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载伊立替康的双响应性温敏凝胶,具有改善的抗肿瘤疗效,无初始突释效应和毒性,可用于肌肉内给药。

Irinotecan-loaded double-reversible thermogel with improved antitumor efficacy without initial burst effect and toxicity for intramuscular administration.

机构信息

College of Pharmacy & Institute of Pharmaceutical Science and Technology, Hanyang University, 55 Hanyangdaehak-ro, Sangnok-gu, Ansan 426-791, Republic of Korea; Department of Pharmacy, Quaid-I-Azam University, Islamabad 45320, Pakistan.

College of Pharmacy & Institute of Pharmaceutical Science and Technology, Hanyang University, 55 Hanyangdaehak-ro, Sangnok-gu, Ansan 426-791, Republic of Korea.

出版信息

Acta Biomater. 2017 May;54:239-248. doi: 10.1016/j.actbio.2017.03.007. Epub 2017 Mar 8.

Abstract

UNLABELLED

Intramuscularly administered, anti-tumour drugs induce severe side effects due to their direct contact with body tissues and initial burst effect. In this study, to solve this problem, a novel double-reversible thermogel system (DRTG) for the intramuscular administration of irinotecan was developed. This irinotecan-loaded DRTG was prepared by dispersing the irinotecan-loaded thermoreversible solid lipid nanoparticles (SLNs) in the thermoreversible hydrogel. In DRTG, the former was solid at 25°C but converted to liquid at 36.5°C; in contrast, the latter existed in a liquid form but transformed to gel state in the body. The DRTG was easily administered intramuscularly. Its particle size and drug content were not noticeably changeable, resulting that it was stable at 40°C for at least 6months. Compared to the irinotecan-loaded solution and conventional hydrogel, the DRTG significantly delayed drug release, leading to a reduced burst effect. Moreover, it showed decreased C and maintained the sustained plasma concentrations at a relatively low level for the long period of 60h in rats, resulting in ameliorated side effects of the anti-tumour drug. Furthermore, it gave significantly improved anti-tumour efficacy in tumour-bearing mice compared to the hydrogel but, unlike the conventional hydrogel, induced no body weight loss and local damage to the muscle. Thus, this DRTG with improved antitumor efficacy without initial burst effect and toxicity could provide a potential pharmaceutical system for the intramuscular administration of irinotecan.

STATEMENT OF SIGNIFICANCE

Intramuscularly administered, anti-tumour drugs induce severe side effects due to their direct contact with body tissues and initial burst effect. To solve this problem, we developed a novel double-reversible thermogel system (DRTG) for the intramuscular administration of irinotecan. Unlike the conventional hydrogel, the DRTG is a dispersion of the irinotecan-loaded thermoreversible solid lipid nanoparticles in the thermoreversible hydrogel. In DRTG, the former was solid at 25°C but converted to liquid at 36.5°C; in contrast, the latter existed in a liquid form but transformed to gel state in the body. This DRTG gave significantly improved anti-tumour efficacy in tumour-bearing mice compared to the hydrogel but, unlike the conventional hydrogel, induced no body weight loss and local damage to the muscle.

摘要

目的

肌内注射的抗肿瘤药物由于直接与身体组织接触和初始突释效应而引起严重的副作用。

方法

为了解决这个问题,我们开发了一种新型的伊立替康肌内给药双重可逆热凝胶系统(DRTG)。与传统水凝胶不同,DRTG 是伊立替康载热可逆固体脂质纳米粒在热可逆水凝胶中的分散体。在 DRTG 中,前者在 25°C 时为固态,但在 36.5°C 时转变为液态;而后者则以液态形式存在,但在体内转变为凝胶状态。

结果

与水凝胶相比,DRTG 显著提高了荷瘤小鼠的抗肿瘤疗效,但与传统水凝胶不同,DRTG 不会导致体重减轻和肌肉局部损伤。

结论

这种具有改善的抗肿瘤疗效、无初始突释效应和毒性的 DRTG 可为伊立替康的肌内给药提供一种有潜力的药物传递系统。

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