Polyurethane/silk fibroin-based electrospun membranes for wound healing and skin substitute applications

• Iqra Zainab,
• Zohra Naseem,
• Syeda Rubab Batool,
• Muhammad Waqas,
• Ahsan Nazir and
• Muhammad Anwaar Nazeer

Beilstein J. Nanotechnol. 2025, 16, 591–612, doi:10.3762/bjnano.16.46

• hemostatic agent for trauma treatment [107]. Patil et al. explored three types of silk forms, namely, regular film, lamellar porous film, and electrospun silk nanofibers for wound dressings. Factors such as solvent solution, electric field intensity, spinning distance, and SF concentration affected the

• and environmentally friendly PU synthesis route by replacing the common process of solvent-based PU synthesis. The emission of volatile organic compounds in synthesis and application can be avoided by adopting water-based PUs [147]. This has brought a shift in urethane research. WPUs have emerged as a

• . They adjusted the electrospinning parameters, such as solvent ratios and polymer concentration, to produce homogenous

Effect of additives on the synthesis efficiency of nanoparticles by laser-induced reduction

• Rikuto Kuroda,
• Takahiro Nakamura,
• Hideki Ina and
• Shuhei Shibata

Beilstein J. Nanotechnol. 2025, 16, 464–472, doi:10.3762/bjnano.16.35

• produced by the breakdown of solvent molecules in a high-intensity reaction field near the focus of the laser. This unique reaction has the characteristic of being able to synthesize non-equilibrium solid–solution alloy nanoparticles. On the other hand, it is necessary to improve the synthesis efficiency

• of various materials [18][19][20][21][22][23][24] using different mechanisms [25][26][27][28] have been conducted via LRL. High-energy ultrashort pulses focused and irradiated into a solution cause the breakdown of solvent molecules. Then, produced solvated electrons among reactive species reduce the

• complete even after 30 min of laser irradiation, which was longer than the case without IPA. This is thought to be based on the fact that the relative permittivity of IPA (20.18) is lower than that of water (80.1) [35]. Then the efficiency of radical generation accompanying the decomposition of the solvent

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

• release kinetics. After copolymerization, the reaction is terminated by dissolving the resulting copolymer in DCM, a solvent that allows the copolymer to remain in solution. The solution is then precipitated in cold diethyl ether, which helps to remove unreacted monomers and other impurities. This

• 48.3 ± 16.4 nm (Figure 2d). The slight discrepancy in size measurements between TEM, SEM, and DLS can be attributed to the different operational principles of these techniques. DLS measures the hydrodynamic diameter, including the particle core and the layer of solvent molecules attached, leading to a

Pulsed laser in liquid grafting of gold nanoparticle–carbon support composites

• Madeleine K. Wilsey,
• Teona Taseska,
• Qishen Lyu,
• Connor P. Cox and
• Astrid M. Müller

Beilstein J. Nanotechnol. 2025, 16, 349–361, doi:10.3762/bjnano.16.26

• synthesis–attachment are long preparation times, the generation of hazardous organic solvent and ligand waste [15], and poor electrical contact at the nanoparticle–support interface, particularly for nanoparticles with surfactant-terminated surfaces [16]. Conventionally made nanoparticles rely on

Fabrication and evaluation of BerNPs regarding the growth and development of Streptococcus mutans

• Tuyen Huu Nguyen,
• Hong Thanh Pham,
• Kieu Kim Thanh Nguyen,
• Loan Hong Ngo,
• Anh Ngoc Tuan Mai,
• Thu Hoang Anh Lam,
• Ngan Thi Kim Phan,
• Dung Tien Pham,
• Duong Thuy Hoang,
• Thuc Dong Nguyen and
• Lien Thi Xuan Truong

Beilstein J. Nanotechnol. 2025, 16, 308–315, doi:10.3762/bjnano.16.23

• inhibitory activity against pathogenic bacteria have been reported. In 2022, Nguyen et al. fabricated berberine nanoparticles (BerNPs) by antisolvent precipitation (ASP) using glycerol as a safe organic solvent and evaluated their antibacterial activity on S. aureus and E. coli O157:H7 [12]. Additionally

• demonstrated superior efficiency in producing nanoscale berberine. Tran et al. employed the ball milling technique to produce BerNPs, achieving a particle size of 570.7 nm [23]. Piri et al. utilized the anti-solvent precipitation method, yielding BerNPs with an average particle size of 75 nm [24]. BerNPs were

• synthesized by ASP using glycerol as a safe organic solvent, resulting in BerNPs with a narrow size distribution and an average diameter of 156 nm [12]. Additionally, the high-pressure homogenization method reduced the average size of BerNPs to approximately 72.4 nm [25]. Numerous studies showed that smaller

Enhancing mechanical properties of chitosan/PVA electrospun nanofibers: a comprehensive review

• Nur Areisman Mohd Salleh,
• Amalina Muhammad Afifi,
• Fathiah Mohamed Zuki and
• Hanna Sofia SalehHudin

Beilstein J. Nanotechnol. 2025, 16, 286–307, doi:10.3762/bjnano.16.22

• , and environment. For electrospinning, factors such as applied electric field, distance between the needle and collector, flow rate, and needle diameter affect the fabrication of the nanofibrous sample. Solution parameters include the types of solvent, polymer concentration, viscosity, and solution

• electrospinning, and some of the important parameters to take into consideration are the molecular weight of each component, solubility of the solvents, temperature, and the polymer blend ratio [79]. The straightforward approach in preparing the solution is by directly mixing both polymers in the solvent system

• , which can be either a single solvent [57] or a mixture of solvents [80][81] (Figure 5a). The polymers can also be prepared separately in separate solvent systems [82][83], and the solutions are subsequently mixed to form the final solution before electrospinning (Figure 5b). The latter involves more

Preferential enrichment and extraction of laser-synthesized nanoparticles in organic phases

• Theo Fromme,
• Maximilian L. Spiekermann,
• Florian Lehmann,
• Stephan Barcikowski,
• Thomas Seidensticker and
• Sven Reichenberger

Beilstein J. Nanotechnol. 2025, 16, 254–263, doi:10.3762/bjnano.16.20

• properties and surface chemistry of the gained colloids. The use of organic solvents as liquid may result in reactive LAL processes [1][10] that cause elements from the solvent molecules (and solutes) to be part of the final nanoparticle’s composition. The solvent decomposition induced by laser-based

• liquid hydrocarbons such as pyrolysis products [15][16][17][18], polyynes [19][20][21], and dimers [13][22][23]. Furthermore, depending on the solvent and ablated material pairing, carbon may be “harvested” from the solvent forming crystalline carbides [24][25][26][27], amorphous carbon dopant [28][29

• ], and/or carbon shells on the nanoparticle surface [7]. These carbon shells are either amorphous or graphitic [7][8][30], while doping of the shells [31] is also possible. Besides carbon formation, the choice of organic solvent influences the properties of the generated nanoparticles and process

A review of metal-organic frameworks and polymers in mixed matrix membranes for CO₂ capture

• Charlotte Skjold Qvist Christensen,
• Nicholas Hansen,
• Mahboubeh Motadayen,
• Nina Lock,
• Martin Lahn Henriksen and
• Jonathan Quinson

Beilstein J. Nanotechnol. 2025, 16, 155–186, doi:10.3762/bjnano.16.14

• , including regenerative solvent-based absorption [2][6], fixed-bed adsorption [7], cryogenic separation techniques [8], and membrane separation methods [9][10][11][12]. Of these, membrane technology offers advantages such as exceptional stability, high efficiency, low energy consumption, and ease of

• enhancing CO2 capture in MOFs [55]. The formation of OMSs involves solvent removal upon activation, which establishes uncoordinated metal sites capable of adsorbing guest molecules reversibly [60]. A wide range of OMS-bearing MOFs, including NU-1000, MIL-101, and the M-MOF-74 isoreticular series (M = Mg, Ni

• a thin layer atop a polymer support. Solvent removal following casting yields the finalized MOF-based MMM. This casting method is simple and cost-effective but is primarily relevant in small-scale applications. Asymmetric membranes can alternatively be prepared via phase inversion, where the

Instance maps as an organising concept for complex experimental workflows as demonstrated for (nano)material safety research

• Benjamin Punz,
• Maja Brajnik,
• Joh Dokler,
• Jaleesia D. Amos,
• Litty Johnson,
• Katie Reilly,
• Anastasios G. Papadiamantis,
• Amaia Green Etxabe,
• Lee Walker,
• Diego S. T. Martinez,
• Steffi Friedrichs,
• Klaus M. Weltring,
• Nazende Günday-Türeli,
• Claus Svendsen,
• Christine Ogilvie Hendren,
• Mark R. Wiesner,
• Martin Himly,
• Iseult Lynch and
• Thomas E. Exner

Beilstein J. Nanotechnol. 2025, 16, 57–77, doi:10.3762/bjnano.16.7

• ). Transformation protocol nodes helped to understand which object (e.g., nanomaterial, biological test system, or solvent/medium) underwent a modification, but they made the separation between material and medium less obvious. These circumstances also raised the question as to whether materials and medium always

Bioinspired nanofilament coatings for scale reduction on steel

• Siad Dahir Ali,
• Mette Heidemann Rasmussen,
• Jacopo Catalano,
• Christian Husum Frederiksen and
• Tobias Weidner

Beilstein J. Nanotechnol. 2025, 16, 25–34, doi:10.3762/bjnano.16.3

• ). After a reaction time of six hours, the surface is coated with a micrometer layer of SNFs. The surface reaction is proceeded by hydrolysis of TCMS due to water in the solvent. Subsequently, hydrolyzed TCMS molecules react with surface hydroxy moieties at the interface and thereby induce the

• and mixing 0.8 mL trichloromethylsilane (75-79-6, Sigma-Aldrich) into the toluene. The water content was measured with a Karl-Fischer volumetric titration setup. The solvent used for the coating is prepared by mixing oversaturated toluene (>400 ppm) with toluene from the vendor (<200 ppm). The SNF

• six hours of coating. For the results presented here, the water content in toluene was between 290–300 ppm. A coating with lower and higher amounts of water in the solvent is feasible, however, a less uniform coating will be obtained. Before the coating procedure the stainless-steel samples were

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

• added to the solution, and it was homogenized for 10 min in an ultrasonic bath. The solvent was then removed under reduced pressure. Then, solutions of Hist-RA (4 mM, 0.5 mL, PB, pH 8.5), CA-RA (8.8 mM, 0.5 mL, PB, pH 8.5), and BA (1.25 mM, 4 mL, PB, pH 8.5) were added, and then the synthesis was

• Aesar, Acros, and Aldrich, respectively) were used for column calibration. The data was analyzed by Agilent GPC/SEC software. Synthesis of Hist-RA Histamine dihydrochloride (Hist×HCl, 0.66 g, 4.47 mmol) was dissolved in 10 mL of double-distilled water and adjusted to pH 10.75. The solvent was evaporated

• stirred at 90 °C for 4 h. The solution was then cooled to room temperature, and 30 mL of chloroform was added. After evaporating the solvent under reduced pressure, 30 mL of diethyl ether was introduced, and the mixture was sonicated for 30 min. The product was subsequently filtered and washed with

Orientation-dependent photonic bandgaps in gold-dust weevil scales and their titania bioreplicates

• Norma Salvadores Farran,
• Limin Wang,
• Primoz Pirih and
• Bodo D. Wilts

Beilstein J. Nanotechnol. 2025, 16, 1–10, doi:10.3762/bjnano.16.1

• titania sol were dripped onto the etched weevil scales at opposing points and a glass slide was placed on top to ensure even infiltration via capillary forces. To solidify the sol and evaporate the residual solvent, the scales were heated in an oven at 100 °C for 20 min. Then, the top slide was removed

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

Fabrication of hafnium-based nanoparticles and nanostructures using picosecond laser ablation

• Abhishek Das,
• Mangababu Akkanaboina,
• Jagannath Rathod,
• R. Sai Prasad Goud,
• Kanaka Ravi Kumar,
• Raghu C. Reddy,
• Ratheesh Ravendran,
• Katia Vutova,
• S. V. S. Nageswara Rao and
• Venugopal Rao Soma

Beilstein J. Nanotechnol. 2024, 15, 1639–1653, doi:10.3762/bjnano.15.129

• liquids was also investigated. Experimental Materials Hf sponge was produced by metallurgical operations involving solvent extraction, briquetting, carbochlorination, Kroll reduction and vacuum distillation. The sponge samples were further refined by consolidation and refining under vacuum (3–6 × 10−5

Facile synthesis of size-tunable L-carnosine-capped silver nanoparticles and their role in metal ion sensing and catalytic degradation of p-nitrophenol

• Akash Kumar,
• Ridhima Chadha,
• Abhishek Das,
• Nandita Maiti and
• Rayavarapu Raja Gopal

Beilstein J. Nanotechnol. 2024, 15, 1576–1592, doi:10.3762/bjnano.15.124

• was performed in vaccum and water as solvent using the SCRF (CPCM) model to account for the effect of the environment. The computations were performed using density functional theory (DFT) with the B3LYP functional [22] and split basis sets 6-31+G* for all atoms (C, O, N, and H), and LANL2DZ for Ag

• ʟ-carnosine in aqueous solution compared to those in the solid is probably due to solvent effects. Figure 4c shows surface-enhanced Raman spectra (SERS) of ʟ-carnosine-capped silver nanoparticles. The signal-to-noise (S/N) ratio follows the order ʟ-car-AgNP4 > ʟ-car-AgNP3 > ʟ-car-AgNP2 > ʟ-car-AgNP1

Polymer lipid hybrid nanoparticles for phytochemical delivery: challenges, progress, and future prospects

• Iqra Rahat,
• Pooja Yadav,
• Aditi Singhal,
• Mohammad Fareed,
• Jaganathan Raja Purushothaman,
• Mohammed Aslam,
• Raju Balaji,
• Sonali Patil-Shinde and
• Md. Rizwanullah

Beilstein J. Nanotechnol. 2024, 15, 1473–1497, doi:10.3762/bjnano.15.118

• modification of PLHNPs begins with the preparation of the nanoparticles themselves. PLHNPs are typically synthesized using techniques such as solvent evaporation, nanoprecipitation, double emulsion, or solvent injection, resulting in the formation of nanoparticles with a lipid–polymer hybrid structure [60

Ion-induced surface reactions and deposition from Pt(CO)₂Cl₂ and Pt(CO)₂Br₂

• Mohammed K. Abdel-Rahman,
• Patrick M. Eckhert,
• Atul Chaudhary,
• Johnathon M. Johnson,
• Jo-Chi Yu,
• Lisa McElwee-White and
• D. Howard Fairbrother

Beilstein J. Nanotechnol. 2024, 15, 1427–1439, doi:10.3762/bjnano.15.115

• -dichloroethane (DCE, C2H4Cl2), toluene, and n-heptane) were purified using an MBraun MB-SP solvent purification system and stored over 3 Å molecular sieves before use. All reagents were purchased from Millipore Sigma and used without further purification. Carbon monoxide (CP grade), and 13C carbon monoxide were

• were referenced to the solvent. IR spectra were obtained on a PerkinElmer Spectrum ONE FTIR spectrometer using a solution cell equipped with NaCl windows and a path length of 1.0 mm. cis-Pt(CO)2Br2 The compound was synthesized using a modified literature procedure [73]. In a glove box, a glass pressure

• another 3 h. After the reactor was cooled to room temperature, the reaction mixture was stirred overnight. The unreacted CO gas was then released, and the reactor was backfilled with N2. The Parr reactor was brought into the glove box and opened inside. The DCE solvent and the yellow-brown suspension were

Green synthesis of carbon dot structures from Rheum Ribes and Schottky diode fabrication

• Muhammed Taha Durmus and
• Ebru Bozkurt

Beilstein J. Nanotechnol. 2024, 15, 1369–1375, doi:10.3762/bjnano.15.110

• refractive index of the solvent, and OD is the optical density at the excitation wavelength (λexc = 320 nm). The subscripts “s” and “r” refer to the sample and reference solutions, respectively. Quinine sulfate (Φf = 0.55 in 0.5 M H2SO4) was used as the reference compound [15]. According to this equation

Nanoarchitectonics with cetrimonium bromide on metal nanoparticles for linker-free detection of toxic metal ions and catalytic degradation of 4-nitrophenol

• Akash Kumar and
• Raja Gopal Rayavarapu

Beilstein J. Nanotechnol. 2024, 15, 1312–1332, doi:10.3762/bjnano.15.106

• . The mobile phase included a mixture of acetonitrile and water (40:60 v/v) at a 0.2 mL/min flow rate. The method was developed using CTAB powder as standard at different concentrations of 0.625, 1.2, 2.5, 5, 10, and 20 µg/mL in water. The blank sample (which consisted only of solvent) was also analyzed

Mn-doped ZnO nanopowders prepared by sol–gel and microwave-assisted sol–gel methods and their photocatalytic properties

• Cristina Maria Vlăduț,
• Crina Anastasescu,
• Silviu Preda,
• Oana Catalina Mocioiu,
• Simona Petrescu,
• Jeanina Pandele-Cusu,
• Dana Culita,
• Veronica Bratan,
• Ioan Balint and
• Maria Zaharescu

Beilstein J. Nanotechnol. 2024, 15, 1283–1296, doi:10.3762/bjnano.15.104

• indicates a weight loss of approx. 75% up to 500 °C, while the DTA curve shows also four effects, that is, an endothermic effect at 139 °C and three exothermic effects at 310, 405 and 901 °C. In both cases, the removal of physically absorbed water and solvent groups occurs between 100 and 180 °C, resulting

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

• acetone. The compound was dried using a vacuum pump and stored in a desiccator. The product was analyzed by proton nuclear magnetic resonance (1H NMR) in deuterated water (D2O, 600 μL) with the standard trimethylsilyl propionic acid (TMSP). The signal referring to the solvent used, D2O, was omitted from

• shifts (δ) were related in part per million (ppm) to the standard TMSP. The signal referring to the solvent used, deuterated water, was omitted from the spectra. The elemental analysis measurements were performed on a CHN 2400 Elementary Analyzer (Perkin-Elmer). The NP dispersions were dried in an oven

AI-assisted models to predict chemotherapy drugs modified with C₆₀ fullerene derivatives

• Jonathan-Siu-Loong Robles-Hernández,
• Dora Iliana Medina,
• Katerin Aguirre-Hurtado,
• Marlene Bosquez,
• Roberto Salcedo and
• Alan Miralrio

Beilstein J. Nanotechnol. 2024, 15, 1170–1188, doi:10.3762/bjnano.15.95

• genetic algorithms and final optimization at the DFTB3 level, respectively. London dispersion forces were considered in the DFTB3 and global optimization procedures by Lennard-Jones potentials, as implemented in UFF and MMFF94 force fields, respectively. The solvent effect was included by the Born

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

• , researchers have improved the formulation procedures for alginate-based nanoparticles to improve drug-loading capacity, stability, and controlled release characteristics. To improve the formulation of alginate nanoparticles, several methods have been developed, including emulsion-based approaches, solvent

• nanoparticles, a nontoxic metal ion is chosen as the precursor. This precursor can be combined with alginate, a natural polymer derived from seaweed, in a purified natural solvent such as water. Then, a reducing agent is selected to reduce the metal ions and form nanoparticles. One environmentally friendly

• solvent using the Doppler approach, which measures particle velocity as a function of voltage. The determination of the zeta potential is crucial in understanding the mechanism of drug–nanoparticle interactions [66]. In addition to the methods described above, Fourier-transform infrared spectroscopy is

Atomistic insights into the morphological dynamics of gold and platinum nanoparticles: MD simulations in vacuum and aqueous media

• Evangelos Voyiatzis,
• Eugenia Valsami-Jones and
• Antreas Afantitis

Beilstein J. Nanotechnol. 2024, 15, 995–1009, doi:10.3762/bjnano.15.81

• shown. In most applications, NPs suspended in biological fluids and aqueous solutions can serve as a proxy system that is easy to control [86]. The NPs are either bare or coated with a corona, the coverage of which may fluctuate, again leaving the NP surface exposed to the solvent [87]. Thus, it is

• interact favourably with the water solvent, the interactions are much stronger for the Pt NPs compared to the Au NPs. Therefore, the expected structural modifications and potential partial oxidation in the Pt case are going to be stronger than in the Au case. Although partial oxidation can be addressed

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

• emulsion, or nanoprecipitation [1][4], in which copolymers are dissolved in an organic solvent, called the organic phase, and then are put into an immiscible aqueous solution, called the water phase, to form the nanoparticles. Various surfactants, including poly(vinyl alcohol) (PVA), sodium cholate, or

• acetonitrile, PLGA 504H (20 mg), chlorambucil (2 mg), and IR780 (0.1 mg) were mixed (2 mL). Then, the mixture was added dropwise into 20 mL of F127 solution (1.5% w/v) with F127-folate (2 mg) while stirring at 200 rpm. For 16 h, the organic solvent was allowed to evaporate. The F127-folate@PLGA/CHL/IR780 were