期刊文献+

生物材料作为口服胰岛素载体的稳定性及缓释作用

Stability and sustained release of biomaterials as oral insulin vector
下载PDF
导出
摘要 目的:探讨生物材料作为载体,在保持口服胰岛素制备与消化过程中的生物活性及建立满足人体生理需求的胰岛素的释放速率的模式中的应用。方法:用计算机检索中国期刊全文数据库(CNKI:1989/2009)和Medline database(1989/2009),按纳入和排除标准,对文献进行筛选,资料收集和质量评价,共纳入31篇文章。从常用口服胰岛素载体生物材料、保持口服胰岛素在制备与消化过程中的生物活性及建立满足人体生理需求的胰岛素的释放速率模式3方面进行总结。结果:以生物材料作为载体包埋胰岛素,可避免胰岛素被胃肠蛋白酶降解,提高其在胃肠道内的稳定性,并有利于肠道黏膜对胰岛素的摄取和转运,在人体内递药过程中又能实现靶向控制药物释放,提高药物的生物利用度,满足人体生理需求的胰岛素的释放速率模式,实现了胰岛素的持续释放。结论:在胰岛素载体材料的研究过程中,生物材料以其优势发展迅速。随着研究的进一步深入,作为口服胰岛素载体的生物材料将向临床实际应用方向发展。 OBJECTIVE: To investigate the bioactivity of biomaterials during oral insulin preparation and digestion, and to study the application of biomaterial to establish release velocity style that was satisfactory for human physiological drive. METHODS: Based on inclusion and exclusion criteria, articles were retrieved from CNKI and Medline database from 1989 to 2009, and a total of 31 articles were included in the final analysis. This study was summarized according to three fields: common biomaterials for oral insulin vector, bioactivity of oral insulin during preparation and digestion, and insulin release velocity style that was satisfactory for human physiological drive. RESULTS: Biomaterial vector which were used to coated insulin could prevent insulin degradation by erepsin and enhance insulin stability. In addition, biomaterial vector benefited for uptake and transport of intestinal tract mucosa to insulin, target-control of drug release, enhancement of drug bioavailability, and establishment of insulin release velocity style for human physiological drive so as to realize sustained release of insulin. CONCLUSION: Performance of biomaterials has been developed rapidly. With the further study, biomaterials as oral insulin vector will develop for clinical application.
出处 《中国组织工程研究与临床康复》 CAS CSCD 北大核心 2009年第42期8357-8360,共4页 Journal of Clinical Rehabilitative Tissue Engineering Research
  • 相关文献

参考文献31

  • 1Prego C,Garcia M,Torres D,et al.Transmucosal macromolecular drug delivery.J Control Release.2005;101 (1-3):151-162.
  • 2Simon M,Wittmar M,Bakowsky U,et al.Self-assembling nanocomplexes from insulin and water-soluble branched polyesters,poly[(vinyl-3-(diethylamino)-propylcarbamate-co(vinyl acetate)-co-(vinyl alcohol)]-graft-poly(L-lactic acid):a novel carrier for transmucosal delivery of peptides.Bioconjug Chem.2004; 15(4):841-849.
  • 3Simon M,Wittmar M,Kissel T,et al.lnsulin containing nanocomplexes formed by self-assembly from biodegradable amine-modified poly(vinyl alcohol)-graft-poly(L-lactide):bioavailability and nasal tolerability in rats.Pharm Res.2005; 22(11):1879-1886.
  • 4Mastrandrea LD,Quattrin T.Clinical evaluation of inhaled insulin.Adv Drug Deliv Rev.2006;58(9-10):1061-1075.
  • 5查刘生,高海峰,杨武利,蒋新国,府寿宽.聚合物纳米粒子用于给药载体[J].高分子通报,2002(3):24-32. 被引量:23
  • 6des Rieux A,Fievez V,Garinot M,et al.Nanoparticles as potential oral delivery systems of proteins and vaccines:a mechanistic approach.J Control Release.2006; 116(1):1-27.
  • 7Takeuchi H,Yamamoto H,Kawashima Y.Mucoadhesive nanoparticulate systems for peptide drug delivery.Adv Drug Deliv Rev.2001 ;47(1):39-54.
  • 8Kato Y,Onishi H,Machida Y.Application of chitin and chitosan derivatives in the pharmaceutical field.Curr Pharm Biotechnol.2003;4(5):303-309.
  • 9Aksungur P,Sungur A,Unal S,et al.Chitosan delivery systems for the treatment of oral mucositis:in vitro and in vivo studies.J Control Release.2004;98(2):269-279.
  • 10Sugamori T,Iwase H,Maeda M,et al.Local hemostatic effects of microcrystalline partially deacetylated chitin hydrochloride.J Biomed Mater Res.2000;49(2):225-232.

二级参考文献74

  • 1王剑红,陆彬,胥佩菱,包定元,张自然.肺靶向米托蒽醌明胶微球的研究[J].药学学报,1995,30(7):549-555. 被引量:25
  • 2陆彬.药物新剂型和新技术[M].北京:人民卫生出版社,1998.521.
  • 3NewRRC KirbyCJ.包含中链单酸甘油酯的疏水性制剂[P].中华人民共和国国家知识产权局发明专利公开说明书,公开号:CN 1224360A.1999-7-28.
  • 4[1]Henriksen I,Vagen SR,Sande SA,et al.Interaction between liposomes and chitosan Ⅱ:effect of selected parameters on aggregation and leakage[J].Int J Pharm,1997,146(2):193-203.
  • 5[2]Kas HS.Chitosan:properties,preparations and application to microparticulate systems[J].J Microencapsulation,1997,14(6):689-711.
  • 6[3]Henriksen I,Smistad G,Karlsen J.Interaction between liposomes and chitosan[J].Int J Pharm,1994,101(3):227-236.
  • 7[4]Aspeden TJ,Mason JDT,Jones NS,et al.Chitosan as a nasal delivery system:the effect of chitosan solutions on in vitro and in vivo mucociliary transport rates in human turbinates and volunteers[J].J Pharm Sci,1997,86(4):509-513.
  • 8[5]Kotze AF,Lueben HL,Leeuw BJ,et al.Comparison of the effect of different chitosan salts and N-trimethyl chitosan chloride on the permeability of intestinal epithelial cells (Caco-2)[J].J Controlled Release,1998,51(1):35-46.
  • 9[6]Lehr C,Bouwstra JA,Schacht EA,et al.In vitro evaluation of mucoadhesive properties of chitosan and some other natural polymers[J].Int J Pharm,1992,78(1):43-48.
  • 10[7]He P,Davis SS,Illum L.In vitro evaluation of mucoadhesive properties of chitosan microspheres[J].Int J Pharm,1998,166(1):75-88.

共引文献58

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部