CN101147743A - 人参皂甙Compound-K在制药中的新应用 - Google Patents
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Abstract
本发明提供结构式如右的人参皂甙Compound-K在制备预防或治疗关节炎的药物中的应用。
Description
技术领域
本发明涉及一种人参皂甙Compound-K在制药中的新应用,特别涉及一种人参皂甙Compound-K在制备预防或治疗关节炎的药物中的应用。
背景技术
中国专利(公开号CN1570133A)公开了人参皂甙Compound-K的结构及其制备方法,以及其在抗肿瘤方面的一些应用,其具有如下结构:
但其在预防或治疗关节炎的应用却未见报道。
发明内容
本发明的目的在于研究人参皂甙Compound-K在其他领域应用的可能性,从而提供其在制药中的新用途。
本发明提供了人参皂甙Compound-K在制备预防或治疗关节炎的药物中的应用。
具体实施方式
实施例1 初测毒
人参皂甙Compound-K,静脉注射360mg/kg剂量,小鼠活动正常,未见异常。
实施例2 人参皂甙Compound-K对角叉菜胶诱发小鼠足跖肿胀的影响
1、实验目的:观察待测样品对角叉菜胶致小鼠急性炎症的影响。
2、材料和试剂:
1)药物:人参皂甙Compound-K,剂量为10mg/kg,5mg/kg,2.5mg/kg。
消炎痛,10mg/kg。
角叉菜胶,用双蒸水配制成1%浓度。
2)动物:
昆明种小鼠60只
体重:19-21g
性别:雄性
每组动物数:10只
实验室温度:24~26℃,相对湿度:60~70%
3、实验方法:
动物先分成大剂量组:10mg/kg,iv;中剂量组:5mg/kg,iv;小剂量组:2.5mg/kg,iv;消炎痛组:10mg/kg,po;空白对照组:生理盐水10mg/kg,iv。按上述方法给药三天,致炎前先用排水法测各组小鼠右后足跖的体积一次,末次给药一小时后在小鼠右后足跖中部皮下注射1%角叉菜胶0.1ml致炎,以后每隔一小时测足跖体积1次,小鼠致炎前及致炎后不同时间右后足跖体积的差值即为肿胀值,计算肿胀率及抑制率,组间差异以t检验进行比较。
En=致炎后不同时间的肿胀值
Eo=致炎前的肿胀值
C=对照组的肿胀率
T=治疗组的肿胀率
4、结果
结果见表1。人参皂甙Compound-K可明显地抑制角叉菜胶致小鼠足跖急性炎症,其中高剂量组作用最强,4h时作用最好,对小鼠急性炎症的抑制率可达65.66%,消炎痛组与小剂量组作用相当。
表1人参皂甙Compound-K对角叉菜胶致小鼠急性炎症的影响(%,n=10,x±s)
致炎后不同时间的肿胀值ml | |||||
0h | 1h | 2h | 4h | 6h | |
致炎对照 | 1.52±0.11 | 2.56±0.30(68.76±18.85) | 2.62±0.18(72.65±8.90) | 2.74±0.22(80.47±10.57) | 2.62±0.18(73.23±16.83) |
高剂量10mg/kg | 1.56±0.17 | 2.18±0.18(40.81±10.14)**<40.64> | 2.19±0.20(41.56±13.38)**<42.79> | 1.98±0.20(27.64±8.46)**<65.66> | 1.91±0.22(23.58±15.23)**<67.80> |
中剂量5mg/kg | 1.47±0.13 | 2.36±0.23(60.97±18.09)<11.33> | 2.35±0.16(60.97±18.41)<16.08> | 2.12±0.22(45.04±18.30)**<44.03> | 2.19±0.19(49.81±17.26)**<31.98> |
低剂量2.5gmg/kg | 1.49±0.15 | 2.36±0.22(66.63±7.82)<14.70> | 2.43±0.23(64.26±14.54)<12.30> | 2.33±0.17(61.75±11.27)**<29.40> | 2.22±0.15(53.48±11.12)**<31.64> |
消炎痛1mg/kg | 1.47±0.14 | 2.44±0.19(67.11±17.30)<2.39> | 2.35±0.20(60.95±18.36)<16.11> | 2.21±0.11(51.04±14.09)**<36.57> | 2.26±0.11(55.36±19.90)*<24.41> |
*P<0.05,**P<0.01与致炎对照组比较 ()内为肿胀率(%) < >内为抑制(%)
实施例3 人参皂甙Compound-K对角叉菜胶诱发大鼠足跖肿胀的影响
1、实验目的:观察待测样品对角叉菜胶致大鼠急性炎症的影响。
2、材料和试剂:
1)药物:人参皂甙Compound-K,剂量为10mg/kg,5mg/kg,2.5mg/kg。
消炎痛,1mg/kg。
角叉菜胶,用双蒸水配制成1%浓度。
2)动物:
大鼠,SD系
体重:130~150g
性别:雄性
每组动物数:8只
实验室温度:24~26℃,相对湿度:60~70%
3、实验方法:
动物先分成大剂量组:10mg/kg,iv;中剂量组:5mg/kg,iv;小剂量组:2.5mg/kg,iv;消炎痛组:1mg/kg,po;空白对照组:生理盐水10mg/kg,iv。动物先分组,按上述方法给药三天,致炎前先用排水法测各组大鼠右后足跖的体积一次,末次给药一小时后在大鼠右后足跖中部皮下注射1%角叉菜胶0.1ml致炎,以后每隔一小时测足跖体积1次,计算肿胀率及抑制率方法同上,组间差异以t检验进行比较。
4、结果
结果见表2,人参皂甙Compound-K可明显地抑制角叉菜胶致大鼠足跖急性炎症,其中高剂量组作用最强,对大鼠急性炎症的抑制率最高可达78.23%,消炎痛组作用介于高剂量和低剂量之间。
表2 人参皂甙Compound-K对角叉菜胶致大鼠急性炎症的影响(%,n=10,x±s)
致炎后不同时间的肿胀值ml | ||||||
0h | 1h | 2h | 3h | 4h | 5h | |
致炎对照 | 1.40±0.10 | 1.73±0.18(23.51±10.11) | 1.85±0.15(32.24±15.29) | 1.98±0.16(41.70±14.21) | 1.94±0.18(38.84±15.35) | 1.91±0.21(37.07±17.47) |
高剂量10mg/kg | 1.42±0.10 | 1.51±0.10(6.38±7.44)**<72.87> | 1.62±0.11(13.87±8.55)**<56.96> | 1.65±0.16(16.06±12.41)**<67.49> | 1.58±0.14(11.51±9.76)**<70.38> | 1.53±0.12(8.07±10.88)**<78.23> |
中剂量5mg/kg | 1.39±0.12 | 1.55±0.11111.87±6.23)**<49.57>1.59±0.08 | 1.64±0.09(18.56±9.77)*<42.44>1.71±0.13 | 1.77±0.12(28.09±11.34)*<32.62>1.79±0.14 | 1.66±0.13(20.11±11.20)**<48.22>1.71±0.12 | 1.62±0.11(17.13±10.13)**<53.80>1.74±0.12 |
低剂量2.5gmg/kg | 1.33±0.08 | (20.22±9.99)<13.97> | (29.40±12.71)<8.80> | (34.80±14.01)<76.54> | (29.49±13.86)<24.08> | (31.22±14.12)<75.78> |
消炎痛1mg/kg | 1.34±0.15 | 1.68±0.10(22.51±10.19)<4.23> | 1.72±0.16(25.65±14.10)<20.44> | 1.82±0.17(33.28±13.54)<20.77> | 1.77±0.22(28.45±15.71)<26.76> | 1.69±0.15(23.04±11.45)<37.84> |
*P<0.05,**P<0.01与致炎对照组比较 ( )内为肿胀率(%) < >内为抑制率(%)
实施例4 人参皂甙Compound-K对佐剂诱导的大鼠佐剂性关节炎的影响
(一)人参皂甙Compound-K对佐剂诱导的大鼠佐剂性关节炎的预防作用。
1、材料和试剂:
1)药物:人参皂甙Compound-K,剂量为10mg/kg,5mg/kg,2.5mg/kg。
消炎痛:1mg/kg。
雷公藤:1.5mg/kg。
弗氏完全佐剂:购于Sigma公司,每只大鼠右后足跖中部皮下注射0.1ml致炎
2)动物:
大鼠,SD系
体重:130~150g
性别:雄性
每组动物数:8只
实验室温度:24~26℃,相对湿度:60~70%
2、实验方法:
动物先分成大剂量组:10mg/kg,iv;中剂量组:5mg/kg,iv;小剂量组:2.5mg/kg,iv;消炎痛组:1mg/kg,po;雷公藤组:1.5mg/kg,po;空白对照组:生理盐水10mg/kg,iv。动物致炎前先用排水法测右后足跖的体积一次,然后在大鼠右后足跖中部皮下注射弗氏完全佐剂0.1ml致炎,致炎后次日按上述分组,并开始给药15天,每隔一定时间测足跖体积,计算肿胀率及抑制率同上,组间差异以t检验进行比较。
3、结果
结果见表3,人参皂甙Compound-K可预防大鼠佐剂性的关节炎,其中高剂量组作用略高于雷公藤组,与消炎痛组相当。
表3 人参皂甙Compound-K对角叉菜胶致大鼠佐剂性关节炎的预防作用(%,n=10,x±s)
致炎后不同天数的肿胀值ml | ||||||||
0day | 2day | 4day | 6day | 9day | 11day | 13day | 15day | |
空白对照 | 1.22±0.09 | 1.28±0.07 | 1.29±0.04 | 1.29±0.07 | 1.29±0.06 | 1.27±0.05 | 1.28±0.04 | 1.29±0.03 |
致炎对照 | 1.23±0.10 | 2.33±0.31(72.36±14.49) | 2.33±0.31(89.52±22.12) | 2.33±0.36(89.34±21.13) | 2.13±0.38(72.42±18.87) | 2.18±0.31(77.92±25.66) | 2.25±0.27(82.72±14.20) | 2.22±0.24(80.63±16.37) |
高剂量10mg/kg | 1.29±0.08 | 2.17±0.14(51.03±8.03)**<29.48> | 2.17±0.14(68.94±10.49)*<22.99> | 2.21±0.15(71.90±9.64)<19.52> | 2.03±0.15(58.23±11.44)<19.59> | 1.98±0.14(54.48±12.39)*<30.08> | 2.03±0.13(58.04±10.97)**<29.83> | 1.99±0.18(55.42±14-65)**<37.26> |
中剂量5mg/kg | 1.25±0.06 | 2.10±0.21(46.63±11.66)**<35.56> | 2.10±0.21(68.35±15.68)*<23.65> | 2.16±0.18(73.31±17.73)<17.94> | 1.97±0.21(57.60±13.83)<20.45> | 1.95±0.18(55.81±11.54)*<28.37> | 2.00±0.18(59.74±11.82)**<27.79> | 1.96±0.21(57.08±14-00)**<29.21> |
低剂量2.5gmg/kg | 1.24±0.08 | 2.14±0.15(56.65±17.83)<27.71> | 2.14±0.15(73.11±15.82)<18.33> | 2.11±0.10(70.87±14.91)<20.67> | 1.95±0.17(57.25±14.42)<20.95> | 2.00±0.26(61.69±21.61)<20.82> | 2.00±0.15(61.24±13.26)**<25.97> | 1.96±0.20(58.02±15-52)*<28.05> |
雷公藤1.5mg/kg | 1.24±0.05 | 1.90±0.07(53.58±3.97)<25.95> | 2.24±0.18(80.76±9.19)<9.78> | 2.30±0.62(85.26±46.85)<4.57> | 2.12±0.46(70.92±33.95)<2.06> | 1.98±0.35(59.06±25.35)<24.20> | 2.03±0.25(63.51±17.33)<23.22> | 2.01±0.20(61.57±12.50)*<23.64> |
消炎痛1mg/kg | 1.23±0.11 | 1.85±0.09(52.34±15.07)<27.67> | 2.08±0.13(70.99±17.35)<20.69> | 2.17±0.17(78.32±23.41)<12.34> | 2.06±0.23(69.44±27.12)<4.11> | 1.86±0.13(52.68±12.02)*<32.39> | 1.86±0.13(53.00±15.57)**<35.93> | 1.86±0.13(52.00±1.27)**<35.50> |
*P<0.05,**P<0.01与致炎对照组比较 ( )内为肿胀率(%) < >内为抑制率(%)
(二)人参皂甙Compound-K对佐剂诱导的大鼠佐剂性关节炎的治疗作用。
1、材料和试剂:
1)药物:人参皂甙Compound-K,剂量为10mg/kg,5mg/kg,2.5mg/kg。
消炎痛:1mg/kg。
雷公藤:1.5mg/kg。
弗氏完全佐剂:购于Sigma公司,每只大鼠右后足跖中部皮下注射0.1ml致炎
2)动物:
大鼠,SD系
体重:130~150g
性别:雄性
每组动物数:8只
实验室温度:24~26℃,相对湿度:60~70%
2、实验方法:
动物先分成大剂量组:10mg/kg,iv;中剂量组: 5mg/kg,iv;小剂量组:2.5mg/kg,iv;消炎痛组:1mg/kg,po;雷公藤组:1.5mg/kg,po;空白对照组:生理盐水10mg/kg,iv。动物致炎前先用排水法测右后足跖的体积一次,然后在大鼠右后足跖中部皮下注射弗氏完全佐剂0.1ml致炎,致炎后20日起按上述分组,并开始给药8天,每隔一定时间测足跖体积,计算肿胀率及抑制率同上,组间差异以t检验进行比较。
3、结果
结果见表4,人参皂甙Compound-K可治疗大鼠佐剂性关节炎,其中高剂量组作用最强,26day时作用最好,抑制率最高可达36.15%,明显高于消炎痛组和雷公藤组。
表4人参皂甙Compound-K对角叉菜胶致大鼠佐剂性关节炎的治疗作用(%,n=10,x±s)
致炎后不同天数的肿胀值ml | ||||||
0day | 19day | 21day | 23day | 26day | 30day | |
空白对照 | 1.16±0.06 | 1.25±0.08 | 1.27±0.07 | 1.28±0.08 | 1.31±0.06 | 1.32±0.07 |
致炎对照 | 1.11±0.07 | 2.19±0.25(98.38±19.60) | 2.28±0.22(106.21±17.63) | 2.28±0.23(106.50±15.80) | 2.34±0.28(112.23±21.37) | 2.27±0.28(105.15±18.04) |
高剂量10mg/kg | 1.05±0.09 | 1.97±0.24(88.85±23.27)<9.69> | 1.81±0.33(72.69±29.97)*<31.57> | 1.80±0.21(72.50±22.18)**<31.92> | 1.79±0.24(71.66±24.46)**<36.75> | 1.80±0.26(71.17±17.97)**<32.32> |
中剂量5mg/kg | 1.10±0.09 | 2.00±0.12(81.36±13.10)<17.31> | 2.03±0.20(84.07±18.91)*<20.85> | 2.01±0.23(81.81±14.58)**<23.19> | 2.00±0.19(81.48±11.30)**<27.40> | 2.03±0.25(83.77±17.65)*<20.33> |
低剂量2.5gmg/kg | 1.06±0.09 | 1.96±0.16(84.26±14.31)<14.36> | 2.00±0.07(89.42±18.47)<15.81> | 1.91±0.08(80.92±16.84)**<24.02> | 1.92±0.08(81.13±10.03)**<27.71> | 1.96±0.16(84.80±19.66)*<19.36> |
雷公藤1.5mg/kg | 1.16±0.05 | 2.03±0.14(75.70±13.13)*<23.06> | 1.98±0.08(71.88±11.09)**<32.33> | 2.06±0.16(79.07±16.20)**<25.75> | 2.08±0.11(80.82±13.76)**<27.99> | 2.07±0.16(79.28±14.25)**<24.61> |
消炎痛1mg/kg | 1.14±0.05 | 2.04±0.20(80.03±17.69)<18.65> | 2.11±0.17(85.98±15.49)*<19.05> | 2.11±0.17(86.16±15.90)*<19.09> | 2.15±0.16(89.32±16.25)*<20.41> | 2.18±0.23(92.39±20.26)<12.14> |
*P<0.05,**P<0.01与致炎对照组比较 ( )内为肿胀率(%) < >内为抑制率(%)
实施例5 人参皂甙Compound-K对II型胶元(CII)诱导的大鼠关节炎的影响
1、材料和试剂:
1)药物:
药物:人参皂甙Compound-K,剂量为10mg/kg,5mg/kg,2.5mg/kg。
Enbrel:9mg/kg, 皮下注射,每4天一次。
雷公藤:1.5mg/kg。
致炎剂:II型胶元溶解在0.1mol/L醋酸中,使终浓度为2mg/ml胶元溶液,4℃过夜,次日将II型胶元溶液滴加至冷的不完全弗氏佐剂中,充分乳化(II型胶元液:弗氏不完全佐剂=1∶1),使II型胶元终浓度为1mg/ml。II型胶元乳剂4℃冰箱保存备用。
免疫方法:每只大鼠分5点背部皮内注射免疫,每点0.1ml,共5ml(含有II型胶元量为0.5mg),7天后以同样的方法追加免疫一次。对照组注射0.1mol/L醋酸及不完全弗氏佐剂乳化液,注射前及免疫后20天起用排水法测定右后足踝部关节的肿胀度。
2)动物:
大鼠,SD系
体重:140~160g
性别:雄性
每组动物数:8只
实验室温度:24~26℃,相对湿度:60~70%
2.人参皂甙Compound-K对II型胶元(CII)诱导的关节炎的预防作用
2.1实验方法:
将预先已溶解在0.1mol/L醋酸并放置过夜的II型胶元,调整浓度为2mg/ml后以1∶1的比例慢慢滴加至弗氏不完全佐剂中,充分乳化后在每个大鼠背部5点皮内注射,每点0.1ml(每鼠共0.5ml,含胶元0.5mg)进行首次免疫,于第7天同法进行第二次免疫,此即为致炎动物。相似的方法处理正常对照组动物,但免疫组分中不含胶元。
动物分成大剂量组:人参皂甙Compound-K10mg/kg,iv;中剂量组:人参皂甙Compound-K5mg/kg,iv;小剂量组:人参皂甙Compound-K2.5mg/kg,iv;雷公藤组:1.5mg/kg,po;Enbrel组:9mg/kg,sc;空白对照组:生理盐水10mg/kg,iv。给药组动物首次免疫时开始给药,于第一次免疫后8天停止给药。用排水法测量免疫前和首次免疫后20、22、24、27、29天的足踝关节肿胀值,计算肿胀率及抑制率同上,组间差异以t检验进行比较。实验结束,取足踝关节作病理检查。
2.2结果
结果见表5。人参皂甙Compound-K可明显地预防II型胶元诱导的关节炎,其中高剂量组作用最强,其作用明显高于雷公藤组,与enbrel组相当。
表5人参皂甙Compound-K对II型胶元(CII)诱导的关节炎的预防作用(%,n=8,x±s)
致炎后不同天数的肿胀值ml | ||||||
0day | 20day | 22day | 24day | 27day | 29day | |
空白对照 | 1.09±0.05 | 1.10±0.05 | 1.12±0.02 | 1.10±0.06 | 1.10±0.06 | 1.10±0.06 |
致炎对照 | 1.12±0.05 | 1.59±0.33(52.50±32.54) | 1.58±0.31(51.56±29.84) | 1.59±0.32(52.53±31.73) | 1.59±0.26(50.64±25.40) | 1.48±0.30(43.85±26.39) |
高剂量10mg/kg | 1.08±0.07 | 1.37±0.26(35.19±19.75)<32.97> | 1.30±0.23(27.06±19.03)<47.51> | 1.31±0.21(27.16±16.39)<48.29> | 1.32±0.19(28.05±14.52)<44.61> | 1.32±0.23(28.86±19.06)<34.19> |
中剂量5mg/kg | 1.11±0.06 | 1.43±0.23(37.27±15.30)<29.01> | 1.41±0.22(35.00±15.12)<32.11> | 1.45±0.17(35.95±11.21)<31.56> | 1.41±0.23(34.66±13.01)<31.57> | 1.39±0.18(31.12±13.81)<29.04> |
低剂量2.gmg/kg | 1.09±0.04 | 1.39±0.24(40.29±18.03)<23.26> | 1.38±0.24(38.98±18.96)<24.39> | 1.37±0.24(38.92±15.07)<25.92> | 1.35±0.22(36.93±13.02)<27.08> | 1.33±0.17(31.75±13.70)<27.60> |
enbrel9mg/kg | 1.06±0.04 | 1.38±0.20(36.48±15.50)<30.52> | 1.36±0.22(35.30±14.25)<31.53> | 1.34±0.21(33.88±13.57)<35.50> | 1.34±0.20(32.16±15.12)<36.49> | 1.31±0.16(27.63±10.87)<36.99> |
雷公藤1.5mg/kg | 1.03±0.05 | 1.43±0.24(46.48±16.88)<11.47> | 1.35±0.19(37.22±16.50)<27.82> | 1.36±0.19(38.09±14.10)<27.49> | 1.36±0.20(39.06±13.00)<22.87> | 1.37±0.19(40.19±11.80)<8.33> |
*P<0.05,**P<0.01与致炎对照组比较 ( )内为肿胀率(%) < >内为抑制率(%)
3.人参皂甙Compound-K对II型胶元(CII)诱导的关节炎的治疗作用
3.1实验方法:
将II型胶原(CII)与弗氏不完全佐剂研磨成乳剂,分别在每个大鼠背部皮内注射免疫,至19天大鼠足关节大部分开始肿胀,挑选足关节出现肿胀的致敏大鼠40只,随即分为5组,每组8只,分别为至炎对照组;人参皂甙Compound-K10mg/kg,iv;中剂量组:人参皂甙Compound-K5mg/kg,iv;小剂量组:人参皂甙Compound-K2.5mg/kg,iv;Enbrel组:9mg/kg,sc;雷公藤组1.5mg/kg;空白对照组:生理盐水10mg/kg,iv。连续给药8天。用排水法测量致炎前及症状开始后(20天后)不同时间的足肿胀值,计算肿胀率及抑制率,以组间差异以t检验进行比较。
3.2结果
结果见表6,人参皂甙Compound-K可治疗II型胶元诱导的关节炎,其中高剂量组作用最强,3 1day时作用最好,抑制率最高达27.67%,高于雷公藤组,与enbrel组相当。
表6人参皂甙Compound-K对II型胶元(CII)诱导的关节炎的治疗作用(%,n=8,x±s)
致炎后不同天数的肿胀值ml | |||||||
0day | 20day | 22day | 23day | 25day | 28day | 31day | |
空白对照 | 1.03±0.07 | 1.01±0.12 | 1.01±0.08 | 1.07±0.10 | 1.06±0.06 | 1.04±0.09 | 1.04±0.08 |
致炎对照 | 1.08±0.06 | 1.67±0.09(54.03±10.64) | 1.73±0.18(60.23±20.06) | 1.75±0.14(62.26±18.40) | 1.75±0.20(61.69±18.90) | 1.64±0.17(51.64±17.41) | 1.61±0.07(49.00±8.66) |
高剂量10mg/kg | 1.04±0.19 | <1.52±0.19(47.22±18.60)<12.61> | 1.54±0.12(50.43±9.45)<16.28> | 1.54±0.10(50.25±22.06)<19.28> | 1.54±0.12(50.62±21.43)<17.95> | 1.44±0.13(40.23±16.26)<22.09> | 1.38±0.11(35.44±22.50)<27.67> |
中剂量5mg/kg | 1.03±0.05 | 1.52±0.21(48.97±27.82<9.35> | 1.56±0.15(52.77±21.55)<12.39> | 1.58±0.13(53.62±14.27)<13.87> | 1.56±0.19(52.06±18.56)<15.62> | 1.49±0.28(44.84±25.91)<13.17> | 1.45±0.13(41.34±13.83)<15.64> |
低剂量2.5gmg/kg | 1.03±0.05 | 1.48±0.11(43.79±12.08<18.95> | 1.53±0.06(48.22±10.27)<19.94> | 1.56±0.06(51.23±9.82)<17.70> | 1.56±0.16(51.66±18.36)<16.26> | 1.45±0.10(41.04±10.92)<20.52> | 1.42±0.10(37.86±11.18)<22.73> |
enbrel9mg/kg | 1.00±0.08 | 1.51±0.11(51.65±15.35<4.41> | 1.48±0.15(49.63±25.60)<17.61> | 1.48±0.12(49.20±19.86)<20.98> | 1.46±0.11(46.43±15.37)<24.74> | 1.36±0.09(37.24±17.23)<27.88> | 1.35±0.08(36.24±14.64)<26.03> |
雷公藤1.5mg/kg | 1.00±0.12 | 1.50±0.17(51.18±18.93<5.28> | 1.52±0.09(54.14±23.10)<10.12> | 1.55±0.12(56.57±23.30<9.13> | 1.48±0.11(49.69±22.81<19.45> | 1.39±0.12(41.18±22.50<20.25> | 1.37±0.12(38.71±22.60)<20.99> |
*P<0.05,**P<0.01与致炎对照组比较 ( )内为肿胀率(%) < >内为抑制率(%)
Claims (1)
1.一种人参皂甙Compound-K在制备预防或治疗关节炎的药物中的应用。
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CN106692168A (zh) * | 2015-07-28 | 2017-05-24 | 复旦大学 | 人参皂苷compound K在制药中的用途 |
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US8855759B2 (en) * | 2007-10-09 | 2014-10-07 | The Hong Kong Polytechnic University | Method of treating a rheumatic disorder using combination of transcutaneous electrical nerve stimulation and a ginsenoside |
KR101401658B1 (ko) | 2011-06-16 | 2014-06-02 | 한국생명공학연구원 | 진세노사이드 컴파운드 k 또는 이의 유도체로 된 항균제 |
CN115177614A (zh) * | 2021-04-01 | 2022-10-14 | 长春藤生物科技股份有限公司 | 正丁基苯酞的应用 |
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