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结肠靶向给药系统研究进展 总被引:18,自引:1,他引:18
通过查阅国内外文献综述近年来国内外结肠靶向给药的研究动态,结肠靶向给药系统的几种类型:pH依赖型,时滞释药型和菌群触发型及其所使用的材料。介绍了结肠的特殊生理结构和功能,阐明药物在结肠的吸收和作用机理。 相似文献
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通过查阅献资料,综述了近几年来国内外口服结肠靶向药给系统的研究情况,介绍了口服结肠靶向给药的概念及其优点和结肠靶向给药系统的几种类型:pH依赖型,时滞释药型,菌群触发型及其使用的材料。 相似文献
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新型结肠靶向给药系统 总被引:1,自引:0,他引:1
结肠靶向给药系统已取得一定进展,主要包括:前体药物、pH依赖型、时滞型及菌群触发型等。恰当的结肠给药系统要求释药机制只与结肠的特定生理因素相关。随着研究深入,近年来研发出一些新的结肠给药系统,它们设计原理独特、靶向性强、适合于工业化生产。本文将在回顾以往给药系统的基础上,对这些新的给药系统的制备及其体内外评价进行详细描述。 相似文献
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结肠吸收及结肠靶向给药 总被引:4,自引:0,他引:4
目的:对目前结肠吸收及其靶向给药方面的研究进行综述。方法:讨论药物结肠吸收特点和结肠靶向给药方法。结果:结肠是多肽药物口服的最佳吸收部位和缓控释制度口服持续吸收的重要部位。结肠靶向制剂可用于结肠局部病患的治疗和多肽药物的口服给药。结论:结肠吸收及其靶向给药是有意义而又有许多有待研究的领域。 相似文献
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结肠靶向给药系统的研究 总被引:7,自引:1,他引:7
20年前 ,人们对用于溃疡性结肠炎的药物吡柳磺胺 (Sulf_asalazine)的作用方式已经有了充分的了解 ,并且发现口服轻泻剂只有到达大肠后才发挥作用。因此 ,人们对结肠靶向给药产生了兴趣 ,并且不断地开发各种结肠靶向给药系统[1]。升结肠和大部分横结肠只有口服途径能接触到 ,直肠给药很少能把药物运送到结肠 ,所以发展口服结肠靶向给药系统具有重要意义。口服结肠靶向给药系统中的药物在上消化道中不释放 ,只有当药物到达人体回盲部后 ,才能使给药系统把药物释放出来 ,并且在结肠部发挥局部或全身治疗作用。1结肠靶向给… 相似文献
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口服结肠靶向给药系统在药物转运和治疗结肠局部疾病方面具有重要作用。本文总结了口服结肠靶向给药系统近年来的研究概况,并对结肠靶向药物制剂的体内、外评价方法作一介绍。 相似文献
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口服结肠靶向给药系统(oral colon targetting drug deliv-ery system,OCTDDS))将治疗结肠疾病的药物靶向输送至结肠,不仅降低常规的口服或直肠给药的毒副作用,且能将药物输送至病灶处,减少给药剂量,提高患者的顺应性;还能提高多肽、蛋白等类药物口服给药的生物利用度。笔者将近年有关口服结肠给药系统的研究综述如下。1口服结肠释药系统的应用1.1时控给药根据时辰药理学原理,应用药剂手段使药物在一定的时滞后释放,使之与人的生理周期相匹配,可用于治疗哮喘、高血压、心绞痛、消化道溃疡及风湿性关节炎等具有节律性的疾病。结肠靶向给药… 相似文献
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《Drug delivery》2013,20(3):258-265
AbstractTargeting drug system (TDS) or targeted drug delivery system (TDDS) is a new kind of drug delivery system which could make drug to be directly concentrated on the target site with high curative effects and low side-effects. As the quintessence of Chinese culture, traditional Chinese medicine (TCM) has a large advantage in many disease clinical treatments, especially in cancer, hypertension and many other intractable diseases owing to their low toxicity and side-effects relative to western medicine. This article reviews literatures on development of TCM-targeted preparations which were published in the past 10 years. TDS including active-targeting, passive-targeting and physical-chemical-targeting preparations were introduced through domestic and overseas literatures to reveal the unique advantages of TCM-targeting preparations in drug delivery system. In this article, we have reviewed some kinds of TCM-targeting preparations and indicated that great attention should be paid to the research on the TCM-targeting preparations. 相似文献
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Rajpurohit H Sharma P Sharma S Bhandari A 《Indian journal of pharmaceutical sciences》2010,72(6):689-696
The colon targeted drug delivery has a number of important implications in the field of pharmacotherapy. Oral colon targeted drug delivery systems have recently gained importance for delivering a variety of therapeutic agents for both local and systemic administration. Targeting of drugs to the colon via oral administration protect the drug from degradation or release in the stomach and small intestine. It also ensures abrupt or controlled release of the drug in the proximal colon. Various drug delivery systems have been designed that deliver the drug quantitatively to the colon and then trigger the release of drug. This review will cover different types of polymers which can be used in formulation of colon targeted drug delivery systems. 相似文献
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The bioactive alkaloids (e.g. vincristine, hydroxycamptothecin, ligustrazine, and so on) from traditional Chinese medicine (TCM) have exerted potent efficacies (e.g. anti-tumor, anti-inflammation, immunosuppression, etc.). However, a series of undesirable physicochemical properties (like low solubility and weak stability) and baneful pharmacokinetic (PK) profiles (e.g. low bioavailability, short half time, rapid clearance, etc.) have severely restricted their applications in clinic. In addition, some side effects (like cumulative toxicities caused by high-frequency administration and their own toxicities) have recently been reported and also confined their clinical uses. Therefore, developments in drug delivery of such alkaloids are of significance in improving their drug-like properties and, thus, treatment efficiencies in clinic. Strategies, including (i) specific delivery via liposomes; (ii) sustained delivery via nanoparticles, gels, and emulsions; and (iii) transdermal delivery via ethosomes, solid lipid nanoparticles, and penetrating enhancers, have been reported to improve the pharmacokinetic and physicochemical characters of problematic TCM alkaloids, decline their adverse effects, and thus, boost their curative efficacies. In this review, the recent reports in this field were comprehensively summarized with the aim of providing an informative reference for relevant readers. 相似文献
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