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聚乙烯醇-果胶水凝胶薄膜用于控制恩诺沙星的释放。

Polyvinyl alcohol-pectin cryogel films for controlled release of enrofloxacin.

机构信息

Institute of Applied Biotechnology-CINDEFI, CONICET-CCT La Plata, School of Sciences, University of La Plata, 1900 Plata, Argentina.

出版信息

Appl Biochem Biotechnol. 2012 Jul;167(5):1421-9. doi: 10.1007/s12010-012-9554-6. Epub 2012 Jan 26.

Abstract

The release of enrofloxacin entrapped in polyvinyl alcohol (PVA) cryogel at pH 5.5 showed a first-order kinetic, releasing 69.7% of the antibiotic after 4.5 h at 37 °C. In order to slow down the fluoroquinolone release rate, high-methoxylated pectin was added into the cryogel (PVA-P). A film containing 1.0% (w/v) HM pectin and 5.0 μg/ml enrofloxacin released only 3.7% of the antibiotic after 4.5 h. Since the FTIR spectrum showed that most of the interactions between PVA-P matrix and enrofloxacin were due to polar groups (carboxylate and amine), a two-layer film system was designed to modulate the releasing rate of the drug. The top film equilibrated with 0.75 or 1.5 M NaCl release up to 41.9% and 89.0% of the enrofloxacin in 4 h, respectively. The release rate of enrofloxacin was found dependent on NaCl concentration in the upper gel layer. The two-layer cryogel system showed attractive features for transcutaneous antibiotic delivery.

摘要

在 pH 5.5 下,恩诺沙星被包埋在聚乙烯醇 (PVA) 水凝胶中的释放呈现一级动力学,在 37°C 下 4.5 小时后释放了 69.7%的抗生素。为了减缓氟喹诺酮类抗生素的释放速度,将高甲氧基果胶添加到水凝胶 (PVA-P) 中。含有 1.0%(w/v)HM 果胶和 5.0μg/ml 恩诺沙星的薄膜在 4.5 小时后仅释放了 3.7%的抗生素。由于傅里叶变换红外光谱(FTIR)显示 PVA-P 基质与恩诺沙星之间的大多数相互作用是由于极性基团(羧酸盐和胺),因此设计了双层膜系统来调节药物的释放速度。顶部薄膜与 0.75 或 1.5 M NaCl 平衡,在 4 小时内分别释放了 41.9%和 89.0%的恩诺沙星。恩诺沙星的释放速度取决于上层凝胶层中的 NaCl 浓度。这种双层水凝胶系统在经皮抗生素传递方面具有吸引力。

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