Pegylated recombinant human granulocyte colony-stimulating factor for primary prophylaxis of neutropenia in patients with cervical cancer receiving concurrent chemoradiotherapy: a prospective study.

BACKGROUND: This study aimed to investigate the efficacy and safety of pegylated recombinant human granulocyte colony-stimulating factor (PEG-rhG-CSF) for primary prophylaxis of neutropenia in patients with cervical cancer receiving concurrent chemoradiotherapy. METHODS: In this prospective, single-center, single-arm study, we enrolled patients (18-70 years) with 2018 International Federation of Gynecology and Obstetrics (FIGO) stage IIIC1r-IVA and IVB (distant metastasis only with inguinal lymph node metastasis) cervical cancer. Eligible patients should have normal function of the bone marrow (absolute neutrophil count (ANC) ≥ 2.0 × 109/L) and adequate hepatic and renal functions. Key exclusion criteria included: previous chemotherapy and/or radiotherapy; a history of bone marrow dysplasia or other hematopoietic abnormalities. All patients underwent radical radiotherapy (pelvic radiotherapy or extended-field irradiation) plus brachytherapy. The chemotherapy regimen included four cycles of 3-weekly paclitaxel and cisplatin. PEG-rhG-CSF was administered 48-72 h after each treatment cycle. Salvage granulocyte colony-stimulating factor (G-CSF) was only permitted in certain circumstances. The primary endpoint was the incidence of grade 3-4 neutropenia. The secondary endpoints included frequency of febrile neutropenia (FN), chemotherapy completion rate in cycles 2-4, time to complete radiotherapy, and safety. RESULTS: Overall, 52 patients were enrolled in this study from July 2019 to October 2020. The incidence of grade 3-4 neutropenia was 28.8%, with an average duration of grade 3-4 neutropenia persistence of 3.85 days (1-7 days). The incidence rate of FN was 3.8%. The chemotherapy completion rate was 94.2%, 82.7%, and 75.0% for cycles 2-4, respectively. The incidences of grade 3-4 neutropenia for cycles 1-4 were 9.6% (5/52), 8.2% (4/49), 14.0% (6/43), and 2.6% (1/39), respectively. All patients completed radiotherapy within 8 weeks (median, 48 days; range: 41-56 days), except one patient who withdrew consent and did not receive radiotherapy. Severe non-hematologic toxicity was not observed in any patient. CONCLUSION: PEG-rhG-CSF is an effective and safe prophylactic treatment for neutropenia in patients with cervical cancer undergoing concurrent chemoradiotherapy. TRIAL REGISTRATION: Chinese Clinical Trial Registry, ChiCTR1900024494. Date of Registration:13/July/2019.

Joint effects of micro-sized polystyrene and chlorpyrifos on zebrafish based on multiple endpoints and gut microbial effects.

Microplastics often co-occur with a variety of organic contaminants in aquatic environment and pose combined risks to aquatic wildlife. Here, we investigated joint effects of micro-sized polystyrene (mPS, 5 µm) and an organophosphate pesticide chlorpyrifos on zebrafish, using multiple endpoints at both fish individual and gut microbiota levels. It was revealed that mPS ingested by zebrafish accumulated in gut and liver, and caused oxidative stress, hyperactive swimming performance and histological damages in fish, and induced disorders and diversity alterations of the gut microbial community. More importantly, mPS exhibited considerable adsorption capacity against chlorpyrifos, and those adsorbing chlorpyrifos presented greater effects on fish individuals but no different effects on gut microbiota compared to single mPS exposure. Together with body residues of chlorpyrifos in zebrafish, it was proposed that the joint effects between mPS and chlorpyrifos were attributed to the chlorpyrifos released from mPS within zebrafish. The present results provided a comprehensive understanding of joint effects of mPS and contaminants co-occurring in the environment and emphasized the importance of considering the adsorbed chemicals in toxicological studies of microplastics.

Microplastic Impacts on Microalgae Growth: Effects of Size and Humic Acid.

Research has already demonstrated the toxic effects of microplastics (MPs) on different biota. However, the underlying toxic mechanism of MPs remains to be elucidated, especially the effect of particle size and the presence of dissolved organic matter in water. This study investigated the impact on Scenedesmus obliquus exposed in five types of polystyrene particle suspensions with different sizes and surface charges, in the presence and absence of humic acid (HA). Results indicated that the 50% growth inhibition rate of S. obliquus showed no significant difference between the five types of MPs, but the toxic mechanism varied with particle size. Larger size MPs caused adverse effects by blocking the light transport and affecting photosynthesis, while smaller ones destroyed the cell wall by adsorbing onto the algae surface. Also, the addition of HA significantly alleviated the toxicity of smaller size MPs, but not of the larger ones. Scanning electron microscopy images and the reactive oxygen species assay demonstrated that the HA could form a corona on the surface of MPs, reduce the affinity to microalgae, and minimize the adverse effect. Together, these findings identified important factors in determining the toxicity of MPs, providing valuable data for risk assessment of MPs.

A new configuration of polar organic chemical integrative sampler with nylon membranes to monitor emerging organophosphate ester contaminants in urban surface water.

Organophosphate ester contaminants, including organophosphate pesticides (OPPs) and organophosphate flame retardants (OPFRs) are ubiquitous in surface water and pose a significant risk to aquatic organisms, thus it is important to develop effective methods for long-term monitoring of these emerging compounds. Polar organic chemical integrative sampler (POCIS) has become a promising monitoring tool for waterborne contaminants, yet recent studies found that the commonly used polyethersulfone (PES) membrane strongly sorbed some moderately hydrophobic compounds, resulting in long lag-phase for chemical accumulation in POCIS. In the present study, 0.45-µm nylon membranes was selected as POCIS diffusion-limiting membrane to design a new POCIS-Nylon configuration for analyzing moderately hydrophobic OPPs and OPFRs in water. The POCIS-Nylon had negligible lag-phase due to low sorption of OPPs and OPFRs to nylon membrane. Meanwhile, linear accumulation time and sensitivity for target contaminants using POCIS-Nylon retained similar to the traditional POCIS. Water velocity and chemical concentration had little impact on sampling rate (Rs), validating that the POCIS-Nylon was suitable for various water conditions. Finally, the occurrence of OPPs and OPFRs in urban waterways of Guangzhou, China was evaluated using the POCIS-Nylon with Rs values that were calibrated in the laboratory. The average concentration of OPPs was 4.97 ± 1.35 ng/L (range: 2.64 ± 1.28-6.54 ± 0.18 ng/L) and the average concentration of OPFRs was 400 ± 88 ng/L (range: 316 ± 24-615 ± 36 ng/L) across nine sampling sites. The present study provides a way to resolve the inherent challenge of accumulating hydrophobic substances by POCIS.

Bioaccumulation of highly hydrophobic organohalogen flame retardants from sediments: application of toxicokinetics and passive sampling techniques.

Highly hydrophobic organohalogen flame retardants (HHOFRs) are found ubiquitously in the environment; therefore, a better understanding of their bioavailability is needed. In the current study, bioaccumulation testing using the oligochaete, Lumbriculus variegatus, and passive sampling (solid-phase microextraction (SPME)) were performed to study the bioaccumulation potential of HHOFRs, including decabromodiphenyl ether (deca-BDE), decabromodiphenyl ethane (DBDPE), and dechlorane plus (DP), in laboratory-spiked and field-collected sediments. The HHOFRs were bioavailable to L. variegatus even though their biota-sediment accumulation factors were low (0.016 ± 0.002 to 0.48 ± 0.082 g organic carbon/g lipid, syn-DP > anti-DP > deca-BDE > DBDPE). Hydrophobicity and stereoisomerism affected HHOFR bioavailability. Meanwhile, HHOFR concentrations on the SPME fibers (Cf) correlated with those in biota (Cb), suggesting the potential application of SPME in bioavailability prediction for those compounds. The log Cf to log Cb correlation for deca-BDE and DP had a greater intercept than that for polychlorinated biphenyls (data obtained from the literature) although the slopes were similar, while data for DBDPE fell on the regression line for PCBs, implying some uncertainty in application of SPMEs across chemical classes. The increasing sorptive ability of proteins for HHOFRs in comparison to the less-brominated BDEs suggested that protein-binding should be considered when estimating bioaccumulation potential of HHOFRs in benthic invertebrates.

Determining buffering capacity of polydimethylsiloxane-based passive dosing for hydrophobic organic compounds in large-volume bioassays.

Polydimethylsiloxane (PDMS) is the most widely used material for passive dosing. However, the ability of PDMS to maintain constant water concentrations of chemicals in large-volume bioassays was insufficiently investigated. In this study, we proposed a kinetic-based method to determine the buffering capacity of PDMS for maintaining constant water concentrations of hydrophobic organic contaminants (HOCs) in large-volume bioassays. A good correlation between log Kow and PDMS-water partitioning coefficients (log KPW) was observed for HOCs with log Kow values ranging from 3.30 to 7.42. For low-molecular-weight HOCs, volatile loss was identified as the primary cause of unstable water concentrations in passive dosing systems. Slow desorption from PDMS resulted in a reduction of water concentrations for high-molecular-weight HOCs. The volume ratio of PDMS to water (RV) was the key factor controlling buffering capacity. As such, buffering capacity was defined as the minimum RV required to maintain 90% of the initial water concentration and was determined to be 0.0076-0.032 for six representative HOCs. Finally, passive dosing with an RV of 0.014 was validated to effectively maintain water concentrations of phenanthrene in 2-L and 96-h toxicity tests with adult mosquitofish. By determining buffering capacity of PDMS, this study recommended specific RV values for cost-efficient implementation of passive dosing approaches in aquatic toxicology, particularly in large-volume bioassays.

Effects of erythromycin on biofilm formation and resistance mutation of Escherichia coli on pristine and UV-aged polystyrene microplastics.

Microplastics (MPs) and antibiotics co-occur widely in the environment and pose combined risk to microbial communities. The present study investigated the effects of erythromycin on biofilm formation and resistance mutation of a model bacterium, E. coli, on the surface of pristine and UV-aged polystyrene (PS) MPs sized 1-2 mm. The properties of UV-aged PS were significantly altered compared to pristine PS, with notable increases in specific surface area, carbonyl index, hydrophilicity, and hydroxyl radical content. Importantly, the adsorption capacity of UV-aged PS towards erythromycin was approximately 8-fold higher than that of pristine PS. Biofilms colonizing on UV-aged PS had a greater cell count (5.6 × 108 CFU mg-1) and a higher frequency of resistance mutation (1.0 × 10-7) than those on pristine PS (1.4 × 108 CFU mg-1 and 1.4 × 10-8, respectively). Moreover, erythromycin at 0.1 and 1.0 mg L-1 significantly (p < 0.05) promoted the formation and resistance mutation of biofilm on both pristine and UV-aged PS. DNA sequencing results confirmed that the biofilm resistance was attributed to point mutations in rpoB segment of the bacterial genome. qPCR results demonstrated that both UV aging and erythromycin repressed the expression levels of a global regulator rpoS in biofilm bacteria, as well as two DNA mismatch repair genes mutS and uvrD, which was likely to contribute to increased resistance mutation frequency.

Influence of ultraviolet-aging and adsorbed pollutants on toxicological effects of polyvinyl chloride microplastics to zebrafish.

Microplastics (MPs) undergo various aging processes and interact with diverse pollutants in the environment. In the present study, we investigated the influence of ultraviolet (UV) aging on the adsorption of organic pollutants by polyvinyl chloride microplastics (mPVC) and explored toxicity variations among pristine, aged, and pollutant-loaded mPVCs to zebrafish. Irradiation of UV for 30 d significantly changed the physiochemical properties of mPVC, leading to more oxygen-containing groups and free radicals (1O2, ·O2-, and ·OH) on mPVC surfaces. The aging process reduced the adsorption of mPVC against a hydrophobic compound chlorpyrifos (CPF) but enhanced the adsorption against a moderately hydrophilic compound erythromycin (ERY). Ingestion of CPF- and ERY-loaded mPVCs resulted in bioaccumulation of the two compounds in zebrafish, suggesting a carrier effect of mPVCs. In toxicity tests, the aged mPVC caused severer gut damages, stronger oxidative stresses, and greater interference with the gut microbiota in zebrafish than the pristine mPVC. The CPF and ERY-loaded mPVCs produced lower oxidative stresses in zebrafish than mPVCs alone, due to fewer radicals on mPVC surfaces after the adsorption of organic contaminants. Notably, the CPF and ERY-loaded mPVCs presented greater effects on fish swimming behaviors and gut microbial compositions, which was associated with the released CPF and ERY from mPVCs within the zebrafish. Overall, the present study demonstrated significant influences of UV-aging and the adsorbed pollutants on the toxicological effects of MPs and highlighted the necessity to perform toxicity studies of MPs using more environmentally relevant MPs.

New insights into the photo-degraded polystyrene microplastic: Effect on the release of volatile organic compounds.

Excessive use of plastics leads to the ubiquity of plastic waste in the environment. Weathering can cause changes in the properties of plastics and lead to the release of various chemicals especially the volatile organic compounds (VOCs). Possible photodegradation pathway of polystyrene (PS) microplastics (MPs) was proposed and verified by the detection of VOCs. Headspace solid phase microextraction (HS-SPME) was employed to investigate the release behavior of VOCs from PS MPs exposed to simulated ultraviolet (UV). Results indicated that although the physicochemical properties of the PS MPs showed no significantly change after UV-irradiation, a variety of toxic VOCs, such as benzene, toluene, and phenol were detected from the irradiated MPs. UV irradiation progressively enhanced the release amount of VOCs with total concentration up to 66 µg g-1 after 30 d of exposure, about 2.4 times higher than that stored in the darkness (27 µg g-1). Some compounds (e.g., benzene and toluene) showed an upward trend over irradiation time, while others (e.g., styrene and 2-propenylbenzene) reduced over time. Results also found that the size of MPs could affect the release amounts but without consistent pattern for different VOCs detected in the headspace of the vial. In general, current study provided a new insight on the photo-aging process of MPs.

Combined effects of nanosized polystyrene and erythromycin on bacterial growth and resistance mutations in Escherichia coli.

Toxicological effects of nanoplastics have been demonstrated in a variety of organisms, yet their impacts on bacteria, especially on the antibiotic resistance evolution remain under explored. Herein, we report individual and combined effects of nano-polystyrene (nano-PS) and erythromycin (ERY) on growth and resistance mutations of Escherichia coli. The toxicity of nano-PS was dependent on size and functional modifications, with 30 nm and amino-modified PS (PS-NH2, 200 nm) showing the greatest toxicity. Adsorption of nano-PS onto bacterial surface and the subsequent increase of intracellular ROS or the probable mechanical damage were considered as the primary toxic mechanisms. Furthermore, nano-PS increased the bacterial resistance mutations, which was due to the oxidative damage to DNA and the SOS response. In addition, PS-NH2 presented synergistic effects with ERY while non-modified PS had no impact, although both of them showed adsorption capacity to ERY. This was likely because the positively charged PS-NH2 acted as a carrier of ERY and enhanced the interactions between ERY and the bacteria. Our findings raised the concerns about the risk of nanoplastics in accelerating the bacterial resistance evolution, and highlighted the necessity of including combined effects of nanoplastics and co-contaminants in risk assessment.

Airway scope for tracheal intubation in the lateral position.

BACKGROUND: Tracheal intubation in the lateral position is difficult because the laryngeal view is compromised during direct laryngoscopy. The Airway Scope facilitates intubation even when laryngeal views are poor with direct laryngoscopy, as they often are in the lateral position. We thus compared the efficacy of the Airway Scope in supine patients with those in the left- and right-lateral positions. METHODS: Anesthetized adults were randomly assigned to supine, left-lateral, or right-lateral position (n = 43 for each group). Laryngeal views were obtained in the designated position with a Macintosh laryngoscope, and patients' tracheas were subsequently intubated with the Airway Scope. Specifically, we tested the hypothesis that the time required for intubation in the left- and right-lateral positions is not increased by >10 seconds compared with tracheal intubation in the supine position. RESULTS: Overall intubation success was 100% in the 2 lateral positions, and 98% in the supine position. Intubation times were similar in the left-lateral (24 [5] seconds, mean [SD]), right-lateral (24 [6] seconds), and supine (22 [7] seconds) positions. The numbers of required intubation attempts were similar in the 2 lateral positions and in the supine and left-lateral positions. However, more intubation attempts were required in the supine position than in the right-lateral position (P = 0.004). The incidences of airway complications were similar in each position; no hypoxia, dental injury, or esophageal intubation was observed. Modified Cormack-Lehane and the percentage of glottic opening scores obtained with the Macintosh laryngoscope did not differ between the 2 lateral positions, but the modified Cormack-Lehane and percentage of glottic opening scores were superior in the supine position (all P < 0.001) compared with either of the lateral positions. CONCLUSIONS: Despite worse laryngoscopic views in either lateral position than when patients were supine, intubation with the Airway Scope offered high success rates. Furthermore, intubation time using the Airway Scope in either lateral position was not longer by >10 seconds than in the supine position. The Airway Scope thus seems to be a useful tool when tracheal intubation is required in a laterally positioned patient.

Bioavailability of hydrophobic organic contaminants in sediment with different particle-size distributions.

Few studies have been conducted examining the distribution of different-sized particles in sediment and its potential impact on bioavailability of sediment-associated contaminants. In the current study, three sediments composed of different particle sizes, i.e., fine (0-180 µm), combined (0-500 µm), and coarse (180-500 µm), were used to evaluate the bioaccumulation potential and toxicokinetic rates of four hydrophobic organic contaminants (HOCs) including two polychlorinated biphenyls (PCB-101 and PCB-118), a metabolite of an organochlorine insecticide (p,p'-DDE), and a polybrominated diphenyl ether (BDE-47) to the benthic oligochaete Lumbriculus variegatus. Two chemical approaches, Tenax extraction and matrix-solid phase microextraction (SPME), were also used to measure bioavailability of the sediment-associated HOCs. The uptake and elimination rates of HOCs by L. variegatus from coarse sediment were greater than those from fine sediment, although the biota-sediment accumulation factors (BSAFs) were not significantly different among sediments with different particle sizes. The freely dissolved HOC concentrations measured by matrix-SPME were greater in coarse sediment, however, no difference was found in uptake and desorption rates for the matrix-SPME and Tenax extraction measurements. Although BSAFs in L. variegatus were the same among sediments, kinetic rates of HOCs for organisms and freely dissolved HOC concentrations were lower in fine sediment, suggesting that sediment ingestion may also play a role in organism uptake, especially for HOCs in fine sediment.

Measuring bioconcentration factors of sediment-associated fipronil in Lumbriculus variegatus using passive sampling techniques.

Fipronil and its degradates have been detected ubiquitously in aquatic environment worldwide, yet little is known about its bioaccumulation potential. The goal of the present study was to measure bioconcentration factor (BCF) of sediment-associated fipronil in a benthic invertebrate, Lumbriculus variegatus using passive sampling techniques. Three passive samplers including polymethyl methacrylate (PMMA) film, poly(dimethylsiloxane) fiber and polyacrylate fiber were evaluated. PMMA film was identified as the preferred method and was applied to determine fipronil log KOC (3.77 ±â€¯0.04). BCF of sediment-associated fipronil in L. variegatus was obtained through measuring freely dissolved concentration (Cfree). Because fipronil degraded in sediment, time weighted average (TWA) Cfree was estimated for calculating BCFTWA (1855 ±â€¯293 mL/g lipid). Fipronil BCF was also measured in a water-only bioaccumulation test of L. variegatus under constant exposure condition. This BCF value (1892 ±â€¯76 mL/g lipid) was comparable with the BCFTWA, validating effectiveness of the passive sampling method for the measurement of sediment Cfree. Fipronil was bioaccumulative in L. variegatus according to the USEPA's criteria. The combination of Cfree and TWA concentration measurements was demonstrated to properly determine BCF value for moderately hydrophobic and degradable chemicals in sediment.

Determining equilibrium partition coefficients between lipid/protein and polydimethylsiloxane for highly hydrophobic organic contaminants using preloaded disks.

Bioaccumulation of hydrophobic organic contaminants is of great concern and understanding their partitioning to biological phases is crucial for estimating their bioaccumulation potential. The estimation, however, was of large uncertainty for highly hydrophobic organic contaminants (HHOCs) with log KOW>9 due to the challenge of quantifying their water concentrations. In the present study, partition coefficients between polydimethylsiloxane (PDMS) and storage lipid (KSL,PDMS), membrane lipid (KML,PDMS) and protein (Kpro,PDMS) were measured for 21 polychlorinated biphenyls (PCBs), 14 polybrominated diphenyl ethers (PBDEs), dechlorane plus (DP) and decabromodiphenyl ethane (DBDPE), covering log KOW from 5.07 to 11.6, using a preloaded PDMS depletion method. The values of KSL,PDMS, KML,PDMS and Kpro,PDMS were in the ranges of 5.36-52.5, 0.286-11.8 and 0.067-2.62g/g, respectively, being relatively constant although their KOW values extend more than six orders of magnitude. The relative sorption capacity of the biological phases showed storage lipid was the dominant sorption phase in biota, followed by membrane lipid and protein was the lowest. The KPDMS,pro values of the compounds with log KOW<9 were similar (0.382-14.9g/g) regardless of the thickness of preloaded PDMS disks (58-209µm). For HHOCs, however, KPDMS,pro values dropped when thinner PDMS disks were used, as a result of slow diffusion of HHOCs in PDMS. The KPDMS,pro values of HHOCs measured by 58-µm PDMS disks ranged from 1.78 to 6.85g/g, which was consistent with compounds with log KOW<9. This validated that partition coefficients between PDMS and biological phases were independent of chemical hydrophobicity, showing the advantage of using PDMS-based methods to directly estimate bioaccumulation potential of HHOCs.

[Structure analysis on growth solid-liquid boundary layer of BSO crystal at real time].

The micro Raman spectra of solid-liquid boundary layer, the melts and crystal side, were measured at real time, concerning BSO crystal grown with zone-melting method. The structure characters in boundary layer, melts and crystal were analyzed. The process, of which the growth unit structure changed while they transited from melts through boundary layer to crystal lattice, was analyzed. The results show that, there exists Bi3O4 and [SiO4] bonding structure in the melts of BSO crystal. While in the solid-liquid boundary layer, the Bi3O4 molecular units converge into [BiO7] octahedron monomer of polymer in form, the monomer or the polymer converge with the [SiO4] structure units, then all these converged structure enter into crystal lattice sites.

Two polyoxometalate-based coordination polymers constructed from Mn(II)-4,4'-bipyridine-N,N'-dioxide building blocks and Keggin-type clusters: Syntheses, crystal structures and spectral properties.

Two polyoxometalate-based coordination polymers {[Mn2(dpdo)4(H2O)6](GeMo12O40)(H2O)4}n (1) and {[Mn2(dpdo)4(H2O)6](GeW12O40)(H2O)3}n (2) (dpdo=4,4'-bipyridine-N,N'-dioxide) have been synthesized and characterized by IR, elemental analysis, XRPD, TG technique and X-ray crystallography. The polymers 1 and 2 are basically isostructural and feature a 3D supramolecular framework decorated with Keggin-type polyanion clusters based on one-dimension polymeric chains, which formed through the coordination interaction of Mn(II) and dpdo. The luminescent properties of the polymers were investigated in the solid state at room temperature.

Sorption of PBDE in low-density polyethylene film: implications for bioavailability of BDE-209.

The coefficients of partitioning (K(pew) ) between low-density polyethylene (LDPE) film (50-µm thickness) and water for 23 polybrominated diphenyl ether (PBDE) congeners were determined based on a regression analysis of sorption kinetics over an extended exposure period (up to 365 d). A curvilinear relationship between log K(pew) and log K(OW) (octanol-water partition coefficient) was obtained for the target BDE congeners with the turning point at log K(OW) approximately 8. Previously obtained dietary uptake efficiencies of BDE congeners in common carp (Cyprinus carpio) were also found to relate curvilinearly to log K(OW) . In addition, field-measured relative abundances of BDE-209 compiled from previous investigations conducted in the Pearl River Delta of South China were significantly (p < 0.001) higher in abiotic samples (n = 79 from 11 matrices) than in biotic samples (n = 73 from 12 matrices), suggesting the likelihood for reduced bioavailability of BDE-209 in certain biota. Finally, a molecular-scale analysis indicated that the curvilinear relationship between log K(pew) and log K(OW) can be attributed to the energy barrier that a molecule has to overcome as it attempts to diffuse into the LDPE structure, which can become significant for larger molecules. Similarly, the reduced bioavailability of BDE-209 in many biological species can be regarded as a reflection of the magnitude of molecular interactions between cell membranes and BDE-209.

Desorption of hydrophobic compounds from laboratory-spiked sediments measured by Tenax absorbent and matrix solid-phase microextraction.

Tenax extraction and matrix solid-phase microextraction (matrix-SPME) were used to study desorption of hydrophobic contaminants (HOC) from sediments. 14C-labeled hexachlorobiphenyl, DDE, permethrin, chlorpyrifos, and phenanthrene were individually spiked into sediments differing in physical characteristics. Sequestration of the HOCs into sediment was observed for all compounds, and desorption was described by rapid, slow, and very slow rates. The freely dissolved HOC concentration in the sediment porewater was estimated by matrix-SPME, and serial sampling was used to ensure equilibrium was achieved among sediment, porewater and matrix-SPME fiber. Differences in partitioning of the HOCs between sediment and porewater for the different sediments were reduced by replacing the HOC concentration in sediment with the rapidly desorbing fraction. The significantly lower porewater concentration determined from matrix-SPME, than predicted from equilibrium partitioning theory (EPT), showed that only a small fraction of sediment HOCs were available for equilibrium and the predictability of EPT can be improved with the consideration of sequestration in sediment. A good correlation was noted between sediment concentration in the rapidly desorbing fraction measured by Tenax extraction, and SPME fiber concentration as determined by matrix-SPME. Thus, the two methods both tracked the readily desorbed contaminant equally well though Tenax extraction measures the accessible pool, and matrix-SPME measures the chemical activity of the HOCs.