Effect Of Conjugation Research Articles

Effects of Conjugation with Basil Seed Gum on Physicochemical, Functional, Foaming, and Emulsifying Properties of Albumin, Whey Protein Isolate and Soy Protein Isolate

Protein conjugation with the Maillard reaction has received considerable attention in the past decades in terms of improving functional properties. This study evaluated the changes in the techno-functional properties of whey protein isolate (WPI), soy protein isolate (SPI), and albumin (Alb) after conjugation with basil seed gum (BSG). The conjugates were developed via the Maillard reaction. Various analyses including FT-IR, XRD, SEM, SDS-PAGE, DSC, RVA, rheology, zeta potential, emulsion, and foaming ability were used for evaluating conjugation products. Conjugation between proteins (WPI, SPI, Alb) and BSG was validated by FT-IR spectroscopy. XRD results revealed a decrease in the peak of BSG after conjugation with proteins. SDS-PAGE demonstrated the conjugation of WPI, SPI, and Alb with BSG. DSC results showed that conjugation with BSG reduced the Tg of WPI, SPI, and Alb from 210.21, 207.21, and 210.90 °C to 190.30, 192.91, and 196.66 °C, respectively. The emulsion activity and emulsion stability of protein/BSG conjugates were increased significantly. The droplet size of emulsion samples ranged from 112.1 to 239.3 nm on day 3. Nanoemulsions stabilized by Alb/BSG conjugate had the smallest droplet sizes (112.1 and 143.3 nm after 3 and 17 days, respectively). The foaming capacity of WPI (78.57%), SPI (61.91%), and Alb (71.43%) in their mixtures with BSG increased to 107.14%, 85.71%, and 85.71%, respectively, after making conjugates with BSG. The foam stability of WPI (39.34%), SPI (61.57%), and Alb (53.37%) in their mixtures with BSG (non-conjugated condition) increased to 77.86%, 77.91%, and 72.32%, respectively, after formation of conjugates with BSG. Conjugation of BSG to proteins can improve the BSG applications as a multifunctional stabilizer in pharmaceutical and food industries.

Designing p‐π Conjugated Naphthoquinone‐Derivatives as High‐Performance Cathodes for Aqueous Proton Batteries

Abstract1,4‐naphthoquinone (NQ) is anticipated to emerge as a promising electrode material for designing high‐performance aqueous proton batteries (APBs), attributed to its high theoretical capacity and flexible designability. However, its high solubility and sluggish kinetics are not conducive to long‐term cycling stability and high‐rate capability. Herein, a unique molecular structure design strategy is proposed to construct effective p‐π conjugated structures by inducing the p‐electrons in substituent groups and 𝜋‐electrons on naphthalene rings. Theoretical calculations and experimental results indicate that the p‐π conjugation effect of 2,3‐dichloro‐1,4‐naphthoquinone (2Cl‐NQ) and 1‐hydroxy‐1,4‐naphthoquinone (1OH‐NQ) greatly reduces molecular polarity and expands the π‐conjugate system, which endows them with minimal solubility and superior structural stability, thereby achieving excellent cycling stability with 99.53% and 98.62% capacity retention after 1800 cycles, respectively. Moreover, the p‐π conjugated structures induce a narrowed bandgap, improving electronic conductivity and redox kinetics, thereby significantly enhancing their rate capability. When coupling with perylene‐3,4,9,10‐tetracarboxylic dianhydride (PTCDA) anode, the full battery of 2Cl‐NQ//PTCDA exhibits a high specific capacity of 173 mAh g−1 at 15 A g−1, maintaining 73.2% capacity retention after 40 000 cycles and demonstrating exceptional cycling performance even at −20 °C. This work provides valuable insights and guidance for designing high‐performance energy storage materials for APBs.

Molecular Design of Imino Anion Acceptors Enables Long‐Life Fluoride Ion Batteries

AbstractAnion acceptors (AAs) enable to dissolve metal fluoride salts and achieve reversible fluorination and defluorination in fluoride ion batteries (FIBs). However, most reported strategies only focus on boron‐ and alcohol‐based AAs with strong Lewis acidity and excessive hydrogen bond (HB) strength, which often leads to the uncontrollable mass loss of active materials and the inferior reduction stability of electrolyte. Although amino and imine groups possess preferable anti‐reductive property, their HB strengths are apparently too weak to dissociate fluoride salts. Here a novel strategy is proposed for molecular structure design toward imino AAs by introducing double bonds and pyridine‐N into the five‐membered‐ring of pyrrolidine. Therein the conjugation effect, inductive effect, and α effect are synergistically utilized to enhance the Lewis acidity of imino group. Theoretical calculations and experiments prove that 1,2,4‐triazole AA retains the reduction stability in the maximum extent while increasing the HB strength of imino group. Based on this imino AA, the electrolyte achieves an unprecedented wide electrochemical stability window (5.5 V), enabling highly reversible cycling of fluorination and defluorination for CuF2||Pb full cells (>300 cycles) with a Cu+‐mediated two‐step redox mechanism, for PbF2‐Pb||PbF2‐Pb symmetric cells (1600 h) with low overpotential, and for PbF2||Pb asymmetric cells with high coulombic efficiency.

Porphyrin-based Vinylene-linked 3D Covalent Organic Framework with Unprecedented cya Topology for Photocatalytic H2O2 Production.

Designing and realizing new topologies represent one of the most important ways toward developing new structures and functionalities for molecule-based frameworks including SOFs, MOFs, and COFs. Herein, Aldol condensation between 5,10,15,20-tetrayl(tetrakis(([1,1':3',1''-terphenyl]-4,4''-dicarbaldehyde)))-porphyrin (TTEP) and 2,4,6-trimethyl-1,3,5-triazine (TMT) affords the vinylene-linked 3D covalent organic framework Por-COF-cya. Powder X-ray diffraction (PXRD) in combination with structural simulation reveals its high crystalline structure with an unprecedented cya topology in the molecule-based frameworks reported thus far. Por-COF-cya displayed polycrystallinity and possessed high permanent porosity. Especially, the incorporation of light-harvesting porphyrin unit and vinylene linkages in Por-COF-cya enables a conjugation effect within the framework, endowing it with a photocatalytic H2O2 production rate of 2209 μmol g-1h-1 in pure aqueous solution under visible-light irradiation (λ > 400 nm). Inclusion of the guest molecules TTF into the pores of Por-COF-cya results in a donor-acceptor system TTF@Por-COF-cya, enhancing the photocatalytic activity with H2O2 production rate of 6994 μmol g-1h-1. This work paves a new way for the development of new topological functional molecule-based frameworks toward diverse application potentials.

Near-IR nanolignin sensitizers based on pyrene-conjugated chlorin and bacteriochlorin for ROS generation, DNA intercalation and bioimaging.

Near-infrared (NIR) fluorescent agents are extensively used for biomedical imaging due to their ability for deep tissue penetration. Tetrapyrrole-based photosensitizers are promising candidates in this regard. Further, the extended conjugation of such macromolecules with chromophores can enhance their fluorescence efficiency and DNA intercalation ability. Herein, pyrene-conjugated NIR photosensitizers, such as chlorin (PyChl) and bacteriochlorin (PyBac), were synthesized from the corresponding pyrene-porphyrin (PyP). The correlation between the theoretical and experimental optical properties (absorption and fluorescence spectroscopy results) was determined using the DFT/TD-DFT computational approach. Next, studies on the photophysical properties, reactive oxygen species (ROS) production, and DNA binding were conducted on these macrocycles to study the effect of pyrene conjugation on the pyrrolic ring. Furthermore, each photosensitizer was loaded into lignin nanoparticles (LNPs) using the solvent-antisolvent method to accomplish fluorescence-guided imaging. The developed near-IR chlorin- and bacteriochlorin-doped lignin nanocarriers (PyChl-LNCs and PyBac-LNCs) exhibited significant in vitro singlet oxygen generation upon red LED light exposure. Moreover, these macrocycle-loaded nanolignin sensitizers showed good fluorescence-guided bioimaging with fungal cells (Candida albicans). Further, the nanoprobes exhibited pH-dependent release profiles for biological applications. These nanolignin sensitizers demonstrated promising potential to be utilized in near-IR image-guided photodynamic therapy.

Effect of soybean phosphatidylethanolamine-tamarind gum Maillard conjugate on physicochemical stability of water-in-oil emulsions

Effect of soybean phosphatidylethanolamine-tamarind gum Maillard conjugate on physicochemical stability of water-in-oil emulsions

Curcumin-carbon dots suppress periodontitis via regulating METTL3/IRE1α signaling.

This study aimed to investigate the effects of curcumin-carbon dot conjugates (CUR-CD) on periodontitis. Porphyromonas gingivalis lipopolysaccharide (LPS) was used to establish periodontitis mode in vivo and in vitro. Histological analysis was conducted using hematoxylin and eosin (HE) staining. Bone morphogenetic protein 2 (BMP2) and secreted phosphoprotein 1 (OPN) expression was determined using immunohistochemistry. mRNA levels were detected using reverse transcription quantitative real-time PCR (RT-qPCR). Protein expression was determined using Western blot. N6-methyladenosine (m6A) enrichment was determined using methylated RNA immunoprecipitation (MeRIP) assay. Cytokine release was determined using enzyme-linked immunosorbent assay (ELISA) assay. Osteogenic differentiation was detected using alkaline phosphatase (ALP) staining. The results showed that CUR-CD inhibited the inflammatory response, as well as promoted bone healing in vivo and osteogenic differentiation in vitro. Moreover, CUR-CD downregulated methyltransferase 3 (METTL3), which inhibited m6A modification of endoplasmic reticulum to nucleus signaling 1 (IRElα) and downregulated IRElα expression. However, overexpression of IRElα reversed the effects of CUR-CD, stimulating inflammatory response and inhibiting bone healing and osteogenic differentiation. Collectively, CUR-CD inhibits the progression of periodontitis via downregulating IRElα. Therefore, CUR-CD may be an alternative strategy for periodontitis.

Significantly improve capacitive properties of alicyclic polyimide dielectrics at high temperatures via hard/soft segment engineering

The demand for high energy storage density and efficiency of polymer film capacitors at high temperatures is urgently increasing in the electronics and electrical field. However, most traditional high temperature resistant polymers exhibit the low bandgap and high conductive loss because of the presence of conjugated aromatic structures, resulting in a significant decrease in the energy storage performance at high temperatures and high fields. In this paper, a series of alicyclic polyimide dielectric films containing hard segment of phenyl imide and soft segment of cyclohexyl imide are designed and prepared. On the one hand, the introduction of non-coplanar alicyclic ring into main-chain of polyimide can break long distance conjugation effect, weaken the intermolecular and intramolecular charge transfer interaction and improve the bandgap. On the other hand, the physical crossing point formed by the soft segments can sharply increase Young's modulus of the polyimide films. As a result, the terpolymer polyimide film (CPI90) with copolymerization ratio of phenyl/cyclohexyl dianhydride of 9:1 achieves a highest discharge energy density (Ud) of 5.59 J cm−3 at 150 °C. Importantly, the CPI90 film can obtain the Ud of 2.74 J cm−3 at 200 °C. In addition, the CPI90 film possesses a good self-healing ability attributing to a small ratio for the carbon to hydrogen and oxygen. This work offers a new strategy for synergistically promoting the bandgap and Young's modulus of polymer dielectrics via molecular and hard/soft segment engineering.

Structure-performance relationship and molecular structure optimization design of acid phosphate ester extractants

The extraction performance of acid phosphate ester extractants (PEEs) decreases significantly as the acidity of the aqueous phase increases. Therefore, finding PEEs suitable for high-acid environments has become critical to addressing their performance attenuation. However, the unclear structure-performance relationship of PEEs has led to a lack of guidance in experimental synthesis, significantly impeding the emergence of new acid-resistant PEEs. To tackle these issues, ten novel phenyl phosphate ester extractants were designed based on the molecular formula of phosphodiester (R1R2P(=O)OH) and the conjugation effect of the benzene ring. The relationship between the intrinsic extraction performance of acid PEEs and substituent groups (phenoxy, alkoxy, and alkyl) was quantitatively established by calculating the Gibbs free energy changes of three primary reactions (dimer dissociation, monomer acid ionization, and metal coordination) during divalent cobalt ion extraction. Additionally, the impact of different substitution sites (para, meta, and ortho) of the benzene ring on the extraction performance of acid PEEs was studied. The results indicated that introducing phenoxy groups into traditional acid PEEs (P204 and P507) can effectively enhance the extractants’ acid ionization ability and thermodynamic driving force. The extraction performance of acid PEEs is positively correlated with the number of phenoxy groups, and carbon chain substitution at the meta-position of the benzene ring is the most advantageous. By screening five low-toxicity and low-cost phenolic hydroxyl reagents currently available on the market, design a phenyl phosphate ester extractant ([(CH3)3CCH2C(CH3)2C6H4O]2P(=O)OH, P-4TO) that combines cost and performance advantages. Furthermore, the transition state theory was used to confirm the feasibility of preparing P-4TO, which provided a comprehensive theoretical research method for the future design and synthesis of efficient PEEs.

Adjusting the Coordination Configuration by Changing Electrostatic Potential: Introducing N/O/S Heteroatoms Based on the Electronic Effect.

Energetic coordination compounds (ECCs) have demonstrated unique advantages in regulating the physicochemical properties of energetic materials through the design of organic ligands. The fundamental approach involves altering the electron cloud density distribution of organic ligands to modify the characteristics of coordination sites and, thus, achieve new coordination configurations. In this study, Mulliken charge distribution and surface electrostatic potential analysis were used to elucidate the effects of pyridinic N, pyrrolic N, oxazolic O, and thiazolic S on the electron cloud density of carbohydrazide groups through the induction effect and conjugate effect. Furthermore, three AgClO4-based ECCs were synthesized based on 1H-imidazole-4-carbohydrazide, oxazole-4-carbohydrazide, and thiazole-4-carbohydrazide. Single-crystal X-ray diffraction analysis revealed that [Ag(IZ-4-CA)ClO4]n has a one-dimensional (1D) chain structure, while Ag2(OZCA)2(ClO4)2 and Ag2(SZCA)2(ClO4)2 exhibit zero-dimensional structures. The 1D structure, with good planarity, results in [Ag(IZ-4-CA)ClO4]n having lower mechanical sensitivity (IS = 21 J, FS = 80 N). The introduction of oxazolic O enhances oxygen balance (OB), leading to a higher predicted detonation velocity and pressure for Ag2(OZCA)2(ClO4)2 (D = 6.4 km s-1, P = 23.6 GPa). Although the introduction of thiazolic S is unfavorable for improving oxygen balance, Ag2(SZCA)2(ClO4)2 exhibits the highest initial decomposition temperature among the three, at 232 °C. Additionally, initiation tests demonstrated that three ECCs can successfully detonate cyclotrimethylenetrinitramine (RDX), indicating good initiation capabilities.

Self-assembling chimeric polypeptides as drug-carrying nanoparticles for anti-cancer chemotherapy

Abstract. Chemotherapy is often limited by unfavorable pharmacokinetics and pharmacodynamics that result in dose-limiting cytotoxicity. Therefore, self-assembling nanoparticles have been of particular interest to address these limitations by altering the physicochemical properties of payloads. Amphiphilic chimeric polypeptides (CPs) capable of versatile payload conjugation and spontaneous self-assembly into monodisperse micelles were designed, recombinantly synthesized, and characterized in this study. Doxorubicin (Dox) was also conjugated onto CPs to determine the effectiveness of pH-mediated release and the effects of payload conjugation on CP morphology. The designed CP consisted of a hydrophilic elastin-like polypeptide that enabled non-chromatographic polypeptide purification, an aspartic acid linker, a short Cys-rich segment for drug conjugation, and a hydrophobic domain that promoted the spontaneous formation of CP nanoparticles. Additionally, bio-orthogonal conjugation of chemotherapeutics onto CPs through short acid-labile chemical linkers enabled controlled pH-mediated release of conjugated chemotherapeutics and enhanced self-assembly. Results indicated that CP and Dox-CP nanoparticles had critical aggregation concentrations of 3.24 and 0.58 M and hydrodynamic radii of 57.09 and 72.86 nm, respectively. Dox-CP also released 76.8% of conjugated chemotherapeutics after 24 hours in late endosome pH and was effective against triple-negative breast cancer cells. These favorable characteristics and the independent self-assembly of the designed CP will enable targeted chemotherapeutic delivery regardless of payload hydrophobicity.

Reducing the Сardiotoxicity of Daunorubicin by Conjugation with Natural Sesquiterpene Lactones

We present the results of a histological study into the cardiotoxicity of conjugates of daunorubicin with dehydrocostus lactone and epoxyisoalantolactone in mature male mice of the C57BL/6 line. The effect of conjugates on the morphology of cardiomyocytes and the structure of the left ventricular myocardium in mice was studied.

Pea protein-p-coumaric acid conjugate-based antioxidant film: The relationship between protein structure and film properties after covalent bonding

In this study, pea protein isolates (PPI) have been used to make conjugates by covalent binding with p-coumaric acid (p-CA), and the effect of conjugation on PPI structural characteristics and the structural, optical, mechanical, and physicochemical properties of conjugate-based films were investigated. The conjugation with p-CA unfolds the tertiary structure of PPI and significantly reduces the surface charge. A tendency of aggregation with increasing p-CA addition was proposed. The conjugate-based films show stronger tensile strength (TS) and better water barrier properties than PPI-based films. However, no significant improvement of the elongation at break (EAB) and thermal stability was found for conjugate-based films. FTIR spectroscopic and zeta-potential analyses indicated that such improved film properties could be attributed to the enhancement of hydrogen bonds and weakening of electrostatic repulsion between conjugate-conjugate. Additionally, the conjugates impart the antioxidant activity to the films as confirmed by DPPH scavenging capacity. This study demonstrates the potential of using pea protein-phenolic acid conjugate to make PPI-based films with improved mechanical properties, water barrier properties, and antioxidant activity.

Potent Effects of Lenalidomide-Conjugated Anti-CD38 Antibody-Drug Conjugate (TE-1146) on Multiple Myeloma Cells Isolated from Patients

Potent Effects of Lenalidomide-Conjugated Anti-CD38 Antibody-Drug Conjugate (TE-1146) on Multiple Myeloma Cells Isolated from Patients

Computational Study of SmI2-Catalyzed Intermolecular Couplings of Cyclopropyl Ketones: Links between the Structure and Reactivity.

SmI2-catalyzed intermolecular coupling reactions of cyclopropyl ketones with alkenes or alkynes offer an efficient strategy for furnishing diverse five-membered ring-containing molecular architectures. This study presents a systematic computational investigation to reveal the structure-reactivity relationships in these reactions. The reactivity of aryl cyclopropyl ketones is enhanced by the stabilized ketyl radical and cyclopropyl fragmentation, arising from the conjugation effect of the aryl ring, despite an obstacle emerging from the gauche styrene intermediate that elevates the energy barrier for radical trapping. By contrast, alkyl cyclopropyl ketones lack conjugation and exhibit high barriers for reduction and fragmentation but undergo facile radical trapping due to the minimal steric hindrance. Interestingly, ortho-substituted phenyl cyclopropyl ketones exhibit superior reactivity due to a balance between the moderate conjugation, promoting cyclopropyl fragmentation, and the pretwisted nature of the ortho-substituted phenyl that circumvents the hindrance posed by the gauche intermediate and facilitates the radical trapping. The markedly enhanced reactivity of bicyclo[1.1.0]butyl (BCB) ketones arises from facile fragmentation of the strained BCB motif. Bicyclo[2.1.0]pentyl (BCP) ketones, less strained than BCB ketones, are computationally verified to undergo efficient couplings with various partners, and this can be attributed to their stable fragmentation intermediates that facilitate radical trapping. Our findings provide insights that can aid in designing related reactions.

Synthesis, photophysical properties, and photocytotoxic effects of porphyrin-diphenylalanine conjugates on HeLa cells

Photodynamic therapy (PDT) triggers selective cell death through intensive oxidative stress induced by the generation of reactive species by a photosensitizer (PS) excited by light. In this work, we report the synthesis of four novel porphyrins conjugated to the self-assembling dipeptide L,L-diphenylalanine (FF), effectively inhibiting cervical tumor cell growth. The PS were prepared using the classical A3B strategy, with functionalized and non-functionalized porphyrins obtained in moderate yields over 3 to 4 steps. Absorption and fluorescence studies indicate that the FF attached to the porphyrin ring influences their aggregation at micromolar concentrations. The compounds were efficiently internalized by HeLa cells after 4 h of incubation. Cytotoxicity tests performed in the 1.25–5.0 µmol L−1 range showed that cell viability was reduced to 70 % after irradiation (650 nm). A correlation between cell permeation and the cell death mechanism promoted by the porphyrin was observed.

Enhancement of carbon nanotubes/kerosene nanofluids on mixed convective heat transfer in rectangular enclosures

With the objective of understanding how the mixed convective and the geometrical parameters together influence the nanofluid behavior (enhancement or deterioration) and finding the best configuration of the moving walls for engineering purposes, this paper investigates the single lid-driven mixed convective flow of carbon nanotubes/kerosene nanofluids confined in vertical and horizontal cavities with non-uniform boundary conditions applied to the vertical walls. The findings of this paper can provide crucial conclusions into the behavior and optimization of nanofluids in mixed convective flows in enclosed systems for engineering applications. The system of the governing equations is tackled by a validated in-house code, where we compared the code accuracy with previous experimental and numerical works. The governing parameters are -50 ≤ Pe ≤ 50, 0.5 ≤ A ≤ 4, and 0 ≤ φ ≤ 3%. The effective nanofluid properties are calculated using special experimental models. The outcomes revealed that the carbon nanotube effect on heat transfer depends on the aspect ratio. The greater the aspect ratio, the more pronounced the negative impact of the nanotube concentration where Nusselt number is reduced by 4.49% and 16.17% for φ = 0.01 and 0.03, respectively, in the case of Pe = 0 and A = 4. The Peclet number also has a significant impact on the heat transfer, especially for higher aspect ratios, and diminishes the critical aspect ratio where the nanofluid's behavior changes. An augmentation in the aspect ratio and Peclet number brings about an augmentation in the Nusselt number. Additionally, the Peclet number can reverse the conjugated effect of carbon nanotube volume fraction and aspect ratio on nanofluid enhancement. When Pe = 50 in C1, heat transfer rate is 1.75% and 1.11% enhanced for φ = 0.01 and 0.03, respectively, and A = 4. Moving horizontal walls exhibits higher heat transfer enhancement compared to vertical ones.

Upgrading of nitrate to hydrazine through cascading electrocatalytic ammonia production with controllable N-N coupling

Nitrogen oxides (NOx) play important roles in the nitrogen cycle system and serve as renewable nitrogen sources for the synthesis of value-added chemicals driven by clean electricity. However, it is challenging to achieve selective conversion of NOx to multi-nitrogen products (e.g., N2H4) via precise construction of a single N-N bond. Herein, we propose a strategy for NOx-to-N2H4 under ambient conditions, involving electrochemical NOx upgrading to NH3, followed by ketone-mediated NH3 to N2H4. It can achieve an impressive overall NOx-to-N2H4 selectivity of 88.7%. We elucidate mechanistic insights into the ketone-mediated N-N coupling process. Diphenyl ketone (DPK) emerges as an optimal mediator, facilitating controlled N-N coupling, owing to its steric and conjugation effects. The acetonitrile solvent stabilizes and activates key imine intermediates through hydrogen bonding. Experimental results reveal that Ph2CN* intermediates formed on WO3 catalysts acted as pivotal monomers to drive controlled N-N coupling with high selectivity, facilitated by lattice-oxygen-mediated dehydrogenation. Additionally, both WO3 catalysts and DPK mediators exhibit favorable reusability, offering promise for green N2H4 synthesis.

Depuration of Asian Green Mussels Using Chitooligosaccharide-Epigallocatechin Gallate Conjugate: Shelf-Life Extension, Microbial Diversity, and Quality Changes during Refrigerated Storage

The effect of chitooligosaccharide-EGCG conjugate (CEC) at different concentrations (0, 1, and 2%; w/v) and depuration times (DT; 3, and 6 h) on the total viable count and Vibrio spp. count of Asian green mussels (AGMs) was studied. Depurated samples showed a reduction in both microbial counts as compared to fresh AGMs (without depuration) and AGMs depurated using water (CON). A similar TVC was noticed at both DTs; however, a lower VC was attained at a DT of 3, irrespective of CEC concentrations (p < 0.05). AGMs were depurated for 3 h using 1 and 2% CEC (CE1 and CE2, respectively) solutions and stored for 6 days at 4 °C. The CE2 sample showed the lowest microbial counts as compared to fresh AGMs, CON, and CE1 throughout the storage (p < 0.05). CE2 extended the shelf-life of AGMs by 4 days, which was also supported by the lower peroxide value (0.48 mg cumene hydroperoxide/kg sample) and TBARS (0.94 mmol MDA eqv/kg sample) when compared with other samples. Moreover, CE2 had a lower total volatile nitrogen base (TVB; 4.72 mg N/100 g) and trimethylamine (TMA; 3.59 mg N/100 g) on day 4. Furthermore, 2% CEC was able to maintain the DHA content; however, a slightly lower EPA was noticed as compared to the CON. Next-generation sequencing suggested that the CON had a larger microbial community, especially Vibrio sp., than the CE2. All the treated samples showed similar likeness scores to the cooked CE2 and CON on day 0. However, slightly lower likeness was attained when CE2 was stored for 4 days, but the likeness score was higher than the acceptable limit (5). No difference in cooking loss was noticed between CON and CE2 samples on day 0. Nevertheless, cooking loss was increased on day 4. Thus, depuration using CEC solution enhanced the shelf-life of AGMs by 4 days without having negative impact on consumer acceptability and textural properties.

211At radiolabeled APBA-FAPI for enhanced targeted-alpha therapy of glioma

Fibroblast activation protein-α (FAPα) is highly expressed in tumor-associated cells and has become one of the most attractive targeting sites in cancer diagnosis and therapy. To ameliorate the rapid metabolism of FAPα inhibitor (FAPI), here, a multifunctional binding agent was introduced to simultaneously achieve 211At radiolabeling and tumor retention prolongation of corresponding radiolabeled drug. 211At-APBA-FAPI was successfully synthesized by conjugating 211At with the designed FAPI carrier in satisfactory radiochemical yield (>60 %). 211At-APBA-FAPI exhibited excellent in vitro stability, significant tumor affinity and specific killing effect on FAPα-positive U87MG cells. Molecular docking reveals that FAPI decorated with albumin binder can bind with FAPα protein via multiple intermolecular interactions with a considerable binding energy of −9.66 kcal/mol 211At-APBA-FAPI exhibits good targeting in murine xenograft models, showing obviously longer tumor retention than previously-reported radioastatinated compound. As a result, 211At-APBA-FAPI presents pronounced therapeutic effect with ignorable normal organs/tissues biotoxicity. All these indicate that introducing a multifunctional binding agent can effectively enhance the availability of FAPI for 211At conjugation and tumoricidal effect, providing vital hints for the translation of targeted-alpha therapy based on radiolabeled FAPI derivatives.