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Centrifugation is a time-consuming step which increases the turnaround time (TAT) in laboratories. A few studies have addressed the effect of altering centrifugation settings on analytical quality for clinical chemistry analytes, and most of these studies have used collection tubes with gel separators. However, gel separator tubes may be unsuitable for some laboratories because they are slightly more expensive than tubes without gel separators and are not appropriate for some special tests. The aim of this study was to investigate the effect of centrifugation conditions on clinical chemistry analytes.

The nitrate concentration in the subsoil moisture of the vadose zone is an important indicator for future groundwater quality, which is classically determined via centrifugation. Batch extraction is an inexpensive and easy alternative method, but whether these methods measure the same soil water, nitrogen species, and nitrate concentrations is unclear, in particular for loess soils. Two experiments were carried out to assess the differences in nitrate and other anion concentrations between centrifugated soil moisture (centrifugated at different speeds and times) and batch extractions (using double-distilled water and 0.01 M CaCl2). Batch extraction resulted in lower nitrate (−20%) and chloride (−15%) concentrations than centrifugation, mainly due to anion exclusion, where soil microporosity controls the contribution of diffusion, denitrification, and leaching processes. Vice versa, batch extraction overestimated the concentration of nutrients that occur as precipitates in or sorb the soil matrix, such as sulphate (+50%) and ammonium (+96%). Batch extractions can only be used as a proxy to determine actual nitrate concentrations of soil water. However, they are useful to monitor changes in nitrate leaching over time in response to (policy) measures taken. They can also be used as "early warning indicator" and to improve the reliability of spatial explicit monitoring networks. [ABSTRACT FROM AUTHOR]

Aim: A force of 400 g at 2700 revolutions per minute (RPM) results in an optimum leukocyte and platelet-rich fibrin (L-PRF). Most of centrifuges with varying characteristics generate a g-force in excess of 700 g at 2700 RPM. In this context, the study explores the effect of the original centrifugation protocol and a modified protocol tailor-made to lower the RPM to generate a g-force of ~ 400 g on platelet concentration, clot size and growth factors release in L-PRF prepared in two different commercially available centrifuges. Materials and Methods: Twenty five subjects each were assigned to the following groups; R1 and R2 where L-PRF was obtained from two laboratory swing-out centrifuges (Remi 8C® and Remi C854®, Mumbai, India), respectively. PRF was obtained from each subject within a group using two protocols; Original (O) protocol: conforming to the original centrifugation cycle (2700 RPM for 12 min) and Modified (M) protocol. Clot size, growth factor estimation, and platelet counts were measured at 20, 40, and 60 min from all the L-PRF clots, respectively. Results: At the third time period (40–60 min), there were no significant differences in clot sizes with the original protocol (P = 0.09), but a highly significant difference was noticed with the modified protocol in both the centrifuges (P = 0.001). Our results showed an increased concentration of vascular endothelial growth factor and epidermal growth factor with modified protocol than with original protocol with both the centrifuges (P = 0.001). By the end of second and third time periods, more platelet concentration was observed with modified protocol than with the original protocol in both the centrifuges (P = 0.001). Conclusion: This study infers that the centrifuge type and relative centrifugal force can affect the quality and quantity of cells and growth factors and an optimum relationship between g-force and RPM should be maintained to obtain L-PRF with adequate cell viability and optimum growth factor release.

Aim: A force of 400 g at 2700 revolutions per minute (RPM) results in an optimum leukocyte and platelet-rich fibrin (L-PRF). Most of centrifuges with varying characteristics generate a g-force in excess of 700 g at 2700 RPM. In this context, the study explores the effect of the original centrifugation protocol and a modified protocol tailor-made to lower the RPM to generate a g-force of ~ 400 g on platelet concentration, clot size and growth factors release in L-PRF prepared in two different commercially available centrifuges. Materials and Methods: Twenty five subjects each were assigned to the following groups; R1 and R2 where L-PRF was obtained from two laboratory swing-out centrifuges (Remi 8C® and Remi C854®, Mumbai, India), respectively. PRF was obtained from each subject within a group using two protocols; Original (O) protocol: conforming to the original centrifugation cycle (2700 RPM for 12 min) and Modified (M) protocol. Clot size, growth factor estimation, and platelet counts were measured at 20, 40, and 60 min from all the L-PRF clots, respectively. Results: At the third time period (40–60 min), there were no significant differences in clot sizes with the original protocol (P = 0.09), but a highly significant difference was noticed with the modified protocol in both the centrifuges (P = 0.001). Our results showed an increased concentration of vascular endothelial growth factor and epidermal growth factor with modified protocol than with original protocol with both the centrifuges (P = 0.001). By the end of second and third time periods, more platelet concentration was observed with modified protocol than with the original protocol in both the centrifuges (P = 0.001). Conclusion: This study infers that the centrifuge type and relative centrifugal force can affect the quality and quantity of cells and growth factors and an optimum relationship between g-force and RPM should be maintained to obtain L-PRF with adequate cell viability and optimum growth factor release. [ABSTRACT FROM AUTHOR]

Centrifugation separates particles within the specimen according to their shape, dimensions, and density and basically can be defined as a separation method. The centrifuge is an essential device in medical laboratories to prepare the serum, plasma, and urine samples for analysis. It is basically an electric device composed of the stationary (motor) and the motile (rotor) part. The centrifugation depends on two main variables: relative centrifugal force (RCF) and centrifugation time. The physical impact separating the specimen into its components in the centrifuge known as RCF is expressed as the multiples of gravitational acceleration (×g). RPM, defined as the number of rotations of the centrifuge per minute, shows the speed of the centrifuge. RCF value can be calculated by using RPM, and the centrifuge radius. Because models and sizes of centrifuges vary considerably, the use of gravity (g) forces instead of RPM is suggested. The centrifuges can be classified according to their usage, speed, technical specifications, and rotor type. An accurate and precise centrifugation process is essential to prevent errors in the preanalytical phase. The purpose of this document is to ensure the standardization of a good, precise protocol for the centrifugation process among the medical laboratories. [ABSTRACT FROM AUTHOR]

CENP-E (centromere protein E) and CENP-F (centromere protein F), also known as mitosin, are large, multi-functional proteins associated with the outer kinetochore. CENP-E features a well-characterized kinesin motor domain at its N-terminus and a second microtubule-binding domain at its C-terminus of unknown function. CENP-F is important for the formation of proper kinetochore-microtubule attachment and, similar to CENP-E, contains two microtubule-binding domains at its termini. While the importance of these proteins is known, the details of their interactions with microtubules have not yet been investigated. We have biochemically and structurally characterized the microtubule-binding properties of the amino- and carboxyl-terminal domains of CENP-F as well as the carboxyl-terminal (non-kinesin) domain of CENP-E. CENP-E's C-terminus and CENP-F's N-terminus bind microtubules with similar affinity to the well-characterized Ndc80 complex, while CENP-F's C-terminus shows much lower affinity. Electron microscopy analysis reveals that all of these domains engage the microtubule surface in a disordered manner, suggesting that these factors have no favored binding geometry and may allow for initial side-on attachments early in mitosis.

：Objective To observe and compare the growth factor release levels of platelet-rich fibrin (PRF) prepared under different centrifugation conditions and its effect on the proliferation and migration of fibroblasts. Methods The whole blood of SD rats was obtained by cardiac blood sampling，and the leukocyte-rich PRF (L-PRF)，advanced PRF (A-PRF)，and advanced PRF+（A-PRF+）were obtained by three centrifugal procedures of 708 g 12 min，208 g 14 min, and 208 g 8 min. The PRF diaphragm was pressed and placed in DMEM/F12 medium which was then collected at 1h，6h, 1 d, 3 d，and 5 d，respectively. The platelet-derived growth factor (PDGF-Ab)，transforming growth factor β (TGFβ)，and vascular endothelial growth factor（VEGF）in the culture medium were detected by ELISA. Skin fibroblasts were isolated and cultured from the dorsal skin of SD rats，and then were divided into the L-PRF group，A-PRF group, A-PRF+ group, and blank group, which were cultured in L-PRF，A-PRF，and A-PRF+ conditioned medium and 10% FBS medium, respectively. CCK-8 cell proliferation assay was used to detect cell proliferation，and Transwell chamber assay was used to detect cell migration. Results The overall release levels of PDGF-Ab，TGF-β and VEGF in A-PRF and A-PRF+ medium were higher than those in L-PRF medium within 5 days after preparation（all P<0. 05）. The cell proliferation abili‐ ties of the A-PRF+ group，A-PRF group，and L-PRF group were higher than that of blank group on day 3 and 5，and the cell proliferation abilities of the A-PRF+ group and A-PRF group were higher than that of L-PRF group on day 3（all P< 0. 05）. The numbers of transmembrane cells in the L-PRF group, A-PRF group，and A-PRF+ group were higher than that in the blank group，and the numbers of transmembrane cells in the A-PRF group and A-PRF+ group were higher than that in the L-PRF group（all P<0. 05). Conclusion The effects of A-PRF+ and A-PRF prepared by reducing the relative cen‐ trifugal force on the growth factor release and promoting the proliferation and migration of fibroblasts were significantly stron‐ ger than that of L-PRF，and the effects of A-PRF+ obtained by appropriately shorting the centrifugal time were stronger. [ABSTRACT FROM AUTHOR]

CNT nanofluids are getting attention in heat transfer applications due to their very high thermal conductivity in comparison with conventional fluids. For commercial exploitation of CNT nanofluids as heat transfer media, they must have long-term stability. In this study, the two-step method was modified to prepare dynamically stable CNT nanofluids by utilizing commercial grade multiwalled carbon nanotubes and SDBS as a surfactant. The modified technique consists of separation of coarse agglomerates of CNT from the CNT nanofluids by applying centrifugal action after its preparation. The effect of relative centrifugal force was also studied for the very first time on the stable concentration of CNT nanofluids. The stability of CNT nanofluids was analyzed by measurement of their CNT concentration and Zeta potential. Results showed that CNT nanofluids possess good stability and remain stable for more than 15 months. In addition to stability, thermo-physical properties such as thermal conductivity, density, and viscosity of CNT nanofluids were also measured. The results of this study elucidated the effect of RCF on the stable concentration of CNT nanofluids. It is expected that the results obtained in this study may significantly contribute to the proper tailoring of CNT nanofluids, by providing long-term stable CNT nanofluids which are suitable for industrial heat transfer applications. [ABSTRACT FROM AUTHOR]

Highlights: [•] Scientific and clinical need to determine free antibiotic for PK/PD optimisation. [•] Ultrafiltration is appropriate to determine free drug concentrations routinely. [•] Physiological conditions, 37°C and pH 7.4, should be aimed. [•] High relative centrifugal forces result in false low free concentrations. [ABSTRACT FROM AUTHOR]

Nogo-A is a transmembrane protein originally discovered in myelin, produced by postnatal CNS oligodendrocytes. Nogo-A induces growth cone collapse and inhibition of axonal growth in the injured adult CNS. In the intact CNS, Nogo-A functions as a negative regulator of growth and plasticity. Nogo-A is also expressed by certain neurons. Neuronal Nogo-A depresses long-term potentiation in the hippocampus and modulates neurite adhesion and fasciculation during development in mice. Here we show that Nogo-A is present in neurons derived from human midbrain (Lund human mesencephalic (LUHMES) cell line), as well as in embryonic and postnatal mouse midbrain (dopaminergic) neurons. In LUHMES cells, Nogo-A was upregulated threefold upon differentiation and neurite extension. Nogo-A was localized intracellularly in differentiated LUHMES cells. Cultured midbrain (dopaminergic) neurons from Nogo-A knock-out mice exhibited decreased numbers of neurites and branches when compared with neurons from wild-type (WT) mice. However, this phenotype was not observed when the cultures from WT mice were treated with an antibody neutralizing plasma membrane Nogo-A. In vivo, neither the regeneration of nigrostriatal tyrosine hydroxylase fibers, nor the survival of nigral dopaminergic neurons after partial 6-hydroxydopamine lesions was affected by Nogo-A deletion. These results indicate that during maturation of cultured midbrain (dopaminergic) neurons, intracellular Nogo-A supports neurite growth initiation and branch formation., (Copyright © 2013 IBRO. Published by Elsevier Ltd. All rights reserved.)

Objectives: The aim of this study was to examine lumbar CSF-VEGF levels from elderly patients with ventriculomegaly to evaluate the possible circadian or periodic concentration profile and relevance to the prediction of drainage response., Methods: Lumbar CSF samples were collected in 1-h interval over 35 h from 22 patients with ventriculomegaly. CSF-VEGF levels were measured to elucidate the possible circadian or periodic concentration profiles. These VEGF levels were evaluated for correlations with clinical response to CSF drainage, ventricle size and other clinical information., Results: The 35-h CSF-VEGF levels demonstrated a periodic concentration pattern with significant episodic fluctuation with 3-5h intervals. CSF-VEGF levels in non-responder group in which patients did not show clinical improvement with CSF drainage were significantly higher than these in responder group., Conclusion: VEGF variation in hydrocephalus patients suggests its possible pathophysiological role in hydrocephalus. The periodic concentration pattern of CSF-VEGF must be considered when choosing the most appropriate time for sample collection or clinical manipulation. Increased VEGF level in patients who showed no improvement with CSF drainage suggests that a possible greater ischemic or vascular injury may play a role in these patients. Pending further studies, these results suggest that high VEGF levels have a potential application in predicting non-responder patients with CSF drainage and so reducing the morbidity and cost of drainage and shunting in these patients., (Copyright © 2013. Published by Elsevier B.V.)