CN1024753C - 避孕植入剂的制造方法 - Google Patents

避孕植入剂的制造方法 Download PDF

Info

Publication number
CN1024753C
CN1024753C CN88104894A CN88104894A CN1024753C CN 1024753 C CN1024753 C CN 1024753C CN 88104894 A CN88104894 A CN 88104894A CN 88104894 A CN88104894 A CN 88104894A CN 1024753 C CN1024753 C CN 1024753C
Authority
CN
China
Prior art keywords
implant
eva
vinyl acetate
weight
desogestrel
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
CN88104894A
Other languages
English (en)
Other versions
CN1031323A (zh
Inventor
享德里克·德·尼思
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Akzo Nobel NV
Organon NV
Original Assignee
Akzo N
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=19850428&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CN1024753(C) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Akzo N filed Critical Akzo N
Publication of CN1031323A publication Critical patent/CN1031323A/zh
Application granted granted Critical
Publication of CN1024753C publication Critical patent/CN1024753C/zh
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0087Galenical forms not covered by A61K9/02 - A61K9/7023
    • A61K9/0092Hollow drug-filled fibres, tubes of the core-shell type, coated fibres, coated rods, microtubules or nanotubes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/56Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
    • A61K31/57Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0019Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
    • A61K9/0024Solid, semi-solid or solidifying implants, which are implanted or injected in body tissue

Abstract

本发明涉及一种由a)含避孕药的EVA聚合物的芯核材料和b)包封芯核材料的EVA聚合物的膜组成的用于皮下或局部植入的避孕植入剂的制造方法。

Description

本发明涉及一种皮下或局部植入时在相当长时间内能释放避孕剂的聚合物材料植入剂。更确切地说,本发明涉及一种如此小的植入剂,以致于它可用普通的皮下注射针进行皮下植入。
对于开发新的要求最少的医学指导的长效避孕药物有着广泛的需求。对于世界上医学基础差和计划生育组织工作不足的地方,这是特别需要的。
在至少2年,但最好是4到5年内,能以实际恒定量释放避孕剂的这类植入剂是一种新的发展,它确实满足了需求。然而,主要的问题是,为了保证4年内的释放量,植入剂的聚合物材料必须经常含有大量的避孕剂,这即导致了只能用外科手术植入极大的植入剂,或必须被同时植入几个较小的植入剂。
目前,对于多个(较小)植入剂的皮下植入的需要并未引起注意。
从理论上讲,只要是生物相容的,任何聚合物材料都适于开发植入剂,具有孕酮作用的任何材料也一样。在这方面可参见,例如美国专利No.3,279,996(Long    et    al.),在此专利中所描述的植入剂含有一种被聚硅氧烷膜包封的活性物质,还可参见荷兰专利167,850(Zaffaroni),该专利描述的一种植入剂是将活性物质含在一个聚合物中,含活性物质的这种高聚物被一种完全控制释放速度的聚合物膜所包封。然而,如果限定植入剂的大小,如果要求植入剂有一定刚度以便容易植入,而且,如果希望达到至少2年,最好是长 达4到5年的避孕物质释放期,那么所有可行的理论解决办法看来都是失败的。
本发明的植入剂可看作是一种已知的释放体系,它本身是由调节释放速度膜包封的活性物质的芯核所组成。然而,所用聚合物的选择,避孕物质的选择和植入剂的大小都要相互匹配,以便得到一种完全满足上述规定要求的独特的释放体系。
本发明的植入剂是圆柱体或基本上是圆柱体,最大截面约2mm,最好是1.5和2.0mm,其长度可变。然而,为了实用,植入剂的长度不得超过5cm。长度最好是1到4cm。本发明植入剂的这些尺寸是如此小,以致于可用普通皮下注射针进行皮下植入。
本发明植入剂的特征是:
a)乙烯和醋酸乙烯酯共聚物(下称EVA)的芯核材料的分子量要使其熔融指数高于10克/10分钟,且醋酸乙烯酯的含量以重量计为20%或更高;这种芯核材料是作为活性避孕物质的3-酮-去氧孕烯、D-炔诺孕酮或孕二烯酮的基体材料,避孕药的量要足以长期持续恒量释放,每天至少释放15-30μg活性物质,和
b)包封芯核材料的膜,厚度为50-25μm,也是由EVA材料构成,但具有熔融指数低于10克/10分钟的分子量,且乙烯酯的重量含量低于20%,此植入剂是圆柱体或基本是圆柱体,最大外径约为2mm,长度约小于5cm。
在本发明范围内可采用的避孕活性物质是一类活性很强的孕激素,特别是3-酮-去氧孕烯、D-炔诺孕酮或孕二烯酮。这些避孕物质已证明有孕酮作用,每天剂量约15-30μg。
这种芯核材料能含大约75%重量的活性物质,而对EVA芯核材料的效用无重大影响。然而,最好含有约50-60%的重量。
本发明使用的芯核材料是具有高于10克/10分钟,并且最好是25到30克/10分钟熔融指数的EVA聚合物。芯核材料中醋酸乙烯酯含量按重量计高于20%,最好是高于25%。
用作芯核材料的最宜的EVA聚合物是,例如,由ICI销售的标号为28-150,28-399和28-400的Evalane
Figure 881048941_IMG1
,由Atochem销售的28,420,特别是28,25和33,25,以及由杜邦销售的标号为310,250,230,220,和210的Elvax
Figure 881048941_IMG2
膜聚合物也是一种EVA聚合物,但它的分子量比芯核材料的分子量高。这种膜材料的熔融指数低于10克/10分钟,最好小于或等于8克/10分钟;醋酸乙烯酯的含量按重量计低于20%。
用作膜的适宜的EVA聚合物是,例如,标号为501/502(熔融指数2,醋酸乙烯含量为7.5%),554/555(4,12.5%),540(10,18%)特别是571(8,15%)的Evatane ,标号为450,460,470,550,560,650,660,670,750,760和770的Elvax 和由Atochem销售的1080VN5,特别是1040VN4的Evatane
Figure 881048941_IMG5
(通过膜)释放避孕物质的性能,很大程度是由EVA膜中醋酸乙烯酯的含量决定的。
本发明植入剂是借助于所谓同轴挤压的方法获得的。在这种方法中,借助于同轴挤压头,使这两种EVA聚合物以予先调整的层厚度被同轴挤出。
这种同轴挤压方法意味着,酯类聚合物均以熔融态通过同轴挤压头。在此同时,熔融的芯核材料中含有活性物质。
由于这种同轴挤压方法在两种聚合物界面上产生了一个接触层。该接触层可能全部或部分地决定了同轴挤出物的优良的药物释放性质, 但不管怎样,由于活性物质在芯核聚合物中消失,它防止了两种聚合物层在一段时期后彼此松开。两种聚合物层松开会从根本上干扰释放方式。
同轴挤压方法本身是已知工艺,因此将不进一步描述它。
具有最大外径约2mm,最好是约1.5-2.0mm粗的同轴细丝是用同轴挤压方法得到的。然后用常规技术把细丝切断,最长约5cm。
如果需要的话,植入剂的园型末端可用惰性聚合物如聚乙烯、聚丙烯或制膜用的EVA聚合物,或还可用如(医用级)聚硅氧烷粘合剂再保护起来,不过,这显然是不必要的。例如,此保护层可以通过将其表面浸入特定聚合物的熔融体或溶液中而获得。如果必要,该末端也可微烧或捏压密封。
除上述组合外,本发明的植入剂的另一实例是上述植入剂整个外表面用聚硅氧烷薄层包住。所选择的聚硅氧烷应使释放方式不受到任何明显的影响。这并不是打算用此形成第二个释放速度调节层。因之该层是极其纤薄的,甚至约为20-50μm的数量级,不过稍微厚些也是允许的。
此保护层可通过将植入剂浸没在聚硅氧烷的细管中而获得。
本发明的植入剂在上述每种情况下均应含有足够量的活性物质。当在人体中使用时,植入剂可含有实际上恒定释放的期限最少一年的活性物质。这大致意味着,芯核材料必须含有5-15mg的3-酮-去氧孕烯、D-炔诺孕酮或孕二烯酮。植入剂每增加一年的释放期,必须追加活性物质的数量约5-15mg。因之,对于5年的释放期而言,需要25-75mg的活性物质。
本发明的植入剂最好用作皮下植入剂,但也可用于局部植入,例如用于子宫或子宫颈部。
实例1
在一可加热的混磨机中,于80℃将1∶1(重量比)的活性物质3-酮-去氧孕烯和EVA芯核材料(熔融指数400g/10min,醋酸乙烯酯含量按重量计为28%)-Evatane
Figure 881048941_IMG6
28-400相混合。将含有3-酮-去氧孕烯的聚合物片按尺寸压延,然后用挤压机及所谓切断机加工成粒料。
将予定作为芯核的含3-酮-去氧孕烯的粒料和予定作为膜的EVA粒料Evatane -571(熔融指数8g/10min,醋酸乙烯酯含量依重量计15%)分别放入同轴挤压机的两个加料斗中,于约100℃下挤出同轴细丝。当正确选择和调整喷丝头的形状、芯核及外皮材料加入喷丝头的进料速度,以及丝的卷绕速度时,即可以得到外径为1.9mm及表皮厚度为150μm的同轴细丝。在水浴中冷却被挤出的同轴细丝,然后以0.25N的拉伸速度卷绕在滚筒上,细丝的挤出速度为2.3米/秒。典型的制备条件为:
温度(℃)    压力(巴)
挤压机(模筒)    100    60-173
挤压机(模芯)    80    5-46
喷丝头    100
然后将挤出的细丝切成所需的长度。若需要的话再将切断的细丝包于聚硅氧烷中,其方法是使聚硅氧烷管材(尺寸:内/外径为1.57/2.41mm)先在环己烷中溶胀,然后将所需长度的同轴细丝填入,最后于真空中干燥。将所得到的植入剂的两端用聚硅氧烷粘合剂(医用级)封闭。有聚硅氧烷外层的植入剂的外径为2.5mm,无聚硅氧烷外层的植入剂的外径为1.9mm。
于37℃下,在250ml去离子水中检验这种植入剂释放出的3-酮-去氧孕烯。将其放入300ml的锥形瓶中并以150次/分振摇,振幅2.5cm。
结果:
表1
从有及没有聚硅氧烷外层的3cm的植入剂中离体释放出的3-酮-去氧孕烯。
释放量(微克/日.厘米)
天数    无聚硅氧烷外层    有聚硅氧烷外层
1    10.0    6.7
2    10.7    9.7
3    11.3    10.0
4    10.3    9.7
7    10.3    9.3
9    10.0    9.7
10    10.0    9.7
14    10.3    9.7
实际上聚硅氧烷外层对释放形式并无影响。
表2
用这种方法制备的有聚硅氧烷外层的植入剂(3cm)离体释放出的3-酮-去氧孕烯。该植入剂用热处理的方法消毒(20分钟,120℃)
天数    释放量(微克/日.厘米)
2    57.0*
5    14.7
10    10.3
20    11.3
30    10.3
40    10.0
50    10.0
90    9.0
100    9.3
200    8.7
300    8.3
376    8.3
400    7.7
471    7.7
500    8.0
550    7.7
600    8.0
650    7.0
700    6.3
750    6.0
800    6.3
*因热处理消毒,3-酮-去氧孕烯的释放量增大。
表3
体内释放
皮下植入用此方法制备的植入剂(见表2的植入剂)后,3-酮-去氧孕烯在血浆中的平均浓度(3只狗)
天数    血浆中的浓度(pmol/ml.)
1    2.11*
2    0.81
3    0.62
7    0.66
14    0.46
21    0.53
28    0.49
35    0.56
42    0.56
51    0.56
56    0.54
63    0.59
70    0.60
77    0.59
84    0.59
91    0.63
*因热处理消毒,3-酮-去氧孕烯的释放量增大。
实例2
在一个10mm的挤压机中于100℃将活性物质3-酮-去氧孕烯和Evatane
Figure 881048941_IMG8
28-400以重量比1∶1掺混。
用切粒机将所得挤出物切成粒料,然后真空下于135℃加热一小时。
按照和实例1中所述的相同的方法,使用上述含3-酮-去氧孕烯粒料作芯核材料及不含3-酮-去氧孕烯的Evatane
Figure 881048941_IMG9
571粒料作膜材料,挤出同轴细丝。同轴丝的膜厚度为135μm,植入剂的外径为1.65mm。聚硅氧烷管材的尺寸为:1.47(内径)×1.95mm(外径)。4cm长的植入剂的两端用医用级聚硅氧烷粘合剂密封。有聚硅氧烷外层的植入剂的外径为2.05mm。
该同轴丝的典型的制备条件为:
温度(℃)    压力(巴)
挤压机(模筒)    80-100    50-160
挤压机(模芯)    70-85    60-70
喷丝头    100
表4
这种4cm长的植入剂离体释放出的3-酮-去氧孕烯,该植入剂用X射线消毒(25KGY)
天数    释放量(微克/日.厘米)
1    10.0*
2    7.8
3    7.8
4    7.5
10    8.0
20    7.8
30    7.3
40    7.3
50    7.3
100    6.0
150    6.5
200    6.0
250    5.5
300    5.8
350    5.3
400    5.0
450    4.6
500    4.3
550    4.0
*用r-射线消毒代替热消毒时,3-酮-去氧孕烯的增值小。
实例3
类似于实例2制出同轴细丝,但此时膜厚度是90μm,植入剂的外径也是约为1.65mm。为包上聚硅氧烷外层仍是使用聚硅氧烷管材(1.47×1.95mm)。并且两端仍用医用级聚硅氧烷粘合剂密封。有聚硅氧烷外层的植入剂的外径为2.05mm。
同轴细丝的典型制备条件为:
温度(℃)    压力(巴)
挤压机(模筒)    75-100    160-150
挤压机(模芯)    60-100    150-110
喷丝头    125
植入剂的长度是3cm。
表5
在玻璃器皿中从这种未消毒的植入剂中释放出的3-酮-去氧孕烯:
天数    释放量(微克/日.厘米)
1    13.7
6    9.7
9    9.7
10    10.7
20    10.7
30    9.3
40    9.0
50    8.7
60    9.7
70    9.3
80    9.0
90    9.3
100    8.3
110    9.0
实例4
实例4
按照实例2所述的方法制备同轴细丝。
细丝组成为:Evatane
Figure 881048941_IMG10
28.25作芯核材料及Evatane 1040VN4作膜材料。
其它数据为:
膜厚度    75μm;
芯核材料含按重量计60%的3-酮-去氧孕烯;
植入剂外径1.7mm;
植入剂长度3.0cm;
包括聚硅氧烷外层的外径:2.05mm。
植入剂两端用聚硅氧烷粘合剂密封。
表6
未消毒的植入剂的体外释放量:
天数    释放量(微克/日.厘米)
1    24.7
5    22.0
10    13.7
20    12.8
30    12.3
40    11.0
50    11.3
60    11.3
70    11.0
80    11.0
90    10.7
100    10.3
110    10.3
120    8.3
130    10.0
140    8.7
150    8.3
160    9.3
实例5
使用和例4所述的同样的方法和材料。
详细规格:
芯核材料:Evatane
Figure 881048941_IMG12
28.25;
膜材料:Evatane
Figure 881048941_IMG13
1040 VN4
膜厚度:60μm
芯核含60%(按重量计)3-酮-去氧孕烯:
外径:2.0mm;
长度4.0cm;
无聚硅氧烷外层;
植入剂两端不封闭。
表7
体外的释放量:
天数    释放量(微克/日.厘米)
1    43.9
5    27.8
10    24.9
20    21.3
30    21.1
40    18.9
50    19.1
60    17.4
70    15.4
80    16.1
90    18.5
100    16.8
110    16.5
120    16.3

Claims (4)

1、一种制造植入剂的方法,该方法包括将熔融指数高于10克/10分钟和醋酸乙烯酯含量为20%(重量)或更多的乙烯/醋酸乙烯酯共聚物(以下称EVA)的芯核材料与活性避孕物质3-酮-去氧孕烯、D-炔诺孕酮或孕二烯酮混合,其数量为足以长时期恒定地每天至少释放约15-30μg活性物质,同轴挤压该混合物与熔融指数低于10克/10分钟和醋酸乙烯酯含量少于20%(重量)的EVA,形成具有膜厚度为50-250μm的包封芯核的植入剂,该植入剂为最大外径约2mm和长度小于5cm的园柱体或大体为园柱体。
2、权利要求1的方法,其中作为芯核材料使用的EVA的熔融指数为25-30克/10分钟和醋酸乙烯酯含量大于25%(重量)。
3、权利要求1的方法,其中作为膜材料用的EVA的熔融指数小于或等于8克/10分钟和醋酸乙烯酯含量小于20%(重量)。
4、权利要求1-3的任一方法,其中3-酮-去氧孕烯用作避孕物质。
CN88104894A 1987-08-08 1988-08-06 避孕植入剂的制造方法 Expired - Lifetime CN1024753C (zh)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
NL8701868 1987-08-08
NL8701868 1987-08-08

Publications (2)

Publication Number Publication Date
CN1031323A CN1031323A (zh) 1989-03-01
CN1024753C true CN1024753C (zh) 1994-06-01

Family

ID=19850428

Family Applications (1)

Application Number Title Priority Date Filing Date
CN88104894A Expired - Lifetime CN1024753C (zh) 1987-08-08 1988-08-06 避孕植入剂的制造方法

Country Status (19)

Country Link
US (3) US4957119A (zh)
EP (1) EP0303306B1 (zh)
JP (1) JP2571831B2 (zh)
KR (1) KR950008763B1 (zh)
CN (1) CN1024753C (zh)
AT (1) ATE86484T1 (zh)
AU (1) AU603475B2 (zh)
CA (1) CA1309949C (zh)
DE (2) DE3879031T2 (zh)
DK (1) DK173166B1 (zh)
ES (1) ES2054784T3 (zh)
FI (1) FI93421C (zh)
HK (1) HK1002020A1 (zh)
IE (1) IE61730B1 (zh)
MX (1) MX9203817A (zh)
NL (1) NL980027I2 (zh)
NZ (1) NZ225399A (zh)
PT (1) PT88220B (zh)
ZA (1) ZA885034B (zh)

Families Citing this family (94)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5114719A (en) * 1987-04-29 1992-05-19 Sabel Bernhard A Extended drug delivery of small, water-soluble molecules
US5156164A (en) * 1988-10-13 1992-10-20 Leveen Harry H Iodine contraceptive sponge
BE1002600A3 (fr) * 1988-11-23 1991-04-09 Wildemeersch Dirk Dispositif intra-uterin perfectionne.
IE71202B1 (en) * 1990-12-17 1997-02-12 Akzo Nv Progestagen-only contraceptive
WO1993017662A1 (en) * 1992-03-02 1993-09-16 Daratech Pty. Ltd. Improved implants
DE69329407T2 (de) * 1992-06-02 2001-05-03 Bard Inc C R Verfahren und Implantatvorrichtung für Langzeitwirkstoffabgabe
US5368588A (en) * 1993-02-26 1994-11-29 Bettinger; David S. Parenteral fluid medication reservoir pump
US5443461A (en) * 1993-08-31 1995-08-22 Alza Corporation Segmented device for simultaneous delivery of multiple beneficial agents
US5681817A (en) 1994-02-04 1997-10-28 The Medical College Of Hampton Roads Treatment of ovarian estrogen dependent conditions
US5660848A (en) * 1994-11-02 1997-08-26 The Population Council, Center For Biomedical Research Subdermally implantable device
US5521166A (en) * 1994-12-19 1996-05-28 Ortho Pharmaceitical Corporation Antiprogestin cyclophasic hormonal regimen
DE19539361A1 (de) * 1995-10-23 1997-04-24 Basf Ag Verfahren zur Herstellung von mehrschichtigen, festen Arzneiformen zur oralen oder rektalen Verabreichung
US5733565A (en) * 1996-02-23 1998-03-31 The Population Council, Center For Biomedical Research Male contraceptive implant
CN1088993C (zh) * 1996-10-11 2002-08-14 上海市计划生育科学研究所 含孕二烯酮的长效皮下避孕埋植剂
US6203813B1 (en) 1997-01-13 2001-03-20 Lance L. Gooberman Pharmaceutical delivery device and method of preparation therefor
TW358031B (en) * 1997-04-11 1999-05-11 Akze Nobel N V Drug delivery system for 2 or more active substances
DE19744135C1 (de) * 1997-09-29 1999-03-25 Schering Ag Beschichtete medizinische Implantate, Verfahren zu ihrer Herstellung und ihre Verwendung zur Restenoseprophylaxe
ATE313422T1 (de) 1998-05-01 2006-01-15 Duramed Pharmaceuticals Inc Verfahren zur spritzgussherstellung von vorrichtungen mit kontrollierter wirkstofffreisetzung und damit hergestellte vorrichtung
US6117441A (en) * 1998-07-02 2000-09-12 The Population Council, Inc. Silicone core long term androgen delivery implant
AU4957999A (en) * 1998-07-17 2000-02-07 Pharmacia & Upjohn Company Subcutaneous medroxyprogesterone acetate for contraception
US6117442A (en) * 1998-11-12 2000-09-12 Leiras Oy Drug delivery device, especially for the delivery of androgens
US6063395A (en) * 1998-11-12 2000-05-16 Leiras Oy Drug delivery device especially for the delivery of progestins and estrogens
US6217895B1 (en) 1999-03-22 2001-04-17 Control Delivery Systems Method for treating and/or preventing retinal diseases with sustained release corticosteroids
CA2267743C (en) * 1999-03-30 2011-07-26 Robert F. Casper Low dose estrogen interrupted hormone replacement therapy
US6375972B1 (en) * 2000-04-26 2002-04-23 Control Delivery Systems, Inc. Sustained release drug delivery devices, methods of use, and methods of manufacturing thereof
AU9177501A (en) * 2000-08-23 2002-03-04 Akzo Nobel Nv Novel testosterone ester formulation for human use
EP1545705A4 (en) 2000-11-16 2010-04-28 Microspherix Llc FLEXIBLE AND / OR ELASTIC BRACHYTHERAPY SEED OR STRAND
EP1387670B1 (en) 2001-05-11 2008-10-15 Ortho-McNeil-Janssen Pharmaceuticals, Inc. Immune modulation device for use in animals
HUP0400390A2 (hu) 2001-07-02 2004-09-28 Akzo Nobel N.V. Tetrahidrokinolin-származékok és ezeket tartalmazó gyógyszerkészítmények
WO2003017971A1 (en) * 2001-08-31 2003-03-06 Schering Oy Drug delivery system
ES2252540T3 (es) 2001-09-04 2006-05-16 Akzo Nobel N.V. Tieno (2,3-d) pirimidinas glicino-sustituidas con actividad agonistas combinada lh y fsh.
TWI228508B (en) 2001-09-04 2005-03-01 Akzo Nobel Nv Thieno[2,3-d]pyrimidines with combined LH and FSH agonistic activity
BR0307218A (pt) * 2002-01-24 2004-12-07 Smart Drug Systems Inc Composição farmacêutica com liberação prolongada
JP2005519964A (ja) * 2002-03-11 2005-07-07 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ スルファターゼ阻害プロゲストゲンのみの避妊レジメン
TWI297685B (en) 2002-04-04 2008-06-11 Organon Nv Non-steroidal progesterone receptor modulators
US8871241B2 (en) * 2002-05-07 2014-10-28 Psivida Us, Inc. Injectable sustained release delivery devices
BR0309844A (pt) * 2002-05-07 2005-02-15 Control Delivery Sys Inc Processos para formação de um dispositivo para a distribuição de droga
PT2561860T (pt) * 2002-05-31 2018-05-08 Titan Pharmaceuticals Inc Dispositivo polimérico implantável para a libertação prolongada de buprenorfina
DE60309895T2 (de) * 2002-08-28 2007-10-18 Casper, Robert-Frederic, Toronto Estrogenersatztherapie
US7795280B2 (en) 2002-11-07 2010-09-14 N.V. Organon Indoles useful in the treatment of androgen-receptor related diseases
TWI306855B (en) 2002-12-20 2009-03-01 Organon Nv Tetrahydroquinoline derivatives
TWI322012B (en) 2002-12-20 2010-03-21 Organon Nv Tetrahydroquinoline derivatives
ZA200507877B (en) 2003-03-31 2007-01-31 Titan Pharmaceuticals Inc Implantable polymeric device for sustained release of dopamine agonist
CA2523859C (en) 2003-04-29 2011-08-02 The General Hospital Corporation Methods and devices for the sustained release of multiple drugs
TWI336627B (en) * 2003-05-23 2011-02-01 Organon Nv Drug delivery system,and use and manufacturing method thereof
ZA200509063B (en) * 2003-05-30 2007-03-28 Titan Pharmaceuticals Inc Impiantable polymeric device for sustained release of nalmefene
JP2007524616A (ja) * 2003-06-20 2007-08-30 ヴァイラル・ジェノミックス・インコーポレーテッド Hivを処置するための組成物および方法
WO2005070445A2 (en) * 2004-01-13 2005-08-04 Vasogenix Pharmaceuticals, Inc. Methods for treating acute myocardial infarction by calcitonin gene related peptide and compositions containing the same
WO2005070444A2 (en) * 2004-01-13 2005-08-04 Vasogenix Pharmaceuticals, Inc. Methods for treating acute myocardial infarction by calcitonin gene related peptide and compositions containing the same
CA2552677A1 (en) * 2004-01-13 2005-07-28 Vasogenix Pharmaceuticals, Inc. Controlled release cgrp delivery composition for cardiovascular and renal indications
TWI434676B (zh) * 2004-03-19 2014-04-21 Merck Sharp & Dohme 可用x射線看出之藥物遞送裝置
TW200531977A (en) 2004-03-25 2005-10-01 Akzo Nobel Nv Progesterone receptor modulators
TW200602317A (en) 2004-04-23 2006-01-16 Akzo Nobel Nv Novel androgens
EP1629844B2 (en) 2004-07-13 2012-04-18 Bayer Schering Pharma Oy A longterm delivery system with controlled initial burst
PT1781264E (pt) 2004-08-04 2013-10-16 Evonik Corp Métodos para o fabrico de dispositivis de administração e dispositivos para a mesma
US11246913B2 (en) 2005-02-03 2022-02-15 Intarcia Therapeutics, Inc. Suspension formulation comprising an insulinotropic peptide
JP2008543863A (ja) * 2005-06-15 2008-12-04 ハイドラ バイオサイエンシズ インコーポレイテッド 精子の運動亢進のモジュレーター及びその利用
EP1743638A1 (en) 2005-07-15 2007-01-17 Laboratorios Del Dr. Esteve, S.A. Pharmaceutical formulations of substituted pyrazoline compounds
PL2359808T3 (pl) 2006-08-09 2013-10-31 Intarcia Therapeutics Inc Osmotyczne systemy dostawcze i zespoły tłokowe
US7989442B2 (en) 2006-09-27 2011-08-02 N.V. Organon Progesterone receptor modulators
CN101209238B (zh) * 2006-12-27 2012-05-09 辽宁省计划生育科学研究院 含孕二烯酮的生物降解型长效皮下避孕埋植剂及其制备
MX2009011123A (es) 2007-04-23 2009-11-02 Intarcia Therapeutics Inc Formulaciones de suspensiones de peptidos insulinotropicos y sus usos.
US8063037B2 (en) 2007-05-07 2011-11-22 N. V. Organon Progesterone receptor modulators
CN101130057B (zh) * 2007-07-06 2011-04-27 复旦大学 胸腺五肽长效植入剂及其制备方法
AR066166A1 (es) 2007-09-21 2009-07-29 Organon Nv Sistema de suministro de droga
US20100303841A1 (en) * 2007-11-27 2010-12-02 Nira Hochman Adjuvant
JP5502751B2 (ja) 2007-12-20 2014-05-28 エボニック コーポレイション 低残留溶媒濃度を有する微粒子を調製するためのプロセス
EP2240155B1 (en) 2008-02-13 2012-06-06 Intarcia Therapeutics, Inc Devices, formulations, and methods for delivery of multiple beneficial agents
NZ598686A (en) 2009-09-28 2014-05-30 Intarcia Therapeutics Inc Rapid establishment and/or termination of substantial steady-state drug delivery
CN102740830A (zh) * 2009-12-23 2012-10-17 普西维达公司 缓释递送装置
US20120208755A1 (en) 2011-02-16 2012-08-16 Intarcia Therapeutics, Inc. Compositions, Devices and Methods of Use Thereof for the Treatment of Cancers
US10028858B2 (en) 2011-07-11 2018-07-24 Medicines360 Intrauterine systems, IUD insertion devices, and related methods and kits therefor
AR089765A1 (es) * 2012-01-23 2014-09-17 Bayer Oy Un sistema para el suministro de un farmaco
US10188426B2 (en) 2013-02-06 2019-01-29 Mark SILLENDER Embryo transfer catheter and method
EP2953678B1 (en) 2013-02-06 2020-03-25 Sillender, Mark Therapeutic substance transfer catheter
US10413504B2 (en) 2013-12-11 2019-09-17 Merck Sharp & Dohme Corp. Intravaginal ring drug delivery system
WO2015086489A1 (en) 2013-12-11 2015-06-18 Merck Sharp & Dohme B.V. Drug delivery system for delivery of anti-virals
US9889085B1 (en) 2014-09-30 2018-02-13 Intarcia Therapeutics, Inc. Therapeutic methods for the treatment of diabetes and related conditions for patients with high baseline HbA1c
WO2016149561A1 (en) * 2015-03-17 2016-09-22 Oak Crest Institute Of Science Subdermal implants for the sustained delivery of water-soluble drugs
AU2016270984B2 (en) 2015-06-03 2021-02-25 Intarcia Therapeutics, Inc. Implant placement and removal systems
CN109310743A (zh) 2016-05-16 2019-02-05 因塔西亚制药公司 胰高血糖素受体选择性多肽及其使用方法
USD860451S1 (en) 2016-06-02 2019-09-17 Intarcia Therapeutics, Inc. Implant removal tool
USD840030S1 (en) 2016-06-02 2019-02-05 Intarcia Therapeutics, Inc. Implant placement guide
WO2018064544A1 (en) 2016-09-29 2018-04-05 Gesea Biosciences Inc. Bioerodible contraceptive implant and methods of use thereof
EP3565580B1 (en) 2017-01-03 2024-03-06 i2o Therapeutics, Inc. Continuous administration of exenatide and co-adminstration of acetaminophen, ethinylestradiol or levonorgestrel
US11571328B2 (en) 2018-04-09 2023-02-07 Medicines360 IUD insertion devices
EP3801462A4 (en) 2018-05-24 2022-03-16 Celanese EVA Performance Polymers LLC IMPLANTABLE DEVICE FOR EXTENDED RELEASE OF A MACROMOLECULAR DRUG COMPOUND
SG11202005949UA (en) * 2018-05-24 2020-07-29 Celanese Eva Performance Polymers Corp Implantable device for sustained release of a macromolecular drug compound
US20200261258A1 (en) 2019-02-19 2020-08-20 Medicines360 Devices, systems, methods and kits for insertion and removal of iuds
BR102020007749A2 (pt) 2020-04-17 2021-11-03 Edson Luiz Peracchi Implante subcutâneo reabsorvível de longa duração com liberação controlada de substância farmacologicamente ativa pré-concentrada em polímero para tratamento da endometriose
EP4159207A4 (en) 2020-05-29 2024-04-17 Peracchi Edson Luiz LONG-LASTING SUBCUTANEOUS IMPLANT WITH SUSTAINED RELEASE OF PRE-CONCENTRATED PHARMACOLOGICAL ACTIVE SUBSTANCE IN POLYMER FOR THE TREATMENT OF CHRONIC ADRENALINE INSUFFICIENCY OR HYPOCORTISOLISM
BR102020013862A2 (pt) 2020-07-07 2022-01-18 Edson Luiz Peracchi Implante subcutâneo reabsorvível de longa duração com liberação sustentada de substância farmacologicamente ativa pré-concentrada em polímero para tratamento da doença de parkinson
EP4316464A1 (en) 2021-03-29 2024-02-07 Edson Luiz Peracchi Long-lasting resorbable subcutaneous implant with prolonged release of pre-concentrated pharmacologically active substance in polymer for the treatment of hypothyroidism, and method
CN113209050A (zh) * 2021-05-14 2021-08-06 浙江恒冀制药有限责任公司 基于生物相容性聚合物的长效体内皮埋或内植缓释制剂

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3903880A (en) * 1972-08-17 1975-09-09 Alza Corp Intrauterine device for managing the reproductive process
US3926188A (en) * 1974-11-14 1975-12-16 Alza Corp Laminated drug dispenser
US4582052A (en) * 1982-03-23 1986-04-15 Repromed, Inc. Povidone-iodine dispensing fiber
NZ200564A (en) * 1982-05-10 1987-03-06 Ahi Operations Ltd Device for slowly releasing chemicals into body cavities of animals
US4601714A (en) * 1983-07-07 1986-07-22 Burnhill Michael S Vaginal device
US4629621A (en) * 1984-07-23 1986-12-16 Zetachron, Inc. Erodible matrix for sustained release bioactive composition
US4596576A (en) * 1984-10-12 1986-06-24 Akzo N.V. Release system for two or more active substances
US4720384A (en) * 1985-05-03 1988-01-19 E. I. Du Pont De Nemours And Company Manufacture of hollow fine tubular drug delivery systems
US4673565A (en) * 1985-05-03 1987-06-16 E. I. Du Pont De Nemours And Company Pharmaceutical compositions containing hollow fine tubular drug delivery systems

Also Published As

Publication number Publication date
HK1002020A1 (en) 1998-07-24
MX9203817A (es) 1992-08-01
DE3879031T2 (de) 1993-06-24
DE3879031D1 (de) 1993-04-15
IE882118L (en) 1989-02-08
IE61730B1 (en) 1994-11-30
JP2571831B2 (ja) 1997-01-16
FI93421C (fi) 1995-04-10
EP0303306B1 (en) 1993-03-10
FI883594A0 (fi) 1988-08-01
ZA885034B (en) 1989-03-29
FI883594A (fi) 1989-02-09
ES2054784T3 (es) 1994-08-16
PT88220A (pt) 1989-06-30
PT88220B (pt) 1995-03-01
NL980027I1 (nl) 1998-12-01
DK438688A (da) 1989-02-09
NL980027I2 (nl) 1999-02-01
JPS6470410A (en) 1989-03-15
AU2044988A (en) 1989-03-02
CN1031323A (zh) 1989-03-01
KR890003360A (ko) 1989-04-14
US5088505A (en) 1992-02-18
US5150718A (en) 1992-09-29
DK438688D0 (da) 1988-08-05
EP0303306A1 (en) 1989-02-15
NZ225399A (en) 1990-09-26
US4957119A (en) 1990-09-18
AU603475B2 (en) 1990-11-15
FI93421B (fi) 1994-12-30
DE19975054I2 (de) 2000-04-13
CA1309949C (en) 1992-11-10
KR950008763B1 (en) 1995-08-08
ATE86484T1 (de) 1993-03-15
DK173166B1 (da) 2000-02-28

Similar Documents

Publication Publication Date Title
CN1024753C (zh) 避孕植入剂的制造方法
CN1049787A (zh) 胃逗留装置
CN1170604C (zh) 含有可相容的抗菌剂的电转运装置
CN1549703A (zh) 药物输送体系
CN1062290A (zh) 低雌激素的口服避孕药
CN1794974A (zh) 药物递送体系
CN1268879A (zh) 基于胶原蛋白的生物相容性的能吸收紫外线的光学透明的聚合材料及其制造方法
CN1089867A (zh) 低熔和/或挥发性活性物膏药
CN101036633A (zh) 一种奥美拉唑肠溶微丸胶囊及其制备方法
CN1933820A (zh) 基于聚乙烯乙酸乙烯酯共聚物的药物递送系统
CN1127529A (zh) 人白细胞介素-10的激动剂和拮抗剂
CN1809643A (zh) 在膜蛋白中插入弗林蛋白酶切割位点及其用途
CN1094284A (zh) 基于去甲基甲地孕酮衍生物的新颖组合物及其生产方法
CN1896107A (zh) 类天蚕素a-马盖宁杂合基因工程抗菌肽
CN1840177A (zh) 胸腺肽α1注射液及其制备方法
CN1035986C (zh) 持久释放的丸药组合物的制备方法
CN1589133A (zh) 不透射线的缓释药物系统
CN1265798C (zh) 含有藻酸盐的药物组合物
CN101036784A (zh) 一种乙型肝炎治疗性细胞毒性t细胞表位疫苗及其制备方法
CN1638747A (zh) 持续释放药物组合物
CN1184960C (zh) 多颗粒药剂、构成它的颗粒、制备它的方法和装置
CN1899287A (zh) 一种治疗焦虑症的缓释药物组合物及其制备方法
CN101073562A (zh) 一种牛磺酸眼用即型凝胶
CN1208057C (zh) 复方莪术油制剂及其制备方法
CN1957864A (zh) 一种TiNi形状记忆合金宫内节育器的制作方法

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C15 Extension of patent right duration from 15 to 20 years for appl. with date before 31.12.1992 and still valid on 11.12.2001 (patent law change 1993)
OR01 Other related matters
ASS Succession or assignment of patent right

Owner name: ORGANON NV

Free format text: FORMER OWNER: AKZO NOVEL N.V. CORP.

Effective date: 20070309

C41 Transfer of patent application or patent right or utility model
C56 Change in the name or address of the patentee

Owner name: AKZO NOVEL N.V. CORP.

Free format text: FORMER NAME OR ADDRESS: AKZO N. V.

CP03 Change of name, title or address

Address after: Holland Arnhem

Patentee after: AKZO NOBEL N.V.

Address before: Holland Arnhem

Patentee before: Akzo N

TR01 Transfer of patent right

Effective date of registration: 20070309

Address after: Holland

Patentee after: N.V. ORGANON

Address before: Holland Arnhem

Patentee before: AKZO NOBEL N.V.

C17 Cessation of patent right
CX01 Expiry of patent term