Preparation Techniques Research Articles

A comparative evaluation of sample preparation techniques for the therapeutic monitoring of carbamazepine in human plasma by RPLC/DAD

A comparative evaluation of sample preparation techniques for the therapeutic monitoring of carbamazepine in human plasma by RPLC/DAD

Cell-Mediated Immune Responses May Play Roles in Osteochondral Allograft Transplantation Osteointegration Failures.

Prolonged and incomplete osteochondral allograft (OCA) osteointegration is consistently cited as a major mechanism for OCA treatment failure. Subrejection immune responses may play roles in this mode of failure. Preimplantation OCA preparation techniques, including subchondral bone drilling, thorough irrigation, and autogenous bone marrow aspirate concentrate saturation, may dampen immune responses and improve OCA osteointegration. This study sought to further characterize potential immune system contributions to OCA transplantation treatment failures by analyzing donor-recipient ABO and Rh-factor mismatches and histological and immunohistochemical assessments of transplanted OCA tissues recovered from revision surgeries. Using a dedicated registry, OCA transplant recipients with documented treatment failures who met inclusion criteria (n = 33) as well as age-, body mass index-, and joint-matched patients with successful outcomes (n = 70) were analyzed to compare matched cohorts of patients with successful versus failed OCA transplantation outcomes. Tissues recovered from 18 failed OCA transplants and portions of 7 nonimplanted OCA controls were further analyzed to provide contributing evidence for potential immune response mechanisms. For patients analyzed, no statistically significant differences in proportions for treatment success versus failure based on mismatches for ABO type, Rh factor, or both were noted. Further, no statistically significant differences in proportions for histological immune response presence or absence based on mismatches for ABO type, Rh factor, or both were noted. Twelve (67%) of the failed OCA tissues contained lymphocyte aggregations in the subchondral bone, which were comprised of combinations of CD3 + , CD4 + , CD8 + , and CD20+ lymphocytes. The mechanisms of failure for these 12 OCA transplants involved insufficient OCA osteointegration. Results of this study suggest that T- and B-cell-mediated subrejection immune responses may play roles in OCA transplant treatment failures independent of donor-recipient blood type mismatch effects.

Review—Self-Supporting Electrocatalysts for HER in Alkaline Water Electrolysis

Abstract Hydrogen is a prime candidate for replacing fossil fuels. Electrolyzing water to produce hydrogen stands out as a particularly clean method, garnering significant attention from researchers in recent years. Among the various techniques for electrolyzing water to produce hydrogen, alkaline electrolysis holds the most promise for large-scale industrialization. The key to advancing this technology lies in the development of durable and cost-effective electrocatalysts for the hydrogen evolution reaction (HER). Self-supporting electrode is an electrode structure in which a catalyst layer is formed directly on a substrate (such as carbon cloth, nickel foam, stainless steel, etc.) without using a binder and with good structural stability. In contrast to traditional nanocatalysts, self-supporting electrocatalysts offer significant advantages, including reduced resistance, enhanced stability, and prolonged usability under high currents. This paper reviews recent advancements in HER electrochemical catalysts for alkaline water electrolysis, focusing on the utilization of hydrogen-evolving catalysts such as metal sulfides, phosphides, selenides, oxides, and hydroxides. With self-supported electrocatalysts as the focal point, the paper delves into progress made in their preparation techniques, structural design, understanding of reaction mechanisms, and strategies for performance enhancement. Ultimately, the future development direction of promoting hydrogen evolution by self-supported electrocatalysts in alkaline water electrolysis is summarized.

A new polyazomethine-based pyrazole moiety and its reinforced nanocomposites @ ZnO for antimicrobial applications

ABSTRACT A new class of biologically active polyazomethine/pyrazole and their related nanocomposites, polyazomethine/pyrazole/zinc oxide nanoparticles, have been successfully synthesized through the polycondensation technique in the form of polyazomethine pyrazole (PAZm/Py4–6) and polyazomethine/pyrazole/zinc oxide nanoparticles (PAZm/Py/ZnOa-c). The polymeric nanocomposites were prepared with a 5% loading of zinc oxide nanofiller using the same preparation technique, in addition to the help of ultrasonic radiation. The characteristics of the new polymers, such as solubility, viscometry, and molecular weight, were examined. All the polymers were completely soluble in the following solvents: concentrated sulfuric acid, formic acid, dimethylformamide, dimethyl sulfoxide, and tetrahydrofuran. Furthermore, the weight loss of the polyazomethine pyrazole (4, 5, and 6) at 800 °C was 67%, 95%, and 86%, respectively, which indicates the thermal stability of these polymers. At 800 °C, the polyazomethine/pyrazole/zinc oxide nanoparticles (a, b, and c) lost 74%, 68%, and 75% of their weight, respectively. This shows that adding zinc oxide nanoparticles made these compounds more stable at high temperatures. The X-Ray diffraction pattern of the polyazomethine pyrazole (PAZm/Py4–6) shows a number of sharp peaks with varying intensities. The polymers that were studied had straight crystal structures. Furthermore, the measurements of polyazomethine/pyrazole/zinc oxide nanoparticles (PAZm/Py/ZnOa-c) indicate a good merging of zinc oxide nanoparticles into the matrix of polymers. The antimicrobial activity of polymers and polymer nanocomposites was tested against some selected bacteria and fungi. The synthesized polymer (c) shows the highest activity against the two types of gram-negative bacteria selected. Most tested compounds were found to be effective against gram-positive bacteria except polyazomethine pyrazole (PAZm/Py5) and polyazomethine pyrazole (PAZm/Py6), which do not exhibit any activity. The synthesized polymers and their related nanocomposites were tested for their ability to kill the chosen fungi. All of them were effective against Aspergillus flavus, but only polyazomethine pyrazole (PAZm/Py4) and polyazomethine/pyrazole/zinc oxide (PAZm/Py/ZnOc) were effective against Candida albicans.

Research Progress on Taxus Extraction and Formulation Preparation Technologies

Taxus, as a globally prevalent evergreen tree, contains a wealth of bioactive components that play a crucial role in the pharmaceutical field. Taxus extracts, defined as a collection of one or more bioactive compounds extracted from the genus Taxus spp., have become a significant focus of modern cancer treatment research. This review article aims to delve into the scientific background of Taxus extracts and their considerable value in pharmaceutical research. It meticulously sifts through and compares various advanced extraction techniques such as supercritical extraction, ultrasound extraction, microwave-assisted extraction, solid-phase extraction, high-pressure pulsed electric field extraction, and enzymatic extraction, assessing each technology’s advantages and limitations across dimensions such as extraction efficiency, extraction purity, economic cost, operational time, and environmental impact, with comprehensive analysis results presented in table form. In the area of drug formulation design, this paper systematically discusses the development strategies for solid, liquid, and semi-solid dosage forms based on the unique physicochemical properties of Taxus extracts, their intended medical uses, and specific release characteristics, delving deeply into the selection of excipients and the critical technical issues in the drug preparation process. Moreover, the article looks forward to the potential directions of Taxus extracts in future research and medical applications, emphasizing the urgency and importance of continuously optimizing extraction methods and formulation design to enhance treatment efficacy, reduce production costs, and decrease environmental burdens. It provides a comprehensive set of preparation techniques and formulation optimization schemes for researchers in cancer treatment and other medical fields, promoting the application and development of Taxus extracts in pharmaceutical sciences.

Innovative Solid-Phase Extraction Strategies for Improving the Advanced Chromatographic Determination of Drugs in Challenging Biological Samples

In the past few decades, considerable scientific strides have been made in the subject of drug analysis in human biological samples. However, the risk caused by incorrect drug plasma levels in patients still remains an important concern. This review paper attempts to investigate the advances made over the last ten years in common sample preparation techniques (SPT) for biological samples based on solid sorbents, including solid-phase extraction (SPE) and solid-phase micro-extraction (SPME), and in particular in the field of molecularly imprinted polymers (MIPs), including non-stimuli-responsive and stimuli-responsive adsorbents. This class of materials is known as ‘smart adsorbents’, exhibiting tailored responses to various stimuli such as magnetic fields, pH, temperature, and light. Details are provided on how these advanced SPT are changing the landscape of modern drug analysis in their coupling with liquid chromatography-mass spectrometry (LC-MS) analytical techniques, a general term that includes high-performance liquid chromatography (HPLC) and ultra-high performance liquid chromatography (UHPLC), as well as any variation of MS, such as tandem (MS/MS), multiple-stage (MSn), and high-resolution (HRMS) mass spectrometry. Some notes are also provided on coupling with less-performing techniques, such as high-performance liquid chromatography with ultraviolet (HPLC-UV) and diode array detection (HPLC-DAD) detection. Finally, we provide a general review of the difficulties and benefits of the proposed approaches and the future prospects of this research area.

Biomechanical and histological comparison of two suture configurations for soft tissue grafts: speedtrap™ versus krackow stitch.

To compare 2 different graft preparation techniques to determine biomechanical strength and resultant tissue trauma evaluated by histology. Twelve common flexors of the finger's tendons were prepared with either tubulization (SpeedTrap™) or transtendon stiches (Orthocord™). The stiffness, resistance and energy at maximum load were tested for biomechanical assessment in both groups. After load testing, Samples were stained with hematoxylin and eosin (HE) to evaluate histological damage. We observe that the time to prepare tendons with SpeedTrap™ was 8.3 times faster (1:25min) than traditional ones (15:02min). In all cases, the mean values for SpeedTrap™ were higher in terms of strength, stiffness and energy at maximum load than for traditional suture but without significant difference (p > 0.05). The Krackow stitch produces greater structural damage to the collagen fibers while SpeedTrap™ maintains better organized arrangement of the fibers after tubulization preparation. With the results obtained, we can conclude that the tubulization technique allows faster graft preparation with less structural damage to the manipulated tissue without altering the biomechanical resistance provided by the transtendon suture technique.

Thymus schimperi Ronniger plant flowers extracted dye-sensitized solar cells

Abstract Today’s energy demand is highly increased with the world’s population growth and technological advancement. Natural dye-sensitized solar cells (N-DSSCs) are attracting research areas as an alternative and renewable energy source due to their simple preparation technique, availability, cost-effectiveness, and environmentally friendliness. In the present work, we have successfully fabricated DSSC from Thymus schimperi Ronniger plant flowers for the first time. The solvents used for extraction of the flower dye were deionized water and its mixture with ethanol. The Thymus schimperi Ronniger flowers extracted dye solutions and sensitized photoanodes were characterized by FTIR and UV-Vis characterization techniques. The crystallinity of TiO2 film was analyzed by the XRD technique and shows pure anatase phase behavior. The photoelectrochemical solar cell performance parameters, like, short circuit current density (JSC), open circuit voltage VOC), fill factor (FF), and efficiency were evaluated from the current density-voltage (J-V) measurement using a Keithley 2450 source meter. DSSC sensitized with extracted dye solution by the mixture of water and ethanol showed better performance (1.37%) as compared with that of extracted dye solution by Deionized water alone (1,02%). 

Keywords: Renewable energy, Dye-sensitized solar cells, Thymus Schimperi Ronniger, photoelectrochemical

Liquid-phase microextraction approach using supramolecular solvent formed in aqueous systems based on di(2-ethylhexyl)phosphoric acid salt: Spectrophotometric determination of antipyrine in saliva

In this study, di(2-ethylhexyl)phosphoric acid salt was investigated as a double-chain anionic surfactant for supramolecular solvent formation in a liquid-phase microextraction procedure for the first time. Inorganic electrolytes (sodium salts) were shown to be coacervation agents, due to their salting-out property in solution of sodium di(2-ethylhexyl)phosphate, obtained by deprotonation of the acid. The physico-chemical properties of the newly synthesised solvents were studied. Sodium carbonate and sodium phosphate were found to be the most suitable coacervation agents, due to their alkaline nature and low viscosity of the supramolecular solvent phases they produce. The extraction ability of the novel solvent was demonstrated in liquid-phase microextraction of a colored derivative of antipyrine from saliva for further spectrophotometric determination. The extraction recovery was found to be 70 %. The proposed green sample preparation technique enabled the exclusion of traditional toxic solvents and reduction of reagent consumption. The satisfactory analytical performance of the procedure was validated with real sample analysis. The calibration graph was linear over the concentration range of 0.03 to 0.5 mmol/L. The limit of detection (3σ) and limit of quantification (10σ), calculated from blank tests, were 0.01 and 0.03 mmol/L, respectively.

Immobilization properties and reaction mechanism of municipal solid waste incineration fly ash with alkali activation technology

Municipal solid waste incineration fly ash (MSWIFA) needs proper treatment prior to security landfilling because of considerable amounts of heavy metals and soluble chloride. Nowadays, alkali activation technology has become an effective solidification/stabilization (S/S) technology for MSWIFA. But few studies have been systematically carried out on the preparation techniques and reaction mechanism of MSWIFA S/S body. The effects of the technical parameters (alkali activator, sodium silicate modulus, alkali equivalent, water-solid ratio, curing regime) on the immobilization properties (compressive strength and heavy metal leaching toxicity) of MSWIFA S/S bodies were studied in this work. The hydration characteristics and reaction mechanism were also explored in depth based on the structure properties and microstructure characterization. Ca2+, Na+, SiO42−, [Al(OH)4]-, OH− dissociated from MSWIFA and alkali activator solution chemical reaction to form the silicates, aluminates and aluminosilicates with lower polymerization, and promoted the gel hydration products formation via depolycondensation. Lower Ca/Si molar ratio was conductive to the formation of amorphous substance, compactness of matrix pore structure and immobilization properties. Compared to the hydration products including halite, sylvine, glauberite, gypsum, calcite crystal, C–S–H gel contributed much more to the pore structure and strength improvement of MSWIFA S/S bodies. These findings will provide valuable theoretical basis for MSWIFA management and resource utilization promotion.

Exploring advanced strategies in SPME-HPLC-DAD: Enhancing analytical precision and diverse applications in modern era

In analytical chemistry, the synergy between innovative sample preparation techniques and advanced chromatographic methods has paved the way for unprecedented advancements in the analysis of complex samples. Solid Phase Microextraction (SPME) stands out as a powerful tool for extraction, and preconcentration. When coupled with High-Performance Liquid Chromatography (HPLC) equipped with a Diode Array Detector (DAD), the integrated SPME-HPLC-DAD system emerges as a sophisticated analytical platform, offering enhanced sensitivity, selectivity, and versatility for various applications. Desorption is accomplished by either depositing organic solvent in the desorption chamber or else by flowing the mobile phase through the desorption chamber specificity. An ordinary description, along with a visual illustration, has been thoroughly provided for concepts of developed well-known enhanced thin film SPME cartridges (Figure 2). The tabular representation is also available with proper description like technique name, targeted analyte, column used, mobile phase used, %RSD, extraction recovery, LOD, and data acquired R2 also considered Based on the information available in the present study. Discussed SPME with HPLC-DAD brings a great turning point by successfully utilization in biomedical sciences, environmental monitors, food safety, and clinical analysis This cost-effective, readily available technique is both environmentally friendly and stable, allowing for rapid, reliable, and accurate measurements across a wide range of analyte concentrations, thanks to the utilization of hyphenated techniques. The different strategies of SPME with HPLC -DAD and possible future apllications have been incorporated in the review. The understanding of these techniques is still limited and challenging.

Thermoset droplet curing performance in the microbond test

ABSTRACT Users of the microbond test assume that a microbond resin droplet’s properties are equivalent to a macroscale specimen. However, there is currently no standardised methodology for determining the cure state of droplet specimens used in the microbond test. In this paper, we present a technique for microbond test users to better understand the properties of thermoset droplet specimens. Utilising a conventional benchtop spectrometer, a novel sample preparation technique involving curing epoxy droplets on thin-steel filaments allowed for high-throughput determination of the microbond droplet cure state. The parity between steel filament and glass fibre microbond samples was confirmed by infrared microspectroscopy. It is shown that cure schedules used in manufacturing composite parts produced microbond droplets with degrees of cure lower than that of bulk matrix specimens subjected to an identical thermal history. Testable microbond droplets could only be prepared for commercial resin systems when introducing a room temperature pre-curing time of at least 2 h. It is concluded that microbond testing should be supported by some droplet cure state characterisation methods to ensure that interfacial effects are not artefacts of droplet sample preparation.

A bioinspired MXene-based flexible sensory neuron for tactile near-sensor computing

Multifunctional near-sensor computing sensory neurons based on the integration of flexible sensors and memristors hold promise to achieve unprecedented development in large-scale neuromorphic perception circuits and human-machine interaction systems. However, the traditional sensory-memory integrated systems are based on the integration of different device modules, which are subjected to redundant analog-to-digital conversion circuits and poor flexibility. Here, an all MXene-based flexible sensory neuron fabricated by a room temperature energy-efficient, and controllable oxidation preparation technique is reported. The near-sensor computing system is seamlessly integrated a MXene-based pressure sensor array for acquisition of tactile signals with a flexible MXene-based memristor array for simulating the implementation of perceived behavior. The tactile sensor array shows a wide range (0.1–100 kPa), high linear sensitivity (23.9 kPa−1), and the memristor array exhibits repeatable and stable bipolar resistive switching behavior (retention >100 cycles, endurance >103 s) and excellent flexibility (R=1.0 mm). As a conceptual demonstration, our devices realize high-precision recognition of handwritten digit recognition (93.21%) and human motion (97.96%), which demonstrate the feasibility for real-time health monitoring based on signals collected by sensors and artificial neural networks constructed by the memristors. The MXene-based sensor-memristor system offers a prominent contribution towards advanced application of intelligence in electronic skin and wearable electronic equipment.

The Digitization of Photographic Spectra in the Dominion Astrophysical Observatory Plate Collection with Commercial Scanners: A Pilot Study

Commercial flatbed scanners have the potential to deliver a quick and efficient means of capturing the scientific content of spectra recorded on photographic plates. We discuss the digitization of selected spectra in the Dominion Astrophysical Observatory (DAO) photographic plate collection with commercial scanners. In this pilot study, emphasis is placed on assessing if the information on the plates can be recovered using Epson V800 and 12000XL scanners; the more complicated issues associated with the shortcomings of photographic materials, such as correcting for nonlinearity, are deferred to a future study. Spectra of Vega (α Lyr) that were recorded over ∼4 decades with the DAO 1.8 m telescope are examined. These spectra sample a range of photographic emulsions, plate preparation techniques, calibration information, observing techniques, and spectrograph configuration. A scanning density of 2400 elements per inch recovers information in the spectra. Differences in the modulation transfer function (MTF) of the two scanners are found, with the Epson 12000XL having a superior MTF. Comparisons with a CCD spectrum of Vega confirm that moderately weak features are faithfully recovered in photographic spectra that have been digitized with the 12000XL scanner. The importance of scanning the full plate to cover the light profile of the target and calibration information is emphasized. Lessons learned from these experiments are also presented.

Technique of corneal allogenic ring segment preparation using femtosecond laser: preclinical study on human corneal grafts.

To describe a new technique for preparing corneal allogenic ring segments (CAIRSs) using femtosecond laser technology. Hospital Foundation Adolphe de Rothschild-Noémie de Rothschild institute, Paris, France. Preclinical study conducted on human corneal grafts. The corneal grafts were mounted on an artificial chamber pressurizer (ACP) with preset constant pressure, and the FSL was used to create a circular annulus with specific dimensions. The resulting CAIRSs were analyzed for their thickness and width after air drying. A total of 25 CAIRSs were prepared using the FSL. The mean width and thickness of the CAIRSs were 803 ± 77 μm and 83 ± 16 μm, respectively. Statistical analysis revealed no significant differences in width among the various quadrants of each CAIRS or between different CAIRSs. Significantly thicker CAIRSs were obtained with a higher ACP pressure. The technique of CAIRS preparation using FSL technology and controlled artificial anterior chamber pressure demonstrated reproducibility and precision. This approach holds the potential for customizing and personalizing CAIRSs based on individual corneal characteristics.

Scanning Electron Microscopy.

Scanning electron microscopy (SEM) remains distinct in its ability to allow topographical visualization of structures. Key elements to consider for successful examination of biological specimens include appropriate preparative and imaging techniques. Chemical processing induces structural artifacts during specimen preparation, and several factors need to be considered when selecting fixation protocols to reduce these effects while retaining structures of interest. Particular care for proper dehydration of specimens is essential to minimize shrinkage and is necessary for placement under the high-vacuum environment required for routine operation of standard SEMs. Choice of substrate for mounting and coating specimens can reduce artifacts known as charging, and a basic understanding of microscope settings can optimize parameters to achieve desired results. This article describes fundamental techniques and tips for routine specimen preparation for a variety of biological specimens, preservation of labile or fragile structures, immune-labeling strategies, and microscope imaging parameters for optimal examination by SEM. © 2024 The Authors. Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1: Chemical preparative techniques for preservation of biological specimens for examination by SEM Alternate Protocol 1: Practical considerations for the preparation of soft tissues Alternate Protocol 2: Removal of debris from the exoskeleton of invertebrates Alternate Protocol 3: Fixation of colonies grown on agar plates Alternate Protocol 4: Stabilization of polysaccharide structures with alcian blue and lysine Alternate Protocol 5: Preparation of non-adherent particulates in solution for SEM Support Protocol 1: Application of thin layer of adhesive on substrate to improve adherence Support Protocol 2: Poly-L-lysine coating specimen substrates for improved adherence Support Protocol 3: Microwave processing of biological specimens for examination by SEM Basic Protocol 2: Critical point drying of specimens Alternate Protocol 6: Chemical alternative to critical point drying Basic Protocol 3: Sputter coating Alternate Protocol 7: Improved bulk conductivity through "OTOTO" Basic Protocol 4: Immune-labeling strategies Alternate Protocol 8: Immune-labeling internal antigens with small gold probes Alternate protocol 9: Quantum dot or fluoronanogold preparations for correlative techniques Basic Protocol 5: Exposure of internal structures by mechanical fracturing Basic Protocol 6: Exposure of internal structures of tissues by fracturing with liquid nitrogen Basic Protocol 7: Anaglyph production from stereo pairs to produce 3D images.

Enhancing Odor Analysis with Gas Chromatography-Olfactometry (GC-O): Recent Breakthroughs and Challenges.

Gas chromatography-olfactometry (GC-O) has made significant advancements in recent years, with breakthroughs in its applications and the identification of its limitations. This technology is widely used for analyzing complex odor patterns. The review begins by explaining the principles of GC-O, including sample preparation, separation methods, and olfactory evaluation techniques. It then explores the diverse range of applications where GC-O has found success, such as food and beverage industries, environmental monitoring, perfume and aroma development, and forensic analysis. One of the major breakthroughs in GC-O analysis is the improvement in separation power and resolution of odorants. Techniques like rapid GC, comprehensive two-dimensional GC, and multidimensional GC have enhanced the identification and quantification of odor-active chemicals. However, GC-O also has limitations. These include the challenges in detecting and quantifying trace odorants, dealing with matrix effects, and ensuring the repeatability and consistency of results across laboratories. The review examines these limitations closely and discusses potential solutions and future directions for improvement in GC-O analysis. Overall, this review presents a comprehensive overview of the recent advances in GC-O, covering breakthroughs, applications, and limitations. It aims to promote the wider usage of GC-O analysis in odor analysis and related industries. Researchers, practitioners, and anyone interested in leveraging the capabilities of GC-O in analyzing complex odor patterns will find this review a valuable resource. The article highlights the potential of GC-O and encourages further research and development in the field.

Search for new green natural solid phases for sample preparation for PAHs determination in seafood samples followed by LC and GC–MS/MS analysis

Polycyclic aromatic hydrocarbons (PAHs) are carcinogenic organic pollutants found in various environments, notably aquatic ecosystems and the food chain, posing significant health risks. Traditional methods for detecting PAHs in food involve complex processes and considerable reagent usage, raising environmental concerns. This study explores eco-friendly approaches suing solid phases derived from natural sources in matrix solid phase dispersion. We aimed to develop, optimize, and validate a sample preparation technique for seafood, employing natural materials for PAH analysis. Ten natural phases were compared with a commercial reference phase. The methodology involved matrix solid phase dispersion and pressurized liquid extraction, followed by liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS). Three solid phases (perlite, sweet manioc starch, and barley) showed superior performance in LC-MS/MS and were further evaluated with gas chromatography-tandem mass spectrometry (GC–Ms/MS), confirming perlite as the most effective phase. Validation followed Brazilian regulatory guidelines and European Community Regulation 2021/808/EC. The resulting method offered advantages in cost-effectiveness, reduced environmental impact, cleaner extracts, and enhanced analytical performance compared to the reference solid phase and LC-MS/MS. Proficiency analysis confirmed method reliability, with over 50% alignment with green analytical chemistry principles. In conclusion, this study developed an environmentally sustainable sample preparation technique for seafood analysis using natural solid phases, particularly perlite, for PAH determination.

Fixation for Knee Cartilage Injuries – An International Delphi Consensus Statement

PURPOSEThe purpose of this study was to establish consensus statements via a Delphi process on cartilage fixation techniques and indications. METHODSA consensus process on knee cartilage injuries utilizing a modified Delphi technique was conducted. Seventy-nine surgeons across 17 countries participated in these consensus statements. Fourteen questions were generated on cartilage fixation, with three rounds of questionnaires and final voting occurring. Consensus was defined as achieving 80-89% agreement, whereas strong consensus was defined as 90-99% agreement, and unanimous consensus was defined as 100% agreement with a proposed statement. RESULTSOf the 14 total questions and consensus statements on cartilage fixation developed from three rounds of voting, zero achieved unanimous consensus, eight achieved strong consensus, three achieved consensus, and three did not achieve consensus. CONCLUSIONThe statements achieving strong consensus related to indications and contraindications, the expectation that younger patients experience better outcomes, an agreement that procedures should be done as soon as possible but no limit on timeframe, cartilage preparation techniques, and the use of fragment stability to guide cartilage fixation techniques. The statements that did not achieve consensus related to the minimum size of cartilage fragments that can be fixed, if purely cartilaginous lesions can be fixed, and the fixation techniques. Level of EvidenceLevel V Expert Opinion.

Green sorbents in sample preparation techniques – naturally occurring materials and biowastes

Green sorbents in sample preparation techniques – naturally occurring materials and biowastes