Ultrathin water layers on mannosylated gold nanoparticles

• Maiara A. Iriarte Alonso,
• Jorge H. Melillo,
• Silvina Cerveny,
• Yujin Tong and
• Alexander M. Bittner

Beilstein J. Nanotechnol. 2025, 16, 2183–2198, doi:10.3762/bjnano.16.151

• inorganic surfaces, usually modified with organic layers, and probed by Fourier-transform infrared spectroscopy (FTIR), vibrational sum frequency generation (VSFG), and atomic force microscopy (AFM). For VSFG and AFM, we systematically varied the relative air humidity (RH). DLS and ZP yield particle size

• and stability in solution, in terms of hydrodynamic diameter and NP surface charge, respectively. Spectroscopy techniques were used to analyze the chemical composition of the organic ligands locally. We used FTIR for the molecular fingerprint infrared region to find the characteristic peaks of the

• indeed yields an independent estimate of the shell thickness. This analysis gives values consistent with the ~1.5 nm thickness extracted from single-particle measurements. Analysis of the chemical groups The nature of the coating layer of PEG AuNPs and dimanno-AuNPs was characterized by FTIR (only in dry

Microplastic pollution in Himalayan lakes: assessment, risks, and sustainable remediation strategies

• Sameeksha Rawat,
• S. M. Tauseef and
• Madhuben Sharma

Beilstein J. Nanotechnol. 2025, 16, 2144–2167, doi:10.3762/bjnano.16.148

• understanding the full contamination profile in remote ecosystems [33]. An overview of MP sampling and analysis methods is given in Figure 3. 4.2 Analytical techniques for microplastic characterization 4.2.1 Spectroscopy. One of the key methods of analyzing MPs is spectroscopy. Fourier-transform infrared (FTIR

• ) spectroscopy is used regularly to identify the chemical structure of MPs [34]. One of the most important developments for nanoplastic detection in complex environmental matrices is micro-FTIR to analyze particles smaller than 10 µm [35]. Raman spectroscopy improves on FTIR by using higher resolution and the

• intervention and possibility of error [39]. Microscopy and spectroscopy tend to be combined to increase reliability. For instance, Raman or FTIR spectroscopy is applied to identify polymers following SEM to examine the shape of particles. This ensures both chemical and physical characteristics are captured [40

Rapid synthesis of highly monodisperse AgSbS₂ nanocrystals: unveiling multifaceted activities in cancer therapy, antibacterial strategies, and antioxidant defense

• Funda Ulusu,
• Adem Sarilmaz,
• Yakup Ulusu,
• Faruk Ozel and
• Mahmut Kus

Beilstein J. Nanotechnol. 2025, 16, 2105–2115, doi:10.3762/bjnano.16.145

• separate interaction exists between 6 sulfur atoms and silver and antimony atoms. Also, the obtained diffraction peaks are neat and intense, indicating the absence of other secondary phase peaks, and proving the successful synthesis of the desired structure. FTIR analysis was carried out in the range of

• specificity. Integration with emerging nanomedicine approaches such as theranostics, controlled drug delivery, and precision oncology could further advance the translational potential of AgSbS2 NCs. Synthesis procedure (a), XRD pattern (b), crystal geometry (c), and FTIR spectrum (d) of the synthesized NCs

Stereodiscrimination of guests in chiral organosilica aerogels studied by ESR spectroscopy

• Sebastian Polarz,
• Yasar Krysiak,
• Martin Wessig and
• Florian Kuhlmann

Beilstein J. Nanotechnol. 2025, 16, 2034–2054, doi:10.3762/bjnano.16.140

• m2·g−1. The meso-macroporous structure was also found by mercury intrusion porosimetry (Figure 2c). The FTIR spectrum is consistent with the proposed composition (Figure 2d). The vibrations at ν = 3000–3600 cm−1 are characteristic for NH and OH groups. At 2982 cm−1, one sees the CH groups. Amide

Beyond the shell: exploring polymer–lipid interfaces in core–shell nanofibers to carry hyaluronic acid and β-caryophyllene

• Aline Tavares da Silva Barreto,
• Francisco Alexandrino-Júnior,
• Bráulio Soares Arcanjo,
• Paulo Henrique de Souza Picciani and
• Kattya Gyselle de Holanda e Silva

Beilstein J. Nanotechnol. 2025, 16, 2015–2033, doi:10.3762/bjnano.16.139

• -sectional imaging, and attenuated total reflectance with Fourier transform infrared (ATR-FTIR) spectroscopy provided compelling evidence for the successful formation of the intended core–shell structure. The resulting nanofibers exhibited surface hydrophobicity, suggesting potential for anti-adhesive

• to increased water ingress through the pores, facilitating access to the core [58]. This possibility is also described by Wang and Xu (2018), who successfully prepared tea polyphenol-loaded porous core–shell fibers by controlling coaxial electrospinning parameters [56]. ATR-FTIR spectroscopy has been

• widely used to evaluate the integrity of core–shell structures and confirm the presence of the core material within electrospun fibers. A well-formed core–shell structure is indicated by FTIR spectra showing the absence of characteristic core bands and the exclusive presence of shell bands [59][60][61

Self-assembly and adhesive properties of Pollicipes pollicipes barnacle cement protein cp19k: influence of pH and ionic strength

• Shrutika Sawant,
• Anne Marie Power and
• J. Gerard Wall

Beilstein J. Nanotechnol. 2025, 16, 1863–1872, doi:10.3762/bjnano.16.129

• concentration environment exhibited the highest fluorescence, though more detailed investigation using methods such as attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy or circular dichroism (CD) will be necessary to confirm an elevated β-sheet content in these fibrils. A similar

On the road to sustainability – application of metallic nanoparticles obtained by green synthesis in dentistry: a scoping review

• Lorena Pinheiro Vasconcelos Silva,
• Joice Catiane Soares Martins,
• Israel Luís Carvalho Diniz,
• Júlio Abreu Miranda,
• Danilo Rodrigues de Souza,
• Éverton do Nascimento Alencar,
• Moan Jéfter Fernandes Costa and
• Pedro Henrique Sette-de-Souza

Beilstein J. Nanotechnol. 2025, 16, 1851–1862, doi:10.3762/bjnano.16.128

• investigation of antimicrobial activity against these microorganisms indicates the potential dental applications of green-synthesized metallic nanoparticles. To characterize the green-synthesized metallic nanoparticles, the selected studies used mainly Fourier-transform infrared spectroscopy (FTIR, 36.73%; n

• structural, optical, and chemical properties. FTIR enables the identification of functional groups involved in the reduction and stabilization of nanoparticles, typically derived from phytochemicals in plant extracts used as reducing agents [52][56]. UV–vis spectroscopy is widely employed to monitor

• potential cytotoxicity of these nanoparticles within the complex and dynamic oral environment [15][20]. A significant number of selected studies (n = 23; 24.1%) also failed to perform advanced physicochemical characterizations, such as FTIR, SEM, or XRD, which are essential for confirming nanoparticle

Electrical, photocatalytic, and sensory properties of graphene oxide and polyimide implanted with low- and medium-energy silver ions

• Josef Novák,
• Eva Štěpanovská,
• Petr Malinský,
• Vlastimil Mazánek,
• Jan Luxa,
• Ulrich Kentsch and
• Zdeněk Sofer

Beilstein J. Nanotechnol. 2025, 16, 1794–1811, doi:10.3762/bjnano.16.123

• interconnected carbon network. Such changes have significant implications for the material’s properties, particularly its electrical conductivity, as a denser carbon structure typically lowers resistivity and enhances conductive pathway. Structure analysis by Raman and FTIR spectroscopies Comprehensive

• analyzed by Fourier-transform infrared spectroscopy (FTIR) [30] (Figure 8). The FTIR spectra were normalized to the signal at 715 cm−1. The spectra consist of several regions of interest, namely, the 715 cm−1 wavenumber region corresponding to C=O bonding and the 1083 cm−1 peak attributed to C–O–C

• evaluated using CasaXPS software. The structural analysis of irradiated GO and PI was investigated through Raman and attenuated total reflectance Fourier-transform infrared (ATR-FTIR) spectroscopies. Raman spectroscopy was conducted using a Renishaw inVia Raman microscope (England) equipped with a Nd:YAG

Prospects of nanotechnology and natural products for cancer and immunotherapy

• Jan Filipe Andrade Santos,
• Marcela Bernardes Brasileiro,
• Pamela Danielle Cavalcante Barreto,
• Ligiane Aranha Rocha and
• José Adão Carvalho Nascimento Júnior

Beilstein J. Nanotechnol. 2025, 16, 1644–1667, doi:10.3762/bjnano.16.116

• spectroscopy, TEM, DLS, X-ray diffraction (XRD), and Fourier-transform infrared (FTIR) spectroscopy, revealing a polygonal or oval morphology. To evaluate the antitumor effects, cytotoxicity assays, cellular uptake assays, apoptosis detection, ROS production, qRT-PCR, and Western blotting for gene and protein

Dendrimer-modified carbon nanotubes for the removal and recovery of heavy metal ions from water

• Thao Quynh Ngan Tran,
• Huu Trung Nguyen,
• Subodh Kumar and
• Xuan Thang Cao

Beilstein J. Nanotechnol. 2025, 16, 1522–1532, doi:10.3762/bjnano.16.107

• spectroscopy was specifically used to confirm the Diels–Alder reaction on the surface of CNTs, and other characterization techniques (SEM, EDX, XRD, TGA, and FTIR) were applied to confirm the successive growth of the dendrimers. Highly dendrimerized CNTs were found to be more effective in removing heavy metal

• functionalization process did not alter the intrinsic structure of the materials as the peak profile of all the samples is similar to that of bare CNTs. Moreover, the absence of any extra peaks further confirms that the washing process has effectively removed the residual substrates and DES. FTIR spectroscopy has

• provided additional insights into the functionalization process (Figure 1c). The FTIR spectrum of CNTs-MA shows a peak around 1745 cm−1 corresponding to the C=O stretching of the carboxyl groups due to the introduction of MA, thus indicating successful covalent grafting onto the surface of CNTs. After

Cross-reactivities in conjugation reactions involving iron oxide nanoparticles

• Shoronia N. Cross,
• Katalin V. Korpany,
• Hanine Zakaria and
• Amy Szuchmacher Blum

Beilstein J. Nanotechnol. 2025, 16, 1504–1521, doi:10.3762/bjnano.16.106

• not drawn to scale, and certain sections of ligand molecules may be omitted. Figure 2 provides a legend with the more detailed structural formulae of the IONP surfaces for each preparation. FTIR analysis of IONP-PPA shows a very weak bump in the spectrum at 2122 cm−1, which may be attributed to the

• amides [57]. While FTIR provides some evidence of PPA coupling to the IONP surface, it is not conclusive; thus, we turned to an indirect means of detection by utilizing the CuAAC coupling reaction to bind Cy5-azide dye to the alkyne groups on the IONP surface, if present. The dye can then be detected

• -3,4-DHBA through its amine group, leaving the alkyne solution-accessible. The FTIR spectrum of the EDC/NHS-free PPA control (Figure 3A.ii) does not show the presence of the 2120 cm−1 alkyne ν(C≡C) band, which may suggest a lower PPA loading than IONP-PPA. We also do not observe the 1635 cm−1 amide ν(C

Laser processing in liquids: insights into nanocolloid generation and thin film integration for energy, photonic, and sensing applications

• Akshana Parameswaran Sreekala,
• Pooja Raveendran Nair,
• Jithin Kundalam Kadavath,
• Bindu Krishnan,
• David Avellaneda Avellaneda,
• M. R. Anantharaman and
• Sadasivan Shaji

Beilstein J. Nanotechnol. 2025, 16, 1428–1498, doi:10.3762/bjnano.16.104

• substrates using 750 rpm for 10 s. FTIR analysis revealed that the functional groups and atomic bonding were involved in physical, rather than chemical, interactions, as no new bonds were formed or broken [111]. These results support the notion that NPs can be combined with various materials, including

Synthesis and antibacterial properties of nanosilver-modified cellulose triacetate membranes for seawater desalination

• Lei Wang,
• Shizhe Li,
• Kexin Xu,
• Wenjun Li,
• Ying Li and
• Gang Liu

Beilstein J. Nanotechnol. 2025, 16, 1380–1391, doi:10.3762/bjnano.16.100

• and Discussion Structure of membrane material To verify the target structure of the synthesized material, Fourier-transform infrared spectroscopy (FTIR) and nuclear magnetic resonance spectroscopy (NMR) were conducted, with the spectra depicted in Figure 1 and Figure 2, respectively. The FTIR bands

• absorption bands in the FTIR spectrum of PCTA and Ag@PCTA. This is because the functional groups in the PDA structure including –OH, –NH2, and C=O, which have band positions at 3200–3600 cm−1, 3300–3500 cm−1, and 1660–1700 cm−1, respectively, coincided with those of CTA. Moreover, the modifying agents (PDA

• and Ag) are present in extremely low quantities relative to the CTA matrix. (For specific details on the content of the modifying layers, please refer to Supporting Information File 1.) The sensitivity of FTIR spectroscopy depends on the concentration of the absorbed species and the path length of the

Functional bio-packaging enhanced with nanocellulose from rice straw and cinnamon essential oil Pickering emulsion for fruit preservation

• Tuyen B. Ly,
• Duong D. T. Nguyen,
• Hieu D. Nguyen,
• Yen T. H. Nguyen,
• Bup T. A. Bui,
• Kien A. Le and
• Phung K. Le

Beilstein J. Nanotechnol. 2025, 16, 1234–1245, doi:10.3762/bjnano.16.91

• and enhanced food safety [30]. Results and Discussion Physicochemical properties FTIR spectroscopy (Figure 1a) was used to study the PVA/glycerol biopackaging (BP), NC-reinforced BP (rBP), and PE-CEO-containing rBP (rCBP) composite films. BP exhibited characteristic peaks at 3330 cm−1 (O–H stretching

• reinforcing effect of nanocellulose within the polymer matrix [41]. The presence of PE-CEO slightly decreases tensile strength and elongation at break to 24.82 MPa and 190%, respectively [43]. FTIR spectra of the biopackaging films containing different concentrations of CEO are shown in Figure 2a. The

• cast onto a mold and dried at 70 °C for 12 h. All concentrations were based on the mass of PVA. Characterization Physicochemical properties Fourier transform infrared spectroscopy (FTIR) spectra were recorded in the range of 4000–500 cm−1 using a Bruker ALPHA II spectrometer (Germany) at a spectral

Chitosan nanocomposite containing rotenoids: an alternative bioinsecticidal approach for the management of Aedes aegypti

• Maria A. A. Bertonceli,
• Vitor D. C. Cristo,
• Ivo J. Vieira,
• Francisco J. A. Lemos,
• Arnoldo R. Façanha,
• Raimundo Braz-Filho,
• Gustavo V. T. Batista,
• Luis G. M. Basso,
• Sérgio H. Seabra,
• Thalya S. R. Nogueira,
• Felipe F. Moreira,
• Arícia L. E. M. Assis,
• Antônia E. A. Oliveira and
• Kátia V. S. Fernandes

Beilstein J. Nanotechnol. 2025, 16, 1197–1208, doi:10.3762/bjnano.16.88

• with smaller size, improved polydispersity index, and enhanced stability, evidenced by a higher zeta potential. FTIR analysis confirmed rotenoid incorporation into the nanocomposite and suggested hydrogen bonding or potential covalent interaction with chitosan functional groups. Bioassays demonstrated

• between the rotenoids and the nanocomposite matrix was obtained through Fourier-transform infrared (FTIR) spectroscopy. Figure 3A shows the FTIR spectra of CS/TPP-β-CD, CS/TPP-β-CD loaded with rotenoids (CS/TPP-β-CD-rot), and pure rotenoids. All three spectra display a broad absorption band in the 3600

• the production of smaller, more uniform nanoparticles, with better polydispersity indices and increased stability, in comparison to conventional ionic gelation method. FTIR analysis confirmed the incorporation of rotenoids into the nanocomposite and revealed characteristic spectral features that

Piezoelectricity of hexagonal boron nitrides improves bone tissue generation as tested on osteoblasts

• Sevin Adiguzel,
• Nilay Cicek,
• Zehra Cobandede,
• Feray B. Misirlioglu,
• Hulya Yilmaz and
• Mustafa Culha

Beilstein J. Nanotechnol. 2025, 16, 1068–1081, doi:10.3762/bjnano.16.78

• drop-casting 1 μL of hBN suspension (prepared in deionized water) onto a TEM grid. Fourier-transform infrared spectroscopy (FTIR, Shimadzu IRAffinity-1S) and Raman spectroscopy (Renishaw, 532 nm laser) were used to analyze chemical bonds and assess crystallinity. UV–visible spectroscopy (Varian Cary UV

• using a variety of techniques including FTIR, Raman, UV–vis, DLS, and PRFM to confirm their physicochemical properties. Characterization of hexagonal boron nitrides The TEM images of the synthesized hBNs are shown in Supporting Information File 1, Figure S3 (a) and (b). As seen, hBNs have platelet-like

• morphology with varying sizes between 50–100 nm, consistent with the literature [42]. Three characteristic peaks of hBNs on the FTIR spectrum in Supporting Information File 1, Figure S3 (c) appeared at 1363, 785, and 661 cm−1, attributed to the in-plane B–N stretching vibration, B–N bonding, and B–N–B out-of

Supramolecular hydration structure of graphene-based hydrogels: density functional theory, green chemistry and interface application

• Hon Nhien Le,
• Duy Khanh Nguyen,
• Minh Triet Dang,
• Huyen Trinh Nguyen,
• Thi Bang Tam Dao,
• Trung Do Nguyen,
• Chi Nhan Ha Thuc and
• Van Hieu Le

Beilstein J. Nanotechnol. 2025, 16, 806–822, doi:10.3762/bjnano.16.61

• microscopy and energy-dispersive X-ray spectroscopy were performed using a JSM-IT200 system (JEOL). Samples were coated with Pt before the SEM-EDS analysis. X-ray diffraction was performed on a D8 Advance instrument (Bruker). Fourier-transform infrared spectroscopy (FTIR) was characterized with a FT/IR-6600

• to the surface and the hydrogen bonding of interfacial hydration layers on the hydrophilic nanostructures. Crystallography, functional group, aqueous dispersibility and hydration lubrication Dry powder of the GO-SG-ZH nanocomposite was analyzed using XRD and FTIR. In Figure 6a, the XRD pattern

• of GO and SG nanomaterials had amorphous structures which did not give obvious peaks in the XRD pattern. Regarding the FTIR spectrum in Figure 6b, most of obvious peaks are attributed to functional groups of nanosilica. The vibration band at 3772.1 cm−1 is assigned to silanol groups on the nanosilica

Changes of structural, magnetic and spectroscopic properties of microencapsulated iron sucrose nanoparticles in saline

• Sabina Lewińska,
• Pavlo Aleshkevych,
• Roman Minikayev,
• Anna Bajorek,
• Mateusz Dulski,
• Krystian Prusik,
• Tomasz Wojciechowski and
• Anna Ślawska-Waniewska

Beilstein J. Nanotechnol. 2025, 16, 762–784, doi:10.3762/bjnano.16.59

• transmission electron microscopy (TEM). Composition studies using XRD, magnetic properties using dc and ac magnetometry, and extensive spectral analysis using Fourier-transform infrared spectroscopy (FTIR), Raman, and electron paramagnetic resonance (EPR) were also performed. Considering that the AB-Fortis

• proved that most likely the cores of the nanoparticles are composed of FeO(OH). However, the results of the magnetic measurements do not allow resolving the issues related to the type of FeO(OH) polymorph. Therefore, additional studies such as FTIR, Raman, and XPS were performed, and their results will

• be presented later in the FTIR and Raman results and analysis and XPS results and analysis sections. Dissolved samples The evolution of the magnetic properties of FS0 with the dissolution time is shown in Figure 8. Figure 8a depicts ZFC–FC relations measured at 50 Oe for all our samples. It can be

Synthesis of a multicomponent cellulose-based adsorbent for tetracycline removal from aquaculture water

• Uyen Bao Tran,
• Ngoc Thanh Vo-Tran,
• Khai The Truong,
• Dat Anh Nguyen,
• Quang Nhat Tran,
• Huu-Quang Nguyen,
• Jaebeom Lee and
• Hai Son Truong-Lam

Beilstein J. Nanotechnol. 2025, 16, 728–739, doi:10.3762/bjnano.16.56

• concentration of 60 mg·L–1 at pH 6–7, reaching equilibrium after 12 h. The surface characteristics and structural properties of PGC were determined using various material characterization techniques, including FTIR, SEM, EDX, and BET. Verification experiments under optimal conditions confirmed that the

• will be applied in the synthesis of an adsorbent for TC removal from water. Material characterization FE-SEM and FTIR results Figure 2 presents comparative field-emission SEM (FE-SEM) images and FTIR spectra of commercial CMC and PGC. Notably, the FE-SEM analysis of PGC (Figure 2d–f) reveals

• aligns with the subsequent EDX results. The FTIR spectrum (Figure 2g) of commercial CMC displays distinct adsorption bands at 3219, 2875, 1424, 1325, 1053, 1029 and 893 cm−1. The broad band from 3219 to 3406 cm−1 corresponds to O‒H stretching vibrations, reflecting the abundance of hydroxy and carboxyl

Efficiency of single-pulse laser fragmentation of organic nutraceutical dispersions in a circular jet flow-through reactor

• Tina Friedenauer,
• Maximilian Spellauge,
• Alexander Sommereyns,
• Verena Labenski,
• Tuba Esatbeyoglu,
• Christoph Rehbock,
• Heinz P. Huber and
• Stephan Barcikowski

Beilstein J. Nanotechnol. 2025, 16, 711–727, doi:10.3762/bjnano.16.55

Aprepitant-loaded solid lipid nanoparticles: a novel approach to enhance oral bioavailability

• Mazhar Hussain,
• Muhammad Farooq,
• Muhammad Asad Saeed,
• Muhammad Ijaz,
• Sherjeel Adnan,
• Zeeshan Masood,
• Muhammad Waqas,
• Wafa Ishaq and
• Nabeela Ameer

Beilstein J. Nanotechnol. 2025, 16, 652–663, doi:10.3762/bjnano.16.50

• analysis. APT-loaded SLNs were prepared by the precipitation method and characterized by physicochemical studies including particle size and zeta potential measurements, drug content, encapsulation efficiency and solubility studies, Fourier-transform infrared spectroscopy (FTIR), scanning electron

• the crystal state into an amorphous state after SLN preparation. FTIR results indicated compatibility between APT and the polymers. XRD, TGA, and DSC results indicated no physical interaction between drug and polymers. In vitro drug release studies showed that APT-CD-NP4 yielded the maximum drug

• , and zeta potential measurements. Also Fourier-transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), solubility, in vitro dissolution, and in vivo and stability studies were carried out. Result and Discussion Physicochemical evaluation The solubility of APT in the SLNs was 24-fold higher

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

• applications without affecting the structure or bioactivity. The effective encapsulation of STZ was confirmed by FTIR, and the nanofibers showed high cytocompatibility in cell viability tests. STZ was released from nanofibers over 6 h, and its antibacterial activity was demonstrated through the formation of a

Nanomaterials in targeting amyloid-β oligomers: current advances and future directions for Alzheimer's disease diagnosis and therapy

• Shiwani Randhawa,
• Trilok Chand Saini,
• Manik Bathla,
• Rahul Bhardwaj,
• Rubina Dhiman and
• Amitabha Acharya

Beilstein J. Nanotechnol. 2025, 16, 561–580, doi:10.3762/bjnano.16.44

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

• Fourier-transform infrared spectroscopy (FTIR) spectrum of produced Ag@ZnO NRs. Different groups and bonds were examined using the FTIR spectrum. Ag doping changes the bond length of the sample, resulting in a minor shift in peak location toward higher wavelengths. The distinctive stretching mode of the

• Zn–O bond is responsible for a significant vibrational band in the FTIR spectra, ranging from 450 to 550 cm−1. The presence of a hydroxy residue, which is caused by ambient moisture, is indicated by a large peak at 3433 cm−1 (stretching) and at 1330 to 1720 cm−1 (bending). Peaks present at 2922 and

• 2854 cm−1 relate to the stretching vibration of carbon and hydrogen bonds. The peaks at 1030 and 1380 cm−1 are related to vibrational or in-plane bending of residual ethanol which was used for washing the nanoparticles and KBr pellet die set (used for pellet making for FTIR) [18][19]. Optical study of

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

• with passing energy at 80 eV, and the binding energy spectrum was recorded from 0 to 1,400 eV. The functional group interaction of PEG–PCL nanoparticles was assessed using Fourier-transform infrared (FTIR) spectroscopy (Thermo Scientific, Nicolet 6700). An amout of 5 mg of PEG, PCL, and PEG–PCL

• undergoing undesirable chemical changes. The functional group interactions between PEG and PCL to form PEG–PCL nanoparticles were investigated using FTIR spectroscopy (Figure 3). The FTIR spectrum of PEG–PCL nanoparticles reveals several characteristic peaks indicating their chemical structure and successful

• method. Physicochemical characterization of PEG–PCL nanoparticles: a) hydrodynamic radius and PDI, b) zeta potential, c) SEM, d) TEM, and e) XPS analysis. FTIR spectrum of PEG–PCL nanoparticles showing functional group interaction between parent compounds (PEG and PCL). Optimization of PEG–PCL