tailor-made

量身定制
  • 文章类型: Journal Article
    多糖(PSAs)是以碳水化合物为基础的大分子,广泛应用于生物医学领域,无论是在它们的纯形式或与其他材料的混合物/纳米复合材料。结构之间的关系,属性,和功能激发了科学家通过结合独特的分子结构和有针对性的整体特性,为各种生物医学应用设计多功能PSA。多种策略,例如共轭,嫁接,交联,和功能化,已经探索过控制它们的机械性能,电导率,亲水性,降解性,流变学特征,和刺激反应。例如,定制的PSA以其在组织工程中的全球生物医学应用而闻名,药物/基因递送,和再生医学。此外,超分子工程和化学的显着进步为面向任务的生物材料合成和定制生物材料的制造铺平了道路。这些材料可以协同地结合生物学和化学的益处来解决重要的生物医学问题。在这里,我们根据PSA的综合方法对它们进行分类和总结,并探索用于定制其化学结构的主要策略。然后,我们使用实际示例强调PSA的各种属性。最后,我们彻底描述了量身定制的PSA的生物医学应用,以及他们当前面临的挑战和潜在的未来方向。
    Polysaccharides (PSAs) are carbohydrate-based macromolecules widely used in the biomedical field, either in their pure form or in blends/nanocomposites with other materials. The relationship between structure, properties, and functions has inspired scientists to design multifunctional PSAs for various biomedical applications by incorporating unique molecular structures and targeted bulk properties. Multiple strategies, such as conjugation, grafting, cross-linking, and functionalization, have been explored to control their mechanical properties, electrical conductivity, hydrophilicity, degradability, rheological features, and stimuli-responsiveness. For instance, custom-made PSAs are known for their worldwide biomedical applications in tissue engineering, drug/gene delivery, and regenerative medicine. Furthermore, the remarkable advancements in supramolecular engineering and chemistry have paved the way for mission-oriented biomaterial synthesis and the fabrication of customized biomaterials. These materials can synergistically combine the benefits of biology and chemistry to tackle important biomedical questions. Herein, we categorize and summarize PSAs based on their synthesis methods, and explore the main strategies used to customize their chemical structures. We then highlight various properties of PSAs using practical examples. Lastly, we thoroughly describe the biomedical applications of tailor-made PSAs, along with their current existing challenges and potential future directions.
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  • 文章类型: Journal Article
    背景:扩增/乳房固定术是整容手术中最复杂的程序之一,关于采取最适当的方法来避免重大并发症并实现预期结果的辩论仍在进行中。本研究旨在通过使用植入物引导的量身定制的乳房固定术技术来管理中度乳房下垂和肥大,从而为该主题提供进一步的贡献。
    方法:对我们的数据库进行了回顾性分析,从2016年11月至2021年12月,共有194名女性接受了量身定制的切除模式乳房固定术加植入物治疗.研究中包括的所有患者均表现为乳腺发育不全和上下垂,分类为RegnaultII级。在第一年的后续访问中,患者接受了一份匿名的书面调查问卷,调查了他们对美容效果的自我认知和总体满意度.
    结果:研究中提出的技术显示出良好的安全性,总并发症发生率为8.2%,总再手术率低至4.6%。主要问题包括伤口开裂,植入物暴露,乳头坏死未报告。患者自我报告的结果在长期随访中显示出很高的满意度和稳定的结果。
    结论:所描述的方法确保了适当的重塑以及所需的乳房体积的增加,从而最大限度地减少了由于伤口裂开或来自断流皮肤边缘的任何类型的组织坏死而导致的植入物暴露的机会。本文所述的外科手术是安全可靠的。
    方法:本期刊要求作者为每篇文章分配一定程度的证据。对于这些循证医学评级的完整描述,请参阅目录或在线作者说明www。springer.com/00266.
    BACKGROUND: Augmentation/mastopexy represents one of the most complex procedures in the setting of cosmetic surgery, and there is still an ongoing debate about the most suitable approach to undertake to avoid major complications and deliver the desired result. The present study aims to offer a further contribute to the topic by presenting our personal experience with an implant-guided tailor-made mastopexy technique to manage moderate breast ptosis and hypotrophy.
    METHODS: A retrospective analysis of our database was carried out, and a total of 194 women who underwent a tailor-made resection pattern mastopexy plus implant from November 2016 to December 2021 were enrolled. All patients included in the study presented breast hypoplasia and ptosis classified as Regnault grade II. At the first-year follow-up visit, patients received an anonymous written questionnaire that addressed their self-perception of cosmetic results and overall satisfaction.
    RESULTS: The technique presented in the study showed a favorable safety profile with a total complication rate accounting for an 8.2% and an overall reoperation rate as low as 4.6%. Major concerns including wound dehiscence, implant exposure, and nipple necrosis are not reported. Patients\' self-reported outcomes revealed high satisfaction rates and stable results in the long-term follow-up.
    CONCLUSIONS: The described approach ensures proper reshaping together with the desired increased breast volume minimizing the chance of implant exposure due to wound dehiscence or any sort of tissue necrosis from devascularized skin edges. The surgical procedure described herein is safe and reliable.
    METHODS: This journal requires that authors assign a level of evidence to each article. For a full description of these Evidence-Based Medicine ratings, please refer to the Table of Contents or the online Instructions to Authors www.springer.com/00266 .
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  • 文章类型: Journal Article
    基于生物基多胺和聚碳酸酯的非异氰酸酯聚氨酯(NIPU)是常规聚氨酯(PU)的可持续替代品。本文公开了一种控制完全不含生物基异氰酸酯的聚氨酯的交联密度的新方法,由先前在scCO2和不同二胺中碳酸化的甘油三酯合成,如乙二胺(EDA),六亚甲基二胺(HMDA)和PriamineTM-1075(衍生自二聚脂肪酸)。作为封顶物质,水或生物醇以这样的方式使用,使得可以调节交联密度以适合预期应用的要求。首先对NIPU合成程序进行了优化,建立聚合动力学并提出合成NIPU的最佳条件。然后,碳酸大豆油(CSBO)的活性聚合位点的部分阻断的影响,使用单官能胺,对NIPUS的物理性质进行了探讨。最后,使用混合NIPU实现具有目标交联密度的完全生物基NIPU的合成,使用部分碳酸化油和H2O或乙醇作为阻断剂以非常精确的方式获得所需的物理性质。
    Non-isocyanate polyurethanes (NIPUs) based on biobased polyamines and polycarbonates are a sustainable alternative to conventional polyurethanes (PU). This article discloses a novel method to control the crosslinking density of fully biobased isocyanate-free polyurethanes, synthesized from triglycerides carbonated previously in scCO2 and different diamines, such as ethylenediamine (EDA), hexamethylenediamine (HMDA) and PriamineTM-1075 (derived from a dimerized fatty acid). As capping substances, water or bioalcohols are used in such a way that the crosslinking density can be adjusted to suit the requirements of the intended application. An optimization of the NIPU synthesis procedure is firstly carried out, establishing the polymerization kinetics and proposing optimal conditions set for the synthesis of the NIPUs. Then, the influence of the partial blocking of the active polymerization sites of the carbonated soybean oil (CSBO), using monofunctional amines, on the physical properties of the NIPUS is explored. Finally, the synthesis of fully biobased NIPUs with a targeted crosslinking density is achieved using hybrid NIPUs, employing partially carbonated oil and H2O or ethanol as blockers to achieve the desired physical properties in a very precise manner.
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  • 文章类型: Journal Article
    未经评估:开发了在线干预Runfitcheck,以刺激成年新手跑步者的伤害预防行为。
    UNASSIGNED:这项研究评估了Runfitcheck对成年新手跑步者的伤害预防行为的有效性。
    UNASSIGNED:在成年新手跑步者中进行了一项随机对照试验。干预组可以使用Runfitcheck干预措施,对照组照常进行跑步活动.一,三,入学五个月后,参与者回顾性地报告了他们在损伤预防行为方面所做的工作(如(i)使用(个性化)训练计划进行操作;(ii)进行力量和技术锻炼;以及(iii)在跑步前进行常规热身).使用相对风险(RR)和95%置信区间(95CI)分析行为变化。
    UNASSIGNED:干预组(n=715)更频繁地搜索有关热身程序的信息(RR1.211;95CI1.080-1.357),并在他们的热身程序中增加了更多的力量练习(RR1.228;95CI1.092-1.380)。与对照组相比,干预组进行更频繁的跑步技术练习(n=696)(RR1.134;95CI1.015-1.267),但力量锻炼较少(RR0.865(95CI0.752-0.995)。在注册时没有执行任何热身程序的跑步者组中(n=272),干预组比对照组更频繁地开始常规热身(RR1.461;95CI1.084-1.968).使用培训计划没有发现明显的结果。
    UNASSIGNED:在线干预Runfitcheck在刺激成年新手跑步者的伤害预防行为方面是有效的,主要与热身有关.
    UNASSIGNED:NL6225,2007年4月24日注册-回顾性注册,https://www.trialregister.nl/试用/6225。
    UNASSIGNED: The online intervention Runfitcheck was developed to stimulate injury-preventive behaviour among adult novice runners.
    UNASSIGNED: This study evaluated the effectiveness of Runfitcheck on injury-preventive behaviour among adult novice runners.
    UNASSIGNED: A randomised controlled trial was conducted among adult novice runners. The intervention group had access to the Runfitcheck intervention, the control group performed their running activities as usual. One, three, and five months after enrolment, participants reported retrospectively what they had done regarding injury-preventive behaviour (operationalised as (i) using a (personalised) training schedule; (ii) performing strength and technique exercises; and (iii) performing a warm-up routine prior to running). Relative Risks (RR) and 95% Confidence Interval (95%CI) were used to analyse behavioural change.
    UNASSIGNED: The intervention group (n=715) searched more often for information about a warm-up routine (RR 1.211; 95%CI 1.080-1.357), and added more often strength exercises to their warm-up routine (RR 1.228; 95%CI 1.092-1.380). The intervention group performed more often running technique exercises compared to the control group (n=696) (RR 1.134; 95%CI 1.015-1.267), but less often strength exercises (RR 0.865 (95%CI 0.752-0.995). Within the group of runners that did not perform any warm-up routine at enrolment (n=272), the intervention group started to perform a regular warm-up routine more often than the control group (RR 1.461; 95%CI 1.084-1.968). No significant results were found for using a training schedule.
    UNASSIGNED: The online intervention Runfitcheck was effective in stimulating aspects of injury-preventive behaviour in adult novice runners, mostly related to a warm-up routine.
    UNASSIGNED: NL6225, Registered April 24th 2007 - Retrospectively registered, https://www.trialregister.nl/trial/6225.
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  • 文章类型: Journal Article
    动静脉移植物(AVG)的两端通过手术与上肢血管吻合,以进行血液透析治疗。然而,上肢血管的大小在不同的个体之间有很大的差异。
    根据术前计算机断层扫描血管造影扫描量化的颈部血管的形状和大小,通过三维(3D)打印机将乙烯-乙酸乙烯酯(EVA)基AVG制成H形,然后灭菌。这项研究调查了这种新型3D打印AVG在体外和体内的功能。
    这种3D打印的AVG可以轻松植入兔子的颈总动脉和颈总静脉,并在体内发挥功能。手术过程很快,不需要缝合。失血很少,手术后至少1周未发现血肿。植入的AVG内的血流速度为14.9±3.7cm/s。此外,体外表征实验表明,这种基于EVA的生物材料具有生物相容性,并且在血液透析针插管后比ePTFE具有更好的恢复性能。
    通过3D打印技术,基于EVA的AVG可以定制以适应特定的容器尺寸。这种3D打印的AVG在体内运行,我们的结果实现了个性化的血管植入。需要进一步的大型动物研究来检查长期通畅性。
    UNASSIGNED: The two ends of arteriovenous graft (AVG) are anastomosed to the upper limb vessels by surgery for hemodialysis therapy. However, the size of upper limb vessels varies to a large extent among different individuals.
    UNASSIGNED: According to the shape and size of neck vessels quantified from the preoperative computed tomography angiographic scan, the ethylene-vinyl acetate (EVA)-based AVG was produced in H-shape by the three-dimensional (3D) printer and then sterilized. This study investigated the function of this novel 3D-printed AVG in vitro and in vivo.
    UNASSIGNED: This 3D-printed AVG can be implanted in the rabbit\'s common carotid artery and common jugular vein with ease and functions in vivo. The surgical procedure was quick, and no suture was required. The blood loss was minimal, and no hematoma was noted at least 1 week after the surgery. The blood flow velocity within the implanted AVG was 14.9 ± 3.7 cm/s. Additionally, the in vitro characterization experiments demonstrated that this EVA-based biomaterial is biocompatible and possesses a superior recovery property than ePTFE after hemodialysis needle cannulation.
    UNASSIGNED: Through the 3D printing technology, the EVA-based AVG can be tailor-made to fit the specific vessel size. This kind of 3D-printed AVG is functioning in vivo, and our results realize personalized vascular implants. Further large-animal studies are warranted to examine the long-term patency.
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  • 文章类型: Journal Article
    修改纸张等易于获得的资源以规避昂贵或密集的样品预处理可能是资源贫乏地区样品分析的答案。因此,介绍了一种将样品采集与亲和样品预处理相结合的新型纸上装置。通用智能亲和采样器是通过简单的KIO4介导的纤维素氧化产生的,使纸张功能化。随后是链霉亲和素的固定化。链霉亲和素作为生物素化抗体的通用锚,能够简单地制备量身定制的亲和采样器。使用模型蛋白(人绒毛膜促性腺激素,hCG)和生物素化的抗hCG抗体用于亲和捕获。在实验室环境中,表演得到了证明,并且与没有bmAb的结合相比,实现了靶结合的14倍增加。用bmAb处理的采样器捕获的hCG的回收率被确定为33%并且与先前描述的亲和捕获方法相当。将智能亲和采样器应用于含有hCG的人血清显示R2为0.98(200-1000pgmL-1),精度≤9.1%RSD,估计检出限为65pgmL-1。尽管在临床环境中应用于真实样本之前需要进一步优化和验证,该装置用于测定复杂样品中低丰度生物标志物的潜力已得到证实.
    The modification of an easily available resource like paper to circumvent expensive or intensive sample pretreatment could be the answer to sample analysis in resource-poor regions. Therefore, a novel on-paper device combining sample collection with affinity sample pretreatment is introduced here. Universal smart affinity samplers are produced by a simple KIO4-mediated oxidation of cellulose, which functionalizes the paper. This is followed by immobilization of streptavidin. Streptavidin serves as a universal anchor for biotinylated antibodies, enabling simple preparation of tailor-made affinity samplers. The functionality of the device was tested using a model protein (human chorionic gonadotropin, hCG) and biotinylated anti-hCG antibodies for affinity capture. In a laboratory setting, the performance was demonstrated, and a 14-fold increase of target binding compared to binding without bmAb was achieved. The recovery of hCG captured with bmAb-treated samplers was determined to be 33% and comparable to previously described affinity capture approaches. Application of the smart affinity samplers to human serum containing hCG showed an R2 of 0.98 (200-1000 pg mL-1), precision of ≤ 9.1% RSD, and estimated limit of detection of 65 pg mL-1. Although further optimization and validation are necessary prior to application to real samples in clinical settings, the potential of the device for use in determination of low abundant biomarkers in complex samples has been demonstrated.
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  • 文章类型: Journal Article
    Mannosylerythritol lipids (MELs) are a type of glycolipid biosurfactant produced by basidiomycetous yeasts, most notably those belonging to the genera Pseudozyma and Ustilago. Mannosylerythritol lipids are environmentally friendly and possess many unique functions, such as gene delivery, bio-activation, and human skin repair, and thus have potential applications in cosmetic, pharmaceutical, agriculture, food, and environmental industries. However, MELs will require overcoming same issues related to the commercialization, e.g., expansion of the structure and function variety and cost reduction. In the past decade, various studies have attempted to tailor production of targeted MELs in order to expand the utility of these biosurfactants. Moreover, the rapid development of genomic sequencing techniques will enhance our ability to modify MEL producers. In this review, we focus on current research into the tailored production of MELs, including conventional and advanced approaches.
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  • 文章类型: Journal Article
    Despite the introduction of evidence based guidelines and practical courses, the incidence of postpartum hemorrhage shows an increasing trend in developed countries. Substandard care is often found, which implies an inadequate implementation in high resource countries. We aimed to reduce the gap between evidence-based guidelines and clinical application, by developing a strategy, tailored to current barriers for implementation.
    The development of the implementation strategy consisted of three phases, supervised by a multidisciplinary expert panel. In the first phase a framework of the strategy was created, based on barriers to optimal adherence identified among professionals and patients together with evidence on effectiveness of strategies found in literature. In the second phase, the tools within the framework were developed, leading to a first draft. In the third phase the strategy was evaluated among professionals and patients. The professionals were asked to give written feedback on tool contents, clinical usability and inconsistencies with current evidence care. Patients evaluated the tools on content and usability. Based on the feedback of both professionals and patients the tools were adjusted.
    We developed a tailored strategy to improve guideline adherence, covering the trajectory of the third trimester of pregnancy till the end of the delivery. The strategy, directed at professionals, comprehending three stop moments includes a risk assessment checklist, care bundle and time-out procedure. As patient empowerment tools, a patient passport and a website with patient information was developed. The evaluation among the expert panel showed all professionals to be satisfied with the content and usability and no discrepancies or inconsistencies with current evidence was found. Patients\' evaluation revealed that the information they received through the tools was incomplete. The tools were adjusted accordingly to the missing information.
    A usable, tailored strategy to implement PPH guidelines and practical courses was developed. The next step is the evaluation of the strategy in a feasibility trial.
    Clinical trial registration: The Fluxim study, registration number: NCT00928863 .
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  • 文章类型: Journal Article
    OBJECTIVE: To examine the efficacy of rehabilitation for elderly individuals with dementia at intermediate facilities between hospitals and home, based on the policies for elderly individuals to promote community-based care at home and dehospitalization.
    METHODS: Participants were older adults with dementia newly admitted to intermediate facilities. A total of 158 in the intervention group who claimed Long-Term Care Insurance for three consecutive months, and 54 in the control group were included in the analysis. The interventions were carried out in a tailor-made manner to meet individual needs. The personal sessions were carried out three times a week for 3 months after admission by physical, occupational or speech therapists. Outcome measures were cognitive tests (Hasegawa Dementia Scale revised [HDS-R] and Mini-Mental State Examination), and observational assessments of dementia severity, activities of daily living (ADL), social activities, behavioral and psychological symptoms of dementia (BPSD) using a short version of the Dementia Disturbance Scale (DBD13), depressive mood, and vitality.
    RESULTS: Significant improvement in the intervention group was shown in cognitive function measured by HDS-R (interaction F[1, 196] = 5.190, P = 0.024), observational evaluation of dementia severity (F[1,198] = 9.550, P = 0.002) and BPSD (DBD13; F[1,197] = 4.506, P = 0.035). Vitality, social activities, depressive mood and ADL were significantly improved only in the intervention group, although interaction was not significant.
    CONCLUSIONS: Significant improvement by intervention was shown in multiple domains including cognitive function and BPSD. Cognitive decline and worsening of BPSD are predictors of care burden and hospitalization, thus intensive rehabilitation for dementia was beneficial for both individuals with dementia and their caregivers.
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