pump

  • 文章类型: Journal Article
    在牙科植入物中实现对液体释放的微创和精确控制对于治疗功能至关重要,例如递送抗生素以防止生物膜形成。注入干细胞以促进骨整合,和管理其他生物医学。然而,由于缺乏无线和小型化的流体控制机制,在牙科植入物中实现可控的液体货物释放仍然具有挑战性。在这里,无线微型泵和阀门,允许远程激活牙科植入物中的液体货物输送,由外部磁场(<65mT)驱动和控制,已报告。流体通道中的磁体-螺杆机构用作活塞泵,与设计用于打开和关闭流体通道的柔性电磁阀一起,是提议的。通过在牙科植入物中存储和释放高达52µL的液体来展示该机制。液体货物直接输送到植入物-骨界面,传统上难以进入的地区。牙科体模和猪颌骨内部的金属植入物进一步显示了按需液体递送。该机制有望在植入后以最小的侵入性控制液体释放,为在各种生物工程应用中实现治疗剂的长期和靶向递送的可植入装置铺平了道路。
    Enabling minimally invasive and precise control of liquid release in dental implants is crucial for therapeutic functions such as delivering antibiotics to prevent biofilm formation, infusing stem cells to promote osseointegration, and administering other biomedicines. However, achieving controllable liquid cargo release in dental implants remains challenging due to the lack of wireless and miniaturized fluidic control mechanisms. Here wireless miniature pumps and valves that allow remote activation of liquid cargo delivery in dental implants, actuated and controlled by external magnetic fields (<65 mT), are reported. A magnet-screw mechanism in a fluidic channel to function as a piston pump, alongside a flexible magnetic valve designed to open and close the fluidic channel, is proposed. The mechanisms are showcased by storing and releasing of liquid up to 52 µL in a dental implant. The liquid cargos are delivered directly to the implant-bone interface, a region traditionally difficult to access. On-demand liquid delivery is further showed by a metal implant inside both dental phantoms and porcine jawbones. The mechanisms are promising for controllable liquid release after implant placement with minimal invasion, paving the way for implantable devices that enable long-term and targeted delivery of therapeutic agents in various bioengineering applications.
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  • 文章类型: Journal Article
    被动记录数据的能力,基于图像的可穿戴传感器可以简化数据读出,并消除了在皮肤上集成电子元件的要求。这里,我们开发了一种皮肤应变驱动的微流体泵(SAMP),它利用不对称的纵横比通道来记录流体域中的人类活动。建立了描述SAMP作为可穿戴微流控设备的工作机制的分析模型。使用来自聚二甲基硅氧烷(PDMS)的软光刻实现SAMP的制造。结果表明,基准实验结果与理论预测结果吻合良好。SAMP安装在人体皮肤上,对志愿者进行的实验表明,SAMP能够通过观察稳定的液体弯月面来记录流体域中数百个循环的人类活动。概念验证实验进一步表明,SAMP可以量化单个手腕活动重复或区分三种不同的肩部活动。
    The capability to record data in passive, image-based wearable sensors can simplify data readouts and eliminate the requirement for the integration of electronic components on the skin. Here, we developed a skin-strain-actuated microfluidic pump (SAMP) that utilizes asymmetric aspect ratio channels for the recording of human activity in the fluidic domain. An analytical model describing the SAMP\'s operation mechanism as a wearable microfluidic device was established. Fabrication of the SAMP was achieved using soft lithography from polydimethylsiloxane (PDMS). Benchtop experimental results and theoretical predictions were shown to be in good agreement. The SAMP was mounted on human skin and experiments conducted on volunteer subjects demonstrated the SAMP\'s capability to record human activity for hundreds of cycles in the fluidic domain through the observation of a stable liquid meniscus. Proof-of-concept experiments further revealed that the SAMP could quantify a single wrist activity repetition or distinguish between three different shoulder activities.
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  • 文章类型: Journal Article
    BACKGROUND: The first pump for intrathecal administration of baclofen was implanted in 1984. Over thirty years, intrathecal prolonged infusion of muscle relaxants has occupied a worthy niche among all methods for correction of non-focal drug-resistant disabling muscle spasticity. However, this method has not become routine despite high awareness of specialists in Russia and abroad, as well as undeniable advantages for restoring the daily activity, improving the walking pattern and providing care and quality of life in people with limited mobility. This is due to scrupulous analysis of adverse events and accurate attitude towards its use.
    The purpose of this review was to systematize data on indications, selection criteria, pump implantation technique, subsequent patient management and treatment outcomes over a 30-year history.
    METHODS: A review of national and foreign literature was performed.
    CONCLUSIONS: Prolonged intrathecal baclofen therapy is perspective for long-term treatment of severe spasticity interfering with quality of life and self-care if oral muscle relaxants are contraindicated or ineffective. This procedure is effective for impaired articulation, chewing and spastic pain syndrome. One can reduce the incidence of side effects via correct dosage of the drug, and tolerance to therapy can be reduced by timely elimination of problems with catheter.
    Начавшись с первой имплантированной помпы для интратекального введения баклофена в 1984 г., за 30 лет использования метод интратекальной пролонгированной инфузии миорелаксантов занял достойную нишу среди способов коррекции нефокальной резистентной инвалидизирующей мышечной спастичности. Однако метод не стал рутинным, несмотря на высокую информированность специалистов как в России, так и за рубежом, и неоспоримые преимущества для восстановления повседневной активности и улучшения стереотипа ходьбы у пациентов с высоким уровнем функциональных возможностей, а также для обеспечения ухода и качества жизни маломобильных больных, что обусловлено скрупулезным анализом нежелательных явлений и взвешенным отношением к его использованию.
    UNASSIGNED: Систематизация информации по показаниям, критериям отбора на операцию, технике проведения имплантации помпы, последующему ведению пациентов и результатам лечения за 30-летний период применения метода.
    UNASSIGNED: Выполнен повествовательный обзор отечественной и зарубежной литературы.
    UNASSIGNED: Изучение источников литературы позволяет сделать вывод о перспективности пролонгированного интратекального введения баклофена в долгосрочной терапии выраженной спастичности, нарушающей качество жизни и самообслуживание, при непереносимости или неэффективности пероральных миорелаксантов. Процедура эффективна при нарушении артикуляции, жевания, спастическом болевом синдроме. Частоту побочных эффектов можно снизить за счет корректной дозировки препарата, а толерантность к терапии — своевременным устранением проблем с катетером.
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  • 文章类型: Journal Article
    本文介绍了一种确定卫星容积式机器(泵和电机)几何工作容积的方法。这些机器的工作机构是由两个非圆齿轮(转子和曲率)和圆齿轮(卫星)组成的卫星机构。提出了卫星机制的两种变体。在第一种机制中,转子的滚动线是围绕一个圆的正弦曲线。在第二种机制中,转子的滚动线是围绕一个圆的双正弦曲线。提出了一种根据转子旋转角度计算工作室面积的方法,根据转子的数学公式,曲率和卫星滚动线。已经示出,卫星机构的第二变型有利地特征在于工作室的最大面积与该工作室的最小面积之间的较大差异。已经提出了新的数学公式,以根据该室面积的最大值和最小值计算轴(转子)的任何旋转角度的工作室面积。因此,可以确认,几何工作体积取决于工作室的最大和最小面积以及卫星机构的高度。对没有齿轮的机构(由机构元件的滚动线限定的区域)和有齿轮的实际机构都进行了工作室面积的分析。还检测到这些字段的值的差异。
    This article describes a method for determining the geometric working volume of satellite positive displacement machines (pump and motor). The working mechanism of these machines is satellite mechanism consisting of two non-circular gears (rotor and curvature) and circular gears (satellites). Two variants of the satellite mechanism are presented. In the first mechanism, the rolling line of the rotor is a sinusoid \"wrapped\" around a circle. In the second mechanism, the rolling line of the rotor is a double sinusoid \"wrapped\" around a circle. A method for calculating the area of the working chamber as a function of the rotor rotation angle is presented, based on mathematical formulae of the rotor, the curvature and the satellite rolling lines. It has been shown that the second variant of the satellite mechanism is advantageously characterised by a larger difference between the maximum area of the working chamber and the minimum area of this chamber. New mathematical formulas have been proposed to calculate the area of the working chamber for any angle of rotation of the shaft (rotor) based on the maximum and minimum values of the area of this chamber. It was thus confirmed that the geometric working volume depends on the maximum and minimum area of a working chamber and on the height of the satellite mechanism. The analyses of the area of the working chamber were carried out both for the mechanism without gears (the area delimited by the rolling lines of the elements of the mechanism) and for the real mechanism with gears. Differences in the values of these fields were also detected.
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  • 文章类型: Case Reports
    甲状旁腺功能减退是Sanjad-Sakati综合征儿童最常见的内分泌特征。治疗包括活性维生素D和钙补充。这里,我们报告1例新生儿Sanjad-Sakati综合征,出生后出现严重的低钙血症,对PTH皮下泵输注有反应.从出生的第一天起,该孩子出生35周时患有低钙血症。标准的药物治疗对新生儿无效,需要给予异常高剂量的口服和IV钙和维生素D类似物2个月。因此,开始间歇性皮下注射PTH,导致钙水平的初步改善,虽然这被证明是短暂的。随后,通过美敦力Vio泵进行连续输液的切换,不幸的是导致医源性高钙血症,需要高钙血症的管理。稍后,对于甲状旁腺功能减退症患者,继续以较低的剂量恢复碳酸钙和阿法骨化醇,并且继续具有平均需求.PTH皮下输注在难治性低钙血症病例中非常有效,并且可以显着影响治疗过程并促进出院,如我们的病例所示。需要仔细的剂量和监测以避免医源性高钙血症。
    Hypoparathyroidism is the most common endocrinological feature in children with Sanjad-Sakati syndrome. Treatment includes active vitamin D and calcium supplementation. Here, we report a case of a newborn with Sanjad-Sakati syndrome who had severe hypocalcemia since birth who responded to PTH subcutaneous pump infusion. The child was born at 35 weeks with hypocalcemia since the first day of life. The standard medical treatment proved ineffective for the newborn, necessitating the administration of unusually high doses of oral and IV calcium and vitamin D analogue for a 2 months. As a result, intermittent subcutaneous injections of PTH were commenced, resulting in an initial improvement in calcium levels, although this proved to be short-lived. Subsequently, a switch to continuous infusion via a Medtronic Vio pump was made, which unfortunately resulted in iatrogenic hypercalcemia, requiring management of hypercalcemia. Later, calcium carbonate and alfacalcidol were resumed at a lower dosage and continued to have average requirements for patients with hypoparathyroidism. PTH subcutaneous infusion can be highly effective in refractory hypocalcemia cases and can significantly impact the treatment course and facilitate hospital discharge as seen in our case. Careful dosage and monitoring are required to avoid iatrogenic hypercalcemia.
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  • 文章类型: Journal Article
    这项体外研究的目的是评估将输注管线连接到中心静脉导管的旋塞的垂直水平对微量输注中的启动流体输送的影响。在标准化条件下测量启动流体输送,其中注射器出口和液体流量传感器定位在心脏水平(0cm)处并以1ml/h的设定流速暴露于10mmHg的模拟CVP。流量和腔内压力是用输液管连接到主要放置在垂直水平0厘米的旋塞测量的。+30厘米和-30厘米或主要放置在0厘米,其次,在连接输液管之后,位移到+30厘米和-30厘米。打开置于零位的旋塞阀10s后和打开主要连接在零位的旋塞阀10s后,二次位移至+30cm和-30cm的垂直水平的启动流体输送相似(-10.52[-13.85至-7.19]微升;-8.84[-12.34至-5.33]微升和-11.19[-13.71至-8.67]微升(p=0.469))。以360秒输送的流体与65%相关(零水平),计算输注量的71%(+30cm)和67%(-30cm)(p=0.395)。将旋塞主要放置在+30cm和-30cm处的启动流体输送导致在10s时出现34.39[33.43至35.34]微升和-24.90[-27.79至-22.01]微升的大的顺行和逆行流体体积,分别(p<0.0001)。主要放置在+30cm和-30cm处的旋塞输送的流体在360s时产生140%和35%的计算体积,分别(p<0.0001)。注射器输液泵应理想地连接到位于心脏水平的旋塞,以便在旋塞打开后最小化顺行和逆行流体体积的量。
    The purpose of this in vitro study was to evaluate the impact of the vertical level of the stopcock connecting the infusion line to the central venous catheter on start-up fluid delivery in microinfusions. Start-up fluid delivery was measured under standardized conditions with the syringe outlet and liquid flow sensors positioned at heart level (0 cm) and exposed to a simulated CVP of 10 mmHg at a set flow rate of 1 ml/h. Flow and intraluminal pressures were measured with the infusion line connected to the stopcock primarily placed at vertical levels of 0 cm, + 30 cm and - 30 cm or primarily placed at 0 cm and secondarily, after connecting the infusion line, displaced to + 30 cm and - 30 cm. Start-up fluid delivery 10 s after opening the stopcock placed at zero level and after opening the stopcock primarily connected at zero level and secondary displaced to vertical levels of + 30 cm and - 30 cm were similar (- 10.52 [- 13.85 to - 7.19] µL; - 8.84 [- 12.34 to - 5.33] µL and - 11.19 [- 13.71 to - 8.67] µL (p = 0.469)). Fluid delivered at 360 s related to 65% (zero level), 71% (+ 30 cm) and 67% (- 30 cm) of calculated infusion volume (p = 0.395). Start-up fluid delivery with the stopcock primarily placed at + 30 cm and - 30 cm resulted in large anterograde and retrograde fluid volumes of 34.39 [33.43 to 35.34] µL and - 24.90 [- 27.79 to - 22.01] µL at 10 s, respectively (p < 0.0001). Fluid delivered with the stopcock primarily placed at + 30 cm and - 30 cm resulted in 140% and 35% of calculated volume at 360 s, respectively (p < 0.0001). Syringe infusion pumps should ideally be connected to the stopcock positioned at heart level in order to minimize the amounts of anterograde and retrograde fluid volumes after opening of the stopcock.
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  • 文章类型: Journal Article
    背景:肝动脉输液泵(HAIP)化疗是不可切除的肝内胆管癌(iCCA)患者的有效治疗方法。HAIP化疗需要插入胃十二指肠动脉的导管和皮下泵。可以使用开放式或机器人方法来放置导管。
    目的:本研究旨在比较机器人与开放式HAIP放置在不可切除iCCA患者的围手术期结果。
    方法:我们分析了2020年1月至2022年9月在阿姆斯特丹UMC进行机器人或开放式HAIP放置的PUMP-II试验中包含的不可切除iCCA患者,伊拉斯谟MC,UMC乌得勒支.主要结果是功能恢复时间(TTFR)。
    结果:总计,进行了22个机器人和28个开放式HAIP放置。TTFR中位数为机器人放置后2天,而开放式HAIP放置后5天(p<0.001)。机器人组中的一名患者(4.5%)由于巨大的肿瘤靠在固定肝脏的肺门上而转变为开放。术后并发症相似-机器人放置后36%(8/22)与开放放置后39%(11/28)(p=1.000)。机器人组住院时间中位数为3天,比5天更短(p<0.001)。所有22名机器人患者在术后开始HAIP化疗,即开放组的93%(26/28)(p=0.497)。开始HAIP化疗的中位时间为14天与18天(p=0.153)。
    结论:在不可切除的iCCA患者中,机器人HAIP置入是一种安全有效的手术,与开放式HAIP置入相比,TTFR和住院时间明显缩短。
    BACKGROUND: Hepatic arterial infusion pump (HAIP) chemotherapy is an effective treatment for patients with unresectable intrahepatic cholangiocarcinoma (iCCA). HAIP chemotherapy requires a catheter inserted in the gastroduodenal artery and a subcutaneous pump. The catheter can be placed using an open or robotic approach.
    OBJECTIVE: This study aimed to compare perioperative outcomes of robotic versus open HAIP placement in patients with unresectable iCCA.
    METHODS: We analyzed patients with unresectable iCCA included in the PUMP-II trial from January 2020 to September 2022 undergoing robotic or open HAIP placement at Amsterdam UMC, Erasmus MC, and UMC Utrecht. The primary outcome was time to functional recovery (TTFR).
    RESULTS: In total, 22 robotic and 28 open HAIP placements were performed. The median TTFR was 2 days after robotic placement versus 5 days after open HAIP placement (p < 0.001). One patient (4.5%) in the robotic group underwent a conversion to open because of a large bulky tumor leaning on the hilum immobilizing the liver. Postoperative complications were similar-36% (8/22) after robotic placement versus 39% (11/28) after open placement (p = 1.000). The median length of hospital stay was shorter in the robotic group-3 versus 5 days (p < 0.001). All 22 robotic patients initiated HAIP chemotherapy post-surgery, i.e. 93% (26/28) in the open group (p = 0.497). The median time to start HAIP chemotherapy was 14 versus 18 days (p = 0.153).
    CONCLUSIONS: Robotic HAIP placement in patients with unresectable iCCA is a safe and effective procedure and is associated with a significantly shorter TTFR and hospital stay than open HAIP placement.
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  • 文章类型: Journal Article
    泵或阀门的气穴侵蚀失效导致核反应堆的低效率和使用寿命缩短。本文回顾了核电工业和学术研究领域中有关泵和阀门气蚀的工作。泵和阀门材料的气蚀机理与表面层的微观结构和力学性能有关。奥氏体不锈钢的抗气蚀能力可以比铁素体钢高十倍。材料的气蚀与硬度有关,韧性,和马氏体相变能力。还回顾了冲蚀磨损和冲蚀腐蚀研究。冲蚀磨损主要受材料表面硬度的影响。冲刷腐蚀行为与元素组成密切相关。本文总结了改善泵阀气蚀的措施。可以通过添加元素和涂层来增强金属材料的抗气蚀性。附着力,包含内容,和残余应力影响涂层材料的空化侵蚀。
    The cavitation erosion failure of pumps or valves induces the low efficiency and reduced service life of nuclear reactors. This paper reviews works regarding the cavitation erosion of pumps and valves in the nuclear power industry and academic research field. The cavitation erosion mechanisms of materials of pumps and valves are related to the microstructure and mechanical properties of the surface layer. The cavitation erosion resistance of austenitic stainless steel can be ten times higher than that of ferritic steel. The cavitation erosion of materials is related to the hardness, toughness, and martensitic transformation capacity. Erosion wear and erosion-corrosion research is also reviewed. Erosion wear is mainly influenced by the hardness of the material surface. Erosion-corrosion behavior is closely connected with the element composition. Measures for improving the cavitation erosion of pumps and valves are summarized in this paper. The cavitation erosion resistance of metallic materials can be enhanced by adding elements and coatings. Adhesion, inclusion content, and residual stress impact the cavitation erosion of materials with coatings.
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  • 文章类型: Journal Article
    位移控制系统效率高,在工业中得到广泛应用。液压系统中的致动器运动的精确控制通常在工业应用中是必需的,例如用于飞行控制的固定翼飞机中的控制表面的运动以及飞机制动系统。为了满足这一需求,本研究的目的是开发高保真模型以实现精确控制.这项工作的重点是对用于控制线性致动器速度的静液压传动进行建模。使用可变排量泵改变进入致动器的流量。该研究包括检查开环系统的稳定性和性能。此外,该研究涉及比例积分微分PID和H∞控制器的设计,然后分析了具有两个控制器的闭环系统的稳定性和性能。此外,考虑了乘性不确定性,并使用PID和H∞控制器验证了系统的鲁棒性。在目前的研究中,不确定的参数,例如执行器效率,泵速,考虑和粘性摩擦系数,并允许其规定值偏差±5%。考虑不确定性可确保即使在设计参数在指定范围内变化的情况下,系统也能正常运行。比较了开环系统的系统响应,带PID控制器的闭环系统,和具有H∞控制器的闭环系统。结果表明,开环系统在实际应用中保持稳定,但在输入跟踪和干扰抑制方面表现不佳。PID控制器的引入显著增强了系统对参考输入的响应;然而,它在超调和稳定时间方面的干扰抑制能力仍然不令人满意。配备PID控制器的系统未能满足鲁棒性要求。相反,H∞控制器的使用产生了优异的响应,满足了鲁棒性标准。
    Displacement-controlled systems have high efficiency and are widely used in industry. Accurate control of the actuator motion in hydraulic systems is usually a necessity in industrial applications such as the motion of control surfaces in fixed-wing airplanes for flight control as well as the aircraft brake systems. To address this need, the current study was conducted with the goal of developing a high-fidelity model to achieve precise control. This work focused on modeling a hydrostatic transmission that is used for controlling a linear actuator velocity. The flow entering the actuator was changed using a variable displacement pump. The study included examining the stability and performance of the open-loop system. Additionally, the study involved the design of the proportional-integral-derivative PID and H∞ controllers, followed by the analysis of the stability and performance of the closed-loop system with both controllers. Furthermore, the multiplicative uncertainty is taken into account and the robustness of the system is verified using controllers PID and H∞. In the current study,Uncertain parameters such as actuator efficiency, pump speed, and viscous friction coefficient were considered and allowed for a ±5% deviation from their stated values. Taking uncertainty into account ensures that the system performs properly even in case where the design parameters vary within the specified range. The system response is compared for the cases of open-loop system, closed-loop system with PID controller, and closed-loop system with H∞ controller. The results demonstrated that the open-loop system remains stable for real-world applications but shows insufficient performance in terms of input tracking and disturbance rejection. The introduction of the PID controller significantly enhanced the system\'s response to a reference input; however, its disturbance rejection capabilities in terms of overshoot and settling time were still unsatisfactory. The system equipped with the PID controller failed to meet the robustness requirements. Conversely, the utilization of H∞ controllers yielded superior responses and fulfilled the robustness criteria.
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  • 文章类型: Journal Article
    类器官是自组织的成体或多能干细胞的3D培养物,其具有包围限定的充满流体的管腔的上皮膜。这些类器官已被证明具有广泛的器官型组织类型,但是结构的封闭性质限制了进入管腔和细胞膜的顶端表面。为了增加类器官的潜在应用,需要新技术来提供进入类器官腔和上皮细胞膜顶表面的通道,以进行新的生物医学研究。本章详细介绍了一种利用双管拉玻璃毛细管和基于压力的泵进入类器官的管腔和顶端表面的方法。类器官灌注系统使用三轴显微操纵器来定位双管毛细管,以通过毛细管的尖端刺穿类器官。双筒毛细管的每个筒由基于压力的泵独立地控制,以允许将材料注射到管腔中和从管腔中移除。此外,用定制设计的PDMS类器官支架固定类器官。本文介绍了类器官灌注系统组件的设计及其使用细节,可用作进行广泛类器官研究的基础,包括但不限于在类器官培养过程中修改腔内容物和顶端细胞膜相互作用。在正常静态的类器官腔内的生理流动的重述,以及机械应变对类器官细胞发育的影响。
    Organoids are 3D cultures of self-organized adult or pluripotent stem cells with an epithelial membrane enclosing a defined fluid-filled lumen. These organoids have been demonstrated with a wide range of organotypic tissue types, but the enclosed nature of the structure restricts access to the lumen and apical surface of the cell membrane. To increase the potential applications of organoids, new technologies are required to provide access to the lumen of the organoid and apical surface of the epithelial cell membrane to enable new biomedical studies. This chapter details a method to access the lumen and apical surface of an organoid utilizing a double-barrel pulled glass capillary and pressure-based pump. The organoid perfusion system uses a three-axis micromanipulator to position the double-barrel capillary to pierce the organoid with the tip of the capillary. Each barrel of the double-barrel capillary is controlled independently with the pressure-based pump to allow injection and removal of material into and from the lumen. Additionally, the organoid is immobilized with a custom-designed PDMS organoid holder. The design of the components for the organoid perfusion system and details on their use are presented here and can be utilized as the basis to enable a wide range of organoid studies including but not limited to modifying luminal contents and apical cell membrane interactions during organoid cultures, recapitulation of physiological flow within the normally static organoid lumen, and effects of mechanical strain on organoid cell development.
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