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用于吉西他滨膀胱内给药的微乳剂。

Microemulsions for intravesical delivery of gemcitabine.

作者信息

Tsai Yi-Hung, Hsieh Yi-Hang, Huang Yaw-Bin, Chang Jui-Sheng, Huang Chi-Te, Wu Pao-Chu

机构信息

Graduate Institute of Clinical Pharmacy, Kaohsiung Medical University, Taiwan.

出版信息

Chem Pharm Bull (Tokyo). 2010 Nov;58(11):1461-5. doi: 10.1248/cpb.58.1461.

Abstract

The objective of this work was to develop a safe and effective delivery vehicle for topical treatment of gemcitabine. The physicochemical properties, drug release rate, drug level in plasma and bladder, and histological changes of tissue after drug administration were investigated. The electrical conductivity, mean size, and viscosity of drug-loaded microemulsions were 0.8-102.0 µS/cm, 116.8-322.5 nm, and 42.9-105.0 cps×10³, respectively. Gemcitabine loaded microemulsions showed a slower and sustained release. After intravesical administration of aqueous control and microemulsions treated, the drug concentrations in plasma were 15.11 µg/ml and 2.81-12.82 µg/ml, respectively, and the accumulation in bladder were 18.27 µg and 9.12-64.16 µg, respectively. Microemulsions slightly decreased the systemic absorption and significantly enhanced the accumulation in bladder tissue. Moreover, the preliminary toxicity studies revealed no overt adverse histological changes or tissue irritation by the microemulsion application. Therefore, the microemulsions were suggested to be a promising drug carrier for intravesical chemotherapy.

摘要

这项工作的目的是开发一种用于吉西他滨局部治疗的安全有效的给药载体。研究了给药后载药微乳的物理化学性质、药物释放速率、血浆和膀胱中的药物水平以及组织的组织学变化。载药微乳的电导率、平均粒径和粘度分别为0.8 - 102.0 μS/cm、116.8 - 322.5 nm和42.9 - 105.0 cps×10³。载吉西他滨微乳显示出较慢且持续的释放。膀胱内给予水性对照和微乳处理后,血浆中的药物浓度分别为15.11 μg/ml和2.81 - 12.82 μg/ml,膀胱中的蓄积量分别为18.27 μg和9.12 - 64.16 μg。微乳略微降低了全身吸收,并显著增强了在膀胱组织中的蓄积。此外,初步毒性研究表明,应用微乳未观察到明显的不良组织学变化或组织刺激。因此,微乳被认为是膀胱内化疗有前景的药物载体。

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