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Enhanced absorption of new oral cyclosporin microemulsion formulation, Neoral, in liver transplant recipients with external biliary diversion.

作者信息

Trull A K, Tan K K, Tan L, Alexander G J, Jamieson N V

机构信息

Department of Clinical Biochemistry, Addenbrooke's Hospital, Cambridge, United Kingdom.

出版信息

Transplant Proc. 1994 Oct;26(5):2977-8.

PMID:7940939
Abstract
摘要

相似文献

1
Enhanced absorption of new oral cyclosporin microemulsion formulation, Neoral, in liver transplant recipients with external biliary diversion.
Transplant Proc. 1994 Oct;26(5):2977-8.
2
Pharmacokinetics of a microemulsion formulation of cyclosporine in pediatric liver transplant recipients.
Transplant Proc. 1996 Aug;28(4):2270-2.
3
Microemulsion technology in the reformulation of cyclosporine: the reason behind the pharmacokinetic properties of Neoral.环孢素重新配方中的微乳剂技术:新山地明药代动力学特性背后的原因。
Clin Transplant. 1996 Aug;10(4):364-73.
4
Cyclosporine neoral in liver transplant recipients.肝移植受者中的新山地明(环孢素软胶囊)
Transplant Proc. 1994 Dec;26(6):3184-7.
5
Conversion from cyclosporine Sandimmun to cyclosporine neoral in liver transplant patients with cholestasis or external biliary drainage.肝移植伴胆汁淤积或外部胆管引流患者从环孢素(山地明)转换为环孢素(新山地明)的情况。
Transplant Proc. 1995 Aug;27(4):2506-7.
6
Change of conventional cyclosporine to neoral cyclosporine formulation in long-term liver transplant recipients.长期肝移植受者中传统环孢素转换为新山地明(Neoral)环孢素制剂的情况。
Transplant Proc. 1996 Dec;28(6):3348-50.
7
Absorption of cyclosporin from conventional and new microemulsion oral formulations in liver transplant recipients with external biliary diversion.肝移植受者行外胆道分流术后常规和新型微乳剂口服制剂中环孢素的吸收情况
Br J Clin Pharmacol. 1995 Jun;39(6):627-31. doi: 10.1111/j.1365-2125.1995.tb05722.x.
8
Cyclosporine Neoral in liver transplant recipients.肝移植受者使用新山地明(环孢素软胶囊)。
Transplant Proc. 1994 Oct;26(5):2949-52.
9
Absorption of cyclosporine Neoral early after liver transplantation: is it possible to abandon intravenous cyclosporine A application?
Transplant Proc. 1996 Aug;28(4):2239-40.
10
Oral cyclosporine pharmacokinetics in pediatric renal and liver transplant recipients.
Transplant Proc. 1994 Oct;26(5):2779-80.

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1
Inclusion of Digestible Surfactants in Solid SMEDDS Formulation Removes Lag Time and Influences the Formation of Structured Particles During Digestion.在固体自微乳化药物传递系统(SMEDDS)制剂中加入可消化表面活性剂可消除滞后时间,并影响消化过程中结构化颗粒的形成。
AAPS J. 2017 May;19(3):754-764. doi: 10.1208/s12248-016-0036-6. Epub 2017 Jan 23.
2
Transforming lipid-based oral drug delivery systems into solid dosage forms: an overview of solid carriers, physicochemical properties, and biopharmaceutical performance.将基于脂质的口服药物传递系统转化为固体剂型:固体载体、理化性质和生物药剂学性能概述。
Pharm Res. 2013 Dec;30(12):2993-3017. doi: 10.1007/s11095-013-1107-3. Epub 2013 Jun 18.
3
Low dose lipid formulations: effects on gastric emptying and biliary secretion.
低剂量脂质制剂:对胃排空和胆汁分泌的影响。
Pharm Res. 2007 Nov;24(11):2084-96. doi: 10.1007/s11095-007-9363-8. Epub 2007 Jul 27.
4
Relative bioavailability of cyclosporin from conventional and microemulsion formulations in heart-lung transplant candidates with cystic fibrosis.囊性纤维化心肺移植候选者中常规制剂和微乳剂制剂中环孢素的相对生物利用度。
Eur J Clin Pharmacol. 1995;48(3-4):285-9. doi: 10.1007/BF00198313.