changxin 2012-12-25 15:03 IP:重庆
这个任务要求提供一种测试方法,能够简单的检测出血友病A 中凝血因子Ⅷ和血友病B 中凝血因子IX在血液中的水平。因为现在市面上所使用的测试方法都不太方便,都不适用于诊所,而且患者也不能在家里进行自我检测。这个任务要求提供一个半定量的测试方式,需要提供可靠的血液中凝血因子水平的资料,然后根据情况分为正常,轻微,严重三种疾病状态。   “征稿件请直接上传网址:https://www.innocentive.com”   TAGS: Engineering/Design, Chemistry, Global Health, Nature, Life Sciences, Food/Agriculture, Theoretical-IP Transfer   AWARD: $25,000 USD | DEADLINE: 2/21/13 | ACTIVE SOLVERS: 27 | POSTED: 12/21/12   The Seeker requires a test that could easily be used to monitor the level of blood coagulation factors FVIII or FIX present in hemophilia A and B patients, respectively. Today, many tests are commercially available, but none are suited for convenient testing either by care providers in the clinic or by hemophilia patients at home. A semi-quantitative test is required that would provide reliable information on the blood levels of FVIII or FIX relative to a state considered as ‘Normal’, ‘Mild’ or ‘Severe’ state of disease.   This Challenge requires only a written proposal.   Detailed Description & Requirements   Background   Hemophilia A and B are inherited coagulation diseases that severely impact the quality of life of persons afflicted. Hemophilia A is caused by lack of coagulation factor VIII (FVIII), while in hemophilia B patients lack coagulation factor IX (FIX). Although the diseases are to a large extent manageable using clotting factor supplement therapies, FVIII and FIX treatment needs to be monitored in order to ensure that it meets the requirements of the individual patients’ plasma level of the coagulations factor to be supplemented. Current tests require tedious laboratory analysis, not allowing patients to achieve the frequency of testing that would facilitate good management of their disease.   The Problem   Hemophilia patients are expected to benefit from daily monitoring of their disease status (i.e. measurements of FVIII or FIX levels) to check the efficacy of their therapy and the current status of their disease.   [更多]
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gonggong 2013-07-26 11:49 IP:重庆
海洋生物医药的开发新技术。目前我国海洋生物医药的开发程度还不高,但国家对这一领域的重视程度在不断加深。海洋规划已经提到,要发展海洋生物产品精深开发的理论、技术与装备。寻求重点开发基于功能基因、功能酶和活性物质等功效因子的生物材料和生物制品;研究海洋药物的成药机理和开发技术,开展细菌等微生物和微藻的开发利用。海洋生物医药、新型海洋生物制品以及新型海洋生物材料都将成为我们重点研究方向   [更多]
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xwguilin 2013-07-27 11:17 IP:南宁
求购一种化工中间体或医药中间体的鉴别方法(提供中间体的样品)   [更多]
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¥20.00
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wuji 2013-10-15 11:12 IP:重庆
灵芝子实体为木质素,材质较坚硬,按传统的提取方法是:醇提、水提和酶解水提。但醇提成本高,花工大,一般很少使用;水提工效低,而且还有些灵芝成分未充分提取,技术有待改进;酶解水提时间长,一般要先经10~15h的酶解,再结合水提,时间长、工效低。要用何种方法能促使灵芝组织松动,便于提取,而所提取的灵芝有效成分得到充分利用。   [更多]
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wrx159 2022-02-09 10:17 IP:北京
求购氯雷他定糖浆(开瑞坦)药品标准,需要开发票   [更多]
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¥100.00
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qjp13139897 2019-10-29 15:37 IP:合肥
Oseltamivir Phosphate Capsules”《 USP42-NF37 》的药典标准一份.   [更多]
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¥50.00
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cutechen 2017-08-07 11:04 IP:重庆
如果哪位老师有请联系我QQ:3567666905   [更多]
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¥1000.00
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taideng 2013-01-17 10:34 IP:重庆
方法的要求:可采用HPLC、GC等常用方法。不能采用毛细管电泳方法。 药物名称及结构式: [中文通用名]:甘磷酸胆碱 [英文通用名]:Choline Alfoscerate [商品名]:Gliatilin、Delecit、Brezal [化学结构式]: 分子式:C8H20NO6P 分子量:257.23 [CAS  RN]:28319-77-9 [英文化学名]:Ethanaminium, 2-[[(2,3-dihydroxypropoxy)hydroxyphosphinyl]oxy]-N,N,N-trimethyl-, hydroxide, inner salt, (R)- [CAS]   [更多]
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lyj19721101 2013-05-06 16:46 IP:马鞍山
最近做磷霉素氨丁三醇这个产品,有个水解杂质达到1%,标准是0.2%,有没有一个好的方案把它精制掉?杂质和产品的极性非常接近.都是易溶于水,微溶于醇,不溶于醚.曾用醇重结晶,可以达到0.5%,还是不好.请找一个能够解决问题的简单点的方案,如果效果明显,这50元全是你的,如果有点作用,就大家分一分,麻烦大家劳神想一想,想到一定要告诉我啊.上次我出的赏金半个月就发放出去了,这次.......,速度啊   [更多]
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¥42.00
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taideng 2013-01-18 13:33 IP:重庆
我公司需要麻醉、精神类的药品用户核查制度和流向跟踪核查制度的范本吗?如有请投标   [更多]
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