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

• -Eud-F-Alg NPs. Surface composition of nanoparticles The surface composition of the nanoparticles was characterized with ATR-FTIR (Figure 2). For Alg nanoparticles, distinctive bands were observed at 1567 and 1405 cm−1, which were assigned to asymmetric and symmetric stretching vibrations of

• position was detected (from 1567 to 1608 cm−1). This was attributed to weak interactions between alginate and Eudragit polymer, which were also observed in other studies [37]. Taken together, it can be concluded from the results of microscopy and FTIR analysis that the Alg nanoparticles were coated with

• reflectance Fourier-transform infrared spectroscopy (ATR-FTIR) was used. Freeze-dried nanoparticles were directly placed on an ATR crystal, and the infrared spectrum of the samples was obtained in the range of 4000–400 cm−1 using a FTIR spectrophotometer (Bruker/Vertex70, USA). Particle size and zeta

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

• quantitative estimation of the unbound drug. Physical characterization techniques The functional group and structural analysis of GO and GO–Chl nanoconjugate were studied using a Fourier-transform infrared spectrometer (Cary 630 FTIR, Agilent, CA, USA) in ATR mode and a Raman spectrophotometer (Ranishaw win

• characteristic band at around 343 nm, in GO–Chl, could be related to the binding of Chl to GO [42]. The functional groups in GO and GO–Chl nanoconjugates were analyzed by FTIR spectroscopy. Supporting Information File 1, Figure S1b shows the FTIR spectrum of GO, Chl, and GO–Chl in the range of 500–3800 cm−1

• /IG ratio (0.882) is observed for the GO–Chl sample compared to that of GO (0.929). This indicates a possible conversion of the sp3 carbon to sp2 carbon due to the reducing environment imparted by the amino functionalities present on the Chl, which was also corroborated by FTIR data [47]. Furthermore

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

• [24][28], which shows that ball grinding does not alter the crystal structure of berberine. FTIR spectroscopy results show that the characteristic peaks of BerNPs coincide with that of the raw berberine at 1597, 1507, 1363, 1276, 1103, and 1035 cm−1 [24]. These results demonstrate that ball grinding

• , and ldh, thereby preventing biofilm development [40]. Conclusion In this study, BerNPs were fabricated using ball milling with zirconium balls. Analysis through FE-SEM, UV–vis, XRD, and FTIR revealed that the nanoparticles predominantly exhibited a crystalline structure, with an average size of 40–65

• temperature, and analyzed at a voltage of 10 kV [24]. X-ray diffraction analysis was used to evaluate the crystalline structure of berberine and BerNPs. FTIR spectra were analyzed to identify typical functional groups and chemical bonds in raw berberine and BerNPs [28]. Determination of minimum inhibitory

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

• after exposure to irradiation, X-ray powder diffraction (XRPD) was used. The stability of TMZ under these conditions was determined unsing attenuated total reflectance Fourier-transform infrared (ATR-FTIR) and UV–vis spectroscopy. Most of the procedures and techniques were used in our previous study [43

• -FA-TMZ (Figure 4d), but are slightly shifted to 3346, 3389, 3423, 2921, and 2853 cm−1, serving as a spectroscopic evidence for the existence of non-covalent interactions (electrostatic, hydrogen bond, and/or van der Waals forces) between CNs and TMZ. From comparison of the ATR-FTIR spectrum of TMZ

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

• formed may not fully represent the structure of the fabricated MOF-based MMMs. While electron microscopy offers a highly detailed qualitative analysis of specific regions within the membrane, methods such as Fourier-transform infrared spectroscopy (FTIR), nuclear magnetic resonance (NMR) spectroscopy

• , and X-ray diffraction (XRD) provide information about the bulk MOF-based MMM [140][141][142]. FTIR yields information about the functional groups within the sample [140], and will differ between the pristine MOF, polymer membrane, and MOF-based MMM [118][121][122][124][128][131]. In this way, it is

• possible to compare how various modifications to the MOF-based MMM system change the functional groups within the final membrane [122][125][128]. Similar to FTIR, NMR provides insights into the chemical nature of the membrane but offers more detailed information about its chemical structure [141]. XRD

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

• radiation (λ = 1.5410 Å) operating at 40 kV and 30 mA. Data were collected in scanning mode in steps between 4° and 75° (2θ) with a step size of 0.05°/s. The basal distance was obtained using Bragg's Law. Fourier-transform infrared spectroscopy (FTIR) spectra were collected on a Perkin Elmer Frontier FTIR

• observed in Figure 3. The FTIR spectra of the bentonite before and after modification with niobium are shown in Figure 4. It can be observed that for the BE samples and all those modified with NbOPO4 (Figure 4a), the spectra show a narrow band in the region of 3638 cm−1, associated with the (Al–OH–Al

• clay (a), bentonite modified with NbOX (BeOx) (b), and bentonite modified with NbPh (BePh) (c). The structures were obtained with the Vesta program using the COD 1100106, COD 1534619, and COD 1517684 for montmorillonite, niobium oxide, and niobium phosphate, respectively. FTIR spectra for the bentonite

Characterization of ZnO nanoparticles synthesized using probiotic Lactiplantibacillus plantarum GP258

• Prashantkumar Siddappa Chakra,
• Aishwarya Banakar,
• Shriram Narayan Puranik,
• Vishwas Kaveeshwar,
• C. R. Ravikumar and
• Devaraja Gayathri

Beilstein J. Nanotechnol. 2025, 16, 78–89, doi:10.3762/bjnano.16.8

• nanoparticles (ZnO NPs), utilizing lactic acid bacteria isolated from curd as the key biological agent. Bacteria function as agents for both reduction and capping processes, which aids the synthesis of ZnO NPs. Various characterization techniques including XRD, FTIR, UV–vis, TEM, SEM-EDX, and zeta potential

• the scattering angle. Using this formula, we determined an average crystallite size of around 25 nm for the 2θ angle of 35.8°. This measurement provided valuable insight into the dimensions of the ZnO NPs and is depicted in Figure 2a. FTIR analysis The FTIR spectra of ZnO NPs were examined in the

• wurtzite structure. Similarly, in another study, Suba et al. [22] also described the biosynthesis of hexagonal ZnO NPs using Lactiplantibacillus spp. Valuable insights into the synthesis process were obtained through FTIR spectroscopy. The peak at 484 cm−1 confirms the occurrence of Zn–O linkages

Natural nanofibers embedded in the seed mucilage envelope: composite hydrogels with specific adhesive and frictional properties

• Agnieszka Kreitschitz and
• Stanislav N. Gorb

Beilstein J. Nanotechnol. 2024, 15, 1603–1618, doi:10.3762/bjnano.15.126

• impossible. The complicated preparation procedures and analysis give us often an information limited to just one factor, for example, to specific chemical composition or topology (AFM, FTIR, or Raman microscopy) [45]. Ideally, the comparison of data from diverse visualisation techniques can provide us with

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

• ʟ-carnosine in synthesizing tunable plasmonic silver nanoparticles (ʟ-car-AgNPs). The formation of ʟ-car-AgNPs was confirmed via UV–vis optical absorption spectroscopy, showing single and double plasmonic peaks, depending on the synthesis conditions. Physicochemical characterization using TEM, FTIR

• . The functionalization of AgNPs with ʟ-carnosine was validated through Fourier-transform infrared spectroscopy (FTIR, Thermo Scientific Nicolet iS5, USA). For this, 10 mg of air-dried nanopowder was placed over a diamond, and the software (OMNIC™) was run over the spectral range of 400–4000 cm−1. The

• -carnosine and ʟ-car-AgNPs and 100 s for ʟ-carnosine in aqueous solution. DFT calculations Theoretical insights into the FTIR and Raman measurements were obtained through molecular structure optimization of ʟ-carnosine, its anionic form, and probable ʟ-carnosine–(Ag)4 complexes. The structure optimization

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

• 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

• Cl LMM and C KVV Auger transitions. Reaction cross sections for Pt(CO)2X2 dissociation. Supporting Information FTIR spectra of Pt(12CO)2Cl2, Pt(13CO)2Cl2, and Pt(CO)2Br2, evolution of film contrast as a function of Ar+ dose, the decay of the C 1s X-ray photoelectron intensity as a function of Ar

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

• synthesis, which is commonly used in the literature. TEM and zeta potential measurements were used to determine morphology and sizes of the CDs, and XRD, XPS, and FTIR and micro-Raman spectroscopy were used for structural characterization. Optical characterization of the CDs was done by absorption and

• Cary Eclipse fluorescence spectrophotometer were used for transmission electron microscopy (TEM), zeta potential measurements, X-ray diffractometry (XRD), Fourier-transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), micro-Raman spectroscopy, PVD thermal evaporation, scanning

• and the thickness of coated CDs film were 1 cm2 and ca. 566 nm, respectively. Results and Discussion Structural and optical characterization of synthesized CDs The morphological and chemical structures of the CDs obtained from Rheum ribes were determined by TEM, FTIR, XRD, and XPS analyses. TEM shows

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

• , surface capping, and linker molecules are required to degrade 4-nitrophenol. Therefore, this study analyzed the impact of size, shape, metal type, and nanoparticle concentration on converting 4-nitrophenol to 4-aminophenol. Characterization of CTAB-capped nanoparticles UV–vis, DLS, Zeta, FTIR, XRD, and

• TEM analyses Physicochemical characterization was performed using optical spectroscopy, DLS, FTIR, XRD, and TEM analyses. Figure 2a shows the synthesized isotropic silver and gold nanospheres with plasmon bands at 410 nm (AgNS) and 525 nm (AuNS). The anisotropic tunable gold nanorods with longitudinal

• of the metal nanoparticles and form a cationic layer around them [28]. CTAB-AgNS, CTAB-AuNS, CTAB-AuNR1, and CTAB-AuNR2 were analyzed for functional group identification using FTIR (Figure 2d). CTAB contains a long alkyl chain that typically results in peaks at 2920 and 2850 cm−1 in the FTIR spectrum

Interaction of graphene oxide with tannic acid: computational modeling and toxicity mitigation in C. elegans

• Romana Petry,
• James M. de Almeida,
• Francine Côa,
• Felipe Crasto de Lima,
• Diego Stéfani T. Martinez and
• Adalberto Fazzio

Beilstein J. Nanotechnol. 2024, 15, 1297–1311, doi:10.3762/bjnano.15.105

• biological medium. In the Fourier-transform infrared spectroscopy (FTIR) analysis (Figure 2a), we observed bands between 3000 and 4000 cm−1 related to –OH strength in all spectra. GO spectra presented fingerprint bands at 1734, 1625, 1390, 1230, and 1068 cm−1, which correspond to C=O stretching vibrations

• spectroscopy (XploRA PLUS, Horiba), FTIR spectroscopy (IRSpirit Shimadzu), and XPS (K-Alpha XPS Thermo Fisher Scientific) were used to assess changes in the morphology and surface chemistry of GO while interacting with TA. For AFM analysis, 10 mg·L−1 GO was incubated in EPA medium for 24 h with and without 10

• mg·L−1 TA. Then, to avoid salt interference, the suspension was washed three times with deionized water and dripped on mica substrate. The incubation procedure was repeated for spectroscopy analysis. For Raman and FTIR analysis, the suspensions were dried using the speed-vacuum method at room

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

• methods. Fourier-transform infrared spectroscopy Figure 1 shows the FTIR spectra of as-prepared gels obtained by SG and MW. The broad band in the 3600–2500 cm−1 region can be assigned to overlapping characteristic vibrations of C–H, N–H, and O–H bonds. The small bands at 2972, 2866, and 2747 cm−1 are

• characteristic to vibrations of C–H bonds in CH2 and CH3 groups. The bands are shifted from their position in the spectrum of pure zinc acetate [42]. The asymmetric and symmetric stretchings of C=O in COO– groups occur in the FTIR spectra at 1580 and 1418 cm−1, respectively. The symmetric stretching of the C–O

• characteristic of Mn–O bond vibrations [44]. Based on the FTIR spectra, we can assume that during the gelation process a zinc-based gel with a structure similar to the one reported by Moezzi [46] was obtained. The primary distinction between the samples prepared by the two methods discussed in this article (SG

Enhanced catalytic reduction through in situ synthesized gold nanoparticles embedded in glucosamine/alginate nanocomposites

• Chi-Hien Dang,
• Le-Kim-Thuy Nguyen,
• Minh-Trong Tran,
• Van-Dung Le,
• Nguyen Minh Ty,
• T. Ngoc Han Pham,
• Hieu Vu-Quang,
• Tran Thi Kim Chi,
• Tran Thi Huong Giang,
• Nguyen Thi Thanh Tu and
• Thanh-Danh Nguyen

Beilstein J. Nanotechnol. 2024, 15, 1227–1237, doi:10.3762/bjnano.15.99

• synthesizing gold nanoparticles (AuNPs) within a glucosamine/alginate (GluN/Alg) nanocomposite via an ionotropic gelation mechanism in aqueous environment. The resulting nanocomposite, AuNPs@GluN/Alg, underwent thorough characterization using UV–vis, EDX, FTIR, SEM, TEM, SAED, and XRD analyses. The spherical

• 0 to 140 min. Physicochemical characterizations of AuNPs@GluN/Alg nanocomposite The samples synthesized under optimal conditions underwent physicochemical characterization and were used for the catalytic reduction of organic dyes. FTIR spectra of blank GluN/Alg and AuNPs@GluN/Alg were acquired using

• a Bruker Tensor 27 FTIR spectrophotometer, which scanned wavelengths from 500 to 4000 cm−1. KBr pellets were used for the measurements. For morphological investigations of the nanocomposites, scanning electron microscopy (SEM) was performed using a SEM-S4800 instrument; transmission electron

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

• are sensitive to two factors, such as pH and temperature, can be engineered to enhance targeting efficacy while minimizing systemic side effects [31][32]. Here, a strategy for the production and application of DOX-SNPs is proposed. FTIR, SEM, and zeta potential measurements were performed to

• Centrifugen, USA). The precipitated nanostructures were redispersed in distilled water utilizing a sonicator and dried with a lyophilizer. Then, the nanostructures were stored at 4 °C. Characterization studies Functional group analysis was carried out by Fourier-transform infrared (FTIR) spectroscopy

• nanostructures, and analyses of the characteristic peaks in the FTIR spectrum were performed. The FTIR spectra of SNPs and DOX-SNPs are given in Figure 2. From these spectra, the intensity of The FTIR spectra of SNPs and DOX-SNPs are given in Figure 2. The intensity of the OH peaks around 3370 cm−1 increased

Direct electron beam writing of silver using a β-diketonate precursor: first insights

• Katja Höflich,
• Krzysztof Maćkosz,
• Chinmai S. Jureddy,
• Aleksei Tsarapkin and
• Ivo Utke

Beilstein J. Nanotechnol. 2024, 15, 1117–1124, doi:10.3762/bjnano.15.90

• Raman or FTIR spectroscopy [5][8][37], to study the nature of the desorbed and incorporated molecular fragments ideally during the irradiation process. Up to now, only silver pentafluoropriopionate allowed for three-dimensional growth [30]. However, the use of this compound required relatively high

Facile synthesis of Fe-based metal–organic frameworks from Fe₂O₃ nanoparticles and their application for CO₂/N₂ separation

• Van Nhieu Le,
• Hoai Duc Tran,
• Minh Tien Nguyen,
• Hai Bang Truong,
• Toan Minh Pham and
• Jinsoo Kim

Beilstein J. Nanotechnol. 2024, 15, 897–908, doi:10.3762/bjnano.15.74

• and yield of the as-prepared MIL-100(Fe) materials, including thermogravimetric analysis (TGA), Fourier-transform infrared (FTIR) spectroscopy, powder X-ray diffraction (PXRD) measurements, determination of textural properties, scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy

• -100Fe@Fe2O3 materials was collected using a field-emission scanning electron microscope Leo-Supra 55 (Carl Zeiss STM, Germany). An attenuated total reflectance (ATR) setup was adopted to record the Fourier-transform infrared (FTIR) spectra of all samples on a Frontier spectrometer (PerkinElmer, USA) in

• MIL-100(Fe) crystals in the prepared M-100Fe@Fe2O3 samples increases in the following order: M-100Fe@Fe2O3#0.90 < M-100Fe@Fe2O3#1.35 < M-100Fe@Fe2O3#1.80 < M-100Fe@Fe2O3#2.25. This result aligns well with the XRD data shown in Figure 2. Figure 4 exhibits ATR-FTIR spectra of Fe2O3, MIL-100(Fe), and as

Electron-induced ligand loss from iron tetracarbonyl methyl acrylate

• Hlib Lyshchuk,
• Atul Chaudhary,
• Thomas F. M. Luxford,
• Miloš Ranković,
• Jaroslav Kočišek,
• Juraj Fedor,
• Lisa McElwee-White and
• Pamir Nag

Beilstein J. Nanotechnol. 2024, 15, 797–807, doi:10.3762/bjnano.15.66

• use. 1H nuclear magnetic resonance spectra (NMR) were obtained on a Bruker 400 MHz spectrometer. 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. Synthesis The compound was synthesized according to

• fragments from the reaction Fe(CO)4(η2-C4H6O2) + e−. Supporting Information Supporting Information contains details of the DFT calculation, ion yield curves for dissociative ionization, and FTIR, NMR and UV–vis spectra of the sample. Supporting Information File 16: Additional experimental data. Funding

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

• scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR), mechanical tests, investigation of salt dissolution from the scaffolds, examination of their antibacterial activity against four different bacterial strains (Escherichia coli, Pseudomonas aeruginosa, Bacillus subtilis, and

• FTIR analysis, we used an energy-dispersive X-ray spectroscopy (EDX) detector during the SEM measurements to show the presence of salts in the fibers. The EDX spectra were taken at a voltage of 15 kV. Mechanical properties A mechanical testing machine (4952, Instron, USA) and the associated software

• in Table 1. The presence of Sr(NO3)2 changed the viscosity and conductivity properties of the solutions. In the case of 20 PSI + 5 Sr(NO3)2 and 20 PSI + 7.5 Sr(NO3)2, a higher voltage was necessary for fiber preparation based on the viscosity decrease. On the FTIR spectra (Figure 1B, Figure 1C), the

Green synthesis of biomass-derived carbon quantum dots for photocatalytic degradation of methylene blue

• Dalia Chávez-García,
• Mario Guzman,
• Viridiana Sanchez and
• Rubén D. Cadena-Nava

Beilstein J. Nanotechnol. 2024, 15, 755–766, doi:10.3762/bjnano.15.63

• catalytic activity in MB degradation, while those prepared with water as a solvent did not show significant catalytic activity. The samples were also characterized using UV–visible spectra, Fourier-transform infrared spectroscopy (FTIR), Raman spectroscopy, dynamic light scattering (DLS), and

• underlines the influence of biomass source and synthesis parameters on the resulting CQD dimensions. Fourier-transform infrared spectroscopy The surface chemical groups of the samples were analyzed using FTIR spectroscopy. Figure 3a displays the FTIR spectrum of the CQDs synthesized with grape pomace. Since

• oxidation process enhances the solubility of CQDs in water. The spectrum also shows low-intensity signals in the range of 1800 to 2500 cm−1, which are characteristic of aromatic compounds [22][27]. In Figure 3b, the FTIR spectrum of the CQDs synthesized from watermelon peel is shown. Similar characteristics

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

• diffraction (XRD), and FTIR, respectively, to establish physicochemical properties of the synthesized nanomaterials. Results Synthesis, optical spectroscopy, and zeta potential Anisotropic gold nanoparticles of makura shape were synthesized using seed-mediated approach as shown in Figure 1a. The Au seeds were

• shifted in the case of surfactant-capped gold nanoparticles when compared to the FTIR spectra of pure surfactants (CTAB, MTAB, and DTAB). Pure surfactants (CTAB, MTAB, and DTAB) generally show two bands at 719 and 731 cm−1, whereas surfactant-capped gold nanoparticles only show one band at 669 cm−1 as

• confirmed through FTIR spectroscopy. C–H scissoring vibrations of H3C–N+ and C–N+ stretching are relatively less intense and slightly shifted in surfactant-capped gold nanoparticles with an appearance of a single band at 669 cm−1 as shown in Figure 5a. This is clear proof of the containments that surfactant

Laser synthesis of nanoparticles in organic solvents – products, reactions, and perspectives

• Theo Fromme,
• Sven Reichenberger,
• Katharine M. Tibbetts and
• Stephan Barcikowski

Beilstein J. Nanotechnol. 2024, 15, 638–663, doi:10.3762/bjnano.15.54

• tetrahydrofurane (THF) at a total energy input of 2250 J comparing fs-, ps-, and ns-pulsed lasers using FTIR spectroscopy. They found a significant decrease in the dominant C–O–C bond at 1070 cm−1 after ablation, which indicates cleavage of the C–O–C bonds in THF. C–H and C–C bonds were detected before and after

AFM-IR investigation of thin PECVD SiO_x films on a polypropylene substrate in the surface-sensitive mode

• Hendrik Müller,
• Hartmut Stadler,
• Teresa de los Arcos,
• Adrian Keller and
• Guido Grundmeier

Beilstein J. Nanotechnol. 2024, 15, 603–611, doi:10.3762/bjnano.15.51

• correlation between the IR wavelength of the laser and the thermal expansion of the material enables the recording of IR absorption spectra with this technique which correspond to the spectra of bulk IR spectroscopy [2][3][4]. Compared to ATR-FTIR spectroscopy, AFM-IR provides a drastic improvement in terms

Radiofrequency enhances drug release from responsive nanoflowers for hepatocellular carcinoma therapy

• Yanyan Wen,
• Ningning Song,
• Yueyou Peng,
• Weiwei Wu,
• Qixiong Lin,
• Minjie Cui,
• Rongrong Li,
• Qiufeng Yu,
• Sixue Wu,
• Yongkang Liang,
• Wei Tian and
• Yanfeng Meng

Beilstein J. Nanotechnol. 2024, 15, 569–579, doi:10.3762/bjnano.15.49

• hydrated state [31]. The DLS depicted size is the closest to that in vivo. The Fourier-transform infrared (FTIR) spectrum of CUR exhibited vibrational absorption peaks at 1207 cm−1 and 3330 cm−1 corresponding to C=O and –OH, respectively, in the phenolic hydroxy group (Figure 2f). Similarly, for bis(4

• ) molecule, while the peaks at 874 cm−1 and 1217.3 cm−1 resulted from the vibrations of P–N and P=N in HCCP. The FTIR spectrum of the CUR-Fe@MnO2 NFs revealed an absorption peak corresponding to the Fe–O bond in the Fe3O4 NCs at 584 cm−1. A new absorption peak at 963 cm−1 indicated the formation of P–O– CUR

• , respectively). f) FTIR spectra of HCCP, CUR, HPS, and the CUR-Fe@MnO2 NFs. g) XRD patterns of the Fe3O4 NCs, curcumin, CUR-Fe NPs, and CUR-Fe@MnO2 NFs. h) Hysteresis loop of the Fe3O4 NCs and CUR-Fe@MnO2 NFs, indicating that they were superparamagnetic. a) T1/T2-mapping MR imaging of CUR-Fe@MnO2 NFs at pH 5.0