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    • 1. 发明授权
    • Polymer coated ceria nanoparticles for selective cytoprotection
    • 用于选择性细胞保护的聚合物包被的二氧化铈纳米颗粒
    • US09119391B1
    • 2015-09-01
    • US12169179
    • 2008-07-08
    • Jesus Manuel PerezAtul AsatiSudip NathCharalambos Kaittanis
    • Jesus Manuel PerezAtul AsatiSudip NathCharalambos Kaittanis
    • A01N59/16A61K9/14A01N1/02
    • A01N1/02A61K9/5161A61K33/00
    • Methods, systems and compositions are disclosed wherein normal, non-transformed, healthy biological cells are protected from oxidative stress, radiation therapy and chemotherapy while diseased, transformed cells, such as, cancer cells, are provided no protection by the biocompatible, polymer coated nanoceria composition of the present invention. The polymer-coated nanoceria preparation herein exhibits no toxicity to normal cells and exhibits pH-dependent antioxidant properties at neutral or physiological pH values, between approximately 6.5 to approximately 11.0 and is inactive as an antioxidant at acidic pH values between approximately 2.0 to approximately 6.4. Improved therapeutic agents and cytoprotecting devices are based on the newly discovered, pH dependent properties of polymer-coated nanoceria that provide selective cytoprotection.
    • 公开了方法,系统和组合物,其中正常的,未转化的,健康的生物细胞免受氧化应激,放射疗法和化学疗法,而患病的转化细胞,例如癌细胞,不提供生物相容的聚合物包被的纳米囊的保护 本发明的组合物。 本文所述的聚合物包被的纳米制品在正常细胞中没有毒性,并且在中性或生理学pH值(约6.5至约11.0之间)具有pH依赖性抗氧化剂性质,并且在约2.0至约6.4之间的酸性pH值下作为抗氧化剂无活性。 改进的治疗剂和细胞保护装置基于提供选择性细胞保护的聚合物包被的纳米囊的新发现的pH依赖性质。
    • 2. 发明授权
    • Cerium-oxide nanoparticle based device for the detection of reactive oxygen species and monitoring of chronic inflammation
    • 基于氧化铈纳米颗粒的器件,用于检测活性氧物质和监测慢性炎症
    • US08795733B1
    • 2014-08-05
    • US13602611
    • 2012-09-04
    • Jesus Manuel PerezCharalambos KaittanisAtul AsatiSantimukul Santra
    • Jesus Manuel PerezCharalambos KaittanisAtul AsatiSantimukul Santra
    • A61K9/14
    • A61K49/0093A61K49/0004A61K49/0054A61K49/1854A61K49/1857A61K49/1863
    • A polymer-coated cerium oxide based device and system is disclosed for detecting reactive oxygen species and monitoring chronic inflammation. The device and system encapsulate free therapeutic nanoparticle elements not present in a living body in a prosthetic or implantable unit. Embodiment one is a two-chamber structure with a reactive oxygen species (ROS) scavenging component on one end and at the opposite end is an imaging agent consisting of at least one of a fluorophore capable of fluorescence emission, a chemiluminescent agent, a magnetic relaxation agent and an X-ray contrast agent. Embodiment two is a single chamber device consisting of a multifunctional nanocomposite with a ROS-scavenging nanoparticle constituent (nanoceria) and a multimodal reporting nanoparticle component (i.e. Dex-IO-DiR). The device and system are utilized in treatment of diseases with a pro-inflammatory component, including, but not limited to, Crohn's disease, ulcerative colitis, inflammatory bowel disease, cystic fibrosis, arthritis, and cancer chemotherapy.
    • 公开了一种用于检测活性氧物质并监测慢性炎症的聚合物涂覆的氧化铈基装置和系统。 该装置和系统封装在假体或可植入单元中不存在于生物体中的游离的治疗性纳米颗粒元件。 实施方案一是在一端具有活性氧(ROS)清除组分的两室结构,相对端是由能够发荧光的荧光团,化学发光剂,磁弛豫中的至少一种构成的成像剂 药剂和X射线造影剂。 实施方案二是由具有ROS清除纳米颗粒组分(纳米碳)和多峰报告纳米颗粒组分(即Dex-IO-DiR)的多功能纳米复合材料组成的单室装置。 该装置和系统用于治疗具有促炎成分的疾病,包括但不限于克罗恩病,溃疡性结肠炎,炎症性肠病,囊性纤维化,关节炎和癌症化疗。
    • 3. 发明授权
    • Cerium oxide nanoparticle-based device for the detection of reactive oxygen species and monitoring of chronic inflammation
    • 基于氧化铈纳米粒子的器件,用于检测活性氧物质和监测慢性炎症
    • US08795731B1
    • 2014-08-05
    • US12924976
    • 2010-10-08
    • Jesus Manuel PerezCharalambos KaittanisAtul AsatiSantimukul Santra
    • Jesus Manuel PerezCharalambos KaittanisAtul AsatiSantimukul Santra
    • A61K9/14
    • A61K49/0019A61B5/411A61B5/686A61K9/0024A61K9/5138A61K45/06A61K49/0032A61K49/0034
    • A polymer-coated cerium oxide based device and system is disclosed for detecting reactive oxygen species and monitoring chronic inflammation. The device and system encapsulate free therapeutic nanoparticle elements not present in a living body in a prosthetic or implantable unit. Embodiment one is a two-chamber structure with a reactive oxygen species (ROS) scavenging component on one end and at the opposite end is an imaging agent consisting of at least one of a fluorophore capable of fluorescence emission, a chemiluminescent agent, a magnetic relaxation agent and an X-ray contrast agent. Embodiment two is a single chamber device consisting of a multifunctional nanocomposite with a ROS-scavenging nanoparticle constituent (nanoceria) and a multimodal reporting nanoparticle component (i.e. Dex-IO-DiR). The device and system are utilized in treatment of diseases with a pro-inflammatory component, including, but not limited to, Crohn's disease, ulcerative colitis, inflammatory bowel disease, cystic fibrosis, arthritis, and cancer chemotherapy.
    • 公开了一种用于检测活性氧物质并监测慢性炎症的聚合物涂覆的氧化铈基装置和系统。 该装置和系统封装在假体或可植入单元中不存在于生物体中的游离的治疗性纳米颗粒元件。 实施方案一是在一端具有活性氧(ROS)清除组分的两室结构,相对端是由能够发荧光的荧光团,化学发光剂,磁弛豫中的至少一种构成的成像剂 药剂和X射线造影剂。 实施方案二是由具有ROS清除纳米颗粒组分(纳米碳)和多峰报告纳米颗粒组分(即Dex-IO-DiR)的多功能纳米复合材料组成的单室装置。 该装置和系统用于治疗具有促炎成分的疾病,包括但不限于克罗恩病,溃疡性结肠炎,炎症性肠病,囊性纤维化,关节炎和癌症化疗。
    • 5. 发明申请
    • Differential Tumor Cell Cytotoxicity Via Contact With Coated Cerium Oxide Nanoparticles
    • 通过与涂覆的氧化铈纳米颗粒接触的差异肿瘤细胞的细胞毒性
    • US20160074334A1
    • 2016-03-17
    • US14862548
    • 2015-09-23
    • Jesus Manuel PerezAtul AsatiSantimukul SantraCharalambos Kaittanis
    • Jesus Manuel PerezAtul AsatiSantimukul SantraCharalambos Kaittanis
    • A61K9/50A61K33/24
    • A61K33/24A61K9/5138A61K9/5161
    • Differential surface-charge-dependent localization of nanoceria in normal cells and cancer cells plays a critical role in the toxicity profile of a nanoceria particle. Engineered surface-coated cerium oxide nanoparticles with different surface charges that are positive, negative and neutral provide therapeutic results for normal and cancer cell lines. Results show that nanoceria with a positive or neutral charge enters most of the cell lines studied, while nanoceria with a negative charge internalizes mostly in the cancer cell lines. Moreover, upon entry into the cells, nanoceria is localized to different cell compartments (e.g. cytoplasm and lysosomes) depending on the nanoparticle surface charge. The internalization and subcellular localization of nanoceria plays a key role in the nanoparticle cytotoxicity profile, exhibiting significant toxicity when they localize in the lysosomes of the cancer cell lines. In contrast, minimal toxicity is observed when they localize into the cytoplasm or do not enter the cells.
    • 正常细胞和癌细胞中纳米囊的差异表面电荷依赖性定位在纳米颗粒的毒性特征中起关键作用。 具有正,负和中性的不同表面电荷的工程表面包覆的氧化铈纳米颗粒为正常和癌细胞系提供治疗结果。 结果表明,具有阳性或中性电荷的纳米药物进入研究的大部分细胞系,而具有负电荷的纳米药物主要在癌细胞系中内化。 此外,在进入细胞后,根据纳米颗粒的表面电荷,将纳米片定位于不同的细胞区室(例如细胞质和溶酶体)。 纳米颗粒的内化和亚细胞定位在纳米颗粒细胞毒性谱中起关键作用,当它们定位在癌细胞系的溶酶体中时显示出显着的毒性。 相比之下,当它们定位到细胞质中或不进入细胞时,观察到最小的毒性。
    • 6. 发明申请
    • Application Device for Inducing Cytotoxicity to Tumor Cells Via Coated Cerium Oxide Nanoparticles
    • 通过涂覆的氧化铈纳米颗粒诱导肿瘤细胞的细胞毒性的应用装置
    • US20160074434A1
    • 2016-03-17
    • US14862559
    • 2015-09-23
    • Jesus Manuel PerezAtul AsatiSantimukul SantraCharalambos Kaittanis
    • Jesus Manuel PerezAtul AsatiSantimukul SantraCharalambos Kaittanis
    • A61K33/24A61K9/50
    • A61K33/24A61K9/5138A61K9/5161
    • Differential surface-charge-dependent localization of nanoceria in normal cells and cancer cells plays a critical role in the toxicity profile of a nanoceria particle. Engineered surface-coated cerium oxide nanoparticles with different surface charges that are positive, negative and neutral provide therapeutic results for normal and cancer cell lines. Results show that nanoceria with a positive or neutral charge enters most of the cell lines studied, while nanoceria with a negative charge internalizes mostly in the cancer cell lines. Moreover, upon entry into the cells, nanoceria is localized to different cell compartments (e.g. cytoplasm and lysosomes) depending on the nanoparticle surface charge. The internalization and subcellular localization of nanoceria plays a key role in the nanoparticle cytotoxicity profile, exhibiting significant toxicity when they localize in the lysosomes of the cancer cell lines. In contrast, minimal toxicity is observed when they localize into the cytoplasm or do not enter the cells.
    • 正常细胞和癌细胞中纳米囊的差异表面电荷依赖性定位在纳米颗粒的毒性特征中起关键作用。 具有正,负和中性的不同表面电荷的工程表面包覆的氧化铈纳米颗粒为正常和癌细胞系提供治疗结果。 结果表明,具有阳性或中性电荷的纳米药物进入研究的大部分细胞系,而具有负电荷的纳米药物主要在癌细胞系中内化。 此外,在进入细胞后,根据纳米颗粒的表面电荷,将纳米片定位于不同的细胞区室(例如细胞质和溶酶体)。 纳米颗粒的内化和亚细胞定位在纳米颗粒细胞毒性谱中起关键作用,当它们定位在癌细胞系的溶酶体中时显示出显着的毒性。 相比之下,当它们定位到细胞质中或不进入细胞时,观察到最小的毒性。
    • 7. 发明授权
    • Oxidase activity of polymeric coated cerium oxide nanoparticles
    • 聚合物涂覆的氧化铈纳米粒子的氧化酶活性
    • US08883519B1
    • 2014-11-11
    • US12704678
    • 2010-02-12
    • J. Manuel PerezAtul AsatiSantimukul SantraCharalambos KaittanisSudip Nath
    • J. Manuel PerezAtul AsatiSantimukul SantraCharalambos KaittanisSudip Nath
    • G01N33/553G01N33/543
    • G01N33/9413B82Y15/00G01N33/5432
    • Methods, systems, compositions include biocompatible polymer coated nanoceria that function as aqueous redox catalyst with enhanced activity at an acidic to moderately alkaline pH value between 1 and 8. The compositions are used as oxidizing agents for decomposition, decontamination or inactivation of organic contaminants, such as, pesticides and chemical warfare agents. Another use includes nanoceria as targetable nanocatalyst prepared by conjugating various targeting ligands to the nanoparticle coating to form a colorimetric or fluorescent probe in immunoassays and other molecule binding assays that involve the use of a molecule in solution that changes the color of the solution or emits a fluorescent signal, where localization of nanoceria to organs or tissue is assessed by treatment with an oxidation sensitive dye or other detection devices. Versatility and uses of the nanoceria compositions are controlled by pH value, choice of dye substrate and thickness of the polymer coating on the ceria nanoparticles.
    • 方法,系统,组合物包括在1至8之间的酸性至中等碱性pH值下具有增强活性的作为水性氧化还原催化剂的生物相容性聚合物包衣纳米片。该组合物用作有机污染物的分解,去污或灭活的氧化剂, 作为农药和化学战剂。 另一种用途包括将纳米囊作为可靶向的纳米催化剂,其通过将各种靶向配体与纳米颗粒涂层结合而形成可靶向的纳米催化剂,以在免疫测定和其它分子结合测定中形成比色或荧光探针,其涉及使用溶液中的分子,其改变溶液的颜色或发射 荧光信号,其中通过用氧化敏感染料或其他检测装置处理来评估纳米器官对器官或组织的定位。 通过pH值,染料底物的选择和二氧化铈纳米粒子上聚合物涂层的厚度来控制纳米材料组合物的多功能性和用途。
    • 9. 发明授权
    • Nanoparticle-mediated methods for antimicrobial susceptibility testing of bacteria
    • 纳米粒子介导的细菌抗菌药敏试验方法
    • US09057094B1
    • 2015-06-16
    • US12258785
    • 2008-10-27
    • J. Manuel PerezCharalambos KaittanisSudip Nath
    • J. Manuel PerezCharalambos KaittanisSudip Nath
    • C12Q1/18B82Y30/00A61K49/18
    • C12Q1/18A61K49/1821B82Y15/00B82Y30/00
    • A method of testing bacterial cells for antimicrobial susceptibility includes preparing a suspension of the bacterial cells in a non-nutrient medium, mixing with the suspension an antimicrobial, a carbohydrate usable by the bacterial cells, metallic nanoparticles, and a lectin, and incubating the mixture while monitoring a parameter of the nanoparticles responsive to use of the carbohydrate by the bacterial cells. More broadly stated, the invention includes a method of testing an agent for its effect on cell metabolism by preparing a suspension of cells in a non-nutrient medium, mixing the suspension with the agent, adding a carbohydrate usable by the cells, metallic nanoparticles, and a lectin with binding specificity for the added carbohydrate, and monitoring a nanoparticle parameter responsive to the cells.
    • 测试细菌细胞用于抗微生物敏感性的方法包括在非营养培养基中制备细菌细胞的悬浮液,与悬浮液混合抗微生物剂,由细菌细胞可用的碳水化合物,金属纳米颗粒和凝集素,并将混合物 同时监测响应于细菌细胞使用碳水化合物的纳米颗粒的参数。 更广泛地说,本发明包括通过制备非营养培养基中的细胞悬浮液,将悬浮液与试剂混合,加入细胞可用的碳水化合物,金属纳米颗粒, 以及对加入的碳水化合物具有结合特异性的凝集素,以及响应于细胞监测纳米颗粒参数。