854 research outputs found
ENVIRONMENT, EQUITY AND WATERSHED MANAGEMENT
This paper presents a methodology for incorporating environmental and social equity objectives in an economic analysis of watershed management. Empirical results indicate that restricting agricultural pollution notably increases farm costs. The equity objective also adversely affects economic efficiency, but the cost increase due to social equity is less significant.Environmental Economics and Policy,
Graphical User Interface Development and Design to Support Airport Runway Configuration Management
The objective of this effort was to develop a graphical user interface (GUI) for the National Aeronautics and Space Administration's (NASA) System Oriented Runway Management (SORM) decision support tool to support runway management. This tool is expected to be used by traffic flow managers and supervisors in the Airport Traffic Control Tower (ATCT) and Terminal Radar Approach Control (TRACON) facilities
Towards a Soft Robotic Skin for Autonomous Tissue Palpation
Manual palpation is commonly used to localize tumors and other features buried deep inside organs during open surgery. This approach is not feasible in minimally invasive or robotic surgery, as the contact with the tissue is mediated by instruments. To address this problem, we propose a soft robotic skin (SRS) that can be deployed from a small incision and create a stiffness map in a single step. Such a skin is composed of a matrix of soft robotic tactile elements (SRTEs), each one able to expand and record the tissue response during expansion. In this paper, we firstly prove the feasibility of palpation using a single SRTE. Then, we present and test a soft-suction based anchoring mechanism able to keep the SRS in the desired position in contact with the tissue, allowing surgeons to palpate different sides of the organ. Finally, we detail a calibration method for the SRTE, and assess the feasibility of identifying lumps buried inside a soft tissue phantom, and then inside a chicken liver during an ex-vivo trial. Experimental results show that the SRTE was able to differentiate simulated lumps (up to 3.25 mm deep) from healthy tissue in both the phantom and the ex-vivo trials. These results, added to the ability of the suction gripper to compensate for the expansion forces of each SRTE, are paving the way for soft robotic autonomous tools that can be used for intraoperative mapping of tissue cancers
Penicillin-Induced Epileptiform Ecog Activity in Gerbils: Effects of Physical Exercise and a Diospyros Kaki Extract
Mongolian gerbils (28 males) were divided into four groups, control (C), treadmill-exercised
(Ex), treated with the extract of Diospyros kaki (Dk), and treated with the Dk extract plus
exercised (Ex+Dk) groups. Animals of the respective groups were running-exercised for
30 min per day during 8 weeks, and the Dk extract (dose 20mg/kg) was given by gavage
during five days per week within the same period. After the treatment and exercise period,
an epilepsy model was produced by penicillin G injection (500 IU) into the left somatomotor
cortex, and electrocorticogram (ECoG) was recorded during 120 min. The mean frequency of
spike/wave complexes was significantly smaller in the Ex and Ex+Dk groups from the 65th
min of the observation period and, in the Dk group, from the 75th min than the respective
value in the C group (P < 0.01, P < 0.05, and P < 0.01, respectively). The differences in the
amplitude values and latency to onset of the spike/wave events among all groups usally did
not reach the significance level (P > 0.05), but, visin late stages of the observation period,
an antiseisure effect of the Dk extract was obvious. Thus, both the running exercise and
Dk extract applications inhibit penicillin-induced epileptiform activity by altering the spike/
wave frequency or severity of seizures observed in ECoG recordings. Further studies are
needed to determine the effects of physical activity of different intensities and forms and to
analyze the active compounds in the Dk extract.Монгольські піщанки (28 самців) були поділені на
чотири групи – контрольну (C), піддану тренуванню
на тредбані (Ex), групу з уведенням екстракту Diospyros kaki (східної хурми, група Dk) та групу з уведенням
вказаного екстракту, комбінованим із тренуванням
(Ex+Dk). Тварин відповідних груп тренували, примушуючи
бігати 30 хв на день протягом восьми тижнів; екстракт
Dk (20 мг/кг) уводився перорально п’ять днів на тиждень
протягом того самого періоду. Після періоду тренування
та введення екстракту у щурів індукували модельну
епілепсію за допомогою ін’єкції 500 МО пеніциліну G у
ліву соматомоторну кору і відводили електрокортикограму
(ЕКоГ) протягом 20 хв. У групах Ex та Ex+Dk середня
частота виникнення комплексів пік/хвиля була вірогідно
меншою, ніж у контролі, починаючи з 65-ї хв періоду
спостереження; те саме відмічалося в групі Dk починаючи
з 75-ї хв вказаного періоду (P < 0.01, P < 0.05 та P < 0.01
відповідно). Відмінності значень амплітуди ЕКоГ та
латентного періоду до появи комплексів пік/хвиля в усіх
групах звичайно не досягали рівня вірогідності (P > 0.05),
але на пізній ділянці періоду спостереження антисудомний
вплив екстракту Dk був очевидним. Отже, тренування бігом
та уведення екстракту хурми східної пригнічує індуковану
пеніциліном епілептиформну активність, змінюючи частоту
комплексів пік/хвиля та інтенсивність судомної активності,
що спостерігається в ЕКоГ. Потрібні подальші дослідження
для того, щоб визначити ефекти фізичної активності
різної інтенсивності та форми та проаналізувати активні
компоненти екстракту хурми
A novel method for spectrophotometric determination of pregabalin in pure form and in capsules
<p>Abstract</p> <p>Background</p> <p>Pregabalin, a γ-amino-n-butyric acid derivative, is an antiepileptic drug not yet official in any pharmacopeia and development of analytical procedures for this drug in bulk/formulation forms is a necessity. We herein, report a new, simple, extraction free, cost effective, sensitive and reproducible spectrophotometric method for the determination of the pregabalin.</p> <p>Results</p> <p>Pregabalin, as a primary amine was reacted with ninhydrin in phosphate buffer pH 7.4 to form blue violet colored chromogen which could be measured spectrophotometrically at λ<sub>max </sub>402.6 nm. The method was validated with respect to linearity, accuracy, precision and robustness. The method showed linearity in a wide concentration range of 50-1000 μg mL<sup>-1 </sup>with good correlation coefficient (0.992). The limits of assays detection was found to be 6.0 μg mL<sup>-1 </sup>and quantitation limit was 20.0 μg mL<sup>-1</sup>. The suggested method was applied to the determination of the drug in capsules. No interference could be observed from the additives in the capsules. The percentage recovery was found to be 100.43 ± 1.24.</p> <p>Conclusion</p> <p>The developed method was successfully validated and applied to the determination of pregabalin in bulk and pharmaceutical formulations without any interference from common excipients. Hence, this method can be potentially useful for routine laboratory analysis of pregabalin.</p
Spectrofluorimetric determination of sertraline in dosage forms and human plasma through derivatization with 9-fluorenylmethyl chloroformate
<p>Abstract</p> <p>Background</p> <p>Sertraline is primarily used to treat major depression in adult outpatients as well as obsessive-compulsive, panic and social anxiety disorders in both adults and children. A survey of the literature reveals that most of the reported methods are either insufficiently sensitive or tedious and require highly sophisticated and dedicated instrumentation. The proposed method is considered to be specific for determination of SER in presence of its metabolite (deaminated form).</p> <p>Results</p> <p>A sensitive, simple and specific spectrofluorimetric method was developed for the determination of sertraline (SER) in pharmaceutical formulations and biological fluids. The method is based on its reaction with 9-fluorenylmethyl chloroformate (FMOC-Cl) in borate buffer of pH 8.0 to yield a highly fluorescent derivative peaking at 315 nm after excitation at 265 nm. The different experimental parameters affecting the development and stability of the reaction product were carefully studied and optimized. The fluorescence concentration plot was rectilinear over the range of 0.05-1.0 μg mL<sup>-1 </sup>with a lower detection limit of 5.34 × 10<sup>-3 </sup>μg mL<sup>-1 </sup>and limit of quantitation of 0.016 μg mL<sup>-1</sup>.</p> <p>Conclusions</p> <p>The proposed method was successfully applied to the analysis of commercial tablets and the results obtained were in good agreement with those obtained using the reference method. Furthermore, the method was applied for the determination of SER in spiked and real human plasma. The mean % recovery (n = 3) was 94.33 ± 1.53 and 92.00 ± 2.65, respectively. A proposal of the reaction pathway was postulated.</p
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