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一种温敏型自修复脂质体水凝胶系统作为抗结核药物载体用于局部骨结核治疗。

A thermo-responsive and self-healing liposome-in-hydrogel system as an antitubercular drug carrier for localized bone tuberculosis therapy.

机构信息

Xiangya School of Pharmaceutical Sciences, Central South University, Changsha, Hunan 410013, China.

Xiangya School of Pharmaceutical Sciences, Central South University, Changsha, Hunan 410013, China; Department of Pharmacy, The Third Xiangya Hospital of Central South University, Changsha, Hunan 410013, China.

出版信息

Int J Pharm. 2019 Mar 10;558:101-109. doi: 10.1016/j.ijpharm.2018.12.083. Epub 2019 Jan 8.

Abstract

Isoniazid (INH) is a first-line therapy for bone tuberculosis (TB), but its clinic benefits are limited by severe side-effects after long-time administration. While nano-drug delivery systems present as promising strategies for INH delivery, the therapeutic efficacies are usually suboptimal due to ineffective drug accumulation at diseased sites. Local delivery system can achieve high drug concentration at focus sites with minimal systemic exposure, and herein we aimed to employ this strategy to develop a novel liposome-in-hydrogel system for localized treatment of bone TB. To achieve sustainable drug release, a derivative of INH called DINH was loaded because of its hydrophobicity, as well as its better activity and higher biosafety than INH. The hybrid system was demonstrated for thermo-responsive and self-healing properties via phase transition test and rheological studies, which were particularly useful for intra-articular administration. In vivo microdialysis studies revealed that the system can rapidly release drug into synovial fluid to reach effective inhibitory concentrations after localized injection, followed by a steady-state drug release. The optical image studies were performed to study its long-term behavior in vivo, which suggested a sustained drug release profile for several days. This work provides a promising drug delivery system for bone TB therapy.

摘要

异烟肼(INH)是治疗骨结核(TB)的一线药物,但由于长期使用会产生严重的副作用,其临床疗效受到限制。虽然纳米药物递送系统是 INH 递送的有前途的策略,但由于在病变部位药物积累效果不佳,治疗效果通常并不理想。局部给药系统可以在最小的全身暴露下在病灶部位实现高药物浓度,我们旨在利用这一策略开发一种新型脂质体-水凝胶系统,用于局部治疗骨结核。为了实现可持续的药物释放,我们加载了 INH 的一种衍生物 DINH,因为它具有疏水性,以及比 INH 更好的活性和更高的生物安全性。通过相变试验和流变学研究,该混合系统表现出热响应和自修复特性,这对关节内给药特别有用。体内微透析研究表明,该系统可以在局部注射后迅速将药物释放到滑液中,达到有效的抑制浓度,然后是稳定的药物释放。我们进行了光学图像研究来研究其在体内的长期行为,结果表明该系统可以持续数天释放药物。这项工作为骨结核治疗提供了一种有前途的药物递送系统。

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