Biodegradability Enhancement Research Articles

Efficient pretreatment of industrial estate wastewater for biodegradability enhancement using a micro-electrolysis-circulatory system

A self-made micro-electrolysis-circulatory system with the mixture regime of an upflow bed and reactor was tested for the pretreatment of industrial estate wastewater with a low ratio of biological to chemical oxygen demand (BOD5/COD) at room temperature, 1:1 vol ratio of sponge iron (SFe)/granular activated carbon (GAC), and an intermittent process in aeration and discharge. The system efficiency was evaluated in view of the effects of various processes (hydraulic retention time (HRT), fillers/wastewater ratio (S/L) and aeration). COD reduction of about 51% was obtained for industrial estate wastewater at an S/L ratio of 25%, refluence rate of 16 L/h, HRT of 24 h, and aeration of 60 L/h as the optimal conditions. The considerable change in the calculated BOD5/COD ratio, from 0.07 to 0.49, showed favorable application of the micro-electrolysis-circulatory system for the reductive and oxidative degradation of organic pollutants to enhance wastewater biodegradability. The reusability of the SFe was also investigated after three successive runs. On the basis of the results of Fe leaching, HRT, S/L ratio, scanning electron microscopy observation, and X-ray photoelectron spectroscopic analysis, the corrosion products facilitated by the inherent porosity of SFe played a significant role due to different oxygen conditions in the surface and internal layers. One result from the removal of organic pollutants dominated by the galvanic cell reactions between SFe and GAC was observed, and the integration coagulation in the bulk solution was mainly attributed to the leaching of Fe. The innovative approach described in this study provides a promising and economical technology for pretreatment of industrial wastewater prior to a biological process.

Substantially enhanced anaerobic reduction of nitrobenzene by biochar stabilized sulfide-modified nanoscale zero-valent iron: Process and mechanisms

Nanoscale zero-valent iron (nZVI), although being increasingly used in anaerobic systems for strengthening the removal of various refractory pollutants, is limited by various inherent drawbacks, such as easy precipitation, passivation, poor mass and electron transfer. To address the above issues, biochar stabilized sulfide-modified nZVI (S-nZVI@BC) was added into an up-flow anaerobic sludge blanket (UASB) to investigate the enhancement of anaerobic biodegradation of nitrobenzene (NB) and its impacts on microbial community structure. The results demonstrated that both NB reduction and aniline formation could be substantially facilitated in S-nZVI@BC coupled system compared to other anaerobic ones coupled with nZVI or S-nZVI. The dosage of S-nZVI@BC resulted in the formation of densely packed aggregates, evidently increased the extracellular polymeric substances content, promoted the volatile fatty acids transformation and stimulated the methane yield. Furthermore, species related to fermentation (Bacteroides and Longilinea), methanogenesis (Methanosarcina and Methanomethylovorans), electroactivity (Pelobacter, Thiobacillus and Phaselicystis) as well as reduction (Desulfovibrio) were considerably enriched in S-nZVI@BC coupled system. The activities of electron transport, total adenosine triphosphate, nitroreductase and NAD(P)H, which were closely related to microbial activity and NB transformation, were increased noticeably in S-nZVI@BC coupled anaerobic system. This study demonstrated the promising potential for long-term operation and full-scale application of S-nZVI@BC coupled system for the treatment of NB containing wastewater.

Electrochemical advanced oxidation processes using novel electrode materials for mineralization and biodegradability enhancement of nanofiltration concentrate of landfill leachates

The objective of this study was to implement electrochemical advanced oxidation processes (EAOPs) for mineralization and biodegradability enhancement of nanofiltration (NF) concentrate from landfill leachate initially pre-treated in a membrane bioreactor (MBR). Raw carbon felt (CF) or FeIIFeIII layered double hydroxides-modified CF were used for comparing the efficiency of homogeneous and heterogeneous electro-Fenton (EF), respectively. The highest mineralization rate was obtained by heterogeneous EF: 96% removal of dissolved organic carbon (DOC) was achieved after 8 h of electrolysis at circumneutral initial pH (pH0 = 7.9) and at 8.3 mA cm−2. However, the most efficient treatment strategy appeared to be heterogeneous EF at 4.2 mA cm−2 combined with anodic oxidation using Ti4O7 anode (energy consumption = 0.11 kWh g−1 of DOC removed). Respirometric analyses under similar conditions than in the real MBR emphasized the possibility to recirculate the NF retentate towards the MBR after partial mineralization by EAOPs in order to remove the residual biodegradable by-products and improve the global cost effectiveness of the process. Further analyses were also performed in order to better understand the fate of organic and inorganic species during the treatment, including acute toxicity tests (Microtox®), characterization of dissolved organic matter by three-dimensional fluorescence spectroscopy, evolution of inorganic ions (ClO3−, NH4+ and NO3−) and identification/quantification of degradation by-products such as carboxylic acids. The obtained results emphasized the interdependence between the MBR process and EAOPs in a combined treatment strategy. Improving the retention in the MBR of colloidal proteins would improve the effectiveness of EAOPs because such compounds were identified as the most refractory. Enhanced nitrification would be also required in the MBR because of the release of NH4+ from mineralization of refractory organic nitrogen during EAOPs.

Novel waste-derived biochar from biomass gasification effluent: preparation, characterization, cost estimation, and application in polycyclic aromatic hydrocarbon biodegradation and lipid accumulation by Rhodococcus opacus.

This study evaluated an enhancement of simultaneous polycyclic aromatic hydrocarbon (PAH) biodegradation and lipid accumulation by Rhodococcus opacus using biochar derived cheaply from biomass gasification effluent. The chemical, physical, morphological, thermal, and magnetic properties of the cheaply derived biochar were initially characterized employing different techniques, which indicatedthat the material is easy to separate, recover, and reuse for further application. Batch experiments were carried out to study biochar-aided PAH biodegradation by R. opacus clearly demonstrating its positive effect on PAH biodegradation and lipid accumulation by the bacterium utilizing the synthetic media containing 2-, 3- or 4-ring PAH compounds, at an initial concentration in the range 50-200 mg L-1, along with 10% (w/v) inoculum. An enhancement in PAH biodegradation from 79.6 to 92.3%, 76.1 to 90.5%, 74.1 to 88.2%, and 71.6 to 82.3% for naphthalene, anthracene, phenanthrene, and fluoranthene, respectively, were attained with a corresponding lipid accumulation of 68.1%, 74.2%, 72.4%, and 63% (w/w) of cell dry weight (CDW). From contact angle measurements carried out in the study, enhancement in PAH biodegradation and lipid accumulation due to the biochar was attributed to an improved bioavailability of PAH to the degrading bacterium.

Using scrap zero valent iron to replace dissolved iron in the Fenton process for textile wastewater treatment: Optimization and assessment of toxicity and biodegradability

A Fenton like advanced oxidation process (AOP) employing scrap zerovalent iron (SZVI) and hydrogen peroxide (H2O2) was studied for industrial textile wastewater treatment from a textile manufacturing plant located at Medellín, Colombia (South America). The wastewater effluent studied contains a mixture of organic compounds resistant to conventional treatments. The effect of initial pH and SZVI concentration and H2O2 concentration were studied by a response surface methodology (RSM) Box-Behnken design of experiment (BBD). The combined SZVI/H2O2 process led to reductions of 95% color, 76% of chemical oxygen demand (COD) and 71% of total organic carbon (TOC) at optimal operating conditions of pH = 3, SZVI = 2000 mg/L and [H2O2] = 24.5 mM. Molecular weight distribution measurement (MWD), ultraviolet–visible (UV–Vis) spectroscopy, HPLC, biodegradability and toxicity were used to characterize the pollutants after the treatment process finding that the resulting effluent was polluted mostly by low molecular weight carboxylic acids. A remarkable biodegradability enhancement of the effluent was evidenced by a BOD5/COD ratio increase from 0.22 to 0.4; also, the SZVI/H2O2 process successfully reduced the toxicity from 60% to 20% of dead A. Salina crustaceans.

Enhancement of atrazine biodegradation by marine isolate Bacillus velezensis MHNK1 in presence of surfactin lipopeptide

Atrazine is one of the widely used toxic herbicide and considered as serious environmental contaminant worldwide due to its long term use in crop production. In this study, the effect of surfactin lipopeptide produced by Bacillus velezensis MHNK1 on atrazine biodegradation was investigated. B. velezensis MHNK1 produced 0.83 ± 0.07 g/L of anionic biosurfactant that reduced surface tension from 72.12 ± 0.02 to 33.2 ± 0.61 mN/m and CMC was 40 mg/L with 85.21 ± 1.60% emulsification index. Further, biosurfactant was characterized as surfactin by TLC, HPLC, FTIR, 1H and 13C NMR and LCMS-ESI. B. velezensis MHNK1 showed 87.10 ± 3.10% atrazine biodegradation within 5 days which was revealed by HPLC and MS analysis. Atrazine biodegradation using a combination of B. velezensis MHNK1 (2%) and surfactin (2 CMC) resulted in 100 ± 1.20% degradation within 4 days. Presence of atrazine degrading genes in B. velezensis MHNK1 was also confirmed by PCR. To the best of our knowledge, there are no previous reports available on atrazine degradation using B. velezensis strain and also in combination with surfactin. The results of this study reveal that strain B. velezensis MHNK1 and surfactin can be potential source of ecofriendly application for removal of atrazine from contaminated sites.

Modeling ozonation pretreatment parameters of distillery wastewater for improved biodegradability

In this study, ozonation pretreatment of real distillery wastewater (DWW) for biodegradability enhancement was undertaken. Response surface methodology was used to model the value of effective parameters, including ozonation duration and initial chemical oxygen demand (COD) concentration, and to estimate linear interactions and quadratic effects. The analysis of variance confirmed the adequate description of all the responses by the quadratic model employed. During ozonation, the pH of the DWW increased in acidity from 4.53 to 4.05, indicating the formation of acidic intermediates. A 60% reduction in color was observed signifying the oxidation of the color causing biorecalcitrant aromatic compounds and confirmed by the reduction in ultraviolet absorbance at λmax of 254 nm. Moreover, an increase in change in oxidation state from −0.1 to 0.4 was attributed to the declined aromaticity and the formation of aliphatic structures. From the measurement of the ratio of biochemical: chemical oxygen demand (BOD5:COD), an increase from 0.48 to 0.72 confirmed improved biodegradability. Optimization studies aimed at achieving maximum improved biodegradability at maximum ozone transfer efficiency yielded optimum ozonation pretreatment parameters of initial COD of 4.1 g L−1 and duration of 64 min.

Ozone as a Pretreatment Method for Antibiotic Contaminated Wastewater and Sludge

ABSTRACTThe capability of ozone to reduce the hazardous impact of environmentally persistent antibiotic tiamulin in term of toxicity reduction and enhancement of biodegradability was investigated. Different ozone doses were applied but ozonation was not effective enough to increase the biodegradability of tiamulin in the aqueous phase. The opposite effect was observed in anaerobic digestion experiments, where ozonation as a pretreatment step of antibiotic-contaminated sludge detoxify tiamulin and improves biogas production for 75%. As confirmed by 1H NMR and HPLC-HRMS analyses, the tiamulin molecule completely reacts with ozone at low ozone/COD molar ratio of 0.03, primarily attacking the vinyl double bond with further oxidation of sulfur and nitrogen atom, and gradual decomposition of tiamulin skeleton.

Bioaugmentation effect of Aeromonas hydrophila and Pseudomonas putida on kinetics of activated sludge process in treating pharmaceutical industrial wastewater

AbstractBACKGROUNDPharmaceutical industrial wastewater represents a challenge for biological treatment due to its complex composition. This research investigates the bioaugmentation effect of indigenous bacterial strains on the kinetics of the activated sludge process in the treatment of real high‐strength pharmaceutical industrial wastewater.RESULTSTwo bacterial strains were isolated from pharmaceutical effluent and identified as Aeromonas hydrophila and Pseudomonas putida. The highest removal efficiency of dissolved organic matter from pharmaceutical wastewater was 71.43% within 24 h, obtained by bioaugmented activated sludge with P. putida, at the initial concentration of activated sludge 4.39 ± 0.37 g L−1. The biokinetic parameters of the biodegradation process were calculated using the Endo‐Haldane model, where bioaugmented activated sludge showed higher affinity to pharmaceutical wastewater.CONCLUSIONThe biodegradation process of high‐strength pharmaceutical wastewater showed enhancement through bioaugmentation of activated sludge with indigenous bacterial isolates. Considering the increasingly demand for pharmaceuticals on a global scale, the bioaugmentation potential of A. hydrophila and P. putida could contribute to enhancement of biodegradation through reduction in process time and environmental impact. © 2019 Society of Chemical Industry

Suspended particles enhance biodegradation of oil in sea

Biodegradation patterns of oil in four distinct phases were compared over a 14-day series of exposures. The dispersibility and stability of oil droplets in the water column were important factors affecting oil biodegradation. Due to the stability of oil droplets with particle interactions, oil-suspended particulate matter aggregates (OSA) showed a five-fold enhancement in biodegradation compared to non-dispersed oil. The reduction of total petroleum hydrocarbons was highest in OSA (51.45%), followed by chemically dispersed oil (33.5%), oil film (21.6%), and water-accommodated fractions (WAF, 14.3%). Polycyclic aromatic hydrocarbon (PAH) profiles and percentage weathering plots showed that reductions in PAHs in WAF, oil film, and chemically dispersed oil were mainly due to evaporation (41.5–69.5%) and only partially due to biodegradation (7.4–16.3%). However, the reduction of PAHs in OSA was driven more by biodegradation (36.8%) than evaporation (29.7%). The strong PAH–particle interactions in OSA inhibited evaporation of PAHs and enhanced microorganism biodegradation in the water column.

Nano catalytic ozonation of biomethanated distillery wastewater for biodegradability enhancement, color and toxicity reduction with biofuel production

The effectiveness of O3, O3/Fe2+, and O3/nZVI processes on biomethanated distillery wastewater (BMDWW) was evaluated in terms of biodegradability index (BI) enhancement, biofuel production, COD, color & toxicity reduction. A significant increase in biodegradability, COD, color and toxicity reduction was observed in O3/nZVI compared with O3, O3/Fe2+ due to more hydroxyl radical production. The O3/nZVI pretreated wastewater with enhanced BI (up to 0.71) showed 60% COD removal with additional biogas generation (64% methane content). From the Gas Chromatography Mass Spectrometry (GC-MS) analysis, 18 foremost organic compounds were predominantly detected in the raw distillery wastewater. The disappearance of the corresponding FTIR (Fourier Transform Infrared Spectroscopy) & GC-MS spectra during pretreatment processes signified the degradation or transformation of the recalcitrant present in the distillery wastewater. Subsequent (AnO + AO, AO) of pretreated BMDWW resulted in biodegradation rate enhancement by (1.83, 1.67), (3.5, 2.4) and (4.7, 2.9) times for O3, O3/Fe2+ and O3/nZVI processes respectively.

Synergistic effects of urban tributary mixing on dissolved organic matter biodegradation in an impounded river system

Dams and wastewater may greatly perturb riverine fluxes of dissolved organic matter (DOM) and CO2, yet little is known about the relationships between altered DOM quality and CO2 emission in eutrophic impounded river systems. A basin-wide field survey of surface water CO2 and dissolved organic carbon (DOC) was combined with laboratory incubations to examine how dams and urban tributaries delivering treated wastewater influence longitudinal patterns in DOM properties and CO2 along the impounded Han River traversing Seoul metropolitan area. Fluorescent DOM indices including parallel factor analysis (PARAFAC) components were used to characterize DOM in relation to biodegradable DOC (BDOC). Compared with distinct downstream increases in DOC and CO2, BDOC concentration and its proportion in DOC (%BDOC) were highly variable along the mainstem and peaked at urban tributaries. Longitudinal increases in fluorescence index (FI), biological index (BIX), and two PARAFAC components (C2 and C3) contrasted with general decreases in humification index (HIX) and C1, reflecting increasing downstream inputs of anthropogenic DOM. During a 5-day incubation employing continuous CO2 measurements, the cumulative production of CO2 in the mainstem water mixed with urban tributary water was significantly higher than the level expected for conservative mixing of the two samples, indicating a synergistic enhancement of DOM biodegradation. Molecular formulas identified by Fourier transform-ion cyclotron resonance-mass spectrometry (FT-ICR-MS) revealed more consumed molecules in the mainstem water and more newly produced molecules in the tributary water over the 5-day incubation, implying abundant labile components in the mainstem water discharged from the upstream dam and highly processed tributary DOM limited in immediately biodegradable organic materials. Downstream increases in CO2 and DOC along the Han River, combined with the synergistic effect observed in the mixed water, suggest that mixing wastewater-derived DOM with labile autochthonous DOM can enhance CO2 production in the river system perturbed by impoundment and wastewater.

Treatment of pharmaceutical industrial wastewater by nano-catalyzed ozonation in a semi-batch reactor for improved biodegradability

The study reports the biodegradability enhancement of pharmaceutical wastewater along with COD (Chemical Oxygen Demand) color and toxicity removal via O3, O3/Fe2+, O3/nZVI (nano zero valent iron) processes. Nano catalytic ozonation process (O3/nZVI) showed the highest biodegradability (BI = BOD5/COD) enhancement of pharmaceutical wastewater up to 0.63 from 0.18 of control with a COD, color and toxicity removal of 62.3%, 93% and 82% respectively. The disappearance of the corresponding Fourier transform infrared (FTIR) and gas chromatography–mass spectrometry (GC–MS) peaks after pretreatment indicated the degradation or transformation of the refractory organic compounds to more biodegradable organic compounds. The subsequent aerobic degradation study of pretreated pharmaceutical wastewater resulted in biodegradation rate enhancement of 5.31, 2.97, and 1.22 times for O3/nZVI O3/Fe2+ and O3 processes respectively. Seed germination test using spinach (Spinacia oleracea) seeds established the toxicity removal of pretreated pharmaceutical wastewater.

Development of an integrated treatment strategy for a leather tannery landfill leachate

This study aimed at developing an efficient multistage treatment strategy for a complex industrial landfill leachate: a leather tannery landfill leachate. Based on the leachate physicochemical characteristics, the following treatment train was delineated and tested: (i) initial biological process for removal of biodegradable organics, ammonium and alkalinity, (ii) coagulation/flocculation process for total removal of chromium and partial removal of recalcitrant organics and suspended solids, (iii) advanced oxidation process (AOP) or electrochemical AOP (EAOP) for degradation of recalcitrant organics and biodegradability enhancement, and (iv) final biological polishing step. Two initial biological treatment configurations were applied: one comprising nitrification and the other nitrification-denitrification. Coagulation/flocculation was optimized in terms of pH, coagulant dosage (iron(III) chloride) and flocculant nature and dosage. The following AOPs/EAOPs were tested: Fenton, photo-Fenton with UVA or UVC radiation (PF-UVA or PF-UVC), anodic oxidation (AO), electro-Fenton (EF) and photoelectro-Fenton with UVA radiation (PEF-UVA). The biological nitrification-denitrification was beneficial not only because it avoided the need for alkalinity addition during nitrification and decreased the amount of substrate added during denitrification, as expected. Over and above that, it reduced the acid consumption in the coagulation/flocculation, avoided the application of an additional stage comprising nitrites oxidation to nitrates prior to the AOP/EAOP, and improved the efficiency of Fenton’s reaction based processes. Following nitrification-denitrification, the coagulation/flocculation was maximized at pH 3.0 and 400 mg Fe L−1 with no flocculant addition. The PEF-UVA process was the best AOP/EAOP. The final leachate fulfilled the discharge limits into waterbodies.

Electro-oxidation by graphite anode for naphthenic acids degradation, biodegradability enhancement and toxicity reduction

Electro-oxidation (EO) by using graphite anode and at relatively low current densities was successfully applied for the degradation of commercial naphthenic acids (NAs) mixture in water samples. At current densities of 0.5, 2.5, and 5 mA/cm2, acid extractable fraction (AEF) was removed by 42.2%, 57.0% and 67.9%, respectively, while classical NAs were degraded by 76.9%, 77.6% and 82.4%, respectively. EO reactivity towards NAs increased with increasing the carbon number (n) and was higher for cyclic NAs compared to the acyclic component. Oxidized NAs containing O3 and O4 were also degraded effectively during EO. The biodegradability of organics in the NA mixture was clearly improved by 1.7, 2.5 and 2.7 folds when the samples were pre-treated with EO at current densities of 0.5, 2.5, and 5 mA/cm2, respectively. The aromatic fraction in the commercial NA mixture consisted mainly of single-ring aromatics and was degraded effectively by EO. Biodegradation alone was able to reduce the toxicity of the commercial NA mixture towards Vibrio fischeri; however, the combination of EO with biodegradation resulted in a complete removal of the toxicity, showing a synergistic effect of combining these two processes. Coupling EO with aerobic biodegradation can result in an effective and energy-efficient treatment option for NA-bearing waters such as oil sands process water (OSPW) and refinery effluents.

Cost-efficient improvement of coking wastewater biodegradability by multi-stages flow through peroxi-coagulation under low current load

Cost-effective pretreatment of the highly concentrated and biorefractory coking wastewater to improve biodegradability is of significant importance, while green electrochemical technologies without external chemicals addition are charming but still challenging due to its high energy consumption. In this work, a novel multi-stages flow through peroxi-coagulation (PC) was for the first time developed with graphite felt cathode modified by graphene, showing an excellent performance in removal of 71.5% COD, 72.3% phenol and 59.4% NH3-N and significant biodegradability enhancement with a low energy consumption as 1.2 kWh/m3. Compared with conventional flow PC, this process was more cost-effective due to more intensive .OH production and higher utilization of generated active species. Through UV spectrophotometry and GC-MS analysis, the improvement of biodegradability was attributed to the reduction of both low and high molecular weight compounds content in the coking wastewater. Comparing to the electro-Fenton, electrocoagulation and ozonation process, the proposed PC process was highly cost-effective, providing a promising and new alternative for pretreatment of coking wastewater.

Ozonolysis pre-treatment of waste activated sludge for solubilization and biodegradability enhancement

Handling of waste activated sludge (WAS) has been a great problem due to its low biodegradability which is contributed by the biorecalcitrant bacterial cells from the activated sludge process. Moreover, the sludge is poorly soluble which makes it difficult to subject to a further biological treatment downstream. This study investigated the application of ozonolysis pre-treatment for the solubilization and biodegradability enhancement of municipal WAS. Ozonolysis led to sludge solubilization as was shown by a 50% reduction in total suspended solids (TSS). Subsequently, the dissolved organic carbon (DOC) increased by 25%, and sludge biodegradability increased two-folds. The mechanism of sludge solubilization was explained through cell content analysis which revealed biomass cell wall rapture during ozonolysis leading to the release of the cellular contents including humic substances, proteins, phosphates, nitrates and carbohydrates into the supernatant. The soluble proteins decreased by 98% while carbohydrates increased four-fold. Additionally, sulphates in the supernatant increased from 18 mg/L to 45 mg/L while nitrates increased from 0 mg/L to 85 mg/L indicating oxidation of the organic nitrogen and phosphorus which are constituents of the biomass cell protein; this can provide nutrient balance in the downstream biological treatment method. Thermogravimetric (TGA) analysis showed that the weight loss for ozone-treated WAS was 10% while that for the raw WAS was 20% further indicating that ozonolysis had solubilized the volatile and organic components of the treated WAS. Ozonolysis is a promising technology for the pre-treatment of WAS before anaerobic digestion for stabilization and energy recovery.

Biodegradability enhancement of hydrolyzed polyacrylamide wastewater by a combined Fenton-SBR treatment process

An efficient way to solve the environmental pollution deriving from hydrolyzed polyacrylamide (HPAM)-containing drilling wastewater is urgent. This work adopted a novel method coupling Fenton oxidation with sequencing batch reactor (SBR) to treat gas-field drilling wastewater successively. This Fenton-SBR process reduced COD, HPAM, NH4+-N and total phosphorus (TP) concentrations of drilling wastewater by 98.35%, 87.58%, 94.50% and 93.52%, respectively. While simulated HPAM wastewater with similar HPAM concentration to Fenton-oxidized drilling wastewater was treated only by biological process, and the COD and HPAM removal efficiencies reached 78.26% and 62.95%. The result indicates that the biodegradability of the drilling wastewater was enhanced after Fenton oxidation. Moreover, the analysis on microbial community structure indicates the dominant bacteria in treated drilling wastewater were different from that in treated simulated-wastewater. It can be considered the Fenton-SBR process possesses potential to be applied to treating the drilling wastewater.

Fluorescent Penetration Enhancers Reveal Complex Interactions among the Enhancer, Drug, Solvent, and Skin.

Skin penetration/permeation enhancers facilitate drug delivery through the skin barrier. However, the specific mechanisms that govern the enhancer interactions with the skin, drug, and donor solvent are not fully understood. We designed and synthesized fluorescent-labeled enhancers by attaching 7-nitrobenzo[c][1,2,5]oxadiazol-4-yl (NBD) groups to 6-aminohexanoic acid esters. These NBD esters (applied at a 1% concentration) enhanced the permeation of the model drugs theophylline and hydrocortisone through human skin in vitro up to 6.6- and 3.9-times, respectively. The enhancement effects were strongly affected by the ester chain length (C8-C12) and the polarity of the donor solvent. Using high-performance liquid chromatography with fluorescence detection, no NBD esters were detected in the acceptor buffer, but their hydrolysis product, NBD acid, was detected, whereas both acid and esters were found in the skin. The enhancer hydrolysis occurred in the lower stratum corneum and epidermis; more hydrophilic NBD acid, which is an inactive enhancer, penetrated deeper. This illustrates the principle of biodegradable enhancers. The enhancer concentrations in the skin depended not only on the enhancer chain length and the donor solvent, but also on the drug used. Thus, the drug, when coapplied with the enhancer, modulates the enhancer penetration into the skin and, consequently, its effect. Finally, active (NBD-C8 ester) and inactive (NBD acid) enhancers were visualized in human skin by confocal laser scanning microscopy. Both compounds were found mostly in the stratum corneum intercellular spaces, suggesting that although both are located within the skin barrier lipids, only the active ester is able to effectively interact with the lipids, which was proved by infrared spectroscopy of enhancer-treated stratum corneum. This proof-of-concept study illustrates the use of fluorescent enhancers to obtain insight into the skin penetration/permeation process; interactions among the enhancer, drug, solvent, and skin; and enhancer metabolism.

Enhancement of Crude Oil Biodegradation by Pseudomonas reinekei MT1

One of the greatest challenges facing today is endangering living organisms as a result of environmental pollution caused by petroleum crude oil. Therefore it was necessary, to find out a way to remediate these pollutants biologically. An oil degrading bacterial isolate was isolated from oil polluted soils and optimized for oil biodegradation. Psuedomonas reinekei MT1 was able to produce biosurfactants which play a major role in the availability of oil for bacterial biodegradation. Ps. reinekei MT1 gives maximum oil degradation on 30oC, pH 7, sodium nitrate as nitrogen source and addition of gasoline and triton X100. Oil degradation reaches 69.62% after 15 days of incubation. Salinity decreased oil degradation, although Ps. reinekei MT1 had the ability of growing and degrading oil in salinity reaches 2%, while there was neither bacterial growth nor oil degradation at 3%.