Polyethylene Glycol Molecular Mass Research Articles

Method of hyaluronidase immobilization to produce an oral dosage form

Hyaluronidase is an enzyme that helps maintain an optimal balance of hyaluronic acid in connective tissue and ensures full tissue regeneration. Currently, hyaluronidase drugs are used in various fields of medicine. Meanwhile, there are no oral preparations based on hyaluronidase on the pharmaceutical market due to its low bioavailability in this method of administration. One of the options to increase enzyme bioavailability is electron-beam pegylation, which involves obtaining drugs with a modified pharmacokinetic profile in the direction of increasing enteral bioavailability, as well as having additional protection from the action of proteolytic enzymes. Aim of the study was using the electron beam pegylation method to obtain a laboratory batch of a preparation based on highly purified hyaluronidase, which can be further used in the development of an oral drug product. Material and methods. Hyaluronidase, which was isolated from bovine testicular hyaluronidase and polyethylene glycols of different molecular weight, was used in the experimental study. Experiments were carried out using a pulsed linear accelerator ILU-10 for enzyme electron beam immobilization on a water-soluble polymer matrix of polyethylene glycol molecules. The formation of hyaluronidase and polyethylene glycols conjugates was confirmed by exclusion chromatography. Results. As a result of accelerated electron irradiation of hyaluronidase and polyethylene glycol of molecular mass 1500 Da conjugates of enzyme and polymer matrix were formed. After electron-beam pegylation, the specific activity of the enzyme was retained. Conclusions. A laboratory batch of prototype pharmaceutical substance based on immobilised hyaluronidase on polyethylene glycol was obtained.

Hydration Numbers of Polyethylene Glycols Based on a New Viscosity Model

AbstractDue to the high solubility in water and the structural compatibility of polyethylene glycol with water molecules, it is a good model system for studying the mechanisms of interaction between water and biopolymers. The behavior of biopolymers in living organisms strongly depends on the hydration of macromolecules in the aquatic environment. In this work the effective hydration numbers of polyethylene glycols are determined using a new viscosity model developed for electrolytes and experimental data on the viscosity of dilute aqueous solutions of polyethylene glycols (300–35000). The calculated hydration numbers are in good agreement with the literature data and increase with increasing molecular mass of polyethylene glycol: as the molecular mass increases, starting from a molecular mass of 1000, the chain begins to fold in on itself, forming segment‐segment interactions, trapping additional, more loosely bound water between the segments. Based on the dependence of the intrinsic viscosity on the molecular mass according to the Mark‐Houwink equation, it is shown that PEGs are the flexible polymers and highly soluble in water.

Taurine as Antioxidant in a Novel Cell- and Oxygen Carrier-Free Perfusate for Normothermic Machine Perfusion of Porcine Kidneys

Donor organ-shortage has resulted in the increased use of marginal grafts; however, normothermic machine perfusion (NMP) holds the potential for organ viability assessment and restoration of marginal grafts prior to transplantation. Additionally, cell-, oxygen carrier-free and antioxidants-supplemented solutions could potentially prevent adverse effects (transfusion reactions, inflammation, hemolysis), associated with the use of autologous packed red blood cell (pRBC)-based perfusates. This study compared 6 h NMP of porcine kidneys, using an established pRBC-based perfusate (pRBC, n = 7), with the novel cell- and oxygen carrier-free organ preservation solution Ecosol, containing taurine (Ecosol, n = 7). Despite the enhanced tissue edema and tubular injury in the Ecosol group, related to a suboptimal molecular mass of polyethylene glycol as colloid present in the solution, functional parameters (renal blood flow, intrarenal resistance, urinary flow, pH) and oxygenation (arterial pO2, absence of hypoxia-inducible factor 1-alpha) were similar to the pRBC group. Furthermore, taurine significantly improved the antioxidant capacity in the Ecosol group, reflected in decreased lactate dehydrogenase, urine protein and tubular vacuolization compared to pRBC. This study demonstrates the feasibility of 6 h NMP using a taurine containing, cell- and oxygen carrier-free perfusate, achieving a comparable organ quality to pRBC perfused porcine kidneys.

Polyethylene Glycol Crowder's Effect on Enzyme Aggregation, Thermal Stability, and Residual Catalytic Activity.

Protein stability and performance in various natural and artificial systems incorporating many other macromolecules for therapeutic, diagnostic, sensor, and biotechnological applications attract increasing interest with the expansion of these technologies. Here we address the catalytic activity of lysozyme protein (LYZ) in the presence of a polyethylene glycol (PEG) crowder in a broad range of concentrations and temperatures in aqueous solutions of two different molecular mass PEG samples (Mw = 3350 and 10000 g/mol). The phase behavior of PEG-protein solutions is examined by using dynamic light scattering (DLS) and small-angle X-ray scattering (SAXS), while the enzyme denaturing is monitored by using an activity assay (AS) and circular dichroism (CD) spectroscopy. Molecular dynamic (MD) simulations are used to illustrate the effect of PEG concentration on protein stability at high temperatures. The results demonstrate that LYZ residual activity after 1 h incubation at 80 °C is improved from 15% up to 55% with the addition of PEG. The improvement is attributed to two underlying mechanisms. (i) Primarily, the stabilizing effect is due to the suppression of the enzyme aggregation because of the stronger PEG-protein interactions caused by the increased hydrophobicity of PEG and lysozyme at elevated temperatures. (ii) The MD simulations showed that the addition of PEG to some degree stabilizes the secondary structures of the enzyme by delaying unfolding at elevated temperatures. The more pronounced effect is observed with an increase in PEG concentration. This trend is consistent with CD and AS experimental results, where the thermal stability is strengthened with increasing of PEG concentration and molecular mass. The results show that the highest stabilizing effect is approached at the critical overlap concentration of PEG.

Parameter Estimation of Mark-Houwink Equation of Polyethylene Glycol (PEG) Using Molecular Mass and Intrinsic Viscosity in Water

Polyethylene glycol (PEG) is an ingredient for approved drug products by the Food & Drug Administration. PEG is mostly used as a pharmaceutical adjuvant, ophthalmic and oral acts as an encapsulating agent, plasticizing agent in food packages, modified and/or functionalized materials, among other applications. It is important to know the molecular mass of PEG because it will bring the product configuration for these applications. The use of instrumental techniques is often infeasible due to high investment and operational costs. The viscosimetry by capillary, in the case of a classical technique, simple and inexpensive, allows significant results for the determination of the molecular mass of polymers from the intrinsic viscosity. The objective of the present study was to determine the parameters of the Mark-Houwink equation for PEG using molecular mass and intrinsic viscosity in water at different temperatures. The parameters resulting in “K” between 0.046828 x 10-3 and 0.298291 x 10-3 cm3.g-1 and “α” between 0.40 and 0.70. The viscosimeter by the capillary allowed to obtain significant results for the estimation of the parameters "K" and "α", with a correlation coefficient greater than 98%.

Purification of xylanase from Aspergillus niger NRRL3 extract by an integrated strategy based on aqueous two-phase systems followed by ion exchange chromatography

Xylanases are enzymes that degrade the linear polysaccharide xylan into xylose, thus breaking down hemicellulose, one of the major components of plant cell walls. Xylanases are applied in a wide range of industrial processes, such as in the pulp and paper industry, which demands a higher purity degree compared to other industries. Processes for the purification of this enzyme has been widely reported using different techniques. However, cases involving the use of a simple combination of unit operations are not common. The objective of this work was to design an integrated bioseparation strategy for the purification of a fungal cellulase-free xylanase. The design consisted of a liquid-liquid extraction using two-combined aqueous two-phase system (ATPS) with an ion exchange chromatography. The effect of different parameters such as polymer type (ethylene oxide-propylene oxide copolymer (UCON) and polyethylene glycol (PEG)), PEG molecular mass (600, 1450, 2000 and 4600 g/mol), volume ratio and the addition of sodium chloride on the enzymes -from the Aspergillus niger NRRL3 extract- partition coefficient were analyzed. The partition behavior of the target product was affected for the type and molecular mass of the polymer used. Extraction using UCON/Citrate system combined with a second extraction using PEG1450/Citrate system proved to be the most suitable for the extraction of xylanase and natural fungal pigments. The enzymatic activity recovery and purification factor achieved were 80% and 4, respectively. The proposed systems have the ability to recycle the UCON and Citrate salt for their reuse in new ATPS. The phases of the combined extraction by ATPS and the elution obtained from ion exchange chromatography were characterized by nano-LC–MS/MS, providing a complete profile of the proteins present. The combination of ATPS with ion exchange chromatography using a Q-Sepharose XL column reached a total enzymatic activity recovery of 79.9% and a purification factor of 11. This is the first time that high-quality xylanase free of cellulolytic enzymes is reported using an integrated bioprocess strategy with potential for industrial adoption.

Destressing Yeast for Higher Biofuel Yields: Can Excess Chaotropicity Be Mitigated?

Biofuels have the capacity to contribute to carbon dioxide emission reduction and to energy security as oil reserves diminish and/or become concentrated in politically unstable regions. However, challenges exist in obtaining the maximum yield from industrial fermentations. One challenge arises from the nature of alcohols. These compounds are chaotropic (i.e. causes disorder in the system) which causes stress in the microbes producing the biofuel. Brewer's yeast (Saccharomyces cerevisiae) typically cannot grow at ethanol concentration much above 17% (v/v). Mitigation of these properties has the potential to increase yield. Previously, we have explored the effects of chaotropes on model enzyme systems and attempted (largely unsuccessfully) to offset these effects by kosmotropes (compounds which increase the order of the system, i.e. the "opposite" of chaotropes). Here we present some theoretical results which suggest that high molecular mass polyethylene glycols may be the most effective kosmotropic additives in terms of both efficacy and cost. The assumptions and limitations of these calculations are also presented. A deeper understanding of the effects of chaotropes on biofuel-producing microbes is likely to inform improvements in bioethanol yields and enable more rational approaches to the "neutralisation" of chaotropicity.

Acoustic and viscometric studies of ternary liquid mixtures of aqueous sodium methyl p-hydroxybenzoate with polyethylene glycols at 250C

The various ultrasonic parameters like acoustic impedance, adiabatic compressibility, intermolecular free length, relaxation time, relative association, attenuation and Gibb’s free energy of polyethylene glycols with molecular weight 200 and 600 in aqueous sodium methyl para-hydroxybenzoate is evaluated at 250C from the density, speed of sound and viscosity. Jone-Dole’s equation has been employed to analyze the experimental results of viscosity. The existence of interaction among the fragments of ternary liquid mixtures has been determined from viscosity coefficients. The polyethylene glycols act as the structure builder in water. The viscosity coefficient B surges with escalation in molecular mass of polyethylene glycols. The structure builder property of polyethylene glycols follows the order PEG-600 > PEG-200.

Isolation and Characterization of Polyethylene Glycol (PEG)-Modified Glycol Lignin via PEG Solvolysis of Softwood Biomass in a Large-Scale Batch Reactor

We have developed an environmentally benign large-scale (50 kg wood meal per batch) lignin production plant, operating based on acid-catalyzed polyethylene glycol (PEG) solvolysis of softwood biomass. The motivation for the proposed process was to promote technological innovation in biomass utilization systems in Japanese rural areas based on widely abundant Japanese cedar (sugi) biomass. In this study, the process was evaluated by investigating the effects of the source sugi wood meal size and the solvent PEG molecular mass on the yield, chemical structure, molecular mass, and thermal properties of the resultant PEG-modified lignin derivatives, glycol lignins (GLs). Reducing the source wood meal size and PEG solvent molecular mass not only promoted lignin PEGylation but also the subsequent acid-induced chemical rearrangements of the GLs as demonstrated by chemical analyses, 2D NMR, and size exclusion chromatography (SEC). Reducing the source wood meal size and/or increasing the solvent PEG molecular mass...

Luminal Polyethylene Glycol Alleviates Intestinal Preservation Injury Irrespective of Molecular Size.

Intestinal preservation injury (IPI) and the resulting mucosa injury raise several serious challenges early after intestinal transplantation. The current clinical approach using only vascular perfusion allows the shortest preservation period among the abdominal organs. The experimental addition of luminal polyethylene glycol (PEG) solutions has been repeatedly suggested to alleviate preservation injury, improve graft quality, and prolong the preservation time. We investigated whether the molecular mass of PEG in solution influences the development of intestinal preservation injury. Small intestines of Sprague-Dawley rats were perfused with University of Wisconsin solution. Group 1 underwent vascular perfusion only (clinical control), group 2 received additional luminal PEG3350 Da, group 3 received luminal PEG10000 Da, and group 4 received luminal PEG20000 Da (n = 8/group). Tissue samples were obtained after 4, 8, and 14 hours. We studied the tissue damage (Chiu/Park score, Goblet cells, apoptosis, tight junctions), activation of c-Jun NH2-terminal kinase (JNK), and p38-mitogen-activated protein kinase (MAPK), and we performed Ussing chamber assessments. Mucosal morphologic and electrophysiologic parameters were significantly improved in the groups receiving luminal PEG. There was significantly less apoptotic activity in groups 2, 3, and 4. Both MAPKs revealed an activation peak after 4 hours with group 3 showing lesser p38-MAPK activation. PEG 20 kDa interfered with protein immunodetection. The results indicate that luminal solutions of PEG of medium and large molecular mass significantly delay the onset and development of IPI, providing further evidence that luminal interventions may allow for longer cold storage intervals of intestinal grafts.

Effects of low and high molecular mass PEG incorporation into different types of poly(ether-b-amide) copolymers on the permeation properties of CO2 and CH4

Blend membranes were prepared by incorporating two types of polyethylene glycol (PEG) (molecular masses of 400 and 1000 g mol−1) into three grades of poly(ether-block-amide) (PEBAX), namely PEBAX 1074, PEBAX 1657, and PEBAX 2533. The PEGs, which were used as blending agents, were employed at mass fractions ranging from 10 to 40 wt.% based on the mass of PEBAX. The gas separation performance of each neat or blend membrane, comprising its CO2 and CH4 permeabilities and its ideal CO2/CH4 selectivity, was studied at room temperature (25 °C) and at pressures of 2–8 bar. X-ray diffraction (XRD) and attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR) analyses were used to determine the crystallinities of and the chemical bonds in the prepared membranes, respectively. Scanning electron microscopy (SEM) was also utilized to observe the morphologies of the membranes. The results obtained from experimental investigations showed that the incorporation of low molecular mass PEG significantly increased the permeability but only slightly affected the ideal CO2/CH4 selectivity, while the incorporation of high molecular mass PEG decreased the permeability considerably but sharply increased the ideal CO2/CH4 selectivity. This behavior intensified as the polyether content of the PEBAX was decreased.

Development and Validation of a New Near-Infrared Sensor to Measure Polyethylene Glycol (PEG) Concentration in Water.

A near-infrared absorption based laser sensor has been designed and validated for the real-time measurement of polyethylene glycol (PEG) concentration. The wavelength was selected after the determination of the absorption spectrum of deionised water and PEG solutions using a Varian Cary 6000i spectrophotometer, in order to limit the influence of PEG molecular mass on the absorption measurement. With this new sensor, the water is treated as the attenuating species and the addition of PEG in water reduces the absorbance of the medium. The concept was validated using three different PEG types (PEG 6000, 20,000, and 35,000) and it was found that the results follow Beer Lambert’s law. The influence of temperature was assessed by testing the PEG 20,000 at four different temperatures that could be encountered in a laboratory environment. The data show a slight temperature influence (increase of absorbance by 8% when the temperature rises from about 20° to about 29°). Following the validation phase conducted ex situ, a prototype of an immersible sensor was built and calibrated for in situ measurements.

The 2D Structure of the T. brucei Preedited RPS12 mRNA Is Not Affected by Macromolecular Crowding.

Mitochondrial transcript maturation in African trypanosomes requires RNA editing to convert sequence-deficient pre-mRNAs into translatable mRNAs. The different pre-mRNAs have been shown to adopt highly stable 2D folds; however, it is not known whether these structures resemble the in vivo folds given the extreme “crowding” conditions within the mitochondrion. Here, we analyze the effects of macromolecular crowding on the structure of the mitochondrial RPS12 pre-mRNA. We use high molecular mass polyethylene glycol as a macromolecular cosolute and monitor the structure of the RNA globally and with nucleotide resolution. We demonstrate that crowding has no impact on the 2D fold and we conclude that the MFE structure in dilute solvent conditions represents a good proxy for the folding of the pre-mRNA in its mitochondrial solvent context.

Structures of Bordered Pits Potentially Contributing to Isolation of a Refilled Vessel from Negative Xylem Pressure in Stems of Morus australis Poir.: Testing of the Pit Membrane Osmosis and Pit Valve Hypotheses.

Two hypotheses have been proposed to explain the mechanism preventing the refilling vessel water from being drained to the neighboring functional vessels under negative pressure. The pit membrane osmosis hypothesis proposes that the xylem parenchyma cells release polysaccharides that are impermeable to the intervessel pit membranes into the refilling vessel; this osmotically counteracts the negative pressure, thereby allowing the vessel to refill. The pit valve hypothesis proposes that gas trapped within intervessel bordered pits isolates the refilling vessel water from the surrounding functional vessels. Here, using the single-vessel method, we assessed these hypotheses in shoots of mulberry (Morus australis Poir.). First, we confirmed the occurrence of xylem refilling under negative pressure in the potted mulberry saplings. To examine the pit membrane osmosis hypothesis, we estimated the semi-permeability of pit membranes for molecules of various sizes and found that the pit membranes were not semi-permeable to polyethylene glycol of molecular mass <20,000. For the pit valve hypothesis, we formed pit valves in the intervessel pits in the short stem segments and measured the maximum liquid pressure up to which gases in bordered pits were retained. The threshold pressure ranged from 0.025 to 0.10 MPa. These values matched the theoretical value calculated from the geometry of the pit chamber (0.0692-0.101 MPa). Our results suggest that gas in the pits is retained by surface tension, even under substantial positive pressure to resolve gases in the refilling vessel, whereas the molecule size required for the pit membrane osmosis mechanism in mulberry would be unrealistically large.

Investigation of penetration into woven fabric specimens impregnated with shear thickening fluid

Abstract In this paper, the effect of weight fraction of nano silica (hydrophilic fumed silica particles) and molecular mass of polyethylene glycol (PEG) on the rheological properties such as the critical shear rate of fluids has been studied. Dynamic moduli based on strain and the effects of increasing the molecular weight are presented. Constructed samples with high-molecular-weight PEG have higher initial, final and critical viscosities. Also, higher molecular chains in the polymer and preventing the movement of most of these chains against the relative motion of liquid (viscosity) will cause higher viscosity in samples. Critical shear rate is lower in the provided samples with high-molecular-weight PEG. Polymer branches in these suspensions are absorbed by the surface of the particles. Due to OH bonds in the silica particles and also due to the presence of this bond in PEG, creating a hydrogen bond is likely. Such a hydrogen bond between the polymer yarn and the particle surface causes surface absorption of the particles. To show the effect of molecular weight on fibers, woven fabric specimens impregnated with shear thickening fluid (STF) have been examined by penetration and pressure test diagrams have been investigated. In a sample with higher molecular weight, displacement to yield point is higher and residence to penetration does not show much difference.

Discontinuities in hygroscopic growth below and above water saturation for laboratory surrogates of oligomers in organic atmospheric aerosols

Abstract. Discontinuities in apparent hygroscopicity below and above water saturation have been observed for organic and mixed organic–inorganic aerosol particles in both laboratory studies and in the ambient atmosphere. However, uncertainty remains regarding the factors that contribute to observations of low hygroscopic growth below water saturation but enhanced cloud condensation nuclei (CCN) activity for a given aerosol population. Utilizing laboratory surrogates for oligomers in atmospheric aerosols, we explore the extent to which such discontinuities are influenced by organic component molecular mass and viscosity, non-ideal thermodynamic interactions between aerosol components, and the combination of these factors. Measurements of hygroscopic growth under subsaturated conditions and the CCN activity of aerosols comprised of polyethylene glycol (PEG) with average molecular masses ranging from 200 to 10 000 g mol−1 and mixtures of PEG with ammonium sulfate (AS) were conducted. Experimental results are compared to calculations of hygroscopic growth at thermodynamic equilibrium conducted with the Aerosol Inorganic Organic Mixtures Functional groups Activity Coefficients (AIOMFAC) model, and the potential influence of kinetic limitations on observed water uptake was further explored through estimations of water diffusivity in the PEG oligomers. Particle-phase behavior, including the prevalence of liquid–liquid phase separation (LLPS), was also modeled with AIOMFAC. Under subsaturated relative humidity (RH) conditions, we observed little variability in hygroscopic growth across PEG systems with different molecular masses; however, an increase in CCN activity with increasing PEG molecular mass was observed. This effect is most pronounced for PEG–AS mixtures, and, in fact, an enhancement in CCN activity was observed for the PEG10000–AS mixture as compared to pure AS, as evidenced by a 15 % reduction in critical activation diameter at a supersaturation of 0.8 %. We also observed a marked increase in apparent hygroscopicity for mixtures of higher molecular mass PEG and AS under supersaturated conditions as compared to subsaturated hygroscopic growth. AIOMFAC-based predictions and estimations of water diffusivity in PEG suggest that such discontinuities in apparent hygroscopicity above and below water saturation can be attributed, at least in part, to differences in the sensitivity of water uptake behavior to surface tension effects. There is no evidence that kinetic limitations to water uptake due to the presence of viscous aerosol components influenced hygroscopic growth. For the systems that display an enhancement in apparent hygroscopicity above water saturation, LLPS is predicted to persist to high RH. This indicates a miscibility gap and is likely to influence bulk-to-surface partitioning of PEG at high RH, impacting droplet surface tension and CCN activity. This work provides insight into the factors likely to be contributing to discontinuities in aerosol water-uptake behavior below and above water saturation that have been observed previously in the ambient atmosphere.

Assembly of functional gold nanoparticle on silica microsphere

We demonstrate a controlled synthesis of silica microsphere with the surface-decorated functional gold nanoparticles. Surface of silica microsphere was modified by 3-aminopropypltriethoxysilane and 3-aminopropyldimethylethoxysilane to generate a positive electric field, by which the gold nanoparticles with the negative charges (unconjugated, thiolated polyethylene glycol functionalized with the traceable packing density and conformation) were able to be attracted to the silica microsphere. Results show that both the molecular conjugation on gold nanoparticle and the uniformity in the amino-silanization of silica microsphere influenced the loading and the homogeneity of gold nanoparticles on silica microsphere. The 3-aminopropyldimethylethoxysilane-functionalized silica microsphere provided an uniform field to attract gold nanoparticles. Increasing the ethanol content in aminosilane solution significantly improved the homogeneity and the loading of gold nanoparticles on the surface of silica microsphere. For the gold nanoparticle, increasing the molecular mass of polyethylene glycol yielded a greater homogeneity but a lower loading on silica microsphere. Bovine serum albumin induced the desorption of gold nanoparticles from silica microsphere, where the extent of desorption was suppressed by the presence of high-molecular mass polyethylene glycol on gold nanoparticles. This work provides the fundamental understanding for the synthesis of gold nanoparticle-silica microsphere constructs useful to the applications in chemo-radioactive therapeutics.

PEG-induced molecular crowding leads to a relaxed conformation, higher thermal stability and lower catalytic efficiency of Escherichia coli β-galactosidase

Enzymatic activities were historically assayed in dilute solutions where molecular crowding, molecular confinement and their consequences were not taken into account. Here we report how macromolecular crowding tunes catalytic parameters for the tetrameric β-Galactosidase from Escherichia coli, β-Gal. We detected increases in KM (weaker substrate binding) and a nonlinear variation in Vmax, with a minimum at 25% W/P of the crowding agent (polyethyleneglycol molecular mass 6000, PEG6000) resulting in a linear decrease in the catalytic efficiency (kcat/KM) within the whole [PEG6000] range tested). Presence of crowding agent affected β-Gal structural content and increased its thermal resistance. Steady state fluorescence and Fourier transformed infrared spectroscopic observations are compatible with crowding-induced disordering and restricted internal dynamics as a result of excluded volume and solvent structuring effects. This leads to a non-optimal substrate-binding site and a less conformationally strained protein.

Morphological characteristics of selenium-polyethylene glycol nanocomposites

Hybrid organo-inorganic nanocomposites containing selenium nanoparticles stabilized with polyethylene glycols with different molecular masses were synthesized and studied by the static and dynamic scattering methods. It was shown that the morphological characteristics of nanocomposites can be regulated by varying the molecular mass of polyethylene glycols and the ratio of the selenium-polyethylene glycol components during the synthesis.

Bacterial degradation of a mixture obtained through the chemical modification of polychlorinated biphenyls by polyethylene glycols

Polychlorinated biphenyls (PCBs), also known by the trade name Sovol, are toxic industrial wastes. They have been subjected to chemical treatment by polyethylene glycols (PEGs) and potassium hydroxide. As a result of the interaction of the Sovol with various molecular mass PEGs (MMPEG-4 ∼ 200, MMPEG-22 ∼ 1000), water-soluble mixtures M1 and M2 containing mono(polyethylene glycol)oxy-derivatives (PCB-PEG-4 and PCB-PEG-22), polychlorobiphenylols, and unreacted PCB congeners (PCB 44, PCB 47, PCB 49, PCB 52, and PCB 66) were obtained. It was shown for the first time that mixtures M1 and M2 are susceptible to bacterial degradation without their fractionation. According to the gas-liquid chromatography with flame-ionization and mass-spectrometric detection, the Rhodococcus wratislaviensis KT112-7 strain degraded all of the chemical compounds occurring in the mixtures. In a 5-day experiment, it was found that the KT112-7 strain decomposes mono(polyethylene glycol)oxy-derivatives completely (by 100%) and polychlorobiphenylols and PCB congeners by 90–95% in the M1 and M2 mixtures. The culture medium did not contain transformation products, whereas free chlorine ions were accumulated (72–94% of the maximum possible amount). Thus, the use of the chemical modification and consecutive bacterial degradation provided an effective destruction of technical PCB mixtures with a high content of highly chlorinated congeners.