CPC) technique. This method is especially sensitive to conductive and semiconductive particles, such as metal oxides or corrosion products, as they generate distinct current signals when reduced or oxidized under cathodic conditions. CPC permits the sizing of the particle, and the obtained results are discussed hereinafter. Interestingly, a staircase response was also obtained for the most concentrated sample of particles suggesting a blocking mechanism. The inclusion of cadmium (Cd) in the nZVI residual material resulted in structural changes, shifting from a hexagonal hematite lattice to a face-centered cubic CdFe2O4 phase. Incident photon-to-current efficiency measurements revealed a 10-fold increase in efficiency compared to the original nZVI material. Furthermore, photovoltage measurements as a function of Cd content suggest that Cd alters the semiconductor properties of the FexOy structure. This study highlights the potential of cadmium-doped iron residual materials (Cd-IR) in enhancing the performance of photoelectrochemical solar cells (PSC) and provides insights into the changes in material properties and structure due to Cd incorporation.
本研究探索了一种利用纳米级零价铁(nZVI)纳米颗粒对环境修复过程中产生的残留物质进行再利用的新方法。虽然nZVI已经被评估为去除污染地区的重金属离子,但它还没有提供一个明确的解决方案。我们建议利用残留的nZVI材料在光电化学电池中进行光收集。在这里,我们报道了材料转变为Fe0/FexOy Cd1−xFexOy催化剂,并通过x射线光电子能谱(XPS),电感耦合等离子体(ICP),透射电子显微镜(TEM)和x射线衍射(XRD)研究了它的潜力。另一方面,传统的表征方法也被用来验证阴极粒子库仑法(CPC)技术的通用性。该方法对导电和半导体颗粒(如金属氧化物或腐蚀产物)特别敏感,因为它们在阴极条件下还原或氧化时会产生明显的电流信号。CPC允许对颗粒进行施胶,所得结果将在下文进行讨论。有趣的是,对于浓度最高的颗粒样本,也获得了阶梯响应,这表明存在阻断机制。镉(Cd)在nZVI残余材料中的包合导致结构变化,从六方赤铁矿晶格转变为面心立方CdFe2O4相。入射光子对电流的效率测量显示,与原来的nZVI材料相比,效率提高了10倍。此外,光电压测量作为Cd含量的函数表明Cd改变了FexOy结构的半导体特性。本研究强调了镉掺杂铁残余材料(Cd- ir)在提高光电化学太阳能电池(PSC)性能方面的潜力,并提供了由于镉掺入而导致的材料性能和结构变化的见解。
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引用次数: 0
Green biosynthesis of silver nanoparticles from Citrus aurantium leaves plant as corrosion inhibitor for carbon steel in sulfuric acid 绿色生物合成金柑橘叶片纳米银作为硫酸中碳钢缓蚀剂的研究
Pub Date : 2025-12-05 DOI: 10.1016/j.nxnano.2025.100331
Noor H. Kurshed , Anees A. Khadom , Rusul K. Ismail , Saja Khalil Mohuee , Noor Kadhim Ahmed , A. Alamiery
Citrus aurantium leaves (CAL) and silver nanoparticles (AgNPs) were used in the biosynthesis of a corrosion inhibitor for low-carbon steel in 0.5 M H₂SO₄. The weight loss method was used to investigate the corrosion inhibition performance of the composite (CAL-AgNPs). It was found that the corrosion rate of low-carbon steel increased with temperature increase and decreased with CAL-AgNPs concentration increase. Maximum corrosion inhibition efficiency was 91.3 % at 10 ml/l and 30°C. Adsorption studies indicated that CAL-AgNPs can be adsorbed spontaneously on the metal surface. The adsorption mechanism was primarily physical and followed the Langmuir adsorption isotherm. The kinetics studies confirmed these outcomes, showing a higher activation energy in the presence of CAL-AgNPs compared to the blank solution. This indicated the formation of a protective layer on the metal surface that increased the energy barrier. The FTIR technique was used as a direct method of CAL functional group diagnosis and an indirect one for AgNPs presence. The FTIR spectra showed the stretching for functional groups like alcohols, phenols, N–H of amines, C–H stretching, esters, aldehydes, and carboxylic acids, which are common in capping biomolecules. In addition, spectra in the range of metal-O bonds, such as Ag–O or Ag–N, were observed.
在0.5 M H₂SO₄溶液中,用柑橘金树叶(CAL)和纳米银粒子(AgNPs)合成了一种低碳钢缓蚀剂。采用失重法考察了复合材料(CAL-AgNPs)的缓蚀性能。结果表明,低碳钢的腐蚀速率随温度升高而升高,随CAL-AgNPs浓度的升高而降低。在10 ml/l和30℃条件下,最大缓蚀率为91.3 %。吸附研究表明,CAL-AgNPs可以在金属表面自发吸附。吸附机制以物理吸附为主,遵循Langmuir吸附等温线。动力学研究证实了这些结果,与空白溶液相比,CAL-AgNPs存在时具有更高的活化能。这表明在金属表面形成了一个保护层,增加了能量屏障。FTIR技术被用作CAL功能群诊断的直接方法和AgNPs存在的间接方法。FTIR光谱显示了覆盖生物分子中常见的功能基团如醇、酚、胺的N-H、C-H、酯、醛和羧酸的拉伸。此外,还观察到了Ag-O或Ag-N等金属- o键范围内的光谱。
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引用次数: 0
Carbon-based quantum dots in oncology: Properties and applications in cancer therapy and diagnosis 肿瘤学中的碳基量子点:特性及其在癌症治疗和诊断中的应用
Pub Date : 2025-12-05 DOI: 10.1016/j.nxnano.2025.100328
Kayeen Vadakkan , Sreeshna Karippali
Carbon dots (CDs) are emerging as transformative nanomaterials in the field of cancer diagnostics due to their unique photoluminescence, high biocompatibility, aqueous solubility, and facile surface functionalization. This review presents a comprehensive synthesis of recent advancements in the application of multifunctional CDs for cancer diagnosis. Emphasis is placed on their potential as optical probes for non-invasive bioimaging, fluorescence-guided tumor identification, and early-stage cancer detection. The photophysical properties of CDs- including excitation-dependent emission and size-tunable fluorescence enable high-contrast imaging with reduced photobleaching, which is critical for real-time monitoring of tumor microenvironments. Additionally, CDs offer significant promise in biosensing platforms for detecting cancer biomarkers such as nucleic acids, proteins, and specific antigens with high sensitivity and specificity. Their functionalized surfaces facilitate conjugation with targeting ligands, enabling selective cellular uptake and tumor localization. This review also highlights the advantages of CDs over conventional contrast agents, including reduced toxicity, deeper tissue penetration in the near-infrared range, and the capability for multimodal imaging. Key synthetic routes are compared in terms of yield, scalability, and control over optical properties. Despite these advantages, translational challenges remain, particularly in terms of standardizing synthesis, ensuring reproducibility, and evaluating long-term biocompatibility. Overall, CDs represent a promising frontier in precision diagnostics, offering the potential for integration into next-generation diagnostic nanoplatforms that aim for early, accurate, and minimally invasive cancer detection.
碳点(cd)由于其独特的光致发光、高生物相容性、水溶性和易于表面功能化而成为癌症诊断领域的变革性纳米材料。本文综述了多功能cd在癌症诊断中的应用的最新进展。重点放在他们的潜力,作为光学探针的非侵入性生物成像,荧光引导肿瘤鉴定,和早期癌症检测。CDs的光物理特性-包括激发依赖性发射和大小可调荧光-使高对比度成像和光漂白减少,这对于实时监测肿瘤微环境至关重要。此外,cd在检测癌症生物标志物(如核酸、蛋白质和特异性抗原)的生物传感平台上具有很高的灵敏度和特异性,具有重要的前景。它们的功能化表面有助于与靶向配体结合,实现选择性细胞摄取和肿瘤定位。这篇综述还强调了cd相对于传统造影剂的优势,包括毒性降低,近红外范围内更深的组织穿透,以及多模态成像能力。主要的合成路线在产率、可扩展性和对光学性质的控制方面进行了比较。尽管有这些优势,但翻译方面的挑战仍然存在,特别是在标准化合成、确保可重复性和评估长期生物相容性方面。总的来说,cd代表了精确诊断的一个有前途的前沿,提供了整合到下一代诊断纳米平台的潜力,旨在早期,准确和微创癌症检测。
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引用次数: 0
Bioprospecting of seaweed: Au nanocluster synthesis, characterization and theoretical studies 海藻生物勘探:金纳米团簇的合成、表征及理论研究
Pub Date : 2025-12-05 DOI: 10.1016/j.nxnano.2025.100324
P.R. Nithiasri, J. Aarthi, B. Karthikeyan
Algaes are potential bioprospecting agents due to their abundance secondary metabolites that have antiviral, antibacterial, anticancer, antidiabetic, and antioxidant properties. In addition, they are frequently employed to remove oils, toxic colors, and heavy metals. Recently in this study, we have investigated the environment friendly production of gold nanoclusters utilizing Turbinaria conoides algae extract. Green synthesis of gold nanoparticles is preliminarily confirmed by color change from yellow to ruby red in the reaction mixture, and the broad surface plasmon resonance band centered at 525 nm which indicates the formation of gold nanoparticles (Au NPs). XRD confirmed the crystalline nature of the synthesized Au NPs. FT-IR confirmed the presence of carboxylic, amine, and polyphenolic groups in the algae extract used for the biosynthesis. FE-SEM results reveal the spherical morphology of the Au NPs. Algae extract can act as reducing agent as well stabilizing agent due to its organic molecules like fucoidan and polyphenolic compounds. The produced Au Nps is tested for the photocatalytic degradation of toxic dye and found to be promising. Since the metallic nanoparticles shows less band gap due to the metallic nature the mechanism is discussed WITH combined photocatalytic and inter band transitions. The production of biomedically useful gold nanoclusters using algae-mediated synthesis is therefore one-step, easy, and environmentally benign procedure for the bioprospecting of seaweed algae.
藻类具有丰富的次生代谢物,具有抗病毒、抗菌、抗癌、抗糖尿病和抗氧化等特性,是潜在的生物勘探资源。此外,它们还经常被用来去除油脂、有毒颜色和重金属。在本研究中,我们研究了利用甲藻提取物环保生产金纳米团簇的方法。通过反应混合物的颜色由黄色变为红宝石红色,以及以525 nm为中心的宽表面等离子体共振带,初步证实了金纳米颗粒的绿色合成。XRD证实了合成的金纳米粒子的结晶性质。傅里叶变换红外光谱证实了用于生物合成的藻类提取物中羧基、胺基和多酚基的存在。FE-SEM结果显示了Au纳米粒子的球形形貌。藻类提取物中含有岩藻聚糖和多酚类化合物等有机分子,可作为还原剂和稳定剂。对所制备的金纳米粒子进行了光催化降解有毒染料的试验,发现其具有良好的应用前景。由于金属纳米颗粒具有较小的带隙,因此结合光催化和带间跃迁讨论了其机理。因此,利用藻类介导的合成方法生产生物医学上有用的金纳米团簇是一种一步、简单、环保的方法,可用于海藻的生物勘探。
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引用次数: 0
Hydrophobic starch acetate nanoparticles: A biopolymer-based system for sustained antitubercular drug release 疏水醋酸淀粉纳米颗粒:一种基于生物聚合物的持续抗结核药物释放系统
Pub Date : 2025-01-01 DOI: 10.1016/j.nxnano.2024.100120
Gaurang Rami , Pruthviraj Limbachiya , Mohyuddin Maradiya , Girish Acharya , Jabali Vora
The objective of the research was to evaluate the utilization of starch acetate nanoparticles (SANPs) as drug delivery carriers for antitubercular drugs (Isoniazid, Rifampicin, and Pyrazinamide). The SANPs were synthesized employing ultrasonic-assisted double emulsification solvent evaporation method, permitting effective drug encapsulation. Chemical modification of native starch strengthened its hydrophobicity, as indicated by lower crystallinity in XRD analysis. The TGA validated the thermal stability of SANPs. Morphological investigation indicated a beehive-like structure with constant porosity changed to evenly dispersed spherical nanoparticles when Starch acetate is converted into SANPs. Dynamic light scattering measured the particle sizes of SANPs to be 161 nm. Drug encapsulation brought up the SANPs particle size to 249 nm. Isoniazid, Rifampicin, and Pyrazinamide exhibited 72 %, 83 %, and 75 % encapsulation efficiency at a 2:1 polymer-drug ratio, respectively. In phosphate-buffered saline (pH 7.4), drug release behavior exhibited 55 %, 30 %, and 45 % release of isoniazid, rifampicin, and pyrazinamide over 24 hours. The Korsmeyer-Peppas model demonstrated non-Fickian diffusion for all drug-encapsulated SANPs. Thus, these results contribute to the development of biopolymer-based drug delivery systems for sustainable release of antitubercular drugs.
本研究的目的是评估醋酸淀粉纳米颗粒(SANPs)作为抗结核药物(异烟肼、利福平和吡嗪酰胺)的药物递送载体的应用。采用超声辅助双乳化溶剂蒸发法制备SANPs,实现了有效的药物包封。对天然淀粉进行化学改性,增强了其疏水性,XRD分析表明其结晶度降低。TGA验证了SANPs的热稳定性。形态学研究表明,当醋酸淀粉转化为SANPs时,具有恒定孔隙率的蜂窝状结构转变为均匀分散的球形纳米颗粒。动态光散射测得SANPs的粒径为161 nm。药物包封使SANPs的粒径达到249 nm。异烟肼、利福平和吡嗪酰胺在2:1聚合物药比下的包封率分别为72 %、83 %和75 %。在磷酸盐缓冲盐水(pH 7.4)中,异烟肼、利福平和吡嗪酰胺在24 小时内的释放率分别为55 %、30 %和45 %。Korsmeyer-Peppas模型显示所有药物包封的SANPs都具有非菲克扩散。因此,这些结果有助于开发基于生物聚合物的药物传递系统,以实现抗结核药物的可持续释放。
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引用次数: 0
Critical review of ultra-lightweight foam materials 超轻泡沫材料的关键审查
Pub Date : 2025-01-01 DOI: 10.1016/j.nxnano.2025.100138
Ridhi Saini , Dipen Kumar Rajak , Tilak Joshi , Dwesh Kumar Singh , Venkat A.N. Chilla , Sriram Sathaiah
Ultra-lightweight foam (ULF) materials have emerged as transformative solutions across many industries, driven by the increasing demand for lightweight yet high-performance materials. Characterized by their low density, high porosity, and remarkable thermal insulation properties, including exceptional cushioning and shock absorption capabilities. These attributes make them essential in the aerospace, automotive, medical, and construction sectors, where efficiency and performance are paramount. Current trends in ULF materials highlight a strong commitment to sustainability by utilizing bio-based resources and recycled materials. The ULF materials revolutionize various industries by providing lightweight solutions, contributing to energy savings and reducing environmental impact. As industries increasingly prioritize sustainability and performance, ULF materials stand at the forefront of material science innovation, promising a future marked by enhanced efficiency and environmental responsibility. This review explores the classifications, manufacturing techniques, properties, applications, advantages, and challenges associated with ULF materials. This exploration aims to lighten the enormous possibilities that ULF materials present in achieving a more sustainable and high-performance future across diverse applications.
在对轻质高性能材料需求不断增长的推动下,超轻质泡沫(ULF)材料已成为许多行业的变革性解决方案。其特点是低密度,高孔隙率,和显著的隔热性能,包括特殊的缓冲和减震能力。这些特性使其在航空航天、汽车、医疗和建筑行业中至关重要,这些行业的效率和性能至关重要。目前超低碳材料的发展趋势强调了通过利用生物基资源和回收材料来实现可持续发展的坚定承诺。ULF材料通过提供轻量化解决方案彻底改变了各个行业,有助于节约能源和减少对环境的影响。随着行业越来越重视可持续性和性能,超低密度材料站在材料科学创新的前沿,承诺未来以提高效率和环境责任为标志。本文综述了超高频材料的分类、制造技术、性能、应用、优势和面临的挑战。这一探索的目的是减轻ULF材料在各种应用中实现更可持续和高性能未来的巨大可能性。
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引用次数: 0
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Next Nanotechnology
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