Quantification of lead through rod-shaped silver-doped zinc oxide nanoparticles using an electrochemical approach

• Ravinder Lamba,
• Gaurav Bhanjana,
• Neeraj Dilbaghi,
• Vivek Gupta and
• Sandeep Kumar

Beilstein J. Nanotechnol. 2025, 16, 422–434, doi:10.3762/bjnano.16.33

• three-electrode configuration. The working electrode consisted of the modified Ag@ZnO NRs/Au electrode, a platinum wire used as the counter electrode, and the reference electrode was an Ag/AgCl electrode. A 0.1 M phosphate buffer solution with a pH of 7.0 was used for all measurements. (a) XRD of Ag@ZnO

Engineered PEG–PCL nanoparticles enable sensitive and selective detection of sodium dodecyl sulfate: a qualitative and quantitative analysis

• Soni Prajapati and
• Ranjana Singh

Beilstein J. Nanotechnol. 2025, 16, 385–396, doi:10.3762/bjnano.16.29

• ), cetyltrimethylammonium bromide (CTAB, Cat. No. H5882), sodium dodecyl sulfate (SDS, Cat. No. 7910), Tween 20 (Cat. No. P1379), and Triton X-100 (Cat. No. T8787) were acquired from Sigma-Aldrich (USA). Dichloromethane (DCM, Cat. No. 24532), diethyl ether (Cat. No. 64665), phosphate-buffered saline (PBS, Cat. No. 78529

Development of a mucoadhesive drug delivery system and its interaction with gastric cells

• Ahmet Baki Sahin,
• Serdar Karakurt and
• Deniz Sezlev Bilecen

Beilstein J. Nanotechnol. 2025, 16, 371–384, doi:10.3762/bjnano.16.28

• ) were resuspended in a freshly prepared dissolution medium (2 mL), that is, either simulated gastric fluid (pH 1.2) or phosphate buffer (pH 6.8), in the absence of enzymes. Alg or EudAlg nanoparticle suspensions were incubated for 7 days with a constant shaking of 50 rpm. At the end of specified time

Graphene oxide–chloroquine conjugate induces DNA damage in A549 lung cancer cells through autophagy modulation

• Braham Dutt Arya,
• Sandeep Mittal,
• Prachi Joshi,
• Alok Kumar Pandey,
• Jaime E. Ramirez-Vick,
• Govind Gupta and
• Surinder P. Singh

Beilstein J. Nanotechnol. 2025, 16, 316–332, doi:10.3762/bjnano.16.24

• ). Phosphate-buffered saline (Ca+2, Mg+2 free; PBS; Cat. No. 14200166), Dulbecco’s modified Eagle’s medium: nutrient mixture F-12 (Ham) (1:1) powder (DMEM F-12; Cat. No. 11320033), trypsin–EDTA (Cat. No. 25200056), fetal bovine serum (FBS; Cat. No. A5256701), antibiotic and antimycotic solution (100X; 10,000 U

Radiosensitizing properties of dual-functionalized carbon nanostructures loaded with temozolomide

• Radmila Milenkovska,
• Nikola Geskovski,
• Dushko Shalabalija,
• Ljubica Mihailova,
• Petre Makreski,
• Dushko Lukarski,
• Igor Stojkovski,
• Maja Simonoska Crcarevska and
• Kristina Mladenovska

Beilstein J. Nanotechnol. 2025, 16, 229–251, doi:10.3762/bjnano.16.18

Synthesis and the impact of hydroxyapatite nanoparticles on the viability and activity of rhizobacteria

• Bedah Rupaedah,
• Indrika Novella,
• Atiek Rostika Noviyanti,
• Diana Rakhmawaty Eddy,
• Anna Safarrida,
• Abdul Hapid,
• Zhafira Amila Haqqa,
• Suryana Suryana,
• Irwan Kurnia and
• Fathiyah Inayatirrahmi

Beilstein J. Nanotechnol. 2025, 16, 216–228, doi:10.3762/bjnano.16.17

• method. Following their immobilization on nHA, the phosphate-solubilizing capacity of rhizobacteria was evaluated using Pikovskaya’s medium. A nitrogen-free bromothymol medium was utilized to qualitatively assess the nitrogen-fixing ability of rhizobacteria. Furthermore, rhizobacteria were identified

• seventh day after inoculation, measuring at 2.480 × 107 and 1.040 × 107 CFU/mL, respectively. The qualitative tests of nHA as rhizobacterial carrier demonstrated that rhizobacteria retained their ability to solubilize phosphate and fix nitrogen. Furthermore, both rhizobacteria have been identified. Pd

• Tb-nHA sample. These findings correlate with the higher colony count of the Pd rhizobacterium strain as outlined in Table 2. Phosphate-solubilizing capability of rhizobacteria-nHA The proficiency of rhizobacteria in phosphate solubilization after inoculation on the nHA carrier for 21 days underscores

Probing the potential of rare earth elements in the development of new anticancer drugs: single molecule studies

• Josiane A. D. Batista,
• Rayane M. de Oliveira,
• Carlos H. M. Lima,
• Milton L. Lana Júnior,
• Virgílio C. dos Anjos,
• Maria J. V. Bell and
• Márcio S. Rocha

Beilstein J. Nanotechnol. 2025, 16, 187–194, doi:10.3762/bjnano.16.15

• the stock solutions in a phosphate-buffered saline (PBS) buffer with [Na+] = 150 mM, pH 7.4. The samples used for OT assays consist of biotin-labeled λ DNA molecules (New England Biolabs N3011S) tethered by the ends between a streptavidin-coated coverslip and a streptavidin-coated polystyrene bead (3

Clays enhanced with niobium: potential in wastewater treatment and reuse as pigment with antibacterial activity

• Silvia Jaerger,
• Patricia Appelt,
• Mario Antônio Alves da Cunha,
• Fabián Ccahuana Ayma,
• Ricardo Schneider,
• Carla Bittencourt and
• Fauze Jacó Anaissi

Beilstein J. Nanotechnol. 2025, 16, 141–154, doi:10.3762/bjnano.16.13

• /bjnano.16.13 Abstract Bentonite clay sourced from the Guarapuava region, Brazil, was modified with niobium oxide (BEOx) and niobium phosphate (BEPh) to act as an adsorbent and photocatalyst in the remediation of wastewater containing methylene blue (MB) dye. Additionally, colored materials were evaluated

• for their potential as antibacterial hybrid pigments. The bentonite clay modified with niobium was prepared by a solution containing swelling clay mixed with niobium oxide (NbOx) and niobium phosphate (NbPh) in a water solution; after that, the suspension was calcinated. X-ray diffractometry, X-ray

• generate OH• radicals (strong oxidants), leading to the mineralization of organic pollutants, including textile dyes [8]. In this study, the strategy and objective are to modify bentonite clay with niobium phosphate and niobium oxide by the calcinated method, and then use it as an adsorbent or

Nanocarriers and macrophage interaction: from a potential hurdle to an alternative therapeutic strategy

• Naths Grazia Sukubo,
• Paolo Bigini and
• Annalisa Morelli

Beilstein J. Nanotechnol. 2025, 16, 97–118, doi:10.3762/bjnano.16.10

• transfection has been utilized for macrophage targeting, wherein glucan-encapsulating sphingosine 1-phosphate receptor 2 (S1PR2)-siRNA NCs can attenuate hepatic inflammation and fibrosis. This is achieved by reducing the activation of the NLRP3 inflammasome in mouse models of bile duct ligation (BDL

A nanocarrier containing carboxylic and histamine groups with dual action: acetylcholine hydrolysis and antidote atropine delivery

• Elina E. Mansurova,
• Andrey A. Maslennikov,
• Anna P. Lyubina,
• Alexandra D. Voloshina,
• Irek R. Nizameev,
• Marsil K. Kadirov,
• Anzhela A. Mikhailova,
• Polina V. Mikshina,
• Albina Y. Ziganshina and
• Igor S. Antipin

Beilstein J. Nanotechnol. 2025, 16, 11–24, doi:10.3762/bjnano.16.2

• present in Figures S1 and S2 of Supporting Information File 1. The nanocarrier (p(Hist-CA)) was prepared, using the microemulsion technique [32][33], through the condensation of CA-RA and Hist-RA with phenylboronic acid (BA) in phosphate buffer (PB) at pH 8.5 [34][35]. CA-RA and Hist-RA are amphiphilic

Mechanistic insights into endosomal escape by sodium oleate-modified liposomes

• Ebrahim Sadaqa,
• Satrialdi,
• Fransiska Kurniawan and
• Diky Mudhakir

Beilstein J. Nanotechnol. 2024, 15, 1667–1685, doi:10.3762/bjnano.15.131

• Sigma-Aldrich (St. Louis, MO, USA). Phosphate-buffered saline (PBS, Catalog No. 10010-023), Dulbecco’s modified Eagle’s medium (DMEM, high glucose; Catalog No. 11965092), fetal bovine serum (FBS, Premium Grade; Catalog No. A5670701), penicillin-streptomycin (Catalog No. 15140122), trypan blue (Catalog

Attempts to preserve and visualize protein corona on the surface of biological nanoparticles in blood serum using photomodification

• Julia E. Poletaeva,
• Anastasiya V. Tupitsyna,
• Alina E. Grigor’eva,
• Ilya S. Dovydenko and
• Elena I. Ryabchikova

Beilstein J. Nanotechnol. 2024, 15, 1654–1666, doi:10.3762/bjnano.15.130

• because this is the concentration of serum used in cell cultivation, and we plan to study the protein corona on bio-NPs in culture medium in the future. The sera were diluted with 0.01 M phosphate buffer (PBS), pH 7.4, from Sigma-Aldrich (USA). Prior to the experiments, all serum samples were processed to

Liver-targeting iron oxide nanoparticles and their complexes with plant extracts for biocompatibility

• Shushanik A. Kazaryan,
• Seda A. Oganian,
• Gayane S. Vardanyan,
• Anatolie S. Sidorenko and
• Ashkhen A. Hovhannisyan

Beilstein J. Nanotechnol. 2024, 15, 1593–1602, doi:10.3762/bjnano.15.125

• described in [61]. For the preparation of extracts, the plant powder was mixed with the extragents, that is, 96%, 70% and 50% ethanol, diluted in phosphate buffer (pH 7.4) in a 1:30 (w/v) ratio and exposed to ultrasound at 75 W (ultrasonic homogenizer, Sonic-150W, MRC, Israel). After 24 h of incubation on

• ) according to the attached BioSystems protocols. Determination of glutathione peroxidase activity in liver tissue To determine the activity of liver glutathione peroxidase (GPx) (EC 1.11.1.9), tissue samples weighing 1–2 g were homogenized in 10 mM potassium phosphate buffer (pH 7.2) on ice using a Potter

Electrochemical nanostructured CuBTC/FeBTC MOF composite sensor for enrofloxacin detection

• Thi Kim Ngan Nguyen,
• Tien Dat Doan,
• Huy Hieu Luu,
• Hoang Anh Nguyen,
• Thi Thu Ha Vu,
• Quang Hai Tran,
• Ha Tran Nguyen,
• Thanh Binh Dang,
• Thi Hai Yen Pham and
• Mai Ha Hoang

Beilstein J. Nanotechnol. 2024, 15, 1522–1535, doi:10.3762/bjnano.15.120

• voltammogram in ENR-free blank solution with no electrochemical response for ENR. In phosphate-buffered saline (PBS) containing ENR, there is a peak at 0.85 V on all four electrodes, attributed to the oxidation of ENR during the anodic scanning. No reduction peak was observed, revealing that the

• %), and HCl (37%) were bought from Fisher and Sigma-Aldrich. All chemicals and reagents were of analytical grade and used without further purification. K3[Fe(CN)6] (≥99.5%) and K4[Fe(CN)6] (≥99.5%) were purchased from China. Phosphate-buffered saline (PBS) was prepared by mixing 0.2 M KH2PO4 and 0.2 M

• K2HPO4 in double-distilled water. The pH of the solution used for the optimization of electrolyte solution was changed from 6.0 to 9.0 by controlling the amount of these phosphate salts. Enrofloxacin stock solution was prepared by dissolving ENR powder in double-distilled water. The ENR solutions with

Dual-functionalized architecture enables stable and tumor cell-specific SiO₂NPs in complex biological fluids

• Iris Renata Sousa Ribeiro,
• Raquel Frenedoso da Silva,
• Romênia Ramos Domingues,
• Adriana Franco Paes Leme and
• Mateus Borba Cardoso

Beilstein J. Nanotechnol. 2024, 15, 1238–1252, doi:10.3762/bjnano.15.100

• equipment (Malvern Instruments Ltd., UK – detection angle of 173° and laser wavelength of 633 nm). For DLS measurements, NPs were dispersed in MilliQ water (1.0 mg·mL–1). To determine the zeta potential, the NPs were diluted in 10 Mm of phosphate buffer at a concentration of 1.0 mg·mL–1. All measurements

• penicillin and streptomycin (Sigma-Aldrich) and ii) human plasma. The human plasma was in compliance with ethics in research committee (CEP) of UNICAMP/Brazil. Particularly, the plasma was diluted (final percentage of 5.5%) in phosphate-buffered saline (PBS, pH 7.4, 10 mM) for incubation with particles. The

Synthesis, characterization and anticancer effect of doxorubicin-loaded dual stimuli-responsive smart nanopolymers

• Ömür Acet,
• Pavel Kirsanov,
• Burcu Önal Acet,
• Inessa Halets-Bui,
• Dzmitry Shcharbin,
• Şeyda Ceylan Cömert and
• Mehmet Odabaşı

Beilstein J. Nanotechnol. 2024, 15, 1189–1196, doi:10.3762/bjnano.15.96

• their transition to the active phase of reproduction. The nanomaterials were added to the cell suspension in the wells. For this, complexes of DOX-SNPs were prepared as described in section “Preparation of DOX-SNPs” to equivalents of loaded DOX of 1, 3, and 5 µmol/L in 0.05 mol/L phosphate-buffered

• structure with a low carrying capacity may not provide the desired effect. DOX loading of SNPs was conducted as previously mentioned in section “Preparation of DOX-SNPs”. The DOX-loading capacity of smart nanopolymers was investigated in the concentration range of 1–9 µM (5 mg SNPs in 5 mL 0.05 M phosphate

Recent updates in applications of nanomedicine for the treatment of hepatic fibrosis

• Damai Ria Setyawati,
• Fransiska Christydira Sekaringtyas,
• Riyona Desvy Pratiwi,
• A’liyatur Rosyidah,
• Rohimmahtunnissa Azhar,
• Nunik Gustini,
• Gita Syahputra,
• Idah Rosidah,
• Etik Mardliyati,
• Tarwadi and
• Sjaikhurrizal El Muttaqien

Beilstein J. Nanotechnol. 2024, 15, 1105–1116, doi:10.3762/bjnano.15.89

• liver cell types, there is a particular receptor that could be targeted to specifically deliver antifibrotic drugs, as illustrated in Figure 2b. On the surface of HSCs, the mannose 6-phosphate receptor (M6PR) is probably the most prominent receptor for targeting HSCs. This particular molecule is

• binding protein. This protein is not available in hepatocytes, thus enabling specific targeting to activated HSCs in liver fibrosis [72]. Tan and co-workers also constructed albumin–mannose 6-phosphate-modified solid lipid NPs to deliver matrine to HSCs [73]. The active substance matrine was first loaded

• into the solid lipid NPs using the microemulsion-probe ultrasound method, while mannose 6-phosphate was conjugated to albumin. The mannose 6-phosphate-conjugated albumin was then decorated onto the surface of matrine-loaded solid lipid NPs, and its HSC-targeting efficiency was evaluated in vitro and in

Unveiling the potential of alginate-based nanomaterials in sensing technology and smart delivery applications

• Shakhzodjon Uzokboev,
• Khojimukhammad Akhmadbekov,
• Ra’no Nuritdinova,
• Salah M. Tawfik and
• Yong-Ill Lee

Beilstein J. Nanotechnol. 2024, 15, 1077–1104, doi:10.3762/bjnano.15.88

• controlled amygdalin release, with an increased cytotoxic effect on cancerous cells while sparing normal cells and tissues. Alginate nanoparticles can be applied to ocular DDSs [91]. Kianersi and coworkers investigated alginate-based nanoparticles for betamethasone sodium phosphate delivery in the human eye

Therapeutic effect of F127-folate@PLGA/CHL/IR780 nanoparticles on folate receptor-expressing cancer cells

• Thi Ngoc Han Pham,
• Phuong-Thao Dang-Luong,
• Hong-Phuc Nguyen,
• Loc Le-Tuan,
• Xuan Thang Cao,
• Thanh-Danh Nguyen,
• Vy Tran Anh and
• Hieu Vu_Quang

Beilstein J. Nanotechnol. 2024, 15, 954–964, doi:10.3762/bjnano.15.78

• ligand folate to improve their capacity to target cells expressing the folate receptor. Materials and Methods Chlorambucil (C0253), PLGA 504H (719900), IR780 (425311), Pluronic™ F-127 (P2443), poly(vinyl alcohol) (PVA) (P8136), phosphate buffered saline (PBS) (P4417), dimethyl sulfoxide (DMSO) (472301

Electrospun nanofibers: building blocks for the repair of bone tissue

• Tuğrul Mert Serim,
• Gülin Amasya,
• Tuğba Eren-Böncü,
• Ceyda Tuba Şengel-Türk and
• Ayşe Nurten Özdemir

Beilstein J. Nanotechnol. 2024, 15, 941–953, doi:10.3762/bjnano.15.77

• of calcium and phosphate and the protection of bone marrow are among the characteristics of bone tissue [9][10]. Bone tissue, which is a special form of connective tissue, consists of cells, fibers, and extracellular matrix; histologically, it can be divided into two bone types, namely, woven bone

• -based nanofiber scaffolds for tissue regeneration (Stellenbosch Nanofiber Company, South Africa) [45]. ReBOSSIS consists of β-tricalcium phosphate, PLGA, and silicon-doped calcium carbonate to support bone formation. ReBOSSIS electrospun fibers are distinguished from other market products by a cotton

The effect of age on the attachment ability of stick insects (Phasmatodea)

• Marie Grote,
• Stanislav N. Gorb and
• Thies H. Büscher

Beilstein J. Nanotechnol. 2024, 15, 867–883, doi:10.3762/bjnano.15.72

• . Freshly molted adult and subadult individuals were acquired from laboratory stock and used for imaging as well. Three individuals were chosen for each age group. Tarsi were cut off at the tarso-tibial joint and transferred into 1.5 mL solution of phosphate-buffered saline (PBS) and Triton TM-X100 (Sigma

Electrospun polysuccinimide scaffolds containing different salts as potential wound dressing material

• Veronika Pálos,
• Krisztina S. Nagy,
• Rita Pázmány,
• Krisztina Juriga-Tóth,
• Bálint Budavári,
• Judit Domokos,
• Dóra Szabó,
• Ákos Zsembery and
• Angela Jedlovszky-Hajdu

Beilstein J. Nanotechnol. 2024, 15, 781–796, doi:10.3762/bjnano.15.65

• , USA); Dulbecco's modified Eagle medium (DMEM, Gibco, USA); MEM, no glutamine, no phenol red (Gibco, USA); phosphate-buffered saline (Gibco, USA); fetal bovine serum (FBS, Gibco, USA); penicillin/streptomycin mix (Gibco, USA); ʟ-glutamine (Gibco, USA); non-essential amino acid solution (NEAA, Gibco

• was removed from each well and 200 µL of phosphate-buffered saline was added to eliminate the residual media as well as cells that were either loosely attached or did not attach to the plate. Then, 100 µL of diluted WST-1 reagent was added to the cells and incubated for 4 h. The absorbance values of

Gold nanomakura: nanoarchitectonics and their photothermal response in association with carrageenan hydrogels

• Nabojit Das,
• Vikas,
• Akash Kumar,
• Sanjeev Soni and
• Raja Gopal Rayavarapu

Beilstein J. Nanotechnol. 2024, 15, 678–693, doi:10.3762/bjnano.15.56

• DTAB-AuNM, respectively, over a wavelength range 300–900 nm. Stability of AuNMs (CTAB-AuNM, MTAB-AuNM, and DTAB AuNM) in different media at the ratio (NPs:media) 3:1 where (a), (b), and (c) represent the stability of AuNMs in ethanol (70%), NaCl (0.9%), and 1X phosphate buffer saline (PBS). (a) k-CG

Comparative analysis of the ultrastructure and adhesive secretion pathways of different smooth attachment pads of the stick insect Medauroidea extradentata (Phasmatodea)

• Julian Thomas,
• Stanislav N. Gorb and
• Thies H. Büscher

Beilstein J. Nanotechnol. 2024, 15, 612–630, doi:10.3762/bjnano.15.52

• tarsomeres were fixed in 2.5% glutaraldehyde in (pH 7.4) phosphate-buffered saline (PBS) for 24 h, washed two times in PBS for 30 min each, fixed in 1% aqueous OsO4 for 1 h, and washed two times in double-distilled water, for 30 min each. After fixation, the samples were dehydrated using an ascending ethanol

Cholesterol nanoarchaeosomes for alendronate targeted delivery as an anti-endothelial dysfunction agent

• Horacio Emanuel Jerez,
• Yamila Roxana Simioni,
• Kajal Ghosal,
• Maria Jose Morilla and
• Eder Lilia Romero

Beilstein J. Nanotechnol. 2024, 15, 517–534, doi:10.3762/bjnano.15.46

• 700 mg TPA was isolated from each culture batch. The reproducibility of each TPA extract composition was routinely screened by phosphate content [75] and electrospray-ionization mass spectrometry [76] and ordered according to decrescent abundance as archaeol analog methyl ester of

• Bligh and Dyer method [77] by a colorimetric phosphate microassay [75]. Size and ζ potential of nanovesicles were determined by dynamic light scattering and phase analysis light scattering, respectively, using a Zetasizer Nano ZS apparatus (Malvern Instruments Ltd, UK). To prepare RhPE-labeled

• nanoarchaeosome (nanoARC-Chol (ALN)). (B) Structure of phosphatidylglycerol phosphate methyl ester (PGP-Me). (C) Structure of the four polar archaeolipids composing the total polar lipids from H. tebenquichense. HUVEC viability upon nanovesicle uptake. Viability upon 24 h of incubation with (A) void nanovesicles