药用辅料在制剂中的应用
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
药用辅料包括多种赋形剂与添加剂,是药物制剂的基础材料和重要的组成部分,在制剂成型的发展和生产中起着很重要的作用,它不仅赋予药物一定剂型用于临床,并且与提高药物的疗效,降低毒副作用有很大的关系。此外,在常规剂型的处方设计和确定最佳处方时以及研制开发新剂型、新品种时,都离不开辅料的选择和应用。特别是近一、二十年来,由于新剂型的研究推动了新辅料的开发,新辅料的应用又促进了新剂型的发展。
     本文首先论述了药用辅料在药剂中的重要作用,对辅料与剂型的关系、辅料与吸收的关系以及药用辅料引起的不良反应进行综述。药物和辅料之间相互影响,辅料对药物的实际应用和疗效的发挥,起着积极的关键性的作用,其中溶剂、稀释剂、粘合剂、崩解剂、润滑剂以及土体分散载体材料的水溶性高分子材料等辅料对药物的吸收都有很大的影响。辅料并非惰性或者非活性物质,不合理的应用会引起一系列的不良反应,本文对一些辅料所引起的不良反应和对辅料在儿童用剂型设计中的注意事项进行了综述。
     其次论述了我国辅料在品种规格及使用频率方面、质量标准方面、检测手段方面、科研开发方面、应用研究方面以及生产经营方面和国外药用辅料的差别。通过在品种规格及使用频率上的对比,分析了国产制剂质量较进口产品差的原因;国内辅料缺乏统一的质量标准,虽然出台了《药用辅料GMP指南》,但和国外仍有很大的差距,并且检测方法单一和检测仪器落后,这就造成了辅料质量差异太大;通过对比在辅料开发和应用研究方面的特点以及药用辅料生产企业的状况,发现我国新辅料均属仿制且开发集中于传统老剂型,低水平重复开发较严重,研究的深度也不够,应用机制理论的研究则还是一片空白,有待于进一步巩固和发展,辅料生产厂家的多样化,专门的药用辅料企业过少,这就使我国药用辅料和国外有了更大的差距。
     再者,对药用新辅料在新药新剂型开发中的应用方面进行了综述,列举了药剂辅料在固体制剂包衣与包合物方面的应用、在控释、透皮制剂与靶向制剂中的应用、在缓控释制剂中的应用、在固体分散体与粘膜吸收剂中的应用,详细介绍了羟丙甲纤维素、微晶纤维素、聚丙烯酸树脂等几种药剂中常用的新辅料的具体应用和最新的研究进展。
     最后对我国药剂辅料工业的发展提出了几点建议,希望我国药用辅料生产企业不断在提高产品质量,提高自主的研究开发能力,寻找出适合国内企业发展的道路,使新型辅料不断得到开发与应用,通过产品质量和应用技术的服务提高竞争力实力,顺应生产专业化、品种系列化、应用科学化、服务优质化、市场国际化的发展趋势,使药用辅料在新药新剂型开发中发挥更大作用,以取得更佳社会效益和经济效益。
The pharmaceutical are composed of various diluents bases and adjuncts, which are essential materials and important parts in pharmaceutics. They play a key role in developing dosage forms and pharmaceutical industry production. Pharmaceutical excipients can not only provide some dosage forms of drug, but also increase therapeutic effects and reduce side effects. Further, the optimization and design of formulation as well as the research and development of dosage form all depend strongly on the selection of excipients. The study of new dosage forms advances the development of new excipients in recent forty years, so they have a close relation and depend strongly on each other.
    This review paper discussed the important function of excipients on dosage forms, and described the relationship between excipients and absorption, and the adverse drug reactions caused by excipients as well. There is a positive correlation between drug and excipients, and the excipients play an important and positive role in applications of drugs. Some pharmaceutical excipients, such as solvent, attenuant, adhesive material, disintegrating agent, lubrication and water soluble polymer of solid dispersion, have a considerable impact on drug absorption. Adverse drug reaction could be caused by the non-rational use of some excipients, thereby; the article summarized some adverse drug reactions induced by excipients and the attention for the use of excipients in dosage form design.
    Comparison has been carried out between domestic and foreign excipients, including the description, usage frequency, quality standard, detecting methods, scientific research, application study and production operations.
    Through the contrast research on the description and usage frequency, the causes of domestic preparations inferior to foreign ones were analyzed. Although the Medical Subsidiary GMPGuide was issued, domestic excipients are scant of unified quality standards, and there is still a big gap compared with foreign ones. The detection methods for excipients are single and detecting instruments are backward, which cause a great quality discrepancy among the excipients.
    Through the contrast research on the application study and production operations, the paper finds that domestic excipients are all imitations, and the research is mostly concentrated traditional old dosage form and repeated at low level. Besides the research depth is not inadequate, and theoretical research of application is still blank,which need to be further investigated.
    Application of the excipients in dosage forms development, e.g. in the solid preparation as well as inclusion compound, sustained/controlled release preparations, transdermal and targeting drug delivery systems, solid dispersion and mucosal absorbefacient, were introduced in this review. The article also presents the applications of some new supplementary agents such as hypromellose, cellulose microcrystallisate, polyacrylic resin in detail, and the development suggestions on also were described.
    In the end, the paper gives some advice on the development of supplementary agents industry in China. We hope that China's pharmaceutical excipients manufacturers will improve the product quality constantly, enhance independence innovation ability, find out for the development of domestic enterprises, and enabled new excipients continued development and application. Through the quality.control and the application of technology services, the competitiveness of strength and service competitiveness strength are hoped to be improved and enhanced. Then some measucements, e.g. specialization and multi-variety series of production, application of scientific, and quality service, international market development trends, must to be administered to enable the pharmaceutical excipients play a greater role in development of new dosage form, and achieve better social and economic benefits.
引文
1.杜月莲,高萧枫.新辅料在固体制剂制备中的应用[J].国际医药卫生导报,2004,10(8):60-61
    2. http://info.pharmacy.hc360.com/2006/07/19095440828.shtml
    3.王虎,陈华庭,吕永宁.从苏丹红事件看加强药用辅料监管的必要性[J].食品药品监管,2006,15(2):12
    4.岳伟彪,向慧川加强辅料管理促进辅料开发[J].药学进展,2000,1:38-40
    5.袁松范 药用辅料30年发展动向[J].上海医药情报研究,1997,46(3):12-14
    6.杨继彰 药用辅料的国内外差距[J].上海市医药局科技情报
    7.吕东南,白先群 药用辅料在制剂中的应用概述[J].华夏医学 2001,6(14):986-988
    8.夏军平,张志荣,胡明等 中美两国药用辅料分类管理的比较[J].华西药学杂志 2004,19(6):451~454
    9.齐继成 国内外药用新辅料的研究用及发展趋势[J].化学医药工业信息,1996,12(11):6-12
    10.孙国庆,徐坚,陈琦,等.格列吡嗪缓释片的制备及其释药特性的研究[J].中国药科大学学报,1996,27(11):661
    11.陈挺,陈子晟,包泳初,等.国产HPMC作为盐酸普萘洛尔缓释骨架片基质的研究[J].中国医药工业杂志,1998,29(1):10
    12. Nellore RV, Rekhi GS, Hussain AS, et al. Development of metoprolol tartrate extended-release matrix tablet formulations for regulatory policy consideration. J Con trolled Release, 1998, 50 (1-3): 247
    13. Ebube NK, Hikal AH, Wyandt CM, et al. Sustained release of acetaminophen from heterogeneous mat rixtablets: influence of polymer ratio, polymer lodaing, and coactive on drug release. Pharm Dev Technol, 1997, 2 (2): 161
    14. Amilu S.Formulating for Controlled Release with Methoc Cellulose Ethers. The Colorcon Co. 1993
    15.董志超,蒋雪涛.羟丙基甲基纤维素的物理性质对口服骨架型制剂释放的影响[J].国外医学—合成药、生化药、制剂分册,1995,16(2):103
    16.董志超,蒋雪涛,张恒弼.卡托普利缓释片的试验研究[J].中国医药工业杂志, 1993,24(2):65
    17.董志超,蒋雪涛.羟丙基甲基纤维素在凝胶骨架中的含量与水溶性药物释放机制的关系[J].药学学报,1996,1(31):43
    18.肖大伟,郭宏.丁卡因口腔粘附片的研究[J].江苏药学与临床研究,2002,10(3):4
    19. Podczeck F, Jones BE. The in vitro dissolution of the ophylline from different types of hard shell capsules [J].Drug Dev Ind Pharm, 2002,28(9): 1163
    20. Chiwele I, Jones BE. Podzeck F. The shell dissolution of various empty hard capsules [J].Chem Pharm Bull (Tokyo),2000,48(7):951
    21.郑俊民.药用高分子材料学[M].北京:中国医药科技出版社.2000:112-114
    22. Cole ET, Scott RA, Connor AL, et al. Enteric coated HPMC capsules designed to achieve intestinal targeting [J], Int J Pharm,2002,231 (1): 83
    23.汤钥,朱家壁,甘莉.HPMC胶囊壳对干粉吸入剂性能的影响[J].中国药科大学学报,2004,35(1):32
    24.高佳.羟丙甲纤维素在外用混悬型制剂中的应用[J].中国药师,2002,5(9):543
    25.杨春丽,马晶.盐酸特比萘芬滴眼剂的制备[J].中国医药工业杂志,2000,31(11):490
    26.胡建平,朱月华.利福平眼药中助溶辅料的改进[J].江苏药学与临床研究,2001,9(1):58
    27.王宝庆,陆新汉,唐星,等.乌拉地尔HPMC骨架片的研制及释放度的考察[J].沈阳药科大学学报,2001,18(1):5
    28.程紫骅,康保国,朱家璧.尼莫地平HPMC骨架片的药物释放影响因素研究[J].中国药科大学学报,1998,29(6):418
    29.李嘉熠,董娥,李华,等.盐酸二甲双胍缓释片释药因素考察及处方筛选[J].沈阳药科大学学报,2003,20(2):88
    30.黄东坡,王远,蒋国强,等.盐酸二甲双胍胃漂浮缓释制剂的制备与释药过程研究[J].精细化工,2002,19(10):609
    31.吴琼珠,戴永健,乔善磊.非洛地平口腔黏附片的研究[J].中国药科大学学报,2001,32(1):13-16
    32.向大雄,焕德,罗杰英,等.葛根总黄酮生物黏附性缓释片体外组织黏附力及释放度研究[J].中国药房,2002,13(8):459
    33.张丽华,腾延平,高萍等,微晶纤维素在片剂生产中的应用[J].牡丹江医学院学包,1999,20(1):47-49
    34.王文刚,崔光华,傅宏义,等.离心制粒工艺制备微晶纤维素空白微丸的研究[J].解放军药学学报,2002,18(5):268-271
    35.姜国庆.微晶纤维素的用法对片剂中扑热息痛溶出度的影响[J].佳末斯医学院学报,1997,20(2):22-24。
    36.张金平,王鹤尧,刘桦.阿司匹林片剂粉末直接压片新工艺研究[J].中国新药杂志,2003,12(1):45-46
    37.王国栋,田红林.脉通片片心处方对成品质量影响研究[J].新疆中医药,2004,22(5):13-14
    38. http://www.100md.com/html/DirDu/2006/04/15197/47/41.htm
    39.卡乐康药学实践,2005,1:12
    40.中国抗生素信息网 http://www.antibiotics-cn.com/anti_front/front_report/report_list_home.jsp?id=1827&type_id=1
    41.邵健,杨宇民,徐秉洳.甲壳素和壳聚糖在生物医学方面的应用[J].南通医学院学报,1997,17(1):145
    42. Ilium L,Farraj NF, Davis SS.Chitosan as anovel nasal delivery system for peptide drugs[J].Pharm Res, 1994,11: 1186
    43. Yamamoto A,Tozaki H,Okada N,et al.Colon-specific delivery of peptide drugs and anti-inflammatory drugs using chitosan capsules[J].STP Pharm Sci,2000,10(1):23
    44. SchipperNC,OlssonS,Hoogstraate JA,et al.Chitosan as absorption enhancers for poorly absorbable drugs:Mechanism of absorption enhancement[J]. Pharm Res, 1997, 14:923
    45. Assadang P, Verhoef J,Gerrit B,et al.In vitro evaluation of intestinal absorption of desmopress in using drug-delivery systems based on superporous hydrogels[J].Int J Pharm,2004,269:303
    46. Thanon M, Nihot MT, Jansen M, et al.Mono-N-carboxymethyl chitosan(MCC),a polyampholytic chitosan derivative,enhances the intestinal absorption of low molecular weight heparin across intestinal epithelia in vitro and in vivo[J].J Pharm Sci,2001,90:38.
    47. Bernkop-Schnurch A,Brandt U-M,Clausen A.Synthesis and in vitro evaluation of chitosan-cysteine conjugates[J].Sci Pharm, 1999,67:197
    48. Davide G,Andreas BS.In vitro evaluation of polymeric excipients protecting calcitonin against degradation by intestinal serine proteases[J].Int J Pharm,2003, 252:187
    
    49. Takeuchi H,MatsuiY,YamamotoY.Mucoadhesive liposomes coated with chitosan or carbopol for oval administration of peptide drugs[J].Proc Int Symp Control Rel Bioact Mater, 1999,26:6372
    
    50. Ahn JS ,Choi HK,Chun MK, et al . Release of triamcinolone acefonide from mucoadhesive polymer composed of chitosan and poly (acrylic acid) in vitro [J]. Biomaterials ,2002 ,23 :1411
    51. Vander LI ,Verhoef JC ,Van Aelst AC , et al . Chitosan microparticles for oral vaccination : Preparation ,characterization and preliminary in vivo uptake studies in murine Peyer's patches[J]. Biomaterials ,2001 ,22 :687
    
    52. Peter GS ,Mitzi LM. Immune stimulating activity of two new chitosan containing adjuvant formulations [J] .Vaccine ,2001 ,19 :661
    
    53. Li F ,Liu WG,Yao KD. Preparation of oxidized glucose-cross-linked alkylated chitosan membrane and in vitro studies of pH-sensitive drug delivery behaviour [J] .Biomaterials ,2002 ,23 :343
    
    54. Ijeoma FU,Lubna S ,Mahmoud A ,et al. Quaternary ammonium palmitoyl glycol chitosan-a new polysoap for drug delivery[J]. Int J Pharm ,2001 ,224 :185
    55. Shi XY, Tan TW. Preparation of chitosan/ ethylcellulose complex microcapsule and its application in controlled release of vitamin D2 [J]. Biomaterials, 2002 ,23 :4469
    
    56. Paolo G,Clandia J , Elisabetta G, et al . Formulation and in vivo evaluation of chlorhexidine buccal tablet s prepared using drug - loaded chitosan microspheres [J] . Eur J Pharm Biopharm ,2002 ,53 :233
    57. Shu XZ ,Zhu KJ . Controlled drug release properties of ionically cross-linked
    chitosan beads :the influence of anion structure[J]. Int J Pharm ,2002 , 233 :217
    58. Vandenberg GW ,Drolet C , Scott SL , et al. Factors affecting protein release from alginate-chitosan coacernate microcapsules during production and gastric/ intestinal simulation[J]. J Control Release ,2001,77 :297
    59. Chen LY, Tian ZG, Du YM. Synthesis and pH sensitivity of carboxy methyl chitosan-based polyampholyte hydrogels for protein carrier matrices [J]. Biomaterials, 2004,25:3725
    60.杨季,毕茹,王征 肠溶包衣材料的发展及其应用[J].中国药学杂志,2006,12(41):885-889
    61. Sarah N, Mansoor A. Localized delivery of paclitaxel in solid fumors from biodegradable chitin microparticle formulations[J]. Biomaterials, 2002,23 : 2723
    62. Zhang H, Steven HN. In vitro degradation of chitosan by bacterial enzymes from ratcecal and colonic contents [J]. Biomaterials, 2002,23:2761
    63. Norihito S, Toshihito T ,Masumi U, et al. Chitosan dispersed system for colon-specific drug delivery [J]. Int J Pharm, 2002,245:45.
    64. Tanina B, Susmita M ,Ajay KS, et al. Preparation characterization and biodistribution of ultrafine chitosan nanoparticles[J ]. Int J Pharm ,2002,242 : 93
    65. Kevin AJ ,Marie PF ,Aria M, et al. Chitosan nanoparticles as delivery systems for doxorubicin [J]. J Control Release ,2001,73:255
    66. Mitra S ,Gaur U ,Ghosh PC ,et al. Tumour targeted delivery of encapsulated dextran-doxorubicin conjugate using chitosan nanoparticles as cartier [J]. J Control Release ,2001,74:317
    67. Futoshi S ,Hiroyuki T, Hideki I, et al. In vitro cellular accumulation of gadolinium incorporated into chitosan nanoparticles designed for neutron-capture therapy of cancer [J]. Eur J Pharm Biopharm, 2002,53:57
    68. Vila A ,Sanchez A, Tobio M ,et al. Design of biodegradable particles for protein delivery [J]. J Control Release ,2002,78:15
    69. Angela M ,Campos D ,Alejandro S, et al. Chitosan nanoparticles :a new vehicle for the improvement of the delivery of drugs to the ocular surface. Application to cyclosporin A[J]. Int J Pharm, 2001,224: 159
    70. http://info.pharmacy.hc360.com/2005/06/13105631245.shtml
    71.张巍.药用辅料羟丙甲纤维素(HPMC)的应用[J].中国药学杂志 2002,2(37):65-67
    72.张立超,胡晋红,连佳芳等.丙烯酸树脂在薄膜包衣中的应用[J].中国医院药学杂志,2001,21(5):301-302.
    73. Per Bo rgquist, Gunnar Zack risson, Bernt Nilsson, et al. Simulation and parametric study of a film-coated controlled-release pharmaceutical [J]. Journal of Controlled Release, 2002, 80: 229-245.
    74.张瑜 崔志敏等.磷酸川芎嗪丙烯酸树脂水分散体包衣小丸的体外释放研究[J].中国现代应用药学杂志,2003,20(1):28
    75.张瑜,刘秀霞 卡托普利控释微丸的研制[J].中国医院药学杂志,2003,23(4):211
    76.王志会,孙英华 对乙酰氨基酚缓释微丸的制备与体外释放度考察[J].中国药剂学杂志,2005,3(4):184
    77.佟杰,王东凯 罗红霉素包衣缓释微丸的体外释放研究[J].中国药剂学杂志 2005,3(1):1
    78. Srisagul Sungthongjeen, Ornlaksana Paeratakul,et al. Preparation and in vitro evaluation of a multiple-unit floating drug delivery system based on gas formation technique [J]. International Journal of Pharmaceutics x (2006)x-x(article in press)
    79.唐青华,劳三申,高明珠,等.金蟾定痛微粒丸工艺的研究[J].中成药,1997,19(3):325.
    80.刘善奎,钟延强,刘乃兵,等.盐酸尼卡地平缓释微丸的制备及其稳定性的研究[J].中国药学杂志,1999,4(11):749
    81.徐慧娟,蔡彩霞等 两种包衣方法制备萘普生肠溶微丸的比较研究[J].药学进展,2005,11(9):17
    82.张焱,陈庆华.红霉素肠溶微丸及其特性研究[J].中国医药工业杂志,1996,27(10):450
    83.刘海 红霉素肠溶微丸制备工艺[J].中国医药工业杂志,2003,34(2):84
    84.刘红 沈灵佳等 萘普生肠溶微丸的制备及其体外特性研究[J].中国医院药学杂志,2004,24(2):84
    85.侯惠民 药用辅料应用技术(第二版)[M]上海医药工业研究院药物制剂部:210
    86.曾环想,潘卫三,陈济民,等.吲哚美辛肠溶包衣微丸的制备及其释放度的研究[J].中国药学杂志,1997,32(7):415.
    87.宋洪涛,郭涛,张汝华等.麝香保心丸pH依赖型梯度释药微丸的体外释放度研究[J].中草药,2001,32(11):978-981
    88.郝钦,岗艳云,朱家壁.硝酸异山梨酯脉冲控释微丸的研制[J].中国医药工业杂 志,1999,30(3):109
    89.张莉,陈大为等,法莫替丁脉冲控释微丸胶囊的制备及其体外释放[J].药品评价,2004,5(1):352
    90. M. Zahirul I. Khan, Zeljko Prebeg , A pH-dependent colon targeted oral drug delivery system using methacrylic acid copolymers I. Manipulation of drug release using Eudragit L100-55 and Eudragit S100 combinations[J]. Journal of Controlled Release 58 (1999) 215-222
    91. M. Zahirul I. Khan, A pH-Dependent Colon-Targeted Oral Drug Delivery System Using Methacrylic Acid Copolymers. Ⅱ. Manipulation of Drug Release Using Eudragit L100 and Eudragit S 100 Combinations [J].Drug Development and Industrial Pharmacy, 26(5), 549-554 (2000)
    92. Vishal K. Gupta; Thomas E. Beckert. A novel pH- and time-based multi-unit potential colonic drug delivery system. Ⅰ. Development [J]. Int J Pharm, 213 (2001) 83-91
    93. Amighi K,Timmermans J ,Puigdevall J ,et al. Peroral sustained-release film-coated pellets as a means to overcome physicochemical and biological drug2related problems.Ⅰ In vitro development and evaluation[J]. Drug Dev Ind Pharm ,1998,24 (6):509
    94. Weijia Zheng, James W. McGinity Influence of Eudragit(?) NE 30 D Blended with Eudragit(?) L 30 D-55 on the Release of Phenylpropanolamine Hydrochloride from Coated Pellets[J]. Drug Dev Ind Pharm, 2003,29(3):357-366
    95.胡连栋,唐星等,离心造粒法制备盐酸二甲双胍缓释微丸[J].中国医药工业杂志,2005,36(9):541
    96.王文刚,崔光华等,双嘧达莫缓释微丸的研制及其体外释放特性[J].中国医院药学杂志,2002,22(9):528
    97. A. Akhgari, F. Sadeghi, H. Afrasiabi Garekani et al, Combination of time-dependent and pH-dependent polymethacrylates as a single coating formulation for colonic delivery of indomethacin pellets [J]. International Journal of Pharmaceutics 320 (2006) 137-142
    98. Vishal K. Gupta a,*, Manfred W. Assmus,et al, A novel pH- and time-based multi-unit potential colonic drug delivery system. Ⅱ. Optimization of multiple response variables [J]. International Journal of Pharmaceutics 213 (2001) 93-102
    99.黄合.羟丙基甲基纤维素的速溶方法[J].中国药学杂志,1995,5(30):314
    100.黄合.羟丙基甲基纤维素的速溶方法[J].中成药,1995,2(17):3-4
    101.沈慧凤.药用辅料——羟丙基甲基纤维素(HPMC)在药剂上的应用[J].纤维素醚工业.2003,11(4):7-10
    102 林东武.两种新辅料在片剂生产中的应用[J].现代应用药学杂志,1993,10(2):97-98
    103.肖秋生,蒋永培.羟丙甲基纤维素控释、缓释骨架片研究进展[J].西北药学杂志,2000,15(3):133
    104. VanL SC, Cheskin H. Prediction of drug release rate from hydroxypropyl methylcellulose matrixes. Dru Dev Ind Pharm, 1993,19(3): 1201
    105. Susana T, Pablo P, Paloma MT, et al . Chitosanpoly(acrylic) acid polyionic complex: in vivo study to demonstrate prolonged gastric retention [J]. Biomaterials, 2004,25:917
    106.门晓媛,王一飞 几种药剂辅料的应用进展[J].中国医药工业杂志,2004,35(12):764-767
    107.李华 透皮吸收制剂中辅料的应用进展[J].华西药学杂志,2005,20(1):085-087
    108.刘威,胡佳 高分子辅料在药学研究中的应用[J].辽宁中医学院学报,2005,7(2):125-126
    109.郑宇,涂家生,庞卉 药用粉末可压性研究概况[J].药学进展,2006,3(30):114-119

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700