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    • 82. 发明申请
    • PHARMACEUTICAL WASTE DISPOSAL ASSEMBLY
    • 药物废物处理装置
    • US20160325322A1
    • 2016-11-10
    • US15213950
    • 2016-07-19
    • CACTUS, LLC
    • David A. Maness
    • B09B3/00A61J1/00
    • B09B3/0075A61B50/20A61B50/36A61B50/37A61B50/39A61B90/98A61B2017/00132A61B2050/0054A61J1/00A61J1/14B65D81/264G06F19/00
    • A pharmaceutical waste disposal assembly (10) for disposing of raw pharmaceutical waste includes a receiver body (19) and a first reaction agent (287). The receiver body (19) is configured to receive the pharmaceutical waste. The receiver body (19) includes a body interior wall (921A) that defines a body interior (921B). The first reaction agent (287) is positioned within the body interior (921B) so that the first reaction agent (287) contacts the body interior wall (921A) prior to receiving the pharmaceutical waste. The first reaction agent (287) chemically reacts with the pharmaceutical waste so that the pharmaceutical waste is rendered unrecoverable. The first reaction agent (287) can include at least one of a denaturant and a deterrent. Additionally, the first reaction agent (287) can include activated charcoal.
    • 用于处置原料药废物的药物废物处理组件(10)包括接收器主体(19)和第一反应剂(287)。 接收器主体(19)被配置为接收药物废物。 接收器主体(19)包括限定主体内部(921B)的主体内壁(921A)。 第一反应剂(287)位于主体内部(921B)内,使得第一反应剂(287)在接收药物废物之前与本体内壁(921A)接触。 第一反应剂(287)与药物废物发生化学反应,使得药物废物不可恢复。 第一反应剂(287)可以包括变性剂和威慑物中的至少一种。 另外,第一反应剂(287)可以包括活性炭。
    • 89. 发明申请
    • ALTERNARIA PEPTIDES
    • US20150098969A1
    • 2015-04-09
    • US14403464
    • 2013-05-30
    • Circassia Limited
    • Roderick Peter HafnerPaul LaidlerPascal HickeyMark Larche
    • C07K7/08A61J1/14G01N33/50
    • C07K7/08A61J1/14C07K14/37G01N33/5094
    • Pharmaceutical formulations, which may be used for preventing or treating allergy to moulds of the Alternaria and/or Cladosporium genus, comprising a pharmaceutically acceptable carrier or diluent and a polypeptide or a pharmaceutically acceptable salt thereof selected from at least three of: (a) a polypeptide comprising the amino acid sequence of WSWKIGPAIATGNT (Alt28; SEQ ID NO: 101) or a T cell epitope-containing variant sequence derived from said amino acid sequence, or a said salt thereof; (b) a polypeptide comprising the amino acid sequence of KYRRVVRAGVKVAQTAR (Alt34A; SEQ ID NO: 107) or a T cell epi tope-containing variant sequence derived from said amino acid sequence, or a said salt thereof; (c) a polypeptide comprising the amino acid sequence of KYAGVFVSTGTLGGG (SEQ ID NO: 112) or a T cell epitope-containing variant sequence derived from said amino acid sequence, or a said salt thereof; (d) a polypeptide comprising the amino acid sequence of AEVYQKLKALAKKTYGQ (Alt13A; SEQ ID NO: 83) or a T cell epitope-containing variant sequence derived from said amino acid sequence, or a said salt thereof; (e) a polypeptide comprising the amino acid sequence of SLGFNIKATNGGTLD (Alt01A; SEQ ID NO: 60) or a T cell epi tope-containing variant sequence derived from said amino acid sequence, or a said salt thereof; (f) a polypeptide comprising the amino acid sequence of SAKRMKVAFKLDIEK (Alt06; SEQ ID NO: 72) or a T cell epitope-containing variant sequence derived from said amino acid sequence, or a said salt thereof; (g) a polypeptide comprising the amino acid sequence of DITYVATATLPNYCR (SEQ ID NO: 111) or a T cell epitope-containing variant sequence derived from said amino acid sequence, or a said salt thereof; and (h) a polypeptide comprising the amino acid sequence of GWGVMVSHRSGET (Alt14; SEQ ID NO: 84) or a T cell epi tope-containing variant sequence derived from said amino acid sequence, or a said salt thereof; wherein a T cell epitope-containing variant sequence of a said amino acid sequence is said amino acid sequence having up to seven amino acid modifications, each of which is independently a deletion, substitution or insertion, and each polypeptide is up to 30 amino acids in length.