Macroporous Poly Research Articles

Macroporous Poly(hydromethylsiloxane) Networks as Precursors to Hybrid Ceramics (Ceramers) for Deposition of Palladium Catalysts.

Poly(hydromethylsiloxane) (PHMS) was cross-linked with 1,3,5,7-tetramethyl-1,3,5,7-tetravinylcyclotetrasiloxane (D4Vi) in water-in-oil High Internal Phase Emulsions to form macroporous materials known as polyHIPEs. It was shown that in the process of pyrolysis under Ar atmosphere at 520 °C, the obtained polyHIPEs were converted to ceramers with high yields (82.8-88.0 wt.%). Structurally, the obtained ceramers were hybrid ceramics, i.e., they consisted of Si-O framework and preserved organic moieties. Macropores present in the polyHIPE precursors remained in ceramers. Ceramers contained also micro- and mesopores which resulted from the precursor's mass loss during pyrolysis. Total pore volume and BET specific surface area related to the existence of micro- and mesopores in ceramers depended on the PHMS: D4Vi ratio applied in polyHIPE synthesis. The highest total pore volume (0.143 cm3/g) and specific surface area (344 m2/g) were reached after pyrolysis of the precursor prepared with the lowest amount of D4Vi as compared to PHMS. The composite materials obtained after deposition of PdO nanoparticles onto ceramers followed by reduction of PdO by H2 were active and selective catalysts for phenylacetylene hydrogenation to styrene.

Macroporous hydrogel prepared via aqueous polymerization induced phase separation toward in situ immobilization of yeast

AbstractYeast‐loaded open‐cell macroporous poly(acrylamide) (PAM) hydrogels are prepared by polymerization induced phase separation (PIPS) with potassium persulfate (KPS)‐yeast as a redox initiator in a polyethylene glycol (PEG) aqueous solution. The presence of PEG not only allows the sizes of both void and interconnected pores of the hydrogels controllable, but also enlarges the void. Which makes it possible to embed cells in situ and efficiently transport nutrients inside the hydrogels. Yeasts are herein used to form a redox pair with KPS to run the polymerization of acrylamide (AM) at a mild temperature (less than 31°C), avoiding the cell inactivation during the polymerization. The in situ immobilization causes a uniformly distribution and high immobilization rate (~100%) of yeasts in the hydrogels. The hydrogels are then used to ferment glucose to produce ethanol, exhibiting high fermentation efficiency of 68%. After 10 cycles, the yeast can still maintain 86% of the initial fermentation efficiency. The yeasts maintain 87% and 93% of the initial cell activity after 1 week store at 4°C in dry state and in yeast extract peptone dextrose (YPD) medium, respectively. This study demonstrates that an aqueous PIPS initiated by peroxide‐target cells is an effective platform to efficiently in situ immobilize cells in a hydrogel for high performance fermentation.

Macroporous Polymer Cantilever Resonators for Chemical Sensing Applications

AbstractA novel, cost‐effective strategy for sensing performance enhancement of cantilever‐shaped, mass‐sensitive sensors is presented. The developed strategy relies on the introduction of macroporosity in the recognition unit. The developed sensors are successfully applied in air humidity monitoring as well as in chemical sensing. As mass‐sensitive transducers, polymer microelectromechanical systems (MEMS) in the form of poly(vinylidene fluoride‐trifluoroethylene) [P(VDF‐TrFE)] cantilever resonators are specifically developed. These resonators are modified with a hierarchically structured macroporous poly(2,3′‐bithiophene) film, acting as a sensing layer. The design of the recognition layer takes advantage of the synergistic combination of inverse opal structuring, surface imprinting, and semi‐covalent imprinting of proteins. The resulting cantilever resonators are first successfully tested for air humidity monitoring in the whole relative humidity range (ca.10 – 90%). When the recognition layer is composed of human serum albumin‐imprinted polymer (HSA‐MIP) with a hierarchical structure, it can also be used as a selective chemosensor in a concentration range from 10 pM to 20 µM. The obtained results demonstrate that the macroporosity of the receptor film significantly enhances the sensor performance.

Engineering of Defective MOF-801 Nanostructures within Macroporous Spheres for Highly Efficient and Stable Water Harvesting.

Water harvesting using the metal-organic framework (MOF)-801 is restricted by limited working capacity, powder structuring, and finite stability. To overcome these issues, wecrystallized MOF-801 on the surface of macroporous poly(N-isopropylacrylamide-glycidyl methacrylate) spheres, called P(NIPAM-GMA), through an in situ confined growth strategy, forming spherical MOF-801@P(NIPAM-GMA) composite with temperature-responsive function. By lowering the nucleation energy barrier, the average size of the MOF-801 crystals decreased by 20 times. Thus, abundant defects as adsorption sites for water couldbe installed in the crystals lattices. As a consequence, the composite provides an unprecedented high water harvesting efficiency. The composite wasproduced in the kilogram-scale and can capture 1.60kg H2 O/kg composite/day from 20% RH between 25°C and 85°C. This work provides an effective methodology for improving the adsorption capacity through controlled defects formation as adsorption sites and to improve the kinetics through the design of a composite with macroporous transport channel network. This article is protected by copyright. All rights reserved.

Cryostructuring of Polymeric Systems: 64. Preparation and Properties of Poly(vinyl alcohol)-Based Cryogels Loaded with Antimicrobial Drugs and Assessment of the Potential of Such Gel Materials to Perform as Gel Implants for the Treatment of Infected Wounds.

Physical macroporous poly(vinyl alcohol)-based cryogels formed by the freeze-thaw technique without the use of any foreign cross-linkers are of significant interests for biomedical applications. In the present study, such gel materials loaded with the antimicrobial substances were prepared and their physicochemical properties were evaluated followed by an assessment of their potential to serve as drug carriers that can be used as implants for the treatment of infected wounds. The antibiotic Ceftriaxone and the antimycotic Fluconazole were used as antimicrobial agents. It was shown that the Ceftriaxone additives caused the up-swelling effects with respect to the cryogel matrix and some decrease in its heat endurance but did not result in a substantial change in the gel strength. With that, the drug release from the cryogel vehicle occurred without any diffusion restrictions, which was demonstrated by both the spectrophotometric recording and the microbiological agar diffusion technique. In turn, the in vivo biotesting of such drug-loaded cryogels also showed that these materials were able to function as rather efficient antimicrobial implants injected in the artificially infected model wounds of laboratory rabbits. These results confirmed the promising biomedical potential of similar implants.

Effect of ternary polymer composites of macroporous adsorbents on adsorption properties for heavy metal removal from aqueous solution.

This research is focused on the preparation of macroporous poly(vinyl alcohol) (PVA)/chitosan (CS)/Al2O3 adsorbents for removal of residual metal ions from wastewater. The PVA/CS/Al2O3 adsorbents were characterized by X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET), and energy dispersive X-ray (EDX) techniques to confirm that all compositions were incorporated into the PVA/CS/Al2O3 adsorbents without chemical modification. Furthermore, a comparison of the properties of the PVA/CS/Al2O3 adsorbents suggested that PVA/CS/0.50Al2O3 was the most suitable sample for adsorption study. The adsorption properties of PVA/CS/0.50Al2O3 for the removal of metal ions such as Pb2+, Cu2+, Zn2+, and Ni2+ in aqueous solution adsorbents in both single and quaternary systems were investigated. The results show that the adsorption selectivity of the PVA/CS/0.50Al2O3 adsorbent for these metal ions was provided in the following order: Pb2+ > Cu2+ > Zn2+ > Ni2+. The adsorption isotherm was studied by equilibrium data obtained from batch experiments. It was found that the Freundlich isotherm model was suitable for explaining the adsorption process. Adsorption kinetics were studied, which indicated that the adsorption of Pb2+, Cu2+, and Zn2+ followed a pseudo-second-order kinetic model, while the adsorption of Ni2+ followed a pseudo-first-order kinetic model. In addition, adsorption-desorption cycles were studied to prove the reusability of PVA/CS/0.50Al2O3 adsorbents. The PVA/CS/0.50Al2O3 adsorbents were able to be regenerated and reused. In a continuous adsorption process, a column experiment was simulated in laboratory. The results showed that Cu2+ was the most selective for a fixed-bed column. Thus, PVA/CS/0.50Al2O3 adsorbents could be potential used for toxic metal ion removal from wastewater, in both batch and fixed-bed continuous-flow columns.

DEPENDENCE OF THE RESTORATIVE EFFECT OF MACROPOROUS POLY(N-[2-HYDROXYPROPYL]-METHACRYLAMIDE HYDROGEL ON THE SEVERITY OF EXPERIMENTAL LACERATIVE SPINAL CORD INJURY

restoration of the spinal cord function presents a most severe biomedical issue nowadays. The aim of the study was to detect the macroporous poly(N-[2-hydroxypropyl]-methacrylamide hydrogel (PHPMA-hydrogel, HG) restorative effect dependence on the severity of the laceration spinal cord injury in young organisms. The male rats sample (~1-month-old, ~50 g, inbred Wistar line) was represented with 4 experimental groups: 1) spinal cord lateral hemisection at the level of ~Т12–Т13 segments (Sect; n=11); 2) spinal cord lateral hemiexcision ~1 mm long at the similar level (Exc; n=8); 3) spinal cord lateral hemisection at the similar level with immediate implantation of the hydrogel fragment into the trauma region (HGsect; n=11); 4) spinal cord lateral hemiexcision at the similar level with immediate implantation of the hydrogel fragment into the affected region (HGexс; n=6). The motor function and spasticity of the paretic hindlimb was estimated respectively by the technically modified Basso–Beattie–Bresnahan (ВВВ) and Ashworth, conditionally blinded to individual characteristics of all operated animals and previous study results. The observation lasted for ~5 months. The criteria of non-inclusion were as follows: the ipsilateral hindlimb function level in a week after the injury >9 points ВВВ, and the contralateral hindlimb function level during prolonged period ≤14 points ВВВ. The results were interpreted and presented according to the standardized time scale with interpolatory representation of the motor function and spasticity individual level in certain cases. Asymptotic stage differences between the studied groups and subgroups were stated during the first three weeks as well as in 8 weeks and 3 months after the injury. We found out that in a week after injury the motor function level in group Exc made up 0.9±0.5 points ВВВ, in group HGexc — 3.6±1.2 points, in group Sect — 5.9±1.1 points, in group HGsect — 6.0±1.0 points. In 5 months the motor function level in group Sect made up 9.5±1.0 points ВВВ, in group HGsect — 9.5±1.1 points, in group Exc — 0.8±0.3 points, in group HGexc — 4.5±1.8 points. At the same study stage the spasticity level in groups Sect and HGsect was, respectively, 0.8±0.2 and 0.8±0.3 points Ashworth, in group HGexc — 1.8±0.7 points, in group Exc — 3.6±0.3 points. Throughout the study no significant differences in groups Sect and HGsect have been detected, and in groups Exc і HGexc such differences were detected only in 5 weeks after the injury. The considerable difference of spasticity in groups Sect and HGsect was noted in 1 week after the injury, in groups HGexc and Exc — during first 2 months of the experiment. In groups Sect and Exc reliable difference of both motor function and spasticity level was found at all study stages. In groups HGsect and HGexc considerable difference of the motor function level was characteristic at all stages, except for the end of the 1st and 7th weeks, whereas spasticity level differences throughout the study remained insignificant. So, the tested hydrogel in young organisms shows positive effect only with severe trauma stages accompanied with extensive spinal cord defect.

The Efficacy of Immediate Implantation of Macroporous Poly(N-[2-Hydroxypropyl]-Methacrylamide) Hydrogel after Laceration Spinal Cord Injury in Young Rats

The Efficacy of Immediate Implantation of Macroporous Poly(N-[2-Hydroxypropyl]-Methacrylamide) Hydrogel after Laceration Spinal Cord Injury in Young Rats

3D printed PCL/GelMA biphasic scaffold boosts cartilage regeneration using co-culture of mesenchymal stem cells and chondrocytes: In vivo study

Cartilage injury is difficult to self-repair, which poses a challenge to scaffold design and selection of seeded cells for cartilage tissue engineering. In this study, we presented a biphasic scaffold consisting of a cells-encapsulated biodegradable gelatin methacrylate (GelMA) hydrogel on the upper layer and a macroporous poly(ε-caprolactone) (PCL) scaffold filled with cells-encapsulated GelMA hydrogel on the lower layer to support cartilage regeneration using co-culture of bone marrow mesenchyml stem cells (BMSCs) and costal chondrocytes (CChon). We determined that the synergistic effect of BMSCs and costal chondrocytes was sufficient to induce chondrogenesis, but cartilage regeneration was better under TGF-β3 supplement. Memorably, when implanted in a rat osteochondral defect model for 12 weeks, the PCL/GelMA biphasic scaffolds with cells co-culture showed excellent cartilage regenerative capability, and enabled the Young’s modulus of engineered cartilage comparable to that of native cartilage. Furthermore, the implantation of biphasic scaffold resulted in less mechanical pain than cartilage defects by gait analysis. Together, both in vitro and in vivo results demonstrated that the PCL/GelMA biphasic scaffold with co-culture of BMSCs and chondrocytes is a promising scaffold for cartilage regeneration, which pave a new way to solve the key issues of clinical cartilage repair.

Some factors affecting pore size in the synthesis of rigid polymer monoliths: Theory and its applicability

AbstractMacroporous monoliths represent now widely used materials whose successful application strongly depends on their characteristics. Among those the average pore size is one of the key parameters. In this paper, we consider the applicability of theoretical calculations for the selection of appropriate porogens to generate the materials with required average pore size. A set of macroporous poly(meth)acrylate monoliths was synthesized via thermo‐ and photo‐initiated free radical polymerization and characterized in regards to their average pore size. Additionally, the difference in solubility parameters as well as Hansen's solubility parameter distance between monomers and porogens were calculated for each polymerization mixture using Hildebrand's and Hansen's solubility theories. The theoretical predications and experimental data were compared and analyzed to establish the applicability of theoretical calculations to previse average pore size for different systems. It was found that Hildebrand's theory seems to be poorly appropriate as universal tool, while Hansen's theoretical approach explained better the efficiency of solvents as porogens. The application of oligomers and polymer solutions due to the increase of viscosity as well as the variation of crosslinker amount in the monomer system can be singled out as Hansen's theory limitations at the prediction of the average pore size.

A Natural Rubber Waste Derived Surfactant for High Internal Phase Emulsion Templating of Poly(Dicyclopentadiene)

AbstractThe use of a surfactant derived from the degradation of natural rubber gloves via cross‐metathesis with methyl acrylate and subsequent saponification of the ester group for the stabilization of water in dicyclopentadiene high internal phase emulsions is described. The versatility of the resulting high internal phase emulsion is demonstrated by polymerizing the continuous dicyclopentadiene phase via ring‐opening metathesis polymerization yielding macroporous poly(dicyclopentadiene) foams with a porosity of 82%. The use of the ionic surfactant allows for the preparation of foams, which are resistant to absorb water. This property is hitherto not accessible with protocols involving the use of nonionic surfactants commonly employed in emulsion templating of polymers.

Surface Modification of Hypercrosslinked Vinylbenzyl Chloride PolyHIPEs by Grafting via RAFT

AbstractGrafting of glycidyl methacrylate from the surface of macroporous poly(4‐vinylbenzyl chloride‐co‐divinylbenzene) polyHIPEs (poly high internal phase emulsions) prepared by the polymerization of the continuous phase of high internal phase emulsions is performed. PolyHIPEs are hypercrosslinked using Friedel–Crafts reaction thus increasing specific surface area, and further functionalized with tris(2‐aminoethyl) amine. To the free amino groups reversible addition–fragmentation chain transfer (RAFT) agent 4‐cyano‐4‐[(dodecylsulfanylthiocarbonyl) sulfanyl] pentanoic acid is immobilized and grafting is performed utilizing glycidyl methacrylate. Poly(glycidyl methacrylate) chains of ≈100 units in length are grafted onto the surface of the polyHIPEs. In comparison, non‐hypercrosslinked monoliths allow for substantially lower degree of immobilization of RAFT agent suggesting decreased accessibility of active sites on the polymer surface.

Strong and weak cation-exchange groups generated cryogels films for adsorption and purification of lysozyme from chicken egg white

Here, the macroporous poly(hydroxylmethyl methacrylate/glycidyl methacrylate [p(HEMA-GMA)] cryogels with large porous surface were prepared, and then the epoxy groups of the p(HEMA-GMA) cryogels were systematically modified into strong and weak cationic groups. The effects of initial protein concentrations, adsorption time, pH, salt concentrations and temperatures on adsorption efficiency of cation exchange cryogels for lysozyme were determined. The maximum lysozyme adsorption capacities of strong and weak cation exchange cryogels were found to be 188.3 and 79.7 mg/g cryogel at 25 °C, respectively. The performance of the strong cationic cryogel was evaluated by purification of lysozyme from egg white. The activity of the isolated lysozyme was found to be 21,347 U/mg. The cationic cryogel maintained its expected high adsorption capacity and efficiency of the purification levels during repeated adsorption desorption processes. Finally, the purpose of this work is the design a cation exchange system for purification of lysozyme from egg-white.

Purification of Fab and Fc using papain immobilized cryogel bioreactor separator system

The continuous bed bioreactor systems have been used for the production of protein therapeutics, such as IgG, using immobilized enzyme in biopharmaceutical applications. We developed macroporous poly(hydroxyethyl methacrylate-co-glycidyl methacrylate) cryogel-based bioreactor matrix using sodium dodecyl sulfate as surfactans in the presence of ethylene glycol dimethacrylate as cross linking agent by bulk polymerization. The developed polyGMA immobilized bioreactor with papain enzyme was used for specific fragmentation of immunoglobulin G. The catalysis efficiency for immobilized enzyme were investigated in comparison with free enzyme. The immobilized papain displayed broad catalytic activity over a variety of conditions, with maximal activity around pH 7.0 and 70 °C. The Michaelis-Menten kinetic constant (Km), the maximum reaction velocity (Vmax), and the catalytic efficiency (kcat) for free enzyme were 0.1097 mg/mL, 29.9 mg/mL/min, and 92.01 1/min, respectively, whereas for immobilized enzyme, Km, Vmax, and kcat values were 0.1078 mg/mL, 30.53 mg/mL/min, and 94.3 1/min, respectively. In a further step, after digestion, remarkable digestion products of bioreactor, Fab and Fc fragments, produced with immobilized papain bioreactors were analyzed in two ways by SDS-PAGE and reversed-phase HPLC; it was demonstrated that papain immobilized bioreactor successfully used for the digestion of human IgG with high activity. Therefore, the polyGMA cryogel immobilized with papain exhibited a very effective matrix for the bioreactor which can be considered as an alternative bioreactor matrix with great promise in biopharmaceutical applications.

Cryostructuring of Polymeric Systems †: Application of Deep Neural Networks for the Classification of Structural Features Peculiar to Macroporous Poly(vinyl alcohol) Cryogels Prepared without and with the Additives of Chaotropes or Kosmotropes.

Macroporous poly(vinyl alcohol) cryogels (PVACGs) are physical gels formed via cryogenic processing of polymer solutions. The properties of PVACGs depend on many factors: the characteristics and concentration of PVA, the absence or presence of foreign solutes, and the freezing-thawing conditions. These factors also affect the macroporous morphology of PVACGs, their total porosity, pore size and size distribution, etc. In this respect, there is the problem with developing a scientifically-grounded classification of the morphological features inherent in various PVACGs. In this study PVA cryogels have been prepared at different temperatures when the initial polymer solutions contained chaotropic or kosmotropic additives. After the completion of gelation, the rigidity and heat endurance of the resultant PVACGs were evaluated, and their macroporous structure was investigated using optical microscopy. The images obtained were treated mathematically, and deep neural networks were used for the classification of these images. Training and test sets were used for their classification. The results of this classification for the specific deep neural network architecture are presented, and the morphometric parameters of the macroporous structure are discussed. It was found that deep neural networks allow us to reliably classify the type of additive or its absence when using a combined dataset.

Water-Soluble Chemical Vapor Detection Enabled by Doctor-Blade-Coated Macroporous Photonic Crystals

Water-soluble chemicals, involving a wide range of toxic chemicals in aqueous solutions, remain essential in both daily living or industrial uses. However, most toxicants are evaporated with water through their use and thus cause deleterious effects on the domestic environment and health in humans. Unfortunately, most current low-dose chemical vapor detection technologies are restricted by the use of sophisticated instruments and unable to promptly detect the quantity of diverse toxicants in a single analysis. To address these issues, this study reports the development of simple and fast chemical vapor detection using doctor-blade-coated macroporous poly(2-hydroxyethyl methacrylate)/poly(ethoxylated trimethylolpropane triacrylate) photonic crystals, in which the poly(2-hydroxyethyl methacrylate) has strong affinity to insecticide vapor owing to a favorable Gibbs free energy change for their mixing. The condensation of water-soluble chemical vapor therefore results in a significant reflection peak shift and an obvious color change. The visual colorimetric readout can be further improved by increasing the lattice spacing of the macroporous photonic crystals. Furthermore, the dependence of the reflection peak position on vapor pressure under actual conditions and the reproducibility of vapor detecting are also evaluated in this study.

Macroporous poly(vinyl chloride)-polypyrrole composites with piezoresistive behaviour

Flexible macroporous composites based on commercially ubiquitous poly(vinyl chloride) (PVC) coated with thin layer of conducting polypyrrole (PPy) were investigated for their piezoresistive characteristics. Macroporous discs were achieved via a thermally assisted and solvent free approach employing common salt as sacrificial template. Coating of PPy was obtained via vapor phase oxidative polymerization and two type of composites (PPyF60 and PPyF75) with different compressibility were prepared by varying PVC-salt ratio (1:4 and 1:5). Composite PPyF60 exhibited higher compressive strength (5.34 MPa vs 3.78 MPa) due to less porosity. In terms of piezoresistive behaviour however PPyF75 exhibited higher pressure sensitivity (0.149 kPa−1) and gauge factor (8.22). Both composites showed good signal stability during continuous cyclic strain and dynamic pressure.

Water‐Promoted Heterogeneous Asymmetric Hydrogenation of Quinolines over Ordered Macroporous Poly(ionic liquid) Catalyst

AbstractThe development of air stable solid chiral catalysts for asymmetric hydrogenation is very attractive for the large‐scale production of chiral compounds. Herein, we reported the synthesis of an ordered macroporous poly(ionic liquid) catalyst integrated with VDPEN‐RuOTf as air stable chiral catalyst for asymmetric hydrogenation of quinoline derivatives. Under ambient conditions, the solid catalyst afforded 97% conversion with 90% ee in the asymmetric hydrogenation of 2‐methylquinoline in water. It was found that the activity and enantioselectivity of poly(ionic liquid) catalyst decreases with surface hydrophobicity increasing, suggesting the important role of surface hydrophilicity in obtaining high activity and enantioselectivity in water. Control experiment suggests that water promotes the anti‐air stability of the poly(ionic liquid) catalyst. The combination of poly(ionic liquid) catalyst and water may provide a new approach for designing heterogeneous chiral catalyst with anti‐air stability.

Fabrication of emulsion-templated macroporous poly(ε-caprolactone) towards highly effective and sustainable oil/water separation

A facile synthetic chemical strategy was descripted to produce porous poly(ϵ-caprolactone) (PCL) towards to a highly selective, reusable and degradable oil absorbent. The porous PCL was synthesized by organocatalyzed ring-opening polymerization (ROP) of ϵ-caprolactone (CL) in a tetradecane-in-CL high internal phase emulsion (HIPE). In this method, methanesulfonic acid (MSA) was used as an organocatalyst, and the block copolymer pluronic F127 acted as both emulsifier of the emulsion and initiator for the ROP of CL at a mild condition (37 °C). The molecular structure of copolymers could be tailored by changing the emulsifier concentration. The resulting polymers exhibited a controllable open-cell macroporous structure with HIPE as templates, and could be completely degraded. Absorption experiments showed the porous polymers absorbed gasoline, diesel, olive oil, or tetradecane from the water-oil mixture within 30 s, and the oils could be recovered simply by a centrifugation process at 3000 rpm. The absorbent had a full preservation of both the porous morphology and the absorption capacity in the performed six absorption/desorption cycles. These materials proved effective as oil absorbents for oil/water separation with not only a noticeable selectivity and recyclability performance, but also unprecedented safe disposability thanks to its degradability.

Towards the Development of a 3-D Biochip for the Detection of Hepatitis C Virus.

The early diagnostics of hepatitis C virus (HCV) infections is currently one of the most highly demanded medical tasks. This study is devoted to the development of biochips (microarrays) that can be applied for the detection of HCV. The analytical platforms of suggested devices were based on macroporous poly(glycidyl methacrylate-co-di(ethylene glycol) dimethacrylate) monolithic material. The biochips were obtained by the covalent immobilization of specific probes spotted onto the surface of macroporous monolithic platforms. Using the developed biochips, different variants of bioassay were investigated. This study was carried out using hepatitis C virus-mimetic particles (VMPs) representing polymer nanoparticles with a size close to HCV and bearing surface virus antigen (E2 protein). At the first step, the main parameters of bioassay were optimized. Additionally, the dissociation constants were calculated for the pairs “ligand–receptor” and “antigen–antibody” formed at the surface of biochips. As a result of this study, the analysis of VMPs in model buffer solution and human blood plasma was carried out in a format of direct and “sandwich” approaches. It was found that bioassay efficacy appeared to be similar for both the model medium and real biological fluid. Finally, limit of detection (LOD), limit of quantification (LOQ), spot-to-spot and biochip-to-biochip reproducibility for the developed systems were evaluated.