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    • 1. 发明申请
    • CVS TRANSPLANTATION FOR TREATMENT OF BACTERIAL VAGINOSIS
    • 用于治疗细菌性血管病的CVS移植
    • US20160279182A1
    • 2016-09-29
    • US15174540
    • 2016-06-06
    • The Johns Hopkins University
    • Laura EnsignRichard ConeJustin Hanes
    • A61K35/747A61K9/00
    • A61K35/747A61K9/00A61K9/0034A61K9/0095A61K9/19
    • Methods and materials for treating bacterial vaginosis (“BV”) are provided. Cervicovaginal secretions (“CVS”) from a woman with vaginal microbiota dominated (>50%) by one of the species of lactobacillus typically found in the human vagina, e.g. Lactobacillus crispatus, L. iners, L. gasseri, L jensenii, is transplanted to women with BV as a method for restoring beneficial vaginal microbial communities and/or increasing resistance to sexually transmitted disease. Efficacy can be enhanced, or the properties of the endogenous CVS improved, through administration of an acidifying agent such as lactic acid. The examples demonstrate the role of healthy CVS in disease resistance, and the effect of pH on CVS properties. The examples also describe the collection and transplantation of healthy beneficial CVS into women at risk for, or after treatment for, BV.
    • 提供了治疗细菌性阴道病的方法和材料(“BV”)。 来自阴道微生物群体的女性的阴道分泌物(“CVS”)由人阴道通常存在的乳酸杆菌种之一(> 50%)占主导地位(> 50%)。 将乳酸乳杆菌(Lactobacillus crispatus),L.erers L.,Gasseri,L jensenii移植到具有BV的妇女中,作为恢复有益的阴道微生物群落和/或增加对性传播疾病的抵抗力的方法。 通过施用酸性剂如乳酸,可以提高功效或内源性CVS的性质。 这些实施例证明了健康CVS在抗病性中的作用以及pH对CVS性质的影响。 这些例子还描述了将健康有益的CVS收集和移植到有BV或BV治疗风险的妇女中。
    • 2. 发明申请
    • NANOPARTICLE FORMULATIONS WITH ENHANCED MUCOSAL PENETRATION
    • 具有增强粘膜渗透性的纳米颗粒制剂
    • US20150297531A1
    • 2015-10-22
    • US14373324
    • 2013-01-21
    • The Johns Hopkins University
    • Laura EnsignRichard ConeJustin Hanes
    • A61K9/51A61K31/704A61K9/00
    • A61K9/5146A61K9/0014A61K9/0031A61K9/0034A61K9/0048A61K9/51A61K9/5138A61K9/5153A61K31/704Y10S977/773Y10S977/906
    • Hypotonic formulations were evaluated for delivering water-soluble drugs and for drug delivery with muco-inert (that is, non-adhesive) mucus-penetrating nanoparticles (MPP). Hypotonic formulations markedly increased the rate at which drugs and MPP reached the epithelial surface, including deep into the vaginal folds. Minimally hypotonic formulations, preferably ranging from 20-220 mOsm/kg, provided rapid and uniform delivery of MPP to the entire vaginal surface, with minimal risk of epithelial toxicity. Data also show that there is a higher osmolality in the colon, such that vehicles with an osmolality above that of blood plasma (generally considered isotonic at ˜300 mOsm/kg), still lead to improvements in distribution in the colon due to rapid, osmotically-induced fluid absorption. The range for improved colon distribution with a hypotonic vehicle in the colon is ˜20 mOsm/kg-450 mOsm/kg.
    • 评价低渗制剂用于递送水溶性药物和用粘膜惰性(即非粘性)粘液穿透纳米颗粒(MPP)进行药物递送。 低血糖配方显着增加药物和MPP达到上皮表面的速度,包括深入阴道褶皱。 微创低渗制剂优选范围为20-220mOsm / kg,提供MPP快速均匀地输送到整个阴道表面,具有上皮毒性的最小风险。 数据还显示,在结肠中存在较高的重量克分子渗透浓度,使得重量摩尔渗透压浓度高于血浆的载体(通常被认为是〜300mOsm / kg的等渗)仍然导致由于快速,渗透性而在结肠中分布的改善 吸收液体。 在结肠中用低渗媒介物改善结肠分布的范围为〜20mOsm / kg-450mOsm / kg。