会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 14. 发明申请
    • PASTEURISATION PROCESS FOR MICROBIAL CELLS AND MICROBIAL OIL
    • 微生物细胞和微生物油的固定过程
    • WO2004001021A1
    • 2003-12-31
    • PCT/EP2003/006553
    • 2003-06-20
    • DSM IP ASSETS B.V.SCHAAP, AlbertVERKOEIJEN, Daniel
    • SCHAAP, AlbertVERKOEIJEN, Daniel
    • C12N1/00
    • A61L2/04A23D9/00A23D9/02A23K20/158A23L33/115A23L33/12A61K8/67A61K8/925A61K8/99A61K2800/85A61Q19/00C07C57/03C11B1/10C12N1/005C12P7/6427C12P7/6463C12P7/6472
    • An improved pasteurisation protocol for pasteurising microbial cells is disclosed. The protocol has three stages, a first heating stage, a second plateau stage at which the cells are held at a (maximum and) constant temperature, and a third cooling stage. Both the heating and the cooling stages are rapid, with the temperature of the cells passing through 40 to 80 °C in no more than 30 minutes in the heating stage. The heating rate is at least 0.5 °C/minute and during cooling is at least -0.5 °C/minute. The plateau maximum temperature is from 70 to 85 °C. By plotting the pasteurisation protocol on a time (t, minutes) versus temperature (T, °C) graph, one obtains a trapezium having an area less than 13,000 °C minute. Not only does this result in a smaller energy input (and so a reduction in costs), but a better quality (and less oxidised) oil results having a peroxide value (POV) of less than 1.5 and an anisidine value (AnV) of less than 1.0.
    • 公开了用于巴氏灭菌微生物细胞的改进的巴氏灭菌方案。 该方案具有三个阶段,第一加热阶段,细胞保持在(最大和恒定)温度的第二平台阶段和第三冷却阶段。 加热阶段和冷却阶段都是快速的,在加热阶段,在不超过30分钟内,电池的温度通过40至80℃。 加热速度为至少0.5℃/分钟,冷却时为至少-0.5℃/分钟。 平台最高温度为70〜85℃。 通过在一段时间(t,分钟)与温度(T,°C)图上绘制巴氏消毒方案,可得到面积小于13,000℃分钟的梯形图。 这不仅导致更小的能量输入(并且因此降低成本),而且具有小于1.5的过氧化值(POV)和较小的茴香胺值(AnV)的更好的质量(和较少氧化的)油的结果 比1.0。
    • 16. 发明申请
    • PRECISION THERAPEUTICS
    • 精密治疗
    • WO2016198859A1
    • 2016-12-15
    • PCT/GB2016/051690
    • 2016-06-08
    • GLOBALACORN LTD.KING'S COLLEGE LONDON
    • THANOU, MariaWRIGHT, Michael James LeeCENTELLES, MiguelMILLER, Andrew DavidGEDROYC, WladyslawSPENCE, Paul
    • A61K41/00A61K49/18A61K47/48A61K9/127A61P35/00
    • A61K49/1812A61K9/0007A61K9/127A61K41/0028A61K41/0052A61K47/6911
    • The invention provides a pharmaceutical composition comprising (a combination of): - imaging lipid nanoparticles (imaging LNPs); and - one or more therapeutic agent(s). The one or more therapeutic agent(s) may be separate from said imaging LNPs, and/or entrapped within said imaging LNPs to form theranostic nanoparticles (TNPs). Imaging LNPs (or TNPs) may have receptor-targeting ligands. Post administration, when sufficient imaging LNPs (or TNPs) reach target sites such as cancerous lesions, then targets may become identified using clinically relevant imaging modalities such as MRI. Image-guided hyperthermia (IgFHT) applied to target sites enables imaging LNPs (or TNPs) still in the blood pool, along with (additional) therapeutic agent(s), to partition substantially into target tissues for therapy by means of hyperpermeability and retention (HPR). Confirmation of therapeutic outcomes can be followed by clinically relevant imaging modalities such as MRI.
    • 本发明提供了一种药物组合物,其包含(组合):成像脂质纳米颗粒(成像LNPs); 和 - 一种或多种治疗剂。 所述一种或多种治疗剂可以与所述成像LNP分离,和/或包埋在所述成像LNPs内以形成纳米颗粒(TNPs)。 成像LNPs(或TNP)可能具有受体靶向配体。 后行管理,当足够的成像LNP(或TNP)到达目标部位如癌性病变时,则可以使用临床相关的成像方式(例如MRI)鉴定目标。 应用于靶位点的图像引导热疗(IgFHT)使得仍然在血液池中的LNP(或TNP)与(附加的)治疗剂一起成像以通过高渗透性和保留性将其基本分配到靶组织进行治疗 HPR)。 治疗结果的确认可以跟随临床相关的成像方式,如MRI。
    • 20. 发明申请
    • PUFAS IN EGGS
    • 蜂蜜中的PUFAS
    • WO2003034816A1
    • 2003-05-01
    • PCT/EP2002/011749
    • 2002-10-21
    • DSM N.V.KIES, Arie, KarstSIMONS, Petrus, Cornelis, MariaVAN DOESUM, Johannes, Henricus
    • KIES, Arie, KarstSIMONS, Petrus, Cornelis, MariaVAN DOESUM, Johannes, Henricus
    • A01K45/00
    • A01K45/007
    • A process for improving the survival rate (post-hatching) or hatching rate of chicks from an egg is disclosed, where the polyunsaturated fatty acid (PUFA) content of the egg is increased. Such an increase can also improve growth, feed conversion ratio or the immunological status of the hatched chicks. Improvements in these parameters have been found even when increasing the PUFA content of the egg by as little as 0.01 %. The PUFA is transported across the shell of the egg, by manual injection, and the PUFA can be injected into the egg yolk, into the egg white, or both. Injection can be within 24 hours of the egg being laid. The invention therefore also provides novel eggs, where at least 10% of the arachidonic acid (ARA) inside the eggs is in triglyceride form. The invention also provides eggs that contain one or more PUFAs or lipids in the egg white, or where the egg (or yolk) has at least 120 mg of a PUFA such as ARA. These eggs may be intact, with a shell, or may be without the shell (and therefore in a raw or cooked form). Such eggs can be included into foodstuffs, such as for humans.
    • 公开了一种提高鸡蛋生存率(孵化后)或雏鸡孵化率的方法,其中鸡蛋的多不饱和脂肪酸(PUFA)含量增加。 这样的增加也可以改善孵化雏鸡的生长,饲料转化率或免疫状态。 即使将蛋黄的PUFA含量提高到0.01%,也已经发现了这些参数的改进。 PUFA通过手动注射运输穿过鸡蛋壳,PUFA可以注入蛋黄,蛋白或两者。 注射可以在鸡蛋放置的24小时内。 因此,本发明还提供了新颖的蛋,其中蛋中至少10%的花生四烯酸(ARA)是甘油三酯形式。 本发明还提供在蛋清中含有一种或多种PUFA或脂质的蛋,或者蛋(或蛋黄)具有至少120mg的PUFA如ARA的蛋。 这些蛋可以是完整的,有壳,或者可以没有壳(因此是生的或熟的形式)。 这样的蛋可以包括在食物中,例如人类。