Method and preparation for administration to the mucosa of the oral or
nasal cavity
    1.
    发明授权
    Method and preparation for administration to the mucosa of the oral or nasal cavity 失效
    用于口腔或鼻腔粘膜的方法和制剂

    公开(公告)号:US4250163A

    公开(公告)日:1981-02-10

    申请号:US103558

    申请日:1979-12-13

    摘要: A method for administering a medicament which comprises adhering to the mucosa of the oral or nasal cavity a pharmaceutical preparation comprising(a) a water-swellable and mucosa-adhesive polymeric matrix comprising about 50 to about 95% by weight of a cellulose ether and about 50 to about 5% by weight of a homo- or copolymer of acrylic acid or a pharmaceutically acceptable salt thereof, and(b) dispersed therein, a pharmaceutically effective amount of the medicament,said preparation releasing continuously the medicament at a controlled rate; and causing the released medicament to be absorbed through the mucosa or enterally; said mucosa-adhesive preparation; and process for said preparation.

    摘要翻译: 一种用于施用药物的方法,其包括将口腔或鼻腔的粘膜粘附到药物制剂中,所述药物制剂包含(a)水溶胀性和粘膜粘合性聚合物基质,其包含约50至约95重量%的纤维素醚和约 50至约5重量%的丙烯酸或其药学上可接受的盐的均聚物或共聚物,和(b)其中分散有药物有效量的药物,所述制剂以受控的速率连续释放药物; 并使释放的药物通过粘膜或肠内吸收; 所述粘膜粘合剂制剂; 和所述制备方法。

    Oral sustained release pharmaceutical preparation
    2.
    发明授权
    Oral sustained release pharmaceutical preparation 失效
    口服持续释放药物制剂

    公开(公告)号:US4777033A

    公开(公告)日:1988-10-11

    申请号:US872996

    申请日:1986-06-11

    摘要: This invention is concerned with an oral sustained release pharmaceutical preparation which is prepared as a pharmaceutical preparation comprising lower alkyl ether of cellulose, polyacrylic acid or its pharmaceutically acceptable salt, and active drugs, or a pharmaceutical preparation comprising lower alkyl ether of cellulose, polyacrylic acid or its pharmaceutically acceptable salt, and active drugs together with a foaming agent, so that it may release the active drugs by such slow degrees in the stomach or the intestinal tract as to make it possible to provide an adequate supply of active drugs in enough concentration to display their therapeutic value for many hours.

    摘要翻译: 本发明涉及作为包含纤维素的低级烷基醚,聚丙烯酸或其药学上可接受的盐的药物制剂和活性药物制备的口服持续释放药物制剂,或包含纤维素的低级烷基醚,聚丙烯酸的药物制剂 或其药学上可接受的盐和活性药物与发泡剂一起释放,使得其可以在胃或肠道中以如此缓慢的程度释放活性药物,使得可以提供足够浓度的活性药物的足够供应 显示其治疗价值多小时。

    Method and preparation for administration to the mucosa of the oral or
nasal cavity
    3.
    发明授权
    Method and preparation for administration to the mucosa of the oral or nasal cavity 失效
    用于口腔或鼻腔粘膜的方法和制剂

    公开(公告)号:US4226848A

    公开(公告)日:1980-10-07

    申请号:US17059

    申请日:1979-03-02

    摘要: A method for administering a medicament which comprises adhering to the mucosa of the oral or nasal cavity a pharmaceutical preparation comprising(a) a water-swellable and mucosa-adhesive polymeric matrix comprising about 50 to about 95% by weight of a cellulose ether and about 50 to about 5% by weight of a homo- or copolymer of acrylic acid or a pharmaceutically acceptable salt thereof, and(b) dispersed therein, pharmaceutically effective amount of the medicament,said preparation releasing continuously the medicament at a controlled rate; and causing the released medicament to be absorbed through the mucosa or enterally; said mucosa-adhesive preparation; and process for said preparation.

    摘要翻译: 一种用于施用药物的方法,其包括将口腔或鼻腔的粘膜粘附于药物制剂中,所述药物制剂包含(a)水溶胀性和粘膜粘合性聚合物基质,其包含约50至约95重量%的纤维素醚和约 50至约5重量%的丙烯酸或其药学上可接受的盐的均聚物或共聚物,和(b)分散在其中的药学上有效量的药物,所述制剂以受控的速率连续释放药物; 并使释放的药物通过粘膜或肠内吸收; 所述粘膜粘合剂制剂; 和所述制备方法。

    Wound-dressing material and method for manufacturing the same
    4.
    发明授权
    Wound-dressing material and method for manufacturing the same 有权
    伤口敷料及其制造方法

    公开(公告)号:US08303980B2

    公开(公告)日:2012-11-06

    申请号:US11271903

    申请日:2005-11-14

    IPC分类号: A61F13/00

    摘要: A wound-dressing material being a product comprising chitosan as a base material and kumazasa extract, and a method for manufacturing the wound-dressing material by gelatinizing a mixture solution containing chitosan and kumazasa extract and drying the resulting gel. The wound-dressing material can be applied to humans and animals, and have biocompatibility, antibacterial effects, and low toxicity, and also have flexibility to be formed into various shapes for applying for various wounds.

    摘要翻译: 作为包含壳聚糖作为基料的材料的伤口敷料材料以及金黄假单胞菌提取物,以及通过使含有壳聚糖和锦缕草提取物的混合溶液凝胶化并干燥得到的凝胶来制造伤口敷料的方法。 伤口敷料可以应用于人和动物,并具有生物相容性,抗菌作用和低毒性,并且还具有形成各种形状的灵活性以应用于各种伤口。

    Wound-dressing material and method for manufacturing the same
    5.
    发明申请
    Wound-dressing material and method for manufacturing the same 有权
    伤口敷料及其制造方法

    公开(公告)号:US20060286156A1

    公开(公告)日:2006-12-21

    申请号:US11271903

    申请日:2005-11-14

    IPC分类号: A61L15/00 A61K36/899

    摘要: A wound-dressing material being a product comprising chitosan as a base material and kumazasa extract, and a method for manufacturing the wound-dressing material by gelatinizing a mixture solution containing chitosan and kumazasa extract and drying the resulting gel. The wound-dressing material can be applied to humans and animals, and have biocompatibility, antibacterial effects, and low toxicity, and also have flexibility to be formed into various shapes for applying for various wounds.

    摘要翻译: 作为包含壳聚糖作为基料的材料的伤口敷料材料以及金黄假单胞菌提取物,以及通过使含有壳聚糖和锦缕草提取物的混合溶液凝胶化并干燥得到的凝胶来制造伤口敷料的方法。 伤口敷料可以应用于人和动物,并具有生物相容性,抗菌作用和低毒性,并且还具有形成各种形状的灵活性以应用于各种伤口。