Mohammadreza Mahdavijalal, Homayon Ahmad Panahi, Elham Moniri, Niloufar Torabi Fard
Levels of anticancer agents in cancer patients' body fluids are typically measured to adjust drug dosages or improve treatment results. The goal of this research is to present a new method for extracting bicalutamide (BCT) from biological samples using a responsive polymeric nanoadsorbent that reacts to temperature and near‐infrared radiation (NIR). To achieve this, the surface layers of tungsten disulfide nanosheets are modified using poly (N‐vinylcaprolactam) and three generations of polymeric dendrimers. The adsorbent product is then characterized using thermogravimetric analysis, Fourier transform infrared spectroscopy, field emission scanning electron microscopy, and X‐ray diffraction techniques. The drug loading operation on the proposed adsorbent is studied through central composite design and response surface strategy, with optimization for temperature (25–45°C), pH (5–9), and contact time (2–18 min). Nonlinear kinetic and adsorption isotherm analysis results show the best fit with Langmuir and pseudo‐second‐order models. The drug release process from the BCT‐loaded adsorbent is investigated via an HPLC‐UV system under both NIR‐irradiated and non‐irradiated conditions. The suggested method demonstrates remarkable recovery rates for BCT spikes from urine (95.23%) and plasma (93.33%), respectively. Overall, the recommended strategy can be regarded as a potent analytical tool for evaluating BCT in complex biosamples.
{"title":"Synthesis, characterization, and optimization of dual‐responsive PAMAM nanodendrimers for improved dispersive solid‐phase extraction of cancer agents from complex biological samples","authors":"Mohammadreza Mahdavijalal, Homayon Ahmad Panahi, Elham Moniri, Niloufar Torabi Fard","doi":"10.1002/pat.6570","DOIUrl":"https://doi.org/10.1002/pat.6570","url":null,"abstract":"Levels of anticancer agents in cancer patients' body fluids are typically measured to adjust drug dosages or improve treatment results. The goal of this research is to present a new method for extracting bicalutamide (BCT) from biological samples using a responsive polymeric nanoadsorbent that reacts to temperature and near‐infrared radiation (NIR). To achieve this, the surface layers of tungsten disulfide nanosheets are modified using poly (N‐vinylcaprolactam) and three generations of polymeric dendrimers. The adsorbent product is then characterized using thermogravimetric analysis, Fourier transform infrared spectroscopy, field emission scanning electron microscopy, and X‐ray diffraction techniques. The drug loading operation on the proposed adsorbent is studied through central composite design and response surface strategy, with optimization for temperature (25–45°C), pH (5–9), and contact time (2–18 min). Nonlinear kinetic and adsorption isotherm analysis results show the best fit with Langmuir and pseudo‐second‐order models. The drug release process from the BCT‐loaded adsorbent is investigated via an HPLC‐UV system under both NIR‐irradiated and non‐irradiated conditions. The suggested method demonstrates remarkable recovery rates for BCT spikes from urine (95.23%) and plasma (93.33%), respectively. Overall, the recommended strategy can be regarded as a potent analytical tool for evaluating BCT in complex biosamples.","PeriodicalId":20382,"journal":{"name":"Polymers for Advanced Technologies","volume":"2 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2024-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142208241","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Shahrzad Shakouri, Sajad Arabshahi, Hamid Madanchi, Mohammad Amin Mohammadifar, Anna Abdolshahi
Bigels are innovative and appealing heterogeneous matrices composed of two structured‐gel (hydrogel and oleogel) phases, which suitable for the entrapment of both hydrophilic and lipophilic active agents. As structuring the bigel phases using convenient materials can enhance the main characteristics, this study aimed to develop bigel system based on a hybrid hydrogel consisting of gelatin and carboxymethylcellulose (CMC). The impact of incorporating various concentrations of CMC (0, 0.5, 1, 2, and 3% w/w) into gelatin‐based hydrogel at a constant organogel/hydrogel ratio of 60:40 was investigated on bigel properties. The integration of gelatin and CMC significantly affected the solvent holding capacity (SHC), microstructure, rheology, thermal, and textural properties. The results showed that bigel samples containing gelatin‐CMC had lower SHC compared to gelatin‐based samples. The integration of CMC to bigel formulation resulted in a significant decrease in hardness, cohesiveness, and adhesiveness also smooth texture. Differential scanning calorimeter (DSC) analysis of the bigels showed a descending trend in melting point from 99.07 to 98.60°C for bigel samples as the CMC concentration increased from 0% to 2%. This was followed by an increase in melting temperature (100.95°C) in the bigel containing 3% CMC. Particle size distribution data indicated that the droplet sizes of the bigels increased with the incorporation of CMC into the hydrogel phase, without displaying a distinct concentration‐dependent trend. The rheological characteristics of strain sweep, frequency sweep, and loss factor affected by gelatin/CMC concentration. Overall obtained results highlight that CMC incorporation to gelatin plays a crucial role in bigel offering different textural, rheological and thermal properties. So that carefully selection and optimization of gelatin and CMC concentrations in hydrogel phase are essential for tailoring the mechanical strength and stability of bigels for various applications such as drug delivery, cosmetic, and food industries. Regarding the desired properties of CMC, it could be recommend to use by combination with gelatin to create a structure–function aimed bigels.
{"title":"Effect of carboxymethyl cellulose incorporation to gelatin‐sunflower oil bigel on the physicochemical and structural properties","authors":"Shahrzad Shakouri, Sajad Arabshahi, Hamid Madanchi, Mohammad Amin Mohammadifar, Anna Abdolshahi","doi":"10.1002/pat.6567","DOIUrl":"https://doi.org/10.1002/pat.6567","url":null,"abstract":"Bigels are innovative and appealing heterogeneous matrices composed of two structured‐gel (hydrogel and oleogel) phases, which suitable for the entrapment of both hydrophilic and lipophilic active agents. As structuring the bigel phases using convenient materials can enhance the main characteristics, this study aimed to develop bigel system based on a hybrid hydrogel consisting of gelatin and carboxymethylcellulose (CMC). The impact of incorporating various concentrations of CMC (0, 0.5, 1, 2, and 3% w/w) into gelatin‐based hydrogel at a constant organogel/hydrogel ratio of 60:40 was investigated on bigel properties. The integration of gelatin and CMC significantly affected the solvent holding capacity (SHC), microstructure, rheology, thermal, and textural properties. The results showed that bigel samples containing gelatin‐CMC had lower SHC compared to gelatin‐based samples. The integration of CMC to bigel formulation resulted in a significant decrease in hardness, cohesiveness, and adhesiveness also smooth texture. Differential scanning calorimeter (DSC) analysis of the bigels showed a descending trend in melting point from 99.07 to 98.60°C for bigel samples as the CMC concentration increased from 0% to 2%. This was followed by an increase in melting temperature (100.95°C) in the bigel containing 3% CMC. Particle size distribution data indicated that the droplet sizes of the bigels increased with the incorporation of CMC into the hydrogel phase, without displaying a distinct concentration‐dependent trend. The rheological characteristics of strain sweep, frequency sweep, and loss factor affected by gelatin/CMC concentration. Overall obtained results highlight that CMC incorporation to gelatin plays a crucial role in bigel offering different textural, rheological and thermal properties. So that carefully selection and optimization of gelatin and CMC concentrations in hydrogel phase are essential for tailoring the mechanical strength and stability of bigels for various applications such as drug delivery, cosmetic, and food industries. Regarding the desired properties of CMC, it could be recommend to use by combination with gelatin to create a structure–function aimed bigels.","PeriodicalId":20382,"journal":{"name":"Polymers for Advanced Technologies","volume":"13 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2024-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142208243","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Advanced flexible display materials have drastically sparked considerable interest for heat‐resistant, low dielectric, and transparent polyimide (PI) materials. In light of this, our study aims to develop high‐performance semi‐aromatic PI films, followed by investigate the correlations between bridged‐alkyl/heteroaromatic ring structures and their thermal, dielectric, optical, and mechanical properties. Such PI films, namely AP‐PIs, were synthesized with a one‐step high‐temperature method between 4‐[4‐(4‐aminophenoxy) phenyl]‐2‐(4‐aminophenyl)‐1(2H)‐phthalazinone (DHPZDA) and various commercial alicyclic dianhydrides. The incorporation of rigid phthalazinone structures significantly enhanced thermal resistance and mechanical flexibility, while simultaneously reducing their dielectric constant (Dk), attributed to the large polymer internal free volume. Impressively, the prepared films exhibit exceptional glass transition temperature (Tg) as high as 419°C (DMTA tanδ peak), low Dk as low as 2.71, and elongation at break (ε %) up to 50.4%. Furthermore, AP‐PI films demonstrate reasonable solubility and optical transparency within the UV–visible region. The maximum optical transmittance at 550 nm (T550 nm) could reach 83.01%. These desirable properties position these materials as promising candidates for flexible substrate applications.
{"title":"Heat‐resistant and transparent polyimides derived from alicyclic dianhydrides and phthalazinone‐based diamine","authors":"Bingbing Wang, Lishuai Zong, Jinyan Wang, Yabin Zhang, Wenhua Hou, Xigao Jian","doi":"10.1002/pat.6562","DOIUrl":"https://doi.org/10.1002/pat.6562","url":null,"abstract":"Advanced flexible display materials have drastically sparked considerable interest for heat‐resistant, low dielectric, and transparent polyimide (PI) materials. In light of this, our study aims to develop high‐performance semi‐aromatic PI films, followed by investigate the correlations between bridged‐alkyl/heteroaromatic ring structures and their thermal, dielectric, optical, and mechanical properties. Such PI films, namely AP‐PIs, were synthesized with a one‐step high‐temperature method between 4‐[4‐(4‐aminophenoxy) phenyl]‐2‐(4‐aminophenyl)‐1(2H)‐phthalazinone (DHPZDA) and various commercial alicyclic dianhydrides. The incorporation of rigid phthalazinone structures significantly enhanced thermal resistance and mechanical flexibility, while simultaneously reducing their dielectric constant (<jats:italic>D</jats:italic><jats:sub>k</jats:sub>), attributed to the large polymer internal free volume. Impressively, the prepared films exhibit exceptional glass transition temperature (<jats:italic>T</jats:italic><jats:sub>g</jats:sub>) as high as 419°C (DMTA tanδ peak), low <jats:italic>D</jats:italic><jats:sub>k</jats:sub> as low as 2.71, and elongation at break (<jats:italic>ε</jats:italic> %) up to 50.4%. Furthermore, AP‐PI films demonstrate reasonable solubility and optical transparency within the UV–visible region. The maximum optical transmittance at 550 nm (T<jats:sub>550 nm</jats:sub>) could reach 83.01%. These desirable properties position these materials as promising candidates for flexible substrate applications.","PeriodicalId":20382,"journal":{"name":"Polymers for Advanced Technologies","volume":"32 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2024-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142208254","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Optically clear pressure‐sensitive adhesive (OCA) possesses exceptional optical properties and exhibits pressure‐sensitive adhesion, making it widely utilized in the adhesive layers of various electronic display devices. However, the increasing popularity of foldable mobile phones in recent years has imposed new requirements on the overall performance of OCA. Conventional pressure‐sensitive adhesives can enhance recoverability through cross‐linking but often demonstrate inadequate adhesive strength. In this study, three long‐chain crosslinking agents (CL) were synthesized using hydroxyethyl acrylate (HEA), dicyclohexylmethane diisocyanate (HMDI), polypropylene glycol (PPG), polyether amine (PEA), and hydroxyl‐terminated polybutadiene (R45V). The long‐chain CL agent contains numerous flexible segments that improve the recovery capability of the OCA while maintaining a certain level of adhesion. The optical clear pressure‐sensitive adhesive, crosslinked by three flexible crosslinkers, exhibits a low glass transition temperature (−60 to −40°C) and a low storage modulus (<0.1 MPa), along with an appropriate 180° stripping force (6–8 N/25 mm). Optically transparent pressure‐sensitive adhesives demonstrate excellent recovery properties (>85%), high light transmittance (>92%), and exceptional flexibility. Moreover, compared to market products, the optically transparent pressure‐sensitive adhesive shows superior folding resistance (>100,000 times). This indicates its suitability for applications in flexible optical displays such as foldable mobile phones and wearable electronics.
{"title":"Optically clear pressure‐sensitive adhesive with flexible crosslinking agent for high recovery efficiency, low energy storage modulus, and excellent folding resistance","authors":"Jinbiao Min, Jinqing Qu","doi":"10.1002/pat.6574","DOIUrl":"https://doi.org/10.1002/pat.6574","url":null,"abstract":"Optically clear pressure‐sensitive adhesive (OCA) possesses exceptional optical properties and exhibits pressure‐sensitive adhesion, making it widely utilized in the adhesive layers of various electronic display devices. However, the increasing popularity of foldable mobile phones in recent years has imposed new requirements on the overall performance of OCA. Conventional pressure‐sensitive adhesives can enhance recoverability through cross‐linking but often demonstrate inadequate adhesive strength. In this study, three long‐chain crosslinking agents (CL) were synthesized using hydroxyethyl acrylate (HEA), dicyclohexylmethane diisocyanate (HMDI), polypropylene glycol (PPG), polyether amine (PEA), and hydroxyl‐terminated polybutadiene (R45V). The long‐chain CL agent contains numerous flexible segments that improve the recovery capability of the OCA while maintaining a certain level of adhesion. The optical clear pressure‐sensitive adhesive, crosslinked by three flexible crosslinkers, exhibits a low glass transition temperature (−60 to −40°C) and a low storage modulus (<0.1 MPa), along with an appropriate 180° stripping force (6–8 N/25 mm). Optically transparent pressure‐sensitive adhesives demonstrate excellent recovery properties (>85%), high light transmittance (>92%), and exceptional flexibility. Moreover, compared to market products, the optically transparent pressure‐sensitive adhesive shows superior folding resistance (>100,000 times). This indicates its suitability for applications in flexible optical displays such as foldable mobile phones and wearable electronics.","PeriodicalId":20382,"journal":{"name":"Polymers for Advanced Technologies","volume":"71 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2024-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142208242","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Maryam Aliakbari, Omid Moini Jazani, Majid Moghadam, José Miguel Martín‐Martínez
Epoxy adhesives become very brittle after curing due to their high‐crosslinking degree. For increasing the toughness of epoxy adhesives, the addition of different toughening agents has been proposed. In this study the diglycidyl ether of bisphenol A (DGEBA)/dicyandiamide epoxy network has been modified by adding an emulsion latex containing core–shell rubber particles (CSPs) prepared by means of seeded emulsion polymerization. The CSPs consist of poly (butyl acrylate) (PBA) as core and methyl methacrylate (MMA) copolymerized with glycidyl methacrylate (GMA) as shell. The effects of adding various amounts of the emulsion latex on the mechanical properties, thermal stability, adhesion, and microstructure of the cured epoxy resin were investigated. The CSPs were analyzed by transmission electron microscopy (TEM), Fourier‐transform infrared spectroscopy (FTIR), and differential scanning calorimetry (DSC). The mechanical properties, thermal stability, adhesion to aluminum plates, and microstructure of the cured epoxy resin were investigated by stress–strain, thermal gravimetric analysis (TGA), single lap shear test, and field emission scanning electron microscopy (FESEM), respectively. The addition of 7 wt.% emulsion latex to epoxy enhanced the tensile strength and the toughness of the dumbbell‐shaped samples by 421% and 4388% with respect to neat epoxy, respectively. Furthermore, the single lap shear strength increased in 33% and an increase of 71°C in the initial decomposition temperature of the epoxy was obtained by adding 7 wt.% CSP, without affecting the maximum decomposition temperature. The FESEM micrographs of the fractured surfaces indicated that the major toughening mechanisms were CSP de‐bonding, plastic void growth, and shear bond yielding.
{"title":"Manipulating a novel epoxy‐based composite with core–shell rubber particles for designing a structural adhesive in aluminum–aluminum bonded joints","authors":"Maryam Aliakbari, Omid Moini Jazani, Majid Moghadam, José Miguel Martín‐Martínez","doi":"10.1002/pat.6564","DOIUrl":"https://doi.org/10.1002/pat.6564","url":null,"abstract":"Epoxy adhesives become very brittle after curing due to their high‐crosslinking degree. For increasing the toughness of epoxy adhesives, the addition of different toughening agents has been proposed. In this study the diglycidyl ether of bisphenol A (DGEBA)/dicyandiamide epoxy network has been modified by adding an emulsion latex containing core–shell rubber particles (CSPs) prepared by means of seeded emulsion polymerization. The CSPs consist of poly (butyl acrylate) (PBA) as core and methyl methacrylate (MMA) copolymerized with glycidyl methacrylate (GMA) as shell. The effects of adding various amounts of the emulsion latex on the mechanical properties, thermal stability, adhesion, and microstructure of the cured epoxy resin were investigated. The CSPs were analyzed by transmission electron microscopy (TEM), Fourier‐transform infrared spectroscopy (FTIR), and differential scanning calorimetry (DSC). The mechanical properties, thermal stability, adhesion to aluminum plates, and microstructure of the cured epoxy resin were investigated by stress–strain, thermal gravimetric analysis (TGA), single lap shear test, and field emission scanning electron microscopy (FESEM), respectively. The addition of 7 wt.% emulsion latex to epoxy enhanced the tensile strength and the toughness of the dumbbell‐shaped samples by 421% and 4388% with respect to neat epoxy, respectively. Furthermore, the single lap shear strength increased in 33% and an increase of 71°C in the initial decomposition temperature of the epoxy was obtained by adding 7 wt.% CSP, without affecting the maximum decomposition temperature. The FESEM micrographs of the fractured surfaces indicated that the major toughening mechanisms were CSP de‐bonding, plastic void growth, and shear bond yielding.","PeriodicalId":20382,"journal":{"name":"Polymers for Advanced Technologies","volume":"53 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2024-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142226431","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Graphene quantum dots (GQDs), owing to their unique optical, electrical, and chemical properties, have emerged as promising nanomaterials for various biomedical applications. This review provides a comprehensive overview of the latest advancements in the utilization of GQDs in tissue engineering, wound healing, drug delivery systems, and other biomedical therapies. The inherent properties of GQDs, including high biocompatibility, tunable photoluminescence, and significant surface area, make them ideal candidates for enhancing medical treatments and diagnostics. In tissue engineering, GQDs improve the mechanical and biological performance of scaffolds, promoting cell proliferation and differentiation. For wound healing, GQDs enhance antimicrobial activity and facilitate faster tissue regeneration. Their potential in DDS is highlighted by their ability to deliver therapeutic agents efficiently, ensuring targeted and controlled release. Additionally, GQDs play a crucial role in biomedical therapies, particularly in cancer treatment, by enhancing drug efficacy and reducing side effects. While GQDs offer significant potential in enhancing medical treatments and diagnostics, challenges such as understanding their long‐term biocompatibility, potential cytotoxicity at higher concentrations, and the need for standardized synthesis methods remain critical areas for further research. This review also discusses the future directions and opportunities for GQDs, emphasizing their transformative potential in advancing modern healthcare solutions. The insights presented here contribute to the expanding field of GQD research, highlighting their potential to significantly enhance patient outcomes and drive healthcare innovations.
{"title":"The role of graphene quantum dots in cutting‐edge medical therapies","authors":"Kosar Arab, Aliakbar Jafari, Farangis Shahi","doi":"10.1002/pat.6571","DOIUrl":"https://doi.org/10.1002/pat.6571","url":null,"abstract":"Graphene quantum dots (GQDs), owing to their unique optical, electrical, and chemical properties, have emerged as promising nanomaterials for various biomedical applications. This review provides a comprehensive overview of the latest advancements in the utilization of GQDs in tissue engineering, wound healing, drug delivery systems, and other biomedical therapies. The inherent properties of GQDs, including high biocompatibility, tunable photoluminescence, and significant surface area, make them ideal candidates for enhancing medical treatments and diagnostics. In tissue engineering, GQDs improve the mechanical and biological performance of scaffolds, promoting cell proliferation and differentiation. For wound healing, GQDs enhance antimicrobial activity and facilitate faster tissue regeneration. Their potential in DDS is highlighted by their ability to deliver therapeutic agents efficiently, ensuring targeted and controlled release. Additionally, GQDs play a crucial role in biomedical therapies, particularly in cancer treatment, by enhancing drug efficacy and reducing side effects. While GQDs offer significant potential in enhancing medical treatments and diagnostics, challenges such as understanding their long‐term biocompatibility, potential cytotoxicity at higher concentrations, and the need for standardized synthesis methods remain critical areas for further research. This review also discusses the future directions and opportunities for GQDs, emphasizing their transformative potential in advancing modern healthcare solutions. The insights presented here contribute to the expanding field of GQD research, highlighting their potential to significantly enhance patient outcomes and drive healthcare innovations.","PeriodicalId":20382,"journal":{"name":"Polymers for Advanced Technologies","volume":"2 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2024-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142208255","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
M. Gomathi, Nair Deepa, Aiswarya Muraleedharan, Shanmugavel Uma Maheswari, R. Thirumalaisamy, T. Selvankumar, Arunachalam Chinnathambi, Sulaiman Ali Alharbi
The current study aimed to investigate the drug delivery potential of chitosan‐conjugated Spondias pinnata phytocompounds for anticancer and antibacterial applications. The phytochemical composition of the aqueous extract of S. pinnata plant leaves revealed seven major compounds, including stearic acid, 2H‐Indol‐2‐one, beta amyrin, oleic acid, octadecanoic acid, 7‐hexadecenoic acid, and phytol. Additionally, five minor compounds were identified through GC–MS analysis. SEM analysis of chitosan‐conjugated S. pinnata phytocompounds revealed amorphous particles. This demonstrates the attainment of optimized larger crystallites, which differ in size and shape extensively. The antioxidant potential of both the chitosan‐conjugated S. pinnata phytocompounds and S. pinnata leaf extracts was evaluated via DPPH and ABTS assays, and the results revealed that the chitosan‐conjugated S. pinnata phytocompounds exhibited significant scavenging activity, with IC50 values of 18.20 and 33.15 μg/mL, respectively. Chitosan‐conjugated S. pinnata phytocompounds also demonstrated antibacterial activity against four clinically significant infections, with zones of inhibition ranging from 16 ± 0.07, 19 ± 0.10, 17 ± 0.09, and 19 ± 0.11 mm against Escherichia coli (MTCC 452), Salmonella typhi (MTCC 733), Klebsiella pneumonia (MTCC 39), and Pseudomonas aeruginosa (MTCC 1688), respectively. Furthermore, the cytotoxicity of the chitosan‐conjugated S. pinnata phytocompounds was assessed against A549 lung cancer cells, and the results revealed a significant reduction in cell viability (33.85) at higher concentrations of 150 μg/mL. The IC50 values of S. pinnata leaf extract (149.2 mg/mL) and chitosan‐conjugated S. pinnata (126.4 mg/mL) toward A549 lung cancer cells were recorded. Overall, the results of the present study highlight the therapeutic applications of chitosan‐conjugated S. pinnata phytocompounds, particularly in the context of their anticancer and antibacterial activities.
{"title":"Novel drug delivery materials: Chitosan polymers conjugated with Spondias pinnata phytocompounds for enhanced anti‐microbial and anti‐cancer properties","authors":"M. Gomathi, Nair Deepa, Aiswarya Muraleedharan, Shanmugavel Uma Maheswari, R. Thirumalaisamy, T. Selvankumar, Arunachalam Chinnathambi, Sulaiman Ali Alharbi","doi":"10.1002/pat.6561","DOIUrl":"https://doi.org/10.1002/pat.6561","url":null,"abstract":"The current study aimed to investigate the drug delivery potential of chitosan‐conjugated <jats:italic>Spondias pinnata</jats:italic> phytocompounds for anticancer and antibacterial applications. The phytochemical composition of the aqueous extract of <jats:italic>S. pinnata</jats:italic> plant leaves revealed seven major compounds, including stearic acid, 2H‐Indol‐2‐one, beta amyrin, oleic acid, octadecanoic acid, 7‐hexadecenoic acid, and phytol. Additionally, five minor compounds were identified through GC–MS analysis. SEM analysis of chitosan‐conjugated <jats:italic>S. pinnata</jats:italic> phytocompounds revealed amorphous particles. This demonstrates the attainment of optimized larger crystallites, which differ in size and shape extensively. The antioxidant potential of both the chitosan‐conjugated <jats:italic>S. pinnata</jats:italic> phytocompounds and <jats:italic>S. pinnata</jats:italic> leaf extracts was evaluated via DPPH and ABTS assays, and the results revealed that the chitosan‐conjugated <jats:italic>S. pinnata</jats:italic> phytocompounds exhibited significant scavenging activity, with IC<jats:sup>50</jats:sup> values of 18.20 and 33.15 μg/mL, respectively. Chitosan‐conjugated <jats:italic>S. pinnata</jats:italic> phytocompounds also demonstrated antibacterial activity against four clinically significant infections, with zones of inhibition ranging from 16 ± 0.07, 19 ± 0.10, 17 ± 0.09, and 19 ± 0.11 mm against <jats:italic>Escherichia coli</jats:italic> (MTCC 452), <jats:italic>Salmonella typhi</jats:italic> (MTCC 733), <jats:italic>Klebsiella pneumonia</jats:italic> (MTCC 39), and <jats:italic>Pseudomonas aeruginosa</jats:italic> (MTCC 1688), respectively. Furthermore, the cytotoxicity of the chitosan‐conjugated <jats:italic>S. pinnata</jats:italic> phytocompounds was assessed against A549 lung cancer cells, and the results revealed a significant reduction in cell viability (33.85) at higher concentrations of 150 μg/mL. The IC<jats:sup>50</jats:sup> values of <jats:italic>S. pinnata</jats:italic> leaf extract (149.2 mg/mL) and chitosan‐conjugated <jats:italic>S. pinnata</jats:italic> (126.4 mg/mL) toward A549 lung cancer cells were recorded. Overall, the results of the present study highlight the therapeutic applications of chitosan‐conjugated <jats:italic>S. pinnata</jats:italic> phytocompounds, particularly in the context of their anticancer and antibacterial activities.","PeriodicalId":20382,"journal":{"name":"Polymers for Advanced Technologies","volume":"176 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2024-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142208256","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Abjesh Prasad Rath, P. Santhana Gopala Krishnan, Krishnan Kanny
It is imperative to improve the physical, morphological, and mechanical properties of biodegradable polymers like polylactic acid (PLA), poly (butylene adipate‐co‐terephthalate) (PBAT), and polycaprolactone (PCL) in order to employ them on a larger scale. The development of hybrid nanocomposite materials using nano inclusions can improve desired qualities. Here we introduced an interactive nano reinforcement approach to improve the properties by combining graphene oxide (GO) and carboxyl functionalized MWCNT (f‐MWCNT), to provide for their chemical bonding for synergic reinforcement. A constant filler 2 wt.% was added to the biopolyesters by melt blending process and examined the different physical properties like water absorption, intrinsic viscosity, and hardness. To completely evaluate the functionalization of the nanofillers, wide‐angle X‐ray diffraction (WAXD), Raman spectroscopy and Fourier transform infrared radiation (FTIR) analyses were used. The paired nanoparticles and polymer matrix appear to mix well together, as shown by electron microscopy, which also reveals good dispersion and the creation of a reinforcing network microstructure across the matrix layer. A thorough analysis of the results showed that effective stress transmission, delaying the start of faults and generating microcracks, and dissipating additional mechanical energy all contributed to efficient hybrid network formation, which improved the mechanical properties of hybrid filler nanocomposites except some nanocomposites. These findings offer a viable technique for chemically altering biodegradable polymers, like PLA, PBAT, and PCL for use in biomedical, wastewater management, and agricultural applications.
当务之急是改善聚乳酸（PLA）、聚己二酸丁二醇酯（PBAT）和聚己内酯（PCL）等可生物降解聚合物的物理、形态和机械性能，以便更大规模地使用它们。使用纳米夹杂物开发混合纳米复合材料可以提高所需的质量。在这里，我们引入了一种交互式纳米增强方法，通过将氧化石墨烯（GO）和羧基功能化的 MWCNT（f-MWCNT）结合在一起，使其化学键协同增强，从而改善性能。通过熔融混合工艺，在生物聚酯中添加 2 重量百分比的恒定填料，并检测不同的物理性质，如吸水性、固有粘度和硬度。为了全面评估纳米填料的功能化情况，使用了广角 X 射线衍射（WAXD）、拉曼光谱和傅立叶变换红外辐射（FTIR）分析。电子显微镜显示，配对的纳米颗粒和聚合物基质似乎混合得很好，电子显微镜还显示出良好的分散性，并在整个基质层中形成了增强网络微结构。对结果的全面分析表明，有效的应力传递、延迟故障开始和微裂纹的产生以及耗散额外的机械能都有助于高效混合网络的形成，从而改善了除某些纳米复合材料以外的混合填料纳米复合材料的机械性能。这些发现为化学改变可生物降解聚合物（如聚乳酸、PBAT 和 PCL）提供了一种可行的技术，可用于生物医学、废水管理和农业应用。
{"title":"A comparison of physical, morphological, and mechanical properties of bio‐polyester hybrid nanocomposites","authors":"Abjesh Prasad Rath, P. Santhana Gopala Krishnan, Krishnan Kanny","doi":"10.1002/pat.6566","DOIUrl":"https://doi.org/10.1002/pat.6566","url":null,"abstract":"It is imperative to improve the physical, morphological, and mechanical properties of biodegradable polymers like polylactic acid (PLA), poly (butylene adipate‐co‐terephthalate) (PBAT), and polycaprolactone (PCL) in order to employ them on a larger scale. The development of hybrid nanocomposite materials using nano inclusions can improve desired qualities. Here we introduced an interactive nano reinforcement approach to improve the properties by combining graphene oxide (GO) and carboxyl functionalized MWCNT (f‐MWCNT), to provide for their chemical bonding for synergic reinforcement. A constant filler 2 wt.% was added to the biopolyesters by melt blending process and examined the different physical properties like water absorption, intrinsic viscosity, and hardness. To completely evaluate the functionalization of the nanofillers, wide‐angle X‐ray diffraction (WAXD), Raman spectroscopy and Fourier transform infrared radiation (FTIR) analyses were used. The paired nanoparticles and polymer matrix appear to mix well together, as shown by electron microscopy, which also reveals good dispersion and the creation of a reinforcing network microstructure across the matrix layer. A thorough analysis of the results showed that effective stress transmission, delaying the start of faults and generating microcracks, and dissipating additional mechanical energy all contributed to efficient hybrid network formation, which improved the mechanical properties of hybrid filler nanocomposites except some nanocomposites. These findings offer a viable technique for chemically altering biodegradable polymers, like PLA, PBAT, and PCL for use in biomedical, wastewater management, and agricultural applications.","PeriodicalId":20382,"journal":{"name":"Polymers for Advanced Technologies","volume":"407 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2024-09-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142208257","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Claudia I. Valdés‐Lozano, Jesús A. Claudio‐Rizo, Denis A. Cabrera‐Munguía, Maria I. León‐Campos, Juan J. Mendoza‐Villafaña, Juan J. Becerra‐Rodriguez
The development of hydrogel biomatrices with potential to modulate animal and plant tissue growth is ongoing. In this study, molybdenum bio‐metal–organic frameworks (MOFs) (Mo‐bioMOFs) incorporating essential amino acids such as l‐histidine (Mo‐His), l‐phenylalanine (Mo‐Phe), and l‐tryptophan (Mo‐Trp) were encapsulated in semi‐interpenetrating polymer network (semi‐IPN) hydrogels composed of collagen and starch. The structure and properties of these materials show dependence on the amino acid that constitutes the Mo‐bioMOFs. The biomatrices have a semi‐crystalline surface with increased porosity when using Mo‐His; this system also benefits swelling. Increased crosslinking, acceleration in gelation, and mechanical improvement are observed for the system based on Mo‐Phe. Methylene blue release experiments were conducted, demonstrating that matrices including Mo‐bioMOFs exhibit controlled release profiles, indicating highly stable retention of Mo‐bioMOFs in the semi‐IPN matrix. The biomatrices enhance the metabolism and proliferation of fibroblasts and monocytes, with Mo‐Trp reducing the secretion of inflammatory cytokines like TNF‐α. The biomatrices exhibit gradual and slow mass loss when exposed to collagenase and commercial vegetable substrates. Both leaf and root cells of tomato plants (Solanum lycopersicum) show increased metabolism and growth when exposed to Mo‐Phe and Mo‐His. Notably, the biomatrix containing Mo‐Phe promotes the most substantial plant growth and foliage after 30 days. These biomatrices have potential applications in chronic wound healing and agriculture.
{"title":"Modulation of animal and plant tissue growth with collagen‐starch‐organic molybdenum networks hydrogel biomatrices","authors":"Claudia I. Valdés‐Lozano, Jesús A. Claudio‐Rizo, Denis A. Cabrera‐Munguía, Maria I. León‐Campos, Juan J. Mendoza‐Villafaña, Juan J. Becerra‐Rodriguez","doi":"10.1002/pat.6568","DOIUrl":"https://doi.org/10.1002/pat.6568","url":null,"abstract":"The development of hydrogel biomatrices with potential to modulate animal and plant tissue growth is ongoing. In this study, molybdenum bio‐metal–organic frameworks (MOFs) (Mo‐bioMOFs) incorporating essential amino acids such as <jats:sc>l</jats:sc>‐histidine (Mo‐His), <jats:sc>l</jats:sc>‐phenylalanine (Mo‐Phe), and <jats:sc>l</jats:sc>‐tryptophan (Mo‐Trp) were encapsulated in semi‐interpenetrating polymer network (semi‐IPN) hydrogels composed of collagen and starch. The structure and properties of these materials show dependence on the amino acid that constitutes the Mo‐bioMOFs. The biomatrices have a semi‐crystalline surface with increased porosity when using Mo‐His; this system also benefits swelling. Increased crosslinking, acceleration in gelation, and mechanical improvement are observed for the system based on Mo‐Phe. Methylene blue release experiments were conducted, demonstrating that matrices including Mo‐bioMOFs exhibit controlled release profiles, indicating highly stable retention of Mo‐bioMOFs in the semi‐IPN matrix. The biomatrices enhance the metabolism and proliferation of fibroblasts and monocytes, with Mo‐Trp reducing the secretion of inflammatory cytokines like TNF‐α. The biomatrices exhibit gradual and slow mass loss when exposed to collagenase and commercial vegetable substrates. Both leaf and root cells of tomato plants (<jats:italic>Solanum lycopersicum</jats:italic>) show increased metabolism and growth when exposed to Mo‐Phe and Mo‐His. Notably, the biomatrix containing Mo‐Phe promotes the most substantial plant growth and foliage after 30 days. These biomatrices have potential applications in chronic wound healing and agriculture.","PeriodicalId":20382,"journal":{"name":"Polymers for Advanced Technologies","volume":"51 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2024-09-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142208258","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Although the utilization of recycled polymers is essential to sustain the environment, conventional recycled polymers face limitations in application due to the degradation of their properties caused by impurities. To solve the problem the performance deterioration of these recycled polymers, this study aimed to enhance their compatibility by chemically adding polypropylene‐graft‐maleic anhydride (PP‐g‐MAH) and physically manipulate a screw profile by using an extrusion simulation program. As a result of applying the optimized extrusion process set by the simulation program, significant improvements in the compatibility and dispersion of fillers within the polymer were observed through scanning electron microscopy image analysis. In addition, through detailed analysis of rheological data, the positive impact of adding compatibilizer and changing screw profile on rheological properties was demonstrated. As the compatibility of recycled polymer blends improved, tensile strength increased by approximately two‐fold and thermal conductivity was significantly improved, which were decisive factors in dramatically enhancing the performance of recycled polymers. These improved polymer properties provide an opportunity for recycled polymers to be applied more broadly and will expand the potential for new applications in various industrial fields.
{"title":"Compatibility study of recycled Polypropylene (PP)/Poly(ethylene terephthalate) (PET) blends nanocomposites with PP‐g‐MAH: Modeling of twin screw extrusion","authors":"Dajeong Gwon, Dohyeong Kim, Jaseung Koo","doi":"10.1002/pat.6557","DOIUrl":"https://doi.org/10.1002/pat.6557","url":null,"abstract":"Although the utilization of recycled polymers is essential to sustain the environment, conventional recycled polymers face limitations in application due to the degradation of their properties caused by impurities. To solve the problem the performance deterioration of these recycled polymers, this study aimed to enhance their compatibility by chemically adding polypropylene‐graft‐maleic anhydride (PP‐<jats:italic>g</jats:italic>‐MAH) and physically manipulate a screw profile by using an extrusion simulation program. As a result of applying the optimized extrusion process set by the simulation program, significant improvements in the compatibility and dispersion of fillers within the polymer were observed through scanning electron microscopy image analysis. In addition, through detailed analysis of rheological data, the positive impact of adding compatibilizer and changing screw profile on rheological properties was demonstrated. As the compatibility of recycled polymer blends improved, tensile strength increased by approximately two‐fold and thermal conductivity was significantly improved, which were decisive factors in dramatically enhancing the performance of recycled polymers. These improved polymer properties provide an opportunity for recycled polymers to be applied more broadly and will expand the potential for new applications in various industrial fields.","PeriodicalId":20382,"journal":{"name":"Polymers for Advanced Technologies","volume":"7 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2024-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142226432","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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