热熔压敏胶伤湿止痛膏的实验研究
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摘要
目的:
     通过伤湿止痛膏的两种不同基质(橡胶基质和热熔压敏胶基质)制备工艺研究比较,研制新型sIs热熔压敏胶贴膏剂,找到传统橡胶膏剂的替代品,解决传统橡胶膏剂的工艺缺陷,以及临床使用刺激性大、易引起过敏等问题;制定热熔压敏胶伤湿止痛膏的质量标准,研制出皮肤黏贴性、稳定性较好的热熔压敏胶贴膏剂;通过体外透皮和释放规律实验,对比两种不同基质伤湿止痛膏的释药性能,为研制热熔压敏胶贴膏剂提供依据。
     方法:
     1.工艺研究:了解原橡胶基质工艺;学习新热熔压敏胶基质工艺,以综合粘附性能(初粘力、持黏力、剥离度)和综合物理性能(成型性、弹性、韧性、舒适感、可涂展性)作为评价指标,进行原料选择、用量筛选,以及制备工艺的优选,然后考察热熔压敏胶的载药性能。
     2.质量标准制定:采用薄层色谱法对热熔压敏胶伤湿止痛膏中的颠茄流浸膏进行定性鉴别;按照2010年版《中国药典》一部附录ⅠⅠ贴膏剂项下贴剂重量差异检测方法进行测定;采用HPLC法测定热熔压敏胶伤湿止痛膏中马钱子碱、士的宁的含量,色谱条件—色谱柱:Agilent SB-C18(250mm×4.6mm,5μm);流动相:乙腈Acetonitrile-0.01mol/L庚烷磺酸钠与0.02mol/L KH2P04等量混合溶液(用10%磷酸调PH值至2.8)(21:79);流速1ml/min波长:260nm;柱温:30℃
     3.体外透皮吸收和释放规律研究:采用智能透皮试验仪及释放度测定装置,对两种不同基质的伤湿止痛膏进行离体透皮吸收及释放度试验,用HPLC法测定接受液中马钱子碱、士的宁、硫酸阿托品的含量,分别计算橡胶伤湿止痛膏、热熔压敏胶伤湿止痛膏中硫酸阿托品、马钱子碱、士的宁的释放度和离体透皮率,对两种不同基质贴膏剂的离体透皮率与释放度进行比较。
     结果:
     1.经试验筛选,确定了热熔压敏胶制备原料:骨架材料为SIS1105,增粘剂为松香衍生物,增塑剂为液体石蜡;原料处方为:SIS1105/松香衍生物/液体石蜡(100:120:50);制备工艺条件:反应时温度为120℃,反应时间为30min,涂布温度为90℃;药物加入基质时的最佳温度为105℃。热熔压敏胶基质在贴剂制备中的优势明显大于橡胶基质,新型的SIS热熔压敏胶贴膏剂可以取代传统橡胶膏剂。
     2.质量标准研究:热熔压敏胶伤湿止痛膏中颠茄流浸膏的薄层鉴别图谱清晰,方法简便。本品的重量差异检查符合规定。HPLC法测定热熔压敏胶伤湿止痛膏中士的宁和马钱子碱的含量:士的宁、马钱子碱在色谱中保留时间分别为16.8min、14.0min,被测色谱峰与其他峰分离良好,生马钱子阴性对照样品溶液无干扰;线性范围分别为0.53-53.0μg·mL-1、0.5~50.0μg·mL1(R2=0.9995);精密度试验RSD分别为0.50%、0.81%;稳定性试验RSD分别为0.75%、2.69%,样品溶液在16h内稳定;重复性试验:RSD分别为4.90%、2.63%;回收率试验:平均加样回收率分别为90.68%、100.10%,RSD分别为2.94%、1.18%。3批热熔压敏胶伤湿止痛膏中士的宁含量分别为22.12μg·g-1、22.56μg·g-1、22.93μg·g-1;马钱子碱的含量分别为15.52μg·g-1、15.07μg·g-1、15.84μg·g-1.
     3.体外透皮吸收和释放规律研究:橡胶伤湿止痛膏中马钱子碱、士的宁、硫酸阿托品72h的平均累积透过百分率分别为54.90%,50.24%,46.54%;在30%乙醇生理盐水中24h的释放度分别为92.29%,81.77%,53.28%;热熔压敏胶伤湿止痛膏中马钱子碱、士的宁、硫酸阿托品72h的内平均累积透过百分率分别为53.25%、74.52%、34.32%;在30%乙醇生理盐水中24h的释放度分别为49.62%、82.25%、25.76%。
     结论:制备的热熔压敏胶伤湿止痛膏具有较好的皮肤黏贴性、释放度与皮肤渗透性。通过制备工艺研究、质量标准制定、体外透皮速和释放规律研究,为热熔压敏胶基质用于制备新型的压敏胶贴膏制剂奠定了良好的基础。
Objective:
     In order to develop an new type of SIS Hot-melt pressure sensitive adhesive patch, to find a substitute of the traditional rubber patch, and to solve the problem in life and clinical use that the traditional rubber patch had large excitability and easy to cause allergys; we compered the preparation process of two different stroma of ShangShi ZhiTong Gao Patch;And then drafting quality standards of Hot melt pressure sensitive adhesive ShangShi ZhiTong Gao patch, which is not only have a nice stability and a well adhesion to skin.; Finally conducting a test on the release regularity and the in-vitro transdermal, then contrasted drug release property of two different kinds of ShangShi ZhiTong Gao Patch, the result provide information for the development of hot melt pressure sensitive adhesive patch.
     Methods::
     1The study on process:comprehended the original rubber stromal technology:The new technology used comprehensive adhesion (initial tack, holding tack, peel degree) and comprehensive physical properties (formability, flexibility, toughness, comfort, glide) of pressure-sensitive adhesive as indicators, in order to study on raw material selection> dosage screening test and optimization of the preparation technology, and then examining the drug carrier for pressure sensitive adhesive; Contrasting the rubber stromal and the hot melt pressure sensitive adhesive stromal through the relevant literature.
     2The study on the quality standards for the Preparation:The Atropine Sulfate fluid extract in The New ShangShi ZhiTong Gao Patch were identified by TLC. The weight variation of the preparation were tested according to the method described for adhesive ointment in2010China Pharmacopeia below the relative volumes of appendix I I. The content of atropine sulfate^Strychnine> Brucine in the ShangShi ZhiTong Gao Patch was determined by HPLC. The chromatography conditions were that the Agilent SB-C18(250mmx4.6mm,5μm) column was used; that mobile phase was composed of Acetonitrile-O.Olmol/L sodium1-heptanesulfonate and0.02mol/L KH2PO4equivalent mixture(used10%phosphoric acid regulating PH value to2.8)(21:79); the flow rate was1mL/min with UV detection at260nm, and that the column temperature was30℃
     3The study on the release rate and the in vitro percutaneous absorption rate:The equipment of release and aptitude percutaneous absorption were used to carry out the experiments of two different stroma of ShangShi ZhiTong Gao Patch. The content of Strychnine、Brucine、 Atropine Sulfate released and in vitro permeated from ShangShi ZhiTong Gao Patch were determined by HPLC. Calculated the release rate and the in vitro percutaneous absorption rate of rubber ShangShi ZhiTong Gao Patch and hot melt pressure sensitive adhesive ShangShi ZhiTong Gao Patch, contrasting the drug release property between two different stroma of ShangShi ZhiTong Gao
     Results:
     1Through the experiment selection that determined raw material of Hot melt pressure sensitive adhesive choose SIS1105as skeleton material, rosin derivatives as tackifier, liquid paraffin as plasticizer. And the prescription ratio of raw material was SIS1105:Rosin derivatives:liquid paraffin (100:120:50); The preparation conditions:reaction temperature wasl20℃, reaction time was30min, coating temperature was90℃; and the optimum temperature of medicine mixed in stromal was105℃. Compared to rubber stromal, hot melt pressure sensitive adhesive stromal had obviously superiority. New hot melt pressure sensitive adhesive patch will replace tradition rubber patch.
     2The study on the quality standards:TLC was used to identify Belladonna in Hot melt pressure sensitive adhesive ShangSh ZhiTong Gao Patch preparation. The examination of the weight variation of the patch preparation were right to the regulation. Determined the content by HPLC:the determination of Strychnine and Brucine had shown that retention time of the chromate graphy were16.8min and14.0min, the measured peaks and other peaks well separated; Raw Strychnos negative reference substance sample solution without interference; the liner rang were0.53-53.0μg-g-'and0.5-50.0μg.g-1(R2=0.9995), and the precision RSD were0.50%and0.81%; The Stability RSD were0.75%and2.69%, sample solution was stable within16h; The redupplicate RSD were4.90%and2.63%; And the average recovery were90.68%and100.10%, with RSD were2.94%and1.18%; Three batches of Hot melt pressure sensitive adhesive ShangShi ZhiTong Gao Patch in which the content of Strychnine were22.12μg.g-1,22.56μg.g-1、22.93μg.g-1、 and content of Brucine were15.52μg.g-1、15.07μg.g-1、15.84μg.g-1、
     3The study on the release rate and the in vitro percutaneous rate:The cumulative permeation rate of strychnine. Strychnine, Atropine sulfate from Rubber ShangShi ZhiTong Gao Patch within72hours were54.90%.50.24%,46.54%;and the release rate in the30%ethanol saline were92.29%,81.77%.53.28%in24hours;And the cumulative permeation rate of strychnine, Strychnine, Atropine sulfate from Hot-melt pressure sensitive adhesive ShangShi ZhiTong Gao Patch within72hours were53.25%,74.52%.34.32%;and the release rate in the30%ethanol saline were49.62%,82.25%,25.76%in24hours,
     Conclusion:
     prepared of Hot-melt pressure sensitive adhesive ShangShi ZhiTong Gao have well skin-adhesive, release rate and skin permeability. Through the preparation of technology, studying on in-vitro permeated and release rate of the regularity, drawing up the quality standards, laid a good foundation for development of pressure-sensitive adhesive matrix for Plaster preparations.
引文
[1]祁荣,贺锐锐,李博或,等.经皮给药系统研究新进展[J].中医外治杂志,2007,16(1):3-6
    [2]王光清主编.中国膏药学[M].陕西:陕西科学技术出版社出版,1981:1-8
    [3]梁秉文.中药经皮给药制剂技术[M].北京:化学工业出版社,2006:88
    [4]赵佶.圣济总录[M].北京:人民出版社,1961:182
    [5]吴尚先.理论骈文[M].北京:中国医药科技出版社,2011:14
    [6]张兆旺主编.中药药剂学[M].北京:中国中医药出版社,2003:296
    [7]梁秉文.中药经皮给药制剂技术[M].北京:化学工业出版社,2006:10-19
    [8]刘伟志,秦阿娜,钟伯雄,等.传统膏药制备工艺研究进展[J].中央民族大报,2010(4):74-75
    [9]傅海舰.傣药橡胶膏剂制备工艺的研究[J].中国民族医药杂志,2007,10(10):63
    [10]李华.橡胶膏剂制备工艺比较[J].医药工程设计,2009,30(2):24-25
    [11]陈政权,吴滨,等.中药浸膏对中药橡胶剂黏附力的影响因素分析[N].国际医药卫生导报,2007,13(19):76-78
    [12]赵光贤.橡胶的自粘与增粘[J].世界橡胶工业,2006,33(8):33
    [13]廖瑞玲,林艳芳,彭燕,等.傣药乳结消膏质量标准研究[J].中国民族医药杂志,2002,8(4):37
    [14]崔秀华,崔淑芹,张艳,等.国内巴布剂的研究现状及展望[J].德州学院学报,2010,26(4):80-83
    [15]潘卫三,李华,李嘉煜.中药巴布剂研究的技术难点及解决方案[J].中医外治杂志,2004,13(3):3-4
    [16]张兵锋,李家敏.紫花地丁巴布剂的制备工艺研究[J].宜春学院学报,2009,31(6):47-48
    [17]张兆旺主编.中药药剂学[M].北京:中国中医药出版社,2003:318-319
    [18]常明明.不同压敏胶基质对中药贴剂的适应性研究[D].大连理工大学,2009:5-6
    [19]江海,黄嘉兰.外用透皮贴膏剂基质的分类和运用[A].第五届外用制剂国际年会论文合集[C],2008,204-207
    [20]郑俊民.经皮药物新剂型[M].北京:人民卫生出版社,2006,12:370
    [21]胡婧,罗华菲,王浩.压敏胶骨架型透皮给药系统的生产工艺及设备概况[J].中国医药工业杂志,2010,41(1):46-50
    [22]石磊.新型热熔压敏胶基质及辣椒风湿贴膏剂的研究[D].河南中医学院,2008
    [23]俞振伟,应晓英,梁文权.热熔压敏胶中药物释放性能的研究[J].中国药学杂,2009,44(24):1878-1882
    [24]国家药典委员会.中华人民共和国药典[S].北京:化学工业出版社,2010:附录8
    [25]冷静,傅超美,邹亮.中药经皮给药制剂的研究进展[J].成都大学学报,2008,27(3):183-186
    [26]苗明三,李振国.现代实用中药质量控制技术[M].2003:156
    [27]苏新医学院.中药大辞典[M].上册.上海:上海人民出版社,1977:291
    [28]常新全,丁丽霞,主编.中药活性成分分析手[M].北京:学苑出版社,2006:318
    [29]杜贵友、方文贤,主编,有毒中药现代研究与合理应用[M],北京:人民卫生出版社,2006:305-314
    [30]王亚静.马钱子透皮吸收试验的研究[D].天津大学.2006
    [31]闫小平,郑蕊,官仕杰,等.热熔压敏胶在中药透皮吸收制剂中的研究进展[J].中国中药杂志,2009,34(12):1612-1614
    [32]张娟,肖鲁伟.马钱子碱的镇痛作用及其作用机制的探讨.中国中医药科技[J].2009,16(5):374-375
    [33]景秀荣,李谦.马钱子的作用及其不良反应.山西医药杂志[J].2011,40(1):72-73
    [34]国家药典委员会.中华人民共和国药典[S].北京:化学工业出版社,2010:767
    [35]国家药典委员会.中华人民共和国药典[S].北京:化学工业出版社,2010:1191-1192
    [36]王书杰,张新春,俞学忠,等.风痛宁丸的制备与临床应用.中国医院药学杂志[J].2009.29(5):416-418
    [37]张源潮,刘文波,苏厚恒,等.马钱子胶囊治疗痹证的临床观察,中药药理与临床[J].1998,14(6):39-40
    [38]裴纪文.职利琴.三乌丸治疗类风湿性关节炎226例.陕西中医[J].2008.29(11).1488-1489
    [39]范继宝.马钱子在临床上的应用.中医药学报[J].1985.3:31-35
    [49]覃旭,赵新,唐良华,等.马钱子散对实验性骨折愈合骨痴局部BMP定量表达的影响[J].中国中医骨伤杂志,2009,17(1):17.
    [41]吕启郁.舒筋活络散治疗坐骨神经痛[J].光明中医,2006,21(4):63
    [42]王梅,张颖.马钱子散治疗坐骨神经痛29例临床观察[J].光明中医.2006.21(9):32-33
    [43]汪开治.有毒药用植物颠茄[J].植物杂志.2003.2
    [44]何爱明,卞明燕.颠茄乳膏剂的制备及其活血作用的初探.中外医疗 [J].2005(5):43-44
    [45]许英.莨菪类药物的临床应用[J].中华中西医学杂志[J].2004,2(12):64-65
    [46]高利娥,边红喜.论阿托品的药理作用及临床应用,中国实用医药[J],2009.4(24)137-138
    [47]陈伟,李金兰.复方颠茄合剂的工艺改进.海峡药学[J].2007.19(3):19-21
    [48]国家药典委员会.中华人民共和国药典[S].北京:化学工业出版社,2010:1247
    [49]国家药典委员会.中华人民共和国药典[S].北京:化学工业出版社,2010:705
    [50]徐力,蒋建伟.巴斯特关节止痛膏治疗风寒湿性关节痛33例.中医杂志[J].2006.47(1):41-42
    [51]许帼光,吴耀持.穴敷邦迪辣椒痛可贴的临床疗效观察.上海针灸杂志
    [J].1995.14(4):179-180
    [52]姜霖,韩凤东,赵英男.平痛新联合阿托品用于肾绞痛镇痛的效果观察.临床军医杂志[J].2012.40(1):69-70
    [53]苗明三,李振国.现代实用中药质量控制技术[M].2003
    [54]杜贵友、方文贤主编,有毒中药现代研究与合理应用.人民卫生出版社:286
    [55]期琪.乌头类药物的临床应用及毒性分析[J].中国医药卫生.2005,6(9):102
    [56]王英豪.从化学、药理学和炮制的角度探讨附子[J].光明中医.2009.4
    [57]刘瑶,焦豪妍.川乌毒理与药理现代研究进展[J]. 云南中医中药杂志[J].2010.,31(3):66-67
    [58]黄建明.草乌标准提取物的研究[D].复旦大学.2003
    [59]王琼珺,林向前.珺腰腿痛片质量标准研究.中国药业[J].2008.17(18):28-29
    [60]国家药典委员会.中华人民共和国药典[S].北京:化学工业出版社,2010:548
    [61]国家药典委员会.中华人民共和国药典[S].北京:化学工业出版社,2010:509
    [62]薛文翰,苗春兰.裴正学重用川乌、草乌治疗类风湿性.关节炎.天津中医[J].2000.17(3):2
    [63]陈双全.舒筋止痛液治疗肩周炎100例.陕西中医[J].1997.18(2):64-65
    [64]史永博,史海虹.热敷散配合手法治疗肩周炎30例.现代中医药[J].2007.27(5):66-67
    [65]张云坤.生川、草乌祁蛇酒治疗坐骨神经痛22例.江西中医药[J].1994(25):28
    [66]张爱清.压敏胶粘剂[M].北京:化学工业出版社,2002:572.
    [67]张小红,王浩,侯惠民,等.经皮给药系统中压敏胶的组成及性能的研究进展[J].中国医药工业杂志,2008,39(10):67-772
    [68]俞振伟,应晓英.热熔压敏胶中药物释放性能的研究[J].中国药学杂.2009,44(24):1878-1882
    [69]王宇.卫生用品用热熔压敏胶的研制及影响因素探讨[D].南京林业大学,2009: 4-5
    [70]杨性坤,宋世林.用sIs及SBS制备热熔压敏胶的工艺研究[J],化学与粘合,2001,3:107-109
    [71]江海,黄嘉兰.外用透皮贴膏剂基质的分类和运用[A].第五届外用制剂国际年会论文合集[c],2008,204-207
    [72]郑俊民.经皮药物新剂型[M].北京:人民卫生出版社,2006,12:370
    [73]李红强,曾幸荣,吴伟卿,等.热熔压敏胶的应用现状及发展[J].化学与黏合.2006.28(5):338-341
    [74]陈榕珍,无溶剂型聚丙烯酸酷压敏胶的研究[D],华东师范大学,2006
    [75]任嘉祥,杜奕,李江屏.丙烯酸系热熔压敏胶粘剂的研究.高分子材料科学与工程[J].2000.16(4):139-142
    [76]杨静,薛志云,陶婉蓉.丙烯酸醋热熔压敏胶固化动力学研究.化学世界[J].1997(8):419-421
    [77]殷锦捷,马海云.热熔压敏胶的开发应用,中国粘胶剂[J],12(5):61-63
    [1]国家药典委员会.中华人民共和国药典[S].(一部),北京:化学工业出版社,2010:691.
    [2]汤淮波,张令君,李湘玲.不同溶剂提取马钱子中士的宁与马钱子碱的实验研究[J].中医药导报,2009,15(11):52.
    [3]国家药典委员会.中华人民共和国药典[S].(一部),北京:化学工业出版社,2010:附录8.
    [4]国家药典委员会.中华人民共和国药典[S].(一部),北京:化学工业出版社,2010:47.
    [5]王红梅,张彤,赵婷婷,等.消痛贴膏中润湿剂的透皮促透作用研究[J].时珍国医国药,2009,20(3):686-687.
    [6]官仕杰,闫小平,毛超一,等.微米大黄痤疮乳膏的透皮吸收研究[J].中国中药杂志,2008,33(10):1215-1217.
    [7]杨立平,邓桂明,杨广民.咳喘穴位贴片体外透皮速率和体外释放规律研究[J].中国药房,2009,20(18):1372-1374.
    [8]刘志敏,牛欣,杨学智,等.草乌提取物乌头碱和新乌头碱的透皮速率测定[J].中西医结合学报,2006,4(1):68-69
    [9]胡巍,陈军,蔡宝昌.马钱子碱与士的宁体外经皮渗透性质的考察[J].中国新药杂志,2008,17(12):1053-1056.
    [10]王志强,吴继禹,张秀华.用Excel软件对溶出数据进行多种曲线拟合和处理[J].海峡药学,2006,18(1):47-49

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