Track-etched Polycarbonate Membranes Research Articles

A Novel Method for Separating Full and Empty Adeno-Associated Viral Capsids Using Ultrafiltration.

Adeno-associated viral vectors (AAVs) are the predominant viral vectors used for gene therapy applications. A significant challenge in obtaining effective doses is removing non-therapeutic empty viral capsids lacking DNA cargo. Current methods for separating full (gene-containing) and empty capsids are challenging to scale, produce low product yields, are slow, and are difficult to operationalize for continuous biomanufacturing. This communication demonstrates the feasibility of separating full and empty capsids by ultrafiltration. Separation performance was quantified by measuring the sieving coefficients for full and empty capsids using ELISA, qPCR, and an infectivity assay based on the live cell imaging of green fluorescent protein expression. We demonstrated that polycarbonate track-etched membranes with a pore size of 30 nm selectively permeated empty capsids to full capsids, with a high recovery yield (89%) for full capsids. The average sieving coefficients of full and empty capsids obtained through ELISA/qPCR were calculated as 0.25 and 0.49, indicating that empty capsids were about twice as permeable as full capsids. Establishing ultrafiltration as a viable unit operation for separating full and empty AAV capsids has implications for developing the scale-free continuous purification of AAVs.

Removal of carbamazepine, sulfamethoxazole and aspirin at municipal wastewater treatment plant of Astana, Kazakhstan: paths to increase the efficiency of the treatment process

AbstractBACKGROUNDMedical substances are utilized around the world, and their accumulation in nature is a global concern. This work aimed to identify three priority pharmaceuticals discharged into the domestic sewage stream of Astana city (Kazakhstan). Samples of municipal wastewater were taken before and after the wastewater treatment plant (WWTP) over a period of 13 months. The performed experiments demonstrated that there are seasonal variations in the priority pharmaceuticals – carbamazepine (CBZ), sulfamethoxazole (SMX) and aspirin (ASP) – identified in the wastewaters.RESULTSThe non‐conventional WWTP of Astana city, which includes a sequence of treatment processes, showed 2–100% removal of these compounds with the following influent concentrations from the entering stream: 12.5–185.6 ppb (μg L−1) for CBZ, 2.6–51.2 ppb for SMX and 1.9–199.8 ppb for ASP. Laboratory‐scale experiments revealed that the application of the membrane separation technique, i.e. ultrafiltration, is able to provide improved removal of these pharmaceuticals. The removal of ASP, CBZ and SMX by phase inversion polyethersulfone and track etch (TE) polycarbonate membranes was investigated. Filtration with TE membrane demonstrated 39–97% removal of the primary pharmaceuticals from the wastewater.CONCLUSIONFiltration with TE membrane was recognized as an affordable and efficient supplementary treatment step. The addition of the TE separation process in the Astana WWTP could potentially improve the removal of the studied pharmaceuticals along with other medical substances. The reported results hold substantial significance, particularly for rapidly expanding urban centers and developing nations. This is especially crucial as there is a scarcity of data regarding the treatment of pharmaceuticals in municipal wastewater for these regions. © 2024 Society of Chemical Industry (SCI).

Integration of 2D Nanoporous Membranes in Microfluidic Devices.

2D material-based membranes have emerged as promising candidates for next-generation separation technology due to their exceptional permeability and selectivity. Integration of these membranes into microfluidic devices has offered significant potential for improving the efficiency, throughput, and precision. However, designing compact and reliable microfluidic devices with membranes has many challenges, including complexities in membrane integration, analyte measurement, and contamination issues. Addressing these challenges is critical for unlocking the full potential of membrane-integrated devices. This paper proposes a systematic procedure for integrating membranes into a microfluidic device by creating a pore in the middle layer. Furthermore, an ion transport experiment is carried out across various stacked graphene and poly carbonate track etch membranes in an Ostemer-based device. The resulting device is capable of facilitating the concurrent measurement, a task that is cumbersome in standard macroscopic diffusion cells. The transparency and compactness of the microfluidic device allowed for the in situ and real-time optical characterization of analytes. The integration of microfluidic devices with 2D nanoporous membranes has enabled the incorporation of several analytical modalities, resulting in a highly versatile platform with numerous applications.

Effect of copper doping on the photocatalytic performance of Ni2O3@PC membrane composites in norfloxacin degradation.

In this study, copper (Cu) and nickel oxide (Ni2O3) microtubes (MTs) were synthesized using an electroless template deposition technique within porous polycarbonate (PC) track-etched membranes (TeMs) to obtain Cu@PC and Ni2O3@PC composite membranes, respectively. The pristine PC TeMs featured nanochannels with a pore density of 4 × 107 pores per cm2 and an average pore diameter of 400 ± 13 nm. The synthesis of a mixed composite, combining Cu and Ni2O3 within the PC matrix, was achieved through a two-step deposition process using a Ni2O3@PC template. An analysis of the resultant composite structure (Cu/Ni2O3@PC) confirmed the existence of CuNi (97.3%) and CuO (2.7%) crystalline phases. The synthesized catalysts were characterized by scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD) analysis, and atomic force microscopy (AFM). In photodegradation assessments, the Cu/Ni2O3@PC mixed composite demonstrated higher photocatalytic activity, achieving a substantial 59% degradation of norfloxacin (NOR) under UV light irradiation. This performance surpassed that of both Ni2O3@PC and Cu@PC composites. The optimal pH for maximum NOR removal from the aqueous solution was determined to be pH 5, with a reaction time of 180 min. The degradation of NOR in the presence of these composites adhered to the Langmuir-Hinshelwood mechanism and a pseudo-first order kinetic model. The reusability of the catalysts was also investigated for 10 consecutive runs, without any activation or regeneration treatments. The Cu@PC membrane catalyst demonstrated a marked decline in degradation efficiency after the 2nd test cycle, ultimately catalyzing only 10% of NOR after the 10th cycle. In contrast, the Ni2O3@PC based catalyst demonstrated a more stable NOR degradation efficiency throughout all 10 runs, with 27% NOR removal observed during the final test. Remarkably, the catalytic performance of the Cu/Ni2O3@PC mixed composite remained highly active even after being recycled 4 times. The degradation efficiency exhibited a gradual reduction, with a 17% decrease after the 6th run and a cumulative 35% removal of NOR achieved by the 10th cycle. Overall, the findings indicate that Cu/Ni2O3@PC mixed composite membranes may represent an advancement in the quest to mitigate the adverse effects of antibiotic pollution in aquatic environments and hold significant promise for sustainable water treatment practices.

Multilayer track-etched membrane-based electroosmotic pump for drug delivery.

Herein, we report an electroosmotic pump (EOP) based on a multilayer track-etched polycarbonate (PC) membrane. A remarkable increase of maximum backpressure (198.2-2400mmH2 O) of a fundamental pump unit was obtained at 0.8mA, when the number of PC membranes was increased from 1 to 10. Meanwhile, the corresponding flow rate was increased from 80.3 to 111.7µL/min. Furthermore, multiple pump units were assembled in series to obtain a multistage EOP. For a three-stage EOP (EOP-3), the operating voltage and power can be decreased significantly by 52%-72% under different driving currents, with a minimum power of 26.7µW. Thus, EOP-3 can run stably over 35h at a pulse current of 0.1mA without the generation of gas bubbles. The pump was further integrated into a miniature device, which was successfully used to decrease the blood glucose level of diabetic rats by subcutaneous delivery of fast-acting insulin. This work brings a facile and efficient strategy to enhance the backpressure and lower the operating voltage and power of EOPs, which may find promising applications in drug delivery.

Molecular Detection of Multidrug Resistance and Characterizations of Mutations in Mycobacterium Tuberculosis Using Polycarbonate Track-Etched Membrane Based DNA Bio-Chip.

With the widespread use of rifampicin (RMP) and isoniazid (INH), multidrug resistance (MDR) in Mycobacterium tuberculosis (M.tb) poses a threat to the success of tuberculosis (TB) control programs. We have developed a new polycarbonate track-etched membranes(PC-TEM) based DNA bio-chip designed for rapid detection of mutations conferring MDR inM.tbculture isolates. Bio-chips were designed to contain 14 specific probes for wild type and mutated allele of selected codons within 80bprifampicin resistance determining region of rpoB gene, katGgene andmabA-inhAregulatory region. RMP-resistance-associated gene mutation pointsrpoB 516, 526, 531and533, and the INH-resistance-associated gene mutation pointskatG315andinhA-15were targeted. Bio-chip signal was detected using enhanced chemiluminescence. A total of 50 culture isolates that were sensitive or resistant to RMP and/or INH were analyzed by bio-chip. The results of culture-based drug susceptibility testing (DST)were used as the gold standard and gene sequencing was performed to resolve the discordance. Amongst 50 culture isolates, we have detected 18 MDR, 9 RMP mono-resistant, 6 INH mono-resistant, and 17 fully susceptible isolates. The developed DNA bio-chip has a sensitivity of 90% for RMP and MDR and 100% for INH resistance. The bio-chip has a specificity of 100% for RMP and MDR and 88.8% for INH detection. The identification of mutations using the DNA bio-chip was 100% concordant with the sequencing data for the probes covered by the bio-chip. The detection ofrpoB, katGand inhA gene mutation points by a DNA bio-chip may be used as a rapid, accurate, and economical, clinical detection method for MDR detection in M.tb. This is very valuable for the control of TB epidemics.

Element Composition of Fractionated Water-Extractable Soil Colloidal Particles Separated by Track-Etched Membranes

Membrane fractionation with track-etched membranes was used to size-profile the microelement composition of water-extractable soil colloids (WESCs). The aim of the study is the element composition of narrow WESC fractions of typical chernozems in the range of 0.01–10 µm. Micro-/ultrafiltration through a cascade of track-etched polycarbonate membrane filters with pore sizes of 5, 2, 1, 0.8, 0.4, 0.2, 0.1, 0.05, 0.03, and 0.01 µm at room temperature was used. ICP–AES using direct spraying of obtained fractions without decomposition was used; Al, Ba, Cd, Cr, Cu, Fe, Mn, Si, Sr, Ti, Zn, Ca, K, Mg, Na, P, and S were found. Narrow WESC fractions differ significantly. For macro- and microelements, maximum amounts of Si, Al, Fe, and Ti and their maximum percentages are observed in fractions with sizes above 1 µm, while Ca, Mg, Mn, Cu, Zn, K, and S are accumulated more in fractions with sizes below 1 µm. The developed approach provides preparative isolation of a detailed set of narrow WESC fractions in the micrometer–nanometer range. This provides element soil profiles that reveal distinct differences and the individual character of each fraction as well as trends in changes in the mineral matrix and microelement composition with fraction size.

Highly enantioseparation in membrane-supported one-dimensional metal–organic framework hollow nanotube array prepared via mussel-inspired chemistry

High-enantioselective chiral metal–organic framework (CMOF) nanochannel membranes are of critical importance for chiral enantiomeric separations by taking advantage of their inherent high porosity and intrinsic chirality. However, traditional chiral membranes are still constrained by the permeability-selectivity trade-off, making it challenging to improve both simultaneously. This study described the structure of a new class of membrane-supported one-dimensional MOF hollow nanotube for transport and separation of chiral 1-phenylethanol (PE), utilizing a biomimetic polydopamine (PDA)-mediated counter-diffusion synthesis strategy. The inner cylindrical pore channel surface of polycarbonate track-etched membranes (PCTM) was modified by PDA chemistry to control the nucleation and interfacial growth of CMOF crystals, leading to the development of integrated chromatographic micro-column array membranes PCTM@PDA@Cu2C2D and PCTM@PDA@Cu2C2B with one-dimensional (1D) CMOF hollow nanochannels. Compared to PCTM@PDA@Cu2C2B, it was highlighted that the chiral membrane PCTM@PDA@Cu2C2D possessed the higher loading of Cu2C2D functional layer and more suitable steric chiral microenvironment, thus exhibited more outstanding permeability and selectivity for S-PE enantiomer with an enantiomeric excess value up to 90 % under an optimal guest concentration of 250 ppm at 30 °C for 1 h. The chiral membrane with 1D MOF hollow nanotubes, created by applying a gentle and simple method to introduce CMOF into the surface and pore channels of the substrate membrane, was expected to be utilized for the large-scale production of chiral separation membranes for industrial applications.

(Invited) The Impact of Carbon Nanotube Length and Diameter on Their Global Alignment by Dead-End Filtration

Dead-end filtration on polyvinylpyrrolidone-coated polycarbonate track-etched membranes has proven to be an effective method to prepare macroscopically (3.8 cm²) aligned thin films from solution-based single-wall carbon nanotubes (SWCNTs). However, to make this technique broadly applicable, the role of SWCNT length and diameter on the alignment process must be understood. To date, most groups report the alignment of unsorted large diameter (» 1.4 nm) SWCNTs, but systematic studies on their small diameter (» 0.78 nm) counterparts are rare and in the case of sorted SWCNT species, non-existent. In this work, films are prepared from two series of length sorted fractions comprised of small and large diameter SWCNTs, respectively. The degree of alignment is characterized by cross polarized microscopy, scanning electron microscopy and Raman spectroscopy. For the longest fractions, the two-dimensional order parameter, , values of » 0.66 and » 0.76 are reported for the small and large diameter SWCNTs, respectively, and Raman maps over an area of 2500 μm2 are presented. A comparison of Derjaguin, Landau, Verwey and Overbeek (DLVO) theory calculations with the aligned domain size is then used to propose a law identifying the required length of a carbon nanotube with a given diameter and zeta potential for alignment.

Assembly and Characterization of Length-Sorted, Aligned Boron Nitride/Carbon Nanotube Thin Film Composites Via Slow Vacuum Filtration

Globally aligned single-wall carbon nanotubes (SWCNTs) are a promising, scalable platform for studying fundamental physical phenomena and an important vehicle for optoelectronic device applications. Recent work by Rust et al. [1] has identified nanotube length as an important mediating factor in the degree and scale of SWCNT alignment via slow vacuum filtration (SVF).Building on this work and that of Walker et al. [2,3], we explore the co-assembly of length-sorted SWCNTs and boron nitride nanotubes (BNNTs) atop polycarbonate track-etched membranes. BNNTs have recently gained interest as a chirality-agnostic, wide-bandgap material for encapsulation, insulation, thermal/mechanical robustness, and visible-light transparency, while also having a similar high aspect ratio morphology, making them an exceptional and alignable host matrix for individualized CNT species. To prepare such hybrid assemblies, a polymer-assisted, depletion-based method was first used to length-sort different diameter SWCNT (alkane filled electric-arc, CoMoCAT, metallic-sorted Tuball), and BNNT nanotube populations. Thereafter, we investigated the impacts of tube lengths, relative BN/C fraction, mass loading, and presence of a global director force on the multi-scale assembly behavior. A combination of birefringence microscopy and polarized Raman spectroscopy probed and identified trends in global and local ordering under these conditions.[1] Rust, C., Shapturenka, P., Spari, M., Jin, Q., Li, H., Bacher, A., Guttmann, M., Zheng, M., Adel, T., Hight Walker, A. R., Fagan, J. A., & Flavel, B. S. (2022). The Impact of Carbon Nanotube Length and Diameter on their Global Alignment by Dead-End Filtration. Small (forthcoming).[2] Walker, J. S., Fagan, J. A., Biacchi, A. J., Kuehl, V. A., Searles, T. A., Hight Walker, A. R., & Rice, W. D. (2019). Global Alignment of Solution-Based Single-Wall Carbon Nanotube Films via Machine-Vision Controlled Filtration. Nano Letters, 19(10), 7256–7264.[3] Walker, J. S., Macdermid, Z. J., Fagan, J. A., Kolmakov, A., Biacchi, A. J., Searles, T. A., Walker, A. R. H., & Rice, W. D. (2022). Dependence of Single‐Wall Carbon Nanotube Alignment on the Filter Membrane Interface in Slow Vacuum Filtration. Small, 18, 2105619.

Comparison of microfiltration performances of ePTFE and PCTE membranes in IPA and deionized water

Isopropyl alcohol (IPA) is widely used as a cleaning and drying agent in semiconductor manufacturing. The purity of chemicals is becoming increasingly stricter as the leading-edge node sizes become smaller. The microfiltration of nanoparticles (NPs) in water has been extensively studied by many research groups. However, studies on microfiltration in IPA are rare. In this study, we conducted experiments to determine the filtration of nanoparticles using expanded polytetrafluoroethylene (ePTFE) and polycarbonate track-etched (PCTE) membranes in both deionized water (DIW) and IPA. The zeta potentials (ZP) of the polymers and particles were measured. The Hamaker constant and its effect on particle capture were estimated using Derjaguin–Landau–Verwey–Overbeek theory. The results show that the retention efficiency of the two membranes (five different pore sizes) for Ag NPs (size: 20–100 nm) in IPA was much higher than that in DIW. However, the retention efficiencies of the two membranes in IPA and DIW increase monotonically upon increasing the particle size, which was completely different from the U-shaped curve for aerosol filtration predicted using the previous liquid model. In addition, the absolute ZP value of the NPs and membrane surface in IPA was found to be much smaller than that of DIW.

A novel approach for extracting magnetic properties of double-shell nanotubes of Prussian blue and its Cr analog with the use of a mathematical hysteresis decomposition

This work presents the synthesis and investigation of Prussian blue and its chromium analog nanotubes obtained inside porous polycarbonate track etch (PCTE) membranes by electrochemical deposition. The process yielded nanotubes with outer diameters between 50 and 200 nm and thicknesses of approximately 30 nm. It was found that decreasing nanotube diameter had little or no effect on magnetic properties (critical temperature and coercivity). Additionally, the growing process and the basic properties of double-shell nanotubes are described. These double-shell structures show a two-component magnetic behavior. By using the theoretical model, it is possible to decompose the hysteresis loops into the base constituents and derive the relative concentration of each counterpart.

Experimental and theoretical retentions of sub-10 nm colloidal nanoparticles by large-pore ultrafiltration membranes in isopropanol and water

Effective removal of small colloidal nanoparticles (NPs, e.g., <20 nm), including rigid particles, macromolecules, organics, viruses, antibiotics, hormones, etc., by dead-end filtration, is very important in drinking water, chemical, biopharmaceutical, and semiconductor factories. Most existing operations focused on sieving mechanism-based filtration with small-pore membranes (e.g., <20 nm) to capture these tiny NPs, which unfortunately leads to high energy consumption. This study proposed an emerging method that is to use large pore membranes (i.e., ∼100 nm) to capture NPs down to 2.8 nm. The ultimate goal is to address the grand challenge presented in the United Nations Sustainable Development Goal 12 on energy saving. To capture (or adhere) small NPs by large-pore membranes, the surface electrostatic interactions between NP and membrane should be considered in addition to the sieving mechanism. To examine the feasibility of the proposed method, the retention efficiency of ∼100 nm rated polyvinylidene fluoride (PVDF), polytetrafluoroethylene (PTFE), and polycarbonate track-etched (PCTE, as a model filter) membranes against 2.8 nm ZnS quantum dot (QD), 5 and 10 nm Au and 100 nm PSL in water and isopropanol (IPA, a representative organic solvent) were studied experimentally and theoretically. In the experiments, the electrospray-scanning mobility particle sizer (ES-SMPS) was used to measure the size distribution of these nanosized colloids before and after the membrane to determine the retention efficiency. In the theory, we combined the hydrodynamic particle transport, extended Derjaguin-Landau-Verwey-Overbeek (xDLVO), and Maxwell models to calculate the NP retention. Results showed that the data agreed with the theoretical model very well, and the NP retentions in IPA were higher than that in water due to a significant change of acid-base interaction from repulsion to attraction. The retention of the 10 nm Au NPs and the 2.8 nm NPs could be attained by ∼80 and 35%, respecively, in IPA by the PTFE. This study was the first to show the combined theoretical model can accurately predict the retention of sub-10 nm NPs by different membranes in an organic solvent and water. The model predicts the retention of 5 nm Au NPs can be increased to higher than 99% by increasing the zeta potential of the PTFE about 5 times, thus a sustainable UF cutting significant carbon footprint is foreseeable in near future.

Low-density Pt nanoarray-based hydrogen peroxide sensing platform and its application in trace sarcosine detection

Hydrogen peroxide (H2O2) is an important signaling molecule that regulates many biological processes. It is of great value to realize rapid, accurate, highly sensitive and low-cost H2O2 detection in the immediate detection of trace disease markers. Low-density nanoelectrode arrays have a high signal-to-noise ratio and are advantageous for trace detection. In this paper, low-density Pt nanoelectrode arrays were successfully prepared by a simple method of ion sputtering combined with electrodeposition based on a track-etched polycarbonate membrane template. The arrays had a detection limit as low as 0.03 μM for H2O2 at a constant potential, a sensitivity of 125.9 μA mM−1, and a linear range spanning nearly four orders of magnitude (0.1–655 μM). The developed sarcosine sensors based on these arrays had a very low detection limit (0.08 μM) and wide linear range (0.5–64.5 μM) for the rapid detection of trace amounts of sarcosine in serum. With a wide linear range and low detection limits, this hydrogen peroxide sensing platform has great potential for use in the rapid electrochemical detection of trace substances.

Biofabrication, biochemical profiling, and in vitro applications of salivary gland decellularized matrices via magnetic bioassembly platforms.

Trending three-dimensional tissue engineering platforms developed via biofabrication and bioprinting of exocrine glands are on the rise due to a commitment to organogenesis principles. Nevertheless, a proper extracellular matrix (ECM) microarchitecture to harbor primary cells is yet to be established towards human salivary gland (SG) organogenesis. By using porcine submandibular gland (SMG) biopsies as a proof-of-concept to mimic the human SG, a new decellularized ECM bioassembly platform was developed herein with varying perfusions of sodium dodecyl sulfate (SDS) to limit denaturing events and ensure proper preservation of the native ECM biochemical niche. Porcine SMG biopsies were perfused with 0.01%, 0.1%, and 1% SDS and bio-assembled magnetically in porous polycarbonate track-etched (PCTE) membrane. Double-stranded DNA (dsDNA), cell removal efficiency, and ECM biochemical contents were analyzed. SDS at 0.1% and 1% efficiently removed dsDNA (< 50ng/mg) and preserved key matrix components (sulfated glycosaminoglycans, collagens, elastin) and the microarchitecture of native SMG ECM. Bio-assembled SMG decellularized ECM (dECM) perfused with 0.1-1% SDS enhanced cell viability, proliferation, expansion confluency rates, and tethering of primary SMG cells during 7 culture days. Perfusion with 1% SDS promoted greater cell proliferation rates while 0.1% SDS supported higher acinar epithelial expression when compared to basement membrane extract and other substrates. Thus, this dECM magnetic bioassembly strategy was effective for decellularization while retaining the original ECM biochemical niche and promoting SMG cell proliferation, expansion, differentiation, and tethering. Altogether, these outcomes pave the way towards the recellularization of this novel SMG dECM in future in vitro and in vivo applications.

Functionalized silica nanoparticles coupled with nanoporous membrane for efficient ionic current rectification

In the last few decades, tremendous effort has been dedicated to mimicking the efficient ionic current rectification (ICR) of biological nanopores. Nanoporous membranes and singular nanopores with ICR functionality have been fabricated using advanced, yet costly technologies. We herein demonstrate that a simple, novel, and robust ICR platform can be constructed using 80 nm silica nanoparticles and a piece of 15 nm track-etched polycarbonate membrane. Efficient ICR can be obtained when voltages of different polarities are applied across the membrane, due to the asymmetric electrophoretic migration of silica nanoparticles whose surfaces are modified with different functional groups. The effect of pore size, ionic strength, pH, voltage magnitude, and density of silica nanoparticles on the efficiency of the ICR system has been systematically investigated in this report. Our results clearly show that smaller pore, lower ionic strength, appropriate pH value, higher electrical field strength, lower density of silica nanoparticles can generally enhance the efficiency of the ICR system. The principles of this new ICR system may find many potential applications in controllable drug delivery, energy storage and water purification.

Precise Pore Size Tailoring and Surface Chemistry Modification of Polycarbonate Membranes Using Atomic Layer Deposition

Physical and chemical surface modifications are commonly used in many applications such as energy generation and storage, microelectronics, water purification, gas separation, and medical/plant biology. In recent several years, sequential infiltration synthesis (SIS), a variant of atomic layer deposition (ALD), has emerged as a promising technology that uses self-limiting reactions to create hybrid organic/inorganic materials within the polymer-free volume. Herein, we employed ALD/SIS of Al2O3, SnO2, Ga2O3, TiO2, and In2O3 to precisely tune the pore size and surface characteristics of track-etched polycarbonate membranes. We used in situ Fourier transform infrared spectroscopy to elucidate the chemistry for Al2O3 SIS in polycarbonate and in situ quartz crystal microbalance measurements to probe the extent of Al2O3 infiltration during SIS in polycarbonate thin films. Next, we used scanning electron microscopy, thermogravimetric analysis, and water permeance measurements to probe the pore size reduction and conformality of SIS Al2O3 in the track-etched polycarbonate membranes. We then used water permeance measurements to compare the water flux for a series of membranes with similar pore size but different pore wall chemistry and compared these results with water contact angle measurements. Interestingly, the hydrophilic metal oxide coatings yielded higher water flux values compared to hydrophobic coatings. Finally, we examined ion-selective transport in the modified track-etched polycarbonate membranes and rationalized the results using zeta potential measurements of the ALD metal oxides. Keywords: atomic layer deposition; sequential infiltration synthesis; metal oxides; hydrophilicity/hydrophobicity; permeability; surface charge; ion conductivity/selectivity.

Ultrathin and handleable nanofibrous net as a novel biomimetic basement membrane material for endothelial barrier formation

Many strategies have been adopted to develop porous membranes to reconstitute basement membrane in vitro, which play a key role in the development of in vitro biomimetic models. However, the development of an artificial basement membrane combines cytocompatibility and nano-thickness is still challenging. Herein, a monolayer nanofibrous net patch was fabricated by combining microfabrication and electrospinning as a biomimetic basement membrane material, which was demonstrated for endothelial barrier formation. The nanofibrous net patches with different fiber densities were obtained by controlling electrospinning time. The net was with high porosity and ultrathin thickness approximate to the diameter of nanofibers, which is comparable to that of the native basement membrane. The morphology, proliferation and cell-cell/cell-substrate interactions of endothelial cells on the nanofibrous nets were studied and compared with track-etched polycarbonate membrane and traditional multilayer nanofibers membrane. In addition, the results of TEER measurement and permeability test demonstrated that the endothelial barrier formed on the nanofibrous net patch displayed stronger barrier integrity and function. Therefore, the proposed nanofibrous net patch shows great potential as a novel biomimetic basement membrane, which is promising to be applied for in vitro tissue mimetic applications.

Bioapplications of Magnetic Nanowires: Barcodes, Biocomposites, Heaters.

Magnetic nanowires (MNWs) can have their moments reversed via several mechanisms that are controlled using the composition, length, diameter, and density of nanowires in arrays as-synthesized or as individual nanoparticles in assays or gels. This tailoring of magnetic reversal leads to unique properties that can be used as a signature for reading out the type of MNW for applications as nano-barcodes. When synthesized inside track-etched polycarbonate membranes, the resulting MNW-embedded membranes can be used as biocompatible bandaids for detection without contact or optical sighting. When etched out of the growth template, free-floating MNWs are internalized by cells at 37 °C such that cells and/or exosomes can be collected and detected. In applications of cryopreservation, MNWs can be suspended in cryopreservation agents (CPAs) for injection into the blood vessels of tissues and organs as they are vitrified to -200 °C. Using an alternating magnetic field, the MNWs can then be nanowarmed rapidly to prevent crystallization and uniformly to prevent cracking of specimens, for example, as grafts or transplants. This invited paper is a review of recent progress in the specific bioapplications of MNWs to barcodes, biocomposites, and nanowarmers.

The Cation Role in Ion Transport Selectivity of Gold-Plated Nanotubes

Ion permselectivity is an important ionic transport property exhibited in nanopores and nanotubes. Permselectivity develops due to the strong interactions between ions in solution and the nanopore/nanotube surfaces. Here, we study the ion permselectivity of gold-plated nanotube membranes. Gold-plated membranes were obtained by using an electroless gold plating method to deposit gold nanotubes into the pores and on the faces of track-etched polycarbonate membranes. These membranes have the potential to display cation permselectivity due to the excess surface charge density present on the membrane from chemisorbed Cl- anions. The cation permselectivity of membranes with 9.9 + 0.6 nm diameter nanotubes was studied potentiometrically by using a concentration cell. A new Debye-sphere based model was presented here to describe the extent of permselectivity. However, some ion specific effects with the gold-plated membrane are observed that cannot be interpreted by Debye theory. These ion-specific surface interactions lead to a reduction in the negative surface charge, causing no permselectivity for some cations as demonstrated by their lower than ideal cation transference numbers. Quantification of the surface charge density by XPS indicated the gold-plated membranes are highly charged due to Cl- chemisorption with a surface charge density of ~ 5.3 uC per cm2 corresponding to 3.3 x 1013 Cl--ions per cm2.