• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

The effect of different concentrations of mannitol in solution on small intestinal transit: implications for drug absorption.

作者信息

Adkin D A, Davis S S, Sparrow R A, Huckle P D, Phillips A J, Wilding I R

机构信息

Department of Pharmaceutical Sciences, University of Nottingham, University Park, United Kingdom.

出版信息

Pharm Res. 1995 Mar;12(3):393-6. doi: 10.1023/a:1016256619309.

DOI:10.1023/a:1016256619309
PMID:7617527
Abstract

The aim of the present study was to investigate the effect that different concentrations of mannitol have on small intestinal transit, and whether any observed effect was concentration dependent. Eight, healthy male subjects each received 200ml of radiolabelled purified water, or a 200ml solution of mannitol at three different concentrations; 0.755g/200ml, 1.509g/200ml and 2.264g/200ml, in a randomised, four way cross-over study. Transit of the radiolabelled solutions was followed by gamma scintigraphy. The study demonstrated no significant differences between the gastric emptying times of the four solutions. Rapid gastric emptying was observed in most cases. The mean small intestinal transit times for the 0.755g/200ml, 1.509g/200ml and 2.264g/200ml mannitol solutions was reduced by 11%, 23% and 34% respectively, when compared to the control solution. The intestinal transit data of the four solutions demonstrate that mannitol has a concentration dependent effect on small intestinal transit. Small concentrations of mannitol included in a pharmaceutical formulation could therefore lead to reduced uptake with any drug exclusively absorbed from the small intestine.

摘要

相似文献

1
The effect of different concentrations of mannitol in solution on small intestinal transit: implications for drug absorption.
Pharm Res. 1995 Mar;12(3):393-6. doi: 10.1023/a:1016256619309.
2
The effects of pharmaceutical excipients on small intestinal transit.药用辅料对小肠转运的影响。
Br J Clin Pharmacol. 1995 Apr;39(4):381-7. doi: 10.1111/j.1365-2125.1995.tb04466.x.
3
Assessment of the Effect of Intestinal Permeability Probes (Lactulose And Mannitol) and Other Liquids on Digesta Residence Times in Various Segments of the Gut Determined by Wireless Motility Capsule: A Randomised Controlled Trial.通过无线动力胶囊测定肠道通透性探针(乳果糖和甘露醇)及其他液体对肠道各段食糜停留时间的影响:一项随机对照试验
PLoS One. 2015 Dec 2;10(12):e0143690. doi: 10.1371/journal.pone.0143690. eCollection 2015.
4
Relationship between small-intestinal transit rate and intestinal absorption of (14)C-labelled mannitol and (51)Cr-labelled ethylenediaminetetraacetic acid in healthy subjects.健康受试者小肠转运速率与(14)C标记甘露醇及(51)Cr标记乙二胺四乙酸肠道吸收之间的关系
Scand J Gastroenterol. 1996 Mar;31(3):254-9. doi: 10.3109/00365529609004875.
5
The effect of polyethylene glycol 400 on gastrointestinal transit: implications for the formulation of poorly-water soluble drugs.聚乙二醇400对胃肠道转运的影响:对难溶性药物制剂的启示。
Pharm Res. 2001 Aug;18(8):1146-50. doi: 10.1023/a:1010927026837.
6
The effect of mannitol on the oral bioavailability of cimetidine.甘露醇对西咪替丁口服生物利用度的影响。
J Pharm Sci. 1995 Dec;84(12):1405-9. doi: 10.1002/jps.2600841205.
7
Meal-induced acceleration of tablet transit through the human small intestine.进餐引起的片剂在人体小肠内转运加速。
Pharm Res. 2009 Feb;26(2):356-60. doi: 10.1007/s11095-008-9749-2. Epub 2008 Nov 4.
8
Concentration-dependent effects of polyethylene glycol 400 on gastrointestinal transit and drug absorption.聚乙二醇400对胃肠道转运和药物吸收的浓度依赖性效应。
Pharm Res. 2003 Dec;20(12):1984-8. doi: 10.1023/b:pham.0000008046.64409.bd.
9
Effects of erythromycin on gastric emptying, alcohol absorption and small intestinal transit in normal subjects.红霉素对正常受试者胃排空、酒精吸收及小肠转运的影响。
J Nucl Med. 1993 Apr;34(4):582-8.
10
Analysis of small intestinal transit and colon arrival times of non-disintegrating tablets administered in the fasted state.空腹状态下服用的不崩解片剂的小肠转运时间和结肠到达时间分析。
Eur J Pharm Sci. 2015 Jul 30;75:131-41. doi: 10.1016/j.ejps.2015.03.001. Epub 2015 Mar 11.

引用本文的文献

1
The Use of Physiologically Based Pharmacokinetic Analyses-in Biopharmaceutics Applications -Regulatory and Industry Perspectives.基于生理学的药代动力学分析在生物药剂学应用中的应用——监管和行业视角。
Pharm Res. 2022 Aug;39(8):1681-1700. doi: 10.1007/s11095-022-03280-4. Epub 2022 May 18.
2
Quantification of P-Glycoprotein in the Gastrointestinal Tract of Humans and Rodents: Methodology, Gut Region, Sex, and Species Matter.人及啮齿类动物胃肠道 P 糖蛋白的定量:方法学、肠道区域、性别和物种很重要。
Mol Pharm. 2021 May 3;18(5):1895-1904. doi: 10.1021/acs.molpharmaceut.0c00574. Epub 2021 Apr 22.
3
Tripling the Bioavailability of Rosuvastatin Calcium Through Development and Optimization of an In-Situ Forming Nanovesicular System.

本文引用的文献

1
The pattern of emptying of the human stomach.人类胃部的排空模式。
J Physiol. 1951 Apr;113(2-3):157-68. doi: 10.1113/jphysiol.1951.sp004562.
2
The kinetics of water absorption in the human intestine.人体肠道对水的吸收动力学
Trans Assoc Am Physicians. 1961;74:195-206.
3
Some properties of an alimentary osmoreceptor mechanism.一种消化性渗透感受器机制的某些特性。
通过开发和优化原位形成纳米囊泡系统使瑞舒伐他汀钙的生物利用度提高两倍。
Pharmaceutics. 2019 Jun 11;11(6):275. doi: 10.3390/pharmaceutics11060275.
4
Effects of Drugs and Excipients on Hydration Status.药物和辅料对水合状态的影响。
Nutrients. 2019 Mar 20;11(3):669. doi: 10.3390/nu11030669.
5
Impact of osmotically active excipients on bioavailability and bioequivalence of BCS class III drugs.渗透活性辅料对BCS III类药物生物利用度和生物等效性的影响。
AAPS J. 2013 Oct;15(4):1043-50. doi: 10.1208/s12248-013-9509-z. Epub 2013 Jul 19.
6
Impact of excipient interactions on drug bioavailability from solid dosage forms.辅料相互作用对固体剂型药物生物利用度的影响。
Pharm Res. 2012 Oct;29(10):2639-59. doi: 10.1007/s11095-012-0767-8. Epub 2012 May 19.
7
Multiple peaking phenomena in pharmacokinetic disposition.药代动力学处置中的多重峰现象。
Clin Pharmacokinet. 2010 Jun;49(6):351-77. doi: 10.2165/11319320-000000000-00000.
8
Meal-induced acceleration of tablet transit through the human small intestine.进餐引起的片剂在人体小肠内转运加速。
Pharm Res. 2009 Feb;26(2):356-60. doi: 10.1007/s11095-008-9749-2. Epub 2008 Nov 4.
9
The effect of polyethylene glycol 400 on gastrointestinal transit: implications for the formulation of poorly-water soluble drugs.聚乙二醇400对胃肠道转运的影响:对难溶性药物制剂的启示。
Pharm Res. 2001 Aug;18(8):1146-50. doi: 10.1023/a:1010927026837.
10
Nuclear medicine techniques in the evaluation of pharmaceutical formulations.核医学技术在药物制剂评估中的应用
Pharm World Sci. 1996 Jun;18(3):97-104. doi: 10.1007/BF00417757.
J Physiol. 1956 May 28;132(2):267-88. doi: 10.1113/jphysiol.1956.sp005524.
4
Effect of sodium acid pyrophosphate on ranitidine bioavailability and gastrointestinal transit time.酸性焦磷酸钠对雷尼替丁生物利用度及胃肠转运时间的影响。
Pharm Res. 1993 Jul;10(7):1027-30. doi: 10.1023/a:1018918907670.
5
Relationship of motility to flow of contents in the human small intestine.人体小肠中蠕动与内容物流动的关系。
Gastroenterology. 1982 Apr;82(4):701-6.
6
Evaluation of mannitol for use as a probe marker of gastrointestinal permeability in man.甘露醇用作人体胃肠道通透性探针标志物的评估。
Eur J Clin Invest. 1982 Dec;12(6):485-91. doi: 10.1111/j.1365-2362.1982.tb02230.x.
7
Conservation of mannitol, lactulose, and raffinose by the human colon.人结肠对甘露醇、乳果糖和棉子糖的保留作用。
Am J Physiol. 1981 Nov;241(5):G397-402. doi: 10.1152/ajpgi.1981.241.5.G397.
8
The effect of unabsorbed sucrose and mannitol on the small intestinal flow rate and mean transit time.未吸收的蔗糖和甘露醇对小肠流速及平均转运时间的影响。
Scand J Gastroenterol. 1968;3(6):665-71.
9
The effect of unabsorbed sucrose- or mannitol-induced accelerated transit on absorption in the human small intestine.未吸收的蔗糖或甘露醇诱导的加速转运对人小肠吸收的影响。
Scand J Gastroenterol. 1969;4(1):25-32. doi: 10.3109/00365526909180147.
10
The mechanism of diarrhoea in congenital disaccharide malabsorption.
Acta Paediatr Scand. 1968 Sep;57(5):425-32. doi: 10.1111/j.1651-2227.1968.tb07315.x.