In this study, Ni/Al composites modified with gambier leaf extract (Ni/Al/Ug) were successfully synthesized using the coprecipitation method and then characterized using XRD, FTIR, BET, SEM, TEM, Zeta Potential, UV–Vis DRS, and XPS. The characterization results indicate that the layered Ni/Al structure remains intact after modification, with the presence of polyphenolic groups from Ug bound to the surface. The specific surface area increases, the morphology becomes more porous, and the bandgap energy decreases, thereby enhancing photocatalytic activity. Performance testing showed that Ni/Al–Ug exhibits high selectivity toward Reactive Violet (RV) compared to four other dyes (DY, RY, DO, and RR), attributed to enhanced π–π stacking interactions and electrostatic interactions mediated by Ug. Although the adsorption capacity decreases compared to Ni/Al, the photodegradation efficiency significantly increases, especially under optimal conditions of pH 3 and reaction time of 120 min, with RV degradation reaching 87.63 %. Kinetic studies followed a pseudo-first-order model with a rate constant of 0.01549 min−1, nearly twice that of Ni/Al. Reusability tests demonstrated high stability with 70.53 % efficiency after five cycles. Scavenger tests indicated that hydroxyl radicals (•OH) and superoxide radicals (•O2-) are the dominant reactive species in the photodegradation mechanism. Overall, Ni/Al/Ug has proven to be a selective, efficient, and stable material for the treatment of anionic dye waste.
{"title":"Eco-engineered Ni/Al composites with Uncaria gambir leaf extract: A selective photocatalyst for anionic dye removal","authors":"Jefri Jefri , Najma Annuria Fithri , Yulizah Hanifah , Alfan Wijaya , Amri Amri , Nur Ahmad , Aldes Lesbani","doi":"10.1016/j.nanoso.2026.101614","DOIUrl":"10.1016/j.nanoso.2026.101614","url":null,"abstract":"<div><div>In this study, Ni/Al composites modified with gambier leaf extract (Ni/Al/Ug) were successfully synthesized using the coprecipitation method and then characterized using XRD, FTIR, BET, SEM, TEM, Zeta Potential, UV–Vis DRS, and XPS. The characterization results indicate that the layered Ni/Al structure remains intact after modification, with the presence of polyphenolic groups from Ug bound to the surface. The specific surface area increases, the morphology becomes more porous, and the bandgap energy decreases, thereby enhancing photocatalytic activity. Performance testing showed that Ni/Al–Ug exhibits high selectivity toward Reactive Violet (RV) compared to four other dyes (DY, RY, DO, and RR), attributed to enhanced π–π stacking interactions and electrostatic interactions mediated by Ug. Although the adsorption capacity decreases compared to Ni/Al, the photodegradation efficiency significantly increases, especially under optimal conditions of pH 3 and reaction time of 120 min, with RV degradation reaching 87.63 %. Kinetic studies followed a pseudo-first-order model with a rate constant of 0.01549 min<sup>−1</sup>, nearly twice that of Ni/Al. Reusability tests demonstrated high stability with 70.53 % efficiency after five cycles. Scavenger tests indicated that hydroxyl radicals (•OH) and superoxide radicals (•O<sub>2</sub><sup>-</sup>) are the dominant reactive species in the photodegradation mechanism. Overall, Ni/Al/Ug has proven to be a selective, efficient, and stable material for the treatment of anionic dye waste.</div></div>","PeriodicalId":397,"journal":{"name":"Nano-Structures & Nano-Objects","volume":"45 ","pages":"Article 101614"},"PeriodicalIF":5.45,"publicationDate":"2026-01-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145939010","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Efficient use of bioresources is essential in order to achieve sustainable development goals, and plays an important role in the reduction of any environmental impact and the improvement of resource efficiency. To this end, the present study investigates the process of obtaining microcrystalline cellulose (MCC) and cellulose nanofibers (CNFs) from corn husks (CHs), which are agricultural waste, under “mild” conditions by employing the organosolvent oxidation method using peroxyacetic acid (PAA). The results obtained at an effective hydromodule of CH:PAA 1:18 g/mL, were: MCC yield – 51.60 %, α-cellulose content – 58.73 ± 3 %, residual lignin – 12.92 ± 0.5 %, hemicellulose – 13.8 ± 0.5 %, ash content (SiO2) – 10.73 ± 0.5 %, and moisture content – 3.57 ± 0.5 %. Furthermore, the effective MCC:FA ratio that was used to obtain CNFs from MCCCH using formic acid (FA) was found to be 1/30 g/mL. The CNF yield achieved with this ratio was 68.67 %, and the average particle size was reduced by 177 times in length and 33 times in width, as compared to the initial MCCCH size. The ζ-potential of the resulting MCC was −19.3 mV and the crystallinity index was 80.9 %. The effectiveness of the PAA/FA approach arises from mild oxidation that selectively removes amorphous cellulose, while preserving crystalline regions, thereby maintaining high crystallinity and contributing to favorable material yields. The physicochemical properties of the resulting high-quality cellulose micro- and nanofibers were compared, and found to have been obtained at good efficiency. The MCC and CNFs obtained have excellent potential for use in the medical field as essential components, and in the development of bioplastics and biocomposites, among other applications.
{"title":"Eco-friendly conversion of corn husk agro-waste into microcrystalline cellulose and cellulose nanofibers","authors":"Nazym Sagiyeva , Kydyrmolla Akatan , Ainur Battalova , Gulfaridat Kampitova , Esbol Shaimardan , Ainur Kabdrakhmanova , Sana Kabdrakhmanova , Madiar Beisebekov","doi":"10.1016/j.nanoso.2025.101610","DOIUrl":"10.1016/j.nanoso.2025.101610","url":null,"abstract":"<div><div>Efficient use of bioresources is essential in order to achieve sustainable development goals, and plays an important role in the reduction of any environmental impact and the improvement of resource efficiency. To this end, the present study investigates the process of obtaining microcrystalline cellulose (MCC) and cellulose nanofibers (CNFs) from corn husks (CHs), which are agricultural waste, under “mild” conditions by employing the organosolvent oxidation method using peroxyacetic acid (PAA). The results obtained at an effective hydromodule of CH:PAA 1:18 g/mL, were: MCC yield – 51.60 %, α-cellulose content – 58.73 ± 3 %, residual lignin – 12.92 ± 0.5 %, hemicellulose – 13.8 ± 0.5 %, ash content (SiO<sub>2</sub>) – 10.73 ± 0.5 %, and moisture content – 3.57 ± 0.5 %. Furthermore, the effective MCC:FA ratio that was used to obtain CNFs from MCC<sub>CH</sub> using formic acid (FA) was found to be 1/30 g/mL. The CNF yield achieved with this ratio was 68.67 %, and the average particle size was reduced by 177 times in length and 33 times in width, as compared to the initial MCC<sub>CH</sub> size. The ζ-potential of the resulting MCC was −19.3 mV and the crystallinity index was 80.9 %. The effectiveness of the PAA/FA approach arises from mild oxidation that selectively removes amorphous cellulose, while preserving crystalline regions, thereby maintaining high crystallinity and contributing to favorable material yields. The physicochemical properties of the resulting high-quality cellulose micro- and nanofibers were compared, and found to have been obtained at good efficiency. The MCC and CNFs obtained have excellent potential for use in the medical field as essential components, and in the development of bioplastics and biocomposites, among other applications.</div></div>","PeriodicalId":397,"journal":{"name":"Nano-Structures & Nano-Objects","volume":"45 ","pages":"Article 101610"},"PeriodicalIF":5.45,"publicationDate":"2026-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145880554","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The demand for non-invasive, continuous health monitoring has accelerated research on wearable biosensors for real-time sweat analysis. Conducting polymer nanocomposites (CPNs), particularly those derived from polyaniline (PANI), polypyrrole (PPy), and PEDOT:PSS, have gained prominence owing to their unique combination of electrical conductivity, redox activity, mechanical flexibility, and biocompatibility. Current review broadly survey wearable biosensors, this article specifically highlights the engineering strategies and structure–property relationships of CPNs for sweat-based applications. Recent advances in nanomaterial integrationincluding carbon nanotubes, graphene derivatives, MXenes, and metal nanoparticlesare critically examined for their role in enhancing electron transfer, stability, and analyte selectivity. Fabrication approaches such as electropolymerization, inkjet printing, electrospinning, and 3D printing are compared in terms of scalability, reproducibility, and device durability. Transduction mechanisms like electrochemical, chemiresistive, and colorimetricare discussed. Device-level considerations, including substrate flexibility, microfluidic sweat handling, and wireless data transmission, are also analyzed. Key challenges like dopant leaching, film cracking under mechanical deformation, and signal drift in humid environments are identified, along with strategies for improved stability and performance. By integrating polymer engineering insights with wearable electronics, this review provides a forward-looking framework for designing next-generation sweat biosensors based on conducting polymer nanocomposites.
{"title":"Recent advances in conducting polymer nanocomposites for non-invasive sweat-based biosensors: A review","authors":"Lovepreet Singh , Harshita Jain , Sakshi Sharma , Nishel Saini , Anuradha Kashyap , Vishal Singh","doi":"10.1016/j.nanoso.2025.101609","DOIUrl":"10.1016/j.nanoso.2025.101609","url":null,"abstract":"<div><div>The demand for non-invasive, continuous health monitoring has accelerated research on wearable biosensors for real-time sweat analysis. Conducting polymer nanocomposites (CPNs), particularly those derived from polyaniline (PANI), polypyrrole (PPy), and PEDOT:PSS, have gained prominence owing to their unique combination of electrical conductivity, redox activity, mechanical flexibility, and biocompatibility. Current review broadly survey wearable biosensors, this article specifically highlights the engineering strategies and structure–property relationships of CPNs for sweat-based applications. Recent advances in nanomaterial integrationincluding carbon nanotubes, graphene derivatives, MXenes, and metal nanoparticlesare critically examined for their role in enhancing electron transfer, stability, and analyte selectivity. Fabrication approaches such as electropolymerization, inkjet printing, electrospinning, and 3D printing are compared in terms of scalability, reproducibility, and device durability. Transduction mechanisms like electrochemical, chemiresistive, and colorimetricare discussed. Device-level considerations, including substrate flexibility, microfluidic sweat handling, and wireless data transmission, are also analyzed. Key challenges like dopant leaching, film cracking under mechanical deformation, and signal drift in humid environments are identified, along with strategies for improved stability and performance. By integrating polymer engineering insights with wearable electronics, this review provides a forward-looking framework for designing next-generation sweat biosensors based on conducting polymer nanocomposites.</div></div>","PeriodicalId":397,"journal":{"name":"Nano-Structures & Nano-Objects","volume":"45 ","pages":"Article 101609"},"PeriodicalIF":5.45,"publicationDate":"2026-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145880630","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-30DOI: 10.1016/j.nanoso.2025.101607
Mehanaz Iqbal , Vijayashree N. Hegde , P. Mohan Kumar , P.R. Deepthi
Titanium dioxide (TiO₂) thin films are widely studied for their multifunctionality, with proven applications in photocatalysis, self-cleaning surfaces, and antimicrobial coatings. By tuning composition and microstructure, TiO₂’s optical and catalytic performance under UV and visible light can be optimized. Metal dopants like platinum, silver, and iron enhance light absorption, charge separation, and catalytic activity. Meanwhile, synthesis methods such as sol-gel and hydrothermal processes control critical properties like porosity, crystallinity, and surface area. TiO₂ also exhibits strong bactericidal effects by generating reactive oxygen species under light, disrupting microbial cells. Doping and co-catalyst integration further amplify this antimicrobial action. The formation of heterojunctions with other semiconductors or graphene materials improves both photocatalytic and antibacterial efficiency by minimizing electron-hole recombination. These advancements position TiO₂ thin films as promising materials for environmental remediation, clean energy, water treatment, and healthcare. Ongoing research on doping, film structure, and fabrication continues to drive improvements in their performance and durability.
{"title":"Engineered TiO₂ thin films for photocatalytic, electrochemical, and bactericidal applications: A comprehensive review","authors":"Mehanaz Iqbal , Vijayashree N. Hegde , P. Mohan Kumar , P.R. Deepthi","doi":"10.1016/j.nanoso.2025.101607","DOIUrl":"10.1016/j.nanoso.2025.101607","url":null,"abstract":"<div><div>Titanium dioxide (TiO₂) thin films are widely studied for their multifunctionality, with proven applications in photocatalysis, self-cleaning surfaces, and antimicrobial coatings. By tuning composition and microstructure, TiO₂’s optical and catalytic performance under UV and visible light can be optimized. Metal dopants like platinum, silver, and iron enhance light absorption, charge separation, and catalytic activity. Meanwhile, synthesis methods such as sol-gel and hydrothermal processes control critical properties like porosity, crystallinity, and surface area. TiO₂ also exhibits strong bactericidal effects by generating reactive oxygen species under light, disrupting microbial cells. Doping and co-catalyst integration further amplify this antimicrobial action. The formation of heterojunctions with other semiconductors or graphene materials improves both photocatalytic and antibacterial efficiency by minimizing electron-hole recombination. These advancements position TiO₂ thin films as promising materials for environmental remediation, clean energy, water treatment, and healthcare. Ongoing research on doping, film structure, and fabrication continues to drive improvements in their performance and durability.</div></div>","PeriodicalId":397,"journal":{"name":"Nano-Structures & Nano-Objects","volume":"45 ","pages":"Article 101607"},"PeriodicalIF":5.45,"publicationDate":"2025-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145880629","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-26DOI: 10.1016/j.nanoso.2025.101602
M.M. Arman , Eman S. Mansor
The perovskite nanoparticles LaFeO3 (LFO), La0.5Sm0.5FeO3 (LSFO), and La0.5Nd0.5FeO3 (LNFO) were prepared in a single phase using the citrate method. The X-ray diffraction (XRD) pattern illustrates the nanoparticles were formed in an orthorhombic structure with a crystallite size in the range of 36–40 nm. The FESEM images show the presence of pores in the morphology of the samples, leading to an increase of the surface to volume ratio of the samples. The saturation magnetization of LFO raised from 0.57 emu/g to 1.46 emu/g for LSFO and to 2.44 emu/g for LNFO samples. The sample LNFO has the lowest direct energy gap (1.903 eV). The LNFO exhibited enhanced optical absorbance characteristics in comparison with neat LFO. The degrading capacities of the produced LNFO were investigated at xenon light illumination and in an aqueous congo red (CR) solution. The photocatalytic effectiveness of the LFO, and LNFO were around 85 % and 99.9 % respectively. The condition of degradation was optimized. Our research indicates that LNFO may serve as photocatalysts to break down the congo red dye with a removal percentage of more than 99 % at pH3, dose 1.5 g/L and dye concentration 25 mg/L.
{"title":"Studying the physical properties of LaFeO3, La0.5Sm0.5FeO3, and La0.5Nd0.5FeO3 perovskite nanoparticles with a comparative photocatalytic degradation of Congo Red dye","authors":"M.M. Arman , Eman S. Mansor","doi":"10.1016/j.nanoso.2025.101602","DOIUrl":"10.1016/j.nanoso.2025.101602","url":null,"abstract":"<div><div>The perovskite nanoparticles LaFeO<sub>3</sub> (LFO), La<sub>0.5</sub>Sm<sub>0.5</sub>FeO<sub>3</sub> (LSFO), and La<sub>0.5</sub>Nd<sub>0.5</sub>FeO<sub>3</sub> (LNFO) were prepared in a single phase using the citrate method. The X-ray diffraction (XRD) pattern illustrates the nanoparticles were formed in an orthorhombic structure with a crystallite size in the range of 36–40 nm. The FESEM images show the presence of pores in the morphology of the samples, leading to an increase of the surface to volume ratio of the samples. The saturation magnetization of LFO raised from 0.57 emu/g to 1.46 emu/g for LSFO and to 2.44 emu/g for LNFO samples. The sample LNFO has the lowest direct energy gap (1.903 eV). The LNFO exhibited enhanced optical absorbance characteristics in comparison with neat LFO. The degrading capacities of the produced LNFO were investigated at xenon light illumination and in an aqueous congo red (CR) solution. The photocatalytic effectiveness of the LFO, and LNFO were around 85 % and 99.9 % respectively. The condition of degradation was optimized. Our research indicates that LNFO may serve as photocatalysts to break down the congo red dye with a removal percentage of more than 99 % at pH3, dose 1.5 g/L and dye concentration 25 mg/L.</div></div>","PeriodicalId":397,"journal":{"name":"Nano-Structures & Nano-Objects","volume":"45 ","pages":"Article 101602"},"PeriodicalIF":5.45,"publicationDate":"2025-12-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145836962","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-23DOI: 10.1016/j.nanoso.2025.101603
Julia Mazurenko , Larysa Kaykan , Sijo A K , Antoni Zywczak , Mateusz Marzec , Liliia Turovska , Katarina Hreus
Nickel-substituted copper ferrite nanoparticles were successfully synthesized using a citrate–nitrate sol-gel autocombustion route and evaluated as photocatalysts for the degradation of organic dyes. X-ray diffraction confirmed that all compositions crystallized into a cubic spinel structure (Fd3m), with crystallite sizes in the nanoscale range. X-ray photoelectron spectroscopy revealed that Fe3 + ions were predominant and distributed across tetrahedral and octahedral sites, while Ni2+ and Cu2+ preferentially occupied octahedral positions. BET analysis revealed specific surface areas of 7–16 m2/g, with Cu-rich samples exhibiting higher porosity. Magnetic measurements confirmed magnetic behavior for all Cu1-xNixFe2O4 (0 ≤ x ≤ 1.0) samples, with saturation magnetization increasing from 28.7 emu g−1 to 58.9 emu g−1, ensuring efficient magnetic separation and reusability of the nanoparticles in photocatalytic applications. Optical studies demonstrated a systematic increase in the direct band gap energy from 1.80 eV for CuFe2O4 to 2.29 eV for NiFe2O4, correlating with decreased Urbach energies and suggesting improved structural order with Ni incorporation. Photocatalytic efficiency was investigated using Methylene Blue (MB), Congo Red (CR), and Malachite Green (MG) under visible light and H2O2. The maximum degradation rate was observed for Cu0.8Ni0.2Fe2O4 at pH 10 with kL–H = 0.080 min−1 and 99 % MB removal within 180 min, while CR degradation peaked at x = 0.4 (96 %) and MG at x ≥ 0.4 (kL–H = 0.115 min−1, ∼99 % removal). The catalysts maintained over 95 % activity after five reuse cycles, confirming excellent structural stability and magnetic recoverability. These findings demonstrate that Cu/Ni co-substitution effectively tunes the band structure, enhances redox activity, and enables sustainable photocatalytic performance for wastewater treatment applications.
{"title":"Photocatalytic efficiency of nickel-doped copper ferrite in organic dye decomposition","authors":"Julia Mazurenko , Larysa Kaykan , Sijo A K , Antoni Zywczak , Mateusz Marzec , Liliia Turovska , Katarina Hreus","doi":"10.1016/j.nanoso.2025.101603","DOIUrl":"10.1016/j.nanoso.2025.101603","url":null,"abstract":"<div><div>Nickel-substituted copper ferrite nanoparticles were successfully synthesized using a citrate–nitrate sol-gel autocombustion route and evaluated as photocatalysts for the degradation of organic dyes. X-ray diffraction confirmed that all compositions crystallized into a cubic spinel structure (Fd3m), with crystallite sizes in the nanoscale range. X-ray photoelectron spectroscopy revealed that Fe<sup>3 +</sup> ions were predominant and distributed across tetrahedral and octahedral sites, while Ni<sup>2+</sup> and Cu<sup>2+</sup> preferentially occupied octahedral positions. BET analysis revealed specific surface areas of 7–16 m<sup>2</sup>/g, with Cu-rich samples exhibiting higher porosity. Magnetic measurements confirmed magnetic behavior for all Cu<sub>1-x</sub>Ni<sub>x</sub>Fe<sub>2</sub>O<sub>4</sub> (0 ≤ x ≤ 1.0) samples, with saturation magnetization increasing from 28.7 emu g<sup>−1</sup> to 58.9 emu g<sup>−1</sup>, ensuring efficient magnetic separation and reusability of the nanoparticles in photocatalytic applications. Optical studies demonstrated a systematic increase in the direct band gap energy from 1.80 eV for CuFe<sub>2</sub>O<sub>4</sub> to 2.29 eV for NiFe<sub>2</sub>O<sub>4</sub>, correlating with decreased Urbach energies and suggesting improved structural order with Ni incorporation. Photocatalytic efficiency was investigated using Methylene Blue (MB), Congo Red (CR), and Malachite Green (MG) under visible light and H<sub>2</sub>O<sub>2</sub>. The maximum degradation rate was observed for Cu<sub>0.8</sub>Ni<sub>0.2</sub>Fe<sub>2</sub>O<sub>4</sub> at pH 10 with k<sub>L–H</sub> = 0.080 min<sup>−1</sup> and 99 % MB removal within 180 min, while CR degradation peaked at x = 0.4 (96 %) and MG at x ≥ 0.4 (k<sub>L–H</sub> = 0.115 min<sup>−1</sup>, ∼99 % removal). The catalysts maintained over 95 % activity after five reuse cycles, confirming excellent structural stability and magnetic recoverability. These findings demonstrate that Cu/Ni co-substitution effectively tunes the band structure, enhances redox activity, and enables sustainable photocatalytic performance for wastewater treatment applications.</div></div>","PeriodicalId":397,"journal":{"name":"Nano-Structures & Nano-Objects","volume":"45 ","pages":"Article 101603"},"PeriodicalIF":5.45,"publicationDate":"2025-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145836960","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Osteoarthritis (OA) is a disease that leads to impaired function and chronic pain in joints. Existing medications are symptomatic and have weak joint retention and may cause systemic drug side effects. This review discusses hyalurosomes, lipid vesicles combined with hyaluronic acid (HA), as potential future intra-articular (IA) delivery systems to provide improved targeting of cartilage, longer residence times, and the possibility of combination therapy in OA. The review is performed by a comprehensive search (cut-off: 25 August 2025) via PubMed, Scopus, Web of Science, Embase, publisher platforms (MDPI, Elsevier, SpringerLink), preprint servers, clinical trial registries, regulatory agencies (FDA, EMA, CDSCO), patent databases (Google Patents, WIPO, USPTO), conference proceedings, and gray literature including manufacturer labels and SSEDs. The results show that hyalurosomes exhibit improved IA sustained release, lower systemic exposure, and enhanced cartilage penetration compared to standard liposomes and soluble drugs. Combining visco-supplementation with controlled pharmacotherapy, such as a dual-function design, offers potential pharmacokinetic and pharmacodynamic benefits, including analgesic and chondroprotective effects in preclinical models. However, the limited number of studies may lead to varied findings. The main challenges for clinical translation include scale-up feasibility, sterilization issues, and regulatory uncertainty. Hyalurosomes are a biologically rational delivery system that could help localize multimodal therapy and bring OA treatment closer to disease-modifying options. There is a need to address manufacturing, stability, and uniform preclinical criteria before clinical trials can be used to determine efficacy and facilitate global adoption. Future research should involve controlled animal studies, pharmacokinetics, and patient outcome-focused assessments.
骨关节炎(OA)是一种导致关节功能受损和慢性疼痛的疾病。现有的药物是有症状的,关节保留力弱,可能引起全身药物副作用。这篇综述讨论了透明质体、脂质囊泡与透明质酸(HA)联合作为未来潜在的关节内(IA)递送系统,以提供更好的软骨靶向性、更长的停留时间和OA联合治疗的可能性。通过PubMed、Scopus、Web of Science、Embase、出版商平台(MDPI、Elsevier、SpringerLink)、预印服务器、临床试验注册、监管机构(FDA、EMA、CDSCO)、专利数据库(谷歌Patents、WIPO、USPTO)、会议记录和灰色文献(包括制造商标签和sds)进行综合检索(截止日期:2025年8月25日)。结果表明,与标准脂质体和可溶性药物相比,透明质体表现出更好的IA持续释放,更低的全身暴露和增强的软骨穿透。将黏液补充与控制药物治疗相结合,如双重功能设计,在临床前模型中提供潜在的药代动力学和药效学益处,包括止痛和软骨保护作用。然而,有限的研究数量可能导致不同的发现。临床翻译的主要挑战包括扩大可行性、灭菌问题和监管不确定性。透明质体是一种生物学上合理的传递系统,可以帮助定位多模式治疗,使OA治疗更接近于疾病改善方案。在临床试验用于确定疗效和促进全球采用之前,需要解决生产、稳定性和统一的临床前标准问题。未来的研究应包括对照动物研究、药代动力学和以患者结果为中心的评估。
{"title":"Hyalurosomes nanoformulation strategies for intra-articular and localized drug delivery: Transforming the management of osteoarthritis","authors":"Md. Azhar , Sathvik Belagodu Sridhar , Javedh Shareef , Tarun Wadhwa , Dhanalekshmi Unnikrishnan Meenakshi , Rishabha Malviya","doi":"10.1016/j.nanoso.2025.101605","DOIUrl":"10.1016/j.nanoso.2025.101605","url":null,"abstract":"<div><div>Osteoarthritis (OA) is a disease that leads to impaired function and chronic pain in joints. Existing medications are symptomatic and have weak joint retention and may cause systemic drug side effects. This review discusses hyalurosomes, lipid vesicles combined with hyaluronic acid (HA), as potential future intra-articular (IA) delivery systems to provide improved targeting of cartilage, longer residence times, and the possibility of combination therapy in OA. The review is performed by a comprehensive search (cut-off: 25 August 2025) via PubMed, Scopus, Web of Science, Embase, publisher platforms (MDPI, Elsevier, SpringerLink), preprint servers, clinical trial registries, regulatory agencies (FDA, EMA, CDSCO), patent databases (Google Patents, WIPO, USPTO), conference proceedings, and gray literature including manufacturer labels and SSEDs. The results show that hyalurosomes exhibit improved IA sustained release, lower systemic exposure, and enhanced cartilage penetration compared to standard liposomes and soluble drugs. Combining visco-supplementation with controlled pharmacotherapy, such as a dual-function design, offers potential pharmacokinetic and pharmacodynamic benefits, including analgesic and chondroprotective effects in preclinical models. However, the limited number of studies may lead to varied findings. The main challenges for clinical translation include scale-up feasibility, sterilization issues, and regulatory uncertainty. Hyalurosomes are a biologically rational delivery system that could help localize multimodal therapy and bring OA treatment closer to disease-modifying options. There is a need to address manufacturing, stability, and uniform preclinical criteria before clinical trials can be used to determine efficacy and facilitate global adoption. Future research should involve controlled animal studies, pharmacokinetics, and patient outcome-focused assessments.</div></div>","PeriodicalId":397,"journal":{"name":"Nano-Structures & Nano-Objects","volume":"45 ","pages":"Article 101605"},"PeriodicalIF":5.45,"publicationDate":"2025-12-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145836959","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The alarming rise of antimicrobial resistance (AMR) has prompted the search for alternative strategies beyond conventional antibiotics. Nickel hydroxide nanoparticles (Ni(OH)₂ NPs) are promising antimicrobial agents, yet their practical application is hindered by colloidal instability and potential cytotoxicity. Herein, we report a green and optimized synthesis of Ni(OH)₂ nanoparticles using cottonwood (Ceiba pentandra) honey as a natural bioreductor, followed by surface modification with oligochitosan to enhance stability and biocompatibility. The synthesis parameters were systematically optimized by varying pH, honey concentration, precursor concentration, and reaction time. The optimal conditions (pH 10, 5 % honey, 0.05 M precursor, and 30 min) were selected based on yielded Ni(OH)₂ nanoparticles with the highest UV–Vis absorbance intensity, the strongest Ni–OH fingerprint bands in FTIR, and the most uniform particle morphology. Morphological analyses confirmed the formation of quasi-spherical nanoparticles with the particle size is ∼56 nm. Surface modification with oligochitosan markedly increased the zeta potential (+60.99 mV) and hydrodynamic size, indicating strong electrosteric stabilization. Antibacterial evaluation revealed a substantial enhancement in activity after oligochitosan coating, with minimum inhibitory concentrations (MICs) reduced by 3.62-fold against Staphylococcus aureus and 4.25-fold against Pseudomonas aeruginosa compared to uncoated Ni(OH)₂ nanoparticles. Toxicity evaluation via brine shrimp lethality test indicated improved biocompatibility of the coated nanocomposites. Collectively, this study establishes a sustainable and effective strategy for producing stable, bioactive Ni(OH)₂–oligochitosan nanocomposites with strong potential as next-generation antibacterial materials.
{"title":"Honey-mediated green synthesis and systematic optimization of Ni(OH)₂ nanoparticles with oligochitosan surface modification: Structural characterization, enhanced stability, and antibacterial biocompatibility","authors":"Saidun Fiddaroini , Berlian Zetta Batari , Budi Mulyati , Ahmad Luthfi Fahmi , Yosep Yuswanto Tri Ananda , Andini , Moh. Farid Rahman , Akhmad Sabarudin","doi":"10.1016/j.nanoso.2025.101606","DOIUrl":"10.1016/j.nanoso.2025.101606","url":null,"abstract":"<div><div>The alarming rise of antimicrobial resistance (AMR) has prompted the search for alternative strategies beyond conventional antibiotics. Nickel hydroxide nanoparticles (Ni(OH)₂ NPs) are promising antimicrobial agents, yet their practical application is hindered by colloidal instability and potential cytotoxicity. Herein, we report a green and optimized synthesis of Ni(OH)₂ nanoparticles using cottonwood (<em>Ceiba pentandra</em>) honey as a natural bioreductor, followed by surface modification with oligochitosan to enhance stability and biocompatibility. The synthesis parameters were systematically optimized by varying pH, honey concentration, precursor concentration, and reaction time. The optimal conditions (pH 10, 5 % honey, 0.05 M precursor, and 30 min) were selected based on yielded Ni(OH)₂ nanoparticles with the highest UV–Vis absorbance intensity, the strongest Ni–OH fingerprint bands in FTIR, and the most uniform particle morphology. Morphological analyses confirmed the formation of quasi-spherical nanoparticles with the particle size is ∼56 nm. Surface modification with oligochitosan markedly increased the zeta potential (+60.99 mV) and hydrodynamic size, indicating strong electrosteric stabilization. Antibacterial evaluation revealed a substantial enhancement in activity after oligochitosan coating, with minimum inhibitory concentrations (MICs) reduced by 3.62-fold against <em>Staphylococcus aureus</em> and 4.25-fold against <em>Pseudomonas aeruginosa</em> compared to uncoated Ni(OH)₂ nanoparticles. Toxicity evaluation via brine shrimp lethality test indicated improved biocompatibility of the coated nanocomposites. Collectively, this study establishes a sustainable and effective strategy for producing stable, bioactive Ni(OH)₂–oligochitosan nanocomposites with strong potential as next-generation antibacterial materials.</div></div>","PeriodicalId":397,"journal":{"name":"Nano-Structures & Nano-Objects","volume":"45 ","pages":"Article 101606"},"PeriodicalIF":5.45,"publicationDate":"2025-12-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145836961","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-13DOI: 10.1016/j.nanoso.2025.101601
Nina Bogdanchikova , Jorge Noé Díaz de León , Mario Humberto Farías Sánchez , Gustavo Alonso Hirata Flores , Miguel Ángel Pastrana Corral , Alexey Pestryakov , Diana Garibo Ruiz
In this work, the characterization of Ag nanoparticles (AgNPs) and their applications in nanomedicine are discussed. Several reports in the literature mentioned that AgNPs (Argovit™) possess high biomedical activity, high stability, and low toxicity; however, the reasons for these properties are still unclear. Therefore, five lots of AgNPs prepared under various conditions were investigated via HRTEM, UVvisible spectroscopy, XPS, and luminescence techniques. The results revealed a series of experimental findings inconsistent with the current AgNP model reported, including a Ag core capped by PVP molecules. Here, we propose a novel structural model for AgNP formulations that is in good agreement with the physicochemical characterization, which consists of PVP nanohydrogels incorporating Ag cores and/or Ag cores capped by PVP molecules.
{"title":"Ag nanoparticles via PVP synthesis: Evidence of nanohydrogel formation, characterization, and review of nanomedicine applications","authors":"Nina Bogdanchikova , Jorge Noé Díaz de León , Mario Humberto Farías Sánchez , Gustavo Alonso Hirata Flores , Miguel Ángel Pastrana Corral , Alexey Pestryakov , Diana Garibo Ruiz","doi":"10.1016/j.nanoso.2025.101601","DOIUrl":"10.1016/j.nanoso.2025.101601","url":null,"abstract":"<div><div>In this work, the characterization of Ag nanoparticles (AgNPs) and their applications in nanomedicine are discussed. Several reports in the literature mentioned that AgNPs (Argovit™) possess high biomedical activity, high stability, and low toxicity; however, the reasons for these properties are still unclear. Therefore, five lots of AgNPs prepared under various conditions were investigated via HRTEM, UV<img>visible spectroscopy, XPS, and luminescence techniques. The results revealed a series of experimental findings inconsistent with the current AgNP model reported, including a Ag core capped by PVP molecules. Here, we propose a novel structural model for AgNP formulations that is in good agreement with the physicochemical characterization, which consists of PVP nanohydrogels incorporating Ag cores and/or Ag cores capped by PVP molecules.</div></div>","PeriodicalId":397,"journal":{"name":"Nano-Structures & Nano-Objects","volume":"45 ","pages":"Article 101601"},"PeriodicalIF":5.45,"publicationDate":"2025-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145749793","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-12DOI: 10.1016/j.nanoso.2025.101585
Monica N. Kalbande , Tejaswini G. Panse , Yashika A. Gaidhani , Rupali S. Balpande , Tejas R. Patil , Yoginee S. Pethe , Latika Pinjarkar , Lowlesh N. Yadav , Nischal Puri , Aseel Smerat , Vikrant S. Vairagade
Applications of high-efficiency micro- light-emitting diode (LED) displays are rapidly increasing to realize next-generation displays and augmented reality systems. However, the Light Extraction Efficiency (LEE) still lags in micro-LED arrays primarily due to inherent optical losses and total internal reflection as well as non-uniform angular emission. The current approaches, such as planar gradient-index (GRIN) structures and conventional metasurfaces, are indeed unable to yield uniform and scalable performance for dense LED configurations. This work addresses these limitations by the introduction of innovative nanophotonic structures toward maximizing LEE, uniformity, and brightness in micro-LED arrays. These proposed approaches are: (1) Topology-Optimized GRIN Metastructures, engineered using inverse design to mitigate Fresnel losses and total internal reflection, thus achieving 25–30 % efficiency improvement over planar GRIN systems; (2) Polarization-Tailored Hyperbolic Metamaterial Nanogratings, which increase directional emission by 2-fold and brightness by 30 %; (3) 3D Multi-Layer Metasurfaces integrated with quantum dots, in which peak emission intensity can be amplified by 3 times by adjusting their phases and amplitudes to optimal values; (4) Anti-reflective light-trapping coatings that suppress back-reflection up to 95 % and enhance extraction efficiency by 1.5 fold; and (5) Reconfigurable Nanostructures with Adaptive Quantum Dots capable of dynamically optimizing the light extraction for different conditions, thereby increasing efficiency up to 30–50 %. Together these methods improved LEE, spectral tunability, and angular brightness, validated by numerical simulations and preliminary experiments. These results show transformative impacts which provide scalable high-performance solutions for ultra-bright and energy-efficient micro-LED displays with new benchmarks for display technology innovation for different scenarios.
{"title":"Enhancing the light extraction efficiency in micro light-emitting diodes integrating advanced nanophotonic structures","authors":"Monica N. Kalbande , Tejaswini G. Panse , Yashika A. Gaidhani , Rupali S. Balpande , Tejas R. Patil , Yoginee S. Pethe , Latika Pinjarkar , Lowlesh N. Yadav , Nischal Puri , Aseel Smerat , Vikrant S. Vairagade","doi":"10.1016/j.nanoso.2025.101585","DOIUrl":"10.1016/j.nanoso.2025.101585","url":null,"abstract":"<div><div>Applications of high-efficiency micro- light-emitting diode (LED) displays are rapidly increasing to realize next-generation displays and augmented reality systems. However, the Light Extraction Efficiency (LEE) still lags in micro-LED arrays primarily due to inherent optical losses and total internal reflection as well as non-uniform angular emission. The current approaches, such as planar gradient-index (GRIN) structures and conventional metasurfaces, are indeed unable to yield uniform and scalable performance for dense LED configurations. This work addresses these limitations by the introduction of innovative nanophotonic structures toward maximizing LEE, uniformity, and brightness in micro-LED arrays. These proposed approaches are: (1) Topology-Optimized GRIN Metastructures, engineered using inverse design to mitigate Fresnel losses and total internal reflection, thus achieving 25–30 % efficiency improvement over planar GRIN systems; (2) Polarization-Tailored Hyperbolic Metamaterial Nanogratings, which increase directional emission by 2-fold and brightness by 30 %; (3) 3D Multi-Layer Metasurfaces integrated with quantum dots, in which peak emission intensity can be amplified by 3 times by adjusting their phases and amplitudes to optimal values; (4) Anti-reflective light-trapping coatings that suppress back-reflection up to 95 % and enhance extraction efficiency by 1.5 fold; and (5) Reconfigurable Nanostructures with Adaptive Quantum Dots capable of dynamically optimizing the light extraction for different conditions, thereby increasing efficiency up to 30–50 %. Together these methods improved LEE, spectral tunability, and angular brightness, validated by numerical simulations and preliminary experiments. These results show transformative impacts which provide scalable high-performance solutions for ultra-bright and energy-efficient micro-LED displays with new benchmarks for display technology innovation for different scenarios.</div></div>","PeriodicalId":397,"journal":{"name":"Nano-Structures & Nano-Objects","volume":"45 ","pages":"Article 101585"},"PeriodicalIF":5.45,"publicationDate":"2025-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145749791","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}