Fabrication of nanocrystal forms of ᴅ-cycloserine and their application for transdermal and enteric drug delivery systems

• Hsuan-Ang Tsai,
• Tsai-Miao Shih,
• Theodore Tsai,
• Jhe-Wei Hu,
• Yi-An Lai,
• Jui-Fu Hsiao and
• Guochuan Emil Tsai

Beilstein J. Nanotechnol. 2024, 15, 465–474, doi:10.3762/bjnano.15.42

• antisolvent, and the mixing conditions. During precipitation, different solvents can affect the size, the structure, and the stability of polymorphous particles. To confirm the morphology of DCS nanocrystals, SEM and XRPD analyses were applied for the examination of particle size and structure, respectively

• . As illustrated in Figure 1 and quantified using ImageJ, the particle size of commercial DCS is in the range of several hundred microns, as depicted in Figure 1A. Conversely, the average particle size of DCS nanocrystals is 47.3 ± 9.5 nm, as evidenced in Figure 1B. This observation indicates a

• smaller particle size. In addition, we used Quality by design (QbD) to generate parameters that can be applied to commercial products in the future. The QbD is a systematic approach to drug development that ensures that a product is of high quality and consistently meets the desired characteristics

Comparative electron microscopy particle sizing of TiO₂ pigments: sample preparation and measurement

• Ralf Theissmann,
• Christopher Drury,
• Markus Rohe,
• Thomas Koch,
• Jochen Winkler and
• Petr Pikal

Beilstein J. Nanotechnol. 2024, 15, 317–332, doi:10.3762/bjnano.15.29

• ) pigment is a non-toxic, particulate material in widespread use and found in everyone’s daily life. The particle size of the anatase or rutile crystals are optimised to produce a pigment that provides the best possible whiteness and opacity. The average particle size is intentionally much larger than the

• for product quality assurance by three TiO2 manufacturing companies and present number-based primary particle size distributions (PSDs) obtained in a round-robin study performed on five anatase pigments fabricated by means of sulfate processes in different plants and commonly used worldwide in food

• ; particle sizing; primary particles; Introduction Following the EU definition of nanomaterials as being materials in which more than 50% by number of their primary particles have at least one dimension smaller than 100 nm [1][2], the accurate measurement of particle size distributions (PSDs) has become

Vinorelbine-loaded multifunctional magnetic nanoparticles as anticancer drug delivery systems: synthesis, characterization, and in vitro release study

• Zeynep Özcan and
• Afife Binnaz Hazar Yoruç

Beilstein J. Nanotechnol. 2024, 15, 256–269, doi:10.3762/bjnano.15.24

• between peak broadening and particle size in X-ray analysis. In this equation, the symbols D, K, λ, β, and θ represent the particle size, Scherrer shape factor (here 0.89), X-ray wavelength (0.15418 nm), half-maximum width, and diffraction angle, respectively [43]. Using the X-ray diffraction (XRD

• ) spectrum and Equation 5, the particle size of Fe3O4 NPs was calculated and determined to be 18 nm on average. X-ray patterns showing the distribution of Fe3O4 NPs in their uncoated state are shown in Figure 2a. XRD analysis reveals the presence of seven distinct peaks at 30.13°, 35.48°, 43.12°, 53.6

Assessing phytotoxicity and tolerance levels of ZnO nanoparticles on Raphanus sativus: implications for widespread adoptions

• Pathirannahalage Sahan Samuditha,
• Nadeesh Madusanka Adassooriya and
• Nazeera Salim

Beilstein J. Nanotechnol. 2024, 15, 115–125, doi:10.3762/bjnano.15.11

• to the reflection from (100), (002), (101), (102), (110), (103), (200), (112), and (201) crystal planes of ZnO NPs, respectively. The average size reported in the particle size analyzer for ZnO NPs was 122.4 nm, as shown in Figure 1b, with a polydispersity index of 0.332. The FTIR spectrum of ZnO NPs

• ZnO NPs characterization The PXRD technique provides important insights into the chemical composition, physical characteristics of the material and crystallographic structure, and crystalline particle size based on the scattered X-ray beam intensity [20][21]. The PXRD pattern (Figure 1a) of

• NPs (>30 nm to <50 nm) in the intercellular space, vacuole, and cytoplasm of Triticum aestivum roots when exposed to 15,000 ppm of ZnO NPs has been reported [50]. However, the average particle size in the present study (70 nm) is beyond the size-exclusion limits (5–20 nm) of the cell wall [51]. Hence

Development and characterization of potential larvicidal nanoemulsions against Aedes aegypti

• Jonatas L. Duarte,
• Leonardo Delello Di Filippo,
• Anna Eliza Maciel de Faria Mota Oliveira,
• Rafael Miguel Sábio,
• Gabriel Davi Marena,
• Tais Maria Bauab,
• Cristiane Duque,
• Vincent Corbel and
• Marlus Chorilli

Beilstein J. Nanotechnol. 2024, 15, 104–114, doi:10.3762/bjnano.15.10

• , and after 21 days there was no significant change in particle size, nor in polydispersity index (PdI) and zeta potential. The formulation with HLB 15 exhibited smaller particle size and lower PdI and zeta potential than the HLB 14 formulation. Also, there was no significant variation in these

• aqueous media [37]. According to NTA measurements, the Cym-NE particle size was 145.7 ± 7.7 nm, while the Myr-NE particle size was 126.4 ± 5.6 nm, confirming the nanometric droplet size. Cryogenic transmission electron microscopy Cryogenic transmission electron microscopy (cryo-TEM) is one of the most

Curcumin-loaded nanostructured systems for treatment of leishmaniasis: a review

• Douglas Dourado,
• Thayse Silva Medeiros,
• Éverton do Nascimento Alencar,
• Edijane Matos Sales and
• Fábio Rocha Formiga

Beilstein J. Nanotechnol. 2024, 15, 37–50, doi:10.3762/bjnano.15.4

• hydrodynamic mean particle size of 312 ± 1.89 nm, PdI of 0.305 ± 0.17 and zeta potential of −38 ± 0.93 mV. These particles were able to entrap 88% of curc due to the irregular lipid crystal structure of NLCs [53]. The NLCs proved to be safe for macrophages, which promptly internalized the nanostructures, as

• mannose-conjugated curcumin–chitosan nanoparticles (curc-MCNPs) intended for visceral leishmaniasis [50]. The selected nanoparticles (curc-MCNPs) presented spherical morphology, hydrodynamic mean particle size of 215 nm, PdI of 0.381, zeta potential of +24.37 mV, and entrapment efficiency of 82.12%. Curc

• curc-coated gold nanoparticles (curc-AuNPs) against L. major [125]. The NPs showed spherical morphology, particle size of 22 nm, and adequate polydispersity. Curc-AuNPs revealed IC50 values against L. major promastigotes of 64.79 μg/mL and 29.89 μg/mL in 24 h and 48 h, respectively. Additionally, they

Nanotechnological approaches in the treatment of schistosomiasis: an overview

• Lucas Carvalho,
• Michelle Sarcinelli and
• Beatriz Patrício

Beilstein J. Nanotechnol. 2024, 15, 13–25, doi:10.3762/bjnano.15.2

• use known drugs which have its effectivity attested, and aim to increase the dissolution of the drug in vitro [48][94]. Yang et al. [94] verified that PZQ nanocrystals had a more significant dissolution rate than that of the conventional drug due to the particle size and, consequently, it also showed

• contact the authors and ask for a copy. The available articles were read entirely, and those unrelated to the theme were excluded. For exclusion, the criteria used were: (1) particle size over 999 nm; (2) articles that approach only prophylactic nanoformulations. After that, a search in the references of

Fluorescent bioinspired albumin/polydopamine nanoparticles and their interactions with Escherichia coli cells

• Eloïse Equy,
• Jordana Hirtzel,
• Sophie Hellé,
• Béatrice Heurtault,
• Eric Mathieu,
• Morgane Rabineau,
• Vincent Ball and
• Lydie Ploux

Beilstein J. Nanotechnol. 2023, 14, 1208–1224, doi:10.3762/bjnano.14.100

• interaction of the KE diad with DA [13]. Most of the DA molecules interact with the proteins, thus limiting the binding of proteins with each other or with PDA aggregates. This results in an increase in aggregate (i.e., particle) size. Hence, a rapid decrease in diameter was observed for BSA/DA ratios from

A combined gas-phase dissociative ionization, dissociative electron attachment and deposition study on the potential FEBID precursor [Au(CH₃)₂Cl]₂

• Elif Bilgilisoy,
• Ali Kamali,
• Thomas Xaver Gentner,
• Gerd Ballmann,
• Sjoerd Harder,
• Hans-Peter Steinrück,
• Hubertus Marbach and
• Oddur Ingólfsson

Beilstein J. Nanotechnol. 2023, 14, 1178–1199, doi:10.3762/bjnano.14.98

• performed on these structures to determine their composition and to better understand the effect of different beam currents on the compositions. The respective spectra are shown in Figure 3c. A careful investigation of the SEM images reveals that the particle size gets smaller when the current is increased

• purification of FEBID deposits, where carbon removal led to ≈18% height reduction of the respective nanoparticles [42]. Notwithstanding, changes in the deposition time and in the associated different volume of the deposited material may also contribute to the observed particle size reduction. AFM of FEBID on

• (SiO2 (500 nm)/Si(111)) at different beam currents In order to obtain complementary information on the structures deposited with different beam currents, noncontact AFM was used to investigate the height of the deposits and their particle size. Figure 4a and Figure 4b depict the 2D AFM images and

Curcumin-loaded albumin submicron particles with potential as a cancer therapy: an in vitro study

• Nittiya Suwannasom,
• Netsai Sriaksorn,
• Chutamas Thepmalee,
• Krissana Khoothiam,
• Ausanai Prapan,
• Hans Bäumler and
• Chonthida Thephinlap

Beilstein J. Nanotechnol. 2023, 14, 1127–1140, doi:10.3762/bjnano.14.93

• , Table S1). CUR loading did not change significantly the particle size. The particles were quite monodisperse as indicated by the relatively low PDI values. In addition, the zeta potential values of CUR-HSA-MPs (−15.30 ± 0.02 mV) and HSA-MPs (−14.50 ± 0.06 mV) were similar. The zeta potential analysis of

• . To enhance cell uptake, it is necessary to reduce the particle size. In this case, the size of MnCO3 templates can be reduced by modifying the experimental conditions, such as increasing the salt concentration, decreasing the reaction time and cosurfactant concentration, and changing the solvent type

• Cytation™ 5 Cell Imaging Multi-Mode Reader and analyzed using Gen5 data analysis software (BioTek® Instruments, Inc., Winooski, VT, USA). Particle size and zeta potential Hydrodynamic size, polydispersity index (PDI), and zeta potential of the particles were evaluated using a Zetasizer Nano ZS (Malvern

Sulfur nanocomposites with insecticidal effect for the control of Bactericera cockerelli

• Lany S. Araujo-Yépez,
• Juan O. Tigrero-Salas,
• Vicente A. Delgado-Rodríguez,
• Vladimir A. Aguirre-Yela and
• Josué N. Villota-Méndez

Beilstein J. Nanotechnol. 2023, 14, 1106–1115, doi:10.3762/bjnano.14.91

• different chemical methods [18][19]. Elemental sulfur nanoparticles (SNPs) have already demonstrated significant insecticidal, fungicidal, and bactericidal activity [20][21]. By manipulating particle size and surface area, SNPs can exhibit higher absorption, increase the efficacy of new insecticide

Experimental investigation of usage of POE lubricants with Al₂O₃, graphene or CNT nanoparticles in a refrigeration compressor

• Kayhan Dağıdır and
• Kemal Bilen

Beilstein J. Nanotechnol. 2023, 14, 1041–1058, doi:10.3762/bjnano.14.86

• (XRD) analyses were performed. Characterization of Al2O3 nanoparticles The morphological features of the Al2O3 nanoparticles were investigated with the help of FE-SEM micrograph (Figure 2a). It is seen that the Al2O3 nanoparticles exhibit amorphous nature. Thus, it can be stated that the particle size

• cannot be clearly determined in FE-SEM micrograph, but the primary particle size is smaller than 50 nm. On the other hand, EDS analysis was conducted on the Al2O3 sample to determine the elemental composition and purity of Al2O3 nanoparticles. The result of the EDS analysis is given in Figure 2b and it

Recognition mechanisms of hemoglobin particles by monocytes – CD163 may just be one

• Jonathan-Gabriel Nimz,
• Pichayut Rerkshanandana,
• Chiraphat Kloypan,
• Ulrich Kalus,
• Saranya Chaiwaree,
• Axel Pruß,
• Radostina Georgieva,
• Yu Xiong and
• Hans Bäumler

Beilstein J. Nanotechnol. 2023, 14, 1028–1040, doi:10.3762/bjnano.14.85

• content in this suspension was 5.4 ± 0.02 mg/mL. Analysis by zetasizer showed an average particle size of 781 ± 7 nm, a conductivity of 1.34 ± 0.07 mS/cm, and a zeta potential of −28.0 ± 0.5 mV. The oxygen release method measurement showed a percentage of 81.4% ± 2.13% functional Hb. Light microscopy

• in the uptake of HbMPs. Further research on this topic will be conducted in the future. To be considered as well is a possible mechanism leading to particle uptake by phagocytes based on the particle size. Our own results regarding PMMA-FluoroGreen-COOH particles (microparticles GmbH, Berlin, Germany

• ., hydrophilicity/hydrophobicity) also played a role. Together with the particle composition, this might be a possible explanation for the difference in the results of Champion et al. and our own. Buehler et al. observed a dependence on particle size in their studies of direct Hb/HBOC–CD163 interaction. HBOCs from

Nanoarchitectonics of photothermal materials to enhance the sensitivity of lateral flow assays

• Elangovan Sarathkumar,
• Rajasekharan S. Anjana and
• Ramapurath S. Jayasree

Beilstein J. Nanotechnol. 2023, 14, 988–1003, doi:10.3762/bjnano.14.82

• particle size from 50 to 4.98 nm. In another study, the size-dependent photothermal conversion efficiency of platinum nanomaterials was studied by Depciuch et al. for cancer therapy. Spherical platinum nanoparticles with diameters of 2 and 80 nm were studied regarding the photothermal activity in colon

Upscaling the urea method synthesis of CoAl layered double hydroxides

• Camilo Jaramillo-Hernández,
• Víctor Oestreicher,
• Martín Mizrahi and
• Gonzalo Abellán

Beilstein J. Nanotechnol. 2023, 14, 927–938, doi:10.3762/bjnano.14.76

• alkalinization rate, which (mainly) controls the nucleation and growth processes, and therefore particle size, morphology, and crystallinity [33][36][37]. Attempts to upscale the production of LDHs included incrementing the concentration of the reactants [38][39], the use of large-scale reactors [40][41], byway

• concentration increase (x25M), the formation of a simonkolleite-like Co-based layered hydroxide impurity is observed, indicating phase competition during precipitation related to the thermodynamic stability of the growing phases. In the case of the volumetric scale-up, a reduction of ca. 45% of the particle

• size is observed as the volume increases. This feature is related to changes in the heating process (heat transfer) modifying the alkalinization kinetics and the concomitant precipitation process, even after 48 h of recrystallization. These results suggest that the final LDH morphology (size and

A wearable nanoscale heart sound sensor based on P(VDF-TrFE)/ZnO/GR and its application in cardiac disease detection

• Yi Luo,
• Jian Liu,
• Jiachang Zhang,
• Yu Xiao,
• Ying Wu and
• Zhidong Zhao

Beilstein J. Nanotechnol. 2023, 14, 819–833, doi:10.3762/bjnano.14.67

• bottle was sealed and placed in a shaking mixer and shaken for 3 h. Next, ZnO nanoparticles (Shanghai Keyan Industrial Co., Ltd., particle size 3 ± 5 nm, content ≥99.8%) and GR filler (Shenzhen Turing Evolution Technology Co., Ltd., carbon content 98%, average diameter/thickness ratio = 9500) were added

Nanostructured lipid carriers containing benznidazole: physicochemical, biopharmaceutical and cellular in vitro studies

• Giuliana Muraca,
• María Esperanza Ruiz,
• Rocío C. Gambaro,
• Sebastián Scioli-Montoto,
• María Laura Sbaraglini,
• Gisel Padula,
• José Sebastián Cisneros,
• Cecilia Yamil Chain,
• Vera A. Álvarez,
• Cristián Huck-Iriart,
• Guillermo R. Castro,
• María Belén Piñero,
• Matias Ildebrando Marchetto,
• Catalina Alba Soto,
• Germán A. Islan and
• Alan Talevi

Beilstein J. Nanotechnol. 2023, 14, 804–818, doi:10.3762/bjnano.14.66

• ] software showed a mean particle size of 150 ± 13 nm. Accordingly, the hydrodynamic diameter of the nanoparticles measured by dynamic light scattering (DLS) was in the 100–200 nm range (≈150 nm), with a moderate distribution of sizes as indicated by a polydispersity index (PdI) of 0.204. The zeta potential

• this description has its limitations, it has been widely used to describe drug release from similar lipidic formulations [35][36][37][38]. The mean particle size, PdI, zeta potential, and encapsulation efficiency were selected as parameters to follow the physical stability of the nanoparticle

• with acceptable particle size, PdI, and EE%. Complementary to these results, TEM images showed a spherical configuration. Thermal and crystallographic experiments indicated that BNZ was dispersed into the lipid matrix. The formulations showed a sustained drug release profile for 24 h, achieving a

Silver-based SERS substrates fabricated using a 3D printed microfluidic device

• Phommachith Sonexai,
• Minh Van Nguyen,
• Bui The Huy and
• Yong-Ill Lee

Beilstein J. Nanotechnol. 2023, 14, 793–803, doi:10.3762/bjnano.14.65

• the Ag particles become smaller when the size of the particles increases, resulting in a stronger hot spot effect. However, when the particle size exceeds a critical threshold, the Ag particles come into contact with each other, causing the hot spots to dissipate. Based on these findings, we selected

Silver nanoparticles loaded on lactose/alginate: in situ synthesis, catalytic degradation, and pH-dependent antibacterial activity

• Nguyen Thi Thanh Tu,
• T. Lan-Anh Vo,
• T. Thu-Trang Ho,
• Kim-Phuong T. Dang,
• Van-Dung Le,
• Phan Nhat Minh,
• Chi-Hien Dang,
• Vinh-Thien Tran,
• Van-Su Dang,
• Tran Thi Kim Chi,
• Hieu Vu-Quang,
• Radek Fajgar,
• Thi-Lan-Huong Nguyen,
• Van-Dat Doan and
• Thanh-Danh Nguyen

Beilstein J. Nanotechnol. 2023, 14, 781–792, doi:10.3762/bjnano.14.64

• different magnifications and particle size distributions of AgNPs@Lac/Alg-0.3 (A, B and C) and AgNPs@Lac/Alg-0.7 (D, E and F). Proposed mechanism of AgNPs@Lac/Alg catalysis in reduction of methyl orange and rhodamine B using NaBH4. UV–vis spectra of the catalyst at concentrations of 1.0 μg/mL (A), 2.0 μg/mL

Carboxylic acids and light interact to affect nanoceria stability and dissolution in acidic aqueous environments

• Matthew L. Hancock,
• Eric A. Grulke and
• Robert A. Yokel

Beilstein J. Nanotechnol. 2023, 14, 762–780, doi:10.3762/bjnano.14.63

• Table 2 of Grulke et al. [34], changes in the valence state at the edge and core of the nanoparticles were shown over twelve weeks of dissolution. The Ce3+ concentration increased as the particle size decreased, but only slightly. Figure 7 of Yokel et al. [33] shows little to no change within four weeks

• following identifies the members of the five groups and describes their effect on nanoceria dissolution/stability. Group one includes nanoceria exposed to citric, malic, and isocitric acid. For all three samples stored in the dark, there was an immediate reduction in hydrodynamic particle size, followed by

• slow dissolution over time. The solution color remained yellow for the experimental duration. For the samples exposed to light, there was an immediate reduction in hydrodynamic particle size accompanied by a color change from yellow to clear. The nanoceria particles decreased to 8.4, 7.3, and 10.9 nm

In situ magnesiothermic reduction synthesis of a Ge@C composite for high-performance lithium-ion batterie anodes

• Ha Tran Huu,
• Ngoc Phi Nguyen,
• Vuong Hoang Ngo,
• Huy Hoang Luc,
• Minh Kha Le,
• Minh Thu Nguyen,
• My Loan Phung Le,
• Hye Rim Kim,
• In Young Kim,
• Sung Jin Kim,
• Van Man Tran and
• Vien Vo

Beilstein J. Nanotechnol. 2023, 14, 751–761, doi:10.3762/bjnano.14.62

• microscopy (HR-TEM, JEOL JEM-2100F) were conducted for morphology and particle size investigation. A well-blended mixture of active material, conductive carbon C65, and polyvinylidene fluoride (PVDF) binder with a mass ratio of 75:15:10 in N-methyl-2-pyrrolidone solvent was used for fabricating the working

Control of morphology and crystallinity of CNTs in flame synthesis with one-dimensional reaction zone

• Muhammad Hilmi Ibrahim,
• Norikhwan Hamzah,
• Mohd Zamri Mohd Yusop,
• Ni Luh Wulan Septiani and
• Mohd Fairus Mohd Yasin

Beilstein J. Nanotechnol. 2023, 14, 741–750, doi:10.3762/bjnano.14.61

• temperature field and the gas phase chemistry evolve concurrently inside the flame [24]; thus, particle formation and CNT growth occur almost instantaneously. The rapid particle formation from the surface breakup produces a heterogenous particle size distribution. Consequently, particle bundles can be

• temperatures at lower and higher HAB values. The lowest HAB value shows the highest temperature reading, which linearly decreases with increasing HAB values. The temperature differences are expected to produce different particle size distributions due to aggregation of particles on the surface of the nickel

• wire. The CNT diameters, which often correlate to the particle size, show a similar trend, as discussed in the next section. CNT characterization The diameter of the synthesized CNTs has been measured using the image post-processing software DigimizerTM with 200–300 data points per sample to produce

Metal-organic framework-based nanomaterials as opto-electrochemical sensors for the detection of antibiotics and hormones: A review

• Akeem Adeyemi Oladipo,
• Saba Derakhshan Oskouei and
• Mustafa Gazi

Beilstein J. Nanotechnol. 2023, 14, 631–673, doi:10.3762/bjnano.14.52

Titania nanoparticles for photocatalytic degradation of ethanol under simulated solar light

• Evghenii Goncearenco,
• Iuliana P. Morjan,
• Claudiu Teodor Fleaca,
• Florian Dumitrache,
• Elena Dutu,
• Monica Scarisoreanu,
• Valentin Serban Teodorescu,
• Alexandra Sandulescu,
• Crina Anastasescu and
• Ioan Balint

Beilstein J. Nanotechnol. 2023, 14, 616–630, doi:10.3762/bjnano.14.51

• correlation between specific surface area and particle/crystallite size is most obvious when comparing the TO-850-a sample with those synthesized at lower pressures. When the average particle size increases, the surface area diminishes. X-ray photoelectron spectroscopy (XPS) analysis was performed, and the

On the use of Raman spectroscopy to characterize mass-produced graphene nanoplatelets

• Keith R. Paton,
• Konstantinos Despotelis,
• Naresh Kumar,
• Piers Turner and
• Andrew J. Pollard

Beilstein J. Nanotechnol. 2023, 14, 509–521, doi:10.3762/bjnano.14.42

• prepare the mixed GNPref/graphite samples, 1.2 mg of the as-purchased graphite was mixed with 40 mL of NMP, and the mixture bath was sonicated for 30 min. Sonication was carried out to reduce the particle size while still maintaining the thickness to be graphite-like [29]. The graphite and GNPref