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用于漂浮脉冲给药的中空/多孔果胶酸钙珠的研制。

Development of hollow/porous calcium pectinate beads for floating-pulsatile drug delivery.

作者信息

Badve Shraddha S, Sher Praveen, Korde Aruna, Pawar Atmaram P

机构信息

Department of Pharmaceutics, Bharati Vidyapeeth Deemed University, Poona College of Pharmacy, Pune, India.

出版信息

Eur J Pharm Biopharm. 2007 Jan;65(1):85-93. doi: 10.1016/j.ejpb.2006.07.010. Epub 2006 Jul 21.

Abstract

The purpose of this work was to develop hollow calcium pectinate beads for floating-pulsatile release of diclofenac sodium intended for chronopharmacotherapy. Floating pulsatile concept was applied to increase the gastric residence of the dosage form having lag phase followed by a burst release. To overcome limitations of various approaches for imparting buoyancy, hollow/porous beads were prepared by simple process of acid-base reaction during ionotropic crosslinking. The floating beads obtained were porous (34% porosity), hollow with bulk density<1 and had Ft50% of 14-24 h. In vivo studies by gamma scintigraphy determined on rabbits showed gastroretention of beads up to 5 h. The floating beads provided expected two-phase release pattern with initial lag time during floating in acidic medium followed by rapid pulse release in phosphate buffer. This approach suggested the use of hollow calcium pectinate microparticles as promising floating-pulsatile drug delivery system for site- and time-specific release of drugs acting as per chronotherapy of diseases.

摘要

这项工作的目的是开发空心果胶酸钙珠,用于双氯芬酸钠的漂浮脉冲释放,以进行时辰治疗。应用漂浮脉冲概念来增加具有滞后相随后突发释放的剂型在胃中的滞留时间。为了克服赋予浮力的各种方法的局限性,通过离子交联过程中的简单酸碱反应制备了空心/多孔珠。所获得的漂浮珠是多孔的(孔隙率为34%),空心的,堆积密度<1,Ft50%为14-24小时。通过γ闪烁显像在兔子身上进行的体内研究表明,珠在胃中的滞留时间长达5小时。漂浮珠提供了预期的两相释放模式,即在酸性介质中漂浮时有初始滞后时间,随后在磷酸盐缓冲液中快速脉冲释放。这种方法表明,空心果胶酸钙微粒有望作为一种漂浮脉冲药物递送系统,用于根据疾病的时辰治疗进行药物的位点和时间特异性释放。

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