Extraction Of Am Research Articles

Spotlight on Amniotic Membrane Extract Eye Drops: A Review of the Literature.

To review the literature focusing on the effectiveness of amniotic membrane extract eye drops (AMEDs) in the treatment of ocular surface diseases. PubMed/MEDLINE, Scopus, and CENTRAL databases were searched until March 4, 2024. Overall, we identified 1,121 studies, 26 of which were selected for a full-text review. Twelve studies met the inclusion criteria and were analyzed for clinical improvements, time to resolution of corneal staining, adverse events, and preparation methods. Strength of clinical data was graded according to the Oxford Center for Evidence-Based Medicine. Overall, AMED compounds were used in 296 eyes of 205 patients. Fifty-nine percent of eyes were treated for dry eye disease, 23% for an epithelial defect, and the rest (18%) for other corneal wound healing disorders. Three main types of eye drops preparation were described, that is, lyophilized, homogenized, and fresh AMED. Although the methods of outcome reporting were heterogeneous, all included studies showed various grades of improvement in both signs and symptoms. The overall incidence of ocular side effects was 2.3%. Despite the suboptimal quality of evidence, overall, the available literature suggests that AMED is a valuable tool in the treatment of ocular surface disorders.

Synthesis and study of bistriazolyl-pyrazines as new ligands for An/Ln separations

Herein, we present new hydrophilic tridentate ligands, bistriazolyl pyrazines. Their design was inspired by structurally similar and promising bis-triazolyl-pyridines (PyTri) ligands as well as theoretically derived criteria for the design of tridentate ligands for An/Ln separations suggested by theoretical studies. These ligands have been synthesised, characterised and tested as possible extractants for An/Ln nuclear separations. In addition, UV and fluorescence studies, pKa determination, and crystallographic and theoretical studies have been performed to explain their observed behaviour. Although the results of the solvent extraction studies have shown that these ligands do not possess sufficient selectivity for the extraction of Am vs Eu in i-SANEX conditions, this study presents a valuable test of the criteria for the design of tridentate heterocyclic N-donor ligands for advanced nuclear separation as postulated by theoretical studies a decade ago. Our experimental observations and theoretical studies have found that these criteria might not be the best guidance for designing novel hydrophilic ligands for An/Ln separations in i-SANEX conditions.

Presence of heavy chain-hyaluronan/pentraxin 3 (HC-HA/PTX3) complex in human umbilical cord

The heavy chain (HC)-hyaluronan (HA)/pentraxin 3 (HC-HA/PTX3) complex is formed by tumor necrosis factor-stimulated gene-6 (TSG-6) catalyzing the covalent (ester bond) transfer of HC1 from inter-α-trypsin inhibitor (IαI) to HA followed by tight binding of PTX3. The presence of such a complex has been found in human amniotic membrane (AM) and is considered to be a major matrix component responsible for its anti‑inflammatory and anti‑scarring properties to promote regenerative healing. Because the therapeutic potentials of AM and umbilical cord (UC) are similar, we herein evaluated whether human UC also contains HC-HA/PTX3. Immunostaining of UC cross-sections showed abundant PTX3, HC1, HA, TSG-6, and bikunin. Western blot analysis suggested the presence of HC1 complex bound via a NaOH-sensitive bond and tightly bound to PTX3 multimer in UC and AM extracts but not in chorion and placenta extracts. HC-HA/PTX3 was purified from UC extract by successive runs of density gradient ultracentrifugation and verified the presence of HC1 but not HC2 or HC3 based on western blot analysis. These results suggest the presence of HC-HA/PTX3 complex in UC is similar to AM.

Comprehensive evaluation of ethanol-preserved amniotic extracts: Exploring antioxidant properties, proliferation enhancement, protective efficacy and regeneration potential in wound healing

Amniotic membrane extract (AME) has significant regenerative potential, which has been preserved using various methods over the years. This study explores ethanol (ETOH) as a preservative for AME in regenerative medicine. The study evaluated ETOH-preserved AME at 70 % (ETOH 70 %) and 50 % (ETOH 50 %) concentrations stored at room temperature (RT) and −80 °C. These were compared to phosphate buffer saline (PBS) and Dulbecco's Modified Eagle Medium/Glycerol (DMEM/GLY). In vitro assays included MTT for proliferation, apoptosis assays for protective effects, and scratch assays for migration using adipose stromal cells (ASCs) and fibroblasts. In vivo assessments involved subcutaneous injections in rats, with wound size measured at 4-, 8-, and 11-days post-injury. Histopathological parameters were analyzed after 11 days to evaluate tissue healing and regeneration.The results showed that ETOH preservation, particularly at 50 % and 70 %, exhibited significant antioxidant potential for AME, outperforming traditional methods. ETOH-preserved AME inhibited reactive oxygen species (ROS) and enhanced proliferation rates in ASCs compared to DMEM/GLY (p < 0.01). The ETOH 50 % variant at RT significantly reduced apoptosis and sustained cell proliferation. In vivo, ETOH-preserved AME at 50 % and 70 % accelerated wound closure significantly compared to the control group (p < 0.05). Histopathological analysis revealed improved healing, collagen deposition, and tissue regeneration in treated groups. ETOH preservation is a viable and cost-effective method for maintaining the regenerative potential of AME. This approach offers notable antioxidant, proliferative, and cytoprotective benefits, suggesting its promise for diverse biomedical applications.

6-(6-Methyl-1,2,4,5-Tetrazine-3-yl)-2,2'-Bipyridine: A N-Donor Ligand for the Separation of Lanthanides(III) and Actinides(III).

Here, we report the synthesis of the 6-(6-methyl-1,2,4,5-tetrazine-3-yl)-2,2'-bipyridine (MTB) ligand that has been developed for lanthanide/actinide separation. A multimethod study of the complexation of MTB with trivalent actinide and lanthanide ions is presented. Single-crystal X-ray diffraction measurements reveal the formation of [Ce(MTB)2(NO3)3], [Pr(MTB)(NO3)3H2O], and [Ln(MTB)(NO3)3MeCN] (Ln = Nd, Sm, Eu, Gd). In addition, the complexation of Cm(III) with MTB in solution was studied by time-resolved laser fluorescence spectroscopy. The results show the formation of [Cm(MTB)1-3]3+ complexes, which occur in two different isomers. Quantum chemical calculations reveal an energy difference between these isomers of 12 kJ mol-1, clarifying the initial observations made by time-resolved laser fluorescence spectroscopy (TRLFS). Furthermore, quantum theory of atoms in molecules (QTAIM) analysis of the Cm(III) and Ln(III) complexes was performed, indicating a stronger covalent contribution in the Cm-N interaction compared to the respective Ln-N interaction. These findings align well with extraction data showing a preferred extraction of Am and Cm over lanthanides (e.g., max. SFAm/Eu = 8.3) at nitric acid concentrations <0.1 mol L-1 HNO3.

Influence of Diluent on Extraction Parameters of Systems for Separation Am(III) and Ln(III) Based on 1,10-Phenanthroline-2,9-Diamide.

A systematic study of extraction systems for the separation of f-elements using the tetradentate N,O-donor diamide of 1,10-phenanthroline-2,9-dicarboxylic acid (L) in various molecular and ionic solvents was performed. It was demonstrated that the nature of a diluent has a significant impact on solvent extraction of Am(III) and Ln(III) and the stoichiometry of formed complexes with f-elements. The mechanism of complexation and forms of complexes in different diluents were investigated by radiometric methods, UV-vis titration, and XRD.

Comparative study on corneal epithelium healing: effects of crosslinked hyaluronic acid and amniotic membrane extract eye drops in rats.

Corneal ulcers are common lesions in both human and veterinary medicine. However, only a few studies have evaluated the efficacy of cross-linked hyaluronic acid (X-HA) eye drops on corneal wound healing. To our knowledge, this is the first study to demonstrate and compare the efficacy of amniotic membrane extract eye drops (AMEED) and X-HA for corneal wound healing in rats. A total of 15 male Wistar rats (30 eyes) were used in this study. Then, 10 eyes were treated with X-HA, AMEED, or 0.9% saline. After general and topical anesthesia, a superficial corneal ulcer was created using a corneal trephine. The defect was further polished with a diamond burr. Three groups of 10 eyes each were treated with either one drop of 0.75% X-HA or AMEED or 0.9% saline (control), administered every 12 h for a duration of 72 h. The median epithelial defect area (MEDA), expressed as a percentage of the total corneal surface, was measured at 0, 12, 24, 36, 48, and 72 h. Re-epithelization time scores were also evaluated. The Kruskal-Wallis test was used to compare median times for re-epithelization and histopathologic scores between groups, while the Friedman test (for paired data) was employed to compare results from the serial analysis of MEDA and vascularization scores between groups. MEDA was not significantly different between X-HA and AMEED. However, MEDA was significantly smaller in the X-HA group compared to the control group at 36 h (2.73 interquartile range (IQR) 5.52% x 9.95 IQR 9.10%, P=0.024) and 48 h (0.00 IQR 0.26% x 6.30 IQR 8.54%, P=0.030). The overall time for re-epithelization was significantly lower in the X-HA group (3.00 IQR 3.00) compared to the AMEED (6.5 IQR 3.00) and control (7.00 IQR 1.00) groups (P=0.035). Vascularization, hydropic degeneration, and epithelial-stromal separation were significantly less observed in samples in the X-HA-treated compared to samples in the AMEED- and saline-treated groups. Significantly more corneal epithelium cells were labeled for caspase3 in samples from the AMEED- and saline-treated groups compared to those from the X-HA-treated group. Topical X-HA has been shown to accelerate corneal epithelial healing. AMEED did not decrease corneal re-epithelialization time. X-HA may also potentially be used as an adjunct therapy for treating corneal ulcers in clinical situations.

PHYTOCHEMICAL ANALYSIS AND ANTIMICROBIAL ACTIVITY OF ATLANTIA MONOPHYLLA (AM) EXTRACT

Objective: Plants have long been recognised for their wide range of biological properties, including antibacterial, analgesic, anticancer, antipyretic, and antihypertensive action. They are also a significant source of several chemicals with biological activity. The Rutaceae family consists of a small shrub Atlantia monophylla. It is available all over India. The leaves were employed as an insect repellent and to alleviate swellings. The root bark has been found to contain atalaphyllinine, atalantin, dehydroatalantin, cycloepiatalantin, and atalaphylline 3, 5-dimethyl ether. Essential oil extracted from the leaves was reported to have antimicrobial properties. Methods: To evaluate the phytochemicals Standard chemical methods for each o the compounds were used – like Tannins (0.1% ferric chloride), saponins (2 ml of water)/flavonoids (with NaOH), Alkaloids (Drangandooff reagent), protein (Million’s reagent) steroids (10% sulphuric acid), anthraquinones (aqueous ammonia), Phenols (lead acetate), terpenoids, (3% sulphuric acids) Carbohydrates (Benedict’s reagent). Disc plate method was used to evaluate the antimicrobial activity of the extract Results: The results of this study identified the presence of tannins, flavonoids, alkaloids, proteins, steroids, phenols, terpenoids, and carbohydrates in the AM extract. The microbiological studies revealed better inhibitions of microbes compared to standard drugs. Conclusion: Tannins, flavonoids, proteins, steroids, phenols, terpenoids, carbohydrates and alkaloids were extracted from the AM extract. The extract has significant microbiological action.

The protective effect and bioactive compounds of Astragalus membranaceus against neurodegenerative disorders via alleviating oxidative stress in Drosophila.

Oxidative stress is proposed as a regulatory element in various neurological disorders, which is involved in the progress of several neurodegenerative diseases such as Alzheimer's disease (AD) and Parkinson's disease (PD). Antioxidant drugs are widely used to alleviate neurodegenerative disorders. Astragalus membranaceus (Huangqi, AM) is a commonly used medicinal herb with a wide range of pharmacological effects. Here, the protective effect and mechanism of AM extract (AME) and its bioactive compounds against neurodegenerative disorders via alleviating oxidative stress were detected using adult Drosophila melanogaster. The drug safety was measured by development analysis; oxidative stress resistance ability was detected by survival rate under H2O2 environment; ROS level was detected by DHE staining and gstD1-GFP fluoresence assay; antioxidative abilitiy was represent by measuring antioxidant enzyme activity, antioxidative-related gene expression, and ATP and MFN2 levels. The neuroprotective effect was evaluated by lifespan and locomotion analysis in Aβ42 transgenic and Pink1B9 mutants. AME dramatically increased the survival rates, improved the CAT activity, restored the decreased mRNA expressions of Sod1, Cat, and CncC under H2O2 stimulation, and ameliorated the neurobehavioral defects of the AD and PD. Thirteen small molecules in AM had antioxidant function, in which vanillic acid and daidzein had the most potent antioxidant effect. Vanillic acid and daidzein could increase the activities of SOD and CAT, GSH level, and the expressions of antioxidant genes. Vanillic acid could improve the levels of ATP and MFN2, and mRNA expressions of ND42 and SDHC to rescue mitochondrial dysfunction. Furthermore, vanillic acid ameliorated neurobehavioral defects of PD. Daidzein ameliorated neurobehavioral defect of Aβ-induced AD mode. Taken together, AM plays a protective role in oxidative damage, thereby as a potential natural drug to treat neurodegenerative disorders.

Effects of a human amniotic membrane extract on ARPE-19 cells

BackgroundHuman Amniotic Membrane (hAM) is endowed with several biological activities and might be considered an optimal tool in surgical treatment for different ophthalmic pathologies. We pioneered the surgical use of hAM to treat retinal pathologies such as macular holes, tears, and retinal detachments, and to overcome photoreceptor damage in age-related macular degeneration. Although hAM contributed to improved outcomes, the mechanisms of its effects are not yet fully understood. The characterization and explanation of the effects of hAM would allow the adoption of this new natural product in different retinal pathologies, operative contexts, and hAM formulations. At this end, we studied the properties of a hAM extract (hAME) on the ARPE-19 cells.Methods and resultsA non-denaturing sonication-based technique was developed to obtain a suitable hAME. Viability, proliferation, apoptosis, oxidative stress, and epithelial-mesenchymal transition (EMT) were studied in hAME-treated ARPE-19 cells. The hAME was able to increase ARPE-19 cell viability even in the presence of oxidative stress (H2O2, TBHP). Moreover, hAME prevented the expression of EMT features, such as EMT-related proteins, fibrotic foci formation, and migration induced by different cytokines.ConclusionsOur results demonstrate that the hAME retains most of the properties observed in the whole tissue by others. The hAME, other than providing a manageable research tool, could represent a cost-effective and abundant drug to treat retinal pathologies in the future.

In Vitro Development of Mouse Preantral Follicle with Using Amniotic Membrane Extract-Loaded Hydrogels.

An artificial ovary based on the alginate (ALG) hydrogel has been widely implemented to preserve prepubertal female fertility. However, this platform is not fully capable of successful an ovary microenvironment simulation for follicle development, holding great potential for its improvement. Therefore, this experimental study aimed to evaluate the effect of an amniotic membrane extract (AME) -loaded hydrogel on the mouse preantral follicles in vitro development. In order to have better follicle development, first, the impact of different concentrations of follicle-stimulating hormone (FSH) was evaluated on the mouse preantral follicles encapsulated in ALG. Later, the appropriate dose was adjusted for the follicles encapsulated in the ALG-AME hydrogel. Results demonstrated that 100 mIU/ml FSH showed a significant follicle survival rate compared with 10 mIU/ml FSH (P=0.005). According to MTT assay finding, the rate of weight loss, and rheology evaluations, ALG containing 1 mg/ml AME was identified as an optimal sample of follicle culture instead of other AME concentrations. Follicle diameter significantly increased in the ALG-AME 1 hydrogel compared with the ALG control group without AME (P=0.027). The storage modulus of ALG-AME 1 was 773 Pa and retained the follicle morphology for 13 days. No statistically substantial difference was seen in survival, antrum cavity formation, and competent oocyte in terms of the normal chromosomal arrangement and meiotic spindle rate in comparison with the control group. It can be concluded that ALG-AME 1 could not significantly impact the mouse preantral follicle.

3D-bioprinted GelMA/gelatin/amniotic membrane extract (AME) scaffold loaded with keratinocytes, fibroblasts, and endothelial cells for skin tissue engineering

Gelatin-methacryloyl (GelMA) is a highly adaptable biomaterial extensively utilized in skin regeneration applications. However, it is frequently imperative to enhance its physical and biological qualities by including supplementary substances in its composition. The purpose of this study was to fabricate and characterize a bi-layered GelMA-gelatin scaffold using 3D bioprinting. The upper section of the scaffold was encompassed with keratinocytes to simulate the epidermis, while the lower section included fibroblasts and HUVEC cells to mimic the dermis. A further step involved the addition of amniotic membrane extract (AME) to the scaffold in order to promote angiogenesis. The incorporation of gelatin into GelMA was found to enhance its stability and mechanical qualities. While the Alamar blue test demonstrated that a high concentration of GelMA (20%) resulted in a decrease in cell viability, the live/dead cell staining revealed that incorporation of AME increased the quantity of viable HUVECs. Further, gelatin upregulated the expression of KRT10 in keratinocytes and VIM in fibroblasts. Additionally, the histological staining results demonstrated the formation of well-defined skin layers and the creation of extracellular matrix (ECM) in GelMA/gelatin hydrogels during a 14-day culture period. Our study showed that a 3D-bioprinted composite scaffold comprising GelMA, gelatin, and AME can be used to regenerate skin tissues.

Mesenchymal stem cells derived-exosomes enhanced amniotic membrane extract promotes corneal keratocyte proliferation.

Amniotic membrane extract (AME) and Wharton's jelly mesenchymal stem cells derived-exosomes (WJ-MSC-Exos) are promising therapeutic solutions explored for their potential in tissue engineering and regenerative medicine, particularly in skin and corneal wound healing applications. AME is an extract form of human amniotic membrane and known to contain a plethora of cytokines and growth factors, making it a highly attractive option for topical applications. Similarly, WJ-MSC-Exos have garnered significant interest for their wound healing properties. Although WJ-MSC-Exos and AME have been used separately for wound healing research, their combined synergistic effects have not been studied extensively. In this study, we evaluated the effects of both AME and WJ-MSC-Exos, individually and together, on the proliferation of corneal keratocytes as well as their ability to promote in vitro cell migration, wound healing, and their impact on cellular morphology. Our findings indicated that the presence of both exosomes (3 × 105 Exo/mL) and AME (50 μg/mL) synergistically enhance the proliferation of corneal keratocytes. Combined use of these solutions (3 × 105 Exo/mL + 50 μg/mL) increased cell proliferation compared to only 50 μg/mL AME treatment on day 3 (**** p < 0.0001). This mixture treatment (3 × 105 Exo/mL + 50 μg/mL) increased wound closure rate compared to isolated WJ-MSC-Exo treatment (3 × 105 Exo/mL) (*p < 0.05). Overall, corneal keratocytes treated with AME and WJ-MSC-Exo (3 × 105 Exo/mL + 50 μg/mL) mixture resulted in enhanced proliferation and wound healing tendency. Utilization of combined use of AME and WJ-MSC-Exo can pave the way for a promising foundation for corneal repair research.

The healing power of amniotic membrane extract eye drops. A 100 year old man saved from an Ocular Perforation.

The healing power of amniotic membrane extract eye drops. A 100 year old man saved from an Ocular Perforation.

Theoretical insights into selective extraction of Am(III) from Cm(III) and Eu(III) with asymmetric N-heterocyclic ligands.

Separation of lanthanide (Ln) and minor actinide (MA) elements and mutual separation between minor actinide elements (e.g. Am(III) and Cm(III)) represent a crucial undertaking. However, separating these elements poses a significant challenge owing to their highly similar physicochemical properties. Asymmetric N-heterocyclic ligands such as N-ethyl-6-(1H-pyrazol-3-yl)-N-(p-tolyl)picolinamide (Et-p-Tol-A-PzPy) and N-ethyl-N-(p-tolyl)-1,10-phenanthroline-2-carboxamide (ETPhenAm) have recently received considerable attention in the separation of MAs over Ln from acid solutions. By changing the central skeleton structures of these ligands and introducing substituents with different properties on the side chains, their complexation behavior with Am(III), Cm(III), and Eu(III) may be affected. In this work, we explore four different asymmetric N-containing heterocyclic ligands, namely Et-p-Tol-A-PzPy (L1), N-ethyl-6'-(1H-pyrazol-3-yl)-N-(p-tolyl)-[2,2'-bipyridine]-6-carboxamide (L2), N-ethyl-9-(1H-pyrazol-3-yl)-N-(p-tolyl)-1,10-phenanthroline-2-carboxamide (L3), and ETPhenAm (L4) using density functional theory (DFT). The calculated results demonstrate the potential of ligands L1-L4 for the extraction and separation of Am(III), Cm(III), and Eu(III). Ligand analysis shows that ligand L3 binds more easily to the central metal atom, in line with the stronger extraction capacity of L3. In spite of the higher covalence between the side chain and the central metal atom for complexes with L1-L3, the main chain seems to control the stability of the extraction complexes. The preorganized 1,10-phenanthroline backbone also further enhances the extraction performance of L3 and L4. The difference in coordination ability between the side chain donors of these ligands and metal ions may affect their separation efficiency. This work presents theoretical insights into synthesizing novel ligands for separating trivalent actinides by adjusting N-heterocyclic ligands.

Liquid-liquid extraction of Am(III), Pu(IV), and U(VI) using malonamide and tributyl phosphate in room temperature ionic liquids as diluent

Liquid-liquid extraction of Am(III), Pu(IV), and U(VI) using malonamide and tributyl phosphate in room temperature ionic liquids as diluent

Formation of Complexes of f-Elements with Electron-Withdrawing N-Heterocyclic Diamides: Extraction and Solution Photophysics

To examine the scope of the abnormal aryl strengthening effect (an increase in the extraction of metal ions when an aromatic substituent is introduced into the amide group) on f-metal extraction, a series of tetradentate diamide-type extragents bearing electron-withdrawing pyridine rings in amide moieties of the molecules were tested. The solvent extraction of Am(III)/Eu(III) pairs was investigated under various conditions, the solution chemistry of the lanthanide-extragents systems was studied, and the bonding constants were calculated for complexes of Eu(III) and Tb(III) ions with diamides. The photophysical properties of chemically synthesized ligand/metal (LM) complexes with various LM compositions were additionally studied in depth. The replacement of a phenyl ring by a pyridine one led to a critical reduction in metal affinity, showing the major contribution of electronic nature to the abnormal aryl strengthening effect. However, the pyridine group in the amide side chain provided additional coordination positions for metal ion binding; corresponding complexes with LM2 composition were detected in the system and their stability was calculated. Due to the low stability of the corresponding LM2 complexes, chemical synthesis of the complexes led to the formation of only one metal-containing species with LM composition. The luminescence spectra of europium and terbium complexes of the LM composition were studied. Differences were discovered in the luminescence excitation spectra of europium and terbium complexes with the same ligand. The luminescence quantum yields and luminescence lifetimes of solutions of europium and terbium complexes were determined.

In uence of the nature of the diluent on the extraction capacity of N,N,N',N'-tetrabutyldiglycolamide to Eu(III), Am(III) and Cm(III)

The in uence of HNO3 concentration on the extraction of Eu(III), Am(III) and Cm(III) by N,N,N',N'tetrabutyldiglycolamide in 5 diluents (nitrobenzene, toluene, 1,2-dichloroethane, 1,1,2,2-tetrachloroethane and chloroform) was studied. The dependence of the distribution ratios of the listed metals on the nature of the diluent was examined. The extraction of Eu(III), Am(III) and Cm(III) decreases in the following order: nitrobenzene &gt; m -tri uoromethylnitrobenzene &gt; mixture of n -dodecane and decanol-1 (90 : 10 vol/vol) &gt; tetrachloromethane &gt; 1,2-dichloroethane &gt; benzene &gt; 1,1,2,2-tetrachloromethane &gt; toluene &gt; chloroform. The conditions for the separation of Eu(III)/Am(III) and Am(III)/Cm(III) pairs were determined. The explanation of the observed increase of the Am(III)/Cm(III) separation factors with the increase of the nitric acid concentration in the equilibrium aqueous phase was suggested.

Extraction properties of polyphosphorylated pyridines in nitric acid media

The extraction of U(VI), Th(IV), Am(III), and Eu(III) with solutions of phosphorylated pyridines from nitric acid solutions has been studied. The stoichiometry of the extractable complexes was established. In terms of their extraction ability, these compounds are inferior to bis(diphenylphosphinyl)methane, but they are signi cantly superior to carbamoylmethylphosphine oxides. An increase in the number of phosphine oxide groups in the molecules of phosphorylated pyridines leads to a signi cant decrease in their extraction ability and selectivity in the extraction of Am(III) and Eu(III) from nitric acid solutions.

Structure-activity relationship approach toward the improved separation of actinides(III) over lanthanides(III) using amine-triamide ligands

The efficient separation of trivalent actinides over lanthanides is a major challenge for the partitioning and transmutation (P&T) strategy in spent nuclear fuel reprocessing due to their very similar properties. In this context, the present work reports three amine-triamide NTAamides (nitrilotriacetamides), to investigate the influence of ligand structure on the extraction of Am3+ over Eu3+. Among the three ligands, N,N-diethyl-N′,N′,N″,N″-tetraoctylnitrilotriacetamide shows higher extraction ability for Am3+ compared with that of N,N-dibutyl-N′,N′,N″,N″-tetraoctylnitrilotriacetamide and N,N,N′,N′,N″,N″-hexaoctylnitrilotriacetamide (NTAamide(n-Oct)) in the examined acid range of 0.01–0.50 mol/L HNO3. The structure–activity relationship study reveals that the two unsymmetrical NTAamides with varying alkyl substituted groups have higher extraction efficiency to Am3+ and relatively lower selectivity for Am3+ over Eu3+ than the symmetrical NTAamide(n-Oct) due to the steric hindrance effect. The complexation study by means of slope analysis, ESI-MS, and UV–vis titration suggests the formation of 1:2 metal/NTAamide extracted species. Meanwhile, the NTAamide is identified as a tetradentate ligand by FT-IR and XPS analyses. Furthermore, the analysis of Raman and TRLFS indicates that the NO3− and the H2O molecule do not participate in the inner coordination sphere of Eu3+. By combining the results of solvent extraction and complexation, a neutral complexation extraction model is proposed. Additionally, the stability constants (logβ) and thermodynamic parameters (ΔH, ΔS, and ΔG) regarding the complexation of Eu3+ with NTAamides are also presented.