课题基金 / 基金详情

项目摘要

项目成果

BENJAMIN M BUEHRER的其他基金

相似基金

相关文献

中文摘要
翻译
描述(由申请人提供):糖尿病和糖尿病相关的并存是流行的比例,给我们的医疗系统带来了巨大的负担。尽管在确定1型和2型糖尿病的致病因素和分子机制方面已经取得了重大进展,但寻找有效的治疗方法仍然是一个巨大的挑战。迫切需要新的方法和工具来加速额外疗法的研究和开发。尽管机制不同,但在1型和2型糖尿病患者中,都存在胰岛细胞或胰岛细胞功能的丧失,导致胰岛素产生完全或显著减少。目前,人类胰岛是最具生理学相关性的系统,用于研究调节胰岛素产生/分泌的潜在疗法,以及调节?细胞生长和凋亡的因子。生物技术和制药公司迫切需要新的合同研究平台和工具,以加快他们需要人类胰岛的药物开发计划。第一阶段应用的里程碑是成功的,包括开发高通量药物发现平台,使用“正常”和诱导疾病状态模型进行筛查。在当前的第二阶段应用中,我们将重点关注这些平台的自然进展,包括用于研究的新型3D胰岛微组织(伪胰岛)的商业化,建立其他基于胰岛的分析,包括实施定量高内容成像(QHCI)平台,以及最后使用小型化合物库屏幕验证当前用于合同研究服务的HT分析。这些产品和服务是学术和制药机构迫切需要的新奇产品和服务,具有巨大的商业潜力。
英文摘要
DESCRIPTION (provided by applicant): Diabetes and diabetes-related co-morbidities are at epidemic proportions and an enormous burden to our healthcare system. Although there has been significant progress in defining the causative factors and molecular mechanisms involved in both type 1 and type 2 diabetes, it remains an overwhelming challenge to identify efficacious therapeutic modalities. Novel approaches and tools to accelerate research and development of additional therapeutics are urgently needed. Although the mechanisms are distinct, in both type 1 and type 2 diabetes there is a loss of pancreatic ßcells or ß-cell function, resulting in a complete or significant reduction in insulin production. Human islets are currently the most physiologically relevant system for the examination of potential therapeutics that modulate the insulin production/secretion, and factors that regulate growth and apoptosis of ß-cells. Biotech and pharmaceutical companies are in urgent need of novel contract research platforms and tools to accelerate their drug development programs that require human islets. The milestones of the Phase 1 application were successful and included the development of high throughput drug discovery platforms using "normal" and induced disease state models for screening purposes. In the current phase 2 application we will focus on the natural progression of these platforms which include the commercialization of novel 3D islet microtissues (pseudoislets) for research, establishing additional islet-based assays including, implementation of a quantitative high content imaging (QHCI) platform and finally validation of the current HT assays for contract research services using a small compound library screen. These products and services are novel and urgently needed by academic and pharmaceutical institutes; there is significant commercial potential.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
A novel class of anti-acne therapeutics
  • 批准号:
    9789007
  • 项目类别:
  • 资助金额:
    $74.52万
  • 财政年份:
    2016
  • 负责人:
    BENJAMIN M BUEHRER
  • 依托单位:
Development of a drug discovery platform for human islets
  • 批准号:
    8642796
  • 项目类别:
  • 资助金额:
    $107.27万
  • 财政年份:
    2012
  • 负责人:
    BENJAMIN M BUEHRER
  • 依托单位:
Selective Fyn kinase inhibitors for treatment of metabolic disease
  • 批准号:
    8840938
  • 项目类别:
  • 资助金额:
    $64.34万
  • 财政年份:
    2011
  • 负责人:
    BENJAMIN M BUEHRER
  • 依托单位:
Development of a discovery platform based on microfluidics and fluorescent cell f
  • 批准号:
    8125967
  • 项目类别:
  • 资助金额:
    $35.0万
  • 财政年份:
    2011
  • 负责人:
    BENJAMIN M BUEHRER
  • 依托单位:
国内基金
海外基金
Epac1/2通过蛋白酶体调控中性粒细胞NETosis和Apoptosis在急性肺损伤中的作用研究
  • 批准号:
    LBY21H010001
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2020
  • 负责人:
    郑绪阳
  • 依托单位:
基于Apoptosis/Ferroptosis双重激活效应的天然产物AlbiziabiosideA的抗肿瘤作用机制研究及其结构改造
  • 批准号:
    81703335
  • 项目类别:
    青年科学基金项目
  • 资助金额:
    20.0万元
  • 批准年份:
    2017
  • 负责人:
    卫高菲
  • 依托单位:
双肝移植后Apoptosis和pyroptosis在移植物萎缩差异中的作用和供受者免疫微环境变化研究
  • 批准号:
    81670594
  • 项目类别:
    面上项目
  • 资助金额:
    58.0万元
  • 批准年份:
    2016
  • 负责人:
    陈昊
  • 依托单位:
Serp-2 调控apoptosis和pyroptosis 对肝脏缺血再灌注损伤的保护作用研究
  • 批准号:
    81470791
  • 项目类别:
    面上项目
  • 资助金额:
    73.0万元
  • 批准年份:
    2014
  • 负责人:
    董家鸿
  • 依托单位: