Transport Mechanism Research Articles

Resistance Switching and Carrier Transport Mechanisms of HfO2-Based Ferroelectric Diode

Resistance Switching and Carrier Transport Mechanisms of HfO₂-Based Ferroelectric Diode

Identification and characterization of zinc importers in Corynebacterium diphtheriae.

Corynebacterium diphtheriae is the causative agent of diphtheria, a severe respiratory disease in humans. C. diphtheriae colonizes the human upper respiratory tract, where it acquires zinc, an essential metal required for survival in the host. While the mechanisms for zinc transport by C. diphtheriae are not well characterized, four putative zinc ABC-type transporter loci were recently identified in strain 1737: iutABCD/E (iut), znuACB (znu), nikABCD1 (nik1), and nikABCD2 (nik2). A mutant deleted for all four loci (Δ4) exhibited similar growth to that of the wild-type strain in a zinc-limited medium, suggesting there are additional zinc transporters. Two additional gene loci predicted to be associated with metal import, mntABCD (mnt) and sidAB (sid), were deleted in the Δ4 mutant to construct a new mutant designated Δ6. The C. diphtheriae Δ6 mutant exhibited significantly reduced growth under zinc limitation relative to the wild type, suggesting a deficiency in zinc acquisition. Strains retaining the iut, znu, mnt, or sid loci grew to near-wild-type levels in the absence of the other five loci, indicating that each of these transporters may be involved in zinc uptake. Plasmid complementation with cloned iut, znu, mnt, or nik1 loci also enhanced the growth of the Δ6 mutant. Quantification of intracellular zinc content by inductively coupled plasma mass spectrometry was consistent with reduced zinc uptake by Δ6 relative to the wild type and further supports a zinc uptake function for the transporters encoded by iut, znu, and mnt. This study demonstrates that C. diphtheriae zinc transport is complex and involves multiple zinc uptake systems.IMPORTANCEZinc is a critical nutrient for all forms of life, including human bacterial pathogens. Thus, the tools that bacteria use to acquire zinc from host sources are crucial for pathogenesis. While potential candidates for zinc importers have been identified in Corynebacterium diphtheriae from gene expression studies, to date, no study has clearly demonstrated this function for any of the putative transporters. We show that C. diphtheriae encodes at least six loci associated with zinc import, underscoring the extent of redundancy for zinc acquisition. Furthermore, we provide evidence that a previously studied manganese-regulated importer can also function in zinc import. This study builds upon our knowledge of bacterial zinc transport mechanisms and identifies potential targets for future diphtheria vaccine candidates.

Albendazole oral drug delivery through ASBT-mediated cholic acid derivatives: A win-win for solubility and permeability

This study investigates the transmembrane transport of cholic acids through the primary sodium-dependent cholic acid transporter (ASBT) and explores the synthesis of a series of albendazole cholic acid derivatives (ABZ-CA). These derivatives, incorporating various linker lengths, aim to enhance the solubility and permeability of albendazole (ABZ) simultaneously.We systematically examined the structural and physicochemical properties of ABZ-CA, delving into its transmembrane transport mechanism and assessing its efficacy against Echinococcus multilocularis (E. multilocularis). Our investigation demonstrates the successful preparation of ABZ-CA using amino alcohols as linkers. The apparent solubility ranking of ABZ-CAs is as follows: ABZ-C4 > ABZ > ABZ-C8 ≈ ABZ-C1. This ranking reflects a balance between the solubilization effect induced by the amorphous state of ABZ-CA and the hydrophobic effect resulting from increased linker length.Enhanced absorption of ABZ-CAs is observed throughout all segments of the intestine, indicating a mechanism of passive diffusion. Notably, the optimal site for absorption shifts from the jejunum (ABZ) to the ileum (ABZ-CAs), with ASBT inhibitors significantly reducing the efficiency of transmembrane transport of ABZ-CAs in the ileum. This implies a specific mechanism of active transport reliant on ASBT. Our hypothesis is that ABZ-CAs undergo transmembrane transport in the gastrointestinal tract via a dual mechanism involving both passive diffusion and active transport.In pharmacodynamic studies, the inclusion of cholic acids does not affect the anti-E. multilocularis effect. Therefore, we believe that the formulation of ABZ-CAs not only enhances the solubility of ABZ but also increases its permeability, resulting in a synergistic effect. Moreover, this formulation presents a novel approach for enhancing the solubility and gastrointestinal permeability of BCSII and IV drugs during oral administration, consequently improving their oral bioavailability.

Ethosome: An Innovative Perspective of Drug Delivery.

Ethosome offers a unique solution to the challenges faced by conventional drug delivery systems. In comparison to traditional liposomes and other nanocarriers, ethosomes exhibit a unique ability to improve drug absorption, overcoming a major limitation in the Transdermal Drug Delivery System. Their soft and flexible nano-vesicular structure facilitates faster permeation, resulting in significantly higher transdermal flux. This scientific investigation effectively traverses the changing landscape of ethosomes as an innovative drug delivery system. By conducting a thorough comparative analysis, we uncover the distinct characteristics that set them apart from other nanocarriers, offering insights into their distinct advantages. The study also includes a detailed analysis of the variables that have a complex impact on performance, elucidating transport mechanisms and addressing advanced facets pivotal for refined drug delivery strategies. This comprehensive overview highlights ethosomes as a future of medicine, offering a promising future for the safe and effective treatment of diverse diseases, impacting numerous lives.

Understanding how junction resistances impact the conduction mechanism in nano-networks

Networks of nanowires, nanotubes, and nanosheets are important for many applications in printed electronics. However, the network conductivity and mobility are usually limited by the resistance between the particles, often referred to as the junction resistance. Minimising the junction resistance has proven to be challenging, partly because it is difficult to measure. Here, we develop a simple model for electrical conduction in networks of 1D or 2D nanomaterials that allows us to extract junction and nanoparticle resistances from particle-size-dependent DC network resistivity data. We find junction resistances in porous networks to scale with nanoparticle resistivity and vary from 5 Ω for silver nanosheets to 24 GΩ for WS2 nanosheets. Moreover, our model allows junction and nanoparticle resistances to be obtained simultaneously from AC impedance spectra of semiconducting nanosheet networks. Through our model, we use the impedance data to directly link the high mobility of aligned networks of electrochemically exfoliated MoS2 nanosheets (≈ 7 cm2 V−1 s−1) to low junction resistances of ∼2.3 MΩ. Temperature-dependent impedance measurements also allow us to comprehensively investigate transport mechanisms within the network and quantitatively differentiate intra-nanosheet phonon-limited bandlike transport from inter-nanosheet hopping.

Deciphering vesicle-assisted transport mechanisms in cytoplasm to cilium trafficking

Deciphering vesicle-assisted transport mechanisms in cytoplasm to cilium trafficking

Proton-coupled transport mechanism of the efflux pump NorA.

Efflux pump antiporters confer drug resistance to bacteria by coupling proton import with the expulsion of antibiotics from the cytoplasm. Despite efforts there remains a lack of understanding as to how acid/base chemistry drives drug efflux. Here, we uncover the proton-coupling mechanism of the Staphylococcus aureus efflux pump NorA by elucidating structures in various protonation states of two essential acidic residues using cryo-EM. Protonation of Glu222 and Asp307 within the C-terminal domain stabilized the inward-occluded conformation by forming hydrogen bonds between the acidic residues and a single helix within the N-terminal domain responsible for occluding the substrate binding pocket. Remarkably, deprotonation of both Glu222 and Asp307 is needed to release interdomain tethering interactions, leading to opening of the pocket for antibiotic entry. Hence, the two acidic residues serve as a "belt and suspenders" protection mechanism to prevent simultaneous binding of protons and drug that enforce NorA coupling stoichiometry and confer antibiotic resistance.

Research on multi‐mechanism synergistic effects of gas cross‐scale percolation in tight gas reservoirs of Yanchang oilfield

AbstractRevealing the gas transport patterns at the microscale and nanoscale is of great scientific and engineering significance for unconventional oil and gas exploration and development. This paper first systematically analyzes the properties of gas transport mechanism under different Knudsen number conditions. Second, the coupling modes of the cross‐scale multi‐drive mechanism are systematically categorized, and three typical coupling calculation methods are pointed out. Again, the rationality of the cross‐scale multi‐agency coupling is quantitatively calculated. The results show that (a) Under the influence of Fick's diffusion equation, when Knr > 0, the coupled ‘slip flow–Fick diffusion–Knudsen diffusion’ equation does not converge to the Knudson diffusion equation. (b) The ‘Fick diffusion–Knudsen diffusion’ coupled equation is calculated to be more than 102 times as large as the Knudsen diffusion equation.

Scalar transport after a high-resolution solitary fractal tree based on large-eddy simulation: Implication to urban green infrastructure

Scalar transport is one of the most concerned issues in the urban environment (e.g., pollutants, pollens, and aeolian transport). Vegetations are commonly regarded as scalar-moderation structures in urban areas by influencing airflows, avoiding aeolian erosion and pollution. The morphological multi-scale branch structures of the single tree were usually neglected in previous studies, which, however, can lead to highly inhomogeneous wake. The turbulence generation through the multi-scale branches is not yet clear. The corresponding spatial details of scalar distribution and its mechanism need to be further examined. In this study, the wake after a single fractal tree is investigated using the large-eddy simulation (LES). The spatial characteristics of the wakes are illustrated, indicating susceptible zones in the canopy, first-generation levels of branches, and recirculation regions. Higher-order moments signify the rare, extreme events with strong upward acceleration, removing air masses likely to occur at the canopy shear layer within 3h downstream where h is the characteristic tree height. The quadrant analysis elucidates the scalar transport potential. The scalar distribution and its transport mechanism are visualized, showing dilution and accumulation by the streamwise and vertical velocities. Involving the multi-scale geometries of the tree can provide guidance for urban green infrastructure (UGI) planning, advancing environmental and sustainability development.

Structure–polaronic conductivity relationship in vanadate–phosphate glasses

AbstractThis work provides new insights into the nature of the polaronic transport in xV2O5–(100−x)P2O5, 41 ≤ x ≤ 89 mol% glasses from analysis of their conductivity over a wide range of frequencies and temperatures, and correlation of the electrical parameters to the structural models of these materials. The results show that the linear increase in direct current (DC) conductivity with the increase in V2O5 could be related to the formation of a vanadate subnetwork, which is characterized by a length distribution of V–O bonds and variations in linkages between different vanadate units. Such a structurally complex network offers multiple conduction pathways which are favorable for polaron hopping. The Summerfield scaling of conductivity spectra reveals a temperature‐invariant mechanism of polaron transport for all glasses and the same local structural environment of polarons at higher V2O5 contents due to the same ratio of vanadate units present in the network. Also, this study highlights the similarities and differences in the nature of the polaronic transport of vanadate–phosphate glasses and other polaronically conducting phosphate glasses containing WO3, MoO3, and Fe2O3, and pins down a pivotal role of the glass structure in electrical processes in these materials.

A Macroscopic Interpretation of the Correlation between Electrical Percolation and Mechanical Properties of Poly-(Ethylene Vinyl Acetate)/Zn Composites

Elastic composites were prepared using a procedure involving hot plates and zinc powder that was directly dispersed into an EVA matrix. The correlation between the zinc content and the conductive properties of the material was studied via impedance spectroscopy, the thermal properties of the material were studied via differential calorimetry and the mechanical properties of the composites were studied via tensile strength curves, representing an important advancement in the characterization of this type of composite material. The composites’ tensile strength and elongation at break decrease with the addition of filler since zinc particles act as stress-concentrating centres, while the composites’ hardness and Young’s modulus increase because of an increase in the stiffness of the material. The AC perturbation across the EVA/Zn composites was characterized using an RC parallel equivalent circuit that allowed us to easily measure their resistivity (ρp) and permittivity (εp). The dependence of these electrical magnitudes on the zinc content is correlated with their mechanical properties across the characteristic time constant τp = ρp·εp of this equivalent circuit. The dependence of the mechanical and electrical magnitudes on the zinc content is consistent with the formation of percolation clusters. The addition of graphite particles increases their potential performance. Three possible mechanisms for the electrical transport of the ac-perturbation across the EVA/Zn composites have been identified. Chemical corrosion in acid media causes the loss of zinc surface particles, but their bulk physical properties practically remain constant.

2D–3D heterostructure of PtS2−x /Ga2O3 and their band alignment studies for high performance and broadband photodetector

For deep ultraviolet (UV-C) photodetectors, gallium oxide (Ga2O3) is a suitable candidate owing to its intrinsic ultra-wide band gap and high stability. However, its detection is limited within the UV-C region, which restricts it to cover a broad range, especially in visible and near-infrared (NIR) region. Therefore, constructing a heterostructure of Ga2O3 with an appropriate material having a narrow band gap is a worthwhile approach to compensate for it. In this category, PtS2 group-10 transitional metal dichalcogenide stands at the top owing to its narrow band gap (0.25–1.65 eV), high mobility, and stability for heterostructure synthesis. Moreover, heterostructure with Ga2O3 sensing in UV and PtS2 broad response in visible and IR range can broaden the spectrum from UV to NIR and to build broadband photodetector. In this work, we fabricated a 2D–3D PtS2−x /Ga2O3 heterostructure based broadband photodetector with detection from UV-C to NIR region. In addition, the PtS2−x /Ga2O3 device shows a high responsivity of 38.7 AW−1 and detectivity of 4.8 × 1013 Jones under 1100 nm light illumination at 5 V bias. A fast response of 90 ms/86 ms illustrates the device’s fast speed. An interface study between the PtS2−x and Ga2O3 was conducted using x-ray photoelectron spectroscopy and ultraviolet photoelectron spectroscopy (UPS) which confirmed type-I band alignment. Finally, based on their band alignment study, a carrier transport mechanism was proposed at the interface. This work offers a new opportunity to fabricate large-area high-performance 2D–3D heterostructures based photodetectors for future optoelectronics devices.

How plastic waste management affects the accumulation of microplastics in waters: a review for transport mechanisms and routes of microplastics in aquatic environments and a timeline for their fate and occurrence (past, present, and future)

An increasing global problem is the buildup of improperly handled plastic garbage in the environment. One of the biggest environmental issues facing aquatic ecosystems today is contamination from bulk plastics and plastic detritus. Specifically, microplastics (MPs) and nanoplastics, which are small-scale plastic waste, are now the main causes of pollution in freshwater and marine environments. On the other hand, contamination of aquatic systems is now acknowledged as one of the major environmental hazards facing our world. Currently, concerns have been raised regarding the breakdown of plastic products into micro and nanosized particles, because of the ineffective plastic waste management. To prioritize regions for mitigation policy implementation, it is critical to pinpoint the precise MPs’ transport mechanisms and the locations where trash is created. In order to show the historical and contemporary circumstances as well as forecasts and scenarios of global plastic waste management from now until 2060, we used continent-level data on trash management. This study, finally, presents a potential future scenario of estimates on the destiny, transport, and occurrence of plastic waste in aquatic habitats, highlighting the different factors that trigger the transport of MPs into water and the necessity of rational management of plastic waste.

Role of sea spray aerosol at the air–sea interface in transporting aromatic acids to the atmosphere

Abstract. Aromatic acids are ubiquitous in seawater (SW) and can be transported to the atmosphere via sea spray aerosol (SSA). Despite their importance in affecting the global radiative balance, the contribution of marine aromatic acids and their transport mechanisms through SSA remain unclear. Herein, the distribution of particle size and number concentration of SSA produced in SW containing nine different aromatic acids (i.e., benzoic acids, benzenedicarboxylic acids, hydroxybenzoic acids, vanillic acid, and syringic acid) was studied using a custom-made SSA simulation chamber; moreover, the enrichment of aromatic acids in SSA and their emission flux to the atmosphere were analyzed. Transmission electron microscopy (TEM) images clearly revealed that aromatic acids can be transferred to the nascent SSA. Interestingly, the morphology associated with benzenedicarboxylic-acid-coated particles showed that aromatic acids can promote the growth of other surfaces of sea salt, thus making the sea salt core spherical. Aromatic acids showed a significant enrichment behavior at the air–sea interface, which clearly indicated that SSA represents a source of aromatic acids in the atmosphere. Vanillic acid had the largest global emission flux through SSA (962 t yr−1), even though its concentration in SW was lower. The calculated results indicated that the global annual flux of aromatic acids was affected not only by the concentration in SW, but also by their enrichment factor (EF). These data are critical for further quantifying the contribution of organic acids to the atmosphere via SSA, which may provide an estimate of the potential influence of the atmospheric feedbacks to the ocean carbon cycle.

Thermal analysis of natural convection in rectangular porous fin wetted with CNTs nanoparticles and thermal radiation

AbstractIn the present investigation, the phenomenon of heat conduction in rectangular shaped porous fin wetted with nanofluid (a mixture of carbon nanotube [CNT] with water as base liquid) is examined using the local thermal non‐equilibrium (LTNE) paradigm. The heat transport mechanism involving the nanofluid and solid phases is represented by the dimensional thermal governing ordinary differential equations (TGODEs). These equations are transformed into nonlinear ordinary differential equations (ODEs) using relevant non‐dimensional variables. To solve the resultant dimensionless TGODEs, probabilists collocation method with Hermite polynomials (PCMHPs) is utilized. This study of temperature analysis has examined the characteristics of internal and exterior radiation, convection, and thermal conductivity to determine the attributes affecting heat transfer. For both the nanofluid and solid phase aspects, temperature distribution characteristics are revealed in tables and graphs. Subsequently, it is determined that as surface‐ambient radiation parameter levels decreased, the temperature profile of both solid and nanofluid phase augmented. The temperature variance among the solid and nanofluid phases decreased with an escalation in the wet porous parameter. The numerical outcomes illustrate that the presented PCMHP approach is not only convenient to execute but also provides accurate results.

Development of pH-responsive Eudragit S100-functionalized silk fibroin nanoparticles as a prospective drug delivery system.

Silk fibroin nanoparticles (FNP) have been increasingly investigated in biomedical fields due to their biocompatibility and biodegradability properties. To widen the FNP versatility and applications, and to control the drug release from the FNP, this study developed the Eudragit S100-functionalized FNP (ES100-FNP) as a pH-responsive drug delivery system, by two distinct methods of co-condensation and adsorption, employing the zwitterionic furosemide as a model drug. The particles were characterized by sizes and zeta potentials (DLS method), morphology (electron microscopy), drug entrapment efficiency and release profiles (UV-Vis spectroscopy), and chemical structures (FT-IR, XRD, and DSC). The ES100-FNP possessed nano-sizes of ∼200-350 nm, zeta potentials of ∼ -20 mV, silk-II structures, enhanced thermo-stability, non-cytotoxic to the erythrocytes, and drug entrapment efficiencies of 30%-60%, dependent on the formulation processes. Interestingly, the co-condensation method yielded the smooth spherical particles, whereas the adsorption method resulted in durian-shaped ones due to furosemide re-crystallization. The ES100-FNP adsorbed furosemide via physical adsorption, followed Langmuir model and pseudo-second-order kinetics. In the simulated oral condition, the particles could protect the drug in the stomach (pH 1.2), and gradually released the drug in the intestine (pH 6.8). Remarkably, in different pH conditions of 6.8, 9.5, and 12, the ES100-FNP could control the furosemide release rates depending on the formulation methods. The ES100-FNP made by the co-condensation method was mainly controlled by the swelling and corrosion process of ES100, and followed the Korsmeyer-Peppas non-Fickian transport mechanism. Whereas, the ES100-FNP made by the adsorption method showed constant release rates, followed the zero-order kinetics, due to the gradual furosemide dissolution in the media. Conclusively, the ES100-FNP demonstrated high versatility as a pH-responsive drug delivery system for biomedical applications.

#1288 Bioinformatic analysis of phosphate transporters in peritoneal cells and tissues and phosphate transport kinetics in vitro

Abstract Background and Aims Hyperphosphatemia is frequent in peritoneal dialysis (PD) patients due to limited dialytic clearance, and significantly increases cardiovascular risk. Molecular mechanisms of phosphate removal across the peritoneal membrane remain unclear, PD specific in vitro models for phosphate transport and modulator studies are not established. Method Phosphate transporter expression was assessed by RNAseq in mesothelial cells (HPMC, MeT5A) and human venous and microvascular endothelial cells (HUVEC, HCMEC). Transcriptome profiles of microdissected omental arterioles from 10 children with normal kidney function (NKF), 15 with chronic kidney disease (CKD5), and 10 children on PD were analyzed for phosphate transporter expression. Specific phosphate transporter localization and abundance in parietal peritoneum membranes and in the cell lines were assessed by immunostaining. In Transwell system, a phosphate transport model across polarized monolayers was established. Cell viability and integrity were verified by MTT assay and transepithelial resistance measurement (TER). Results Out of nine identified phosphate transporters, PiT1 (SLC20A1) and PiT2 (SLC20A2) exhibited high expression in all four cell lines, while SLC34A2 was specific in HPMC and SLC34A3 in MeT5A. In human arterioles, four phosphate transporters, SLC34A1, PiT1, PiT2, and SLC17A1, were detected. Arteriolar PiT1 was two-fold more abundant in PD patients treated with low glucose degradation product (GDP) fluids compared to those with CKD5 and NKF. In parietal peritoneal membranes, PiT1 was abundant in mesothelial and endothelial cells, with no difference between children with NKF, CKD5 and low GDP PD treatment. Concentration and time dependent phosphate kinetics across polarized mesothelial cells were studied in Transwells. Upon increased phosphate concentration in medium (1 mM and 2 mM vs. 0.1 mM), cells didn´t show signs of impaired viability, reduced TER or junction dysregulation (ZO-1 abundance) for up to 12 h. Independent of the added phosphate concentration, 60% of expected equilibrium was achieved after 12 h. Addition of PFA (SLC20/34 sodium-phosphate cotransporter inhibitor) alone or in combination with Tenapanor (an NHE3 blocker inhibiting paracellular phosphate transport) reduced phosphate transport across mesothelial cells by 10% and 20%, respectively. Conclusion We describe phosphate transporter expression and localization in peritoneal cells, in arterioles and parietal peritoneal tissues, and the impact of CKD5 and PD. The Transwell system allowed for quantification of phosphate transport across cell barriers and demonstrated the role of peritoneal sodium-phosphate cotransporter and of the paracellular route for phosphate transport across the mesothelial cell barrier. Further, yet unknown phosphate transport mechanisms should be active.

Molecular mechanism of choline and ethanolamine transport in humans.

Human feline leukaemia virus subgroup C receptor-related proteins 1 and 2 (FLVCR1 and FLVCR2) are members of the major facilitator superfamily1. Their dysfunction is linked to several clinical disorders, including PCARP, HSAN and Fowler syndrome2-7. Earlier studies concluded that FLVCR1 may function as a haem exporter8-12, whereas FLVCR2 was suggested to act as a haem importer13, yet conclusive biochemical and detailed molecular evidence remained elusive for the function of both transporters14-16. Here, we show that FLVCR1 and FLVCR2 facilitate the transport of choline and ethanolamine across the plasma membrane, using a concentration-driven substrate translocation process. Through structural and computational analyses, we have identified distinct conformational states of FLVCRs and unravelled the coordination chemistry underlying their substrate interactions. Fully conserved tryptophan and tyrosine residues form the binding pocket of both transporters and confer selectivity for choline and ethanolamine through cation-π interactions. Our findings clarify the mechanisms of choline and ethanolamine transport by FLVCR1 and FLVCR2, enhance our comprehension of disease-associated mutations that interfere with these vital processes and shed light on the conformational dynamics of these major facilitator superfamily proteins during the transport cycle.

Electronic interfacial thermal conductance between metal nano-films in sub-picosecond non-equilibrium transport process

Interfaces play a critical role in nanoscale thermal transport, and understanding thermal transport mechanisms across metal/metal interfaces at the non-equilibrium states is urgently needed for highly integrated electronic structures or devices. In this work, the electronic interfacial thermal conductance hee of two metal interfaces, Au/Pt and Au/Al, was measured by time domain thermoreflectance (TDTR) at the non-equilibrium states and an extended two-temperature model was applied to well describe the interactions of electrons between the metal films. For the Au/Pt structure, the measured hee is 4.4 ± 1.8 GWm−2K−1, which is consistent with the predicted value by the electronic diffuse mismatch model (DMM). While for the Au/Al structure, the measured hee (0.13±0.05 GWm−2K−1) is an order of magnitude smaller than that of Au/Pt and the predicted value of the electronic DMM. The results indicate that even the extremely thin oxide layer at the Au/Al interface can significantly hinder the electron thermal transport across the metal interface. Overall, our findings contribute to revealing the non-equilibrium interfacial thermal transport mechanisms and pave the way for designing the highly integrated electronic devices.

Theoretical limits of energy extraction in active fluids

Active materials form a class of far-from-equilibrium systems that are driven internally and exhibit self-organization, which can be harnessed to perform mechanical work. Inspired by experiments on synthetic active polymer networks, in this paper we examine limits of work extraction from an active viscoelastic medium by analyzing the transport of a particle. The active viscoelastic material possesses an equilibrium density where the active and passive forces are balanced out. In a one-dimensional system, a gliding activation front (AF), which converts a passive to an active medium, provides active energy at a constant rate, which is injected into the system at one end and propagates to the other. We demonstrate that there exists a maximum velocity of the AF, above which the activated region fails to deliver the transport power. We hypothesize and intuitively argue based on the limit cases that the feasibility and the velocity of transport of the particle can be interpreted in terms of the velocity of an equilibration domain wall of the field, which is set by two parameters: (i) a measure of activity, and (ii) the viscoelastic timescale. The phase diagram is divided into “transport” and “no-transport” sectors, namely, for any pair of the two parameters, there exists a threshold velocity of the AF above which the particle transport becomes impossible. Constructing the phase diagram we find that (1) there are regions of the phase diagram for which the threshold velocity of the AF diverges, and (2) larger viscoelastic timescale makes the transport region more accessible and also increases the transport velocity therein. Furthermore, we find that increasing the velocity of AF, results in larger extracted power but smaller transport coefficient; defined as the ratio of the transport velocity and that of the AF. Our model provides a framework for understanding the energetics of transport phenomena in biology and designing efficient mechanisms of transport in synthetic active materials. Published by the American Physical Society 2024