TWI333422B - Oral pharmaceutical preparations comprising ion exchange resins with active substance loading and pseudoplastic gel-former thickeners - Google Patents
Oral pharmaceutical preparations comprising ion exchange resins with active substance loading and pseudoplastic gel-former thickeners Download PDFInfo
- Publication number
- TWI333422B TWI333422B TW092114643A TW92114643A TWI333422B TW I333422 B TWI333422 B TW I333422B TW 092114643 A TW092114643 A TW 092114643A TW 92114643 A TW92114643 A TW 92114643A TW I333422 B TWI333422 B TW I333422B
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- Taiwan
- Prior art keywords
- acid
- preparation
- ion exchange
- cellulose
- intellectual property
- Prior art date
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- 239000013543 active substance Substances 0.000 title description 17
- 239000003456 ion exchange resin Substances 0.000 title description 13
- 229920003303 ion-exchange polymer Polymers 0.000 title description 13
- 239000002562 thickening agent Substances 0.000 title description 2
- 239000008183 oral pharmaceutical preparation Substances 0.000 title 1
- -1 sylvestite Polymers 0.000 claims description 40
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- 238000002360 preparation method Methods 0.000 claims description 25
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- GYDJEQRTZSCIOI-LJGSYFOKSA-N tranexamic acid Chemical compound NC[C@H]1CC[C@H](C(O)=O)CC1 GYDJEQRTZSCIOI-LJGSYFOKSA-N 0.000 description 1
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- UXQDWARBDDDTKG-UHFFFAOYSA-N tromantadine Chemical compound C1C(C2)CC3CC2CC1(NC(=O)COCCN(C)C)C3 UXQDWARBDDDTKG-UHFFFAOYSA-N 0.000 description 1
- 229960000832 tromantadine Drugs 0.000 description 1
- 229960004799 tryptophan Drugs 0.000 description 1
- MSRILKIQRXUYCT-UHFFFAOYSA-M valproate semisodium Chemical compound [Na+].CCCC(C(O)=O)CCC.CCCC(C([O-])=O)CCC MSRILKIQRXUYCT-UHFFFAOYSA-M 0.000 description 1
- 229960000604 valproic acid Drugs 0.000 description 1
- 229960003165 vancomycin Drugs 0.000 description 1
- MYPYJXKWCTUITO-LYRMYLQWSA-N vancomycin Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=C2C=C3C=C1OC1=CC=C(C=C1Cl)[C@@H](O)[C@H](C(N[C@@H](CC(N)=O)C(=O)N[C@H]3C(=O)N[C@H]1C(=O)N[C@H](C(N[C@@H](C3=CC(O)=CC(O)=C3C=3C(O)=CC=C1C=3)C(O)=O)=O)[C@H](O)C1=CC=C(C(=C1)Cl)O2)=O)NC(=O)[C@@H](CC(C)C)NC)[C@H]1C[C@](C)(N)[C@H](O)[C@H](C)O1 MYPYJXKWCTUITO-LYRMYLQWSA-N 0.000 description 1
- MYPYJXKWCTUITO-UHFFFAOYSA-N vancomycin Natural products O1C(C(=C2)Cl)=CC=C2C(O)C(C(NC(C2=CC(O)=CC(O)=C2C=2C(O)=CC=C3C=2)C(O)=O)=O)NC(=O)C3NC(=O)C2NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(CC(C)C)NC)C(O)C(C=C3Cl)=CC=C3OC3=CC2=CC1=C3OC1OC(CO)C(O)C(O)C1OC1CC(C)(N)C(O)C(C)O1 MYPYJXKWCTUITO-UHFFFAOYSA-N 0.000 description 1
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Classifications
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Description
1333422 A7 "____ B7 五、發明說明(). 本發明係關於供口服施藥之醫藥製劑,其包含—或多 種結合於離子交換劑之活性物質。為了改良物理安定性及 接受性,尤其是於動物中,其包含假塑性凝膠形成劑增稠 劑。 5 使活性醫藥物質結合至離子交換樹脂以便使其更容易 施藥係為已長久已知,例如具明顯固有氣味之活性物質 (CH 383 552) »使活性醫藥物質結合至離子交換樹脂以便 於延長期間進行活性物質之均勻釋放亦為已知(DE 30 28 082)。此外,使活性驅蟲劑物質結合至離子交換樹脂以便 10影響活性物質之味道亦為已知(DE 30 28 082)。藉結合至離 子交換樹脂,亦可能掩蔽喳咁酮抗生素之苦味以便容許施 藥至動物(EP-A-295 495)。 上述主題揭示結合至離子交換樹脂之苦味4咐酮_缓 酸衍生物的調配物以及其製法。討論中之離子交換樹脂包 15含弱酸性陽離子型,其基質可為凝膠狀或大孔的。供離子 交換劑用之適合的基礎單體係為可聚合的單體,其可藉適 當的側鏈官能化以提供陽離子交換樹脂。離子交換劑係以 經濟部智慧財產局員工消費合作社印製 商標名 Lewatit®、Amberlite® ' Purolite® 或 Dowex® 為已 知。對應的調配物已揭示於獸醫藥中作為供豬用之飼料藥 20 劑。 八 離子交換劑之通常不佳的表面質地經常在顆粒沉殿於 液悲'懸浮液後造成嚴重的沉降結塊。 本申請人之專利申請案WO 03/007995揭示此等離子 父換劑之安定化作用,其係藉研磨作用使得至少90%顆粒
1333422 A7 B7 五、發明說明(2 ) 1 小於50微米。可能地,由於不規則表面變圓之緣故,形 成的沉積物接著容易地重新攪動。然而’此種研磨操作非 常耗工且使得此製劑之製程明顯地更昂責。 藉使用凝膠形成劑(例如羥乙基纖維素、羥丙基纖維 5素、羥甲基丙基纖維素)使醫藥製劑固化至沉降作用不再 能發生之程度亦是已知的。然而,此種半固態製劑在其自 身重力作用下不再流動。以此等製劑實現液態醫藥形式是 困難的。 再者,已知離子交換樹脂之液態、水性懸浮液可使用 10 假塑性凝膠形成劑(例如聚丙烯酸、黃原膠、黃蓍膠 (tragac’anth)、羧曱基纖維素鈉、黏土)安定。舉例來說',美 國專利US 6 146 622及US 2 002 035 154揭示以聚丙烯酸 (Carbopol 974P)或黃原膠安定之陽離子交換劑的水性懸浮 液。美國專利US 5 612 026揭示一種含陰離子交換劑與黃 15 原膠之飲料混合物。Balkus 等人(Langmuir,12,6277-6281 (1996))發表以黃原膠安定含亂賀客多力士 (hect〇rite)懸浮 液。使用假塑性聚合物對沉降作用安定之水性離子交換懸 浮液之進一步說明可見於日本專利jp 〇5 279 245、JP 05 經濟部智慧財產局員工消費合作社印製 279 246、Sprockel 等人,Drug Dev. Ind. Pharm. 15, 1275- 20 1287 (1989)、歐洲專利 EP 139 881、日本專利 Jp 〇1 〇71 823、JP 01 071 822及JP 63 230 636。此種靜止的懸浮液 狀態具高黏度,藉以防止懸浮的離子交換劑顆粒之沉降作 用。於力量之作用下,系統液化且因而可容易地果取或喷 淋。
本纸張尺度適用中國國家標準(CNS)A4規格(210 X -4- 五、發明說明(3 ) 令人驚舒地,頃發現離子交換劑 ϋ(已以假塑性聚合物增稍)具特佳的口感,並且t懸 化藥後極妥善地被接收及耐受。再者n ; 口服 :組份之沉降作用具安定性且具有針對口服 =動性質。當於胃中吸收後,活性醫藥快逮 離。因此,相較於未結合的活性物質, 力學分布中,有少許的變化。 、醫樂動 因此’本發明係提供: 10 •一種醫藥製劑,其包含—或多種結合於離 性物質,其特徵在於填_子交_係分散於含有t 一種假塑性凝膠形成劑之載體媒介物中。 •醫藥製劑之用途’該醫藥製劑含有裝填活性物質之離子 =換劑及至少-種假塑性凝膠形成劑(由於在獸醫藥物 15 彳用之假塑性凝謬形成劑包含微結晶之纖維素、纖維 素醋(甲基纖維素、經乙基纖維素、經丙基纖維素、声甲 基丙基纖維素、甲基經丙基纖維素、缓甲基纖維辛納)、 黃原穆、黃箸膠、瓜爾豆膠、阿拉伯樹膠'殿粉及殿粉衍 生物(例如叛甲基殿粉)、明穆、高分散的♦石(例如 20 $丙烯酸、硬脂酸銘_土)。亦可能使所述的 凝膠形成劑彼此合併。 高分散的石夕石據發現較佳係用於非水性載體液體 之增 稠作用。為了水性載體液體之增稠作用,較佳使用微結晶 之纖維素、纖維素謎、黃原膠、聚兩稀酸及黏土或所述的 -5- 本紙張尺度適用中國國冢標準(CNS)A4規格(210 X 297公釐了 1333422 A7 B7 五、發明說明(4)· 凝膠形成劑之混合物。於本文中特佳使用微結晶之纖維 素、羧曱基纖維素鈉、黃原膠、聚丙烯酸及黏土。
裝 I I I 舉例來說,離子交換劑樹脂可具有凝膠狀或大孔基 質。供離子交換劑用之適合的基礎單體包含可聚合的單 5 體,其可藉適當的官能化作用以轉化為離子交換樹脂。適 合的單體之實例包含(甲基)丙烯酸酯、(甲基)丙烯腈及笨 乙烯衍生物。其他用以製備基礎聚合物之單體包含聚乙稀 基化合物,例如二乙烯基苯、乙二醇二甲基丙烯酸酯或亞 甲基雙丙烯醯胺。可導致離子交換劑之縮合的樹脂亦適 10 合,實例為具適當官能基團之酚-曱醛樹脂。 碍 可用之離子交換劑為已知。許多離子交換劑類型友其 製法之進一步細節可見於例如Ullmann’s Encyclopedia of Industrial Chemistry(Ullmann 之工業化學大全)(2001 年發 行,第6版較佳的大孔樹脂可具有不同的孔體積。適 15 合的離子交換樹脂之交聯程度應較佳為至多20%,且特佳 者為至多12%。合成的樹脂通常具粒徑為1至300微米, 較佳為10至200微米。習用的市售離子交換樹脂為
Lewatit®、Amberlite®、Dowex®及 Purolite®。 經濟部智慧財產局員工消費合作社印製 為了結合驗性或1%離子活性物質,使用酸性離子交換 20 劑是可能的。 所用之強酸性離子交換劑較佳為以聚(苯乙烯,二乙烯 基苯)績酸為基礎者。可提到之實例包含: • Amberlite IRP 09 : Na型之聚(苯乙烯,二乙烯基苯)磺 酸;通常粒徑:10-25% > 75微米,最大1%大於15〇微 本紙張尺度適用中國國家標準(CNS)A4規格(2Ϊ0 X 297公爱) 1333422 A7 B7 五、發明說明(5 ) · 米,K交換容量:110-135毫克/克,相當於2.75-3.38當 量/公斤》 • PuroliteC 100HMR : Η型之聚(苯乙烯,二乙烯基苯)項 酸;通常粒徑:最大1% > 150微米,交換容量:至少 5 3.2當量/公斤。 • Purolite C 100 MR ·· Na型之聚(苯乙晞,二乙稀基苯)績 酸,相當於 Amberlite IRP 69。 •Lewatit Catalyst K 1481 : Η型之聚(苯乙烯,二乙稀基苯) 磺酸;通常粒徑:最小70% < 30微米,交換容量:5.0 10 •當量/公斤。 • Lewasorb SW 12 : Na型之聚(苯乙烯,二乙烯基笨)續 酸,另外相當於Lewatit K 1481。 就弱酸性離子交換劑而言,可使用特別地以曱基丙缔 酸-二乙烯基苯共聚合物為基礎者。實例包含: 15 · Amberlite IRP 64 : Η型之甲基丙烯酸-二乙烯基笨共聚 合物;通常粒徑:15-30% > 75微米,最大1% > 150微 米,交換容量:最小10當量/公斤。 • Purolite C 115 K MR :鉀型之甲基丙烯酸-二乙烯基苯共 聚合物;通常粒徑:最大1%> 150微米。 20 · Purolite C 115 H MR: Η型之甲基丙烯酸-二乙烯基笨共 聚合物,另外類似Purolite C 115 K MR。 •Lewatit CNP 105 :大孔的甲基丙烯酸-二乙烯基笨共聚 合物’交換容量:最小1.4當量/公斤。 為了結合酸性及陰離子活性物質,使用陰離子交換劑 -7- 本紙張尺度適用中國國家標準(CNS)A4規格_ΰ丨0 X 297公爱了
--------J. I 好丨 線. 經濟部智慧財產局員工消費合作社印製 1333422 A7
是可能的。 所用之陰離子交換劑較佳為具胺及/或録側基團之聚笨 乙烯樹脂。可提到之實例包含: • Purolite A 430 MR:氯化聚(苯乙烯_二乙烯基苯)三甲基 5 銨,交換容量:3.7-4.8當量/公斤。 •Lewatit MP 500:氣化聚(苯乙烯-二乙烯基苯)三▼基 銨,交換容量:最小U當量/公斤。 土 •Lewatit MP 62 WS :氣化聚(苯乙烯-二乙烯基苯)三甲基 錢,交換容量:最小1.7當量/公斤。 10 .Duolite AP143/109;3氯化聚(苯乙稀-二乙烯基苯)三甲基 銨,交換容量:3.7-4.8當量/公斤。 , 可使用具驗性官能(可結合至陽離子交換劑)之活性醫 藥物質。此針對具討厭氣味或造成討厭味道感覺(當口服 施藥時)之藥劑特別適合。此種活性物質可提到之實例包 15含喳咁酮抗生素及相關的抗生素,尤其是揭示於以下文獻 者.美國專利US 4 670 444 (拜耳廠股份有限公司)、US 4 472 405 (Riker Labs)、US 4 730 000 (Abbott)、US 4 861 779 (Pfizer)、US 4 382 892 (Daiichi)、US 4 704 459 經濟部智慧財產局員工消費合作社印製 (Toyama);特例包含如下:賓諾氟沙星(ben〇fl〇xacin)、賓 20 氟沙星(binfloxacin)、欣諾沙星(cinoxacin)、環丙沙星 (ciprofloxacin)、丹謹氟沙星(danofloxacin)、二氟沙星 (difloxacin)、恩諾沙星(enoxacin)、恩羅氟沙星 (enrofloxacin)、氟》羅沙星(fleroxacin)、依巴免沙星 (ibafloxacin)、左旋氟沙星(levofloxacin)、洛美氟沙星 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 1333422 Α7 * Β7五、發明說明(0. (lomefloxacin)、馬柏氟沙星(marbofloxacin)、莫西氟沙星 (moxifloxacin)、諾氟沙星(norfloxacin)、歐說沙星 (ofloxacin)、歐必氟沙星(orbifloxacin)、沛氟沙星 (pefloxacin)、匹培咪迪酸(pipemidic acid)、特馬氟沙星 5 (temafloxacin)、多舒敗沙星(tosufloxacin)、沙拉氟沙星 (sarafloxacin)、斯巴氟沙星(sparfloxacin)。喳啉酮之較佳基團係為具式(I)或(II)者: 經濟部智慧財產局員工消費合作社印製 ο 15
2 R 〇 ο C 〇
① (Π) 20 其中X代表氫、齒素、Cm-烷基、Cm-烷氧基、ΝΗ2 Υ代表以下結構之基團 -9-
本紙張尺度適用_國國家標準(CNS)A4規格(210x297公釐) 經濟部智慧財產局員工消費合作杜印製 1333422 A7 B7 五、發明說明(8)
5 其中 R4代表視需要選用之羥基取代或甲氧基取代之直鏈或分 支鏈CrC4-烷基、環丙基、具1至3個碳原子之醯 基, 10 R5代表氫、曱基、苯基、噻嗯基或吡啶基, R6代表氫或CVCV烷基, ’ R7代表氮或C1-C4-烧基* R8代表氫或CrC4-烷基, 且 15 R1代表具1至3個碳原子之烷基基團、環丙基、2-氟乙 基、曱氧基、4-氟苯基、2,4-二氟苯基或甲基胺基, R2代表氫或視需要選用具1至6個碳原子之甲氧基取代 或2-曱氧基取代之烷基以及環己基、苄基、2-氧基丙 基、苄醯甲基、乙氧基羰基曱基、三甲基乙醯氧基甲 20 基, R3代表氫、甲基或乙基, A 代表氮、=CH-、=C(鹵素)、=C(OCH3)-、=C(CH3)-或 =C(CN), B代表氧、視需要選用之曱基取代或笨基取代之=NH或 -10- 本紙張尺度適用中國國家標準(CNS)A4規格(210x297公釐)
1333422 A7 〃 B7 五、發明說明(9)· CH2, Z代表=CH-或=N- ’ 以及其醫藥上可使用之鹽類及水合物。 式(I)及(II)之化合物亦可以其外消旋或對掌物形式存 5 在。 較佳的化合物為具式(I)者 其中 A 代表=CH-或=C-CN, R1代表視需要選用之鹵素取代的CrC3-烷基或環丙基, 10 R2代表氫或CrC4-烷基, Y代表以下結構之基團
其中 經濟部智慧財產局員工消費合作社印製 R4代表視需要選用之羥基取代的直鏈或分支鏈CrCr烷 20 基、具1至4個碳原子之氧烷基, R5代表氫、甲基或苯基, R6、R7、R8彼此獨立地代表氫或甲基, 以及其醫藥上可使用之鹽類及水合物。 特佳的化合物為具式(I)者 -11- 本纸張尺度適用中國國家標準(CNS)A4規格(210x297公釐) 1333422 A7
其中 A 代表=CH-或=C-CN, R1代表環丙基, R2代表氫、甲基或乙基, 5 γ代表以下結構之基團
經濟部智慧財產局員工消費合作社印製
其中 R代表甲基、視需要選用之羥基取代的乙基, R5代表氫或甲基, R6、R7、R8彼此獨立地代錢或甲基, 以及其醫藥上可使用之鹽類及水合物。 適合的鹽類包含醫藥上可用之鹼性鹽及酸加成鹽。 醫藥上可用之鹽類一詞代表例如氫氣酸、硫酸'醋 酸乙醇酸乳酸、號站酸、檸檬酸、酒石酸、曱烧績 20酸、4-曱笨磺酸、半乳糖醛酸、葡糖醛酸、安邦酸 1C acid) μ胺酸或天門冬胺酸之鹽類。本發明之化 合至酸性或驗性離子交換劑。就醫藥上可用之 全屬越二丨1 ν提及者為驗金屬鹽(例如鈉或鉀鹽)、驗土 金屬鹽(例如鎂或鈉鹽)、鋅鹽、銀鹽及紙鹽。 12- 本纸狀㈣財0 S 15
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C〇〇H 經濟部智慧財產局員工消費合作社印製 A7 B7 五、發明說明(η) 水合物一詞代表氟喳啉酮本身之水合物及其鹽類之水 合物。 特佳的氟喳啉酮包含揭示於WO 97/31001之化合物, 尤其是具下式之8-氰基-1-環丙基-7-((lS,6S)-2,8-二吖雙環-5 [4·3 ·0]壬-8-基)-6-氟-1,4-二氮-4-氧基-3-啥琳缓酸(普拉多氟 沙星(pradofloxacin)) 10 再者,特佳使用恩羅氟沙星(enrofloxacin),1-環丙基-7-(4-乙基-1-六氮σ比π井基)-6-^-1,4-二氮-4-氣基-3-啥咐嗣叛 15 酸: 20 .〇 CH.
A 再者,亦適合者為其他具有適合的驗性官能之活性物 質,尤其是揭示於以下文獻者:美國專利US 3 536 713、 -13- 本紙張尺度適用中國國家標準(CNS)A4規格(210x297公釐) 1333422 A7 " B7 五、發明說明(12) 經濟部智慧財產局員工消費合作社印製 US 3 714 159、US 3 682 930 ' US 3 177 252 ;特例包含以 下活性物質:安美西林(ampicillin)、阿莫西林 (amoxicillin)、西華樂林(cephazolin)、頭抱替安 (cefotiam)、雪娣若欣(ceftizoxime)、頭抱他秦 5 (cefotaxim)、頭孢地秦(cef〇dizim)、頭孢曲松(ceftriaxon)、 頭抱塔齊定(ceftazidim)、西蘇羅錠(cefsuldin)、苯甘頭抱 菌素(cefalexin)、秀克刻樂 (cefaclor)、賜福力 (cefadroxil)、頭抱新 g旨(cefpodoximproxetil)、頭抱塔美匹 否西(cefetametpivoxil)、頭抱秦(cefixim)、頭抱布婦 10 (ceftibuten)、羅拉卡倍芙(loracarbef)、亞胺培南 (imipenem)、胺曲南(azreonam)、鏈黴素(streptomycin)’、新 黴素(neomycin)、卡那黴素(kanamycin)、大觀黴素 (spectinomycin)、四環黴素、氧基四環黴素、四環黴素 (doxyxycline)、美滿黴素(minocycline)、紅徽素 15 (erythromycin)、克拉黴素(clarithromycin)、羅紅徵素 (roxithromycin)、阿奇黴素(azithromycin)、螺徽素 (spiramycin)、達淨續胺(sulfadiazin)、美嗤續胺 (sulfamethoxazole)、硫稀(sulfalene)、三美多普寧 (trimethoprim)、特索普寧(tetroxoprim)、甲頌建嗤 20 (metronidazole)、尼摩拉嗤(nimorazole)、替硝嗤 (tinidazole)、林可黴素(lincomycin)、克林達黴素 (clindamycin)、萬古徵(vancomycin)、替考拉寧 (teicoplanin)、異於驗酿(isoniazid)、敵癖新邁 (pyrazinamide)、乙胺丁醇(ethambutol)、利福平 -14- 本纸張尺度適用申國國家標準(CNS)A4規格(210x297公釐) 1333422 A7 〃 B7 五、發明說明(13) 經濟部智慧財產局員工消費合作社印製 (rifampicin)、克徵唾(clotrimazole)、益康吐(econazole)、 異康吐(isoconazole)、歐康嗤(〇xic〇nazole)、比風那唾 (bifonazole)、替康吐(tioconazole)、(fenticonazole)、0米康 唾(miconazole)、酮那吐(ketoconazole)、依特那唆 5 (itraconazole)、氟康唾(fluconazole)、特比那芬 (terbinafine)、那地芬(naftifine)、安莫芬(amorofine)、氟胞 嘧啶(flucytosine)、兩性黴素 B(amphotericin B)、寧司泰 定(nystatin)、氯奎寧(chloroquine)、美爾奎寧 (mefloquine)、奎寧、普來馬奎寧(primaqUine)、鹵泛曲林 10 (halofantrine)、普羅苦亞呢(proguanil)、乙胺嘧啶 (pyrimethamine)、美拉梭普羅(melarsoprol)、尼夫替莫 (nifurtimox)、幫達名定(pentamidine)、金剛烷胺 (amantadine)、託曼塔定(tromantadine)、阿昔洛韋 (aciclovir)、甘昔洛韋(gancicl〇vir)、阿糖腺昔 15 (vidarabine)、地丹諾辛(didanosine)、扎西他濱 (zalcitabine)、派拉替(pyrantel)、馬苯達吃(mebendazole)、 阿苯達唑(albendazole)、替苯達唑(tiabendazole)、二乙基 卡巴馬秦(diethylcarbamazine)、比敏尼(pyrvinium) ' 奥薩 姆奎寧(oxamniquine)、安布索(ambroxol) '洛普丁胺 20 (loperamide)、凱多芬(ketotifen)、甲氧氣普胺 (metoclopramide)、氟比錠(flupirtin)。 亦可能使酸及陰離子活性物質結合至陰離子交換劑。 可提及之特例包含如下: 阿卡普賽(acamprosate)、阿克羅芬那(aceclofenac)、愛斯美 -15- 本纸張尺度適用中國國家標準(CNS)A4規格(210x297公釐) 1333422 A7 B7 五、發明說明(14) 經濟部智慧財產局員工消費合作社印製 特辛(acemetacin)、乙醯基半胱胺酸、乙醢基水楊酸、阿維 A(acitretin)、第三代 A 酸(adapalene)、亞蘭德酸(alendronic acid)、酿胺三洛酸(amidotrizoic acid)、4-胺基水楊酸、阿 莫西林(amoxicillin)、安美西林(ampicillin)、抗壞血酸、阿 5 伐他汀(atorvastatin)、胺曲南(aztreonam)、貝可芬 (baclofen)、貝那普利(benazepril)、节基青徽素、苯紮貝特 (bezafibrate)、生物素、布美坦尼(bumetanide)、坎伐沙坦 (candesartan)、坎任酸鉀(potassium canrenoate)、卡托普利 (captopril)、卡必多巴(carbidopa)、卡玻西典 10 (carbocisteine)、秀克刻樂 (cefaclor)、賜福力 (cefadroxil)、西華力新(cefalexin)、西華馬吐 (cefamandazole)、西華樂林(cefazolin)、頭抱塔美 (cefetamet)、頭抱秦(ceflxim)、頭抱他秦(cefotaxim)、頭抱 替安(cefotiam)、頭抱西汀(cefoxitin)、頭抱新g旨 15 (cefpodoxime)、雪娣丁稀(ceftibutene)、頭孢曲松 (ceftriaxon)、頭抱新輯(cefuroxime)、西立伐他 >’丁 (cerivastatin)、思得寧(cetirizine)、去氧膽酸 (chenodeoxycholic acid)、苯丁酸氮芥(chlorambucil)、西多 福韋(cidofovir)、西司他丁(cilastatin)、西拉普利 20 (cilazapril)、克拉維酸(clavulanic acid)、克羅酸(clodronic acid)、塔肝素鈉(dalteparin Na)、達洛況(diclofenac)、達可 西林(dicloxacillin)、氣氮平酸二鉀(dipotassium clorazepat)、地法前列酮(dinoprost)、依那普利 (enalapril)、依洛沙坦(eprosartan)、依塔酸(etacrynic -16- 本纸張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 1333422 A7 B7 五、發明說明(15) acid)、依地酸(etidronic acid)、菲賓那(felbinac)、菲索芬那 定(fexofenadine)、氟氣西林(flucloxacillin)、福納密酸 (flufenamic acid)、夫比普洛芬(flurbiprofen)、氟伐他·;丁 (fluvastatin)、葉酸、活菲妥(fosfestrol)、麟黴素 5 (fosfomycin)、反丁烯二酸、利尿績胺(furosemid)、加巴喷 丁(gabapentin)、健非布脂(gemfibrozil)、肝素、玻尿酸 (hyaluronic acid)、氫可體松(hydrocortisone)、氫玻珀醋、 依邦酸(ibandronic acid)、布洛芬(ibuprofen)、依洛前列酮 (iloprost)、亞酿胺普利(imidapril)、亞胺培南(imipenem)、 10 p引1r朵美辛(indomethacin)、依塔拉酸(iotalaminic acid)、依 經濟部智慧財產局員工消費合作社印製 妥酸(iotroxic acid)、依沙利酸(ioxaglic acid)、嗣洛芬 (ketoprofen)、左卡巴斯,;丁(levocabastine)、左旋多巴 (levodopa)、左旋曱狀腺納(levothyroxin Na)、硫辛酸 (lipoic acid)、賴諾普利(lisinopril)、洛多沙醢胺 15 (lodoxamide)、龍那洛雷克(lonazolac)、羅拉卡倍芙 (loracarbef)、美非那酸(mefenamic acid)、美洛平 (meropenem)、美沙拉秦(mesalazine)、美思那(mesna)、美 他0米唾(metamizole)、甲胺嗓昤(methotrexate)、美洛西林 (mezlocillin)、莫西普利(moexipril)、白三烯 20 (montelukast)、莫西氟沙星(moxifloxacin)、那普洛先 (naproxen)、鏈徽菌素(natamycin)、那塔尼(nateglinide)、 二布酸鈉(Na dibunate)、依波酸鈉(Na iopodate)、皮可硫酸 納(Na picosulfate)、於驗酸、奥沙拉秦(olsalazine)、清酸 (orotic acid)、苯唾青徽素(oxacillin)、魔咪酸(pamidronic -17- 本紙張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐) 1333422 A7 __ B7 五、發明說明( acid)、維生素 B15 (pangamic acid)、青黴胺 (penicillamine)、培操普利(perindopril)、笨基巴比妥 (phenobarbital)、苯氧基甲基青黴素、必倍西林 (piperacillin)、比瑞塔尼(piretanide)、普伐他 丁 5 (pravastatin)、丙續舒(probenecid)、普固麥(proglumide)、 普批西林(propicillin)、奎那普利(quinapril)、諾和隆鍵 (repaglinide)、諾巴林(reviparin Na)、雷士酸(risedronic acid)、水楊酸 '螺普利(spirapril)、續胺二曱異°惡咕 (sulphasalazine)、他唑巴坦(tazobactam)、替米沙坦 10 (telmisartan)、替加賓(tiagabin)、泰普菲酸(tiaprofenic acid)、替錄酸(tiludronic acid)、丁那肝素鈉(tinzaparin Na)、坦多普利(trandolapril)、妥内散敏(tranexamic acid)、 維生素A酸(tretinoin)、色胺酸、熊去氧膽酸 (ursodeoxycholic acid)、發爾波克酸(valproic acid)、氨已稀 15 酸(vigabatrin)、任娜密威(zanamivir)及洛樂酸(zoledronic acid)。亦可提到者為上述之喳啉羧酸以及其結構上有關的 抗生素。 上述之止痛氟比錠(flupirtin)具有以下結構式:
經濟部智慧財產局員工消費合作社印製
Flupirtin亦可以醫藥上可用的鹽類之形式使用,較佳 -18- 本纸張尺度適用中國國家標準(CNS)A4規格(210x297公爱) 1333422 A7 五、發明說明(17) 10 15 經濟部智慧財產局員工消費合作钍印製 20 為含酸之鹽類,例如氣化氫鹽或馬來酸鹽。 離子交換樹脂係於水或極性有機溶劑中,例如醇類 (例如乙二醇或乙醇)、甘油、酮類(例如丙酮)或其混人物 中,填充活性物質。水及醇/水混合物為特佳。於室^或 升溫下使離子交換劑及活性物質在媒介物中攪拌,直到l 性物質完全地結合為止。離子交換樹脂與活性物質之填充 以及醫藥之調配亦可以單一步驟進行。 當裝載活性物質之離子交換劑欲分散於與水及/或極性 溶劑不混溶之親油性載體媒介物中時,首先其必須自水性 填料媒介物分離及乾燥。接著,經填充的離子交換劑可合 併於載體媒介物中》就親油性載體媒介物而言,舉例來 說,可能使用脂肪油 '石蠟烴油或矽酮油。此中較佳使用 脂肪油,實例為中鏈三酸甘油酯、芝麻油、落花生油或大 豆油。 本發明之醫藥製劑一般而言適用於同時施藥於人類及 動物。其較佳用於動物飼養及繁殖,其係與家畜、生殖家 畜、動物園動物、實驗室動物、試驗動物及寵物有關。 家畜及繁殖家畜包含哺乳動物(例如牛、馬、綿羊、 山羊、路乾、水牛、驢、兔、歐洲淡黃色鹿、馴 生毛動物(例如水貂、栗鼠、浣熊)及禽類(例如雞、 火雞、鴿子及飼養於家中或動物園_之烏類)。 實驗室及試驗動物包含鼠、大鼠、天竺鼠、金倉鼠、 狗及貓。 寵物包含兔、倉鼠、天竺鼠、鼠、馬、爬蟲類、適合 豬鹿) 鵡 •19- % 計 線
X297 公楚) 1333422 A7 B7 五、發明說明(ι〇 的烏類、狗及貓。 魚亦可提及者包含養殖魚類、繁殖魚類、水族槽魚及 觀賞魚(生活於清水及鹽水中之所有年齡層)。養殖魚類包 含例如,裡魚、緩魚、缚魚、白娃、鞋魚、鯛魚、翻車魚、 5 赤睛魚、維魚 '比目魚、歐鲽、大比目魚、日本黃尾錄魚 (Seriola quinqueradiata)、曰本鳗魚(Anguilla japonica)、紅 色海鯛(Pagurus major)、海驢魚(Dicentrarchus labrax)、灰 色鯡魚(Mugilus cephalus)、鰹魚、烏頰魚、海鯛(Sparus auratus)、吳郭魚種、棘籍類魚(例如plagioscion、溝渠餘 10 魚)。本發明之組成物適用於處理魚乾(例如體重為2至4 公分之鯉魚)及鰻魚飼養。 , 本發明之製劑較佳用於寵物,例如倉鼠、兔、天竺 鼠、狗及貓。其特別適用於施藥予貓。 可預防地或者治療地進行施藥。 15 本發明之製劑較佳係口服地施藥。 舉例來說,適用於動物之醫藥製劑係為在消耗期間一 部分用以改良味道者或其目標係用以阻礙活性物質於施藥 後釋放者。 經濟部智慧財產局員工消費合作社印製 為了製備懸浮液,將填充活性物質之樹脂非常均勻地 20分散於液態載體媒介物中,必要時以其他辅助劑(例如潤 濕劑)輔助。使用假塑性凝膠形成劑使懸浮液增稠◊同樣 地可包含額外的輔助劑,例如潤濕劑 '抗氧化劑、防腐 劑、著色劑及風味劑或香料。 本發明之製劑含有具活性物質填料之離子交換劑,以 -20·
1333422 Α7 Β7 五、發明說明(19) 製劑之總重量計,其通常用量為1至50重量%,較佳為5 至30重量%,最佳為5至25重量%。 可提及之載體液包含水、水及可與水混溶的有機溶劑 (例如醇類,例如乙醇、丙二醇、甘油、聚乙二醇)之混合 5 物以及親油性載體液(例如脂肪油、石蠟烴油或矽酮油)。 於本發明之製劑中,適用於所需稠度之載體液存在量以製 劑之總重量計,通常為10至98重量%,較佳為20至90 重量%。 潤濕劑(分散劑)包含: 10 •陰離子界面活性劑,包含乳化劑例如月桂基硫酸鈉、脂 肪醇醚硫酸鹽、單/二烷基聚二醇醚正磷酸酯單乙醇胺 鹽、木質素磺酸鹽或硫代琥珀酸二辛酯, •陽離子界面活性劑,包含乳化劑例如氯化十六烷基三曱 基敍* 15 •兩性界面活性劑,包含乳化劑例如N-月桂基-β-亞胺基 二丙酸二鈉或卵磷脂, 經濟部智慧財產局員工消費合作社印製 •非離子界面活性劑,包含乳化劑例如聚氧乙基化之蓖麻 油、聚氧乙基化之山梨聚糖脂肪酸酯、山梨聚糖脂肪酸 酯、甘油單甘油酯及甘油雙甘油酯 '聚氧乙烯脂肪酸 20 酯、聚氧乙烯脂肪醇酯、烷基酚聚二醇醚、聚乙烯-聚 丙烯團塊共聚合物。 於本發明之製劑中,以製劑之總重量計,潤濕劑之含 量通常為0.01至10重量%,較佳為0.1至2重量%。 其他輔助劑之實例包含: -21- 本紙張尺度適用中國國家標準(CNS)A4規格(210x297公釐) 1333422 A7 B7 五、發明說明(20 ) •防腐劑,例如對-羥基苯甲酸鹽、山梨酸、苯甲酸、丙 酸、甲酸或其鹽類。於本發明之製劑中,以製劑之總重 量計,防腐劑之含量通常為0.05至2重量%,較佳為 0.1至1重量%。 5 •著色劑,例如所有經證實可用於人類或動物中且可為溶 解或懸浮形式之著色劑。於本發明之製劑中,以製劑之 總重量計,著色劑之含量通常為0.001至5重量%,較 佳為0.01至2重量%。 •抗氧化劑,例如亞硫酸鹽或偏雙亞硫酸鹽,例如偏雙亞 10 硫酸鈉、抗壞血酸、丁基化之羥基甲苯、丁基化之羥基 茴香醚、生育酚。於本發明之製劑中,以製劑之總重量 計,抗氧化劑之含量通常為0_001至5重量%,較佳為 0,01至2重量%。 •風味劑或香料,其係為常用於藥物中者,實例為香草 15 醛。於本發明之製劑中,以製劑之總重量計,風味劑或 香料之含量通常為0.001至5重量%,較佳為0.01至2 重量%。 經濟部智慧財產局員工消費合作社印製 本發明之製劑可為半固態(例如糊漿)或液體懸浮液。 使用旋轉式黏度計(例如Haake Rheometer RS 100)測得之 20 屈服點係位於0與2000 Pa間。於300 s·1之黏度總計為介 於 10 與 5000 mPa*s 間。 本發明之製劑較佳為液體懸浮液。屈服點係位於0與 100 Pa間,較佳介於5與50 Pa間。於300 s'1之黏度總計 為介於10與1000 mPa*s間,較佳介於50與500 mPa*s -22- 本紙張尺度適用申國國家標準(CNS)A4規格(210x297公釐) 1333422 A7 B7 五、發明說明(21) 間。 本發明之製劑可分開地或與飼料一起施藥。 飼料包含植物來源之飼料成分(例如乾草、甜菜、榖 類、榖類副產物)、動物來源之飼料成分(例如肉、脂肪、 5 乳品、骨粉、魚產)及飼料成分,例如維生素、蛋白質、 胺基酸(例如DL-甲硫胺酸)、鹽(例如碳酸鈣及氣化鈉)。飼 料亦包含補充、調配及混合的飼料。此等包含在組成物中 可確保均衡飲食之飼料成分(鑒於能量及代白質供應以及 維生素、礦物鹽及微量元素之供應)。 10 製備實施例 , 實施例1 經濟部智慧財產局員工消費合作社印製 將0.18公斤對-羥基苯甲酸甲酯與0.02公斤對-羥基苯 甲酸丙酯溶解於75.0公斤熱水中。伴隨激烈攪拌,將0.3 15 公斤黃原膠(Xantural 180,CK Kelco)與0.3公斤黏土 (Veegum,Vanderbildt)合併於溶液中,並且在70°C攪拌混 合物1小時。於生成的溶膠冷卻後,使6.0公斤普拉多氟 沙星(pradofloxacin)、18.0公斤弱酸性離子交換劑 (Amberlite IRP 64)及1.0公斤香草醛分散於其中。接著以 20 轉子-定子使總批量均質。結果為黏性懸浮液。 實施例2 如實施例1,但使用0.2公斤奶油焦糖香料替代香草 链。 -23- 本紙張尺度適用中國國家標準(CNS)A4規格(210x297公釐) 1333422 A7 B7 五、發明說明(22 ) 實施例3 將0.2公斤山梨酸與0.02公斤抗壞血酸溶解於74.98 公斤熱水中。伴隨激烈攪拌,將0.3公斤黃原膠(Xanturai 5 180,CK Kelco)與 0.3 公斤黏土(Veegum,Vanderbildt)合併 於溶液中’並且在70C搜掉混合物1小時。於生成的溶膠 冷卻後,使6.0公斤普拉多氟沙星、18.0公斤弱酸性離子 交換劑(Amberlite IRP 64)及0.2公斤奶油焦糖香料分散於 其中。接著以轉子-定子使總批量均質。結果為黏性懸浮 10 液。
I 實施例4 如實施例1,但使用0.1公斤香草精香料替代香草 搭。 15 實施例5 經濟部智慧財產局員工消費合作社印製 將0.2公斤山斜酸容解於30·〇公斤丙二醇中。伴隨激 烈攪拌’將〇.7公斤黃原谬(Xantural⑽,CKKelc〇)合併於 此溶液中。於第二容器中,將2.5公斤普拉多氟沙星、 20 0.02公斤抗壞血酸及〇·2公斤香草精香料溶解於61.58公
斤水中。將1〇.〇公斤弱酸性陽離子交換劑(Amberlite IRP 64)分散於溶液中β使用高速攪拌器,將黃原膠/丙二醇分 散液合併於此懸浮液中。接著以轉子_定子使總批量均 質。結果為黏性懸浮液。 -24- 本纸張尺度適用中國國1標準(CNS)A4規格----------------- 1333422 A7 B7 五、發明說明(23 ) 實施例6 將0.2公斤山梨酸溶解於3〇.〇公斤甘油中。伴隨激烈 授拌’將0.5公斤黃原膠(xanturai 180, CK Kelco)合併於此 5溶液中。於第二容器中,將6,0公斤普拉多氟沙星溶解於 48.3公斤水中。將ι〇·〇公斤弱酸性陽離子交換劑 (Ambedite IRP 64)與5_0公斤肉香料分散於溶液中。使用 高速攪拌器’將黃原膠/甘油分散液合併於此懸浮液中。 接著以轉子-定子使總批量均質。結果為黏性懸浮液。 10 實施例7 將5.00公斤恩羅氟沙星(enrof]oxacin)及20.00公斤 Purolite c 100 H MR懸浮於80_00公斤純水中,並且在室 溫下攪拌懸浮液至少8小時。於沉降後,排除上層清液。 15以過濾乾燥器在75°C.乾燥殘餘物。與此同時地,將0.384 公斤山梨酸溶解於146.496公斤熱水中。於第二容器中, 將0.96公斤聚丙烯酸(carbopol 974P,BFGoodrich)分散於 19.20公斤甘油中。將24公斤經乾燥、裝填之離子交換劑 分散於其中。 20 實施你 將5.00公斤普拉多氟沙星及20.00公斤Purolite C 100 H MR懸浮於75 〇〇公斤純水中。接著,伴隨攪拌,合併 〇·25公斤笨曱酸及0.5公斤黏土(Veegum, Vanderbildt),並 -25- 本紙浪尺皮遇用甲國國家標準(CNS)A4規格(2丨〇χ297公釐) 裝— .計_ 4 經濟部智慧財產局員工消費合作社印製 1333422 經濟部智慧財產局員工消費合作社印製 A7 B7 五、發明說明(μ) 且在70°C加熱混合物丨小時以製得液態懸浮液。 實施例9 將0.2公斤山梨酸溶解於3〇 〇公斤甘油中。伴隨激烈 5攪拌,將2.25公斤微結晶纖維素與羧甲基纖維素鈉 (Avicel CL 611,FMC)之混合物合併於此溶液中。於第二容 器中,將6.0公斤普拉多氟沙星、〇〇2公斤抗壞血酸及 0.2公斤香草精香料溶解於54 35公斤水中。將18〇公斤 弱酸性陽離子交換劑(Amberlite IRP 64)分散於溶液中。使 10用高速攪拌器,將凝膠形成劑/丙二醇分散液合併於此懸 浮液中。接著以轉子-定子使總批量均質。結果為黏性懸 浮液。 實施例10
15 將6.〇公斤普拉多氟沙星與18.0公斤Amberlite IRP 64 —起於72公斤水中攪拌16小時。於懸浮的顆粒沉澱 後’排除上層清液,並且70°C乾燥殘餘物。將此填充活性 物質之離子交換劑與1.〇公斤香草醛於72.0公斤中鏈三酸 甘油酯(Miglyol 812)中一起分散。於添加3.0公斤高分散 20矽石(Aerosil 200)後,以轉子-定子使總批量均質。結果為 黏性懸浮液。 實施例11 將2.50公斤氟比錠與7.5公斤Amberlite IRP 69懸浮 -26- 本紙張尺度適用中國國家標準(CNS)A4規格(210x297公釐)
1333422 A7 五'發明說明 25 10 15 經濟部智慧財產局員工消費合作社印製 20 於40.00公斤5〇%(v/v)乙醇中,並且使懸浮物在4〇β(:攪拌 至少12小時。將懸浮液轉移至過濾乾燥器 '過濾且在6〇 C乾燥。伴隨激烈攪拌,經填充之離子交換劑及0.8公斤 羧甲基纖維素鈉(Blanose 7M31CF,Hercules)接續地分散於 29.0公斤純水中。結果為液態懸浮液。 實施例19 將3.〇公斤氟比錠馬來酸酯與12.〇公斤Pur〇iite C 115 kmr —起於60.0〇公斤水中攪拌16小時。於過濾後在 二c乾燥殘餘物。於第二製備容器中,將〇 5公斤山梨酸 岭解於82.24公斤中鏈三酸甘油酯(Migly〇1 812)中。使用 轉子-疋子均質地分散於其中者係為0.25公斤焦糖香料、 0.〇1公斤紅氧化鐵及離子交換劑(裝填活性物質)。伴隨激 …攪拌,添加2.0公斤高分散矽石(Aer〇si丨2〇〇),並且以轉 子-疋子分散組成物。結果為液態懸浮液。 使用轉子-定子將3.0公斤氟比旋馬來酸酷、12.0公斤 urolite c 115 KMR、0.25公斤焦糖香料及0 〇1公斤紅氧 化鐵均勻地分散於62·14公斤水中。接著使批量搜拌16小 時於第—製備谷器中,將〇·1公斤山梨酸溶解於20.0公 醇中,並且將2·5公斤微結晶纖維素與羧甲基纖維 胜鈉(AviCei CL 611)之混合物分散於其中。伴隨激烈攪 ,將此懸浮液添加至含活性物質之懸浮液中,並且以轉 -27- V紙張尺度適用中規格(2丨⑽7
1333422 A7
子-定子使組成物均f。結果_性懸浮液 1摘錄關 於貓之對應試驗結果:
10表1 .本發明實施例1-4,10於|苗中之美味性相較於立即美 味的參考調配物(營養增量描食(nutri-plus Cat),維克 (virbac)動物藥劑,Bad Oldesloe),n=36 經 濟 部 智 慧 財 產 局 員 工 消 費 合 作 社 印 製 生物實施例 美味性試驗 由於良好口感之緣故(亦可歸因於並 醫藥製劑具有極佳美味性(例如於貓中)'。、以下I本發明之 分數:1=無法接受,2=不易施藥,3=適度消耗,4= 谷易施藥,5=極易施藥 15 實施例之組成:參見以上 -28-
本纸張尺度適用中國國家標準(CNS)A4規格(210 X 297公釐)
Claims (1)
- rI333422 A8 B8 C8 專利申請案第92114643號 ROC Patent Αρρϊη. No,92114643 匕14舍為由技亩4il拉阁士 # 士 ϋ ΐ 一· ~一 _ pv〇 ROC Patent Appln. No.92114643 ^Τ^ϊϊίΐϊϊ: ~—苹總觀^丰鋼_(j - (民國98年2月 (Si bm^fced όθ Febfiiary ] 1, 200S 1 I 補充 1. ;種液«藥製劑,其包含結合⑽衫換狀普t」 ’其特徵在於填料離子交換劑 該假塑性凝膠形成劑係選自微結晶之纖維 素、頁原膠、聚丙烯酸、黏土、選自甲基 維素、羥丙基纖維素、曱基羥丙基纖維素、‘ Z基纖維素鋼之纖維素醚、或以上凝膠形成劑之混合 10 2. t申請翻範圍第1項之醫藥製劑,其特徵在於盆包 含黃原膠作為假塑性凝膠形成劑。 、/、° 範圍第1或2項之醫藥製劑,其特徵在於 孩離子父換劑係為酸性離子交換劑。 4. -種如申請專利範圍第i至3·項中任—項之醫藥製劑 之用途’其係用於製備口服施藥之藥物。 15 經濟部智慧財產局員工消費合作社印製 本紙張尺度適用中國 92244B·接 1
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10224086A DE10224086A1 (de) | 2002-05-31 | 2002-05-31 | Pharmazeutische Zubereitungen zur oralen Anwendung enthaltend wirkstoffbeladene Ionentauscherharze sowie strukturviskose Gelbildner als Verdicker |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TW200406230A TW200406230A (en) | 2004-05-01 |
| TWI333422B true TWI333422B (en) | 2010-11-21 |
Family
ID=29432468
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW092114643A TWI333422B (en) | 2002-05-31 | 2003-05-30 | Oral pharmaceutical preparations comprising ion exchange resins with active substance loading and pseudoplastic gel-former thickeners |
Country Status (27)
| Country | Link |
|---|---|
| US (1) | US8545829B2 (zh) |
| EP (1) | EP1513500B1 (zh) |
| JP (2) | JP5350574B2 (zh) |
| KR (3) | KR101258373B1 (zh) |
| CN (1) | CN1671361B (zh) |
| AR (2) | AR039861A1 (zh) |
| AT (1) | ATE421317T1 (zh) |
| AU (1) | AU2003242545B2 (zh) |
| BR (2) | BRPI0311511B1 (zh) |
| CA (1) | CA2487648C (zh) |
| CR (1) | CR7598A (zh) |
| DE (2) | DE10224086A1 (zh) |
| DK (1) | DK1513500T3 (zh) |
| ES (1) | ES2319115T3 (zh) |
| HR (1) | HRP20041219B1 (zh) |
| IL (2) | IL165322A0 (zh) |
| MX (1) | MXPA04011820A (zh) |
| MY (1) | MY140953A (zh) |
| NO (1) | NO333939B1 (zh) |
| PL (1) | PL207269B1 (zh) |
| PT (1) | PT1513500E (zh) |
| RU (1) | RU2380091C2 (zh) |
| SI (1) | SI1513500T1 (zh) |
| TW (1) | TWI333422B (zh) |
| UA (1) | UA84270C2 (zh) |
| WO (1) | WO2003101422A2 (zh) |
| ZA (1) | ZA200409616B (zh) |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| DE102004001558A1 (de) * | 2004-01-10 | 2005-08-18 | Bayer Healthcare Ag | Arzneimittel zur topischen Applikation bei Tieren |
| US20080095842A1 (en) * | 2004-12-06 | 2008-04-24 | Antarkar Amit K | Rapidly Disintegrating Taste Masked Compositions and a Process for Its Preparations |
| DE102005025900A1 (de) * | 2005-06-06 | 2006-12-07 | Basf Ag | Verfahren zur Entfernung von Salzen aus einem Alkoxycarbonylaminotriazin enthaltenden Reaktionsgemisch |
| US20080051332A1 (en) * | 2005-11-18 | 2008-02-28 | Nastech Pharmaceutical Company Inc. | Method of modulating hematopoietic stem cells and treating hematologic diseases using intranasal parathyroid hormone |
| CN100360131C (zh) * | 2006-01-24 | 2008-01-09 | 新昌国邦化学工业有限公司 | 一种掩味恩诺沙星的生产方法 |
| US20070248564A1 (en) * | 2006-04-25 | 2007-10-25 | Roxane Laboratories, Inc. | Formulation of sodium polystyrene sulfonate suspension for the treatment of hyperkalemia |
| CA2661576A1 (en) * | 2006-09-26 | 2008-04-03 | Taro Pharmaceuticals North America, Inc. | Stabilizing compositions for antibiotics and methods of use |
| DE102006049520A1 (de) | 2006-10-20 | 2008-04-24 | Bayer Healthcare Ag | Verfahren zur Herstellung von Pradofloxacin |
| US20080118570A1 (en) * | 2006-11-20 | 2008-05-22 | Zhi Liu | Polymer coated drug-ion exchange resins and methods |
| EP2262536A4 (en) * | 2008-03-26 | 2013-07-03 | Taro Pharmaceuticals North America Inc | STABILIZING LIPID COMPOSITIONS FOR ORAL PHARMACEUTICAL AGENTS |
| AU2011226523C1 (en) | 2010-03-12 | 2016-07-14 | Monsanto Technology Llc | Agrochemical gel compositions |
| ES2588008T3 (es) * | 2010-05-19 | 2016-10-28 | Astellas Pharma Inc. | Composición farmacéutica que contiene solifenacina |
| AU2012326513B2 (en) | 2011-10-19 | 2016-03-17 | R.P. Scherer Technologies, Llc | Two phase pharmaceutical delivery system |
| FR2998305B1 (fr) * | 2012-11-22 | 2015-02-20 | Henkel Ag & Co Kgaa | Substances actives contenant des groupes sulfonates ameliorant la puissance de lavage primaire |
| KR101697095B1 (ko) * | 2015-09-30 | 2017-01-18 | 주식회사 포스코 | 더스트 막힘을 방지할 수 있는 배가스 청정 라인의 실탱크 |
| CN111989314B (zh) | 2018-04-25 | 2024-04-30 | 拜耳动物保健有限责任公司 | 喹诺酮甲酸酯水解的方法 |
| CN114249749B (zh) * | 2022-01-08 | 2024-03-22 | 天象生物药业邢台有限责任公司 | 一种马波沙星甲酸盐的转化方法 |
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| US614622A (en) * | 1898-11-22 | Machine for making billets | ||
| JPS60204713A (ja) * | 1984-03-30 | 1985-10-16 | Zenyaku Kogyo Kk | 水性懸濁組成物 |
| GB8618847D0 (en) | 1986-08-01 | 1986-09-10 | Smith Kline French Lab | Pharmaceutical formulations |
| DE3719764A1 (de) * | 1987-06-13 | 1988-12-22 | Bayer Ag | Ionenaustauscherharze beladen mit chinoloncarbonsaeurederivaten, ihre herstellung und verwendung |
| US5338732A (en) | 1991-06-18 | 1994-08-16 | Bristol-Myers Squibb Company | Megestrol acetate formulation |
| AU2884892A (en) * | 1991-10-28 | 1993-06-07 | Procter & Gamble Company, The | Beverage thickener/emulsifier system |
| JP3207494B2 (ja) * | 1992-04-02 | 2001-09-10 | ロート製薬株式会社 | 水性懸濁製剤 |
| DE4319649A1 (de) * | 1993-03-18 | 1994-09-22 | Asta Medica Ag | Feste Flupirtin enthaltende orale Darreichungsformen mit kontrollierter Wirkstoffabgabe |
| AU715341B2 (en) * | 1996-02-23 | 2000-01-20 | Bayer Intellectual Property Gmbh | Possibly substituted 8-cyano-1-cyclopropyl-7-(2,8- diazabicyclo-(4.3.0)-nonan-8-yl)-6-fluoro-1,4-dihydro-4-oxo- 3-quinolin carboxylic acids and their derivatives |
| US5980882A (en) * | 1997-04-16 | 1999-11-09 | Medeva Pharmaceuticals Manufacturing | Drug-resin complexes stabilized by chelating agents |
| DE19854357A1 (de) * | 1998-11-25 | 2000-05-31 | Bayer Ag | Semi-Hydrochlorid von 8-Cyan-1-cyclopropyl-7-(1S,6S-2,8-diazabicyclo/4.3.0/ -nonan-8-yl)-6-fluor-1,4-dihydro-4-oxo-3-chinolincarbonsäure |
| CZ302919B6 (cs) * | 1999-07-14 | 2012-01-18 | Schering-Plough Ltd. | Vodný farmaceutický prostredek |
| GB9930058D0 (en) | 1999-12-20 | 2000-02-09 | Novartis Ag | Organic compounds |
| GB0020089D0 (en) | 2000-08-15 | 2000-10-04 | Smithkline Beecham Biolog | Vaccine Composition |
| DE10134719A1 (de) * | 2001-07-17 | 2003-02-06 | Bayer Ag | Pharmazeutische Zubereitungen enthaltend wirkstoffbeladene Ionentauscherharze |
| US7001667B2 (en) * | 2002-07-17 | 2006-02-21 | Ppg Industries Ohio, Inc. | Alkyd-based free radical wood coating compositions |
-
2002
- 2002-05-31 DE DE10224086A patent/DE10224086A1/de not_active Withdrawn
-
2003
- 2003-05-19 IL IL16532203A patent/IL165322A0/xx unknown
- 2003-05-19 RU RU2004139022/15A patent/RU2380091C2/ru active
- 2003-05-19 DE DE50311123T patent/DE50311123D1/de not_active Expired - Lifetime
- 2003-05-19 ES ES03755931T patent/ES2319115T3/es not_active Expired - Lifetime
- 2003-05-19 PL PL373456A patent/PL207269B1/pl unknown
- 2003-05-19 SI SI200331534T patent/SI1513500T1/sl unknown
- 2003-05-19 UA UA20041210942A patent/UA84270C2/ru unknown
- 2003-05-19 KR KR1020117031524A patent/KR101258373B1/ko not_active Expired - Lifetime
- 2003-05-19 BR BRPI0311511-9A patent/BRPI0311511B1/pt unknown
- 2003-05-19 DK DK03755931T patent/DK1513500T3/da active
- 2003-05-19 KR KR1020127026888A patent/KR20120123607A/ko not_active Ceased
- 2003-05-19 BR BR0311511-9A patent/BR0311511A/pt active IP Right Grant
- 2003-05-19 AU AU2003242545A patent/AU2003242545B2/en not_active Expired
- 2003-05-19 HR HRP20041219AA patent/HRP20041219B1/hr not_active IP Right Cessation
- 2003-05-19 JP JP2004508780A patent/JP5350574B2/ja not_active Expired - Lifetime
- 2003-05-19 KR KR10-2004-7019371A patent/KR20050010015A/ko not_active Ceased
- 2003-05-19 PT PT03755931T patent/PT1513500E/pt unknown
- 2003-05-19 CN CN038182106A patent/CN1671361B/zh not_active Expired - Lifetime
- 2003-05-19 MX MXPA04011820A patent/MXPA04011820A/es active IP Right Grant
- 2003-05-19 WO PCT/EP2003/005228 patent/WO2003101422A2/de not_active Ceased
- 2003-05-19 CA CA2487648A patent/CA2487648C/en not_active Expired - Lifetime
- 2003-05-19 EP EP03755931A patent/EP1513500B1/de not_active Expired - Lifetime
- 2003-05-19 AT AT03755931T patent/ATE421317T1/de active
- 2003-05-19 US US10/516,344 patent/US8545829B2/en not_active Expired - Fee Related
- 2003-05-28 AR ARP030101867A patent/AR039861A1/es not_active Application Discontinuation
- 2003-05-29 MY MYPI20031984A patent/MY140953A/en unknown
- 2003-05-30 TW TW092114643A patent/TWI333422B/zh not_active IP Right Cessation
-
2004
- 2004-11-22 IL IL165322A patent/IL165322A/en active IP Right Grant
- 2004-11-24 CR CR7598A patent/CR7598A/es not_active Application Discontinuation
- 2004-11-29 ZA ZA200409616A patent/ZA200409616B/xx unknown
- 2004-12-29 NO NO20045700A patent/NO333939B1/no not_active IP Right Cessation
-
2010
- 2010-10-20 JP JP2010235021A patent/JP2011012087A/ja not_active Withdrawn
-
2016
- 2016-08-23 AR ARP160102580A patent/AR105798A2/es unknown
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